PMID-sentid	Pub_year	Sent_text	comp_official_name	comp_offset	protein_name	organism	prot_offset
32867776-10	2020	CONCLUSION: Our results indicate the presence of a novel mechanism mediating a fine balance between defence and counter-defence in which a SIM site is competitively sought for degradation and, as a counter-defence, betaC1 undergoes SUMOylation to escape from its degradation.	sim	139-142	long intergenic non-protein coding RNA 1587	Homo sapiens	215-221
31337732-7	2020	For intermodality agreement, PD MRI also showed higher AC1 (PD MRI: 0.9069, 95% CI 0.8374 to 0.9764; TOF MRA: 0.7983, 95% CI 0.6969 to 0.8996) and PABAK (PD MRI: 0.8735, TOF MRA: 0.7289) than TOF MRA.	pabak	147-152	long intergenic non-protein coding RNA 1587	Homo sapiens	55-58
26951338-3	2016	Furthermore, the application of AC1, AC2, AC3, AC4 on different heavy metal (Cu(2+), Zn(2+), Pb(2+), Cr(3+)) removals was explored to investigate their adsorption properties.	Metals	70-75	long intergenic non-protein coding RNA 1587	Homo sapiens	32-35
30306522-3	2018	In this chapter, I will summarize our work on ACC and IC and provide evidence for calcium-stimulated AC1 as a key molecule for cortical LTP and chronic pain.	Calcium	82-89	long intergenic non-protein coding RNA 1587	Homo sapiens	101-104
31858034-8	2019	The surface of coking coal modified by acids was rougher than that of AC-1.	Coal	22-26	long intergenic non-protein coding RNA 1587	Homo sapiens	70-74
28566698-4	2017	So carbon-exchange of biocrusts (cyanobacteria crusts-AC1/AC2; cyanolichen crust-LC1; chlorolichen crust-LC2; moss crust-MC) utilizing NRW at various temperatures and light-intensities were determined under simulated and insitu mesocosm experiments.	Carbon	3-9	long intergenic non-protein coding RNA 1587	Homo sapiens	54-57
26951338-3	2016	Furthermore, the application of AC1, AC2, AC3, AC4 on different heavy metal (Cu(2+), Zn(2+), Pb(2+), Cr(3+)) removals was explored to investigate their adsorption properties.	Copper	77-79	long intergenic non-protein coding RNA 1587	Homo sapiens	32-35
26951338-3	2016	Furthermore, the application of AC1, AC2, AC3, AC4 on different heavy metal (Cu(2+), Zn(2+), Pb(2+), Cr(3+)) removals was explored to investigate their adsorption properties.	Zinc	85-87	long intergenic non-protein coding RNA 1587	Homo sapiens	32-35
26951338-3	2016	Furthermore, the application of AC1, AC2, AC3, AC4 on different heavy metal (Cu(2+), Zn(2+), Pb(2+), Cr(3+)) removals was explored to investigate their adsorption properties.	Lead	93-95	long intergenic non-protein coding RNA 1587	Homo sapiens	32-35
26951338-3	2016	Furthermore, the application of AC1, AC2, AC3, AC4 on different heavy metal (Cu(2+), Zn(2+), Pb(2+), Cr(3+)) removals was explored to investigate their adsorption properties.	Chromium	101-103	long intergenic non-protein coding RNA 1587	Homo sapiens	32-35
26951338-6	2016	Among the four samples, AC1 exhibits the highest adsorption capacity for Cu(2+); the highest adsorption capacities of Pb(2+) and Zn(2+) are obtained for AC2; that of Cr(3+) are obtained for AC4.	Lead	118-120	long intergenic non-protein coding RNA 1587	Homo sapiens	24-27
26951338-6	2016	Among the four samples, AC1 exhibits the highest adsorption capacity for Cu(2+); the highest adsorption capacities of Pb(2+) and Zn(2+) are obtained for AC2; that of Cr(3+) are obtained for AC4.	Zinc	129-131	long intergenic non-protein coding RNA 1587	Homo sapiens	24-27
27152112-1	2016	A series of 5"-amino-2"-hydroxy-1,3-diaryl-2-propen-1-ones (AC1-AC15) were synthesized by Claisen-Schmidt condensation of 5"-acetamido-2"-hydroxy acetophenone with various substituted aromatic aldehydes.	Aldehydes	193-202	long intergenic non-protein coding RNA 1587	Homo sapiens	60-68
