MW: 611.63
Salt: Na+
CAS: 1476-53-5
TNP NUMBER: TNP00635
IUPAC: 3-hydroxy-2-(4-hydroxy-3-{[4-hydroxy-3-(3-methylbut-2-enyl)phenyl]carbonylamin o}-8-methyl-2-oxochromen-7-yloxy)-5-methoxy-6,6-dimethyl-2H-3,4,5,6-tetrahydro pyran-4-yl aminooate
Smiles: Cc1c2c(c([O-])c(c(o2)=O)NC(=O)c2cc(C\C=C(\C)C)c(cc2)O)ccc1OC1C(O)C(OC(N)=O)C(C(O1)(C)C)OC
THERAPEUTIC CATEGORY: Antibacterial
VET THERAP CATEGORY: Antimicrobial
REFERENCE: 1. D. Lockshon, D.R. Morris Nucleic Acids Res. 11, 2999, (1983) 2. N.R. Cozzarelli Science 207, 953, (1980) 3. Y. Sumiyoshi et al. J. Gen. Virol. 64, 2329, (1983) Merck Merck 13,6755 Beilstein Beil. 18,IV,8125
SOURCE: Antibiotic sunstance produced by Streptomyces spheroides
ACCEPTORS: 11
DONORS: 5
ROTATION BONDS: 10
N+O: 13
Chiral Centers: 4
LogP: 1.2
LogS: -4.84
LIPINSKI: 2
Synonyms: albamycin(capsule);Albamycinsodium;Cathomycinsodium;Cathomycinsodiumlyovac;Monosodiumnovobiocin;Novobiocin,sodiumderiv.;Novobiocinmonosodium;Sodiumalbamycin
CAS:1476-53-5
MF:C31H35N2NaO11
MW:634.61
EINECS:216-023-6
Product Categories:Coumarin-glycosidesAntibiotics;Antibacterial;Antibiotics;Antibiotics A to;Antibiotics by Application;Antibiotics N-SAntibiotics;Antineoplastic and Immunosuppressive AntibioticsAntibiotics;Chemical Structure Class;Inhibits an EnzymeAntibiotics;Interferes with DNA SynthesisSpectrum of Activity;L - ZMore...Close...;Mechanism of Action NOVOBIOCIN SODIUM SALT
Chemical Properties: mp 215-220 C storage temp. 2-8C Merck 13,6755 Xi,Xn Risk Statements 43-36-36/37/38-20/21/22 Safety Statements 36-36/37-26-37/39 WGK Germany 2 RTECS RD5425000 F 8-10 NOVOBIOCIN SODIUM SALT
Usage And Synthesis: NOVOBIOCIN SODIUM SALT
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