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Details

Stereochemistry ABSOLUTE
Molecular Formula C22H24FN5O4
Molecular Weight 441.4555
Optical Activity UNSPECIFIED
Defined Stereocenters 2 / 2
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of BRIVANIB ALANINATE

SMILES

C[C@H](COC1=CN2N=CN=C(OC3=C(F)C4=C(NC(C)=C4)C=C3)C2=C1C)OC(=O)[C@H](C)N

InChI

InChIKey=LTEJRLHKIYCEOX-OCCSQVGLSA-N
InChI=1S/C22H24FN5O4/c1-11-7-15-16(27-11)5-6-17(19(15)23)32-21-20-13(3)18(8-28(20)26-10-25-21)30-9-12(2)31-22(29)14(4)24/h5-8,10,12,14,27H,9,24H2,1-4H3/t12-,14+/m1/s1

HIDE SMILES / InChI

Molecular Formula C22H24FN5O4
Molecular Weight 441.4555
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 2 / 2
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

Substance Class Chemical
Created
by admin
on Fri Dec 15 15:56:19 UTC 2023
Edited
by admin
on Fri Dec 15 15:56:19 UTC 2023
Record UNII
U2Y5OFN795
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
BRIVANIB ALANINATE
INN   USAN   WHO-DD  
INN   USAN  
Official Name English
BRIVANIB L-ALANINE ESTER [MI]
Common Name English
BRIVANIB ALANINATE [USAN]
Common Name English
BRIVANIB ALANINATE [JAN]
Common Name English
Brivanib alaninate [WHO-DD]
Common Name English
(1R)-2-[[4-[(4-Fluoro-2-methyl-1H-indol-5-yl)oxy]-5-methylpyrrolo[2,1-f][1,2,4]triazin-6-yl]oxy]-1-methylethyl (2S)-2-aminopropanoate
Systematic Name English
BMS-582664-02
Code English
BMS-582664
Code English
L-ALANINE, (1R)-2-((4-((4-FLUORO-2-METHYL-1H-INDOL-5-YL)OXY)-5-METHYLPYRROLO(2,1-F)(1,2,4)TRIAZIN-6-YL)OXY)-1-METHYLETHYL ESTER
Common Name English
brivanib alaninate [INN]
Common Name English
Classification Tree Code System Code
FDA ORPHAN DRUG 336311
Created by admin on Fri Dec 15 15:56:19 UTC 2023 , Edited by admin on Fri Dec 15 15:56:19 UTC 2023
NCI_THESAURUS C1967
Created by admin on Fri Dec 15 15:56:19 UTC 2023 , Edited by admin on Fri Dec 15 15:56:19 UTC 2023
EU-Orphan Drug EU/3/11/918
Created by admin on Fri Dec 15 15:56:19 UTC 2023 , Edited by admin on Fri Dec 15 15:56:19 UTC 2023
NCI_THESAURUS C1742
Created by admin on Fri Dec 15 15:56:19 UTC 2023 , Edited by admin on Fri Dec 15 15:56:19 UTC 2023
Code System Code Type Description
PUBCHEM
11154925
Created by admin on Fri Dec 15 15:56:19 UTC 2023 , Edited by admin on Fri Dec 15 15:56:19 UTC 2023
PRIMARY
INN
8879
Created by admin on Fri Dec 15 15:56:19 UTC 2023 , Edited by admin on Fri Dec 15 15:56:19 UTC 2023
PRIMARY
FDA UNII
U2Y5OFN795
Created by admin on Fri Dec 15 15:56:19 UTC 2023 , Edited by admin on Fri Dec 15 15:56:19 UTC 2023
PRIMARY
NCI_THESAURUS
C53397
Created by admin on Fri Dec 15 15:56:19 UTC 2023 , Edited by admin on Fri Dec 15 15:56:19 UTC 2023
PRIMARY
EVMPD
SUB26391
Created by admin on Fri Dec 15 15:56:19 UTC 2023 , Edited by admin on Fri Dec 15 15:56:19 UTC 2023
PRIMARY
USAN
SS-94
Created by admin on Fri Dec 15 15:56:19 UTC 2023 , Edited by admin on Fri Dec 15 15:56:19 UTC 2023
PRIMARY
EPA CompTox
DTXSID20215295
Created by admin on Fri Dec 15 15:56:19 UTC 2023 , Edited by admin on Fri Dec 15 15:56:19 UTC 2023
PRIMARY
DRUG BANK
DB11865
Created by admin on Fri Dec 15 15:56:19 UTC 2023 , Edited by admin on Fri Dec 15 15:56:19 UTC 2023
PRIMARY
ChEMBL
CHEMBL270995
Created by admin on Fri Dec 15 15:56:19 UTC 2023 , Edited by admin on Fri Dec 15 15:56:19 UTC 2023
PRIMARY
MERCK INDEX
m2653
Created by admin on Fri Dec 15 15:56:19 UTC 2023 , Edited by admin on Fri Dec 15 15:56:19 UTC 2023
PRIMARY Merck Index
SMS_ID
100000089608
Created by admin on Fri Dec 15 15:56:19 UTC 2023 , Edited by admin on Fri Dec 15 15:56:19 UTC 2023
PRIMARY
MESH
C509922
Created by admin on Fri Dec 15 15:56:19 UTC 2023 , Edited by admin on Fri Dec 15 15:56:19 UTC 2023
PRIMARY
CAS
649735-63-7
Created by admin on Fri Dec 15 15:56:19 UTC 2023 , Edited by admin on Fri Dec 15 15:56:19 UTC 2023
PRIMARY
CHEBI
167656
Created by admin on Fri Dec 15 15:56:19 UTC 2023 , Edited by admin on Fri Dec 15 15:56:19 UTC 2023
PRIMARY
WIKIPEDIA
BRIVANIB ALANINATE
Created by admin on Fri Dec 15 15:56:19 UTC 2023 , Edited by admin on Fri Dec 15 15:56:19 UTC 2023
PRIMARY
Related Record Type Details
METABOLITE ACTIVE -> PRODRUG
Related Record Type Details
ACTIVE MOIETY