27152112-1	2016	A series of 5"-amino-2"-hydroxy-1,3-diaryl-2-propen-1-ones (AC1-AC15) were synthesized by Claisen-Schmidt condensation of 5"-acetamido-2"-hydroxy acetophenone with various substituted aromatic aldehydes.	5"-amino-2"-hydroxy-1,3-diaryl-2-propen-1-ones	12-58	long intergenic non-protein coding RNA 1587	Homo sapiens	60-68
25937212-8	2015	The selective AC1 inhibitor CB-6673567 and siRNA-mediated deletion of AC1 both blocked the choline-induced cAMP increase, suggesting that calcium-dependent AC1 is required for choline"s action.	Choline	91-98	long intergenic non-protein coding RNA 1587	Homo sapiens	14-17
27152112-1	2016	A series of 5"-amino-2"-hydroxy-1,3-diaryl-2-propen-1-ones (AC1-AC15) were synthesized by Claisen-Schmidt condensation of 5"-acetamido-2"-hydroxy acetophenone with various substituted aromatic aldehydes.	5"-acetamido-2"-hydroxy acetophenone	122-158	long intergenic non-protein coding RNA 1587	Homo sapiens	60-68
26484974-5	2015	AC-1 (TAKETA- G2X) was used as the target for modification.	taketa- g2x	6-17	long intergenic non-protein coding RNA 1587	Homo sapiens	0-4
25937212-8	2015	The selective AC1 inhibitor CB-6673567 and siRNA-mediated deletion of AC1 both blocked the choline-induced cAMP increase, suggesting that calcium-dependent AC1 is required for choline"s action.	Choline	91-98	long intergenic non-protein coding RNA 1587	Homo sapiens	70-73
25937212-8	2015	The selective AC1 inhibitor CB-6673567 and siRNA-mediated deletion of AC1 both blocked the choline-induced cAMP increase, suggesting that calcium-dependent AC1 is required for choline"s action.	Choline	91-98	long intergenic non-protein coding RNA 1587	Homo sapiens	70-73
25937212-8	2015	The selective AC1 inhibitor CB-6673567 and siRNA-mediated deletion of AC1 both blocked the choline-induced cAMP increase, suggesting that calcium-dependent AC1 is required for choline"s action.	Cyclic AMP	107-111	long intergenic non-protein coding RNA 1587	Homo sapiens	14-17
25937212-8	2015	The selective AC1 inhibitor CB-6673567 and siRNA-mediated deletion of AC1 both blocked the choline-induced cAMP increase, suggesting that calcium-dependent AC1 is required for choline"s action.	Cyclic AMP	107-111	long intergenic non-protein coding RNA 1587	Homo sapiens	70-73
25937212-8	2015	The selective AC1 inhibitor CB-6673567 and siRNA-mediated deletion of AC1 both blocked the choline-induced cAMP increase, suggesting that calcium-dependent AC1 is required for choline"s action.	Cyclic AMP	107-111	long intergenic non-protein coding RNA 1587	Homo sapiens	70-73
25937212-8	2015	The selective AC1 inhibitor CB-6673567 and siRNA-mediated deletion of AC1 both blocked the choline-induced cAMP increase, suggesting that calcium-dependent AC1 is required for choline"s action.	Calcium	138-145	long intergenic non-protein coding RNA 1587	Homo sapiens	14-17
25937212-8	2015	The selective AC1 inhibitor CB-6673567 and siRNA-mediated deletion of AC1 both blocked the choline-induced cAMP increase, suggesting that calcium-dependent AC1 is required for choline"s action.	Calcium	138-145	long intergenic non-protein coding RNA 1587	Homo sapiens	70-73
25937212-8	2015	The selective AC1 inhibitor CB-6673567 and siRNA-mediated deletion of AC1 both blocked the choline-induced cAMP increase, suggesting that calcium-dependent AC1 is required for choline"s action.	Calcium	138-145	long intergenic non-protein coding RNA 1587	Homo sapiens	70-73
25937212-8	2015	The selective AC1 inhibitor CB-6673567 and siRNA-mediated deletion of AC1 both blocked the choline-induced cAMP increase, suggesting that calcium-dependent AC1 is required for choline"s action.	Choline	176-183	long intergenic non-protein coding RNA 1587	Homo sapiens	14-17
