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64-75-5 分子结构
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(4S,4aS,5aS,6S,12aS)-4-(dimethylamino)-3,6,10,12,12a-pentahydroxy-6-methyl-1,11-dioxo-1,4,4a,5,5a,6,11,12a-octahydrotetracene-2-carboxamide hydrochloride

ChemBase编号:73266
分子式:C22H25ClN2O8
平均质量:480.8955
单一同位素质量:480.12994345
SMILES和InChIs

SMILES:
c1ccc2c(c1O)C(=O)C1=C([C@]3([C@@H](C[C@@H]1[C@]2(C)O)[C@@H](C(=C(C3=O)C(=O)N)O)N(C)C)O)O.Cl
Canonical SMILES:
CN([C@@H]1C(=C(C(=O)N)C(=O)[C@@]2([C@H]1C[C@H]1C(=C2O)C(=O)c2c([C@@]1(C)O)cccc2O)O)O)C.Cl
InChI:
InChI=1S/C22H24N2O8.ClH/c1-21(31)8-5-4-6-11(25)12(8)16(26)13-9(21)7-10-15(24(2)3)17(27)14(20(23)30)19(29)22(10,32)18(13)28;/h4-6,9-10,15,25,27-28,31-32H,7H2,1-3H3,(H2,23,30);1H/t9-,10-,15-,21+,22-;/m0./s1
InChIKey:
XMEVHPAGJVLHIG-FMZCEJRJSA-N

引用这个纪录

CBID:73266 http://www.chembase.cn/molecule-73266.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
(4S,4aS,5aS,6S,12aS)-4-(dimethylamino)-3,6,10,12,12a-pentahydroxy-6-methyl-1,11-dioxo-1,4,4a,5,5a,6,11,12a-octahydrotetracene-2-carboxamide hydrochloride
IUPAC传统名
tetracycline hydrochloride
别名
四环素 盐酸盐
四环素盐酸盐
Tetracycline hydrochloride
Tetracycline hydrochloride
[4S-(4α,4aα,5aα,6β,12aα]-4-(Dimethylamino)-1,4,4a,5,5a,6,11,12a-octahydro-3,6,10,12,12a-pentahydroxy-6-methyl-1,11-dioxo-2-Naphthacenecarboxamide Hydrochloride
(-)-Tetracycline Hydrochloride
Achromycin
Imex
Tetracyn
CAS号
64-75-5
EC号
200-593-8
MDL号
MFCD00078142
Beilstein号
3844873
默克索引号
149196
PubChem SID
162038186
24900607
24900135
24900496
24900468
24900192
24870588
PubChem CID
54704426
E编码
E701

理论计算性质

理论计算性质

JChem
Acid pKa 2.9185581  质子受体
质子供体 LogD (pH = 5.5) -3.4724553 
LogD (pH = 7.4) -3.695556  Log P -3.4722908 
摩尔折射率 114.1883 cm3 极化性 43.205765 Å3
极化表面积 181.62 Å2 可自由旋转的化学键
里宾斯基五规则 false 

