PMID-sentid	Pub_year	Sent_text	compound_name	comp_offset	prot_official_name	organism	prot_offset
28772354-6	2017	The maximum o-DCB and p-DCB removal efficiencies of 76.34% and 80.43%, respectively, were achieved with 4 g L-1 saponin solution.	4-dichlorobenzene	22-27	immunoglobulin kappa variable 1-16	Homo sapiens	108-111
32251592-3	2020	Neryl acetate has the lowest interaction energy (-87 kcal/mol) against active site of acetylcholinesterase, which is comparable to the ones of methiocarb and pirimicarb (-90 kcal/mol) and reported PDB binder 9-(3-iodobenzylamino)-1,2,3,4-tetrahydroacridine (-112.67 kcal/mol).	4-dichlorobenzene	197-200	Acetylcholine esterase	Drosophila melanogaster	86-106
29170797-6	2018	Limits of detection were in the order of nanograms per liter ranging from 4 ng L-1 for 1,4-dichlorobenzene and 1,2,3,4-tetrachlorobenzene to 8 ng L-1 for 1,2,4,5-tetrachlorobenzene.	4-dichlorobenzene	87-106	immunoglobulin kappa variable 1-16	Homo sapiens	79-82
27273578-2	2016	The spectroscopic and electrochemical measurements suggested that the coupling value of a directly linked PDI dimer (PDI)2 is much larger than those of para- and meta-phenylene-bridged PDI dimers p-(PDI)2 and m-(PDI)2 .	4-dichlorobenzene	152-156	peptidyl arginine deiminase 2	Homo sapiens	196-204
27840215-1	2017	This study was to investigate the inhibition effects of para-substituted cinnamic acid derivatives (4-chlorocinnamic acid, 4-ethoxycinnamic acid and 4-nitrocinnamic acid) on tyrosinase catalyzing the substrates, with the purpose of elucidating the inhibition mechanism of the tested derivatives on tyrosinase by the UV-vis spectrum, fluorescence spectroscopy, copper interacting and molecular docking, respectively.	4-dichlorobenzene	56-60	tyrosinase	Homo sapiens	174-184
27840215-1	2017	This study was to investigate the inhibition effects of para-substituted cinnamic acid derivatives (4-chlorocinnamic acid, 4-ethoxycinnamic acid and 4-nitrocinnamic acid) on tyrosinase catalyzing the substrates, with the purpose of elucidating the inhibition mechanism of the tested derivatives on tyrosinase by the UV-vis spectrum, fluorescence spectroscopy, copper interacting and molecular docking, respectively.	4-dichlorobenzene	56-60	tyrosinase	Homo sapiens	298-308
26975756-7	2016	Moreover, our results indicate that three novel lncRNAs (Snora41, Gm19947, and Scarna3a) in mESCs respond to p-DCB exposure.	4-dichlorobenzene	109-114	small nucleolar RNA, H/ACA box 41	Mus musculus	57-64
26975756-7	2016	Moreover, our results indicate that three novel lncRNAs (Snora41, Gm19947, and Scarna3a) in mESCs respond to p-DCB exposure.	4-dichlorobenzene	109-114	small Cajal body-specific RNA 3A	Mus musculus	79-87
28183024-1	2017	SABRE (Signal Amplification By Reversible Exchange) is a nuclear spin hyperpolarization technique based on the reversible concurrent binding of small molecules and para-hydrogen (p-H2) to an iridium metal complex in solution.	4-dichlorobenzene	164-169	polyhomeotic homolog 2	Homo sapiens	179-183
22386244-0	2012	Human kallikrein 6 inhibitors with a para-amidobenzylanmine P1 group identified through virtual screening.	4-dichlorobenzene	37-41	kallikrein related peptidase 6	Homo sapiens	6-18
26822143-5	2016	This thorough SAR evaluation revealed that the oxidized, para-substituted hydroxamic acids can be recognized as valuable lead structures in the pursuit of novel potent and selective HDAC6 inhibitors.	4-dichlorobenzene	57-61	sarcosine dehydrogenase	Homo sapiens	14-17
26822143-5	2016	This thorough SAR evaluation revealed that the oxidized, para-substituted hydroxamic acids can be recognized as valuable lead structures in the pursuit of novel potent and selective HDAC6 inhibitors.	4-dichlorobenzene	57-61	histone deacetylase 6	Homo sapiens	182-187
