Cellocidin是由许多链霉菌属物种产生的小型中性炔烃,最早是由Suzuki及其同事于1958年发现的。Cellocidin具有广泛的抗菌,抗真菌和抗肿瘤特性,因为它能够与半胱氨酸和谷胱甘肽等内源性硫醇反应。Cellocidin在许多使用放线菌粗提物的生物测定中以弱活性存在,因此是化学和生物测定去重复的有用标准。 Cellocidin is a small neutral alkyne produced by a number of Streptomyces species, first discovered by Suzuki and colleagues in 1958. Cellocidin has a broad antibacterial, antifungal and antitumor profile due to its ability to react with endogenous thiols like cysteine and glutathione. Cellocidin occurs as a weak active in many bioassays using actinomycete crude extracts and is thus a useful standard for chemical and bioassay dereplication.
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Cellocidin
Dangerous GoodsCAS number:543-21-5 molecular formula:C4H4N2O2
overview
compound introduction
Specs
| Chinese alias | 乙炔二羰酰胺 | ||
| English alias | CHEBI:51763 | A830097 | BRN 1756134 | FT-0602756 | Q5058318 | CCG-35858 | SCHEMBL1003846 | 5-SULFO-2-AMINOBENZOICACIDSODIUMSALT | Acetylendicarboxamid | Acetylene diamide | Z1203578096 | 2-Butynediamide | But-2-ynedioic acid diamide | NSC38643 | NSC-38643 | ||
| CAS number | 543-21-5 | molecular formula | C4H4N2O2 |
| molecular weight | 112.09 g/mol | Exact mass | ≥95% |
| PSA | 86.200 Ų | logp | -1.2 |
numbering system
No numbering system information yet
physicochemical properties
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Safety information
pictogram:
GHS07
Signal word:
Warning
Hazard Statement:
H302: 吞食有害
Statement of Preventive Measures:
P501: 将内容物/容器处理到。。。 P264: 处理后要彻底洗手。 P270: 使用本产品时,请勿进食、饮水或吸烟。 P330: 漱口 P301+P317: 如果被吞咽:请寻求医疗帮助。
UN Number:
3462
Packing Group:
III
Production methods and uses
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MSDS
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