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Cat. No. Product Name Information
PC-42653

Ketanserin

5-HT2A antagonist

Ketanserin (R41468) is a high-affinity, non-selective antagonist of 5-HT2 receptor with Ki of 2-3 nM for 5-HT2A and 28 nM for 5-HT2C.
PC-45229

Ziprasidone hydrochloride monohydrate

D2/5-HT2A antagonist

Ziprasidone hydrochloride monohydrate (CP-88059) is a full antagonist of D2 and 5-HT2A receptors with Ki of 6.8 and 0.6 nM, respectively.
PC-43963

Ziprasidone

D2/5-HT2A antagonist

Ziprasidone (CP 88059) is a full antagonist of D2 and 5-HT2A receptors with Ki of 6.8 and 0.6 nM, respectively.
PC-24462

NLX-266

5-HT1A agonist

NLX-266 is a potent, selective, orally available and metabolically stable ERK1/2-biased 5-HT1A receptor agonist with binding pKi of 10.35, >1000-fold selective over adrenergic α1 and dopaminergic D2 receptors.
PC-24453

Brexpiprazole

CAS 913611-97-9

Brexpiprazole (OPC-34712) is an atypical orally active antipsychotic agent and partial agonist of human 5-HT1A and dopamine D2L receptor with Ki of 0.12 nM and 0.3 nM, respectively.
PC-24324

MW073

5-HT2bR inhibitor

MW073 is a highly selective and orally bioavailable inhibitor of 5-HT2b receptor (5-HT2bR) with binding IC50 of 70 nM.
PC-24283

AM1476

5-HT2B inhibitor

AM1476 is a highly selective 5-HT2B receptor (5-HT2BR) inhibitor with IC50 of 5.8 nM, showed only low activity at the5-HT2AR (IC50 >10 000 nM) and 5-HT2CR.
PC-24221

PUC-55

5-HT6R antagonist

PUC-10 is a selective 5-HT6 receptor antagonist high binding affinity (Ki=37.5 nM), induces autophagy in the neuroblastoma SH-SY5Y cell line by inhibiting the mTOR pathway.
PC-24220

PUC-10

5-HT6R antagonist

PUC-10 is a selective 5-HT6 receptor antagonist high binding affinity (Ki=14.6 nM) and IC50 of 32 nM in calcium mobilisation functional assay, induces mTOR-dependent autophagy.
PC-24197

AAZ-A-154

5-HT2R ligand

Zalsupindole (AAZ-A-154) is a potent, highly selective non-hallucinogenic psychLight competitive ligand/antagonist of 5-HT2A receptor (5-HT2AR), exhibits antidepressant-like effects.
PC-24117

Bretisilocin

5-HT2A agonist

Bretisilocin is a potent, selective 5-HT2A receptor agonist with the EC50 of 5.54 nM.
PC-24116

Bretisilocin hydrochloride

5-HT2A agonist

Bretisilocin hydrochloride is a potent, selective 5-HT2A receptor agonist with the EC50 of 5.54 nM.

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