PMID-sentid	Pub_year	Sent_text	compound_name	comp_offset	prot_official_name	organism	prot_offset
26905725-3	2016	Arabidopsis spermine (Spm) synthase (SPMS) gene-deficient mutant was previously shown to be rather resistant to the diamine cadaverine (Cad).	Cadaverine	124-134	spermidine synthase 3	Arabidopsis thaliana	37-41
26905725-3	2016	Arabidopsis spermine (Spm) synthase (SPMS) gene-deficient mutant was previously shown to be rather resistant to the diamine cadaverine (Cad).	Cadaverine	136-139	spermidine synthase 3	Arabidopsis thaliana	37-41
23811823-7	2013	The accumulation of 2-piperidone in the Cyp2e1-null mice was mainly caused by the changes in the biosynthesis and degradation of 2-piperidone because compared with the WT mice, the conversion of cadaverine to 2-piperidone was higher, whereas the metabolism of 2-piperidone to 6-hydroxy-2-piperidone was lower in the Cyp2e1-null mice.	Cadaverine	195-205	cytochrome P450, family 2, subfamily e, polypeptide 1	Mus musculus	40-46
24218586-7	2013	The large majority of neurons activated by low concentrations of cadaverine expresses a particular olfactory receptor, trace amine-associated receptor 13c (TAAR13c).	Cadaverine	65-75	trace amine associated receptor 13c	Danio rerio	119-154
24218586-7	2013	The large majority of neurons activated by low concentrations of cadaverine expresses a particular olfactory receptor, trace amine-associated receptor 13c (TAAR13c).	Cadaverine	65-75	trace amine associated receptor 13c	Danio rerio	156-163
25938752-3	2015	The vaginal DA (VADA) assay is based on the enzyme diamine oxidase which reacts with putrescine and cadaverine to produce H2O2 in a quantitative manner.	Cadaverine	100-110	amine oxidase copper containing 1	Homo sapiens	51-66
25403917-0	2015	Natural variation in the expression of ORGANIC CATION TRANSPORTER 1 affects root length responses to cadaverine in Arabidopsis.	Cadaverine	101-111	organic cation/carnitine transporter1	Arabidopsis thaliana	39-67
25403917-6	2015	OCT1 expression was higher in Cvi than in Ler, and oct1 mutants were more sensitive to cadaverine than wild-type plants.	Cadaverine	87-97	organic cation/carnitine transporter1	Arabidopsis thaliana	51-55
25403917-7	2015	In oct1 mutants transformed with an ectopic copy of OCT1 originating from either Cvi or Ler, the expression level of the transgene, not its accession, correlated with the cadaverine response.	Cadaverine	171-181	organic cation/carnitine transporter1	Arabidopsis thaliana	3-7
25403917-7	2015	In oct1 mutants transformed with an ectopic copy of OCT1 originating from either Cvi or Ler, the expression level of the transgene, not its accession, correlated with the cadaverine response.	Cadaverine	171-181	organic cation/carnitine transporter1	Arabidopsis thaliana	52-56
25403917-8	2015	These results suggest that decreased OCT1 expression confers cadaverine sensitivity in some accessions.	Cadaverine	61-71	organic cation/carnitine transporter1	Arabidopsis thaliana	37-41
23811823-7	2013	The accumulation of 2-piperidone in the Cyp2e1-null mice was mainly caused by the changes in the biosynthesis and degradation of 2-piperidone because compared with the WT mice, the conversion of cadaverine to 2-piperidone was higher, whereas the metabolism of 2-piperidone to 6-hydroxy-2-piperidone was lower in the Cyp2e1-null mice.	Cadaverine	195-205	cytochrome P450, family 2, subfamily e, polypeptide 1	Mus musculus	316-322
23327914-7	2012	RESULTS: (1) The serum contents of TNF-alpha, IL-1, and IL-6 were increased in NTH, putrescine, and cadaverine groups in different degrees at most post injection time points.	Cadaverine	100-110	tumor necrosis factor	Oryctolagus cuniculus	35-44
23327914-15	2012	The obvious correlation between cadaverine group and NTH group was only found in the contents of IL-1 and IL-6 (r(IL-1) = 0.913, P < 0.01; r(IL-6) = 0.883, P < 0.05).	Cadaverine	32-42	interleukin-6	Oryctolagus cuniculus	106-110
23327914-15	2012	The obvious correlation between cadaverine group and NTH group was only found in the contents of IL-1 and IL-6 (r(IL-1) = 0.913, P < 0.01; r(IL-6) = 0.883, P < 0.05).	Cadaverine	32-42	interleukin-6	Oryctolagus cuniculus	144-148
23539494-3	2013	In the presence of Brij 76 (1.5 %), Hg(2+) (7.5 muM), and cadaverine (10 muM) at pH 5.0, this SALDI-MS approach allowed the simultaneous detection of T15, T20, T33, and T40, with limits of detection at the femtomole-to-picomole level and sample-to-sample intensity variation <23 %.	Cadaverine	58-68	latexin	Homo sapiens	73-76
23539494-4	2013	In the presence of Ag(+) (1 muM) and cadaverine (10 muM) at pH 7.0, this technique allowed the detection of randomly sequenced ss- and ds-ODNs at concentrations down to the femtomole level.	Cadaverine	37-47	latexin	Homo sapiens	52-55
29403792-7	2013	The cadaverine, putrescine and 1, 3-diaminopropane levels were significantly higher in U14 model mice plasma than those in normal mice plasma, especially the putrescine and 1, 3-diaminopropane (P<0.01).	Cadaverine	4-14	small nucleolar RNA, C/D box 14C	Mus musculus	87-90
29403792-8	2013	The cadaverine, putrescine and 1, 3-diaminopropane levels were significantly higher in U14 mice model urine than those in normal mice urine, especially the cadaverine and 1, 3-diaminopropane (P<0.01).	Cadaverine	4-14	small nucleolar RNA, C/D box 14C	Mus musculus	87-90
29403792-8	2013	The cadaverine, putrescine and 1, 3-diaminopropane levels were significantly higher in U14 mice model urine than those in normal mice urine, especially the cadaverine and 1, 3-diaminopropane (P<0.01).	Cadaverine	156-166	small nucleolar RNA, C/D box 14C	Mus musculus	87-90
23327914-7	2012	RESULTS: (1) The serum contents of TNF-alpha, IL-1, and IL-6 were increased in NTH, putrescine, and cadaverine groups in different degrees at most post injection time points.	Cadaverine	100-110	interleukin-6	Oryctolagus cuniculus	56-60
18389226-0	2008	CE-LIF determination of salivary cadaverine and lysine concentration ratio as an indicator of lysine decarboxylase enzyme activity.	Cadaverine	33-43	LIF interleukin 6 family cytokine	Homo sapiens	3-6