25913677-7	2015	The observed trend in the HDCl activity was: ClB>1,4-DClB>1,3-DClB>1,2-DClB>1,2,4-TClB.	4-dichlorobenzene	52-60	citramalyl-CoA lyase	Homo sapiens	45-48
24475903-1	2014	SABRE is a nuclear spin hyperpolarization technique based on the reversible association of a substrate molecule and para-hydrogen (p-H2) to a metal complex.	4-dichlorobenzene	116-120	polyhomeotic homolog 2	Homo sapiens	131-135
20069279-6	2010	An increase in renal alpha2u and cell proliferation was observed in DCB- and DL-treated rats but not in C500C-treated rats.	4-dichlorobenzene	68-71	alpha-2u globulin PGCL4	Rattus norvegicus	21-28
17593721-8	2007	Comparison of 1,4- and 1,2-DCB shows that the critical molecular diameter was apparently more important than the condensed state, suggesting that 1,4-DCB sorbed in the liquid state for ENC1.	4-dichlorobenzene	146-153	ectodermal-neural cortex 1	Homo sapiens	185-189
17593721-5	2007	For the solid-phase compounds (1,4-dichlorobenzene (1,4-DCB) and two PAHs), sorption was statistically higher with ENC1, thus demonstrating sorption effects due to both (1) authigenic organic content in the sorbentand (2)the sorbate"s condensed state.	4-dichlorobenzene	31-50	ectodermal-neural cortex 1	Homo sapiens	115-119
16078292-2	2005	Based on the direct measurements of tau(T(n)) of BP(T(n)), the triplet energy transfer (TET) from BP(T(n)) to quenchers (Q), such as carbon tetrachloride (CCl4), benzene (Bz), and p-dichlorbenzene (DCB), was investigated.	4-dichlorobenzene	180-196	C-C motif chemokine ligand 4	Homo sapiens	155-159
17593721-5	2007	For the solid-phase compounds (1,4-dichlorobenzene (1,4-DCB) and two PAHs), sorption was statistically higher with ENC1, thus demonstrating sorption effects due to both (1) authigenic organic content in the sorbentand (2)the sorbate"s condensed state.	4-dichlorobenzene	52-59	ectodermal-neural cortex 1	Homo sapiens	115-119
16078292-2	2005	Based on the direct measurements of tau(T(n)) of BP(T(n)), the triplet energy transfer (TET) from BP(T(n)) to quenchers (Q), such as carbon tetrachloride (CCl4), benzene (Bz), and p-dichlorbenzene (DCB), was investigated.	4-dichlorobenzene	198-201	C-C motif chemokine ligand 4	Homo sapiens	155-159
15988127-4	2005	The hypertrophy was accompanied by small increases of basal PLD activity and strong potentiation of stimulated PLD activity caused by 4beta-phorbol-12beta,13alpha-dibutyrate (PDB) and by phenylephrine.	4-dichlorobenzene	175-178	glycosylphosphatidylinositol specific phospholipase D1	Homo sapiens	111-114
12618297-3	2003	The phorbol ester 4beta-phorbol-12,13-dibutyrate (PDB) induced a concentration-dependent potentiation of synaptic responses in area CA1 that could partially be inhibited by the PKC inhibitor chelerythrine.	4-dichlorobenzene	50-53	carbonic anhydrase 1	Rattus norvegicus	132-135
15900770-7	2005	The highest level of PCB congeners was that of trichlorinated biphenyls (537 ng/g), which maybe due to the relatively low chlorination in the process of p-DCB production.	4-dichlorobenzene	153-158	pyruvate carboxylase	Homo sapiens	21-24
12700395-1	2003	A combination of experimental and simulation approaches was used to analyze clonal growth of glutathione-S-transferase pi (GST-P) enzyme-altered foci during liver carcinogenesis in an initiation-promotion regimen for 1,4-dichlorobenzene (DCB), 1,2,4,5-tetrachlorobenzene (TECB), pentachlorobenzene (PECB), and hexachlorobenzene (HCB).	4-dichlorobenzene	217-236	glutathione S-transferase pi 1	Rattus norvegicus	123-128
