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GPCR/G Protein

Chemical Structure Cat. No. Product Name CAS No.
Lu AF27139 Chemical Structure
BCP44190 Lu AF27139 2097117-06-9
Lu AF27139, a novel rodent-active and CNS-penetrant P2X7 receptor antagonist.
Levalbuterol hydrochloride Chemical Structure
BCP44201 Levalbuterol hydrochloride 50293-90-8‬
Levalbuterol Hydrochloride is the hydrochloride salt form of levalbuterol, a relatively selective sympathomimetic beta-2 adrenergic receptor agonist with bronchodilator activity.
Difelikefalin HCl Chemical Structure
BCP44189 Difelikefalin HCl 2413256-25-2
Difelikefalin is a novel and potent kappa opioid receptor agonist.
D-DOPA Chemical Structure
BCP44158 D-DOPA 5796-17-8
D-dopa is the D-enantiomer of dopa. It is a dopa and a D-tyrosine derivative. It is an enantiomer of a L-dopa. It is a tautomer of a D-dopa zwitterion.
JNJ-54166060 Chemical Structure
BCP44118 JNJ-54166060 1627900-42-8
JNJ-54166060 is a potent P2X7 antagonist.
LY2979165 Chemical Structure
BCP44009 LY2979165 1311385-35-9
LY-2979165 is a metabotropic glutamate receptor agonist prodrug.
Nebracetam Chemical Structure
BCP44037 Nebracetam 116041-13-5
Nebracetam, a nootropic M1-muscarinic agonist, induces a rise of intracellular Ca2+ concentration.
Terfenadine Chemical Structure
BCP43974 Terfenadine 50679-08-8
Terfenadine is a potent open-channel blocker of hERG with a mean IC50 of 204 nM.
Nelivaptan Chemical Structure
BCP43930 Nelivaptan 439687-69-1
Nelivaptan is a non-peptide vasopressin receptor antagonist that is selective for the V1B subtype.
EST64454 HCl Chemical Structure
BCP43797 EST64454 HCl 1950569-11-5
EST64454 is a Highly Soluble σ1 Receptor Antagonist Clinical Candidate for Pain Management.
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