InChI=1S/C66H75Cl2N9O24/c1- 23(2) 12- 34(71- 5) 58(88) 76- 49- 51(83) 26- 7- 10- 38(32(67) 14- 26) 97- 40- 16- 28- 17- 41(55(40) 101- 65- 56(54(86) 53(85) 42(22- 78) 99- 65) 100- 44- 21- 66(4,70) 57(87) 24(3) 96- 44) 98- 39- 11- 8- 27(15- 33(39) 68) 52(84) 50- 63(93) 75- 48(64(94) 95) 31- 18- 29(79) 19- 37(81) 45(31) 30- 13- 25(6- 9- 36(30) 80) 46(60(90) 77- 50) 74- 61(91) 47(28) 73- 59(89) 35(20- 43(69) 82) 72- 62(49) 92/h6- 11,13- 19,23- 24,34- 35,42,44,46- 54,56- 57,65,71,78- 81,83- 87H,12,20- 22,70H2,1- 5H3,(H2,69,82) (H,72,92) (H,73,89) (H,74,91) (H,75,93) (H,76,88) (H,77,90) (H,94,95) /t24- ,34+,35- ,42+,44- ,46+,47+,48- ,49+,50- ,51+,52+,53+,54- ,56+,57+,65- ,66- /m0/s1 |
MYPYJXKWCTUITO-LYRMYLQWSA-N |
CN[C@H] (CC(C) C) C(=O) N[C@@H] 1[C@H] (O) c2ccc(Oc3cc4cc(Oc5ccc(cc5Cl) [C@@H] (O) [C@@H] 5NC(=O) [C@H] (NC(=O) [C@@H] 4NC(=O) [C@H] (CC(N) =O) NC1=O) c1ccc(O) c(c1) - c1c(O) cc(O) cc1[C@H] (NC5=O) C(O) =O) c3O[C@@H] 1O[C@H] (CO) [C@@H] (O) [C@H] (O) [C@H] 1O[C@H] 1C[C@] (C) (N) [C@H] (O) [C@H] (C) O1) c(Cl) c2 |
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Bronsted base
A molecular entity capable of accepting a hydron from a donor (Bronsted acid).
(via organic amino compound )
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antibacterial drug
A drug used to treat or prevent bacterial infections.
bacterial metabolite
Any prokaryotic metabolite produced during a metabolic reaction in bacteria.
antimicrobial agent
A substance that kills or slows the growth of microorganisms, including bacteria, viruses, fungi and protozoans.
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antibacterial drug
A drug used to treat or prevent bacterial infections.
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View more via ChEBI Ontology
(3S,6R,7R,11R,23S,26S,30aS,36R,38aR)- 44- [2- O- (3- amino- 2,3,6- trideoxy- 3- C- methyl- α- L- lyxo- hexopyranosyl)- β- D- glucopyranosyloxy]- 3- (carbamoylmethyl)- 10,19- dichloro- 2,3,4,5,6,7,23,25,26,36,37,38,38a- tetradecahydro- 7,22,28,30,32- pentahydroxy- 6- (N- methyl- D- leucyl)- 2,5,24,38,39- pentaoxo- 1H,22H- 23,36- (epiminomethano)- 8,11:18,21- dietheno- 13,16:31,35- di(metheno)[1,6,9]oxadiazacyclohexadecino[4,5- m][10,2,16]benzoxadiazacyclotetracosine- 26- carboxylic acid
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vancomicina
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ChemIDplus
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vancomycin
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ChemIDplus
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vancomycine
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ChemIDplus
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vancomycinum
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ChemIDplus
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(1S,2R,18R,22S,25R,28R,40S)- 22- (2- amino- 2- oxoethyl)- 48- [2- O- (3- amino- 2,3,6- trideoxy- 3- methyl- α- L- lyxo- hexopyranosyl)- β- D- glucopyranosyloxy]- 5,15- dichloro- 2,18,32,35,37- pentahydroxy- 19- [(N- methyl- D- leucyl)amino]- 20,23,26,42,44- pentaoxo- 7,13- dioxa- 21,24,27,41,43- pentaazaoctacyclo[26.14.2.23,6.214,17.18,12.129,33.010,25.034,39]pentaconta- 3,5,8(48),9,11,14,16,29(45),30,32,34,36,38,46,49- pentadecaene- 40- carboxylic acid
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ChEBI
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(2.2Sp,3.5Sa,2.6Sp)- O4.2,C3.4:C5.4,O4.6:C3.5,C2.7- tricyclo[N- methyl- D- leucyl- 3- chloro- (R)- β- hydroxy- D- tyrosyl- L- asparaginyl- D- 2- (4- {[2- O- (3- amino- 2,3,6- trideoxy- 3- C- methyl- α- L- lyxo- hexopyranosyl)- β- D- glucopyranosyl]oxy}phenyl)glycyl- D- 2- (4- hydroxyphenyl)glycyl- 3- chloro- (R)- β- hydroxy- L- tyrosyl- L- 2- (3,5- dihydroxyphenyl)glycine]
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JCBN
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vancomicin
Note: (2015-03-23) An uncommon spelling variant. |
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ChEBI
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Vancomycin
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KEGG COMPOUND
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VANCOMYCIN
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PDBeChem
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2807
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DrugCentral
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C00016052
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KNApSAcK
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C06689
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KEGG COMPOUND
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CPD-12245
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MetaCyc
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D00212
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KEGG DRUG
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DB00512
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DrugBank
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US3067099
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Patent
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VAN
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PDBeChem
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Vancomycin
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Wikipedia
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View more database links |
1404-90-6
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CAS Registry Number
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KEGG COMPOUND
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1404-90-6
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CAS Registry Number
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ChemIDplus
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3132
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Beilstein Registry Number
|
Beilstein
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3132
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Reaxys Registry Number
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Reaxys
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11028184
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11408222
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11688538
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