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Home > products > 6H-Pyridazino[1,2-a][1,2]diazepine-1-carboxylicacid, 9-[[(1S)-1-(ethoxycarbonyl)-3-phenylpropyl]amino]octahydro-10-oxo-,hydrate (1:1), (1S,9S)-

6H-Pyridazino[1,2-a][1,2]diazepine-1-carboxylicacid, 9-[[(1S)-1-(ethoxycarbonyl)-3-phenylpropyl]amino]octahydro-10-oxo-,hydrate (1:1), (1S,9S)- cas no:92077-78-6

Synonyms: 6H-Pyridazino[1,2-a][1,2]diazepine-1-carboxylicacid, 9-[[(1S)-1-(ethoxycarbonyl)-3-phenylpropyl]amino]octahydro-10-oxo-,monohydrate, (1S,9S)- (9CI);6H-Pyridazino[1,2-a][1,2]diazepine-1-carboxylicacid, 9-[[1-(ethoxycarbonyl)-3-phenylpropyl]amino]octahydro-10-oxo-,monohydrate, [1S-[1a,9a(R*)]]-;Cilazapril monohydrate;(1S,9S)-9-(((S)-1-Carboxy-3-phenylpropyl)amino)octahydro-10-;Cilazapril;Cilazapril monohydrate;UNII-19KW7PI29F;Inhibace;

Identification
Name6H-Pyridazino[1,2-a][1,2]diazepine-1-carboxylicacid, 9-[[(1S)-1-(ethoxycarbonyl)-3-phenylpropyl]amino]octahydro-10-oxo-,hydrate (1:1), (1S,9S)-
CAS92077-78-6
Synonyms6H-Pyridazino[1,2-a][1,2]diazepine-1-carboxylicacid, 9-[[(1S)-1-(ethoxycarbonyl)-3-phenylpropyl]amino]octahydro-10-oxo-,monohydrate, (1S,9S)- (9CI);6H-Pyridazino[1,2-a][1,2]diazepine-1-carboxylicacid, 9-[[1-(ethoxycarbonyl)-3-phenylpropyl]amino]octahydro-10-oxo-,monohydrate, [1S-[1a,9a(R*)]]-;Cilazapril monohydrate;(1S,9S)-9-(((S)-1-Carboxy-3-phenylpropyl)amino)octahydro-10-;Cilazapril;Cilazapril monohydrate;UNII-19KW7PI29F;Inhibace;
Molecular FormulaC22H31N3O5.H2O
Molecular Weight435.58
Safety Data

Safety

A poison by intravenous route. Moderately toxic by subcutaneous and intraperitoneal routes. Human systemic effects by ingestion: dermatitis. When heated to decomposition it emits toxic vapors of NOx.


Toxicity
Organism Test Type Route Reported Dose (Normalized Dose) Effect Source
monkey LD50 oral > 4gm/kg (4000mg/kg)   Cardiovascular Drug Reviews. Vol. 8, Pg. 1, 1990.
mouse LD50 intraperitoneal 1300mg/kg (1300mg/kg)   Cardiovascular Drug Reviews. Vol. 8, Pg. 1, 1990.
mouse LD50 intravenous > 30mg/kg (30mg/kg)   Yakuri to Chiryo. Pharmacology and Therapeutics. Vol. 17, Pg. 1281, 1989.
mouse LD50 subcutaneous > 1gm/kg (1000mg/kg)

skin and appendages (skin): "dermatitis, other: after systemic exposure" skin and appendages (skin): hair: other

Yakuri to Chiryo. Pharmacology and Therapeutics. Vol. 17, Pg. 1281, 1989.
mouse LDLo oral 5gm/kg (5000mg/kg)

behavioral: altered sleep time (including change in righting reflex) behavioral: convulsions or effect on seizure threshold

Yakuri to Chiryo. Pharmacology and Therapeutics. Vol. 17, Pg. 1281, 1989.
rat LD50 intraperitoneal 830mg/kg (830mg/kg)   Cardiovascular Drug Reviews. Vol. 8, Pg. 1, 1990.
rat LD50 intravenous > 30mg/kg (30mg/kg)   Yakuri to Chiryo. Pharmacology and Therapeutics. Vol. 17, Pg. 1281, 1989.
rat LD50 oral > 5gm/kg (5000mg/kg)

gastrointestinal: changes in structure or function of salivary glands gastrointestinal: "hypermotility, diarrhea"

Yakuri to Chiryo. Pharmacology and Therapeutics. Vol. 17, Pg. 1281, 1989.
rat LD50 subcutaneous > 1gm/kg (1000mg/kg)

skin and appendages (skin): "dermatitis, other: after systemic exposure" behavioral: regidity

Yakuri to Chiryo. Pharmacology and Therapeutics. Vol. 17, Pg. 1281, 1989.
women TDLo oral 15mg/kg/22W-I (15mg/kg)

skin and appendages (skin): "dermatitis, other: after systemic exposure"

Lancet. Vol. 345, Pg. 398, 1995.

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