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Details

Stereochemistry ACHIRAL
Molecular Formula C23H30N8O.C4H6O4
Molecular Weight 552.6253
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of RIBOCICLIB SUCCINATE

SMILES

OC(=O)CCC(O)=O.CN(C)C(=O)C1=CC2=CN=C(NC3=NC=C(C=C3)N4CCNCC4)N=C2N1C5CCCC5

InChI

InChIKey=NHANOMFABJQAAH-UHFFFAOYSA-N
InChI=1S/C23H30N8O.C4H6O4/c1-29(2)22(32)19-13-16-14-26-23(28-21(16)31(19)17-5-3-4-6-17)27-20-8-7-18(15-25-20)30-11-9-24-10-12-30;5-3(6)1-2-4(7)8/h7-8,13-15,17,24H,3-6,9-12H2,1-2H3,(H,25,26,27,28);1-2H2,(H,5,6)(H,7,8)

HIDE SMILES / InChI

Molecular Formula C23H30N8O
Molecular Weight 434.5373
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Molecular Formula C4H6O4
Molecular Weight 118.088
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 08:41:07 UTC 2023
Edited
by admin
on Sat Dec 16 08:41:07 UTC 2023
Record UNII
BG7HLX2919
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
RIBOCICLIB SUCCINATE
USAN  
USAN  
Official Name English
Ribociclib succinate [WHO-DD]
Common Name English
BUTANEDIOIC ACID, COMPD. WITH 7-CYCLOPENTYL-N,N-DIMETHYL-2-((5-(1-PIPERAZINYL)-2-PYRIDINYL)AMINO)-7H-PYRROLO(2,3-D)PYRIMIDINE-6-CARBOXAMIDE (1:1)
Common Name English
RIBOCICLIB SUCCINATE [MI]
Common Name English
LEE-011-BBA
Code English
RIBOCICLIB SUCCINATE COMPONENT OF KISQALI FEMARA CO-PACK
Brand Name English
Birociclib [WHO-DD]
Common Name English
LEE011-BBA
Code English
LEE-011 SUCCINATE
Code English
KISQALI FEMARA CO-PACK COMPONENT RIBOCICLIB SUCCINATE
Brand Name English
RIBOCICLIB SUCCINATE [ORANGE BOOK]
Common Name English
KISQALI
Brand Name English
RIBOCICLIB SUCCINATE [USAN]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C2185
Created by admin on Sat Dec 16 08:41:08 UTC 2023 , Edited by admin on Sat Dec 16 08:41:08 UTC 2023
Code System Code Type Description
CAS
1374639-75-4
Created by admin on Sat Dec 16 08:41:08 UTC 2023 , Edited by admin on Sat Dec 16 08:41:08 UTC 2023
PRIMARY
ChEMBL
CHEMBL3545110
Created by admin on Sat Dec 16 08:41:08 UTC 2023 , Edited by admin on Sat Dec 16 08:41:08 UTC 2023
PRIMARY
MERCK INDEX
m12002
Created by admin on Sat Dec 16 08:41:08 UTC 2023 , Edited by admin on Sat Dec 16 08:41:08 UTC 2023
PRIMARY
USAN
DE-30
Created by admin on Sat Dec 16 08:41:08 UTC 2023 , Edited by admin on Sat Dec 16 08:41:08 UTC 2023
PRIMARY
EPA CompTox
DTXSID301027923
Created by admin on Sat Dec 16 08:41:08 UTC 2023 , Edited by admin on Sat Dec 16 08:41:08 UTC 2023
PRIMARY
NCI_THESAURUS
C152210
Created by admin on Sat Dec 16 08:41:08 UTC 2023 , Edited by admin on Sat Dec 16 08:41:08 UTC 2023
PRIMARY
RXCUI
1873978
Created by admin on Sat Dec 16 08:41:08 UTC 2023 , Edited by admin on Sat Dec 16 08:41:08 UTC 2023
PRIMARY
PUBCHEM
57334219
Created by admin on Sat Dec 16 08:41:08 UTC 2023 , Edited by admin on Sat Dec 16 08:41:08 UTC 2023
PRIMARY
FDA UNII
BG7HLX2919
Created by admin on Sat Dec 16 08:41:08 UTC 2023 , Edited by admin on Sat Dec 16 08:41:08 UTC 2023
PRIMARY
EVMPD
SUB184164
Created by admin on Sat Dec 16 08:41:08 UTC 2023 , Edited by admin on Sat Dec 16 08:41:08 UTC 2023
PRIMARY
DAILYMED
BG7HLX2919
Created by admin on Sat Dec 16 08:41:08 UTC 2023 , Edited by admin on Sat Dec 16 08:41:08 UTC 2023
PRIMARY
DRUG BANK
DBSALT002583
Created by admin on Sat Dec 16 08:41:08 UTC 2023 , Edited by admin on Sat Dec 16 08:41:08 UTC 2023
PRIMARY
SMS_ID
100000170331
Created by admin on Sat Dec 16 08:41:08 UTC 2023 , Edited by admin on Sat Dec 16 08:41:08 UTC 2023
PRIMARY
Related Record Type Details
PARENT -> SALT/SOLVATE
Related Record Type Details
ACTIVE MOIETY