25937212-8	2015	The selective AC1 inhibitor CB-6673567 and siRNA-mediated deletion of AC1 both blocked the choline-induced cAMP increase, suggesting that calcium-dependent AC1 is required for choline"s action.	Choline	176-183	long intergenic non-protein coding RNA 1587	Homo sapiens	70-73
25937212-8	2015	The selective AC1 inhibitor CB-6673567 and siRNA-mediated deletion of AC1 both blocked the choline-induced cAMP increase, suggesting that calcium-dependent AC1 is required for choline"s action.	Choline	176-183	long intergenic non-protein coding RNA 1587	Homo sapiens	70-73
25937212-10	2015	Our findings provide the first direct evidence to link activation of alpha7 nAChRs to a cAMP rise via AC1, which defines a new signaling pathway employed by alpha7 nAChRs.	Cyclic AMP	88-92	long intergenic non-protein coding RNA 1587	Homo sapiens	102-105
25863366-13	2015	High ozone levels emitted by AC1 did not allow for simultaneous determination of ROS levels due to high background levels associated with ozone decomposition in the buffer.	Ozone	5-10	long intergenic non-protein coding RNA 1587	Homo sapiens	29-32
25937212-0	2015	Activation of alpha7 nicotinic acetylcholine receptors increases intracellular cAMP levels via activation of AC1 in hippocampal neurons.	Cyclic AMP	79-83	long intergenic non-protein coding RNA 1587	Homo sapiens	109-112
25937212-8	2015	The selective AC1 inhibitor CB-6673567 and siRNA-mediated deletion of AC1 both blocked the choline-induced cAMP increase, suggesting that calcium-dependent AC1 is required for choline"s action.	CB-6673567	28-38	long intergenic non-protein coding RNA 1587	Homo sapiens	14-17
24835595-2	2014	By comparing six polymer (P1, P2, P3, P4, P5 and P6) and five activated carbon (AC1, AC2, AC3, AC4 and AC5) coatings through BAmuE, AC2 exhibited much higher selectivity and efficiency from all the sorbent phases tested, even when compared with the commercial stir bar sorptive extraction with polydimethylsiloxane.	baysilon	294-314	long intergenic non-protein coding RNA 1587	Homo sapiens	80-83
23413977-3	2013	We tested the hypothesis that two dominant grazing resistant bacterial taxa, the ac1 tribe of Actinobacteria (ac1) and filamentous bacteria from the LD2 lineage (Saprospiraceae), profit from such carbon sources during periods of intense HNF predation.	Carbon	196-202	long intergenic non-protein coding RNA 1587	Homo sapiens	81-84
24755265-9	2014	Of the total deaths, 22% occurred in hospital, where the agreement coefficient (AC1) for SCD between PCVA and hospital physician diagnosis was 95.5%, and agreement between InterVA-4 and hospital physician diagnosis was 96.9%.	pcva	101-105	long intergenic non-protein coding RNA 1587	Homo sapiens	80-83
23413977-3	2013	We tested the hypothesis that two dominant grazing resistant bacterial taxa, the ac1 tribe of Actinobacteria (ac1) and filamentous bacteria from the LD2 lineage (Saprospiraceae), profit from such carbon sources during periods of intense HNF predation.	Carbon	196-202	long intergenic non-protein coding RNA 1587	Homo sapiens	110-113
23413977-5	2013	Members of ac1 and LD2 were significantly more enriched after NAG addition to lake water.	Acetylglucosamine	62-65	long intergenic non-protein coding RNA 1587	Homo sapiens	11-14
23413977-5	2013	Members of ac1 and LD2 were significantly more enriched after NAG addition to lake water.	Water	83-88	long intergenic non-protein coding RNA 1587	Homo sapiens	11-14
23532022-5	2013	Similarly, dinapinones AC1 and AC2, consisting of monapinones A and C, dinapinones AD1 and AD2, consisting of monapinones A and D, and dinapinones AE1 and AE2, consisting of monapinones A and E, were atropisomers.	dinapinones	11-22	long intergenic non-protein coding RNA 1587	Homo sapiens	23-26
23532022-5	2013	Similarly, dinapinones AC1 and AC2, consisting of monapinones A and C, dinapinones AD1 and AD2, consisting of monapinones A and D, and dinapinones AE1 and AE2, consisting of monapinones A and E, were atropisomers.	dinapinones	71-82	long intergenic non-protein coding RNA 1587	Homo sapiens	23-26
