您当前所在的位置:首页 > 产品中心 > 产品详细信息
859-18-7 分子结构
点击图片或这里关闭

(2S,4R)-N-[(1R,2R)-2-hydroxy-1-[(2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(methylsulfanyl)oxan-2-yl]propyl]-1-methyl-4-propylpyrrolidine-2-carboxamide hydrochloride

ChemBase编号:132521
分子式:C18H35ClN2O6S
平均质量:442.9983
单一同位素质量:442.19043553
SMILES和InChIs

SMILES:
CCC[C@@H]1C[C@H](N(C1)C)C(=O)N[C@@H]([C@@H]1[C@@H]([C@@H]([C@H]([C@H](O1)SC)O)O)O)[C@@H](C)O.Cl
Canonical SMILES:
CCC[C@H]1CN([C@@H](C1)C(=O)N[C@@H]([C@H]1O[C@H](SC)[C@@H]([C@H]([C@H]1O)O)O)[C@H](O)C)C.Cl
InChI:
InChI=1S/C18H34N2O6S.ClH/c1-5-6-10-7-11(20(3)8-10)17(25)19-12(9(2)21)16-14(23)13(22)15(24)18(26-16)27-4;/h9-16,18,21-24H,5-8H2,1-4H3,(H,19,25);1H/t9-,10-,11+,12-,13+,14-,15-,16-,18-;/m1./s1
InChIKey:
POUMFISTNHIPTI-BOMBIWCESA-N

引用这个纪录

CBID:132521 http://www.chembase.cn/molecule-132521.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
(2S,4R)-N-[(1R,2R)-2-hydroxy-1-[(2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(methylsulfanyl)oxan-2-yl]propyl]-1-methyl-4-propylpyrrolidine-2-carboxamide hydrochloride
IUPAC传统名
lincomycin hydrochloride
别名
Lincocin 盐酸盐
Methyl 6,8-dideoxy-6-(1-methyl-4-propyl-2-pyrrolidinecarboxamido)-1-thio-D-erythro-α-D-galactooctopyranoside 盐酸盐
Lincomycin hydrochloride 盐酸盐
Lincomycin hydrochloride
Lincocin hydrochloride
Methyl 6,8-dideoxy-6-(1-methyl-4-propyl-2-pyrrolidinecarboxamido)-1-thio-D-erythro-α-D-galactooctopyranoside hydrochloride
CAS号
859-18-7
EC号
212-726-7
MDL号
MFCD00083647
Beilstein号
4171650
PubChem SID
162226798
PubChem CID
64710

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 64710 external link

理论计算性质

理论计算性质

JChem
Acid pKa 12.365502  质子受体
质子供体 LogD (pH = 5.5) -2.7498562 
LogD (pH = 7.4) -0.99001026  Log P -0.3168542 
摩尔折射率 102.6663 cm3 极化性 41.491238 Å3
极化表面积 122.49 Å2 可自由旋转的化学键
里宾斯基五规则 true 

分子性质

分子性质

理化性质 安全信息 产品相关信息 生物活性(PubChem)
溶解度
H2O: soluble50 mg/mL, clear, colorless expand 查看数据来源
RTECS编号
RH6315000 expand 查看数据来源
欧盟危险性物质标志
刺激性(Irritant) 刺激性(Irritant) (Xi) expand 查看数据来源
MSDS下载
下载链接 expand 查看数据来源
德国WGK号
2 expand 查看数据来源
危险公开号
36/37/38 expand 查看数据来源
安全公开号
26 expand 查看数据来源
GHS危险品标识
GHS07 expand 查看数据来源
GHS警示词
Warning expand 查看数据来源
GHS危险声明
H315-H319-H335 expand 查看数据来源
GHS警示性声明
P261-P305 + P351 + P338 expand 查看数据来源
个人保护装置
dust mask type N95 (US), Eyeshields, Gloves expand 查看数据来源
保存温度
2-8°C expand 查看数据来源
纯度
≥90% (TLC) expand 查看数据来源
≥95.0% (TLC) expand 查看数据来源
药效
800-900 units per mg expand 查看数据来源
适用性
suitable for cell culture expand 查看数据来源
杂质
≤5% water expand 查看数据来源
Empirical Formula (Hill Notation)
C18H34N2O6S · HCl expand 查看数据来源

详细说明

详细说明

Sigma Aldrich Sigma Aldrich
Sigma Aldrich -  L2774 external link
Biochem/physiol Actions
Lincomycin is a lincosamide antibiotic that forms cross-links within the peptidyl transferase loop region of the 23S rRNA.1Mode of action: inhibits bacterial protein synthesis Antimicrobial spectrum: Gram-positive bacteria
Protocols & Applications
Antibiotic Selector for application, solubility, solution stability, working concentration, and mode of action information
Sigma Aldrich -  L6004 external link
Biochem/physiol Actions
Lincomycin is a lincosamide antibiotic that forms cross-links within the peptidyl transferase loop region of the 23S rRNA.3Mode of action: inhibits bacterial protein synthesis Antimicrobial spectrum: Gram-positive bacteria
Application
Lincomycin hydrochloride is an antibiotic used to study the inhibition of protein synthesis, bacterial antibiotic resistance, and protein and surfactant binding 1,2 Product L6004 is ≥90% (TLC). It is produced by Streptomyces lincolnensis var. lincolnensis and has been used in the treatment of Staphylococcal, Streptococcal, and Bacteroides fragilis infections.
Protocols & Applications
Antibiotic Selector for application, solubility, solution stability, working concentration, and mode of action information
Sigma Aldrich -  62143 external link
Biochem/physiol Actions
Lincomycin is a lincosamide antibiotic that forms cross-links within the peptidyl transferase loop region of the 23S rRNA.3Mode of action: inhibits bacterial protein synthesis Antimicrobial spectrum: Gram-positive bacteria
Other Notes
Review4
Application
Lincomycin hydrochloride is used to study the inhibition of protein synthesis, bacterial antibiotic resistance, and protein and surfactant binding 1,2

参考文献

参考文献

供应商提供 Google Scholar IconGoogle Scholar PubMed iconPubMed Google Books IconGoogle Books
    暂无数据
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