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58001-44-8 分子结构
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(2R,3Z,5R)-3-(2-hydroxyethylidene)-7-oxo-4-oxa-1-azabicyclo[3.2.0]heptane-2-carboxylic acid

ChemBase编号:646
分子式:C8H9NO5
平均质量:199.16076
单一同位素质量:199.04807239
SMILES和InChIs

SMILES:
O1[C@H]2N([C@H](/C/1=C/CO)C(=O)O)C(=O)C2
Canonical SMILES:
OC(=O)[C@@H]1N2[C@H](O/C/1=C\CO)CC2=O
InChI:
InChI=1S/C8H9NO5/c10-2-1-4-7(8(12)13)9-5(11)3-6(9)14-4/h1,6-7,10H,2-3H2,(H,12,13)/b4-1-/t6-,7-/m1/s1
InChIKey:
HZZVJAQRINQKSD-PBFISZAISA-N

引用这个纪录

CBID:646 http://www.chembase.cn/molecule-646.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
(2R,3Z,5R)-3-(2-hydroxyethylidene)-7-oxo-4-oxa-1-azabicyclo[3.2.0]heptane-2-carboxylic acid
IUPAC传统名
clavulanate
别名
Clavulanic Acid
Clavulanate
CAS号
58001-44-8
PubChem SID
46508845
160964109
PubChem CID
5280980

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
DrugBank DB00766 external link
PubChem 5280980 external link
数据来源 数据ID 价格

理论计算性质

理论计算性质

JChem ALOGPS 2.1
Acid pKa 3.3169081  质子受体
质子供体 LogD (pH = 5.5) -3.6880052 
LogD (pH = 7.4) -4.943672  Log P -1.5212076 
摩尔折射率 44.2525 cm3 极化性 17.05212 Å3
极化表面积 87.07 Å2 可自由旋转的化学键
里宾斯基五规则 true 
Log P -1.16  LOG S 0.23 
溶解度 3.37e+02 g/l 

分子性质

分子性质

理化性质 生物活性(PubChem)
溶解度
300 mg/mL (potassium salt) expand 查看数据来源
疏水性(logP)
-1.5 expand 查看数据来源

详细说明

详细说明

DrugBank DrugBank
DrugBank -  DB00766 external link
Item Information
Drug Groups approved
Description Clavulanic acid and its salts and esters. The acid is a suicide inhibitor of bacterial beta-lactamase enzymes from Streptomyces clavuligerus. Administered alone, it has only weak antibacterial activity against most organisms, but given in combination with beta-lactam antibiotics prevents antibiotic inactivation by microbial lactamase. [PubChem]
Indication For use with Amoxicillin, clavulanic acid is suitable for the treatment of infections with Staph. aureus and Bacteroides fragilis, or with beta-lactamase producing H. influenzae and E. coli.
Pharmacology Clavulanic acid, produced by the fermentation of Streptomyces Clavuligerus, is a beta-lactam structurally related to the penicillins. Clavulanic acid is used in conjunction with amoxicillin for the treatment of bronchitis and urinary tract, skin, and soft tissue infections caused by beta-lactamase producing organisms.
Toxicity Gastrointestinal symptoms including stomach and abdominal pain, vomiting, and diarrhea. Rash, hyperactivity, or drowsiness have also been observed in a small number of patients
Affected Organisms
Enteric bacteria and other eubacteria
Biotransformation Hepatic
Absorption 75%
Half Life 1.0 hour
Protein Binding Low (22 to 30%)
External Links
Wikipedia

参考文献

参考文献

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专利

专利

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互联网资源

互联网资源

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