22447680-1	2012	A series of metal-free acene-modified triphenylamine dyes (benzene to pentacene, denoted as TPA-AC1 to TPA-AC5) are investigated as organic sensitizers for application in dye-sensitized solar cells (DSSCs).	Metals	12-17	long intergenic non-protein coding RNA 1587	Homo sapiens	96-99
22952279-6	2012	Ca(2+)-inhibited ACs 5 and 6 are increased in ADPKD cells, while Ca(2+)/CaM-stimulated ACs 1 and 3 are downregulated.	cafestol palmitate	72-75	long intergenic non-protein coding RNA 1587	Homo sapiens	87-98
23535312-6	2013	Moreover, AC1 was useful in the removal of free residual chlorine in tap water.	Chlorine	57-65	long intergenic non-protein coding RNA 1587	Homo sapiens	10-13
23535312-6	2013	Moreover, AC1 was useful in the removal of free residual chlorine in tap water.	Water	73-78	long intergenic non-protein coding RNA 1587	Homo sapiens	10-13
23088424-4	2012	However, PVA/GA/AC composite rods formed with a lower concentration of GA (content ratio GA/AC = 1/6 and GA/PVA = 1/10) have significantly greater S(BET) (~500 m2/g) and V(p) (>0.55 cm3/g) values because of improved accessibility of the AC surface.	Glutaral	13-15	long intergenic non-protein coding RNA 1587	Homo sapiens	92-118
22447680-1	2012	A series of metal-free acene-modified triphenylamine dyes (benzene to pentacene, denoted as TPA-AC1 to TPA-AC5) are investigated as organic sensitizers for application in dye-sensitized solar cells (DSSCs).	Tetradecanoylphorbol Acetate	92-95	long intergenic non-protein coding RNA 1587	Homo sapiens	96-99
22447680-5	2012	The results show that from TPA-AC1 to TPA-AC5 with increasing sizes of the acenes, the absorption and fluorescence spectra are systematically broadened and red-shifted, but the oscillator strength and electron injection properties are reduced.	Tetradecanoylphorbol Acetate	27-30	long intergenic non-protein coding RNA 1587	Homo sapiens	31-34
22447680-5	2012	The results show that from TPA-AC1 to TPA-AC5 with increasing sizes of the acenes, the absorption and fluorescence spectra are systematically broadened and red-shifted, but the oscillator strength and electron injection properties are reduced.	Tetradecanoylphorbol Acetate	38-41	long intergenic non-protein coding RNA 1587	Homo sapiens	31-34
22447680-5	2012	The results show that from TPA-AC1 to TPA-AC5 with increasing sizes of the acenes, the absorption and fluorescence spectra are systematically broadened and red-shifted, but the oscillator strength and electron injection properties are reduced.	anthracene	75-81	long intergenic non-protein coding RNA 1587	Homo sapiens	31-34
22447680-6	2012	The molecular orbital contributions show increasing localization on the bridging acene units from TPA-AC1 to TPA-AC5.	anthracene	81-86	long intergenic non-protein coding RNA 1587	Homo sapiens	102-105
22447680-6	2012	The molecular orbital contributions show increasing localization on the bridging acene units from TPA-AC1 to TPA-AC5.	Tetradecanoylphorbol Acetate	98-101	long intergenic non-protein coding RNA 1587	Homo sapiens	102-105
22447680-6	2012	The molecular orbital contributions show increasing localization on the bridging acene units from TPA-AC1 to TPA-AC5.	Tetradecanoylphorbol Acetate	109-112	long intergenic non-protein coding RNA 1587	Homo sapiens	102-105
22447680-1	2012	A series of metal-free acene-modified triphenylamine dyes (benzene to pentacene, denoted as TPA-AC1 to TPA-AC5) are investigated as organic sensitizers for application in dye-sensitized solar cells (DSSCs).	anthracene	23-28	long intergenic non-protein coding RNA 1587	Homo sapiens	96-99