22328822-7	2012	RESULTS: All of the haplotype variants of LOXL1 (141R-153G, 141R-153D, 141L-153G, and 141L-153D) showed beta-aminopropionitrile-inhibitable amine oxidase activity toward elastin, type I collagen, and cadaverine, indicating that each LOXL1 variant functions as an amine oxidase.	Cadaverine	200-210	lysyl oxidase like 1	Homo sapiens	42-47
20855735-8	2010	By measuring cadaverine production, we discovered that the PA4115 mutant had significantly reduced lysine decarboxylase activity.	Cadaverine	13-23	hypothetical protein	Pseudomonas aeruginosa PAO1	59-65
20855735-10	2010	Cadaverine increased the rate of killing and lysis of the PA4115 mutant in the presence of both antibiotics.	Cadaverine	0-10	hypothetical protein	Pseudomonas aeruginosa PAO1	58-64
20167857-4	2010	However, cadaverine, the most widely used substrate for TGase activity assay, is not isozyme specific.	Cadaverine	9-19	transglutaminase 1	Homo sapiens	56-61
19627092-3	2009	Two examples of enzymatic reactions were investigated: the hydrolysis of arginine to ornithine catalyzed by arginase and the oxidation of cadaverine to 5-aminopentanal by diamine oxidase, in which the substrates have a higher affinity to the macrocycle than the products ("substrate-selective assays").	Cadaverine	138-148	amine oxidase copper containing 1	Homo sapiens	171-186
19627092-9	2009	Through the sequential coupling of a "product-selective" with a "substrate-selective" assay it was furthermore possible to monitor a multistep biochemical pathway, namely the decarboxylation of lysine to cadaverine by lysine decarboxylase followed by the oxidation of cadaverine by diamine oxidase.	Cadaverine	204-214	amine oxidase copper containing 1	Homo sapiens	282-297
20439985-1	2010	In this report, we assessed the steady-state enzymatic activity of lysyl oxidase-like 2 (LOXL2) against the substrates 1,5-diaminopentane (DAP), spermine, and fibrillar type I collagen.	Cadaverine	119-137	lysyl oxidase like 2	Homo sapiens	67-87
20439985-1	2010	In this report, we assessed the steady-state enzymatic activity of lysyl oxidase-like 2 (LOXL2) against the substrates 1,5-diaminopentane (DAP), spermine, and fibrillar type I collagen.	Cadaverine	119-137	lysyl oxidase like 2	Homo sapiens	89-94
20439985-1	2010	In this report, we assessed the steady-state enzymatic activity of lysyl oxidase-like 2 (LOXL2) against the substrates 1,5-diaminopentane (DAP), spermine, and fibrillar type I collagen.	Cadaverine	139-142	lysyl oxidase like 2	Homo sapiens	67-87
20439985-1	2010	In this report, we assessed the steady-state enzymatic activity of lysyl oxidase-like 2 (LOXL2) against the substrates 1,5-diaminopentane (DAP), spermine, and fibrillar type I collagen.	Cadaverine	139-142	lysyl oxidase like 2	Homo sapiens	89-94
20439985-2	2010	We find that both DAP and spermine are capable of activating LOXL2 to the same extent and have similar Michaelis constants (K(m) approximately 1 mm) and catalytic rates (k(cat) approximately 0.02 s(-1)).	Cadaverine	18-21	lysyl oxidase like 2	Homo sapiens	61-66
20439985-5	2010	In addition, we identified an antibody inhibitor (AB0023) of LOXL2 enzymatic function and have found that the inhibition occurs in a non-competitive manner with respect to both spermine and DAP.	Cadaverine	190-193	lysyl oxidase like 2	Homo sapiens	61-66
19821519-7	2010	The porin inhibitor cadaverine was added to study the porin-mediated influx of toluene.	Cadaverine	20-30	porin	Pseudomonas putida	4-9
17826755-3	2007	DESIGN AND METHODS: DAO activity was measured by using cadaverine coupled to O-dianisidine oxidation in 50 healthy individuals.	Cadaverine	55-65	amine oxidase copper containing 1	Homo sapiens	20-23
11942921-5	2002	To relate the effects of polylysine on contractility in smooth muscle to physiologically relevant material, we investigated the ability of naturally occurring positively charged polyamines, histones, cadaverine, putrescine and spermidine to activate the Mg2+ ATPase activity of unphosphorylated smooth muscle myosin.	Cadaverine	200-210	mucin 7, secreted	Homo sapiens	254-257
16936095-8	2006	tTgase activity was assayed by incorporation of biotinylated cadaverine into fibronectin.	Cadaverine	61-71	transglutaminase 2	Homo sapiens	0-6
16936095-8	2006	tTgase activity was assayed by incorporation of biotinylated cadaverine into fibronectin.	Cadaverine	61-71	fibronectin 1	Homo sapiens	77-88
14570723-4	2003	The inhibitory capacity of the antibodies on tTG activity was checked by a fluorometric assay based on the incorporation of monodansyl cadaverine into casein and by tTG-catalysed cross linking of biotinylated cadaverine to gliadin.	Cadaverine	135-145	transglutaminase 2	Homo sapiens	45-48
18251895-8	2007	A biotin-labeled cadaverine incorporation assay showed that TGase activity occurred in S1 (containing soluble proteins), S2 (proteins released by both cell walls and membranes) and S3 (membrane intrinsic proteins) fractions.	Cadaverine	17-27	transglutaminase 1	Homo sapiens	60-65
15972954-6	2005	TSP-2-null mice had reduced tTG activity in skin, as measured by incorporation of fluorescein isothiocyanate-labeled cadaverine, and a threefold increase in acetic acid-extracted dermal collagen.	Cadaverine	117-127	tumor suppressor region 2	Mus musculus	0-5
15138821-7	2004	Both a colorimetric and a radiometric assay for TGase activity, the former carried out in the presence of biotinylated cadaverine and the latter in the presence of polyamines labelled with radioactive isotopes and resulting in the isolation of glutamyl-polyamines, further confirmed that the thylakoid enzyme is indeed a calcium-dependent transglutaminase (Thyl-TGase).	Cadaverine	119-129	transglutaminase15	Zea mays	48-53
15221502-12	2004	This function of diamine oxidase is to be considered as part of a general defence function, of which the prevention of histamine and cadaverine accumulation from the gastrointestinal tract is a well-known aspect.	Cadaverine	133-143	amine oxidase copper containing 1	Homo sapiens	17-32
