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GPCR/G Protein

Chemical Structure Cat. No. Product Name CAS No.
Fluocortolone Chemical Structure
BCP22649 Fluocortolone 152-97-6
Fluocortolone is a glucocorticoid with anti-inflammatory activity used topically for various skin disorders.
Clocortolone pivalate Chemical Structure
BCP22647 Clocortolone pivalate 34097-16-0
Clocortolone Pivalate is a Corticosteroid Hormone Receptor Agonist. It is used for the treatment of dermatitis and is considered a medium-strength corticosteroid. It is unusual among steroids in that it contains a chlorine atom and a fluorine atom.
Solabegron Chemical Structure
BCP31054 Solabegron 252920-94-8
Solabegron (GW 427353) is a selective β3-adrenergic receptor agonist, stimulating cAMP accumulation in Chinese hamster ovary cells expressing the human β3-AR, with an EC50 value of 22 nM. Solabegron (GW 427353) is being developed for the treatment of overactive bladder and irritable bowel syndrome.
Vicagrel Chemical Structure
BCP24464 Vicagrel 1314081-53-2
Vicagrel, an acetate derivative of Clopidogrel, is a P2Y12 platelet inhibitor potentially for the treatment of thrombosis.
J-113863, trans- Chemical Structure
BCP27912 J-113863, trans- 353791-85-2
J 113863 is a potent CCR1 antagonist
PSNCBAM-1 Chemical Structure
BCP27729 PSNCBAM-1 877202-74-9
PSNCBAM-1 is an allosteric, non-competitive antagonist of CB-1 (IC50= 45 and 209 nM) with hypophagic effects in vivo, potentially an anti-obesity agents.
Alarelin Acetate Chemical Structure
BCP27725 Alarelin Acetate 79561-22-1
Alarelin acetate is a synthetic GnRH agonist.
VU-29 Chemical Structure
BCP27694 VU-29 890764-36-0
VU 29 is a potent allosteric potentiator at the rat mGlu5 receptor (EC50 = 9 nM); binds to the MPEP allosteric site (Ki app = 244 nM).
Azaphen 2HCl Chemical Structure
BCP27680 Azaphen 2HCl 24853-80-3
Azafen is a tricyclic antidepressant.It acts as a potent inhibitor of the reuptake of serotonin.
Histrelin Chemical Structure
BCP27657 Histrelin 76712-82-8
Histrelin is a nonapeptide analog of GnRH (gonadotropin-releasing hormone) with added potency. When present in the bloodstream, it can act on gonadotropes. Histrelin can stimulate these cells to release luteinizing hormone and follicle-stimulating hormone. Histrelin is considered a GnRH agonist. It can be used for the treatment of menstruation disorders.
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