22447680-1	2012	A series of metal-free acene-modified triphenylamine dyes (benzene to pentacene, denoted as TPA-AC1 to TPA-AC5) are investigated as organic sensitizers for application in dye-sensitized solar cells (DSSCs).	4,4',4''-tris(3-methylphenyl(phenyl)amino)triphenylamine	38-52	long intergenic non-protein coding RNA 1587	Homo sapiens	96-99
22447680-1	2012	A series of metal-free acene-modified triphenylamine dyes (benzene to pentacene, denoted as TPA-AC1 to TPA-AC5) are investigated as organic sensitizers for application in dye-sensitized solar cells (DSSCs).	Benzene	59-66	long intergenic non-protein coding RNA 1587	Homo sapiens	96-99
22447680-1	2012	A series of metal-free acene-modified triphenylamine dyes (benzene to pentacene, denoted as TPA-AC1 to TPA-AC5) are investigated as organic sensitizers for application in dye-sensitized solar cells (DSSCs).	pentacene	70-79	long intergenic non-protein coding RNA 1587	Homo sapiens	96-99
16447436-2	2005	Activated carbon was oxidized in HNO3 aqueous solution at first (AC1), then treated in the mixture of NaOH and NaCl solution (AC2).	Carbon	10-16	long intergenic non-protein coding RNA 1587	Homo sapiens	65-68
24956524-4	2012	An agarose-carbomer (AC1) hydrogel, already used in SCI repair strategies, was here investigated as a delivery system capable of an effective chABC administration: the material ability to include chABC within its pores and the possibility to be injected into the target tissue were firstly proved.	Sepharose	3-10	long intergenic non-protein coding RNA 1587	Homo sapiens	21-24
19691254-4	2009	The maximum efficiencies of Cr(VI) removal were 97.67 and 99.87% for activated carbon (AC0) and modified activated carbon (AC1), respectively.	chromium hexavalent ion	28-34	long intergenic non-protein coding RNA 1587	Homo sapiens	123-126
19691254-8	2009	The Cr(VI) uptake by AC0 and AC1 followed pseudo first-order and second-order kinetics, but was best described by the pseudo second-order rate model.	chromium hexavalent ion	4-10	long intergenic non-protein coding RNA 1587	Homo sapiens	29-32
16885381-5	2006	Growth of a new aromatase stably transfected MCF-7 cell line (Ac1) was stimulated by conversion of androstenedione into estrogens and was sensitive to aromatase inhibitors.	Androstenedione	99-114	long intergenic non-protein coding RNA 1587	Homo sapiens	62-65
19433063-2	2009	We report the novel benzimidazole analogue AC1-004, obtained from a chemical library using an HRE-dependent cell-based assay in colorectal carcinoma HCT-116 cells.	benzimidazole	20-33	long intergenic non-protein coding RNA 1587	Homo sapiens	43-50
19433063-7	2009	These results suggest the benzimidazole analogue AC1-004 is a novel HIF inhibitor that targets HIF-1alpha via the Hsp90-Akt pathway, and that it can be used as a new lead in developing anticancer drugs.	benzimidazole	26-39	long intergenic non-protein coding RNA 1587	Homo sapiens	49-56
17942301-7	2008	The growth of Ac-1 cells was inhibited by tamoxifen, toremifene and atamestane in vitro with IC(50) values of 1.8+/-1.3 microM, 1+/-0.3 microM and 60.4+/-17.2 microM, respectively.	Tamoxifen	42-51	long intergenic non-protein coding RNA 1587	Homo sapiens	14-18
17942301-7	2008	The growth of Ac-1 cells was inhibited by tamoxifen, toremifene and atamestane in vitro with IC(50) values of 1.8+/-1.3 microM, 1+/-0.3 microM and 60.4+/-17.2 microM, respectively.	Toremifene	53-63	long intergenic non-protein coding RNA 1587	Homo sapiens	14-18
17942301-7	2008	The growth of Ac-1 cells was inhibited by tamoxifen, toremifene and atamestane in vitro with IC(50) values of 1.8+/-1.3 microM, 1+/-0.3 microM and 60.4+/-17.2 microM, respectively.	atamestane	68-78	long intergenic non-protein coding RNA 1587	Homo sapiens	14-18
