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Details

Stereochemistry ACHIRAL
Molecular Formula C14H13BrN2O
Molecular Weight 305.17
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of Tyrphostin AG-1024

SMILES

CC(C)(C)C1=CC(C=C(C#N)C#N)=CC(Br)=C1O

InChI

InChIKey=ABBADGFSRBWENF-UHFFFAOYSA-N
InChI=1S/C14H13BrN2O/c1-14(2,3)11-5-9(4-10(7-16)8-17)6-12(15)13(11)18/h4-6,18H,1-3H3

HIDE SMILES / InChI

Molecular Formula C14H13BrN2O
Molecular Weight 305.17
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Target ID: P08069
Gene ID: 3480.0
Gene Symbol: IGF1R
Target Organism: Homo sapiens (Human)
7.0 µM [IC50]
Target ID: P06213
Gene ID: 3643.0
Gene Symbol: INSR
Target Organism: Homo sapiens (Human)
57.0 µM [IC50]
PubMed

PubMed

TitleDatePubMed
Substance Class Chemical
Created
by admin
on Tue Apr 01 19:01:26 GMT 2025
Edited
by admin
on Tue Apr 01 19:01:26 GMT 2025
Record UNII
NF4XN6A8V9
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
Tyrphostin AG-1024
Common Name English
AG-1024
Preferred Name English
2-[(3-Bromo-5-tert-butyl-4-hydroxyphenyl)methylidene]propanedinitrile
Systematic Name English
AGS-200
Code English
Propanedinitrile, 2-[[3-bromo-5-(1,1-dimethylethyl)-4-hydroxyphenyl]methylene]-
Systematic Name English
2-[[3-Bromo-5-(1,1-dimethylethyl)-4-hydroxyphenyl]methylene]propanedinitrile
Systematic Name English
Code System Code Type Description
PUBCHEM
2044
Created by admin on Tue Apr 01 19:01:26 GMT 2025 , Edited by admin on Tue Apr 01 19:01:26 GMT 2025
PRIMARY
FDA UNII
NF4XN6A8V9
Created by admin on Tue Apr 01 19:01:26 GMT 2025 , Edited by admin on Tue Apr 01 19:01:26 GMT 2025
PRIMARY
EPA CompTox
DTXSID50274350
Created by admin on Tue Apr 01 19:01:26 GMT 2025 , Edited by admin on Tue Apr 01 19:01:26 GMT 2025
PRIMARY
CAS
65678-07-1
Created by admin on Tue Apr 01 19:01:26 GMT 2025 , Edited by admin on Tue Apr 01 19:01:26 GMT 2025
PRIMARY
Related Record Type Details
TARGET -> INHIBITOR