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

Details

Stereochemistry ACHIRAL
Molecular Formula C21H20FN5O4
Molecular Weight 425.413
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of L-870812

SMILES

CN(C)C(=O)C(=O)N(C)C1=NC(C(=O)NCC2=CC=C(F)C=C2)=C(O)C3=NC=CC=C13

InChI

InChIKey=DKMXWAOCNKDQMT-UHFFFAOYSA-N
InChI=1S/C21H20FN5O4/c1-26(2)20(30)21(31)27(3)18-14-5-4-10-23-15(14)17(28)16(25-18)19(29)24-11-12-6-8-13(22)9-7-12/h4-10,28H,11H2,1-3H3,(H,24,29)

HIDE SMILES / InChI

Molecular Formula C21H20FN5O4
Molecular Weight 425.413
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Postexposure protection of macaques from vaginal SHIV infection by topical integrase inhibitors.
2014-03-12
A series of 5-aminosubstituted 4-fluorobenzyl-8-hydroxy-[1,6]naphthyridine-7-carboxamide HIV-1 integrase inhibitors.
2006-06-01
Substance Class Chemical
Created
by admin
on Mon Mar 31 22:01:52 GMT 2025
Edited
by admin
on Mon Mar 31 22:01:52 GMT 2025
Record UNII
O168ONK0IG
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
ETHANEDIAMIDE, (7-((((4-FLUOROPHENYL)METHYL)AMINO)CARBONYL)-8-HYDROXY-1,6-NAPHTHYRIDIN-5-YL)TRIMETHYL-
Preferred Name English
L-870812
Common Name English
ETHANEDIAMIDE, N1-(7-((((4-FLUOROPHENYL)METHYL)AMINO)CARBONYL)-8-HYDROXY-1,6-NAPHTHYRIDIN-5-YL)-N1,N2,N2-TRIMETHYL-
Systematic Name English
N1-(7-(((4-FLUOROBENZYL)AMINO)CARBONYL)-8-HYDROXY-1,6-NAPHTHYRIDIN-5-YL)-N1,N2,N2-TRIMETHYLETHANEDIAMIDE
Systematic Name English
Code System Code Type Description
FDA UNII
O168ONK0IG
Created by admin on Mon Mar 31 22:01:52 GMT 2025 , Edited by admin on Mon Mar 31 22:01:52 GMT 2025
PRIMARY
CAS
410545-90-3
Created by admin on Mon Mar 31 22:01:52 GMT 2025 , Edited by admin on Mon Mar 31 22:01:52 GMT 2025
PRIMARY
PUBCHEM
6918643
Created by admin on Mon Mar 31 22:01:52 GMT 2025 , Edited by admin on Mon Mar 31 22:01:52 GMT 2025
PRIMARY
EPA CompTox
DTXSID00426084
Created by admin on Mon Mar 31 22:01:52 GMT 2025 , Edited by admin on Mon Mar 31 22:01:52 GMT 2025
PRIMARY
Related Record Type Details
ACTIVE MOIETY