18494907-9	2003	Labelled cadaverine as an exogenous substrate for transglutaminase (TGase) could be incorporated into CEs during maturation.	Cadaverine	9-19	transglutaminase 1	Homo sapiens	50-66
18494907-9	2003	Labelled cadaverine as an exogenous substrate for transglutaminase (TGase) could be incorporated into CEs during maturation.	Cadaverine	9-19	transglutaminase 1	Homo sapiens	68-73
14755941-1	2003	Our study showed that the administration in pre-treatment of some polyamines (especially spermine and spermidine and almost null agmatine, putrescine and cadaverine) reduced the contractile effects of angiotensin II (Ang II) in isolated rat aorta.	Cadaverine	154-164	angiotensinogen	Rattus norvegicus	201-215
14755941-1	2003	Our study showed that the administration in pre-treatment of some polyamines (especially spermine and spermidine and almost null agmatine, putrescine and cadaverine) reduced the contractile effects of angiotensin II (Ang II) in isolated rat aorta.	Cadaverine	154-164	angiotensinogen	Rattus norvegicus	217-223
11485548-5	2001	Founder lines with >1000-fold overexpression of ODC in the heart were established, resulting in a 50-fold overaccumulation of putrescine, 4-fold elevation in spermidine, a slight increase in spermine and accumulation of large amounts of cadaverine compared with littermate controls.	Cadaverine	240-250	ornithine decarboxylase, structural 1	Mus musculus	51-54
10379569-4	1999	DAO is the enzyme which catalyzes the oxidation of agmatine, cadaverine, and putrescine with the production of NH and H2O2.	Cadaverine	61-71	D-amino acid oxidase	Bos taurus	0-3
10892867-6	2000	External tTgase activity was measured by the ability to form polymerized fibronectin and the incorporation of biotinylated cadaverine into fibronectin.	Cadaverine	123-133	transglutaminase 2	Homo sapiens	9-15
10892867-11	2000	Incorporation of biotinylated cadaverine was markedly increased when HTM cells were treated with TGF-beta for 24 hours before seeding.	Cadaverine	30-40	transforming growth factor beta 1	Homo sapiens	97-105
11040105-3	2000	In ODC transgenic hearts, putrescine and cadaverine levels were highly elevated ( identical with 35-fold for putrescine), spermidine was increased 3.6-fold, but spermine was essentially unchanged.	Cadaverine	41-51	ornithine decarboxylase, structural 1	Mus musculus	3-6
7625228-2	1995	In the present study the activity of plasmatic histaminase was analysed, with histamine and with cadaverine as substrates, in a group of 23 schizophrenic patients and compared with that of healthy controls (n = 32).	Cadaverine	97-107	amine oxidase copper containing 1	Homo sapiens	47-58
9410884-7	1997	A novel assay was developed to measure externalised tTgase activity which is cell mediated, inhibited by preincubation of cells with anti-tTgase antibody and relies on the incorporation of biotinylated cadaverine into fibronectin.	Cadaverine	202-212	fibronectin 1	Homo sapiens	218-229
7625228-4	1995	On the other hand, when cadaverine was used as substrate plasma histaminase was significantly reduced in female schizophrenics but not in males.	Cadaverine	24-34	amine oxidase copper containing 1	Homo sapiens	64-75
7823945-4	1995	Exogeneous expression of c-myb in transfected cell lines abrogated erythroid differentiation induced by cadaverine or cytosine arabinoside as assessed by hemoglobin production.	Cadaverine	104-114	MYB proto-oncogene, transcription factor	Homo sapiens	25-30
8125959-9	1994	alpha-Difluoromethylornithine, a selective inhibitor of ornithine decarboxylase, inhibited both cadaverine and putrescine export.	Cadaverine	96-106	ornithine decarboxylase 1	Homo sapiens	56-79
8125959-11	1994	The cumulative data suggested that cadaverine formation may be caused by the action of intracellular ornithine decarboxylase upon lysine to produce cadaverine, which is then effluxed from the cell with a high degree of efficiency.	Cadaverine	35-45	ornithine decarboxylase 1	Homo sapiens	101-124
8125959-11	1994	The cumulative data suggested that cadaverine formation may be caused by the action of intracellular ornithine decarboxylase upon lysine to produce cadaverine, which is then effluxed from the cell with a high degree of efficiency.	Cadaverine	148-158	ornithine decarboxylase 1	Homo sapiens	101-124
1458548-3	1992	The observed partitioning ratios go through a minimum value with 1,5-diaminopentane, the best substrate of diamine oxidase of the compounds tested.	Cadaverine	65-83	amine oxidase copper containing 1	Homo sapiens	107-122
7517727-3	1994	With this method and diamine substrates cadaverine or putrescine, or polyamine substrates spermidine or spermine as substrates, DAOX was localized species-independently but substrate-dependently in the basolateral cytoplasm and/or plasma membrane of small intestinal enterocytes of rats, mice and gerbils.	Cadaverine	40-50	amine oxidase, copper containing 1	Rattus norvegicus	128-132
8366761-2	1993	ODC and polyamines (putrescine, spermidine, spermine, and cadaverine) have an essential role in cell proliferation.	Cadaverine	58-68	ornithine decarboxylase 1	Homo sapiens	0-3
1417947-1	1992	Three electrophilic homologous aminoalkylaziridine analogues of putrescine, cadaverine, and 1,3-diaminopropane were synthesized and found to represent a mechanistically distinct class of irreversible inhibitors of diamine oxidase.	Cadaverine	76-86	amine oxidase copper containing 1	Homo sapiens	214-229
1503383-4	1992	Previous radiometric methods for DAO used tritiated putrescine or cadaverine as substrate.	Cadaverine	66-76	amine oxidase copper containing 1	Homo sapiens	33-36
16668466-11	1991	The activity of diamine oxidase, the cadaverine degrading enzyme, started to increase at the third day and reached a maximum between the fourth and fifth day of germination.	Cadaverine	37-47	copper amino oxidase	Glycine max	16-31
1850732-5	1991	Evidence that N-(3-aminopropyl)cadaverine can also act as the amine substrate for deoxyhypusine synthase in intact cells was obtained by incubating putrescine- and spermidine-depleted Chinese hamster ovary cells with [3H]cadaverine.	Cadaverine	31-41	deoxyhypusine synthase	Cricetulus griseus	82-104
