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Cat. No.	Product Name	Field of Application
DC2092	Genistein Featured	Genistein is a highly specific inhibitor of protein tyrosine kinase (PTK).
DC2093	Genistin Featured	Genistin is an isoflavone glycoside found in soy-based products. Can be used as a negative control for the PTK inhibitor Genistein
DCAPI1064	mixtures of three isomers (Gentamicins C1, C2, and C1(subA). Featured	Gentamycin sulfate (Gentacycol)
DC7417	Genz-123346 Featured	Genz-123346 free base is an inhibitor of GL1 synthase that blocks the conversion of ceramide to GL1; IC50 for GM1 inhibition is 14 nM.
DC10161	Gepotidacin Featured	Gepotidacin (GSK2140944) is a novel triazaacenaphthylene bacterial type II topoisomerase inhibitor.
DC7132	GF 109203X Featured	GF109203X is a potent PKC inhibitor with IC50 of 20 nM, 17 nM, 16 nM, and 20 nM for PKCα, PKCβI, PKCβII, and PKCγ, respectively, showing more than 3000-fold selectivity for PKC as compared to EGFR, PDGFR and insulin receptor.
DC21043	GGTI 2417 Featured	GGTI 2417 is the methyl ester prodrug of GGTI-2418, a highly potent, competitive, and selective inhibitor of GGTase I.
DC21044	GGTI 2418 Featured	GGTI 2418 (PTX 100) is a highly potent, competitive, and selective peptidomimetic inhibitor of geranylgeranyltransferase I (GGTI) with IC50 of 9.5 nM, displays 5,600-fold selectivity over FTase.
DC21042	GGTI-2147 Featured	GGTI-2147 is a non-thiol peptidomimetic that inhibits GGTase I and blocks geranyl-geranylation of Rap1A (IC50=0.5 uM).
DC11246	Ghrelin agonist HM01 Featured	Ghrelin agonist HM01 is a novel potent, orally available ghrelin (GHS-R) agonist with Ki of 1.42 nM (human GHS-R1a), induces potent activation of intracellular calcium signaling with EC50 of 1.25 nM.
DC10883	GI254023X Featured	GI254023X is a potent MMP9 and ADAM10 inhibitor with IC50s of 2.5 and 5.3 nM, respectively.
DC10490	GIBH-130 Featured	GIBH-130 is a novel inhibitor of neuroinflammation effective in Alzheimer’s disease models.
DC7432	Givinostat (ITF2357) Featured	Givinostat (ITF2357) is a potent HDAC inhibitor for maize HD2, HD1B and HD1A with IC50 of 10 nM, 7.5 nM and 16 nM. Phase 1/2.
DC10081	GJ103 Featured	GJ103 is an active analog of the read-through compound GJ072.
DC10080	GJ103 (sodium salt) Featured	GJ103 sodium salt is an active analog of the read-through compound GJ072.
DC9855	GK921 Featured	GK921 is a transglutaminase 2 (TGase 2) inhibitor with average GI50 of 0.9 uM in cancer cell lines.
DC8118	GKT137831(Setanaxib) Featured	GKT137831 is a novel and specific dual Nox1/Nox4 inhibitor with Ki of 140±40 nM and 110±30 nM; a potent inhibitor of fibrosis and hepatocyte apoptosis.
DC21049	Glabrescione B Featured	Glabrescione B (GlaB) is a small molecule binding to Gli1 zinc finger and impairing Gli1 activity by interfering with Gli1/DNA interaction, inhibits Hh signaling by impairing Gli1 function; inhibits the growth of Hedgehog-dependent tumor cells in vitro and in vivo, inhibits Gli1-dependent growth of cerebellum-derived normal progenitors; inhibits the growth of Gli-dependent medulloblastoma and tumor-derived stem-like cells; inhibits the growth of Gli-dependent basal cell carcinoma in vitro and in vivo.
DC10130	Glabridin Featured	Glabridin is a bio-available isoflavan isolated from licorice (Glycyrrhiza glabra L.) root extract
DC10818	ABT-493(Glecaprevir) Featured	Glecaprevir is a novel HCV NS3/4A protease inhibitor, with IC50 values ranging from 3.5 to 11.3 nM.
DC11296	GLP-26 Featured	GLP-26 is a novel potent HBV capsid modulator that reduces secreted HBeAg in HepNTCPDL cells transfected with HBV wild type with EC50 of 0.7 uM.
DC8375	GLPG0634 analogue Featured	GLPG0634 (analog) is a pan JAK inhibitor with IC50s of 50-200 nM for JAK1/JAK2/JAK3; more information can be found in the reference patents.
DC11803	GLPG-1690(Ziritaxestat) Featured	GLPG-1690 is a first-in-class, potent, competitive autotaxin inhibitor with Ki/IC50 of 15 nM/131 nM.
DC10753	GLPG-1837(ABBV-974) Featured	GLPG-1837(ABBV-974) is a novel cystic fibrosis transmembrane conductance regulator CFTR potentiator.
DC26048	GLS1 Inhibitor Featured	GLS1 inhibitor is an inhibitor of glutaminase 1
DC21052	GLS 4(Morphothiadin) Featured	GLS4 (Morphothiadin) is a potent inhibitor of HBV capsid assembly, inhibits HBV replication (EC50=62.24 nM) and reduces HBV-DNA levels in HepG.2.2.15 cells (IC50=14 nM), shows efficacy against ADV-resistant HBV mutations.
DC10003	PF-06291874（glucagon receptor antagonists-4） Featured	glucagon receptor antagonists-4 is a highly potent glucagon receptor antagonist.
DC11543	Glumetinib Featured	Glumetinib (SCC 244) is a novel potent and highly selective inhibitor of c-Met kinase with IC50 of 0.42 nM.
DC9529	Glutaminase C-IN-1 Featured	Glutaminase C-IN-1 (968) is an allosteric inhibitor of Glutaminase C that inhibits cancer cell growth without affecting their normal cellular counterparts.
DC11009	GLX351322 Featured	GLX351322 is an inhibitor of NADPH oxidase 4, and inhibits hydrogen peroxide production from NOX4-overexpressing cells with an IC50 of 5 μ M.

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