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| | gougerotin Basic information |
| Product Name: | gougerotin | | Synonyms: | gougerotin;1-(2-Oxo-4-amino-1,2-dihydropyrimidine-1-yl)-4-(N-methyl-Gly-D-Ser-amino)-1,4-dideoxy-β-D-glucopyranulonamide;1-(4-Amino-1,2-dihydro-2-oxopyrimidin-1-yl)-1,4-dideoxy-4-[[(R)-3-hydroxy-2-[[(methylamino)acetyl]amino]-1-oxopropyl]amino]-β-D-glucopyranulonamide;Aspiculamycin;Asteromycin;Z6572500;6-(4-amino-2-keto-pyrimidin-1-yl)-4,5-dihydroxy-3-[[3-hydroxy-2-(sarcosylamino)propanoyl]amino]tetrahydropyran-2-carboxamide;6-(4-amino-2-oxopyrimidin-1-yl)-4,5-dihydroxy-3-[[3-hydroxy-2-[[2-(methylamino)acetyl]amino]propanoyl]amino]oxane-2-carboxamide | | CAS: | 2096-42-6 | | MF: | C16H25N7O8 | | MW: | 443.41 | | EINECS: | | | Product Categories: | | | Mol File: | 2096-42-6.mol |  |
| | gougerotin Chemical Properties |
| Melting point | 211-217° (dec) | | alpha | D27 +53° (c = 0.8) | | Boiling point | 553.74°C (rough estimate) | | density | 1.2429 (rough estimate) | | refractive index | 1.6800 (estimate) | | color | Needles from MeOH |
| Toxicity | LD50 in mice (mg/kg): 57 i.v. (Kanzaki) |
| | gougerotin Usage And Synthesis |
| Uses | Aspiculamycin, a cytosine nucleoside, is an antibiotic. Aspiculamycin has a broad spectrum of antibacterial activity[1]. | | Safety Profile | Poison by intraperitoneal andintravenous routes. When heated to decomposition itemits toxic fumes of NOx. | | References | [1] Arai M, et al. Aspiculamycin, a new cytosine nucleoside antibiotic. I. Producing organism, fermentation and isolation. J Antibiot (Tokyo). 1974 May;27(5):329-33. DOI:10.7164/antibiotics.27.329 |
| | gougerotin Preparation Products And Raw materials |
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