U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry RACEMIC
Molecular Formula C45H48F3N7O6S
Molecular Weight 871.966
Optical Activity ( + / - )
Defined Stereocenters 2 / 3
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of Zomiradomide

SMILES

CC(C)(O)C1=CC2=C(SC(=N2)[C@H]3CC[C@H](CN4CC5(CC(CCNC6=CC=CC7=C6C(=O)N(C8CCC(=O)NC8=O)C7=O)C5)C4)CC3)C=C1NC(=O)C9=CC=CC(=N9)C(F)(F)F

InChI

InChIKey=WDRJGMSUTPVXDH-KBOGUJPVSA-N
InChI=1S/C45H48F3N7O6S/c1-43(2,61)28-17-32-34(18-31(28)51-38(57)30-7-4-8-35(50-30)45(46,47)48)62-40(52-32)26-11-9-24(10-12-26)21-54-22-44(23-54)19-25(20-44)15-16-49-29-6-3-5-27-37(29)42(60)55(41(27)59)33-13-14-36(56)53-39(33)58/h3-8,17-18,24-26,33,49,61H,9-16,19-23H2,1-2H3,(H,51,57)(H,53,56,58)/t24-,26-,33?

HIDE SMILES / InChI

Approval Year

Name Type Language
rac-N-[2 <sup>1</sup> ,2 <sup>4</sup> -trans-(9 <sup>3</sup>R)-1<sup> 5</sup> -(2-hydroxypropan-2-yl)-8 <sup>1</sup> ,8 <sup>3</sup> ,9 <sup>2</sup> ,9 <sup>6</sup> -tetraoxo-8 <sup>1</sup> ,8 3 -dihydro-4 <sup>2</sup> ,7-diaza-1(2)-[1,3]benzothiazola-8(
Preferred Name English
Zomiradomide
INN  
Official Name English
zomiradomide [INN]
Common Name English
N-[2-[trans-4-[[6-[2-[[2-(2,6-Dioxo-3-piperidinyl)-2,3-dihydro-1,3-dioxo-1H-isoindol-4-yl]amino]ethyl]-2-azaspiro[3.3]hept-2-yl]methyl]cyclohexyl]-5-(1-hydroxy-1-methylethyl)-6-benzothiazolyl]-6-(trifluoromethyl)-2-pyridinecarboxamide
Systematic Name English
2-Pyridinecarboxamide, N-[2-[trans-4-[[6-[2-[[2-(2,6-dioxo-3-piperidinyl)-2,3-dihydro-1,3-dioxo-1H-isoindol-4-yl]amino]ethyl]-2-azaspiro[3.3]hept-2-yl]methyl]cyclohexyl]-5-(1-hydroxy-1-methylethyl)-6-benzothiazolyl]-6-(trifluoromethyl)-
Systematic Name English
Code System Code Type Description
NCI_THESAURUS
C190059
Created by admin on Wed Apr 02 11:19:34 GMT 2025 , Edited by admin on Wed Apr 02 11:19:34 GMT 2025
PRIMARY
INN
12914
Created by admin on Wed Apr 02 11:19:34 GMT 2025 , Edited by admin on Wed Apr 02 11:19:34 GMT 2025
PRIMARY
FDA UNII
AQ5UXV5646
Created by admin on Wed Apr 02 11:19:34 GMT 2025 , Edited by admin on Wed Apr 02 11:19:34 GMT 2025
PRIMARY
CAS
2655656-99-6
Created by admin on Wed Apr 02 11:19:34 GMT 2025 , Edited by admin on Wed Apr 02 11:19:34 GMT 2025
PRIMARY