Castanospermine inhibits all forms of α- and β-glucosidases, especially glucosidase l (required for glucoprotein processing by transfer of mannose and glucose from asparagine-linked lipids).

Catechin-7-O-xyloside, a natural product isolated and purified from ultrafine U. davidiana var. japonica ethanol extract, induces apoptosis via endoplasmic reticulum stress and mitochondrial dysfunction in human non-small cell lung carcinoma H1299 cells, suggests that it has anti-cancer activity.

Caulilexin C is a natural product isolated and purified from the herbs of Isatis idigotica, showing inhibitory activity on human Acyl CoA: cholesterol transferase I (hACATI) and on human Acyl CoA: cholesterol transferase 2 (hACAT2) at 100 ug/mL.

Caulilexin C is a natural product isolated and purified from the herbs of Isatis idigotica, showing inhibitory activity on human Acyl CoA: cholesterol transferase I (hACATI) and on human Acyl CoA: cholesterol transferase 2 (hACAT2) at 100 ug/mL.

CCG 2046 is an inhibitor of regulator of G-protein signaling 4 (RGS4).

CCG 2046 is an inhibitor of regulator of G-protein signaling 4 (RGS4).

CCG 2046 is an inhibitor of regulator of G-protein signaling 4 (RGS4).

CCG 2046 is an inhibitor of regulator of G-protein signaling 4 (RGS4).

CCG 2046 is an inhibitor of regulator of G-protein signaling 4 (RGS4).

CCT367766 is an active PROTAC degrader targeting on Pirin protein.

CCT367766 is an active PROTAC degrader targeting on Pirin protein.

CCT367766 is an active PROTAC degrader targeting on Pirin protein.

CCT367766 is an active PROTAC degrader targeting on Pirin protein.

CCT367766 is an active PROTAC degrader targeting on Pirin protein.

CCT128930 is a potent ATP-competitive, selective Akt2 inhibitor with an IC50 of 6 nM and > 28-fold selectivity for Akt2 than the closely related PKA kinase.

CCT128930 is a potent ATP-competitive, selective Akt2 inhibitor with an IC50 of 6 nM and > 28-fold selectivity for Akt2 than the closely related PKA kinase.

CCT128930 is a potent ATP-competitive, selective Akt2 inhibitor with an IC50 of 6 nM and > 28-fold selectivity for Akt2 than the closely related PKA kinase.

CCT128930 is a potent ATP-competitive, selective Akt2 inhibitor with an IC50 of 6 nM and > 28-fold selectivity for Akt2 than the closely related PKA kinase.

CCT128930 is a potent ATP-competitive, selective Akt2 inhibitor with an IC50 of 6 nM and > 28-fold selectivity for Akt2 than the closely related PKA kinase.

CCT128930 is a potent ATP-competitive, selective Akt2 inhibitor with an IC50 of 6 nM and > 28-fold selectivity for Akt2 than the closely related PKA kinase.

CDDO-Im is a synthetic triterpenoid more potent than its parent compound CDDO both in vitro and in vivo and a PPARγ agonist.

CDDO-Im is a synthetic triterpenoid more potent than its parent compound CDDO both in vitro and in vivo and a PPARγ agonist.

CDDO-Im is a synthetic triterpenoid more potent than its parent compound CDDO both in vitro and in vivo and a PPARγ agonist.

CDK2 inhibitor 73 is a selective CDK2 inhibitor with IC50 value of 44nM.

CDK2 inhibitor 73 is a selective CDK2 inhibitor with IC50 value of 44nM.

Ceapin-A7 is a selective blocker of ATF6α signaling in response to ER stress with IC50 of 0.59 μM.

Ceapin-A7 is a selective blocker of ATF6α signaling in response to ER stress with IC50 of 0.59 μM.

Ceapin-A7 is a selective blocker of ATF6α signaling in response to ER stress with IC50 of 0.59 μM.

Ceapin-A7 is a selective blocker of ATF6α signaling in response to ER stress with IC50 of 0.59 μM.

Ceapin-A7 is a selective blocker of ATF6α signaling in response to ER stress with IC50 of 0.59 μM.

Ceapin-A7 is a selective blocker of ATF6α signaling in response to ER stress with IC50 of 0.59 μM.

Cedrelopsin is a natural product isolated and purified from Melicope borbonica with antifungal activity.