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265-02-1

265-02-1 | 1H-1,5-Benzodiazepine

CAS No: 265-02-1 Catalog No: AG002THE MDL No:

Product Description

Catalog Number:
AG002THE
Chemical Name:
1H-1,5-Benzodiazepine
CAS Number:
265-02-1
Molecular Formula:
C9H8N2
Molecular Weight:
144.1732
IUPAC Name:
1H-1,5-benzodiazepine
InChI:
InChI=1S/C9H8N2/c1-2-5-9-8(4-1)10-6-3-7-11-9/h1-7,10H
InChI Key:
ZVAPWJGRRUHKGP-UHFFFAOYSA-N
SMILES:
C1=CNc2c(N=C1)cccc2

Properties

Complexity:
184  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
144.069g/mol
Formal Charge:
0
Heavy Atom Count:
11  
Hydrogen Bond Acceptor Count:
2  
Hydrogen Bond Donor Count:
1  
Isotope Atom Count:
0
Molecular Weight:
144.177g/mol
Monoisotopic Mass:
144.069g/mol
Rotatable Bond Count:
0
Topological Polar Surface Area:
24.4A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
1.2  

Literature

Title Journal
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Synthesis of 1,5-benzodiazepine and its derivatives by condensation reaction using H-MCM-22 as catalyst. Journal of biomedicine & biotechnology 20120101
Randomized, phase III study results of clobazam in Lennox-Gastaut syndrome. Neurology 20111011
Toxicological approach for elucidation of clobazam-induced hepatomegaly in male rats. Regulatory toxicology and pharmacology : RTP 20110801
Ethyl 5,5-dichloro-3-(4-chloro-phen-yl)-3a-methyl-4a-phenyl-3a,4,4a,5-tetra-hydro-3H-aziridino[2,1-d][1,2,4]triazolo[4,3-a][1,5]benzodiazepine-1-carboxyl-ate. Acta crystallographica. Section E, Structure reports online 20110501
Racemic 9,10-dimeth-oxy-3-methyl-6-phenyl-7,7a-dihydro-benzo[b]benzo[4,5]isothia-zolo[2,3-d][1,4]diazepine 12,12-dioxide. Acta crystallographica. Section E, Structure reports online 20110301
[Effect of 1,5-benzodiazepine derivatives on the electrical activity of neurons of the Helix albescens Rossm]. Fiziolohichnyi zhurnal (Kiev, Ukraine : 1994) 20110101
Clobazam as an adjunctive therapy in treating seizures associated with Lennox-Gastaut syndrome. Neuropsychiatric disease and treatment 20110101
Synthesis of substituted 1,4-diazepines and 1,5-benzodiazepines using an efficient heteropolyacid-catalyzed procedure. Molecules (Basel, Switzerland) 20101228
Anti-neuroinflammatory activity of 1,5-benzodiazepine derivatives. Bioorganic & medicinal chemistry letters 20100701
Cytogenetic activity of newly synthesized 1,5-benzodiazepines in normal human lymphocyte cultures. Genetic testing and molecular biomarkers 20100601
New 1,5-benzodiazepine compounds: activity at native GABA(A) receptors. Neuroscience 20100331
Neuropharmacological screening of two 1,5-benzodiazepine compounds in mice. Comptes rendus biologies 20100301
Sodium tetrachloroaurate(III) dihydrate-catalyzed efficient synthesis of 1,5-benzodiazepine and quinoxaline derivatives. Journal of Zhejiang University. Science. B 20100201
Diethyl 1,4-bis-(4-nitro-phen-yl)-1,4-dihydro-1,2,4,5-tetra-zine-3,6-dicarboxyl-ate. Acta crystallographica. Section E, Structure reports online 20100201
[Therapeutic drug monitoring of clobazam]. Therapie 20100101
Z-360, a novel therapeutic agent for pancreatic cancer, prevents up-regulation of ephrin B1 gene expression and phosphorylation of NR2B via suppression of interleukin-1 β production in a cancer-induced pain model in mice. Molecular pain 20100101
Enaminonitrile in heterocyclic synthesis: synthesis and antimicrobial evaluation of some new pyrazole, isoxazole and pyrimidine derivatives incorporating a benzothiazole moiety. European journal of medicinal chemistry 20091201
2-Methyl-2,4-di-4-pyridyl-2,3-dihydro-1H-1,5-benzodiazepine acetic acid solvate. Acta crystallographica. Section E, Structure reports online 20091201
1,5-Benzodiazepine inhibitors of HCV NS5B polymerase. Bioorganic & medicinal chemistry letters 20090501
Treatment of Lennox-Gastaut syndrome: overview and recent findings. Neuropsychiatric disease and treatment 20081201
Efficient TCT-catalyzed synthesis of 1,5-benzodiazepine derivatives under mild conditions. Molecules (Basel, Switzerland) 20080925
Gas-phase fragmentation study of novel synthetic 1,5-benzodiazepine derivatives using electrospray ionization tandem mass spectrometry. Rapid communications in mass spectrometry : RCM 20080701
4-(2-Hydroxyphenyl)-2-phenyl-2,3-dihydro-1H-1,5-benzodiazepine and the 2-(2,3-dimethoxyphenyl)-, 2-(3,4-dimethoxyphenyl)- and 2-(2,5-dimethoxyphenyl)-substituted derivatives. Acta crystallographica. Section C, Crystal structure communications 20070701
New inhibitors of fungal 17beta-hydroxysteroid dehydrogenase based on the [1,5]-benzodiazepine scaffold. Journal of enzyme inhibition and medicinal chemistry 20070201
Strategies for design of non peptide CCK1R agonist/antagonist ligands. Current topics in medicinal chemistry 20070101
Transition metal complexes of quinolino[3,2-b]benzodiazepine and quinolino[3,2-b]benzoxazepine: synthesis, characterization, and antimicrobial studies. Bioinorganic chemistry and applications 20070101
In vitro and in vivo inhibitory effect of stiripentol on clobazam metabolism. Drug metabolism and disposition: the biological fate of chemicals 20060401
Novel benzodiazepine photoaffinity probe stereoselectively labels a site deep within the membrane-spanning domain of the cholecystokinin receptor. Journal of medicinal chemistry 20060209
1H and 13C NMR identification of unexpected 3,4-dihydroquinoxalines in the syntheses of 1,5-benzodiazepine derivatives. Magnetic resonance in chemistry : MRC 20050701
Mechanism of clobazam-induced thyroidal oncogenesis in male rats. Toxicology letters 20031210
[A pharmacological profile of clobazam (Mystan), a new antiepileptic drug]. Nihon yakurigaku zasshi. Folia pharmacologica Japonica 20010801
1,5-Benzodiazepine tricyclic derivatives exerting anti-inflammatory effects in mice by inhibiting interleukin-6 and prostaglandinE(2)production. Pharmacological research 20010501
Biologically active substituted benzodiazepines and their effect on cardiovascular and central nervous system. Bollettino chimico farmaceutico 20010101
1,5-Benzodiazepines. Part XII. Synthesis and biological evaluation of tricyclic and tetracyclic 1,5-benzodiazepine derivatives as nevirapine analogues. European journal of medicinal chemistry 20010101

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