
| Chemical & Physical Properties | |
|---|---|
| CAS Number | 1476-53-5 |
| Catalog No. | 2A-9091174 |
| Chinese Name | 新生霉素(钠盐) |
| Synonyms | MFCD00066541; NOVOBIOCIN SODIUM SALT; Novobiocin sodium; EINECS 216-023-6 |
| Molecular Formula | C31H35N2NaO11 |
| Molecular Weight | 634.61 |
| Purity | 98.00 |
| Density | 1.42g/cm3 |
| Boiling Point | 848.2ºC at 760mmHg |
| Melting Point | 215-220ºC |
| Storage Condition | Sealed, store at 2 ºC -8 ºC |
| Application | Novobiocin sodium is an antibiotic derived from the genus Streptomyces. |
| PubChem ID | 582999 |
| SMILES | COC1C(OC(N)=O)C(O)C(Oc2ccc3c(O)c(NC(=O)c4ccc(O)c(CC=C(C)C)c4)c(=O)oc3c2C)OC1(C)C |
| InChI | InChI=1S/C31H36N2O11.Na/c1-14(2)7-8-16-13-17(9-11-19(16)34)27(37)33-21-22(35)18-10-12-20(15(3)24(18)42-28(21)38)41-29-23(36)25(43-30(32)39)26(40-6)31(4,5)44-29;/h7,9-13,23,25-26,29,34-36H,8H2,1-6H3,(H2,32,39)(H,33,37);/q;+1/p-1/t23-,25+,26-,29-;/m1./s1 |
| InChI Key | YJQPYGGHQPGBLI-TXGFFYAOSA-N |
| Bioactivity | Novobiocin Sodium is an antibiotic compound derived from Streptomyces niveus.Target: AntibacterialNovobiocin, also known as albamycin or cathomycin, is an aminocoumarin antibiotic that is produced by the actinomycete Streptomyces niveus, which has recently been identified as a subjective synonym for S. spheroides a member of the order Actinobacteria . Other aminocoumarin antibiotics include clorobiocin and coumermycin A1. The molecular basis of action of novobiocin, and other related drugs clorobiocin and coumermycin A1 has been examined. Aminocoumarins are very potent inhibitors of bacterial DNA gyrase and work by targeting the GyrB subunit of the enzyme involved in energy transduction. Novobiocin as well as the other aminocoumarin antibiotics act as competitive inhibitors of the ATPase reaction catalysed by GyrB. The potency of novobiocin is considerably higher than that of the fluoroquinolones that also target DNA gyrase, but at a different site on the enzyme. The GyrA subunit is involved in the DNA nicking and ligation activity [1-4]. Related Catalog Signaling Pathways >> Autophagy >> Autophagy Signaling Pathways >> Anti-infection >> Bacterial Natural Products >> Others Research Areas >> Infection References [1]. http://www.ncbi.nlm.nih.gov/pubmed/8231802 [2]. Maxwell, A., DNA gyrase as a drug target. Biochem Soc Trans, 1999. 27(2): p. 48-53. [3]. Lewis, R.J., F.T. Tsai, and D.B. Wigley, Molecular mechanisms of drug inhibition of DNA gyrase. Bioessays, 1996. 18(8): p. 661-71. [4]. Maxwell, A. and D.M. Lawson, The ATP-binding site of type II topoisomerases as a target for antibacterial drugs. Curr Top Med Chem, 2003. 3(3): p. 283-303. Chemical & Physical Properties Density 1.42g/cm3 Boiling Point 848.2ºC at 760mmHg Melting Point 215-220ºC Molecular Formula C31H35N2NaO11 Molecular Weight 634.60600 Flash Point 466.8ºC Exact Mass 634.21400 PSA 202.84000 LogP 4.83860 InChIKey YJQPYGGHQPGBLI-TXGFFYAOSA-N SMILES COC1C(OC(N)=O)C(O)C(Oc2ccc3c(O)c(NC(=O)c4ccc(O)c(CC=C(C)C)c4)c(=O)oc3c2C)OC1(C)C Storage condition -20°C |
