SB 218795

SB 218795 Suppliers list
Company Name: 3B Pharmachem (Wuhan) International Co.,Ltd.  
Tel: 18930552037
Email: 3bsc@sina.com
Company Name: Nanjing Chemlin Chemical Co., Ltd  
Tel: 025-83697070 13770331960
Email: info@chemlin.com.cn
Company Name: Shanghai T&W Pharmaceutical Co., Ltd.  
Tel: +86 21 61551611
Email:
Company Name: EMMX Biotechnology LLC  
Tel: 888-539-0666
Email: info@emmx.com
Company Name: Shanghai YuanYe Biotechnology Co., Ltd.  
Tel: 15026964105
Email: 2881489226@qq.com
SB 218795 Basic information
Product Name:SB 218795
Synonyms:SB 218795;(-)-(R)-N-(ALPHA-METHOXYCARBONYLBENZYL)-2-PHENYLQUINOLINE-4-CARBOXAMIDE;(R)-[[(2-PHENYL-4-QUINOLINYL)CARBONYL]AMINO]-METHYL ESTER BENZENEACETIC ACID;(-)-(R)-N-(α-Methoxycarbonylbenzyl)-2-phenylquinoline-4-carboxamide;Benzeneacetic acid, alpha-(((2-phenyl-4-quinolinyl)carbonyl)amino)-, methyl ester, (alphar)-;Sb 218795r;methyl (2R)-2-phenyl-2-[(2-phenylquinoline-4-carbonyl)amino]acetate;constriction,SB-218795,Neurokinin Receptor,Inhibitor,neurokinin-3,NK receptor,pupillary,inhibit,Tachykinin receptor,SB218795,SB 218795,NK-3
CAS:174635-53-1
MF:C25H20N2O3
MW:396.44
EINECS:
Product Categories:
Mol File:174635-53-1.mol
SB 218795 Structure
SB 218795 Chemical Properties
Boiling point 623.7±55.0 °C(Predicted)
density 1.237±0.06 g/cm3(Predicted)
storage temp. 2-8°C
solubility DMSO: 40 mg/mL, soluble
form solid
pka11.41±0.46(Predicted)
color white
Safety Information
WGK Germany 3
MSDS Information
ProviderLanguage
SigmaAldrich English
SB 218795 Usage And Synthesis
UsesSB 218795 is an NK3 receptor antagonist.
DefinitionChEBI: (2R)-2-[[oxo-(2-phenyl-4-quinolinyl)methyl]amino]-2-phenylacetic acid methyl ester is a member of quinolines.
Biological ActivityPotent, selective and competitive non-peptide NK 3 receptor antagonist (K i = 13 nM at hNK 3 ). Displays 90-fold and 7000-fold selectivity over hNK 2 and hNK 1 receptors respectively. Active in vivo , inhibiting agonist-induced pupillary constriction.
in vivo

SB 218795 (0.25-1 mg/kg; i.v.) inhibits Senktide-induced miosis in rabbits by the maximum inhibition of 78%[2].

IC 50hNK3: 13 nM (Ki); hNK2: 1220 nM (Ki)
SB 218795 Preparation Products And Raw materials
Tag:SB 218795(174635-53-1) Related Product Information
N-Me-D-Phg-OH N-Methyl-1-quinolin-4-ylmethanamine For-D-Phg-OH N-(2-Hydroxyethyl)isonicotinamide, 99 D(-)-Ac-alpha-phenylglycinol CHEMBRDG-BB 9071014 SB 218795 2-methylquinoline-4-carboxamide