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Details

Stereochemistry ABSOLUTE
Molecular Formula C25H29FN2O4S2
Molecular Weight 504.637
Optical Activity UNSPECIFIED
Defined Stereocenters 3 / 3
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of VIQUIDACIN

SMILES

COC1=CC=C2N=CC(F)=C([C@@H](O)CC[C@@H]3CCN(CCSC4=CC=CS4)C[C@@H]3C(O)=O)C2=C1

InChI

InChIKey=USGHRRVFKSLEJT-WVBUVRCRSA-N
InChI=1S/C25H29FN2O4S2/c1-32-17-5-6-21-18(13-17)24(20(26)14-27-21)22(29)7-4-16-8-9-28(15-19(16)25(30)31)10-12-34-23-3-2-11-33-23/h2-3,5-6,11,13-14,16,19,22,29H,4,7-10,12,15H2,1H3,(H,30,31)/t16-,19+,22+/m1/s1

HIDE SMILES / InChI

Molecular Formula C25H29FN2O4S2
Molecular Weight 504.637
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 3 / 3
E/Z Centers 0
Optical Activity UNSPECIFIED

Viquidacin (also known as NXL-101), a quinoline antibacterial agent, was studied as a bacterial DNA gyrase and topoisomerase IV inhibitor. Viquidacin showed potent activity against gram-positive bacteria, including methicillin- and fluoroquinolone-resistant strains. The drug participated in phase I clinical trial. Viquidacin achieved homogeneous and potent bactericidal concentrations in human volunteer plasma. However, further, development was discontinued after QT interval prolongation, which was observed in a healthy volunteer.

Approval Year

PubMed

PubMed

TitleDatePubMed
Mechanism of action of the antibiotic NXL101, a novel nonfluoroquinolone inhibitor of bacterial type II topoisomerases.
2008 Sep
Patents
Substance Class Chemical
Created
by admin
on Sat Dec 16 01:35:18 UTC 2023
Edited
by admin
on Sat Dec 16 01:35:18 UTC 2023
Record UNII
0TA0YE45QE
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
VIQUIDACIN
INN  
INN  
Official Name English
viquidacin [INN]
Common Name English
NXL-101
Code English
3-PIPERIDINECARBOXYLIC ACID, 4-((3S)-3-(3-FLUORO-6-METHOXY-4-QUINOLINYL)-3-HYDROXYPROPYL)-1-(2-(2-THIENYLTHIO)ETHYL)-, (3R,4R)-
Common Name English
(3R,4R)-4-((3S)-3-(3-FLUORO-6-METHOXYQUINOLIN-4-YL)-3-HYDROXYPROPYL)-1-(2-((THIOPHEN-2-YL)SULFANYL)ETHYL)PIPERIDINE-3-CARBOXYLIC ACID
Systematic Name English
NXL 101
Code English
Classification Tree Code System Code
NCI_THESAURUS C258
Created by admin on Sat Dec 16 01:35:18 UTC 2023 , Edited by admin on Sat Dec 16 01:35:18 UTC 2023
NCI_THESAURUS C471
Created by admin on Sat Dec 16 01:35:18 UTC 2023 , Edited by admin on Sat Dec 16 01:35:18 UTC 2023
Code System Code Type Description
NCI_THESAURUS
C152895
Created by admin on Sat Dec 16 01:35:18 UTC 2023 , Edited by admin on Sat Dec 16 01:35:18 UTC 2023
PRIMARY
EPA CompTox
DTXSID30238172
Created by admin on Sat Dec 16 01:35:18 UTC 2023 , Edited by admin on Sat Dec 16 01:35:18 UTC 2023
PRIMARY
SMS_ID
300000034459
Created by admin on Sat Dec 16 01:35:18 UTC 2023 , Edited by admin on Sat Dec 16 01:35:18 UTC 2023
PRIMARY
PUBCHEM
11591505
Created by admin on Sat Dec 16 01:35:18 UTC 2023 , Edited by admin on Sat Dec 16 01:35:18 UTC 2023
PRIMARY
CAS
904302-98-3
Created by admin on Sat Dec 16 01:35:18 UTC 2023 , Edited by admin on Sat Dec 16 01:35:18 UTC 2023
PRIMARY
FDA UNII
0TA0YE45QE
Created by admin on Sat Dec 16 01:35:18 UTC 2023 , Edited by admin on Sat Dec 16 01:35:18 UTC 2023
PRIMARY
INN
8971
Created by admin on Sat Dec 16 01:35:18 UTC 2023 , Edited by admin on Sat Dec 16 01:35:18 UTC 2023
PRIMARY
Related Record Type Details
TARGET -> INHIBITOR
Related Record Type Details
ACTIVE MOIETY