U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ABSOLUTE
Molecular Formula C30H30F2N6O3
Molecular Weight 560.5944
Optical Activity UNSPECIFIED
Defined Stereocenters 1 / 1
E/Z Centers 0
Charge 0
Stereo Comments AXIAL, R

SHOW SMILES / InChI
Structure of SOTORASIB

SMILES

CC(C)C1=NC=CC(C)=C1N2C(=O)N=C(N3CCN(C[C@@H]3C)C(=O)C=C)C4=C2N=C(C(F)=C4)C5=C(F)C=CC=C5O

InChI

InChIKey=NXQKSXLFSAEQCZ-SFHVURJKSA-N
InChI=1S/C30H30F2N6O3/c1-6-23(40)36-12-13-37(18(5)15-36)28-19-14-21(32)26(24-20(31)8-7-9-22(24)39)34-29(19)38(30(41)35-28)27-17(4)10-11-33-25(27)16(2)3/h6-11,14,16,18,39H,1,12-13,15H2,2-5H3/t18-/m0/s1

HIDE SMILES / InChI

Approval Year

Name Type Language
SOTORASIB
USAN   INN  
Official Name English
SOTORASIB [JAN]
Common Name English
SOTORASIB [ORANGE BOOK]
Common Name English
sotorasib [INN]
Common Name English
KRAS MUTANT-TARGETING AMG 510
Common Name English
Sotorasib [WHO-DD]
Common Name English
PYRIDO(2,3-D)PYRIMIDIN-2(1H)-ONE, 6-FLUORO-7-(2-FLUORO-6-HYDROXYPHENYL)-1-(4-METHYL-2-(1-METHYLETHYL)-3-PYRIDINYL)-4-((2S)-2-METHYL-4-(1-OXO-2-PROPEN-1-YL)-1-PIPERAZINYL)-
Systematic Name English
PYRIDO(2,3-D)PYRIMIDIN-2(1H)-ONE, 6-FLUORO-7-(2-FLUORO-6-HYDROXYPHENYL)-1-(4-METHYL-2-(1-METHYLETHYL)-3-PYRIDINYL)-4-((2S)-2-METHYL-4-(1-OXO-2-PROPEN-1-YL)-1-PIPERAZINYL)-, (1R)-
Systematic Name English
AMG-510
Code English
LUMAKRAS
Brand Name English
AMG510
Code English
(1RA)-6-FLUORO-7-(2-FLUORO-6-HYDROXYPHENYL)-4-((2S)-2-METHYL-4-(1-OXOPROP-2-EN-1-YL)PIPERAZIN-1-YL)-1-(4-METHYL-2-(PROPAN-2-YL)PYRIDIN-3-YL)PYRIDO(2,3-D)PYRIMIDIN-2(1H)-ONE
Systematic Name English
(1M)-6-FLUORO-7-(2-FLUORO-6-HYDROXYPHENYL)-1-(4-METHYL-2-(PROPAN-2-YL)PYRIDIN-3-YL)-4-((2S)-2-METHYL-4-(PROP-2-ENOYL)PIPERAZIN-1-YL)PYRIDO(2,3-D)PYRIMIDIN-2(1H)-ONE
Systematic Name English
SOTORASIB [USAN]
Common Name English
6-FLUORO-7-(2-FLUORO-6-HYDROXYPHENYL)-(1M)-1-(4-METHYL-2-(PROPAN-2-YL)PYRIDIN-3-YL)-4-((2S)-2-METHYL-4-(PROP-2-ENOYL)PIPERAZIN-1-YL)PYRIDO(2,3-D)PYRIMIDIN-2(1H)-ONE
Systematic Name English
KRAS G12C INHIBITOR 9
Common Name English
Classification Tree Code System Code
FDA ORPHAN DRUG 654918
Created by admin on Sat Dec 16 14:33:41 UTC 2023 , Edited by admin on Sat Dec 16 14:33:41 UTC 2023
FDA ORPHAN DRUG 653818
Created by admin on Sat Dec 16 14:33:41 UTC 2023 , Edited by admin on Sat Dec 16 14:33:41 UTC 2023
Code System Code Type Description
FDA UNII
2B2VM6UC8G
Created by admin on Sat Dec 16 14:33:41 UTC 2023 , Edited by admin on Sat Dec 16 14:33:41 UTC 2023
PRIMARY
PUBCHEM
137278711
Created by admin on Sat Dec 16 14:33:41 UTC 2023 , Edited by admin on Sat Dec 16 14:33:41 UTC 2023
PRIMARY
CAS
2252403-56-6
Created by admin on Sat Dec 16 14:33:41 UTC 2023 , Edited by admin on Sat Dec 16 14:33:41 UTC 2023
NON-SPECIFIC STEREOCHEMISTRY
DAILYMED
2B2VM6UC8G
Created by admin on Sat Dec 16 14:33:41 UTC 2023 , Edited by admin on Sat Dec 16 14:33:41 UTC 2023
PRIMARY
USAN
HI-164
Created by admin on Sat Dec 16 14:33:41 UTC 2023 , Edited by admin on Sat Dec 16 14:33:41 UTC 2023
PRIMARY
WIKIPEDIA
Sotorasib
Created by admin on Sat Dec 16 14:33:41 UTC 2023 , Edited by admin on Sat Dec 16 14:33:41 UTC 2023
PRIMARY
CAS
2296729-00-3
Created by admin on Sat Dec 16 14:33:41 UTC 2023 , Edited by admin on Sat Dec 16 14:33:41 UTC 2023
PRIMARY
DRUG BANK
DB15569
Created by admin on Sat Dec 16 14:33:41 UTC 2023 , Edited by admin on Sat Dec 16 14:33:41 UTC 2023
PRIMARY
INN
11370
Created by admin on Sat Dec 16 14:33:41 UTC 2023 , Edited by admin on Sat Dec 16 14:33:41 UTC 2023
PRIMARY
SMS_ID
100000183068
Created by admin on Sat Dec 16 14:33:41 UTC 2023 , Edited by admin on Sat Dec 16 14:33:41 UTC 2023
PRIMARY
NCI_THESAURUS
C154287
Created by admin on Sat Dec 16 14:33:41 UTC 2023 , Edited by admin on Sat Dec 16 14:33:41 UTC 2023
PRIMARY
EPA CompTox
DTXSID001099260
Created by admin on Sat Dec 16 14:33:41 UTC 2023 , Edited by admin on Sat Dec 16 14:33:41 UTC 2023
PRIMARY
RXCUI
2550714
Created by admin on Sat Dec 16 14:33:41 UTC 2023 , Edited by admin on Sat Dec 16 14:33:41 UTC 2023
PRIMARY