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79-57-2 分子结构
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(4S,4aR,5S,5aR,6S,12aS)-4-(dimethylamino)-3,5,6,10,12,12a-hexahydroxy-6-methyl-1,11-dioxo-1,4,4a,5,5a,6,11,12a-octahydrotetracene-2-carboxamide

ChemBase编号:477
分子式:C22H24N2O9
平均质量:460.43396
单一同位素质量:460.14818036
SMILES和InChIs

SMILES:
[C@H]12[C@](C(=C3[C@H]([C@@H]1O)[C@](c1c(C3=O)c(ccc1)O)(C)O)O)(C(=O)C(=C([C@H]2N(C)C)O)C(=O)N)O
Canonical SMILES:
CN([C@@H]1C(=C(C(=O)N)C(=O)[C@@]2([C@H]1[C@@H](O)[C@H]1C(=C2O)C(=O)c2c([C@@]1(C)O)cccc2O)O)O)C
InChI:
InChI=1S/C22H24N2O9/c1-21(32)7-5-4-6-8(25)9(7)15(26)10-12(21)17(28)13-14(24(2)3)16(27)11(20(23)31)19(30)22(13,33)18(10)29/h4-6,12-14,17,25,27-29,32-33H,1-3H3,(H2,23,31)/t12-,13-,14+,17+,21-,22+/m1/s1
InChIKey:
IWVCMVBTMGNXQD-PXOLEDIWSA-N

引用这个纪录

CBID:477 http://www.chembase.cn/molecule-477.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,4aR,5S,5aR,6S,12aS)-4-(dimethylamino)-3,5,6,10,12,12a-hexahydroxy-6-methyl-1,11-dioxo-1,4,4a,5,5a,6,11,12a-octahydrotetracene-2-carboxamide
IUPAC传统名
oxytetracycline
商标名
Oxytetracycline anhydrous
Oxytetracycline HCl
Terramycin
别名
Oxytetracycline
Oxytetracycline dihydrate
OGYE Selective Supplement
Oxytetracycline
Oxytetra Selective Supplement
[4S-(4α,4aα,5α,5aα,6β,12aα]-4-(Dimethylamino)-1,4,4a,5,5a,6,11,12a-octahydro-3,5,6,10,12,12a-hexahydroxy-6-methyl-1,11-dioxo-2-naphthacenecarboxamide Dihydrate
5-Hydroxytetracycline Dihydrate
Oxytetracycline Dihydrate
CAS号
79-57-2
6153-64-6
EC号
201-212-8
MDL号
MFCD00003700
Beilstein号
2714587
PubChem SID
46507025
160963940
PubChem CID
5280972
54675779

数据来源

数据来源

所有数据来源 商品来源 非商品来源

理论计算性质

理论计算性质

JChem ALOGPS 2.1
Acid pKa 0.24295226  质子受体 10 
质子供体 LogD (pH = 5.5) -5.5841894 
LogD (pH = 7.4) -7.485068  Log P -4.5983834 
摩尔折射率 115.3982 cm3 极化性 43.880726 Å3
极化表面积 201.85 Å2 可自由旋转的化学键
里宾斯基五规则 false 
Log P -0.99  LOG S -2.52 
溶解度 1.40e+00 g/l 

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
0.6 mg/mL (6.9 mg/mL as HCl salt) expand 查看数据来源
DMSO expand 查看数据来源
Methanol expand 查看数据来源
外观
Pale Yellow Solid expand 查看数据来源
熔点
>178°C (dec.) expand 查看数据来源
182-186 °C (dec.) expand 查看数据来源
比旋光度
[α]20/D -195±3°, c = 1% in 0.1 M HCl expand 查看数据来源
疏水性(logP)
-1.3 expand 查看数据来源
保存条件
-20°C Freezer expand 查看数据来源
RTECS编号
QI7875000 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
德国WGK号
2 expand 查看数据来源
3 expand 查看数据来源
安全公开号
22-24/25 expand 查看数据来源
个人保护装置
Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter expand 查看数据来源
纯度
≥98.0% (NT) expand 查看数据来源
级别
for microbiology expand 查看数据来源
质检报告
下载链接 expand 查看数据来源
有效期
(limited shelf life, expiry date on the label) expand 查看数据来源
Empirical Formula (Hill Notation)
C22H24N2O9 expand 查看数据来源
C22H24N2O9 · 2H2O expand 查看数据来源

详细说明

详细说明

DrugBank DrugBank Sigma Aldrich Sigma Aldrich TRC TRC
DrugBank -  DB00595 external link
Item Information
Drug Groups approved
Description A tetracycline analog isolated from the actinomycete streptomyces rimosus and used in a wide variety of clinical conditions. [PubChem]
Indication Oxytetracycline is indicated for treatment of infections caused by a variety of Gram positive and Gram negative microorganisms including Mycoplasma pneumoniae, Pasteurella pestis, Escherichia coli, Haemophilus influenzae (respiratory infections), and Diplococcus pneumoniae.
Pharmacology Oxytetracycline is known as a broad-spectrum antibiotic due to its activity against such a wide range of infections. It was the second of the tetracyclines to be discovered. Oxytetracycline, like other tetracyclines, is used to treat many infections common and rare. Its better absorption profile makes it preferable to tetracycline for moderately severe acne, but alternatives sould be sought if no improvement occurs by 3 months.
Toxicity Adverse effects may include stomach or bowel upsets and rarely allergic reactions. Very rarely severe headache and vision problems may be signs of dangerous intracranial hypertenion.
Affected Organisms
Enteric bacteria and other eubacteria
Absorption Readily absorbed following oral administration.
External Links
Wikipedia
RxList
Sigma Aldrich -  75965 external link
Biochem/physiol Actions
Antibiotic produced by Streptomyces rimosus.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: Active efflux, ribosome protection, tetracycline inactivation.
Sigma Aldrich -  51239 external link
Components
(per vial sufficient for 500 ml medium) Oxytetracycline 50.0 mg
Biochem/physiol Actions
Oxytetracycline is a protein synthesis inhibitor 2.
Features and Benefits
Added to OGY-Agar (Fluka 75310) Oxytetracycline suppresses the growth of accompanying bacterial flora during culturing yeasts and moulds.
Application
Oxytetracycline is used as an antibacterial selective agent in microbiology studies 1. It is a broad spectrum antibiotic that is active against a wide variety of bacteria. When added to OGY-Agar (Fluka 75310) Oxytetracycline suppresses the growth of accompanying bacterial flora during culturing yeasts and molds.
Toronto Research Chemicals -  O877501 external link
Antibiotic substance isolated from the elaboration products of the actinomycete, Streptomyces rimosus, grown on a suitable medium. Antibacterial.

参考文献

参考文献

供应商提供 Google Scholar IconGoogle Scholar PubMed iconPubMed Google Books IconGoogle Books
  • Finlay, et al.: Science, 111, 85 (1950)
  • Weiss, et al.: Antibiot. Chemother., 7, 374 (1950)
  • Kruse, H., et al.: Microb. Drug. Resist., 5, 135, (1950)
  • van den Bogaard, A., et al.: J. Antimicrob. Chemother., 45, 663 (1950)
  • Nwosu, V., et al.: Res. Microbio
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专利

专利

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