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Protease/Metabolic Enzyme

Chemical Structure Cat. No. Product Name CAS No.
FASN-IN-3 Chemical Structure
BCP35577 FASN-IN-3 2097262-60-5
FASN-IN-3 is an orally-available, reversible, potent, and selective FASN inhibitor, inducing apoptosis, inhibiting anchorage-independent cell growth under lipid-rich conditions, and inhibiting in-vivo xenograft tumor growth.
Dorzolamide Chemical Structure
BCP35353 Dorzolamide 120279-96-1
Dorzolamide is an anti-glaucoma agent, which is a carbonic anhydrase inhibitor.
DMU2105 Chemical Structure
BCP35214 DMU2105 1031063-36-1
DMU2105(CYP1B1 inhibitor 7k) is a potent and specific CYP1B1 inhibitor.
URB 937 Chemical Structure
BCP35209 URB 937 1357160-72-5
URB 937 is a FAAH inhibitor and increases anandamide levels.
SGK3 degrader-1 Chemical Structure
BCP35166 SGK3 degrader-1 2381320-35-8
SGK3 degrader-1 is a potent SGK3 degrader based on PROTAC.
Mardepodect hydrochloride Chemical Structure
BCP35070 Mardepodect hydrochloride 2070014-78-5
Mardepodect hydrochloride is a potent, orally active and selective PDE10A inhibitor with an IC50 of 0.37 nM, with >1000-fold selectivity over other PDEs. Mardepodect hydrochloride can cross the blood-brain barrier.
DGAT-3 Chemical Structure
BCP35050 DGAT-3 701232-20-4
DGAT-3 is a inhibitor of diacylglycerol O-acyltransferase 1 (DGAT1). It is tested pre-clinically as a potential treatment for obesity.
NAcM-OPT Chemical Structure
BCP35044 NAcM-OPT 2089293-61-6
NAcM-OPT is a specific, reversible small molecule inhibitor targeting N-Acetyl-UBE2M interaction with DCN1 with IC50 of 79 nM
LHVS Chemical Structure
BCP34916 LHVS 170111-28-1
LHVS is an irreversible cysteine protease cathepsin S (CatS) inhibitor.
Zatolmilast Chemical Structure
BCP34899 Zatolmilast 1606974-33-7
Zatolmilast(BPN14770) is a phosphodiesterase IV inhibitor.
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