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 |