12700395-1	2003	A combination of experimental and simulation approaches was used to analyze clonal growth of glutathione-S-transferase pi (GST-P) enzyme-altered foci during liver carcinogenesis in an initiation-promotion regimen for 1,4-dichlorobenzene (DCB), 1,2,4,5-tetrachlorobenzene (TECB), pentachlorobenzene (PECB), and hexachlorobenzene (HCB).	4-dichlorobenzene	238-241	glutathione S-transferase pi 1	Rattus norvegicus	93-121
12700395-1	2003	A combination of experimental and simulation approaches was used to analyze clonal growth of glutathione-S-transferase pi (GST-P) enzyme-altered foci during liver carcinogenesis in an initiation-promotion regimen for 1,4-dichlorobenzene (DCB), 1,2,4,5-tetrachlorobenzene (TECB), pentachlorobenzene (PECB), and hexachlorobenzene (HCB).	4-dichlorobenzene	238-241	glutathione S-transferase pi 1	Rattus norvegicus	123-128
11254668-6	2001	Disruption of the dADAR gene results in totally unedited sodium (Para), calcium (Dmca1A), and chloride (DrosGluCl-alpha) channels, a very prolonged recovery from anoxic stupor, a vulnerability to heat shock and increased O2 demands, and neuronal degeneration in aged flies.	4-dichlorobenzene	65-69	Adenosine deaminase acting on RNA	Drosophila melanogaster	18-23
12558164-8	2003	Elevated VTG levels and decreased female GSIs were found in fish exposed to > or = 5 ng EE2/L and in fish exposed to > or = 10 mg p-DCB/L.	4-dichlorobenzene	138-141	vitellogenin	Danio rerio	9-12
11114946-2	2000	We have utilized confocal microscopy to compare phorbol 12, 13 dibutyrate (PDB) - stimulated translocation of PKCalpha in cultured cells derived from rat vascular smooth muscle.	4-dichlorobenzene	75-78	protein kinase C, alpha	Rattus norvegicus	110-118
11106506-7	2000	The binding affinities of a series of para-substituted phenethylamine analogues to MAO A show an increase in affinity of the deprotonated amine with increasing van der Waals volume of the substituent.	4-dichlorobenzene	38-42	monoamine oxidase A	Homo sapiens	83-88
11027971-14	2000	In addition, CHO/HPRT-gene mutation tests with 1,4-DCB and 2,5-DCP yielded negative results for both compounds with and without metabolic activation system.	4-dichlorobenzene	47-54	hypoxanthine guanine phosphoribosyl transferase	Mus musculus	17-21
10218646-12	1999	Cyclocommunin reduced the [3H]phorbol 12,13-dibutyrate ([3H]PDB) binding to cytosolic PKC in a concentration-dependent manner.	4-dichlorobenzene	60-63	protein kinase C, beta	Rattus norvegicus	86-89
10696772-2	2000	In the studies presented here, we measured the ability of 1,4-dichlorobenzene (DCB), 1,2,4,5-tetrachlorobenzene (TeCB), pentachlorobenzene (PeCB), and hexachlorobenzene (HCB) to promote glutathione S-transferase pi (GSTP1-1) positive preneoplastic foci formation in rat liver, following diethylnitrosamine (DEN) initiation.	4-dichlorobenzene	58-77	glutathione S-transferase pi 1	Rattus norvegicus	216-223
10691684-10	2000	The least potent para-substituted sulfonyl compounds had higher AR binding affinities than the most potent meta-substituted sulfonyl compounds.	4-dichlorobenzene	17-21	androgen receptor	Homo sapiens	64-66
18944733-1	1999	ABSTRACT In this study, we found that the inhibition of fungal growth in potato dextrose broth (PDB) medium by the 14-kDa corn trypsin inhibitor (TI) protein, previously found to be associated with host resistance to aflatoxin production and active against various fungi, was relieved when exogenous alpha-amylase was added along with TI.	4-dichlorobenzene	96-99	Bowman-Birk type bran trypsin inhibitor	Zea mays	127-149
18944733-1	1999	ABSTRACT In this study, we found that the inhibition of fungal growth in potato dextrose broth (PDB) medium by the 14-kDa corn trypsin inhibitor (TI) protein, previously found to be associated with host resistance to aflatoxin production and active against various fungi, was relieved when exogenous alpha-amylase was added along with TI.	4-dichlorobenzene	96-99	alpha-amylase	Zea mays	300-313
