Company Name: |
Shenzhen SUNGENING Bio-Medical Co., Ltd.
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Tel: |
0755-28967200 13631290199 |
Email: |
wxf@sungening.com |
Products Intro: |
Product Name:13-Deoxocarminomycin CAS:76034-18-9 Purity:99% HPLC or More Package:10MG;25MG;50MG;100MG
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Company Name: |
Zhejiang Huida Biotech Co., LTD
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Tel: |
0571-89903882 13626641628 |
Email: |
jiangnan@huidabiotech.com |
Products Intro: |
Product Name:13-Deoxycarminomycin CAS:76034-18-9 Purity:99% HPLC Package:10mg;100mg;1g;10g;100g
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| 13-Deoxocarminomycin Basic information |
Product Name: | 13-Deoxocarminomycin | Synonyms: | 13-Deoxocarminomycin;13-deoxycarminomycin;(8S)-10α-[(3-Amino-2,3,6-trideoxy-α-L-lyxo-hexopyranosyl)oxy]-8-ethyl-7,8,9,10-tetrahydro-1,6,8α,11-tetrahydroxy-5,12-naphthacenedione;13-Deoxocarminomycin I;D-788-11;R-20X;Daunorubicin Impurity 4;Antibiotic D 788-11 | CAS: | 76034-18-9 | MF: | C26H29NO9 | MW: | 499.513 | EINECS: | | Product Categories: | | Mol File: | 76034-18-9.mol | |
| 13-Deoxocarminomycin Chemical Properties |
Boiling point | 713.1±60.0 °C(Predicted) | density | 1.57±0.1 g/cm3(Predicted) | solubility | Chloroform (Slightly), DMSO (Slightly) | form | Solid | pka | 6.48±0.60(Predicted) | color | Very Dark Green to Black | Stability: | Light Sensitive |
| 13-Deoxocarminomycin Usage And Synthesis |
Uses | 13-Deoxycarminomycin is used as antitumor agents in preparation of 3''-Deamino-3''-(2"-pyrroline-1"-yl)-5-imine-13-deoxyanthracyclines. 13-Deoxycarminomycin is a doxA gene confers on the transformed host the ability to convert Daunomycin and 13-Dihydrodaunomycin to Doxorubicin. | Definition | ChEBI: 13-deoxycarminomycin is a cytotoxic anthracycline antibiotic that is produced by Streptomyces peucetius var. carminatus (a biochemical mutant of Streptomyces peucetius var. caesius), and is active against P-388 murine leukemia. It has a role as an antineoplastic agent and a bacterial metabolite. It is an anthracycline antibiotic, an aminoglycoside antibiotic, a member of p-quinones, a member of tetracenequinones and a tertiary alcohol. It is a conjugate base of a 13-deoxycarminomycin(1+). It derives from a hydride of a tetracene. |
| 13-Deoxocarminomycin Preparation Products And Raw materials |
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