ChemicalBook > Product Catalog >Biochemical Engineering >Inhibitors >protein tyrosine kinase >CO-1686

CO-1686

CO-1686 Structure
CAS No.
1374640-70-6
Chemical Name:
CO-1686
Synonyms
CS-851;CNX-419;AVL-301;CO-1686;ROCILETINIB;Pyridostadin;CO-1686, >=98%;Clovis CO-1686;CO-1686/CO1686;CO-1686 (AVL-301)
CBNumber:
CB22666396
Molecular Formula:
C27H28F3N7O3
Molecular Weight:
555.55
MOL File:
1374640-70-6.mol
MSDS File:
SDS
Modify Date:
2023/6/8 9:03:09

CO-1686 Properties

Melting point 202 - 205°C (dec.)
Density 1.372±0.06 g/cm3(Predicted)
storage temp. Amber Vial, -20°C Freezer, Under inert atmosphere
solubility DMSO (Slightly), Methanol (Slightly)
form Solid
pka 13.23±0.70(Predicted)
color Off-White
CAS DataBase Reference 1374640-70-6

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS07
Signal word  Warning
Hazard statements  H302-H315-H319-H335
Precautionary statements  P261-P264-P270-P271-P280-P301+P312-P330-P302+P352-P321-P304+P340-P305+P351+P338-P332+P313-P362+P364-P337+P313-P403+P233-P405-P501
Risk Statements  23-25-36
Safety Statements  24
HS Code  29335990
NFPA 704
0
2 0

CO-1686 Chemical Properties,Uses,Production

Description

CO-1686 is an irreversible kinase inhibitor that specifically targets mutant forms of the epidermal growth factor receptor (EGFR) including T790M (Ki = 21.5 nM) with significantly reduced activity at the wild-type form of the receptor (Ki = 303.3 nM). CO-1686 has been shown to inhibit the proliferation of non-small cell lung cancer (NSCLC) cells expressing mutant EGFR with GI50 values ranging from 7-32 nM in vitro, inducing apoptosis. It also demonstrates anti-tumor activity in NSCLC EGFR mutant xenograft and transgenic models dosed orally at 100 mg/kg/day.

Uses

CO 1686 is seen as an irreversible epidermal growth factor receptor (EFGR1) kinase inhibitor.

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CO-1686 Spectrum

CO-1686 AVL-301 CNX-419 CO-1686 (AVL-301) CO-1686/CO1686 N-[3-[[2-[[4-(4-Acetyl-1-piperazinyl)-2-methoxyphenyl]amino]-5-(trifluoromethyl)-4-pyrimidinyl]amino]phenyl]-2-propenamide Clovis CO-1686 CO-1686(free base) Rociletinib(AVL-301,CNX-419,CO-1686) N-(3-(2-(4-(4-acetylpiperazin-1-yl)-2-methoxyphenylamino)-5-(trifluoromethyl)pyrimidin-4-ylamino)phenyl)acrylamide CO-1686, >=98% N-[3-[[2-[4-(4-acetylpiperazin-1-yl)-2-methoxyanilino]-5-(trifluoromethyl)pyrimidin-4-yl]amino]phenyl]prop-2-enamide ROCILETINIB Rociletinib(CO1686) 2-Propenamide, N-[3-[[2-[[4-(4-acetyl-1-piperazinyl)-2-methoxyphenyl]amino]-5-(trifluoromethyl)-4-pyrimidinyl]amino]phenyl]- Rociletinib (CO-1686, AVL-301) Co 1686 N-[3-[[2-[[4-(4-Acetyl-1-piperazinyl)-2-methoxyphenyl]amino]-5-(trifluoromethyl)-4-pyrimidinyl]amino]phenyl]-2-propenamide N-[3-[[2-[[4-(4-Acetyl-1-piperazinyl)-2-methoxyphenyl]amino]-5-(trifluoromethyl)-4-pyrimidinyl]amino]phenyl]-2-propenamide Co 1686 CO-1686(ROCILETINIB) Pyridostadin N-(3-((2-((4-(4-Acetylpiperazin-1-yl)-2-methoxyphenyl)amino)-5-(trifluoromethyl)pyrimidin-4-yl CO1686; CO-1686; CO 1686; AVL301; AVL 301; AVL-301; CNX419; CNX 419; CNX-419; ROCILETINIB. Rociletinib (CO1686,CNX419) CS-851 ROCILETINIB; AVL-301; CNX-419;CO 1686;CO1686 N-(3-((2-((4-(4-Acetylpiperazin-1-yl)-2-methoxyphenyl)amino)-5-(trifluoromethyl)pyrimidin-4-yl)amino)phenyl)prop-2-enamide CO-1686 (Rociletinib, AVL-301) Pyridostadin 3TFA CO-1686 USP/EP/BP Rociletinib (CO-1686, AVL-301, CNX-419) Rociletinib(free base) Pazufloxacin Monomer 1374640-70-6 C27H28F3N7O3 Inhibitors API