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| | coformycin Basic information |
| Product Name: | coformycin | | Synonyms: | (r)-3,4,7,8-tetrahydro-3-beta-d-ribofuranosylimidazo(4,5-d)(1,3)diazepin-8-o;5-d)(1,3)diazepin-8-ol,3,4,7,8-tetrahydro-3-beta-d-ribofuranosyl-imidazo((;coformycin;(8R)-3,4,7,8-Tetrahydro-3-β-D-ribofuranosylimidazo[4,5-d][1,3]diazepin-8-ol;(8R)-3-β-D-Ribofuranosyl-3,6,7,8-tetrahydroimidazo[4,5-d][1,3]diazepin-8-ol;Imidazo[4,5-d][1,3]diazepin-8-ol, 3,4,7,8-tetrahydro-3-β-D-ribofuranosyl-, (8R)-;NSC 277817 | | CAS: | 11033-22-0 | | MF: | C11H16N4O5 | | MW: | 284.27 | | EINECS: | | | Product Categories: | | | Mol File: | 11033-22-0.mol |  |
| | coformycin Chemical Properties |
| Melting point | 182-184 °C | | Boiling point | 692.670±65.00 °C(Press: 760.00 Torr)(predicted) | | density | 1.964±0.14 g/cm3(Temp: 25 °C; Press: 760 Torr)(predicted) | | pka | 12.826±0.20(predicted) |
| | coformycin Usage And Synthesis |
| Description | Coformycin is isolated from Nocardia
interforma along with formycin. Coformycin
shows a synergistic effect with
formycin on Yoshida rat sarcoma cells because
of its strong inhibition of adenosine deaminase,
which inactivates formycin. Coformycin, having
a characteristic seven-membered ring base
moiety, is thought to be a typical example of a
“transition-state analog” in the adenosine deaminase
reaction. 2_x0002_-Deoxycoformycin (19b) has
also been isolated also . | | Definition | ChEBI: An N-glycosyl in which (8R)-3,6,7,8-tetrahydroimidazo[4,5-d][1,3]diazepin-8-ol is attached to ribofuranose via a beta-N3-glycosidic bond. compound The
parent of the class of coformycins. |
| | coformycin Preparation Products And Raw materials |
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