Name | triacsin c |
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Synonyms |
(3E)-1-Oxo-3-[(2E,4E,7E)-2,4,7-undecatrien-1-ylidene]triazane
2E,4E,7E-undecatriene-1-triazine Antibiotic WS-1228A WS 1228A Triacsincapprox. triacsin c from streptomyces sp. Triacsin C 2,4,7-Undecatrienal WS1228A Galloflavin 2E,4E,7E-UNDECATRIENE-1-TRIAZENE 2,4,7-Undecatrienal, 2-nitrosohydrazone, (1E,2E,4E,7E)- 1-hydroxy-3-(E,E,E,-2',4',7'-undecatrienylidine)triazene |
Description | Triacsin C (WS 1228A), a natural intracellular long-chain acyl-CoA synthetases (ACSL) inhibitor, is from Streptomyces aureofaciens. Triacsin C inhibits TAG accumulation into lipid droplets (LD) by suppressing ACSL activity[1]. Triacsin C is found to be highly effective against rotavirus replication[2]. |
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Related Catalog | |
Target |
ACSL[1] |
References |
Density | 0.9±0.1 g/cm3 |
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Boiling Point | 320.7±45.0 °C at 760 mmHg |
Melting Point | 100-102ºC |
Molecular Formula | C11H17N3O |
Molecular Weight | 207.272 |
Flash Point | 147.7±28.7 °C |
Exact Mass | 207.137161 |
PSA | 53.82000 |
LogP | 4.02 |
Vapour Pressure | 0.0±0.7 mmHg at 25°C |
Index of Refraction | 1.485 |
Storage condition | -20°C |
RIDADR | NONH for all modes of transport |
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WGK Germany | 3 |
~% 76896-80-5 |
Literature: Tanaka; Yoshida; Itoh; Imanaka Tetrahedron Letters, 1981 , vol. 22, # 35 p. 3421 - 3422 |
~% 76896-80-5 |
Literature: Tanaka; Yoshida; Itoh; Imanaka Tetrahedron Letters, 1981 , vol. 22, # 35 p. 3421 - 3422 |