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Details

Stereochemistry ACHIRAL
Molecular Formula C16H8N2O5
Molecular Weight 308.2451
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of PIRENOXINE

SMILES

OC(=O)c1cc(O)c2c3nc4ccccc4oc3cc(=O)c2n1

InChI

InChIKey=OKPNYGAWTYOBFZ-UHFFFAOYSA-N
InChI=1S/C16H8N2O5/c19-9-5-8(16(21)22)18-14-10(20)6-12-15(13(9)14)17-7-3-1-2-4-11(7)23-12/h1-6H,(H,18,19)(H,21,22)

HIDE SMILES / InChI

Molecular Formula C16H8N2O5
Molecular Weight 308.2451
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Description
Curator's Comment: description was created based on several sources, including, http://www.fda.gov.tw/MLMS/ShowFile.aspx?LicId=02021053&Seq=007&Type=9

Pirenoxine is an anti-cataract agent which is used in many asian countries under the name Catalin. Although its efficacy is not proved scientifically, the drug may play an important role in cataract prevention. It is supposed that the anti-cataract effect of pirenoxine results from inhibition of sulfhydryl combination of quinoid substances with lens proteins and the inhibition leads to the maintenance of lens transparency.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Preventing
CATALIN

Approved Use

Early stage of senile cataract.
PubMed

PubMed

TitleDatePubMed
[Efficacy of catalin eyed drops in age-related cataract agents].
2010-07-22
Why are physicians not persuaded by scientific evidence? A grounded theory interview study.
2006-07-27
Pirenoxine prevents oxidative effects of argon fluoride excimer laser irradiation in rabbit corneas: biochemical, histological and cytofluorimetric evaluations.
2005-01-14
Contact dermatitis due to pirfenoxone.
2004-06
[Evaluation of effectiveness of Catalin eyedrops in patients with presenile and senile cataract].
2004
Antioxidant protection in cultured corneal cells and whole corneas submitted to UV-B exposure.
2003-10-15
Patents

Patents

Sample Use Guides

Dissolve the granules (0.75 mg) in 15 ml of the vehicle just before use and instill 1-2 drops of the solution, 3-5 times a day
Route of Administration: Other
In Vitro Use Guide
Pirenoxine (1,000 uM) decreased UVC-induced turbidity formation compared to controls after 4 h of UVC exposure. The absolute gamma-crystallin turbidity induced by 4 h of UVC exposure was ameliorated in the presence of catalin equivalent to 1-100 uM of the drug in a concentration-dependent manner. Pirenoxine at 0.03, 0.1, and 0.3 uM significantly delayed 10 mM selenite- and calcium-induced turbidity formation compared to controls on days 0-4.
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:29:17 GMT 2025
Edited
by admin
on Mon Mar 31 18:29:17 GMT 2025
Record UNII
27L0EP6IZK
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
PIRENOXINE
INN   MI   WHO-DD  
INN  
Official Name English
CATALIN-K
Preferred Name English
pirenoxine [INN]
Common Name English
PIRENOXINE [JAN]
Common Name English
PIRENOXINE [MI]
Common Name English
Pirenoxine [WHO-DD]
Common Name English
Classification Tree Code System Code
WHO-VATC QS01XA91
Created by admin on Mon Mar 31 18:29:17 GMT 2025 , Edited by admin on Mon Mar 31 18:29:17 GMT 2025
NCI_THESAURUS C345
Created by admin on Mon Mar 31 18:29:17 GMT 2025 , Edited by admin on Mon Mar 31 18:29:17 GMT 2025
Code System Code Type Description
ECHA (EC/EINECS)
213-872-4
Created by admin on Mon Mar 31 18:29:17 GMT 2025 , Edited by admin on Mon Mar 31 18:29:17 GMT 2025
PRIMARY
PUBCHEM
4846
Created by admin on Mon Mar 31 18:29:17 GMT 2025 , Edited by admin on Mon Mar 31 18:29:17 GMT 2025
PRIMARY
CAS
1043-21-6
Created by admin on Mon Mar 31 18:29:17 GMT 2025 , Edited by admin on Mon Mar 31 18:29:17 GMT 2025
PRIMARY
ChEMBL
CHEMBL1372341
Created by admin on Mon Mar 31 18:29:17 GMT 2025 , Edited by admin on Mon Mar 31 18:29:17 GMT 2025
PRIMARY
RXCUI
228080
Created by admin on Mon Mar 31 18:29:17 GMT 2025 , Edited by admin on Mon Mar 31 18:29:17 GMT 2025
PRIMARY RxNorm
SMS_ID
100000081662
Created by admin on Mon Mar 31 18:29:17 GMT 2025 , Edited by admin on Mon Mar 31 18:29:17 GMT 2025
PRIMARY
INN
5317
Created by admin on Mon Mar 31 18:29:17 GMT 2025 , Edited by admin on Mon Mar 31 18:29:17 GMT 2025
PRIMARY
FDA UNII
27L0EP6IZK
Created by admin on Mon Mar 31 18:29:17 GMT 2025 , Edited by admin on Mon Mar 31 18:29:17 GMT 2025
PRIMARY
NCI_THESAURUS
C66416
Created by admin on Mon Mar 31 18:29:17 GMT 2025 , Edited by admin on Mon Mar 31 18:29:17 GMT 2025
PRIMARY
DRUG CENTRAL
3476
Created by admin on Mon Mar 31 18:29:17 GMT 2025 , Edited by admin on Mon Mar 31 18:29:17 GMT 2025
PRIMARY
EPA CompTox
DTXSID6048335
Created by admin on Mon Mar 31 18:29:17 GMT 2025 , Edited by admin on Mon Mar 31 18:29:17 GMT 2025
PRIMARY
EVMPD
SUB09902MIG
Created by admin on Mon Mar 31 18:29:17 GMT 2025 , Edited by admin on Mon Mar 31 18:29:17 GMT 2025
PRIMARY
MERCK INDEX
m8873
Created by admin on Mon Mar 31 18:29:17 GMT 2025 , Edited by admin on Mon Mar 31 18:29:17 GMT 2025
PRIMARY Merck Index
MESH
C004580
Created by admin on Mon Mar 31 18:29:17 GMT 2025 , Edited by admin on Mon Mar 31 18:29:17 GMT 2025
PRIMARY
WIKIPEDIA
Pirenoxine
Created by admin on Mon Mar 31 18:29:17 GMT 2025 , Edited by admin on Mon Mar 31 18:29:17 GMT 2025
PRIMARY
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SALT/SOLVATE -> PARENT
Related Record Type Details
ACTIVE MOIETY