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Details

Stereochemistry ACHIRAL
Molecular Formula C21H18FN5O
Molecular Weight 375.3989
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of LINIFANIB

SMILES

CC1=CC(NC(=O)NC2=CC=C(C=C2)C3=C4C(N)=NNC4=CC=C3)=C(F)C=C1

InChI

InChIKey=MPVGZUGXCQEXTM-UHFFFAOYSA-N
InChI=1S/C21H18FN5O/c1-12-5-10-16(22)18(11-12)25-21(28)24-14-8-6-13(7-9-14)15-3-2-4-17-19(15)20(23)27-26-17/h2-11H,1H3,(H3,23,26,27)(H2,24,25,28)

HIDE SMILES / InChI

Molecular Formula C21H18FN5O
Molecular Weight 375.3989
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 16:31:41 UTC 2023
Edited
by admin
on Sat Dec 16 16:31:41 UTC 2023
Record UNII
CO93X137CW
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
LINIFANIB
INN   USAN   WHO-DD  
USAN   INN  
Official Name English
RG-3635
Code English
LINIFANIB [USAN]
Common Name English
UREA, N-(4-(3-AMINO-1H-INDAZOL-4-YL)PHENYL)-N'-(2-FLUORO-5-METHYLPHENYL)-
Systematic Name English
1-(4-(3-AMINO-1H-INDAZOL-4-YL)PHENYL)-3-(2-FLUORO-5-METHYLPHENYL)UREA
Systematic Name English
A-741439
Code English
ABT-869
Code English
linifanib [INN]
Common Name English
Linifanib [WHO-DD]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C1967
Created by admin on Sat Dec 16 16:31:41 UTC 2023 , Edited by admin on Sat Dec 16 16:31:41 UTC 2023
NCI_THESAURUS C93259
Created by admin on Sat Dec 16 16:31:41 UTC 2023 , Edited by admin on Sat Dec 16 16:31:41 UTC 2023
FDA ORPHAN DRUG 240807
Created by admin on Sat Dec 16 16:31:41 UTC 2023 , Edited by admin on Sat Dec 16 16:31:41 UTC 2023
FDA ORPHAN DRUG 248007
Created by admin on Sat Dec 16 16:31:41 UTC 2023 , Edited by admin on Sat Dec 16 16:31:41 UTC 2023
Code System Code Type Description
WIKIPEDIA
LINIFANIB
Created by admin on Sat Dec 16 16:31:41 UTC 2023 , Edited by admin on Sat Dec 16 16:31:41 UTC 2023
PRIMARY
USAN
UU-147
Created by admin on Sat Dec 16 16:31:41 UTC 2023 , Edited by admin on Sat Dec 16 16:31:41 UTC 2023
PRIMARY
PUBCHEM
11485656
Created by admin on Sat Dec 16 16:31:41 UTC 2023 , Edited by admin on Sat Dec 16 16:31:41 UTC 2023
PRIMARY
FDA UNII
CO93X137CW
Created by admin on Sat Dec 16 16:31:41 UTC 2023 , Edited by admin on Sat Dec 16 16:31:41 UTC 2023
PRIMARY
INN
9195
Created by admin on Sat Dec 16 16:31:41 UTC 2023 , Edited by admin on Sat Dec 16 16:31:41 UTC 2023
PRIMARY
SMS_ID
100000126073
Created by admin on Sat Dec 16 16:31:41 UTC 2023 , Edited by admin on Sat Dec 16 16:31:41 UTC 2023
PRIMARY
EVMPD
SUB33027
Created by admin on Sat Dec 16 16:31:41 UTC 2023 , Edited by admin on Sat Dec 16 16:31:41 UTC 2023
PRIMARY
NCI_THESAURUS
C71759
Created by admin on Sat Dec 16 16:31:41 UTC 2023 , Edited by admin on Sat Dec 16 16:31:41 UTC 2023
PRIMARY
EPA CompTox
DTXSID40229834
Created by admin on Sat Dec 16 16:31:41 UTC 2023 , Edited by admin on Sat Dec 16 16:31:41 UTC 2023
PRIMARY
CAS
796967-16-3
Created by admin on Sat Dec 16 16:31:41 UTC 2023 , Edited by admin on Sat Dec 16 16:31:41 UTC 2023
PRIMARY
DRUG BANK
DB06080
Created by admin on Sat Dec 16 16:31:41 UTC 2023 , Edited by admin on Sat Dec 16 16:31:41 UTC 2023
PRIMARY
ChEMBL
CHEMBL223360
Created by admin on Sat Dec 16 16:31:41 UTC 2023 , Edited by admin on Sat Dec 16 16:31:41 UTC 2023
PRIMARY
Related Record Type Details
TARGET -> INHIBITOR
Related Record Type Details
METABOLITE ACTIVE -> PARENT
Active: CLK2, CSF1R, DYRK1A, FLT3, GSK3A, GSK3B, JAK2, JAK3, KDR, LIMK1, MAP4K2, MAP4K4, PRKACA, PRKX, ROCK1, STK12, STK6, TAO1, CLK4, MET, PLK4, PLK3, ROCK2, SGK, MARK3, STK3, CDC7, CDK2, CSNK1G2, IRAK3, IRAK4, MINK, MKNK2, RPS6KA5, RPS6KB1, CDC2, CSNK2A1, DYRK3, HIPK4, KIAA1811, MAP4K5, TOPK, CSNK1D, SRPK1, ZAK, PRKG1, PRKG2, FLT4, MARK2, PASK, CDK5
IN-VITRO
METABOLITE ACTIVE -> PARENT
IN-VIVO
PLASMA
Related Record Type Details
ACTIVE MOIETY