Product Name

  • Name

    Moveltipril calcium

  • EINECS
  • CAS No. 85921-53-5
  • Density 1.248g/cm3
  • Solubility
  • Melting Point ~190°
  • Formula C19H30 N2 O5 S . 1/2 Ca
  • Boiling Point 658.9°Cat760mmHg
  • Molecular Weight 835.10
  • Flash Point 352.3°C
  • Transport Information
  • Appearance
  • Safety
  • Risk Codes
  • Molecular Structure Molecular Structure of 85921-53-5 (Moveltipril calcium)
  • Hazard Symbols
  • Synonyms L-Proline,1-[3-[[2-[(cyclohexylcarbonyl)amino]-1-oxopropyl]thio]-2-methyl-1-oxopropyl]-,calcium salt (2:1), [R-(R*,S*)]-; Altiopril calcium; L-Proline,1-[(2S)-3-[[(2R)-2-[(cyclohexylcarbonyl)amino]-1-oxopropyl]thio]-2-methyl-1-oxopropyl]-,calcium salt (2:1); Lowpres; MC 838; Moveltipril calcium
  • PSA 236.16000
  • LogP 4.58920

Moveltipril calcium Chemical Properties

Molecular Structure:

Molecular Formula: 2(C19H29N2O5S).Ca
Molecular Weight: 835.10
Product Name: Moveltipril calcium
Synonyms of Moveltipril calcium (CAS NO.85921-53-5): MC 838 ; Moveltipril calcium salt ; Altiopril calcium ; Calcium (-)-N-(((S)-3-(N-cyclohexylcarbonyl-D-alanyl)thio)-2-methylpropionyl)-L-prolinate ; Lowpres ; MC-838 ; L-Proline, 1-(3-((2-((cyclohexylcarbonyl)amino)-1-oxopropyl)thio)-2-methyl-1-oxopropyl)-, calcium salt (2:1), (R-(R*,S*))-
CAS NO: 85921-53-5
Product Categories: Drug / Therapeutic Agent ; Reproductive Effect

Moveltipril calcium Toxicity Data With Reference

Organism Test Type Route Reported Dose (Normalized Dose) Effect Source
dog LD50 oral > 6gm/kg (6000mg/kg)   Tohoku Journal of Experimental Medicine. Vol. 152, Pg. 363, 1987.
mouse LD50 intraperitoneal 2100mg/kg (2100mg/kg)   Tohoku Journal of Experimental Medicine. Vol. 152, Pg. 363, 1987.
mouse LD50 oral > 10gm/kg (10000mg/kg)   Tohoku Journal of Experimental Medicine. Vol. 152, Pg. 363, 1987.
mouse LD50 subcutaneous 3gm/kg (3000mg/kg)   Tohoku Journal of Experimental Medicine. Vol. 152, Pg. 363, 1987.
rat LD50 intraperitoneal 1300mg/kg (1300mg/kg)   Tohoku Journal of Experimental Medicine. Vol. 152, Pg. 363, 1987.
rat LD50 oral > 10gm/kg (10000mg/kg)   Tohoku Journal of Experimental Medicine. Vol. 152, Pg. 363, 1987.
rat LD50 subcutaneous 3400mg/kg (3400mg/kg)   Tohoku Journal of Experimental Medicine. Vol. 152, Pg. 363, 1987.

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