7689939-6	1993	Two antibodies to human P-selectin KC4.1 and AC1.2 crossreacted with canine platelets whose surface binding, in response to agonists thrombin, calcium ionophore (A23187), phorbol esters and ADP, was similar.	Calcimycin	162-168	long intergenic non-protein coding RNA 1587	Homo sapiens	45-48
16117107-8	2005	In the CW and the AC1 soils, strong correlations were observed between the amount of PAHs biodegraded and the fraction of PAHs removed from the soils using the HPCD extraction.	Polycyclic Aromatic Hydrocarbons	85-89	long intergenic non-protein coding RNA 1587	Homo sapiens	18-21
15533211-7	2004	But in 9 families with left and bilateral CL/P, two-point Zmax for APOC2[AC1/AC2] was 1.701 and multi-point Zmax at APOC2 locus was 1.909.	Phosphorus	45-46	long intergenic non-protein coding RNA 1587	Homo sapiens	73-76
9228084-4	1997	Galphas stimulation of AC1 involved a single site and had an apparent Kact of 0.9 nM.	galphas	0-7	long intergenic non-protein coding RNA 1587	Homo sapiens	23-26
9172642-4	1997	Molecular modeling using the NMR distance and dihedral angle constraints obtained in DMSO-d6 yielded a model showing a well-defined structure for the N-terminal segment Ac-1 to Sta-4, but a flexible structure for the C-terminal segment.	Dimethyl sulfoxide-d6	85-92	long intergenic non-protein coding RNA 1587	Homo sapiens	169-173
9172642-4	1997	Molecular modeling using the NMR distance and dihedral angle constraints obtained in DMSO-d6 yielded a model showing a well-defined structure for the N-terminal segment Ac-1 to Sta-4, but a flexible structure for the C-terminal segment.	xylometazoline	177-180	long intergenic non-protein coding RNA 1587	Homo sapiens	169-173
7691962-4	1993	We show here that T cell clones specific for the N-terminal fragment of myelin basic protein, acetylated Ac1-11, recognize a set of unrelated peptides in the context of the same I-Au molecule.	Gold	180-182	long intergenic non-protein coding RNA 1587	Homo sapiens	105-108
12130572-2	2002	Two N-terminal peptides, ANXA1(Ac2-26) and ANXA1(Ac1-50), inhibited forskolin-evoked ACTH and prolactin release; however, they lacked the potency and full efficacy of the parent molecule (ANXA1(1-346)), whereas other shorter N-terminal sequences were without effect.	Colforsin	68-77	long intergenic non-protein coding RNA 1587	Homo sapiens	49-52
7689939-6	1993	Two antibodies to human P-selectin KC4.1 and AC1.2 crossreacted with canine platelets whose surface binding, in response to agonists thrombin, calcium ionophore (A23187), phorbol esters and ADP, was similar.	Calcium	143-150	long intergenic non-protein coding RNA 1587	Homo sapiens	45-48
7689939-6	1993	Two antibodies to human P-selectin KC4.1 and AC1.2 crossreacted with canine platelets whose surface binding, in response to agonists thrombin, calcium ionophore (A23187), phorbol esters and ADP, was similar.	Phorbol Esters	171-185	long intergenic non-protein coding RNA 1587	Homo sapiens	45-48
7689939-6	1993	Two antibodies to human P-selectin KC4.1 and AC1.2 crossreacted with canine platelets whose surface binding, in response to agonists thrombin, calcium ionophore (A23187), phorbol esters and ADP, was similar.	Adenosine Diphosphate	190-193	long intergenic non-protein coding RNA 1587	Homo sapiens	45-48
34569814-0	2021	Correction for Gnanasekaran et al., "Geminivirus Betasatellite-Encoded betaC1 Protein Exhibits Novel ATP Hydrolysis Activity That Influences Its DNA-Binding Activity and Viral Pathogenesis".	Adenosine Triphosphate	101-104	long intergenic non-protein coding RNA 1587	Homo sapiens	71-77
35580131-10	2022	Gwet"s AC1 using the mode of the blinded raters" assessment of "Decayed", "Missing" and IMPL compared to CLIN ranged from 0.81 to 0.89 (IODP) and 0.87 to 1.00 (IODP+PAN-X), while for "Filled" and DMFT they were 0.29 and 0.36 (IODP) as well as 0.33 and 0.36 (IODP+PAN-X), respectively.	iodp	136-140	long intergenic non-protein coding RNA 1587	Homo sapiens	7-10
