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12650-69-0 分子结构
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9-{[(2E)-4-[(2S,3R,4R)-3,4-dihydroxy-5-{[(2R,3R)-3-[(2S,3S)-3-hydroxybutan-2-yl]oxiran-2-yl]methyl}oxan-2-yl]-3-methylbut-2-enoyl]oxy}nonanoic acid

ChemBase编号:179703
分子式:C26H44O9
平均质量:500.62216
单一同位素质量:500.29853299
SMILES和InChIs

SMILES:
O1[C@@H]([C@H]1CC1[C@H]([C@H]([C@@H](OC1)C/C(=C/C(=O)OCCCCCCCCC(=O)O)/C)O)O)[C@H]([C@@H](O)C)C
Canonical SMILES:
OC(=O)CCCCCCCCOC(=O)/C=C(/C[C@@H]1OCC([C@H]([C@H]1O)O)C[C@H]1O[C@@H]1[C@H]([C@@H](O)C)C)\C
InChI:
InChI=1S/C26H44O9/c1-16(13-23(30)33-11-9-7-5-4-6-8-10-22(28)29)12-20-25(32)24(31)19(15-34-20)14-21-26(35-21)17(2)18(3)27/h13,17-21,24-27,31-32H,4-12,14-15H2,1-3H3,(H,28,29)/b16-13+/t17-,18-,19?,20-,21+,24+,25-,26+/m0/s1
InChIKey:
MINDHVHHQZYEEK-CQLBTRCRSA-N

引用这个纪录

CBID:179703 http://www.chembase.cn/molecule-179703.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
9-{[(2E)-4-[(2S,3R,4R)-3,4-dihydroxy-5-{[(2R,3R)-3-[(2S,3S)-3-hydroxybutan-2-yl]oxiran-2-yl]methyl}oxan-2-yl]-3-methylbut-2-enoyl]oxy}nonanoic acid
IUPAC传统名
9-{[(2E)-4-[(2S,3R,4R)-3,4-dihydroxy-5-{[(2R,3R)-3-[(2S,3S)-3-hydroxybutan-2-yl]oxiran-2-yl]methyl}oxan-2-yl]-3-methylbut-2-enoyl]oxy}nonanoic acid
别名
Bactroban
Eismycin
Mupirocin
Antibiotic BRL 4910A
Antibiotic Y 11633
Pseudomonic acid A
Mupirocin
CAS号
12650-69-0
PubChem SID
164235613
PubChem CID
17571751

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 价格
InterBioScreen
Bio-0065 external link 加入购物车 请登录
数据来源 数据ID
PubChem 17571751 external link

理论计算性质

理论计算性质

JChem
Acid pKa 4.8340716  质子受体
质子供体 LogD (pH = 5.5) 1.7011259 
LogD (pH = 7.4) -0.07094509  Log P 2.4513257 
摩尔折射率 129.3941 cm3 极化性 51.53534 Å3
极化表面积 146.05 Å2 可自由旋转的化学键 17 
里宾斯基五规则 false 

分子性质

分子性质

药理学性质 产品相关信息 生物活性(PubChem)
生物活性机理
Binds to bacterial isoleucyl-tRNA synthetase, which halts the incorporation of isoleucine into bacterial proteins expand 查看数据来源
生物来源
Prod. by Pseudomonas fluorescens expand 查看数据来源
应用领域
Broad spectrum antibiotic effective against gram-positive organisms expand 查看数据来源

详细说明

详细说明

参考文献

参考文献

供应商提供 Google Scholar IconGoogle Scholar PubMed iconPubMed Google Books IconGoogle Books
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  • Chain, E.B. et al., J.C.S. Perkin 1, 1977, 294; 318, (isol, struct, uv, ir, ms, pmr, cmr, stereochem)
  • Feline, T.C. et al., J.C.S. Perkin 1, 1977, 309, (biosynth, cmr)
  • Alexander, R.G. et al., J.C.S. Perkin 1, 1978, 561, (pmr, cmr, cryst struct, abs config)
  • Schmiesing, R.J., Diss. Abstr. Int., B, 1982, 42, 3272, (synth)
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  • Raphael, R.A. et al., Tet. Lett., 1982, 2407, (synth, bibl)
  • O'Hanlon, P.J. et al., J.C.S. Perkin 1, 1983, 2655, (struct, uv, ir, pmr, cmr, ms, synth, Pseudomonic acid D)
  • Snider, B.B. et al., J.O.C., 1983, 48, 3003, (synth)
  • Fleet, G.W.J. et al., Tet. Lett., 1983, 24, 3661, (synth)
  • Sorgi, K.L., Diss. Abstr. Int., B, 1984, 44, 2432, (synth)
  • Sutherland, R. et al., Antimicrob. Agents Chemother., 1985, 27, 495, (props)
  • Mellows, G., Curr. Clin. Pract. Ser., 1985, 16, 3, (rev, chem, metab)
  • Ward, A. et al., Drugs, 1986, 32, 425, (rev, pharmacol)
  • Parenti, M.A. et al., Clin. Pharm., 1987, 6, 761, (rev, pharmacol)
  • Martindale, The Extra Pharmacopoeia, 30th edn., Pharmaceutical Press, 1993, 183
  • Yanagisawa, T. et al., J. Biol. Chem., 1994, 269, 24304, (pharmacol)
  • Negwer, M., Organic-Chemical Drugs and their Synonyms, 7th edn., Akademie-Verlag, 1994, 10508, (synonyms)
  • Class, Y.J. et al., Chem. Rev., 1995, 95, 1843, (rev, synth)
  • Class, Y.J. et al., Tet. Lett., 1995, 36, 7631, (synth)
  • Mantle, P.G. et al., J. Antibiot., 2001, 54, 166-174, (biosynth)
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专利

专利

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