| Use of | Novobiocin Sodium is an antibiotic compound derived from Streptomyces niveus.Target: AntibacterialNovobiocin, also known as albamycin or cathomycin, is an aminocoumarin antibiotic that is produced by the actinomycete Streptomyces niveus, which has recently been identified as a subjective synonym for S. spheroides a member of the order Actinobacteria . Other aminocoumarin antibiotics include clorobiocin and coumermycin A1. The molecular basis of action of novobiocin, and other related drugs clorobiocin and coumermycin A1 has been examined. Aminocoumarins are very potent inhibitors of bacterial DNA gyrase and work by targeting the GyrB subunit of the enzyme involved in energy transduction. Novobiocin as well as the other aminocoumarin antibiotics act as competitive inhibitors of the ATPase reaction catalysed by GyrB. The potency of novobiocin is considerably higher than that of the fluoroquinolones that also target DNA gyrase, but at a different site on the enzyme. The GyrA subunit is involved in the DNA nicking and ligation activity [1-4]. Properties Articles37 Name Novobiocin Sodium Salt Synonym More Synonyms Novobiocin Sodium Salt Biological Activity Description Novobiocin Sodium is an antibiotic compound derived from Streptomyces niveus.Target: AntibacterialNovobiocin, also known as albamycin or cathomycin, is an aminocoumarin antibiotic that is produced by the actinomycete Streptomyces niveus, which has recently been identified as a subjective synonym for S. spheroides a member of the order Actinobacteria . Other aminocoumarin antibiotics include clorobiocin and coumermycin A1. The molecular basis of action of novobiocin, and other related drugs clorobiocin and coumermycin A1 has been examined. Aminocoumarins are very potent inhibitors of bacterial DNA gyrase and work by targeting the GyrB subunit of the enzyme involved in energy transduction. Novobiocin as well as the other aminocoumarin antibiotics act as competitive inhibitors of the ATPase reaction catalysed by GyrB. The potency of novobiocin is considerably higher than that of the fluoroquinolones that also target DNA gyrase, but at a different site on the enzyme. The GyrA subunit is involved in the DNA nicking and ligation activity [1-4]. Related Catalog Signaling Pathways >> Autophagy >> Autophagy Signaling Pathways >> Anti-infection >> Bacterial Natural Products >> Others Research Areas >> Infection References [1]. http://www.ncbi.nlm.nih.gov/pubmed/8231802 [2]. Maxwell, A., DNA gyrase as a drug target. Biochem Soc Trans, 1999. 27(2): p. 48-53. [3]. Lewis, R.J., F.T. Tsai, and D.B. Wigley, Molecular mechanisms of drug inhibition of DNA gyrase. Bioessays, 1996. 18(8): p. 661-71. [4]. Maxwell, A. and D.M. Lawson, The ATP-binding site of type II topoisomerases as a target for antibacterial drugs. Curr Top Med Chem, 2003. 3(3): p. 283-303. Chemical & Physical Properties Molecular Formula C31H35N2NaO11 Exact Mass 634.21400 PSA 202.84000 LogP 4.83860 InChIKey YJQPYGGHQPGBLI-TXGFFYAOSA-N |
| Transport Info | Product name: Novobiocin (sodium salt) |
| Related Products in Specialty Chemicals | ||
|---|---|---|
| 7-Bromo-2,3-dihydro-isoindol-1-one | 200049-46-3 | 2A-9091167 |
| 1,4-DIBROMO-2-CHLOROBENZENE | 3460-24-0 | 2A-9091168 |
| CELLULOSEPHOSPHATE | 9015-14-9 | 2A-9091169 |
| Dimethyl-4-toluidine-N-oxide | 825-85-4 | 2A-9091172 |
| BENZOICACID,2-[[(2'-CYANO[1,1'-BIPHENYL]-4-YL)METHYL]AMINO]-3-NITRO-METHYLESTER | 139481-28-0 | 2A-9091173 |
| Trichloroacetamidinehydrochloride | 42563-97-3 | 2A-9091175 |
| Methyl3-(benzylamino)propanoate | 23574-01-8 | 2A-9091179 |
| 3-(2,4)-Dimethoxybenzylidineanabaseine(DMXB;alsoknownasGTS-21) | 156223-05-1 | 2A-9091180 |
| Chloro(chloromethoxy)methane | 542-88-1 | 2A-0201909 |
| 2,2-Dimethyl-3-pentanol | 3970-62-5 | 2A-9091185 |
| Browse all Specialty Chemicals products » | ||
Phone:
630-322-8886
630-322-8887
Email:
Office Locations:
Chicago, IL, USA
San Francisco, CA, USA