Aplysistatin
| Code | Size | Price |
|---|
| TAR-T30099-5mg | 5mg | £850.00 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Special offer! Add £1 to your order to get a TargetMol CCK-8 Kit. Read more here. | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Quantity:
Prices exclude any Taxes / VAT
Overview
Regulatory Status: RUO
Shipping:
cool pack
Storage:
-20℃
Documents
Further Information
Bioactivity:
Aplysistatin is a bromosesquiterpene derived from sea mollusks.
CAS:
62003-89-8
Formula:
C15H21BrO3
Molecular Weight:
329.234
Purity:
0.98
SMILES:
CC1(C)[C@@H](Br)CC[C@]2(C)O[C@H]3COC(=O)C3=CC[C@@H]12
References
1. Couladouros EA, Vidali VP. Novel stereocontrolled approach to syn- and anti-oxepene-cyclogeranyl trans-fused polycyclic systems: asymmetric total synthesis of (-)-Aplysistatin, (+)-Palisadin A, (+)-Palisadin B, (+)-12-hydroxy-palisadin B, and the AB ring system of adociasulfate-2 and toxicol A. Chemistry. 2004 Aug 6;10(15):3822-35. PubMed PMID: 15281167.
2. Koshimura M, Utsukihara T, Kawamoto M, Saito M, Horiuchi CA, Kuniyoshi M. Biotransformation of bromosesquiterpenes by marine fungi. Phytochemistry. 2009 Dec;70(17-18):2023-6. doi: 10.1016/j.phytochem.2009.08.021. Epub 2009 Sep 21. PubMed PMID: 19772936.
3. Pettit GR, Herald CL, Allen MS, von Dreele RB, Vanell LD, Kao JP, Blake W. The isolation and structure of aplysistatin. J Am Chem Soc. 1977 Jan 5;99(1):262-3. PubMed PMID: 830682.
4. Su H, Yuan Z, Li J, Guo S, Han L, Zhu X, Shi D. [Studies on chemical constituents of Laurencia saitoi]. Zhongguo Zhong Yao Za Zhi. 2009 Apr;34(7):871-4. Chinese. PubMed PMID: 19623985.