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Details

Stereochemistry ACHIRAL
Molecular Formula C4H4N2
Molecular Weight 80.088
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of PYRIDAZINE

SMILES

C1=CC=NN=C1

InChI

InChIKey=PBMFSQRYOILNGV-UHFFFAOYSA-N
InChI=1S/C4H4N2/c1-2-4-6-5-3-1/h1-4H

HIDE SMILES / InChI

Molecular Formula C4H4N2
Molecular Weight 80.088
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Design, synthesis, and structure-activity relationships of a series of 3-[2-(1-benzylpiperidin-4-yl)ethylamino]pyridazine derivatives as acetylcholinesterase inhibitors.
2001 Aug 16
Bis[3,6-bis(6-methyl-2pyridyl)pyridazine-kappa2N2,N3]chlorocopper(II) perchlorate.
2001 Jan
Binuclear complexes as building blocks for polynuclear complexes with high-spin ground states: synthesis and structure of a tetranuclear nickel complex with an S = 4 ground state.
2001 Oct 1
A meso-helical coordination polymer from achiral dinuclear [Cu2(H3CCN)2(micro-pydz)3][PF6]2 and 1,3-bis(diphenylphosphanyl)propane-synthesis and crystal structure of 1 to infinity Cu(mu-pydz)2][PF6 (pydz=pyridazine).
2001 Sep 17
Cross-coupling reactions of phenylmagnesium halides with fluoroazines and fluorodiazines.
2002 Dec 13
Pyridazine based inhibitors of p38 MAPK.
2002 Feb 25
A study by ultraviolet spectroscopy on the self-association of diazines in aqueous solution.
2003 Apr
Synthesis, crystal structures, and thermal and thermodynamic properties of dimorphic copper(I) coordination polymers.
2003 May 5
Mechanism-based inactivation of human recombinant P450 2C9 by the nonsteroidal anti-inflammatory drug suprofen.
2003 Nov
Benzyl vinylogous amide substituted aryldihydropyridazinones and aryldimethylpyrazolones as potent and selective PDE3B inhibitors.
2003 Nov 17
An aminopyridazine-based inhibitor of a pro-apoptotic protein kinase attenuates hypoxia-ischemia induced acute brain injury.
2003 Oct 20
Quaternary salts containing the pentafluorosulfanyl (SF5) group.
2003 Sep 22
Synthesis and chemistry of unusual bicyclic endoperoxides containing the pyridazine ring.
2003 Sep 5
Synthesis of 5-azaindolizine derivatives by the palladium-catalyzed intermolecular formal [3+2] cycloaddition of alkylidenecyclopropanes with 1,2-diazines.
2004 Apr 30
Synthesis and herbicidal activity of novel heterocyclic protoporphyrinogen oxidase inhibitors.
2004 Dec
New developments in the symmetry-adapted algorithm of the Polarizable Continuum Model.
2004 Feb
Structural distortion of pyridazine in the 1(n, pi) excited state: evidence for local excitation.
2004 May 17
Pyridazine derivatives and related compounds. Part 13: Synthesis and antimicrobial activity of some pyridazino[3',4':3,4]pyrazolo[5,1-c]-1,2,4-triazines.
2004 Oct 4
Synthesis of 3-alkylthio-6-allylthiopyridazine derivatives and their antihepatocarcinoma activity.
2005 Apr
Neutral Cu4N12 and Ag4N12 metallacycles with a para-cyclophane framework assembled from copper(I) and silver(I) pyrazolates and pyridazine.
2005 Mar 28
Fully dimensional ab initio description of the structure and energetics of azabenzene-argon complexes.
2005 Oct 15
Vibrational spectra and potential energy distributions for 4,5-dichloro-3-hydroxypyridazine by density functional theory and normal coordinate calculations.
2005 Sep
A pyridazine series of alpha2/alpha3 subtype selective GABA A agonists for the treatment of anxiety.
2006 Apr 20
Use of 4-bromo pyridazine 3,6-dione for building 3-amino pyridazine libraries.
2006 Aug
Synthetic approaches to polypyridyl bridging ligands with proximal multidentate binding sites.
2006 Jan 6
The in vivo metabolism of 3-oxo-5-benzylidene-6-methyl-(4H)-2-(benzoylmethyl)pyridazine in rats.
2006 Jan-Mar
Copper complexes with heterocyclic sulfonamides: synthesis, spectroscopic characterization, microbiological and SOD-like activities: crystal structure of [Cu(sulfisoxazole)2(H2O)4] . 2H2O.
2006 Jul
Kinetics and mechanism of the reactions of Pd(II) complexes with azoles and diazines. Crystal structure of [Pd(bpma)(H2O)](ClO4)2.2H2O.
2006 Jun 28
Vibrational spectroscopy of the pyridazine cation in the ground state.
2006 Mar 2
CoMFA based de novo design of pyridazine analogs as PTP1B inhibitors.
2007 Jul
Silver(I) sulfate coordination polymers with 4,4'-bipyridazine and pyridazino[4,5-d]pyridazine.
2007 Jun
Patents
Substance Class Chemical
Created
by admin
on Sat Dec 16 01:35:27 GMT 2023
Edited
by admin
on Sat Dec 16 01:35:27 GMT 2023
Record UNII
449GLA0653
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
PYRIDAZINE
MI  
Systematic Name English
PYRIDAZINE [MI]
Common Name English
OIZINE
Common Name English
1,2-DIAZINE
Systematic Name English
NSC-90792
Code English
ORTHODIAZINE
Systematic Name English
Code System Code Type Description
FDA UNII
449GLA0653
Created by admin on Sat Dec 16 01:35:27 GMT 2023 , Edited by admin on Sat Dec 16 01:35:27 GMT 2023
PRIMARY
CHEBI
30954
Created by admin on Sat Dec 16 01:35:27 GMT 2023 , Edited by admin on Sat Dec 16 01:35:27 GMT 2023
PRIMARY
ECHA (EC/EINECS)
206-025-5
Created by admin on Sat Dec 16 01:35:27 GMT 2023 , Edited by admin on Sat Dec 16 01:35:27 GMT 2023
PRIMARY
NSC
90792
Created by admin on Sat Dec 16 01:35:27 GMT 2023 , Edited by admin on Sat Dec 16 01:35:27 GMT 2023
PRIMARY
WIKIPEDIA
PYRIDAZINE
Created by admin on Sat Dec 16 01:35:27 GMT 2023 , Edited by admin on Sat Dec 16 01:35:27 GMT 2023
PRIMARY
CAS
289-80-5
Created by admin on Sat Dec 16 01:35:27 GMT 2023 , Edited by admin on Sat Dec 16 01:35:27 GMT 2023
PRIMARY
EPA CompTox
DTXSID7059777
Created by admin on Sat Dec 16 01:35:27 GMT 2023 , Edited by admin on Sat Dec 16 01:35:27 GMT 2023
PRIMARY
PUBCHEM
9259
Created by admin on Sat Dec 16 01:35:27 GMT 2023 , Edited by admin on Sat Dec 16 01:35:27 GMT 2023
PRIMARY
MERCK INDEX
m9350
Created by admin on Sat Dec 16 01:35:27 GMT 2023 , Edited by admin on Sat Dec 16 01:35:27 GMT 2023
PRIMARY Merck Index
MESH
C062482
Created by admin on Sat Dec 16 01:35:27 GMT 2023 , Edited by admin on Sat Dec 16 01:35:27 GMT 2023
PRIMARY
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