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11003-38-6 分子结构
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(3S)-3,6-diamino-N-{[(2S,5S,8E,11S,15S)-15-amino-11-[(4R)-2-amino-3,4,5,6-tetrahydropyrimidin-4-yl]-8-[(carbamoylamino)methylidene]-2-(hydroxymethyl)-3,6,9,12,16-pentaoxo-1,4,7,10,13-pentaazacyclohexadecan-5-yl]methyl}hexanamide; (3S)-3,6-diamino-N-{[(2S,5S,8E,11S,15S)-15-amino-11-[(4R)-2-amino-3,4,5,6-tetrahydropyrimidin-4-yl]-8-[(carbamoylamino)methylidene]-2-methyl-3,6,9,12,16-pentaoxo-1,4,7,10,13-pentaazacyclohexadecan-5-yl]methyl}hexanamide

ChemBase编号:199
分子式:C50H88N28O15
平均质量:1321.41232
单一同位素质量:1320.69839426
SMILES和InChIs

SMILES:
O=C1NC[C@H](N)C(=O)N[C@H](C(=O)N[C@@H](CNC(=O)C[C@@H](N)CCCN)C(=O)N/C(=C/NC(=O)N)/C(=O)N[C@H]1[C@@H]1NC(=NCC1)N)CO.O=C1NC[C@H](N)C(=O)N[C@H](C(=O)N[C@@H](CNC(=O)C[C@@H](N)CCCN)C(=O)N/C(=C/NC(=O)N)/C(=O)N[C@H]1[C@@H]1NC(=NCC1)N)C
Canonical SMILES:
NCCC[C@@H](CC(=O)NC[C@@H]1NC(=O)[C@H](CO)NC(=O)[C@@H](N)CNC(=O)[C@@H](NC(=O)/C(=C\NC(=O)N)/NC1=O)[C@H]1CCN=C(N1)N)N.NCCC[C@@H](CC(=O)NC[C@@H]1NC(=O)[C@H](C)NC(=O)[C@@H](N)CNC(=O)[C@@H](NC(=O)/C(=C\NC(=O)N)/NC1=O)[C@H]1CCN=C(N1)N)N
InChI:
InChI=1S/C25H44N14O8.C25H44N14O7/c26-4-1-2-11(27)6-17(41)32-8-14-20(43)35-15(9-34-25(30)47)21(44)39-18(13-3-5-31-24(29)38-13)23(46)33-7-12(28)19(42)37-16(10-40)22(45)36-14;1-11-19(41)36-15(9-32-17(40)7-12(27)3-2-5-26)21(43)37-16(10-34-25(30)46)22(44)39-18(14-4-6-31-24(29)38-14)23(45)33-8-13(28)20(42)35-11/h9,11-14,16,18,40H,1-8,10,26-28H2,(H,32,41)(H,33,46)(H,35,43)(H,36,45)(H,37,42)(H,39,44)(H3,29,31,38)(H3,30,34,47);10-15,18H,2-9,26-28H2,1H3,(H,32,40)(H,33,45)(H,35,42)(H,36,41)(H,37,43)(H,39,44)(H3,29,31,38)(H3,30,34,46)/b15-9+;16-10+/t11-,12-,13+,14-,16-,18-;11-,12-,13-,14+,15-,18-/m00/s1
InChIKey:
VCOPTHOUUNAYKQ-WBTCAYNUSA-N

引用这个纪录

CBID:199 http://www.chembase.cn/molecule-199.html

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名称和登记号

名称和登记号

名称 登记号
IUPAC标准名
(3S)-3,6-diamino-N-{[(2S,5S,8E,11S,15S)-15-amino-11-[(4R)-2-amino-3,4,5,6-tetrahydropyrimidin-4-yl]-8-[(carbamoylamino)methylidene]-2-(hydroxymethyl)-3,6,9,12,16-pentaoxo-1,4,7,10,13-pentaazacyclohexadecan-5-yl]methyl}hexanamide; (3S)-3,6-diamino-N-{[(2S,5S,8E,11S,15S)-15-amino-11-[(4R)-2-amino-3,4,5,6-tetrahydropyrimidin-4-yl]-8-[(carbamoylamino)methylidene]-2-methyl-3,6,9,12,16-pentaoxo-1,4,7,10,13-pentaazacyclohexadecan-5-yl]methyl}hexanamide
IUPAC传统名
(3S)-3,6-diamino-N-{[(2S,5S,8E,11S,15S)-15-amino-11-[(4R)-2-amino-3,4,5,6-tetrahydropyrimidin-4-yl]-8-[(carbamoylamino)methylidene]-2-(hydroxymethyl)-3,6,9,12,16-pentaoxo-1,4,7,10,13-pentaazacyclohexadecan-5-yl]methyl}hexanamide; (3S)-3,6-diamino-N-{[(2S,5S,8E,11S,15S)-15-amino-11-[(4R)-2-amino-3,4,5,6-tetrahydropyrimidin-4-yl]-8-[(carbamoylamino)methylidene]-2-methyl-3,6,9,12,16-pentaoxo-1,4,7,10,13-pentaazacyclohexadecan-5-yl]methyl}hexanamide
商标名
Ogostal
Caprocin
别名
Capreomycin sulphate
Capreomycin
Capastat
Capastat sulfate
Capreomycin sulfate
Capreomycin
CAS号
11003-38-6
PubChem SID
46508514
160963662
PubChem CID
3000502

数据来源

数据来源

所有数据来源 商品来源 非商品来源
数据来源 数据ID
DrugBank DB00314 external link
PubChem 3000502 external link
数据来源 数据ID 价格

理论计算性质

理论计算性质

JChem
Acid pKa 10.622467  质子受体 14 
质子供体 14  LogD (pH = 5.5) -20.15656 
LogD (pH = 7.4) -17.134743  Log P -11.191733 
摩尔折射率 162.2049 cm3 极化性 63.26125 Å3
极化表面积 378.42 Å2 可自由旋转的化学键 19 
里宾斯基五规则 false 

分子性质

分子性质

理化性质 生物活性(PubChem)
溶解度
Soluble in water as disulfate salt. expand 查看数据来源
疏水性(logP)
-9.609 expand 查看数据来源

详细说明

详细说明

DrugBank DrugBank
DrugBank -  DB00314 external link
Item Information
Drug Groups approved
Description Cyclic peptide antibiotic similar to viomycin. It is produced by Streptomyces capreolus. [PubChem]
Indication Used in the treatment of tuberculosis in combination with other drugs.
Pharmacology Capreomycin is a member of the aminoglycoside family of antibiotics. These antibiotics have the ability to kill a wide variety of bacteria, including bacteria responsible for causing tuberculosis (TB).
Toxicity Hypokalemia, hypocalcemia, hypomagnesemia, and an electrolyte disturbance resembling Bartter's syndrome have been reported to occur in patients with capreomycin toxicity. The subcutaneous median lethal dose (LD50) in mice was 514 mg/kg.
Affected Organisms
Enteric bacteria and other eubacteria
Absorption Not absorbed in significant quantities from the gastrointestinal tract and must be administered parenterally.
Elimination When a 1–g dose of capreomycin was given intramuscularly to normal volunteers, 52% was excreted in the urine within 12 hours.
External Links
Wikipedia
Drugs.com

参考文献

参考文献

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专利

专利

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互联网资源

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