18944733-1	1999	ABSTRACT In this study, we found that the inhibition of fungal growth in potato dextrose broth (PDB) medium by the 14-kDa corn trypsin inhibitor (TI) protein, previously found to be associated with host resistance to aflatoxin production and active against various fungi, was relieved when exogenous alpha-amylase was added along with TI.	4-dichlorobenzene	96-99	Bowman-Birk type bran trypsin inhibitor	Zea mays	146-148
9804164-3	1998	Our results demonstrate that the cysl and cys2 motifs of the CRD of PKD are functionally dissimilar, with the cys2 motif responsible for the majority of [3H]phorbol 12,13-dibutyrate (PDB) binding, both in vivo and in vitro.	4-dichlorobenzene	183-186	protein kinase D1	Homo sapiens	68-71
9950075-6	1998	DCB gave a small (1.7-fold) increase in DNA synthesis (P = 0.03) and a small (1.7- to 2-fold) suppression of both spontaneous (P = 0.022) and TGFbeta1-induced (P = 0.015) apoptosis.	4-dichlorobenzene	0-3	transforming growth factor, beta 1	Rattus norvegicus	142-150
7747284-3	1995	Furthermore, CYP1A1 and CYP1A2 showed relatively high enzymatic activities toward the lower chlorinated benzenes (1,2-dichlorobenzene, 1,4-dichlorobenzene, 1,2,4-trichlorobenzene) and CYP3A4 toward the higher chlorinated benzenes (1,2,3,5-tetrachlorobenzene, pentachlorobenzene).	4-dichlorobenzene	135-154	cytochrome P450 family 1 subfamily A member 1	Homo sapiens	13-19
9325029-5	1997	Western immunoblotting studies demonstrated that DCB induced CYP2B isoenzyme(s) in both rat and mouse liver microsomes.	4-dichlorobenzene	49-52	cytochrome P450, family 2, subfamily b, polypeptide 10	Mus musculus	61-66
9325029-9	1997	The observed species difference in DCB-induced liver tumor formation may reflect the greater sensitivity of the mouse to tumor promotion by a CYP2B inducer.	4-dichlorobenzene	35-38	cytochrome P450, family 2, subfamily b, polypeptide 10	Mus musculus	142-147
9436787-6	1998	Also, MMP inhibitors such as 1,10-phenanthroline and synthetic dipeptides that inactivate the MMP catalytic site negated the 4beta-phorbol-12,13-dibutyrate (PDB)-mediated process extension, further supporting the key role of MMPs in process extension in vitro.	4-dichlorobenzene	157-160	matrix metallopeptidase 9	Homo sapiens	225-229
7747284-3	1995	Furthermore, CYP1A1 and CYP1A2 showed relatively high enzymatic activities toward the lower chlorinated benzenes (1,2-dichlorobenzene, 1,4-dichlorobenzene, 1,2,4-trichlorobenzene) and CYP3A4 toward the higher chlorinated benzenes (1,2,3,5-tetrachlorobenzene, pentachlorobenzene).	4-dichlorobenzene	135-154	cytochrome P450 family 1 subfamily A member 2	Homo sapiens	24-30
7747284-3	1995	Furthermore, CYP1A1 and CYP1A2 showed relatively high enzymatic activities toward the lower chlorinated benzenes (1,2-dichlorobenzene, 1,4-dichlorobenzene, 1,2,4-trichlorobenzene) and CYP3A4 toward the higher chlorinated benzenes (1,2,3,5-tetrachlorobenzene, pentachlorobenzene).	4-dichlorobenzene	135-154	cytochrome P450 family 3 subfamily A member 4	Homo sapiens	184-190
1293313-0	1992	The differential hepatotoxicity and cytochrome P450 responses of Fischer-344 rats to the three isomers of dichlorobenzene.	4-dichlorobenzene	106-121	cytochrome P450, family 2, subfamily g, polypeptide 1	Rattus norvegicus	36-51
7807594-3	1994	In the current study, the regrowth of fibers by adult human oligodendrocytes was examined and was found to be significantly enhanced by the PKC stimulator, 4 beta-phorbol-12,13-didecanoate (PDB); this was accompanied by a 400-500% increase in oligodendroglial PKC activity.	4-dichlorobenzene	190-193	proline rich transmembrane protein 2	Homo sapiens	140-143
