a-37 — TargetMol Chemicals

Cat No.	Product Name	Synonyms	Targets
T23903	CM037	CM-037,A-37,CM 037,A37,A 37	Dehydrogenase
	CM037 (A-37) is a selective ALDH1A1 (acetaldehyde dehydrogenase 1A1) inhibitor (IC50; 4.6 µM) with antitumor activity and may be used in studies to eliminate gynecologic malignancies.		Dehydrogenase
T71646	Frenolicin
	Frenolicin is a selective inhibitor of Prx1 and Grx3 through covalent modification of active-site cysteines.
TP1134	HCGRP-(8-37)	Human α-CGRP (8-37)
	Rat CGRP-(8-37) (VTHRLAGLLSRSGGVVKDNFVPTNVGSEAF) is a highly selective CGRP receptor antagonist
T38034	MAO-IN-M30 dihydrochloride	M 30 dihydrochloride	Monoamine Oxidase
	MAO-IN-M30 dihydrochloride (M 30 dihydrochloride) is a potent and brain selective monoamine oxidase (MAO) inhibitor (EC50 values are 37 and 57 nM for MAO-A and MAO-B, respectively). Also an iron chelator with antioxidant...		Monoamine Oxidase
TP1775L	LL-37, Human acetate(154947-66-7 free base)		Antibacterial
	LL-37, Human acetate is a 37-residue, amphipathic, cathelicidin-derived antimicrobial peptide, which exhibits a broad spectrum of antimicrobial activity.		Antibacterial
T15372	GB1107	(2R,3R,4S,5R,6R)-2-(3,4-dichlorophenyl)sulfanyl-6-(hydroxymethyl)-4-[4-(3,4,5-trifluorophenyl)triazol-1-yl]oxane-3,5-diol	Galectin
	GB1107 is an effective and selective Galectin-3 inhibitor with a Kd of 37 nM.		Galectin
TP1548L	SIYRY acetate(178561-37-0 free base)		Others
	SIYRY acetate(178561-37-0 free base) is a Kb-restricted epitope peptide.		Others
TP1976L	Oxyntomodulin acetate		Glucagon Receptor
	Oxyntomodulin acetate, a 37-amino acid peptide hormone, is a glucagon-like peptide 1 (GLP-1) receptor agonist[1].		Glucagon Receptor
T8721L	I-37 free base( 2359690-13-2(free base))		Raf
	I-37 free base is a novel benzylamino substituted pyridopyrimidinone as SOS1 inhibitor.		Raf
TP1323	CGRP 8-37 (rat)		CGRP Receptor
	CGRP 8-37 (rat) is a CGRP receptor antagonist, a CGRP fragment with potential anti-injury effects that induces arterial relaxation.		CGRP Receptor
TP1134L	HCGRP-(8-37) acetate	HCGRP-(8-37) acetate (119911-68-1 free base)	CGRP Receptor
	HCGRP-(8-37) acetate is a human calcitonin gene-related peptide (hCGRP) fragment acetate and also an antagonist of CGRP receptor.		CGRP Receptor
T17219	Vatalanib free base		VEGFR
	Vatalanib is a VEGFR2/KDR inhibitor (IC50: 37 nM).		VEGFR
TP1410	Cecropin A		Antibacterial , Antibiotic
	Cecropin A is a naturally occurring, linear, cationic, 37-residue antimicrobial peptide.		Antibacterial , Antibiotic
T2412	SRT1720 hydrochloride	SRT1720 HCl,SRT 1720 Hydrochloride	Sirtuin
	SRT1720 hydrochloride (SRT1720 HCl) is a selective activator of SIRT1 (EC1.5: 0.16 μM) and shows less potent activities on SIRT2/SIRT3 (EC1.5s: 37 μM/300 μM).		Sirtuin
T1896	Ro 61-8048		Hydroxylase
	Ro 61-8048 is a potent and selective inhibitor of kynurenine hydroxylase with an IC50 value of 37 nM.		Hydroxylase
T22372	MYF-01-37	1-[3-Methyl-3-[3-(trifluoromethyl)anilino]pyrrolidin-1-yl]prop-2-en-1-one	Others , YAP
	MYF-01-37 (1-[3-Methyl-3-[3-(trifluoromethyl)anilino]pyrrolidin-1-yl]prop-2-en-1-one) is a novel covalent TEAD inhibitor.		Others , YAP
T19083	1-Methylinosine	N1-Methylinosine,Inosine, 1-methyl	Nucleoside Antimetabolite/Analog , Endogenous Metabolite
	1-Methylinosine (N1-Methylinosine) is a modified nucleotide found at position 37 in tRNA 3' to the anticodon of eukaryotic tRNA and has a role as a metabolite.		Nucleoside Antimetabolite/Analog , Endogenous Metabolite
T5124	SRT 1720 dihydrochloride[925434-55-5(free base)]		Sirtuin
	SRT 1720 is a selective activator of SIRT1 (EC1.5: 0.16 μM) and shows less potent activities on SIRT2 (EC1.5: 37 μM) and SIRT3 (EC1.5: 300 μM).		Sirtuin
T3951	NSC632839	F6,Ubiquitin Isopeptidase Inhibitor II	DUB
	NSC-632839 (Ubiquitin Isopeptidase Inhibitor II) is a nonselective isopeptidase inhibitor, which inhibits USP2 (EC50: 45±4 μM), USP7 (EC50: 37±1 μM), and SENP2 (EC50: 9.8±1.8 μM).		DUB
T4342	PF-04929113 Mesylate	PF-04929113 (Mesylate),SNX-5422 Mesylate	HSP , HER
	PF-04929113 Mesylate (SNX-5422 Mesylate), a prodrug of SNX-2112, is an orally available Hsp90 inhibitor (Kd: 41 nM) and also induces Her-2 degradation (IC50: 37 nM).		HSP , HER