1799365-0	1991	Competition of homologous substrates, putrescine and cadaverine, in the reaction catalyzed by pea diamine oxidase.	Cadaverine	53-63	amine oxidase copper containing 1	Homo sapiens	98-113
1799365-1	1991	The determination of diamine oxidase activity with the ninhydrin reagent was used for monitoring of simultaneous oxidation of two homologous substrates, putrescine and cadaverine, which give different colour products (519 and 417 nm).	Cadaverine	168-178	amine oxidase copper containing 1	Homo sapiens	21-36
34331403-8	2021	This genera seems to affect the bile acid metabolism and cadaverine which may account for the improvement in insulin levels.	Cadaverine	57-67	insulin	Homo sapiens	109-116
34600890-6	2021	Docking and site-directed mutagenesis analyses show that both sTAAR365 and mTAAR9 recognize the two amino groups of cadaverine with the conserved Asp3.32 and Tyr6.51 residues.	Cadaverine	116-126	trace amine-associated receptor 9	Mus musculus	75-81
34474093-4	2021	The DAO-1 showed a broad substrate selectivity with tyramine, histamine, putrescine and cadaverine being the most favored substrates.	Cadaverine	88-98	amine oxidase copper containing 1	Homo sapiens	4-9
34560100-2	2021	The polyamines putrescine, agmatine and cadaverine, are produced by pyridoxal 5"-phosphate-dependent L-ornithine, L-arginine and L-lysine decarboxylases (ODC, ADC, LDC), respectively, from both the alanine racemase (AR) and aspartate aminotransferase (AAT) folds.	Cadaverine	40-50	ornithine decarboxylase 1	Homo sapiens	154-157
34250670-5	2021	Exogenous supply of biotin and a pathway intermediate downstream of BIO1, 7,8-diaminopelargonic acid, suppressed this cadaverine sensitivity phenotype.	Cadaverine	118-128	adenosylmethionine-8-amino-7-oxononanoate transaminase	Arabidopsis thaliana	68-72
34250670-6	2021	An in vitro enzyme assay showed cadaverine inhibits the BIO3-BIO1 activity.	Cadaverine	32-42	adenosylmethionine-8-amino-7-oxononanoate transaminase	Arabidopsis thaliana	61-65
34250670-7	2021	Furthermore, cadaverine-treated seedlings displayed reduced biotinylation of Biotin Carboxyl Carrier Protein 1 (BCCP1) of the Acetyl-CoA Carboxylase complex involved in de novo fatty acid biosynthesis, resulting in decreased accumulation of triacylglycerides.	Cadaverine	13-23	chloroplastic acetylcoenzyme A carboxylase 1	Arabidopsis thaliana	77-110
34250670-7	2021	Furthermore, cadaverine-treated seedlings displayed reduced biotinylation of Biotin Carboxyl Carrier Protein 1 (BCCP1) of the Acetyl-CoA Carboxylase complex involved in de novo fatty acid biosynthesis, resulting in decreased accumulation of triacylglycerides.	Cadaverine	13-23	chloroplastic acetylcoenzyme A carboxylase 1	Arabidopsis thaliana	112-117
2758638-1	1989	This simple, rapid liquid-chromatographic assay of urinary polyamines (putrescine, spermidine, spermine, and cadaverine) involves electrochemical detection with a post-column immobilized enzyme, polyamine oxidase (EC 1.4.3.6) from soybean seedlings.	Cadaverine	109-119	polyamine oxidase	Homo sapiens	195-212
35308356-11	2022	The purified Odc1 protein decarboxylated lysine into cadaverine, while the recombinant Odc2 protein preferentially produced putrescine from ornithine but also exhibited low lysine decarboxylating activity.	Cadaverine	53-63	ornithine decarboxylase 1	Homo sapiens	13-17
35177711-4	2022	Here, we used TAAR9 that recognizes important biogenic amines such as cadaverine, spermine, and spermidine as a model for entry tunnel study.	Cadaverine	70-80	trace amine-associated receptor 9	Mus musculus	14-19
35154043-6	2021	In sausages spontaneously fermented and inoculated with Salmonella spp., the presence of cadaverine and putrescine diminished by 62 and 78%, respectively, due to the addition of cava lees.	Cadaverine	89-99	carbonic anhydrase 5A	Homo sapiens	178-182
35154043-7	2021	The addition of cava lees phenolic extract also showed an anti-aminogenic effect (21% for cadaverine and 40% for putrescine), although in a lesser extent than cava lees.	Cadaverine	90-100	carbonic anhydrase 5A	Homo sapiens	16-20
35572636-6	2022	Results: Mice lacking CYP1A1 exhibited an altered gut microbiome, a reduced metabolic shift from lysine to cadaverine in the caecal contents and antimicrobial molecule production (Retnlb, Gbp7, and Gbp3), and they were protected against gut barrier disruption when subjected to MRSA challenge.	Cadaverine	107-117	cytochrome P450, family 1, subfamily a, polypeptide 1	Mus musculus	22-28
35572636-7	2022	These beneficial effects were validated in aryl hydrocarbon receptor (AHR) knockout (KO) mice by cohousing with CYP1A1 KO mice and abrogated after supplementation with cadaverine or Enterococcus faecalis, the primary microbiota genus for cadaverine synthesis.	Cadaverine	168-178	aryl-hydrocarbon receptor	Mus musculus	43-68
35572636-7	2022	These beneficial effects were validated in aryl hydrocarbon receptor (AHR) knockout (KO) mice by cohousing with CYP1A1 KO mice and abrogated after supplementation with cadaverine or Enterococcus faecalis, the primary microbiota genus for cadaverine synthesis.	Cadaverine	168-178	aryl-hydrocarbon receptor	Mus musculus	70-73
35572636-7	2022	These beneficial effects were validated in aryl hydrocarbon receptor (AHR) knockout (KO) mice by cohousing with CYP1A1 KO mice and abrogated after supplementation with cadaverine or Enterococcus faecalis, the primary microbiota genus for cadaverine synthesis.	Cadaverine	238-248	aryl-hydrocarbon receptor	Mus musculus	70-73
35572636-11	2022	Conclusion: This study revealed the unexpected function of host CYP1A1 in microbiota-mediated cadaverine metabolism, with crucial consequences for dysbacteriosis following MRSA-induced abdominal sepsis, indicating that inhibiting CYP1A1 or blocking cadaverine-histamine H4 receptor signaling could be a potential therapeutic target against abdominal sepsis.	Cadaverine	94-104	cytochrome P450 family 1 subfamily A member 1	Homo sapiens	64-70
