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Details

Stereochemistry ACHIRAL
Molecular Formula C24H23ClFN5O5S
Molecular Weight 547.986
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of GILMELISIB

SMILES

COC1=NC=C(C=C1NS(=O)(=O)C2=C(Cl)C=C(F)C=C2)C3=CN4C(=O)C(OCCN(C)C)=CN=C4C=C3

InChI

InChIKey=BXKBZQAZYOZHJY-UHFFFAOYSA-N
InChI=1S/C24H23ClFN5O5S/c1-30(2)8-9-36-20-13-27-22-7-4-15(14-31(22)24(20)32)16-10-19(23(35-3)28-12-16)29-37(33,34)21-6-5-17(26)11-18(21)25/h4-7,10-14,29H,8-9H2,1-3H3

HIDE SMILES / InChI

Molecular Formula C24H23ClFN5O5S
Molecular Weight 547.986
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

Substance Class Chemical
Created
by admin
on Sat Dec 16 18:45:54 GMT 2023
Edited
by admin
on Sat Dec 16 18:45:54 GMT 2023
Record UNII
B9ZBD8SQ96
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
GILMELISIB
INN  
Official Name English
BENZENESULFONAMIDE, 2-CHLORO-N-(5-(3-(2-(DIMETHYLAMINO)ETHOXY)-4-OXO-4H-PYRIDO(1,2-A)PYRIMIDIN-7-YL)-2-METHOXY-3-PYRIDINYL)-4-FLUORO-
Systematic Name English
gilmelisib [INN]
Common Name English
2-CHLORO-N-(5-(3-(2-(DIMETHYLAMINO)ETHOXY)-4-OXO-4H-PYRIDO(1,2-A)PYRIMIDIN-7-YL)-2-METHOXY-3-PYRIDINYL)-4-FLUOROBENZENESULFONAMIDE
Systematic Name English
Code System Code Type Description
INN
11989
Created by admin on Sat Dec 16 18:45:54 GMT 2023 , Edited by admin on Sat Dec 16 18:45:54 GMT 2023
PRIMARY
FDA UNII
B9ZBD8SQ96
Created by admin on Sat Dec 16 18:45:54 GMT 2023 , Edited by admin on Sat Dec 16 18:45:54 GMT 2023
PRIMARY
NCI_THESAURUS
C188554
Created by admin on Sat Dec 16 18:45:54 GMT 2023 , Edited by admin on Sat Dec 16 18:45:54 GMT 2023
PRIMARY
SMS_ID
300000042065
Created by admin on Sat Dec 16 18:45:54 GMT 2023 , Edited by admin on Sat Dec 16 18:45:54 GMT 2023
PRIMARY
PUBCHEM
118612873
Created by admin on Sat Dec 16 18:45:54 GMT 2023 , Edited by admin on Sat Dec 16 18:45:54 GMT 2023
PRIMARY
CAS
1845777-61-8
Created by admin on Sat Dec 16 18:45:54 GMT 2023 , Edited by admin on Sat Dec 16 18:45:54 GMT 2023
PRIMARY
Related Record Type Details
ACTIVE MOIETY