WS009 A
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| Category | Bioactive by-products |
| Catalog number | BBF-01638 |
| CAS | |
| Molecular Weight | 519.52 |
| Molecular Formula | C24H25NO10S |
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Description
WS009 A is an endothelin receptor antagonists isolated from Streptomyces sp. no. 89009. II. The IC50 is 5.8 X 10(-6) mol/L.
Specification
| Synonyms | WS-009A |
Properties
| Appearance | White Powder |
| Melting Point | 170-172°C |
Reference Reading
1. WS009 A and B, new endothelin receptor antagonists isolated from Streptomyces sp. no. 89009. II. Biological characterization and pharmacological characterization of WS009 A and B
S Miyata, M Hashimoto, K Fujie, M Shouho, K Sogabe, S Kiyoto, M Okuhara, M Kohsaka J Antibiot (Tokyo). 1992 Jul;45(7):1041-6. doi: 10.7164/antibiotics.45.1041.
WS009 A and B, produced by Streptomyces sp. No. 89009, were found to be competitive and specific antagonists against endothelin (ET)-1 receptors in in vitro studies and also active in in vivo studies. Furthermore, WS009 A and B were specific antagonists for vascular ET-1 receptors (ETA receptors) and significantly prevented the accumulation of intracellular inositol 1,4,5-triphosphate (IP3) in endothelin treated rat aorta tissues.
2. WS009 A and B, new endothelin receptor antagonists isolated from Streptomyces sp. no. 89009. I. Taxonomy, fermentation, isolation, physico-chemical properties and biological activities
S Miyata, N Ohhata, H Murai, Y Masui, M Ezaki, S Takase, M Nishikawa, S Kiyoto, M Okuhara, M Kohsaka J Antibiot (Tokyo). 1992 Jul;45(7):1029-40. doi: 10.7164/antibiotics.45.1029.
WS009 A and B novel endothelin receptor antagonists, have been isolated from the fermentation broth of Streptomyces sp. No. 89009. These antagonists were purified from the culture filtrate followed by Diaion SP-207, DEAE Toyopearl column chromatography and HPLC. WS009 A and B showed selective activity in an endothelin receptor binding assay with IC50 of 5.8 x 10(-6) M and 6.7 x 10(-7) M, respectively. On the basis of spectroscopic and chemical evidence, the structures of WS009 A and B have been established as 1 and 3, and are highly hydroxylated benz[a]anthraquinone chromophores.
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Bio Calculators
* Our calculator is based on the following equation:
Concentration (start) x Volume (start) = Concentration (final) x Volume (final)
It is commonly abbreviated as: C1V1 = C2V2
* Total Molecular Weight:
g/mol
Tip: Chemical formula is case sensitive. C22H30N4O √ c22h30n40 ╳
