A synthesis of the thromboxane A2 analog,&-(9,11),(11,12)-dideoxa-(9,11)-epithio-(11,12)-methylene-thromboxane A2 is described.
Synthesis of thromboxane A2 analog DL-(9,11), (11,12)-dideoxa-(9,11)-methylene-(11,12)-epithio-thromboxane A2 methyl ester
โ Scribed by Shunji Kosuge; Nobuyuki Hamanaka; Masaki Hayashi
- Publisher
- Elsevier Science
- Year
- 1981
- Tongue
- French
- Weight
- 196 KB
- Volume
- 22
- Category
- Article
- ISSN
- 0040-4039
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โฆ Synopsis
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.
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).
+)-(9,11)-Epithia-(11,12)-methano-thromboxane A2, which
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-