您当前所在的位置:首页 > 产品中心 > 产品详细信息
80214-83-1 分子结构
点击图片或这里关闭

(3R,4S,5S,6R,7R,9R,10E,11S,12R,13S,14R)-6-{[(2S,3R,4S,6R)-4-(dimethylamino)-3-hydroxy-6-methyloxan-2-yl]oxy}-14-ethyl-7,12,13-trihydroxy-4-{[(2R,4R,5S,6S)-5-hydroxy-4-methoxy-4,6-dimethyloxan-2-yl]oxy}-3,5,7,9,11,13-hexamethyl-10-(2,4,7-trioxa-1-azaoctan-1-ylidene)-1-oxacyclotetradecan-2-one

ChemBase编号:119519
分子式:C41H76N2O15
平均质量:837.04654
单一同位素质量:836.52456974
SMILES和InChIs

SMILES:
[C@@H]1([C@@H]([C@H](C[C@H](O1)C)N(C)C)O)O[C@@H]1[C@H]([C@@H]([C@H](C(=O)O[C@@H]([C@]([C@@H]([C@H](/C(=N/OCOCCOC)/[C@@H](C[C@]1(O)C)C)C)O)(O)C)CC)C)O[C@H]1C[C@]([C@H]([C@@H](O1)C)O)(OC)C)C
Canonical SMILES:
COCCOCO/N=C/1\[C@H](C)C[C@@](C)(O)[C@H](O[C@@H]2O[C@H](C)C[C@@H]([C@H]2O)N(C)C)[C@@H](C)[C@H](O[C@@H]2O[C@@H](C)[C@@H]([C@](C2)(C)OC)O)[C@H](C(=O)O[C@@H]([C@@]([C@@H]([C@H]1C)O)(C)O)CC)C
InChI:
InChI=1S/C41H76N2O15/c1-15-29-41(10,49)34(45)24(4)31(42-53-21-52-17-16-50-13)22(2)19-39(8,48)36(58-38-32(44)28(43(11)12)18-23(3)54-38)25(5)33(26(6)37(47)56-29)57-30-20-40(9,51-14)35(46)27(7)55-30/h22-30,32-36,38,44-46,48-49H,15-21H2,1-14H3/b42-31+/t22-,23-,24+,25+,26-,27+,28+,29-,30+,32-,33+,34-,35+,36-,38+,39-,40-,41-/m1/s1
InChIKey:
RXZBMPWDPOLZGW-XMRMVWPWSA-N

引用这个纪录

CBID:119519 http://www.chembase.cn/molecule-119519.html

Collapse All Expand All

名称和登记号

名称和登记号

名称 登记号
IUPAC标准名
(3R,4S,5S,6R,7R,9R,10E,11S,12R,13S,14R)-6-{[(2S,3R,4S,6R)-4-(dimethylamino)-3-hydroxy-6-methyloxan-2-yl]oxy}-14-ethyl-7,12,13-trihydroxy-4-{[(2R,4R,5S,6S)-5-hydroxy-4-methoxy-4,6-dimethyloxan-2-yl]oxy}-3,5,7,9,11,13-hexamethyl-10-(2,4,7-trioxa-1-azaoctan-1-ylidene)-1-oxacyclotetradecan-2-one
IUPAC传统名
(E)-roxithromycin
(3R,4S,5S,6R,7R,9R,10E,11S,12R,13S,14R)-6-{[(2S,3R,4S,6R)-4-(dimethylamino)-3-hydroxy-6-methyloxan-2-yl]oxy}-14-ethyl-7,12,13-trihydroxy-4-{[(2R,4R,5S,6S)-5-hydroxy-4-methoxy-4,6-dimethyloxan-2-yl]oxy}-3,5,7,9,11,13-hexamethyl-10-(2,4,7-trioxa-1-azaoctan-1-ylidene)-1-oxacyclotetradecan-2-one
别名
(3R,4S,5S,6R,7R,9R,11S,12R,13S,14R,E)-6-(((2S,3R,6R)-4-(dimethylamino)-3-hydroxy-6-methyltetrahydro-2H-pyran-2-yl)oxy)-14-ethyl-7,12,13-trihydroxy-4-(((2R,4R,5S,6S)-5-hydroxy-4-methoxy-4,6-dimethyltet rahydro-2H-pyran-2-yl)oxy)-10-(((2-methoxyethoxy)methox y)imino)-3,5,7,9,11,13-hexamethyloxacyclotetradecan-2-one
Abbotic
Antibiotic RU 28965
Azuril
Cirumycin
Macrosil
Roxitrol
Rulide
Roxithromycin
(9E)-9-[O-[(2-Methoxyethoxy)methyl]oxime] Erythromycin
Assoral
Brilid
Claramid
Forilin
Overal
RU 28965
RU 965
Rossitrol
Rotramin
Roxeptin
Roxid
Roxithromycin
Roxithromycin A
Rulid
Surlid
Roxithromycin
CAS号
80214-83-1
PubChem SID
162107641
PubChem CID
6915744

