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127254-12-0 分子结构
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7-[(7S)-7-amino-5-azaspiro[2.4]heptan-5-yl]-8-chloro-6-fluoro-1-[(2S)-2-fluorocyclopropyl]-4-oxo-1,4-dihydroquinoline-3-carboxylic acid

ChemBase编号:72866
分子式:C19H18ClF2N3O3
平均质量:409.8143264
单一同位素质量:409.10047557
SMILES和InChIs

SMILES:
c1(c(c(c2c(c1)c(=O)c(cn2C1[C@H](C1)F)C(=O)O)Cl)N1CC2([C@@H](C1)N)CC2)F
Canonical SMILES:
F[C@H]1CC1n1cc(C(=O)O)c(=O)c2c1c(Cl)c(N1C[C@H](C3(C1)CC3)N)c(c2)F
InChI:
InChI=1S/C19H18ClF2N3O3/c20-14-15-8(17(26)9(18(27)28)5-25(15)12-4-10(12)21)3-11(22)16(14)24-6-13(23)19(7-24)1-2-19/h3,5,10,12-13H,1-2,4,6-7,23H2,(H,27,28)/t10-,12?,13+/m0/s1
InChIKey:
PNUZDKCDAWUEGK-RDWQBYKPSA-N

引用这个纪录

CBID:72866 http://www.chembase.cn/molecule-72866.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
7-[(7S)-7-amino-5-azaspiro[2.4]heptan-5-yl]-8-chloro-6-fluoro-1-[(2S)-2-fluorocyclopropyl]-4-oxo-1,4-dihydroquinoline-3-carboxylic acid
IUPAC传统名
7-[(7S)-7-amino-5-azaspiro[2.4]heptan-5-yl]-8-chloro-6-fluoro-1-[(2S)-2-fluorocyclopropyl]-4-oxoquinoline-3-carboxylic acid
别名
DU 6859A
DU 6859
DU-6859
LS-184401
Sitafloxacin
CAS号
127254-12-0
PubChem SID
162037787
PubChem CID
73011

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 价格
Selleck Chemicals
S2152 external link 加入购物车 请登录
数据来源 数据ID
PubChem 73011 external link

理论计算性质

理论计算性质

JChem
Acid pKa 5.699729  质子受体
质子供体 LogD (pH = 5.5) -0.46243346 
LogD (pH = 7.4) -0.1614805  Log P -0.16889024 
摩尔折射率 99.0881 cm3 极化性 36.969666 Å3
极化表面积 86.87 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

安全信息 产品相关信息 生物活性(PubChem)
保存条件
-20°C expand 查看数据来源
成盐信息
Free Base expand 查看数据来源

详细说明

详细说明

Selleck Chemicals Selleck Chemicals
Selleck Chemicals -  S2152 external link
Research Area: Infection
Biological Activity:
Sitafloxacin is a new-generation, broad-spectrum oral fluoroquinolone antibiotic.It is very active against many Gram-positive, Gram-negative and anaerobic clinical isolates, including strains resistant to other fluoroquinolones, was recently approved in Japan for the treatment of respiratory and urinary tract infections. Sitafloxacin is active against methicillin-resistant staphylococci, Streptococcus pneumoniae and other streptococci with reduced susceptibility to levofloxacin and other quinolones and enterococci. [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
  • Anderson DL.Drugs Today (Barc). 2008 Jul; 44(7):489-501
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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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