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

Details

Stereochemistry ABSOLUTE
Molecular Formula C22H22F3N3O6
Molecular Weight 481.4218
Optical Activity UNSPECIFIED
Defined Stereocenters 1 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of ABT-770

SMILES

CC1(C)NC(=O)N(C[C@@H](COC2=CC=C(C=C2)C3=CC=C(OC(F)(F)F)C=C3)N(O)C=O)C1=O

InChI

InChIKey=IIHFBHZWJNGWRC-INIZCTEOSA-N
InChI=1S/C22H22F3N3O6/c1-21(2)19(30)27(20(31)26-21)11-16(28(32)13-29)12-33-17-7-3-14(4-8-17)15-5-9-18(10-6-15)34-22(23,24)25/h3-10,13,16,32H,11-12H2,1-2H3,(H,26,31)/t16-/m0/s1

HIDE SMILES / InChI

Molecular Formula C22H22F3N3O6
Molecular Weight 481.4218
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 1 / 1
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

PubMed

PubMed

TitleDatePubMed
Analysis of two matrix metalloproteinase inhibitors and their metabolites for induction of phospholipidosis in rat and human hepatocytes(1).
2001-12-15
Patents

Patents

Substance Class Chemical
Created
by admin
on Mon Mar 31 18:18:34 GMT 2025
Edited
by admin
on Mon Mar 31 18:18:34 GMT 2025
Record UNII
I8NWP25THF
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
FORMAMIDE, N-((1S)-1-((4,4-DIMETHYL-2,5-DIOXO-1-IMIDAZOLIDINYL)METHYL)-2-((4'-(TRIFLUOROMETHOXY)(1,1'-BIPHENYL)-4-YL)OXY)ETHYL)-N-HYDROXY-
Preferred Name English
ABT-770
Common Name English
N-((1S)-2-(4,4-DIMETHYL-2,5-DIOXO-1-IMIDAZOLIDINYL)-1-(((4'-(TRIFLUOROMETHOXY)(1,1'-BIPHENYL)-4-YL)OXY)METHYL)ETHYL)-N-HYDROXYFORMAMIDE
Systematic Name English
Code System Code Type Description
FDA UNII
I8NWP25THF
Created by admin on Mon Mar 31 18:18:34 GMT 2025 , Edited by admin on Mon Mar 31 18:18:34 GMT 2025
PRIMARY
PUBCHEM
9869811
Created by admin on Mon Mar 31 18:18:34 GMT 2025 , Edited by admin on Mon Mar 31 18:18:34 GMT 2025
PRIMARY
MESH
C442959
Created by admin on Mon Mar 31 18:18:34 GMT 2025 , Edited by admin on Mon Mar 31 18:18:34 GMT 2025
PRIMARY
CAS
220614-50-6
Created by admin on Mon Mar 31 18:18:34 GMT 2025 , Edited by admin on Mon Mar 31 18:18:34 GMT 2025
PRIMARY
Related Record Type Details
ACTIVE MOIETY