35572636-11	2022	Conclusion: This study revealed the unexpected function of host CYP1A1 in microbiota-mediated cadaverine metabolism, with crucial consequences for dysbacteriosis following MRSA-induced abdominal sepsis, indicating that inhibiting CYP1A1 or blocking cadaverine-histamine H4 receptor signaling could be a potential therapeutic target against abdominal sepsis.	Cadaverine	94-104	cytochrome P450 family 1 subfamily A member 1	Homo sapiens	230-236
3366303-2	1988	Partially purified rat liver ornithine decarboxylase is inhibited by several diamines including putrescine, 1,3-diaminopropane, cadaverine and p-phenylenediamine.	Cadaverine	128-138	ornithine decarboxylase 1	Rattus norvegicus	29-52
3122732-0	1987	Cadaverine supplementation during a chronic exposure to difluoromethylornithine allows an overexpression, but prevents gene amplification, of ornithine decarboxylase in L1210 mouse leukaemia cells.	Cadaverine	0-10	ornithine decarboxylase, structural 1	Mus musculus	142-165
3122732-1	1987	We recently selected a variant mouse L1210 leukaemia-cell line overproducing ornithine decarboxylase (ODC) (EC 4.1.1.17) as a result of chronic exposure to 2-difluoromethylornithine (DFMO) in the presence of micromolar concentrations of cadaverine.	Cadaverine	237-247	ornithine decarboxylase, structural 1	Mus musculus	77-100
3122732-1	1987	We recently selected a variant mouse L1210 leukaemia-cell line overproducing ornithine decarboxylase (ODC) (EC 4.1.1.17) as a result of chronic exposure to 2-difluoromethylornithine (DFMO) in the presence of micromolar concentrations of cadaverine.	Cadaverine	237-247	ornithine decarboxylase, structural 1	Mus musculus	102-105
3122732-5	1987	Omission of cadaverine from the culture medium, but leaving 10 mM-DFMO, resulted in an about 10-fold ODC gene amplification within a few weeks.	Cadaverine	12-22	ornithine decarboxylase, structural 1	Mus musculus	101-104
6436440-1	1984	1-Piperideine, 5-aminopentanoic acid, and its lactam, 2-piperidone, were identified as metabolites of cadaverine in 10,000 g mouse liver supernatants to which diamine oxidase had been added.	Cadaverine	102-112	amine oxidase, copper-containing 1	Mus musculus	159-174
16665078-1	1986	Exposing etiolated pea seedlings to ethylene which inhibited the activity of arginine decarboxylase and S-adenosylmethionine decarboxylase caused an increase in the level of cadaverine.	Cadaverine	174-184	antizyme inhibitor 2	Homo sapiens	77-99
3987688-1	1985	The yeast Candida boidinii when grown on spermidine, diaminopropane, putrescine or cadaverine as sole nitrogen source contains an N-acetyltransferase capable of acetylating the primary amino groups of spermine, spermidine, acetylspermidines, acetylputrescine and alpha, omega-diaminoalkanes.	Cadaverine	83-93	acetyltransferase	Saccharomyces cerevisiae S288C	132-149
3106087-1	1987	When the cyanide complex of the copper protein, pig kidney diamine oxidase, is reduced anaerobically by cadaverine (1,5-diaminopentane), the broad, 480 nm, absorption band characteristic of the resting enzyme is bleached and a new absorption spectrum with features at 457, 429, 403 (shoulder), 360 (shoulder) and 332 nm appears.	Cadaverine	104-114	amine oxidase copper containing 1	Sus scrofa	59-74
3106087-1	1987	When the cyanide complex of the copper protein, pig kidney diamine oxidase, is reduced anaerobically by cadaverine (1,5-diaminopentane), the broad, 480 nm, absorption band characteristic of the resting enzyme is bleached and a new absorption spectrum with features at 457, 429, 403 (shoulder), 360 (shoulder) and 332 nm appears.	Cadaverine	116-134	amine oxidase copper containing 1	Sus scrofa	59-74
3937520-0	1985	Gene expression of ornithine decarboxylase in L1210 leukaemia cells exposed to DL-2-difluoromethylornithine in the presence of cadaverine.	Cadaverine	127-137	ornithine decarboxylase, structural 1	Mus musculus	19-42
3937520-1	1985	Cultured mouse L1210 leukaemia cells treated with DL-2-difluoromethylornithine, an irreversible inhibitor of ornithine decarboxylase (EC 4.1.1.17), in the presence of micromolar concentrations of cadaverine, started to overproduce ornithine decarboxylase after an exposure of several weeks.	Cadaverine	196-206	ornithine decarboxylase, structural 1	Mus musculus	109-132
3841480-1	1985	Hydroxylamine-containing analogues of putrescine and cadaverine have been found effective in inhibiting the mouse liver ornithine decarboxylase, the best among synthesized were 1-aminooxy-3-aminopropane (I50 2.10(-8) M) and 1-aminooxy-4-aminobutane (I50 2.10(-7) M).	Cadaverine	53-63	ornithine decarboxylase, structural 1	Mus musculus	120-143
6615435-2	1983	It was found that both phospholipid-sensitive Ca2+-dependent protein kinase and myosin light-chain kinase (a calmodulin-sensitive species of Ca2+-dependent protein kinase) were inhibited to different degrees by polyamines, with an approximate order of inhibitory potency of spermine = 1, 12-diaminododecane greater than spermidine = 1, 10-diaminodecane much greater than cadaverine = putrescine.	Cadaverine	371-381	myosin light chain kinase	Rattus norvegicus	80-105
6747294-15	1984	The formation of covalent bonds between IgG and C3 and probably C4 was essential for inhibition of immune precipitation, because inhibitors of their formation, such as putrescine, cadaverine, and salicylhydroxamic acid, effectively prevented the inhibition of precipitation.	Cadaverine	180-190	complement C4A (Rodgers blood group)	Homo sapiens	64-66
6148101-5	1984	For both dansylcadaverine and Glc-Glc-Glc(OH)-cadaverine, 5 and 8 mol of donor were incorporated per mol of amidinated and succinylated beta-casein, respectively.	Cadaverine	15-25	casein beta	Homo sapiens	136-147
6425061-3	1984	20 mM lysine, 1,2-diaminoethane, 1,3-diaminopropane, 1,4-diaminobutane or 1,5-diaminopentane are able to dissociate C1 into its two entities, C1q and the calcium-dependent C1r2-C1s2 complex.	Cadaverine	74-92	complement C1q A chain	Homo sapiens	142-145
6430782-2	1984	Dimeric subunits were visualized in UV light as monodansyl cadaverine bound to casein at the position of the transglutaminase activity representing F13A.	Cadaverine	59-69	coagulation factor XIII A chain	Homo sapiens	148-152
