Home - Products - Endocrinology/Hormones - 5-HT Receptor - SB-200646

SB-200646

CAS No. 143797-63-1

SB-200646 ( —— )

Catalog No. M21616 CAS No. 143797-63-1

SB-200646 is a selective and potent?antagonist of 5-HT2B/5-HT2C receptor.

Purity : >98% (HPLC)

COA

Datasheet

HNMR

HPLC

MSDS

Handing Instructions

Size	Price / USD	Stock	Quantity
2MG	138	Get Quote
5MG	196	Get Quote
10MG	295	Get Quote
25MG	498	Get Quote
50MG	716	Get Quote
100MG	981	Get Quote
200MG	Get Quote	Get Quote
500MG	Get Quote	Get Quote
1G	Get Quote	Get Quote

Group Booking Get Quotation Bulk Inquiry Add to Cart

Biological Information

Product Name

SB-200646
Note

Research use only not for human use.
Brief Description

SB-200646 is a selective and potent?antagonist of 5-HT2B/5-HT2C receptor.
Description

SB-200646 is a selective and potent?antagonist of 5-HT2B/5-HT2C receptor.
Synonyms

——
Pathway

Endocrinology/Hormones
Target

5-HT Receptor
Recptor

5-HT2B;5-HT2C
Research Area

——
Indication

——

Chemical Information

CAS Number

143797-63-1
Formula Weight

266.3
Molecular Formula

C15H14N4O??
Purity

>98% (HPLC)
Solubility

DMSO:53 mg/mL (199.02 mM)
SMILES

Cn1ccc2cc(NC(=O)Nc3cccnc3)ccc12
Chemical Name

——

Shipping & Storage Information

Storage

(-20℃)
Shipping

With Ice Pack
Stability

≥ 2 years

Reference

1.Kennett GA et al. In vivo properties of SB 200646A a 5-HT2C/2B receptor antagonist. Br J Pharmacol. 1994 Mar;111(3):797-802.

Calculator

Molecular Weight Calculator

Dilution Calculator

Molarity Calculator

molnova catalog

related products

Setiptiline

A tetracyclic antidepressant (TeCA) that acts as a norepinephrine reuptake inhibitor, α2-adrenergic receptor antagonist.
Velusetrag

Velusetrag (TD-5108) is a potent, selective and oral 5-HT4 receptor agonist with pKi of 7.7.
Cerlapirdine

Cerlapirdine is a selective, potent, full antagonist of the 5-hydroxytryptamine 6 (5-HT6) receptor. Cerlapirdine is already in clinical development for the treatment of cognitive disorders related to Alzheimer's disease and schizophrenia. It works by acting as a selective 5-HT6 receptor antagonist.

Sign In Join Free