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
SMILES
OC(=O)C1=NC2=C(C(O)=C1)C3=NC4=CC=CC=C4OC3=CC2=O
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)
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 |
DescriptionSources: http://www.ncbi.nlm.nih.gov/pubmed/21850160Curator's Comment: description was created based on several sources, including, http://www.fda.gov.tw/MLMS/ShowFile.aspx?LicId=02021053&Seq=007&Type=9
Sources: http://www.ncbi.nlm.nih.gov/pubmed/21850160
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
Primary Target | Pharmacology | Condition | Potency |
---|---|---|---|
Target ID: GO:0036438 Sources: http://www.ncbi.nlm.nih.gov/pubmed/21850160 |
Conditions
Condition | Modality | Targets | Highest Phase | Product |
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Preventing | CATALIN Approved UseEarly stage of senile cataract. |
PubMed
Title | Date | PubMed |
---|---|---|
Antioxidant protection in cultured corneal cells and whole corneas submitted to UV-B exposure. | 2003 Oct 15 |
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[Evaluation of effectiveness of Catalin eyedrops in patients with presenile and senile cataract]. | 2004 |
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Contact dermatitis due to pirfenoxone. | 2004 Jun |
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Pirenoxine prevents oxidative effects of argon fluoride excimer laser irradiation in rabbit corneas: biochemical, histological and cytofluorimetric evaluations. | 2005 Jan 14 |
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Why are physicians not persuaded by scientific evidence? A grounded theory interview study. | 2006 Jul 27 |
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[Efficacy of catalin eyed drops in age-related cataract agents]. | 2010 Jan-Feb |
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
Sources: http://www.ncbi.nlm.nih.gov/pubmed/21850160
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
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admin
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Edited
Fri Dec 15 16:29:13 GMT 2023
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Record UNII |
27L0EP6IZK
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Record Status |
Validated (UNII)
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Record Version |
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WHO-VATC |
QS01XA91
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NCI_THESAURUS |
C345
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213-872-4
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4846
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1043-21-6
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CHEMBL1372341
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228080
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100000081662
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5317
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27L0EP6IZK
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C66416
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3476
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DTXSID6048335
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SUB09902MIG
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m8873
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C004580
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Pirenoxine
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Related Record | Type | Details | ||
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SALT/SOLVATE -> PARENT |
Related Record | Type | Details | ||
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ACTIVE MOIETY |