6615435-2	1983	It was found that both phospholipid-sensitive Ca2+-dependent protein kinase and myosin light-chain kinase (a calmodulin-sensitive species of Ca2+-dependent protein kinase) were inhibited to different degrees by polyamines, with an approximate order of inhibitory potency of spermine = 1, 12-diaminododecane greater than spermidine = 1, 10-diaminodecane much greater than cadaverine = putrescine.	Cadaverine	371-381	calmodulin 1	Rattus norvegicus	109-119
6790686-1	1981	Hog kidney diamine oxidase (DAO) interacted with 1,3-diaminopropane, putrescine and cadaverine to arrest proliferation of cultured mammalian cells.	Cadaverine	84-94	amine oxidase copper containing 1	Homo sapiens	11-26
6408913-4	1983	The oxidative products of cadaverine might be of importance in various physiological and pathophysiological connections associated with elevated diamine oxidase levels.	Cadaverine	26-36	amine oxidase, copper containing 1	Rattus norvegicus	145-160
6805462-6	1982	Spermidine oxidase activity and diamine oxidase activity eluted in a concerted fashion when pregnancy serum was subjected to cadaverine-Sepharose chromatography, gel filtration and ion-exchange chromatography.	Cadaverine	125-135	amine oxidase copper containing 1	Homo sapiens	32-47
6790686-1	1981	Hog kidney diamine oxidase (DAO) interacted with 1,3-diaminopropane, putrescine and cadaverine to arrest proliferation of cultured mammalian cells.	Cadaverine	84-94	amine oxidase copper containing 1	Homo sapiens	28-31
7238568-7	1981	Mouse amniotic fluid was found to contain high levels of a spermine oxidase having a somewhat different specificity than that in FCS, and this enzyme produced a noncytotoxic immune inhibitor from cadaverine, spermidine and spermine.	Cadaverine	196-206	spermine oxidase	Mus musculus	59-75
7435118-1	1980	In the ovaries of pre-pubertal rats stimulated by human chorionic gonadotrophin (hCG) the temporal changes in cadaverine and putrescine formation were investigated.	Cadaverine	110-120	chorionic gonadotropin subunit beta 5	Homo sapiens	81-84
7435118-3	1980	The results show that the ovary stimulated by hCG, in addition to putrescine, forms cadaverine at a highly increased rate.	Cadaverine	84-94	chorionic gonadotropin subunit beta 5	Homo sapiens	46-49
7435118-5	1980	Treatment with aminoguanidine elevated the content of cadaverine in the ovary, suggesting that diamine oxidase has a role as a regulator of the intra-ovary level of cadaverine.	Cadaverine	54-64	amine oxidase copper containing 1	Homo sapiens	95-110
7435118-5	1980	Treatment with aminoguanidine elevated the content of cadaverine in the ovary, suggesting that diamine oxidase has a role as a regulator of the intra-ovary level of cadaverine.	Cadaverine	165-175	amine oxidase copper containing 1	Homo sapiens	95-110
7205597-2	1980	The diamines (1,3-propanediamine, 1,5-pentanediamine, and 1,6-hexanediamine) dramatically decreased neuroblastoma replication and inhibited the rate-limiting enzyme, ornithine decarboxylase.	Cadaverine	34-52	ornithine decarboxylase 1	Homo sapiens	166-189
7190634-0	1980	The dual action of the non-physiological diamines 1,3 diaminopropane and cadaverine on ornithine decarboxylase of HTC cells.	Cadaverine	73-83	ornithine decarboxylase 1	Rattus norvegicus	87-110
110032-5	1979	Treatment with aminoguanidine generally elevated the content of cadaverine, indicating a role of diamine oxidase as a regulator of diamine content.	Cadaverine	64-74	amine oxidase, copper containing 1	Rattus norvegicus	97-112
7228251-8	1980	The formation of NPYR and NPIP from proline, pyrrolidine, putrescine, spermidine and cadaverine was studied in a model experiment, using minced bacon as the reaction medium.	Cadaverine	85-95	neuropeptide Y receptor Y1	Homo sapiens	17-21
486492-8	1979	These experiments indicate that all of the detectable lysine decarboxylase activity in rat and mouse tissues was due to the action of ornithine decarboxylase and that significant cadaverine production in vivo would occur only when ornithine decarboxylase activity is high and lysine concentrations substantially exceed those of ornithine.	Cadaverine	179-189	ornithine decarboxylase, structural 1	Mus musculus	231-254
901422-10	1977	Cadaverine (1,5-diaminopentane) and 1,6-diaminohexane were the most potent inhibitors of ornithine decarboxylase among the amines tested.	Cadaverine	0-10	ornithine decarboxylase, structural 1	Mus musculus	89-112
646807-1	1978	Rat liver ornithine decarboxylase activity was decreased by administration of putrescine (1,4-diaminobutane) or other diamines, including 1,3-diaminopropane, 1,5-diaminopentane and 1,6-diaminohexane.	Cadaverine	158-176	ornithine decarboxylase 1	Rattus norvegicus	10-33
901422-10	1977	Cadaverine (1,5-diaminopentane) and 1,6-diaminohexane were the most potent inhibitors of ornithine decarboxylase among the amines tested.	Cadaverine	12-30	ornithine decarboxylase, structural 1	Mus musculus	89-112
32816235-0	2021	Cadaverine and Spermine Elicit Ca2+ Uptake in Human CP Cells via a Trace Amine-Associated Receptor 1 Dependent Pathway.	Cadaverine	0-10	trace amine associated receptor 1	Homo sapiens	67-100
402498-2	1977	It metabolises also a variety of diamines such as putrescine and cadaverine and is generally accepted to be identical with histaminase.	Cadaverine	65-75	amine oxidase copper containing 1	Homo sapiens	123-134
178010-1	1975	When the diamines putrescine, cadaverine, cystamine and lanthionamine are oxidized by purified pig kidney diamine oxidase in the presence of NADH and either liver or yeast crystalline alcohol dehydrogenase, NADH is oxidized.	Cadaverine	30-40	amine oxidase copper containing 1	Sus scrofa	106-121
4963523-0	1967	The inactivation of pea-seedling diamine oxidase by peroxidase and 1,5-diaminopentane.	Cadaverine	67-85	amine oxidase copper containing 1	Homo sapiens	33-48
4963523-2	1967	The rate of oxidative deamination of 1,5-diaminopentane by pea-seedling extracts, which contain diamine oxidase [diamine-oxygen oxidoreductase (deaminating), EC 1.4.3.6], was increased by adding pyridoxal or pyridoxal phosphate.	Cadaverine	37-55	amine oxidase copper containing 1	Homo sapiens	96-111
