16,16-DIMETHYL PROSTAGLANDIN A2
16,16-DIMETHYL PROSTAGLANDIN A2 Basic information
- Product Name:
- 16,16-DIMETHYL PROSTAGLANDIN A2
- Synonyms:
-
- 9-OXO-15R-HYDROXY-16,16-DIMETHYL-PROSTA-5Z,10,13E-TRIEN-1-OIC ACID
- 16,16-DIMETHYL PROSTAGLANDIN A2
- MOTPSJUHMGPRFZ-QEJIITRLSA-N
- Prosta-5,10,13-trien-1-oic acid, 15-hydroxy-16,16-dimethyl-9-oxo-, (5Z,13E,15R)-
- CAS:
- 41691-92-3
- MF:
- C22H34O4
- MW:
- 362.5
- Mol File:
- 41691-92-3.mol
16,16-DIMETHYL PROSTAGLANDIN A2 Chemical Properties
- 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)
16,16-DIMETHYL PROSTAGLANDIN A2 Usage And Synthesis
Description
16,16-
Uses
16,16-dimethyl Prostaglandin A2 is a PGA2 analog studied for its antiproliferative properties.
Definition
ChEBI: 16,16-dimethyl-PGA2 is a prostanoid.
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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