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58662-84-3

58662-84-3 Structure

58662-84-3 Structure
IdentificationBack Directory
[Name]

Meclonazepam
[CAS]

58662-84-3
[Synonyms]

Ro-11-3128
Meclonazepam
Meclonazepamum
Meclonazepam, 3-Methylclonazepam
(3S)-5-(2-chlorophenyl)-3-methyl-7-nitro-1,3-dihydro-1,4-benzodiazepin-2-one
(S)-5-(2-Chlorophenyl)-1,3-dihydro-3-methyl-7-nitro-2H-1,4-benzodiazepin-2-one
(3S)-5-(2-Chlorophenyl)-1,3-dihydro-3-methyl-7-nitro-2H-1,4-benzodiazepin-2-one
2H-1,4-Benzodiazepin-2-one, 5-(2-chlorophenyl)-1,3-dihydro-3-methyl-7-nitro-, (3S)-
[EINECS(EC#)]

200-001-8
[Molecular Formula]

C16H12ClN3O3
[MOL File]

58662-84-3.mol
[Molecular Weight]

329.74
Chemical PropertiesBack Directory
[Boiling point ]

522.1±50.0 °C(Predicted)
[density ]

1.46
[storage temp. ]

-20°C
[solubility ]

DMF: 25 mg/ml; DMSO: 25 mg/ml; DMSO:PBS (pH 7.2) (1:1): 0.5 mg/ml; Methanol: 1 mg/ml
[form ]

A crystalline solid
[pka]

11.24±0.70(Predicted)
[color ]

White to off-white
Hazard InformationBack Directory
[Uses]

Meclonazepam-d4, is the labeled analogue of Meclonazepam (M202790), a drug of a benzodiazepine class similar in structure to Clonazepam (C587080). It has sedative and anxiolytic properties. It has also shown to have anti-parasitic effects against the parasitic worm Schistosoma mansoni.
[in vivo]

Meclonazepam (0.1-5.6 mg/kg) exhibits anxiolytic effect in gerbils[1].
Meclonazepam (40 and 80 mg/kg) Has highly significant effect on the immature schistosomes[2].

Animal Model:Adult experimentally naive male Mongolian gerbils (Meriones unguiculatus)[1]
Dosage:0.1, 0.3, 1.0, 3.0, 5.6 mg/kg
Administration:Administration intraperitoneally (IP) 5 min prior to training onset.
Result:The ED50 of 0.77-0.78 mg/kg at the 5 min post-injection (p.i.).
Animal Model:CB6F1 mice were infected with single-sex male S. mansoni cercariae 28 days before treatment[2]
Dosage:40 and 80 mg/kg
Administration:Administered by gavage either as single drugs or in a sequence consisting of 1 dose of Praziquantel (PZQ), a 5-min interval, 1 dose of Ro, a 15-min interval, a second dose of PZQ.
Result:PZQ had no significant effect on the immature schistosomes, whereas Ro 11-3128 was highly effective.
[IC 50]

Schistosome
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