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
PubChem 6915744 external link

理论计算性质

理论计算性质

JChem
Acid pKa 12.454023  质子受体 16 
质子供体 LogD (pH = 5.5) -0.23886713 
LogD (pH = 7.4) 1.3162447  Log P 2.9999793 
摩尔折射率 211.2376 cm3 极化性 85.90249 Å3
极化表面积 216.89 Å2 可自由旋转的化学键 13 
里宾斯基五规则 false 

分子性质

分子性质

理化性质 安全信息 药理学性质 产品相关信息 生物活性(PubChem)
溶解度
Chloroform expand 查看数据来源
外观
White Solid expand 查看数据来源
熔点
111-118°C expand 查看数据来源
保存条件
-20°C Freezer expand 查看数据来源
MSDS下载
下载链接 expand 查看数据来源
生物活性机理
Binds to the 50S subunit of ribosome expand 查看数据来源
Protein synthesis inhibitor expand 查看数据来源
质检报告
下载链接 expand 查看数据来源
应用领域
Antibiotic expand 查看数据来源
Immunomodulator expand 查看数据来源
Shows a similar range of antibacterial activity to Erythromycin BDQ81-E but is much more active in vivo expand 查看数据来源

详细说明

详细说明

TRC TRC
Toronto Research Chemicals -  R700850 external link
Semisynthetic Erythromycin derivative. Antibacterial.

参考文献

参考文献

供应商提供 Google Scholar IconGoogle Scholar PubMed iconPubMed Google Books IconGoogle Books
  • Jones, R.N., et al.: Antimicrob. Agents Chemother., 24, 209 (1983)
  • Barry, A.L., et al.: Eur. J. Clin. Microbiol., 5, 536 (1983)
  • Grassi, C., et al.: Chemioterapia, 6, 41 (1983)
  • Fr. Pat., 1981, Roussel, 2 473 525; CA, 96, 123219, (synth)
  • Jones, R.N. et al., Antimicrob. Agents Chemother., 1983, 24, 209, (props)
  • Barlam, T. et al., Antimicrob. Agents Chemother., 1984, 25, 529, (props)
  • Chantot, J.-F. et al., J. Antibiot., 1986, 39, 661, (props)
  • Young, R.A. et al., Drugs, 1987, 37, 8, (rev, pharmacol)
  • Phillips, I. et al., J. Antimicrob. Chemother., Suppl. B, (Eds.), 1987, 20, (book)
  • Gharbi-Benarous, J. et al., Magn. Reson. Chem., 1990, 28, 846, (pmr, cmr, conformn)
  • Gharbi-Benarous, J. et al., J. Med. Chem., 1991, 34, 1117, (pmr, cmr, conformn)
  • Peruche, B. et al., Pharm. Ztg., 1992, 137, 32; 34; 36; 38; 40, (rev)
  • Martindale, The Extra Pharmacopoeia, 30th edn., Pharmaceutical Press, 1993, 201
  • Markham, A. et al., Drugs, 1994, 48, 297, (rev)
  • Konno, S. et al., Int. Arch. Allergy Appl. Immunol., 1994, 105, 308, (pharmacol)
  • Negwer, M., Organic-Chemical Drugs and their Synonyms, 7th edn., Akademie-Verlag, 1994, 11688, (synonyms)
  • Infection (Munich), Suppl. 1, 1995, 23, (rev)
正在搜索,请耐心等待...(如果遇到网页错误或者长时间没有结果,请刷新页面[F5])

专利

专利

PubChem iconPubChem Patent Google Patent Search IconGoogle Patent

互联网资源

互联网资源

百度图标百度 google iconGoogle