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Substance Name: Mopidamol [INN:BAN]
RN: 13665-88-8
UNII: 4Q0IWP8B8O
InChIKey: FOYWNSCCNCUEPU-UHFFFAOYSA-N

Note

  • A phosphodiesterase inhibitor which inhibits platelet aggregation. Formerly used as an antineoplastic.

Molecular Formula

  • C19-H31-N7-O4

Molecular Weight

  • 421.499
 

Classification Codes

  • Antineoplastic Agents
  • Drug / Therapeutic Agent
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Names and Synonyms

Name of Substance

  • Mopidamol
  • Mopidamol [INN:BAN]

MeSH Heading

  • Mopidamol

Synonyms

  • 2,2',2'',2'''-((4-Piperidinopyrimido(5,4-d)pyrimidine-2,6-diyl)dinitrilo)tetraethanol
  • 2,2',2',2'''-((4-Piperidinopyrimido(5,4-d)pyrimidine-2,6-diyl)dinitrilo)tetraethanol
  • 2,6-Bis(diethanolamino)-4-piperidinopyrimido(5,4-d)pyrimidine
  • BRN 0587985
  • Compound RA-233
  • EINECS 237-145-6
  • Mopidamol
  • Mopidamolum
  • Mopidamolum [INN-Latin]
  • R-A 233-BS
  • RA 233
  • Rapenton
  • UNII-4Q0IWP8B8O

Systematic Names

  • 2,2',2'',2'''-((4-Piperidinopyrimido(5,4-d)pyrimidine-2,6-diyl)dinitrilo)tetraethanol
  • Ethanol, 2,2',2'',2'''-((4-(1-piperidinyl)pyrimido(5,4-d)pyrimidine-2,6-diyl)dinitrilo)tetrakis-
  • Ethanol, 2,2',2'',2'''-((4-piperidinopyrimido(5,4-d)pyrimidine-2,6-diyl)dinitrilo)tetra-
  • Mopidamol

Registry Numbers

CAS Registry Number

  • 13665-88-8

FDA UNII

  • 4Q0IWP8B8O

System Generated Number

  • 0013665888

Structure Descriptors

InChI

1S/C19H31N7O4/c27-10-6-25(7-11-28)18-20-14-15-16(22-18)17(24-4-2-1-3-5-24)23-19(21-15)26(8-12-29)9-13-30/h14,27-30H,1-13H2

InChIKey

FOYWNSCCNCUEPU-UHFFFAOYSA-N

Smiles

c12c(N3CCCCC3)nc(N(CCO)CCO)nc1cnc(n2)N(CCO)CCO

Toxicity

Organism Test Type Route Reported Dose (Normalized Dose) Effect Source
guinea pig LD50 oral 3gm/kg (3000mg/kg)   Medicamentos de Actualidad. Vol. 17, Pg. 89, 1981.
mouse LD50 intravenous 148mg/kg (148mg/kg)   Medicamentos de Actualidad. Vol. 17, Pg. 89, 1981.
mouse LD50 oral 465mg/kg (465mg/kg)   German Offenlegungsschrift Patent Document. Vol. #2931573,
rat LD50 intraperitoneal 408mg/kg (408mg/kg)   Medicamentos de Actualidad. Vol. 17, Pg. 89, 1981.
rat LD50 oral 3gm/kg (3000mg/kg)   Medicamentos de Actualidad. Vol. 17, Pg. 89, 1981.

Physical Properties

Physical Property Value Units Temp (deg C) Source
Melting Point 157.5 deg C   EXP
log P (octanol-water) 0.190 (none)   EST
Atmospheric OH Rate Constant 2.85E-10 cm3/molecule-sec 25 EST

Physical property data is provided to ChemIDplus by SRC, Inc.