ChemicalBook--->CAS DataBase List--->41691-92-3

41691-92-3

41691-92-3 Structure

41691-92-3 Structure
IdentificationBack Directory
[Name]

16,16-DIMETHYL PROSTAGLANDIN A2
[CAS]

41691-92-3
[Synonyms]

MOTPSJUHMGPRFZ-QEJIITRLSA-N
16,16-DIMETHYL PROSTAGLANDIN A2
9-OXO-15R-HYDROXY-16,16-DIMETHYL-PROSTA-5Z,10,13E-TRIEN-1-OIC ACID
Prosta-5,10,13-trien-1-oic acid, 15-hydroxy-16,16-dimethyl-9-oxo-, (5Z,13E,15R)-
[Molecular Formula]

C22H34O4
[MDL Number]

MFCD00065727
[MOL File]

41691-92-3.mol
[Molecular Weight]

362.5
Chemical PropertiesBack Directory
[Boiling point ]

526.9±50.0 °C(Predicted)
[density ]

1.078±0.06 g/cm3(Predicted)
[storage temp. ]

Store at -20°C
[solubility ]

DMF: >75 mg/ml (from PGA1); DMSO: >50 mg/ml (from PGA1); Ethanol: >100 mg/ml (from PGA1); PBS pH 7.2: >2.4 mg/ml (from PGA1)
[pka]

4.75±0.10(Predicted)
Safety DataBack Directory
[Symbol(GHS) ]

Flame (GHS02)Exclamation Mark (GHS07)
GHS02,GHS07
[Signal word ]

Danger
[Hazard statements ]

H225-H302-H319-H336
[Precautionary statements ]

P210-P240-P241-P242-P243-P261-P264-P270-P271-P280-P301+P312-P330-P303+P361+P353-P304+P340-P305+P351+P338-P337+P313-P370+P378-P403+P233-P403+P235-P405-P501
Hazard InformationBack Directory
[Description]

16,16-dimethyl PGA2 is a metabolism-resistant analog of PGA2 with a prolonged in vivo half-life. It inhibits the proliferation of Sendai virus in cultured African green monkey kidney cells by >90% at a concentration of 4 μg/ml. Daily infusion of 10 μg of 16,16-dimethyl PGA2 methyl ester into mice infected with influenza A virus increased survival by 40%. Similar treatment of mice inoculated with erythroleukemia cells delayed tumor growth and increased survival time.
[Uses]

16,16-dimethyl Prostaglandin A2 is a PGA2 analog studied for its antiproliferative properties.
[Definition]

ChEBI: 16,16-dimethyl-PGA2 is a prostanoid.
[storage]

Store at -20°C
[References]

[1] M. G. SANTORO. Prostaglandin A Compounds as Antiviral Agents[J]. Science, 1980, 209 4460. DOI: 10.1126/science.6157190
[2] M. G. SANTORO. Antiviral activity of a synthetic analog of prostaglandin A in mice infected with influenza A virus[J]. Archives of Virology, 1988, 99 1-2: 89-100. DOI: 10.1007/bf01311026
[3] S MARINI. Growth inhibition of Friend erythroleukaemia cell tumours in vivo by a synthetic analogue of prostaglandin A: an action independent of natural killer-activity[J]. British Journal of Cancer, 1990, 61 3: 394-399. DOI: 10.1038/bjc.1990.86
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