4963523-6	1967	This inactivation only occurred when 1,5-diaminopentane was the substrate and depended on a second thermolabile factor in the extract besides the diamine oxidase.	Cadaverine	37-55	amine oxidase copper containing 1	Homo sapiens	146-161
4963523-8	1967	Purified diamine oxidase, when catalysing the oxidation of 1,5-diaminopentane, was rapidly inactivated in the presence of peroxidase.	Cadaverine	59-77	amine oxidase copper containing 1	Homo sapiens	9-24
4963523-12	1967	It is suggested that peroxidase catalyses the further oxidation of the product of the oxidative deamination of 1,5-diaminopentane to a compound that inactivates diamine oxidase.	Cadaverine	111-129	amine oxidase copper containing 1	Homo sapiens	161-176
4963469-0	1967	Oxidative deamination of 2-hydroxy derivatives of putrescine and cadaverine by pea-seedling and pig-kidney diamine oxidase.	Cadaverine	65-75	amine oxidase copper containing 1	Sus scrofa	107-122
32816235-9	2021	Calcium imaging assays after TAAR1 knockdown in these cells with a specific siRNA against TAAR1 showed a consistent reduction in the responses of these cells to cadaverine and spermidine, but not to spermine, suggesting that TAAR1 is activated by cadaverine and spermidine, but not spermine.	Cadaverine	247-257	trace amine associated receptor 1	Homo sapiens	90-95
32816235-9	2021	Calcium imaging assays after TAAR1 knockdown in these cells with a specific siRNA against TAAR1 showed a consistent reduction in the responses of these cells to cadaverine and spermidine, but not to spermine, suggesting that TAAR1 is activated by cadaverine and spermidine, but not spermine.	Cadaverine	247-257	trace amine associated receptor 1	Homo sapiens	90-95
808238-2	1975	The procedure is based upon the binding of histaminase to cadaverine, a diamine substrate for the enzyme, which is coupled to Sepharose.	Cadaverine	58-68	amine oxidase copper containing 1	Homo sapiens	43-54
808238-4	1975	The purification technique has the following characteristics: (1) in optimal experiments, 3000-fold purification of enzyme was obtained; (2) the yield of enzyme was as great as 25%; (3) the binding of histaminase to the amine groups of the cadaverine appears to represent a true "affinity" phenomenon since enzyme bound to DEAE-cellulose under neutral pH conditions was eluted at much lower concentrations of NaCl (less than 0.4 M).	Cadaverine	240-250	amine oxidase copper containing 1	Homo sapiens	201-212
33545502-6	2021	Moreover, L-tryptophan, cadaverine and D-pantothenic acid could serve as the diagnostic biomarker for NTCP deficiency.	Cadaverine	24-34	solute carrier family 10 (sodium/bile acid cotransporter family), member 1	Mus musculus	102-106
32816235-6	2021	The zebrafish TAAR13c was the only receptor known to bind a polyamine-cadaverine.	Cadaverine	70-80	trace amine associated receptor 13c	Danio rerio	14-21
32816235-9	2021	Calcium imaging assays after TAAR1 knockdown in these cells with a specific siRNA against TAAR1 showed a consistent reduction in the responses of these cells to cadaverine and spermidine, but not to spermine, suggesting that TAAR1 is activated by cadaverine and spermidine, but not spermine.	Cadaverine	161-171	trace amine associated receptor 1	Homo sapiens	29-34
32816235-9	2021	Calcium imaging assays after TAAR1 knockdown in these cells with a specific siRNA against TAAR1 showed a consistent reduction in the responses of these cells to cadaverine and spermidine, but not to spermine, suggesting that TAAR1 is activated by cadaverine and spermidine, but not spermine.	Cadaverine	161-171	trace amine associated receptor 1	Homo sapiens	90-95
32816235-9	2021	Calcium imaging assays after TAAR1 knockdown in these cells with a specific siRNA against TAAR1 showed a consistent reduction in the responses of these cells to cadaverine and spermidine, but not to spermine, suggesting that TAAR1 is activated by cadaverine and spermidine, but not spermine.	Cadaverine	161-171	trace amine associated receptor 1	Homo sapiens	90-95
33144591-12	2020	TMA and cadaverine inhibited LPS-stimulated TNF-alpha and IL-6 secretion by primary human monocytes.	Cadaverine	8-18	tumor necrosis factor	Homo sapiens	44-53
33144591-12	2020	TMA and cadaverine inhibited LPS-stimulated TNF-alpha and IL-6 secretion by primary human monocytes.	Cadaverine	8-18	interleukin 6	Homo sapiens	58-62
31638822-8	2020	One or two secondary glutamine residues of only P-H, P-D P32, P-C and statherin were hierarchically susceptible to the reaction with monodansyl-cadaverine.	Cadaverine	133-154	statherin	Homo sapiens	48-79
32488317-3	2020	METHODS AND RESULTS: Condensation of ortho-aminobenzaldehyde (oABA) with delta-1-pyrroline and delta-1-piperideine, the autocyclization products of the DAO-oxidized natural substrates putrescine and cadaverine, generates new quinazoline fluorophores with absorption and excitation maxima of 430 and 460 nm, respectively, and peak emission at 620 nm.	Cadaverine	199-209	amine oxidase copper containing 1	Homo sapiens	152-155
32488317-8	2020	CONCLUSIONS: Incubation of DAO with the natural substrates putrescine and cadaverine and oABA generates novel fluorophores increasing the detection limit compared to absorption measurements at least tenfold.	Cadaverine	74-84	D-amino acid oxidase	Mus musculus	27-30
29274298-6	2018	This allows monitoring the dynamic progress of the conversion of lysine to cadaverine with a temporal resolution of ~30 s. Moreover, the method only requires to sample the very early onset of the reaction (<0.5% of substrate conversion where the host itself is required only at muM concentrations) at comparatively low reaction rates, thus saving enzyme material and reducing NMR acquisition time.	Cadaverine	75-85	latexin	Homo sapiens	281-284
33405720-11	2019	The incorporation of fluorescently labeled cadaverine derivatives for the detection of active TGase 2 was in accordance with the results of the expression analysis.	Cadaverine	43-53	transglutaminase 2, C polypeptide	Mus musculus	94-101
