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| | saframycin A Basic information |
| Product Name: | saframycin A | | Synonyms: | saframycin A;N-[[(6S)-7α-Cyano-1,5,6,7,9,10,13,14,14aα,15-decahydro-2,11-dimethoxy-3,12,16-trimethyl-1,4,10,13-tetraoxo-6α,15α-epimino-4H-isoquino[3,2-b][3]benzazocin-9β-yl]methyl]-2-oxopropionamide;NSC 325663;Propanamide, N-[[(6S,7R,9R,14aS,15R)-7-cyano-1,5,6,7,9,10,13,14,14a,15-decahydro-2,11-dimethoxy-3,12,16-trimethyl-1,4,10,13-tetraoxo-6,15-imino-4H-isoquino[3,2-b][3]benzazocin-9-yl]methyl]-2-oxo- | | CAS: | 66082-27-7 | | MF: | C29H30N4O8 | | MW: | 562.57 | | EINECS: | | | Product Categories: | | | Mol File: | 66082-27-7.mol |  |
| | saframycin A Chemical Properties |
| Melting point | 120-122 °C | | density | 1.440±0.10 g/cm3(Temp: 25 °C; Press: 760 Torr)(predicted) | | pka | 11.770±0.46(predicted) |
| | saframycin A Usage And Synthesis |
| Uses | Saframycin A has the effect of anti-Gram-positive bacteria. Saframycin A also has weak activity against Gram-negative bacteria and mycobacteria. Saframycin A has the effect of inhibiting mouse lymphocyte L-1210 with an ID50 of 0.0056 μM[1]. | | References | [1] Ryo Tanifuji, et al. Chemo-enzymatic Total Syntheses of Jorunnamycin A, Saframycin A, and N-Fmoc Saframycin Y3. J Am Chem Soc. 2018 Aug 29;140(34):10705-10709. |
| | saframycin A Preparation Products And Raw materials |
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