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Details

Stereochemistry ACHIRAL
Molecular Formula C19H16ClNO4
Molecular Weight 357.788
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of RILOPIROX

SMILES

CC1=CC(=O)N(O)C(COC2=CC=C(OC3=CC=C(Cl)C=C3)C=C2)=C1

InChI

InChIKey=UDYUIWXQUBNDHC-UHFFFAOYSA-N
InChI=1S/C19H16ClNO4/c1-13-10-15(21(23)19(22)11-13)12-24-16-6-8-18(9-7-16)25-17-4-2-14(20)3-5-17/h2-11,23H,12H2,1H3

HIDE SMILES / InChI

Molecular Formula C19H16ClNO4
Molecular Weight 357.788
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Rilopirox (HOE 351) is a fungicidal antimycotic that was developed as an intravaginal antifungal with a long skin retention time and a strong killing effect on pathogenic yeasts. Its very low water solubility makes rilopirox a good candidate for an intravaginal antifungal. Potential applications may be in mucosal candida infections, tinea versicolor and seborrheic dermatitis. In addition, it has been suggested that rilopirox could be effective against oropharyngeal Candida infections, for example in AIDS patients. There is no information on current development of rilopirox.

Originator

Approval Year

PubMed

PubMed

TitleDatePubMed
[The in vitro properties of a new hydroxypyridone antimycotic rilopirox, with special reference to its anti-Candida activity].
1999-02
The hydroxypyridones: a class of antimycotics of its own.
1997-11
Patents

Patents

Substance Class Chemical
Created
by admin
on Mon Mar 31 17:58:49 GMT 2025
Edited
by admin
on Mon Mar 31 17:58:49 GMT 2025
Record UNII
595T4D0KQ3
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
rilopirox [INN]
Preferred Name English
RILOPIROX
INN  
INN  
Official Name English
Classification Tree Code System Code
NCI_THESAURUS C514
Created by admin on Mon Mar 31 17:58:49 GMT 2025 , Edited by admin on Mon Mar 31 17:58:49 GMT 2025
Code System Code Type Description
EVMPD
SUB10317MIG
Created by admin on Mon Mar 31 17:58:49 GMT 2025 , Edited by admin on Mon Mar 31 17:58:49 GMT 2025
PRIMARY
FDA UNII
595T4D0KQ3
Created by admin on Mon Mar 31 17:58:49 GMT 2025 , Edited by admin on Mon Mar 31 17:58:49 GMT 2025
PRIMARY
MESH
C066307
Created by admin on Mon Mar 31 17:58:49 GMT 2025 , Edited by admin on Mon Mar 31 17:58:49 GMT 2025
PRIMARY
SMS_ID
100000080584
Created by admin on Mon Mar 31 17:58:49 GMT 2025 , Edited by admin on Mon Mar 31 17:58:49 GMT 2025
PRIMARY
ChEMBL
CHEMBL2105325
Created by admin on Mon Mar 31 17:58:49 GMT 2025 , Edited by admin on Mon Mar 31 17:58:49 GMT 2025
PRIMARY
NCI_THESAURUS
C75204
Created by admin on Mon Mar 31 17:58:49 GMT 2025 , Edited by admin on Mon Mar 31 17:58:49 GMT 2025
PRIMARY
EPA CompTox
DTXSID90146320
Created by admin on Mon Mar 31 17:58:49 GMT 2025 , Edited by admin on Mon Mar 31 17:58:49 GMT 2025
PRIMARY
INN
6015
Created by admin on Mon Mar 31 17:58:49 GMT 2025 , Edited by admin on Mon Mar 31 17:58:49 GMT 2025
PRIMARY
PUBCHEM
71778
Created by admin on Mon Mar 31 17:58:49 GMT 2025 , Edited by admin on Mon Mar 31 17:58:49 GMT 2025
PRIMARY
CAS
104153-37-9
Created by admin on Mon Mar 31 17:58:49 GMT 2025 , Edited by admin on Mon Mar 31 17:58:49 GMT 2025
PRIMARY
Related Record Type Details
ACTIVE MOIETY