33405720-12	2019	The presence of an irreversible inhibitor of TGase 2 led to attenuated incorporation of the cadaverines, which verified the catalytic action of TGase 2.	Cadaverine	92-103	transglutaminase 2, C polypeptide	Mus musculus	45-52
33405720-12	2019	The presence of an irreversible inhibitor of TGase 2 led to attenuated incorporation of the cadaverines, which verified the catalytic action of TGase 2.	Cadaverine	92-103	transglutaminase 2, C polypeptide	Mus musculus	144-151
31509528-7	2019	xlAZIN2 did not behave as an antizyme inhibitor, but it rather acts as an authentic decarboxylase forming cadaverine, due to its higher affinity to L-lysine than to L-ornithine as substrate; so, in accordance with this, it should be named as lysine decarboxylase (LDC) or lysine/ornithine decarboxylase (LODC).	Cadaverine	106-116	antizyme inhibitor 2 S homeolog	Xenopus laevis	0-7
31509528-7	2019	xlAZIN2 did not behave as an antizyme inhibitor, but it rather acts as an authentic decarboxylase forming cadaverine, due to its higher affinity to L-lysine than to L-ornithine as substrate; so, in accordance with this, it should be named as lysine decarboxylase (LDC) or lysine/ornithine decarboxylase (LODC).	Cadaverine	106-116	ornithine decarboxylase, structural 1	Mus musculus	279-302
31088617-4	2019	In this study, we introduced an ATP regeneration system using polyphosphate kinase (ppk) into systems containing cadaverine decarboxylase (CadA) and PdxY for a sufficient supply of PLP, which resulted in enhanced cadaverine production.	Cadaverine	113-123	pyridoxal phosphatase	Homo sapiens	181-184
31367038-6	2019	We reveal a connection between polyamine and lysine metabolism during stress situations, in the form of a promiscuous enzymatic reaction in which the first enzyme of the polyamine pathway, Spe1p, decarboxylates lysine and forms an alternative polyamine, cadaverine.	Cadaverine	254-264	ornithine decarboxylase SPE1	Saccharomyces cerevisiae S288C	189-194
30718646-7	2019	Trace amino acid receptors (TAARs), namely, TAAR1, TAAR8 and TAAR9 were instrumental in provoking the cadaverine-evoked effects.	Cadaverine	102-112	trace amine associated receptor 1	Homo sapiens	44-49
30718646-7	2019	Trace amino acid receptors (TAARs), namely, TAAR1, TAAR8 and TAAR9 were instrumental in provoking the cadaverine-evoked effects.	Cadaverine	102-112	trace amine associated receptor 8	Homo sapiens	51-56
30718646-7	2019	Trace amino acid receptors (TAARs), namely, TAAR1, TAAR8 and TAAR9 were instrumental in provoking the cadaverine-evoked effects.	Cadaverine	102-112	trace amine associated receptor 9	Homo sapiens	61-66
30021117-2	2018	However, ODC also has minor activity towards cell metabolite C6 lysine and yields C5 cadaverine.	Cadaverine	85-95	ornithine decarboxylase 1	Homo sapiens	9-12
30021117-7	2018	This corresponds to four-fold decrease in cadaverine yield compared to the native ODC.	Cadaverine	42-52	ornithine decarboxylase 1	Homo sapiens	82-85
29080172-2	2018	Here we describe the methods used in a Quantitative Trait Loci (QTL) study that allowed the identification of ORGANIC CATION TRANSPORTER 1 (OCT1) as a determinant of root growth response to cadaverine treatment in Arabidopsis thaliana.	Cadaverine	190-200	organic cation/carnitine transporter1	Arabidopsis thaliana	110-138
29941999-2	2018	TAAR13c, the zebrafish olfactory receptor activated by the death-associated odor cadaverine, appears to possess an allosteric binding site for cadaverine, which was assumed to block progress of the ligand towards the internal orthosteric binding-and-activation site.	Cadaverine	81-91	trace amine associated receptor 13c	Danio rerio	0-7
29941999-2	2018	TAAR13c, the zebrafish olfactory receptor activated by the death-associated odor cadaverine, appears to possess an allosteric binding site for cadaverine, which was assumed to block progress of the ligand towards the internal orthosteric binding-and-activation site.	Cadaverine	143-153	trace amine associated receptor 13c	Danio rerio	0-7
29080172-2	2018	Here we describe the methods used in a Quantitative Trait Loci (QTL) study that allowed the identification of ORGANIC CATION TRANSPORTER 1 (OCT1) as a determinant of root growth response to cadaverine treatment in Arabidopsis thaliana.	Cadaverine	190-200	organic cation/carnitine transporter1	Arabidopsis thaliana	140-144
28102357-1	2017	The death-associated odor cadaverine, generated by bacteria-mediated decarboxylation of lysine, has been described as the principal activator of a particular olfactory receptor in zebrafish, TAAR13c.	Cadaverine	26-36	trace amine associated receptor 13c	Danio rerio	191-198
28102357-2	2017	Low concentrations of cadaverine activated mainly TAAR13c-expressing olfactory sensory neurons, suggesting TAAR13c as an important element of the neuronal processing pathway linking cadaverine stimulation to a strongly aversive innate behavioral response.	Cadaverine	22-32	trace amine associated receptor 13c	Danio rerio	50-57
28102357-2	2017	Low concentrations of cadaverine activated mainly TAAR13c-expressing olfactory sensory neurons, suggesting TAAR13c as an important element of the neuronal processing pathway linking cadaverine stimulation to a strongly aversive innate behavioral response.	Cadaverine	22-32	trace amine associated receptor 13c	Danio rerio	107-114
28102357-2	2017	Low concentrations of cadaverine activated mainly TAAR13c-expressing olfactory sensory neurons, suggesting TAAR13c as an important element of the neuronal processing pathway linking cadaverine stimulation to a strongly aversive innate behavioral response.	Cadaverine	182-192	trace amine associated receptor 13c	Danio rerio	107-114
27303024-6	2016	Transgenic tobacco (Nicotiana tabacum) hairy roots and Arabidopsis (Arabidopsis thaliana) plants expressing LcL/ODC enhanced the production of a Lys-derived alkaloid, anabasine, and cadaverine, respectively, thus, confirming the function of LcL/ODC in plants.	Cadaverine	182-192	ornithine decarboxylase-like	Nicotiana tabacum	112-115