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Cat. No. Product name CAS No.
DC21060 GNX-865

GNX-865 is a potent mitochondrial permeability transition pore (mPTP) inhibitor with EC50 of 105 uM (mitochondrial swelling).

1223568-82-8
DC22100 GO289 Featured

GO289 (GO-289, GO 289) is a potent and selective inhibitor of casein kinase 2 (CK2) with IC50 of 7 nM in in vitro kinase assays, shows minor effects on CKIδ and CKIα activity in vitro.

694522-87-7
DC20393 Golgicide A Featured

Golgicide A is a potent, highly specific, reversible inhibitor of the cis-Golgi ArfGEF GBF1, inhibits the effect of shiga toxin on protein synthesis with IC50 of 3.3 uM.

1139889-93-2
DC12542 GOT1 inhibitor 2c Featured

GOT1 inhibitor 2c is a first-in-class, non-covalent inhibitor of glutamate oxaloacetate transaminase 1 (GOT1) with IC50 of 8.2 uM..

732973-87-4
DC9375 GPDA Featured

GPDA(Glycylproline p-nitroanilide tosylate) is the substarate of X-Prolyl dipeptidyl-aminopeptidase in the enzyme assay.

65096-46-0
DC21902 GPR139 agonist AC4

GPR139 agonist AC4 is a novel small molecule GPR139 receptor agonist with EC50 of 220 nM in calcium mobilization assay in CHO-GPR139 cells. .

1147746-85-7
DC20394 GPR39 modulator 3

GPR39 modulator 3 is a Hedgehog pathway inhibitor that has high cellular potency (EC50=5 nM) in the reporter gene assay, activates the orphan receptor GPR39 and potently reduces of Gli1 and Ptch1 mRNA levels.

1582736-28-4
DC20395 GPR39 modulator 7

GPR39 modulator 7 is a Hedgehog pathway inhibitor that has high cellular potency (EC50=20 nM) in the reporter gene assay, activates the orphan receptor GPR39 and potently reduces of Gli1 and Ptch1 mRNA levels.

1582736-32-0
DC20076 GPR4 antagonist 3(NE 52-QQ57 ) Featured

GPR4 antagonist 3 is a selective, and orally available GPR4 antagonist with an IC50 of 70 nM. Anti-inflammatory activities.

1401728-56-0
DC11143 GPR40 AgoPAM AP5

GPR40 AgoPAM AP5 is a potent, selective GPR40 AgoPAM (full agonist with positive allosteric modulation) with hIP1 EC50 of 0.8 nM, high selectivity over the GPR120 receptor (EC50>30 uM).

1623194-37-5
DC22224 Gpr52 antagonist E7

Gpr52 antagonist E7 (Scabertopin) is a novel Gpr52-specific small molecule antagonist, reduces mutant HTT levels and rescues Huntington's disease-associated phenotypes in cellular and mouse models..

185213-52-9
DC21064 GR-127935 hydrochloride Featured

GR-127935 potent and selective 5-HT1B/1D receptor antagonist with pKi of 8.5 for both guinea pig 5-HT1D and rat 5-HT1B receptor.

148642-42-6
DC8820 GR148672X

GR148672X is a specific TGH inhibitor.

263890-70-6
DC21065 GR-64349

GR-64349 is a potent and selective tachykinin NK2 receptor agonist with EC50 of 3.7 nM, displays >1000- and >300-fold selectivity over NK1 and NK3 receptors, respectively..

137593-52-3
DC21066 GR73632 Featured

GR-73632 is a potent and selective tachykinin NK1 receptor agonist with EC50 of 2 nM, promotes differentiation but not survival of rat chromaffin cells in vitro..

133156-06-6
DC9918 Gracillin

Gracillin is a kind of steroidal saponin isolated from the root bark of wild yam Dioscorea nipponica with antitumor agent.

19083-00-2
DC12095 GRGDSP TFA

GRGDSP (TFA) is an integrin inhibitor.

DC22629 GRL-0617 Featured

GRL-0617 is a potent, noncovalent SARS-CoV papain-like protease (PLpro) inhibitor with IC50 of 0.6 uM, Ki of 0.49 uM.

1093070-16-6
DC23564 GS 462808

GS 462808 is a potent Late INa current inhibitor with IC50 of 1.33 uM.

1354198-41-6
DC21070 GS-1

GS-1 is a close structural analog of GS-5806 that acts an RSV fusion inhibitor.

1353625-49-6
DC21068 GS-493

GS-493 is a novel potent, selective SHP2 inhibitor with IC50 of 71±15 nM in enzyme assay.

1710337-31-7
DC23381 GS-626510

GS-626510 (GS-6510, GS 6510, GS 626510) is a novel BET family bromodomains inhibitor with Kd of 0.5-2.8 nM for BRD2/3/4, and BRDT.

1637770-13-8
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