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
DMSO expand 查看数据来源
H2O: soluble10 mg/mL (as a stock solution. Stock solutions should be filtered sterilized and stored at -20°C. Stable at 37°C for 4 days.) expand 查看数据来源
Methanol expand 查看数据来源
Water expand 查看数据来源
外观
powder expand 查看数据来源
Yellow Solid expand 查看数据来源
熔点
>215°C (dec.) expand 查看数据来源
215-220 °C (dec.) expand 查看数据来源
220-223 °C(lit.) expand 查看数据来源
220-223°C expand 查看数据来源
比旋光度
[α]20/D -245±9°, c = 1% in methanol expand 查看数据来源
-247 (c=1, 0.1M HCl) expand 查看数据来源
保存条件
-20°C expand 查看数据来源
-20°C Freezer expand 查看数据来源
保存注意事项
Air & Light Sensitive expand 查看数据来源
RTECS编号
QI9100000 expand 查看数据来源
欧盟危险性物质标志
X expand 查看数据来源
刺激性(Irritant) 刺激性(Irritant) (Xi) expand 查看数据来源
有害性(Harmful) 有害性(Harmful) (Xn) expand 查看数据来源
MSDS下载
下载链接 expand 查看数据来源
下载链接 expand 查看数据来源
下载链接 expand 查看数据来源
下载链接 expand 查看数据来源
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
36-63 expand 查看数据来源
63-36/37/38-64 expand 查看数据来源
安全公开号
26-36 expand 查看数据来源
26-36/37-60 expand 查看数据来源
TSCA收录
expand 查看数据来源
GHS危险品标识
GHS07 expand 查看数据来源
GHS08 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
H315-H319-H335-H361-H362 expand 查看数据来源
H361-H319 expand 查看数据来源
GHS警示性声明
P261-P263-P281-P305 + P351 + P338 expand 查看数据来源
P261-P305 + P351 + P338 expand 查看数据来源
P280-P281-P305+P351+P338-P308+P313-P405-P501A 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
-20°C expand 查看数据来源
2-8°C expand 查看数据来源
纯度
≥95% expand 查看数据来源
≥95% (European Pharmacopoeia HPLC assay) expand 查看数据来源
≥96.0% (HPLC) expand 查看数据来源
96% expand 查看数据来源
级别
Biotechnology Performance Certified expand 查看数据来源
VETRANAL™, analytical standard expand 查看数据来源
成盐信息
HCl expand 查看数据来源
hydrochloride expand 查看数据来源
质检报告
下载链接 expand 查看数据来源
适用性
cell culture tested expand 查看数据来源
meets USP testing specifications expand 查看数据来源
suitable for cell culture expand 查看数据来源
杂质
endotoxin, tested expand 查看数据来源
无菌消毒
γ-irradiated expand 查看数据来源
Pharmacopeia Traceability
traceable to BP 480 expand 查看数据来源
traceable to PhEur T060000 expand 查看数据来源
traceable to USP 1651009 expand 查看数据来源
Empirical Formula (Hill Notation)
C22H24N2O8 · HCl expand 查看数据来源
分类
Genuine Natural Compounds expand 查看数据来源

