A synthesis of the thromboxane A2 analog, a-(9,11), (11,12)-dideoxa-(9,11)-methylene-(11,12)-epithio-thromboxane A2 methyl ester 2, is described.
Synthesis of thromboxane A2 analog DL-(9,11), (11,12)-dideoxa-(9,11)-epithio-(11,12)-methylene-thromboxane A2
โ Scribed by Shuichi Ohuchida; Nobuyuki Hamanaka; Masaki Hayashi
- Publisher
- Elsevier Science
- Year
- 1981
- Tongue
- French
- Weight
- 263 KB
- Volume
- 22
- Category
- Article
- ISSN
- 0040-4039
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โฆ Synopsis
A synthesis of the thromboxane A2 analog,&-(9,11),(11,12)-dideoxa-(9,11)-epithio-(11,12)-methylene-thromboxane A2 is described.
๐ SIMILAR VOLUMES
The thromboxane A2 analog, dl-(9,11),( 11,12)-dideoxa-(9,11),(11,12)dimethylene thromboxane A2 (TX A2) has been synthesized; the compound showed high agonist activities on platelet aggregation and the aorta contracting activities. In 1975, Samuelsson et al. discovered a new family of arachidonic aci
A synthesis of nitrogen containing thromboxane A2 analog, c-(9,11)methano-(11,12)-amino thromboxane A2 (a is described. Thromboxane A2 (TXA~) 1s an extremely unstable substance possessing very important biological actlvltles (platelet aggregation and vasoconstrlctlon).
The thromboxane A1 (TXAI) analogue (1) has been synthesised from the ketone (2). Thromboxane AZ (TXAZ), an unstable (t% 32sec. at 37O) metabolite of the prostaglandin endo-
+)-(9,11)-Epithia-(11,12)-methano-thromboxane A2, which