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Details

Stereochemistry ACHIRAL
Molecular Formula C29H32N8O
Molecular Weight 508.6174
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of IDRX-42

SMILES

CN1C=C(C=N1)C2=CC=C(CNC3=NC=NC(=C3)C4=CN=C5C=C(OCCCN6CCCC6)C=CN45)C=C2

InChI

InChIKey=LVMAULGVWBINFP-UHFFFAOYSA-N
InChI=1S/C29H32N8O/c1-35-20-24(18-34-35)23-7-5-22(6-8-23)17-30-28-16-26(32-21-33-28)27-19-31-29-15-25(9-13-37(27)29)38-14-4-12-36-10-2-3-11-36/h5-9,13,15-16,18-21H,2-4,10-12,14,17H2,1H3,(H,30,32,33)

HIDE SMILES / InChI

Molecular Formula C29H32N8O
Molecular Weight 508.6174
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 18:08:42 UTC 2023
Edited
by admin
on Sat Dec 16 18:08:42 UTC 2023
Record UNII
Y6UHU32G5Z
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
IDRX-42
Code English
4-Pyrimidinamine, N-[[4-(1-methyl-1H-pyrazol-4-yl)phenyl]methyl]-6-[7-[3-(1-pyrrolidinyl)propoxy]imidazo[1,2-a]pyridin-3-yl]-
Systematic Name English
M-4205
Code English
[4-(Methyl-1H-pyrazol-4-yl)-benzyl] -(6-[7-(3-pyrrolidin-1-yl-propoxy)-imidazo[1,2-a] pyridin-3-yl]-pyrimidin-4-yl]-amine
Systematic Name English
Classification Tree Code System Code
FDA ORPHAN DRUG 892122
Created by admin on Sat Dec 16 18:08:43 UTC 2023 , Edited by admin on Sat Dec 16 18:08:43 UTC 2023
Code System Code Type Description
PUBCHEM
155587867
Created by admin on Sat Dec 16 18:08:43 UTC 2023 , Edited by admin on Sat Dec 16 18:08:43 UTC 2023
PRIMARY
FDA UNII
Y6UHU32G5Z
Created by admin on Sat Dec 16 18:08:43 UTC 2023 , Edited by admin on Sat Dec 16 18:08:43 UTC 2023
PRIMARY
CAS
2590556-80-0
Created by admin on Sat Dec 16 18:08:43 UTC 2023 , Edited by admin on Sat Dec 16 18:08:43 UTC 2023
PRIMARY
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M4205 is planned for clinical development for the treatment of patients with unresectable metastatic or recurrent gastrointestinal stromal tumors (GIST). GIST are the most common human sarcomas and driven by activating mutations in cKIT (~80%) and the related PDGFRA (~5% to 10%) receptor tyrosine kinases