详细说明

详细说明

Selleck Chemicals Selleck Chemicals Sigma Aldrich Sigma Aldrich TRC TRC
Selleck Chemicals -  S2574 external link
Research Area: Infection
Biological Activity:
Tetracycline hydrochloride is a hydrochloride salt of tetracycline that is a broad-spectrum polyketide antibiotic. Tetracycline binds to the 30S subunit of microbial ribosomes. Tetracycline inhibits protein synthesis by blocking the attachment of charged aminoacyl-tRNA. Thus tetracycline prevents introduction of new amino acids to the nascent peptide chain. The action is usually inhibitory and reversible upon withdrawal of the drug. Resistance to the tetracycline results from changes in permeability of the microbial cell envelope. In susceptible cells, the tetracycline is concentrated from the environment and does not readily leave the cell. In resistant cells, the drug is not actively transported into the cell or leaves it so rapidly that inhibitory concentrations are not maintained. Tetracycline hydrochloride is used in the treatment of bacterial infections, such as urinary tract infections, acne, gonorrhea, chlamydia, and others.[1]References on Tetracycline HCl[1] http://en.wikipedia.org/wiki/Tetracycline, ,
Sigma Aldrich -  T9823 external link
Biochem/physiol Actions
Mode of Action: Inhibits protein synthesis (elongation) by preventing binding of aminoacyl-tRNA to the 30S subunit. Antimicrobial spectrum: Gram-negative and Gram-positive bacteria.Mode of Resistance: Loss of cell wall permeability.
Tetracycline inhibits bacterial protein synthesis elongation at the level of aminoacyl-tRNA binding to the 30S ribosome. Tetracycline passively diffuses through porin channels in the bacterial cell membrane. It also binds to the bacterial 50S ribosomal subunit which may alter the cytoplasmic membrane, causing intracellular components to leak from bacterial cells1. Mode of resistance is loss of cell wall permeability.
Application
Tetracycline is a broad spectrum polyketide antibiotic. It is used clinically to treat bacterial infections such as Rocky Mountain spotted fever, typhus fever, tick fevers, Q fever and Brill-Zinsser disease. It is used to treat upper respiratory infections and acne1. It is used to study multidrug resistance2 as well as potential side effects such as acute pancreatitis3. It has been used in target and resistance based mechanistic studies of novel antibiotics4.
Protocols & Applications
Antibiotic Selector for application, solubility, solution stability, working concentration, and mode of action information
Sigma Aldrich -  T7660 external link
Application
Used in tetracycline controlled gene expression systems (gene switches) such a the tet-on and tet-off systems. Recommended for use in cell culture applications at 10 mg/L.
Biochem/physiol Actions
Mode of Action: Inhibits protein synthesis (elongation) by preventing binding of aminoacyl-tRNA to the 30S subunit. Antimicrobial spectrum: Gram-negative and Gram-positive bacteria.Mode of Resistance: Loss of cell wall permeability.
Protocols & Applications
Antibiotic Selector for application, solubility, solution stability, working concentration, and mode of action information
Sigma Aldrich -  74749 external link
Biochem/physiol Actions
Mode of Action: Inhibits protein synthesis (elongation) by preventing binding of aminoacyl-tRNA to the 30S subunit. Antimicrobial spectrum: Gram-negative and Gram-positive bacteria.Mode of Resistance: Loss of cell wall permeability.
Sigma Aldrich -  87130 external link
Biochem/physiol Actions
Mode of Action: Inhibits protein synthesis (elongation) by preventing binding of aminoacyl-tRNA to the 30S subunit. Antimicrobial spectrum: Gram-negative and Gram-positive bacteria.Mode of Resistance: Loss of cell wall permeability.
Sigma Aldrich -  31741 external link
Biochem/physiol Actions
Mode of Action: Inhibits protein synthesis (elongation) by preventing binding of aminoacyl-tRNA to the 30S subunit. Antimicrobial spectrum: Gram-negative and Gram-positive bacteria.Mode of Resistance: Loss of cell wall permeability.
法律信息
VETRANAL 商标 Sigma-Aldrich Co. LLC
Sigma Aldrich -  T4062 external link
Biochem/physiol Actions
Mode of Action: Inhibits protein synthesis (elongation) by preventing binding of aminoacyl-tRNA to the 30S subunit. Antimicrobial spectrum: Gram-negative and Gram-positive bacteria.Mode of Resistance: Loss of cell wall permeability.
Mode of Action: inhbit bacterial protein synthesis elongation at the level of aminoacyl-tRNA binding to the 30S ribosome. Antimicrobial spectrum: Gram-negative and Gram-positive bacteria. Mode of Resistance: Loss of cell wall permeability.
Sigma Aldrich -  T3383 external link
Biochem/physiol Actions
Mode of Action: Inhibits protein synthesis (elongation) by preventing binding of aminoacyl-tRNA to the 30S subunit. Antimicrobial spectrum: Gram-negative and Gram-positive bacteria.Mode of Resistance: Loss of cell wall permeability.
包装
25, 100 g in poly bottle
Sigma Aldrich -  T8032 external link
Application
建议以 10-20μg/ml 的量用于分子生物学应用。
Biochem/physiol Actions
Mode of Action: Inhibits protein synthesis (elongation) by preventing binding of aminoacyl-tRNA to the 30S subunit. Antimicrobial spectrum: Gram-negative and Gram-positive bacteria.Mode of Resistance: Loss of cell wall permeability.
Reconstitution
直接在样品瓶中用无菌水 (10mg/ml) 制备储存液。储存液在 2-8°C 下保存不应超过一周;四环素在水溶液中会发生水解。
Toronto Research Chemicals -  T291400 external link
Antibiotic substance produced by Streptomyces spp. Antiamebic; antibacterial; antirickettsial.

参考文献

参考文献

供应商提供 Google Scholar IconGoogle Scholar PubMed iconPubMed Google Books IconGoogle Books
  • Weiss, et al.: Antibiot. Chemother., 7, 374 (1957)
  • Goldenthal, E.I., et al.: Toxicol. Appl. Pharmacol., 18, 185 (1957)
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专利

专利

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