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Details

Stereochemistry ACHIRAL
Molecular Formula C8H6N2O
Molecular Weight 146.146
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of PHTHALAZINONE

SMILES

O=C1NN=CC2=C1C=CC=C2

InChI

InChIKey=IJAPPYDYQCXOEF-UHFFFAOYSA-N
InChI=1S/C8H6N2O/c11-8-7-4-2-1-3-6(7)5-9-10-8/h1-5H,(H,10,11)

HIDE SMILES / InChI

Molecular Formula C8H6N2O
Molecular Weight 146.146
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Modifying a proton conductive membrane by embedding a "barrier".
2010-10-21
Azelastine hydrochloride, a dual-acting anti-inflammatory ophthalmic solution, for treatment of allergic conjunctivitis.
2010-09-07
Synthesis and biological evaluation of novel phthalazinone derivatives as topically active phosphodiesterase 4 inhibitors.
2009-10-01
Regioselective synthesis of N-aminoisoindolones and mono-N- and di-N,N'-substituted phthalazones utilizing hydrazine nucleophiles in a palladium-catalyzed three-component cascade process.
2008-11-07
Azelastine hydrochloride: a review of pharmacology, pharmacokinetics, clinical efficacy and tolerability.
2007-10
Design and syntheses of novel phthalazin-1(2H)-one derivatives as acetohydroxyacid synthase inhibitors.
2006-11-29
Microwave-assisted cyclic amidine synthesis using TiCl4.
2006-08-21
Anti-HIV activity of stilbene-related heterocyclic compounds.
2006-08-01
Azamerone, a terpenoid phthalazinone from a marine-derived bacterium related to the genus Streptomyces (Actinomycetales).
2006-06-08
Synthesis and molluscicidal activity of some 1,3,4-triaryl-5-chloropyrazole, pyrano[2,3-c]pyrazole, pyrazolylphthalazine and pyrano[2,3-d]thiazole derivatives.
2006-06
Vasorelaxant activity of phthalazinones and related compounds.
2006-05-15
Phthalazinones 2: Optimisation and synthesis of novel potent inhibitors of poly(ADP-ribose)polymerase.
2006-02-15
Some pyrrole substituted aryl pyridazinone and phthalazinone derivatives and their antihypertensive activities.
2004-12
Some pyridazinone and phthalazinone derivatives and their vasodilator activities.
2004-01
Human liver aldehyde oxidase: inhibition by 239 drugs.
2004-01
Enzymatic oxidation of phthalazine with guinea pig liver aldehyde oxidase and liver slices: inhibition by isovanillin.
2004
Synthesis and structural characterization of 1-(D-glycosyloxy)phthalazines.
2003-10-31
Novel selective phosphodiesterase (PDE4) inhibitors. 4. Resolution, absolute configuration, and PDE4 inhibitory activity of cis-tetra- and cis-hexahydrophthalazinones.
2002-06-06
Novel phthalazinone and benzoxazinone containing thiazolidinediones as antidiabetic and hypolipidemic agents.
2001-10-16
Novel selective PDE4 inhibitors. 1. Synthesis, structure-activity relationships, and molecular modeling of 4-(3,4-dimethoxyphenyl)-2H-phthalazin-1-ones and analogues.
2001-08-02
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 20:51:09 GMT 2025
Edited
by admin
on Mon Mar 31 20:51:09 GMT 2025
Record UNII
463ZJB0EI2
Record Status Validated (UNII)
Record Version
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Name Type Language
PHTHALAZINONE
Systematic Name English
NSC-10432
Preferred Name English
1(2H)-PHTHALAZINONE
Systematic Name English
1-HYDROXYPHTHALAZINE
Systematic Name English
1-OXOPHTHALAZINE
Systematic Name English
1-PHTHALAZINONE [USP IMPURITY]
Common Name English
NSC-52567
Code English
PHTHALAZIN-1-ONE
Systematic Name English
1-PHTHALAZINOL
Systematic Name English
Code System Code Type Description
ECHA (EC/EINECS)
204-319-8
Created by admin on Mon Mar 31 20:51:09 GMT 2025 , Edited by admin on Mon Mar 31 20:51:09 GMT 2025
PRIMARY
PUBCHEM
8394
Created by admin on Mon Mar 31 20:51:09 GMT 2025 , Edited by admin on Mon Mar 31 20:51:09 GMT 2025
PRIMARY
CHEBI
34023
Created by admin on Mon Mar 31 20:51:09 GMT 2025 , Edited by admin on Mon Mar 31 20:51:09 GMT 2025
PRIMARY
FDA UNII
463ZJB0EI2
Created by admin on Mon Mar 31 20:51:09 GMT 2025 , Edited by admin on Mon Mar 31 20:51:09 GMT 2025
PRIMARY
NSC
10432
Created by admin on Mon Mar 31 20:51:09 GMT 2025 , Edited by admin on Mon Mar 31 20:51:09 GMT 2025
PRIMARY
EPA CompTox
DTXSID4025903
Created by admin on Mon Mar 31 20:51:09 GMT 2025 , Edited by admin on Mon Mar 31 20:51:09 GMT 2025
PRIMARY
CAS
119-39-1
Created by admin on Mon Mar 31 20:51:09 GMT 2025 , Edited by admin on Mon Mar 31 20:51:09 GMT 2025
PRIMARY
HSDB
4310
Created by admin on Mon Mar 31 20:51:09 GMT 2025 , Edited by admin on Mon Mar 31 20:51:09 GMT 2025
PRIMARY
NSC
52567
Created by admin on Mon Mar 31 20:51:09 GMT 2025 , Edited by admin on Mon Mar 31 20:51:09 GMT 2025
PRIMARY
Related Record Type Details
PARENT -> IMPURITY
CHROMATOGRAPHIC PURITY (HPLC/UV)
USP