35580131-10	2022	Gwet"s AC1 using the mode of the blinded raters" assessment of "Decayed", "Missing" and IMPL compared to CLIN ranged from 0.81 to 0.89 (IODP) and 0.87 to 1.00 (IODP+PAN-X), while for "Filled" and DMFT they were 0.29 and 0.36 (IODP) as well as 0.33 and 0.36 (IODP+PAN-X), respectively.	iodp	160-164	long intergenic non-protein coding RNA 1587	Homo sapiens	7-10
35580131-10	2022	Gwet"s AC1 using the mode of the blinded raters" assessment of "Decayed", "Missing" and IMPL compared to CLIN ranged from 0.81 to 0.89 (IODP) and 0.87 to 1.00 (IODP+PAN-X), while for "Filled" and DMFT they were 0.29 and 0.36 (IODP) as well as 0.33 and 0.36 (IODP+PAN-X), respectively.	dmft	196-200	long intergenic non-protein coding RNA 1587	Homo sapiens	7-10
35580131-10	2022	Gwet"s AC1 using the mode of the blinded raters" assessment of "Decayed", "Missing" and IMPL compared to CLIN ranged from 0.81 to 0.89 (IODP) and 0.87 to 1.00 (IODP+PAN-X), while for "Filled" and DMFT they were 0.29 and 0.36 (IODP) as well as 0.33 and 0.36 (IODP+PAN-X), respectively.	iodp	226-230	long intergenic non-protein coding RNA 1587	Homo sapiens	7-10
35580131-10	2022	Gwet"s AC1 using the mode of the blinded raters" assessment of "Decayed", "Missing" and IMPL compared to CLIN ranged from 0.81 to 0.89 (IODP) and 0.87 to 1.00 (IODP+PAN-X), while for "Filled" and DMFT they were 0.29 and 0.36 (IODP) as well as 0.33 and 0.36 (IODP+PAN-X), respectively.	iodp	258-262	long intergenic non-protein coding RNA 1587	Homo sapiens	7-10
33264998-6	2021	The N2O emission, H2S emission, and H2SO4 consumption in H2SO-VM1 were 28, 93 and 39% lower than those in H2SO4-AC1, respectively.	sulfuric acid	106-111	long intergenic non-protein coding RNA 1587	Homo sapiens	112-115
1717980-4	1991	The AC1 channel can be activated from the intracellular side by protein kinase C activators such as diacylglycerol and phorbolester and by cGMP but not by Ca2+, inositol 1,4,5-triphosphate, or cAMP.	Diglycerides	100-114	long intergenic non-protein coding RNA 1587	Homo sapiens	4-7
1717980-4	1991	The AC1 channel can be activated from the intracellular side by protein kinase C activators such as diacylglycerol and phorbolester and by cGMP but not by Ca2+, inositol 1,4,5-triphosphate, or cAMP.	Cyclic GMP	139-143	long intergenic non-protein coding RNA 1587	Homo sapiens	4-7
1717980-4	1991	The AC1 channel can be activated from the intracellular side by protein kinase C activators such as diacylglycerol and phorbolester and by cGMP but not by Ca2+, inositol 1,4,5-triphosphate, or cAMP.	Cyclic AMP	193-197	long intergenic non-protein coding RNA 1587	Homo sapiens	4-7
34277574-1	2021	The synthesis and characterization of three aromatic oligoamides, constructed from the same pyridyl carboxamide core but incorporating distinct end groups of acetyl (Ac) 1, tert-butyloxycarbonyl (Boc) 2 and amine 3 is reported.	aromatic oligoamides	44-64	long intergenic non-protein coding RNA 1587	Homo sapiens	158-171
35125087-15	2022	The bioassay guided isolation afforded four molecules AC-1 to AC-4 from chloroform fraction.	Chloroform	72-82	long intergenic non-protein coding RNA 1587	Homo sapiens	64-66
35125087-26	2022	cadamba afforded four pure molecules AC-1 to AC-4 with identification of fourteen new compounds.	cadamba	0-7	long intergenic non-protein coding RNA 1587	Homo sapiens	47-49
33477701-3	2021	Two compounds selected at the end of the computational analysis, i.e., ZINC2429155 (also named STL1) and ZINC1447881 (also named AC1), have been tested in an experimental assay, together with IQO as a positive control and quercetin as a negative control.	methyl 4-((7-((3-chlorobenzyl)oxy)-4-oxo-4H-chromen-3-yl)oxy)benzoate	105-116	long intergenic non-protein coding RNA 1587	Homo sapiens	129-132