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| | cinerubine B Basic information |
| Product Name: | cinerubine B | | Synonyms: | cinerubine B;Cinerubin B;1-Naphthacenecarboxylic acid, 4-[[[2''',3''-anhydro]-O-3,6-dideoxy-α-L-erythro-hexopyranos-4-ulos-1-yl-(1→4)-O-2,6-dideoxy-α-L-lyxo-hexopyranosyl-(1→4)-2,3,6-trideoxy-3-(dimethylamino)-α-L-lyxo-hexopyranosyl]oxy]-2-ethyl-1,2,3,4,6,11-hexahydro-2,5,7,10-tetrahydroxy-6,11-dioxo-, methyl ester, (1R,2R,... | | CAS: | 35906-51-5 | | MF: | C42H51NO16 | | MW: | 825.85 | | EINECS: | | | Product Categories: | | | Mol File: | 35906-51-5.mol |  |
| | cinerubine B Chemical Properties |
| Melting point | 173°C | | Boiling point | 762.31°C (rough estimate) | | density | 1.2494 (rough estimate) | | refractive index | 1.6220 (estimate) | | solubility | Dichloromethane: soluble
DMSO: soluble
Ethanol: soluble
Methanol: soluble | | pka | 6.20±0.70(Predicted) |
| | cinerubine B Usage And Synthesis |
| Uses | Cinerubine B is an antimitotic antibiotic from Streptomyces. | | References | [1] LEONARDO JOSE SILVA. Actinobacteria from Antarctica as a source for anticancer discovery.[J]. ACS Applied Electronic Materials, 2020: 13870. DOI: 10.1038/s41598-020-69786-2
[2] Y MATSUZAWA. Structure-activity relationships of anthracyclines relative to cytotoxicity and effects on macromolecular synthesis in L1210 leukemia cells.[J]. Journal of Antibiotics, 1981, 34 12: 1596-1607. DOI: 10.7164/antibiotics.34.1596 |
| | cinerubine B Preparation Products And Raw materials |
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