7801330-7	1994	These results suggest that p-DCB is activated by a cytochrome P-450-dependent metabolic reaction and that the hepatotoxicity is caused by inadequate rates of detoxification of the resulting metabolite in mice depleted of hepatic GSH by BSO treatment.	4-dichlorobenzene	27-32	cytochrome P450, family 21, subfamily a, polypeptide 1	Mus musculus	51-67
7869420-11	1994	Treatment with 50 nM 4 beta-phorbol-12,13-dibutyrate (PDB) caused a delayed downregulation of PKC-delta levels after 8 hr without modulating the expression of other PKC isozymes in 1-day OLG; in the 3-day-old and 6-day-old OLG, PDB downmodulated PKC-beta I, -delta and epsilon isozymes with only a minor effect on PKC-alpha and no reduction in PKC-zeta.	4-dichlorobenzene	54-57	protein kinase C, alpha	Rattus norvegicus	94-97
7869420-11	1994	Treatment with 50 nM 4 beta-phorbol-12,13-dibutyrate (PDB) caused a delayed downregulation of PKC-delta levels after 8 hr without modulating the expression of other PKC isozymes in 1-day OLG; in the 3-day-old and 6-day-old OLG, PDB downmodulated PKC-beta I, -delta and epsilon isozymes with only a minor effect on PKC-alpha and no reduction in PKC-zeta.	4-dichlorobenzene	54-57	protein kinase C, alpha	Rattus norvegicus	314-323
3165303-1	1988	Protein kinase C (PK-C) levels were determined using [3H]phorbol-12,13-dibutyrate (PDB) binding and the in vitro phosphorylation of histone H I (III-S), in autopsied human frontal cortex of age- and postmortem time-matched normal and Alzheimer patients.	4-dichlorobenzene	83-86	proline rich transmembrane protein 2	Homo sapiens	0-16
1715830-3	1991	The objective of this study was to show that the presence of alpha 2u-globulin (alpha 2u) is essential for the development of this syndrome in rats exposed to 2,2,4-trimethylpentane (TMP), 1,4-dichlorobenzene (DCB), isophorone (IP), PS-6 unleaded gasoline (UG), and d-limonene (d-L).	4-dichlorobenzene	189-208	alpha2u globulin	Rattus norvegicus	61-78
1715830-3	1991	The objective of this study was to show that the presence of alpha 2u-globulin (alpha 2u) is essential for the development of this syndrome in rats exposed to 2,2,4-trimethylpentane (TMP), 1,4-dichlorobenzene (DCB), isophorone (IP), PS-6 unleaded gasoline (UG), and d-limonene (d-L).	4-dichlorobenzene	189-208	alpha2u globulin	Rattus norvegicus	61-69
1715830-3	1991	The objective of this study was to show that the presence of alpha 2u-globulin (alpha 2u) is essential for the development of this syndrome in rats exposed to 2,2,4-trimethylpentane (TMP), 1,4-dichlorobenzene (DCB), isophorone (IP), PS-6 unleaded gasoline (UG), and d-limonene (d-L).	4-dichlorobenzene	210-213	alpha2u globulin	Rattus norvegicus	61-78
1715830-3	1991	The objective of this study was to show that the presence of alpha 2u-globulin (alpha 2u) is essential for the development of this syndrome in rats exposed to 2,2,4-trimethylpentane (TMP), 1,4-dichlorobenzene (DCB), isophorone (IP), PS-6 unleaded gasoline (UG), and d-limonene (d-L).	4-dichlorobenzene	210-213	alpha2u globulin	Rattus norvegicus	61-69
1715830-10	1991	It is thus concluded that the presence of alpha 2u is causal to the development of renal disease in rats exposed to TMP, DCB, IP, UG, d-L, and lindane.	4-dichlorobenzene	121-124	alpha2u globulin	Rattus norvegicus	42-50
2398390-3	1990	The administration of the PKC-activating phorbol esters 4-beta-phorbol-12,13-dibutyrate (PDB) and phorbol-12-myristate-13-acetate (PMA) resulted in a dose-related inhibition of growth of human glioma cell lines in vitro as measured by 3H-thymidine uptake.	4-dichlorobenzene	89-92	proline rich transmembrane protein 2	Homo sapiens	26-29
