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Details

Stereochemistry ACHIRAL
Molecular Formula C22H30N6O
Molecular Weight 394.5132
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of JNJ-2408068

SMILES

CC1=CC=C(O)C(CN2C(NC3CCN(CCN)CC3)=NC4=C(C)C=CC=C24)=N1

InChI

InChIKey=RDQSNNMSDOHAPG-UHFFFAOYSA-N
InChI=1S/C22H30N6O/c1-15-4-3-5-19-21(15)26-22(25-17-8-11-27(12-9-17)13-10-23)28(19)14-18-20(29)7-6-16(2)24-18/h3-7,17,29H,8-14,23H2,1-2H3,(H,25,26)

HIDE SMILES / InChI

Molecular Formula C22H30N6O
Molecular Weight 394.5132
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Substituted benzimidazoles with nanomolar activity against respiratory syncytial virus.
2003 Nov
Selection of a respiratory syncytial virus fusion inhibitor clinical candidate, part 1: improving the pharmacokinetic profile using the structure-property relationship.
2007 Sep 20
Substance Class Chemical
Created
by admin
on Sat Dec 16 04:37:30 GMT 2023
Edited
by admin
on Sat Dec 16 04:37:30 GMT 2023
Record UNII
AB821DL88A
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
JNJ-2408068
Common Name English
R-170591
Code English
3-PYRIDINOL, 2-((2-((1-(2-AMINOETHYL)-4-PIPERIDINYL)AMINO)-4-METHYL-1H-BENZIMIDAZOL-1-YL)METHYL)-6-METHYL-
Systematic Name English
2-((2-((1-(2-AMINOETHYL)-4-PIPERIDINYL)AMINO)-4-METHYL-1HBENZIMIDAZOL-1-YL)METHYL)-6-METHYL-3-PYRIDINOL
Common Name English
Code System Code Type Description
FDA UNII
AB821DL88A
Created by admin on Sat Dec 16 04:37:30 GMT 2023 , Edited by admin on Sat Dec 16 04:37:30 GMT 2023
PRIMARY
PUBCHEM
511013
Created by admin on Sat Dec 16 04:37:30 GMT 2023 , Edited by admin on Sat Dec 16 04:37:30 GMT 2023
PRIMARY
EPA CompTox
DTXSID50185654
Created by admin on Sat Dec 16 04:37:30 GMT 2023 , Edited by admin on Sat Dec 16 04:37:30 GMT 2023
PRIMARY
CAS
317846-22-3
Created by admin on Sat Dec 16 04:37:30 GMT 2023 , Edited by admin on Sat Dec 16 04:37:30 GMT 2023
PRIMARY
Related Record Type Details
ACTIVE MOIETY