2803280-2	1989	4-beta-phorbol-12,13-dibutyrate (PDB), an activator of protein kinase C (PKC), enhanced the potassium-evoked overflow of 14C.	4-dichlorobenzene	33-36	protein kinase C, gamma	Rattus norvegicus	55-71
2803280-2	1989	4-beta-phorbol-12,13-dibutyrate (PDB), an activator of protein kinase C (PKC), enhanced the potassium-evoked overflow of 14C.	4-dichlorobenzene	33-36	protein kinase C, gamma	Rattus norvegicus	73-76
1692643-9	1990	Binding of d-limonene and 1,4-dichlorobenzene to alpha 2u-globulin did not alter the degradation of the protein, whereas binding of d-limonene-1,2-oxide, 2.5-dichlorophenol, and isophorone decreased alpha 2u-globulin degradation by 33%.	4-dichlorobenzene	26-45	alpha2u globulin	Rattus norvegicus	49-66
2471290-0	1989	Involvement of reversible binding to alpha 2u-globulin in 1,4-dichlorobenzene-induced nephrotoxicity.	4-dichlorobenzene	58-77	alpha2u globulin	Rattus norvegicus	37-54
2471290-5	1989	Gel filtration chromatography of a 116,000g supernatant prepared from kidneys of 1,4-[14C]DCB-treated rats showed that radiolabel coeluted with alpha 2u-globulin as one sharp peak as opposed to a multipeak pattern observed for 1,2-[14C]DCB; the maximal quantity of radiolabel for 1,4-DCB was twice that for 1,2-DCB.	4-dichlorobenzene	280-287	alpha2u globulin	Rattus norvegicus	144-161
2471290-8	1989	1,4-DCB and, to a minor extent, 2,5-dichlorophenol, the major metabolite of 1,4-DCB, were reversibly bound to renal alpha 2u-globulin from 1,4-DCB-treated rats.	4-dichlorobenzene	0-7	alpha2u globulin	Rattus norvegicus	116-133
2471290-8	1989	1,4-DCB and, to a minor extent, 2,5-dichlorophenol, the major metabolite of 1,4-DCB, were reversibly bound to renal alpha 2u-globulin from 1,4-DCB-treated rats.	4-dichlorobenzene	76-83	alpha2u globulin	Rattus norvegicus	116-133
2471290-8	1989	1,4-DCB and, to a minor extent, 2,5-dichlorophenol, the major metabolite of 1,4-DCB, were reversibly bound to renal alpha 2u-globulin from 1,4-DCB-treated rats.	4-dichlorobenzene	76-83	alpha2u globulin	Rattus norvegicus	116-133
2471290-11	1989	Nephrotoxicity and biochemical alterations induced by 1,4-DCB resemble those of unleaded gasoline and suggest that a similar mechanism is involved in the induction of alpha 2u-globulin nephropathy in male rats.	4-dichlorobenzene	54-61	alpha2u globulin	Rattus norvegicus	167-184
3165303-1	1988	Protein kinase C (PK-C) levels were determined using [3H]phorbol-12,13-dibutyrate (PDB) binding and the in vitro phosphorylation of histone H I (III-S), in autopsied human frontal cortex of age- and postmortem time-matched normal and Alzheimer patients.	4-dichlorobenzene	83-86	proline rich transmembrane protein 2	Homo sapiens	18-22
3426217-5	1987	Chloride was released in stoichiometric amounts when P. putida CB1-9 was grown on either chlorobenzene or 1,4-dichlorobenzene.	4-dichlorobenzene	106-125	cannabinoid receptor 1	Homo sapiens	63-66
33179677-8	2020	Most probably these dianions transfer electrons to C6H4Cl2 producing the {BIII(CN)[SubPc(CN)2] 3-} - radical anions which form sigma-bonded diamagnetic dianions in {crypt(K+)}2{BIII(CN)[SubPc(CN)2]}22- 3C6H4Cl2 (3).	4-dichlorobenzene	51-58	calcium voltage-gated channel subunit alpha1 B	Homo sapiens	74-78
33179677-8	2020	Most probably these dianions transfer electrons to C6H4Cl2 producing the {BIII(CN)[SubPc(CN)2] 3-} - radical anions which form sigma-bonded diamagnetic dianions in {crypt(K+)}2{BIII(CN)[SubPc(CN)2]}22- 3C6H4Cl2 (3).	4-dichlorobenzene	51-58	calcium voltage-gated channel subunit alpha1 B	Homo sapiens	177-181
6698918-9	1984	Sensitivities for dichlorobenzenes and dichlorotoluenes were 8 ng/g for fat, 2 ng/g for tissue, and 0.4 ng/mL for blood.	4-dichlorobenzene	18-34	FAT atypical cadherin 2	Rattus norvegicus	72-78