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比阿培南

比阿培南

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?比阿培南名称


















中文名

比阿培南
英文名

biapenem
中文别名


比亚培南




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6-[[(4R,5S,6S)-2-羧基-6-((1R)-1-羟乙基)-4-甲基-7-氧代-1-氮杂双环[3.2.0]庚-2-烯-3-基]硫]-6,7-双氢-5H-哌唑酮[1,2-a][1,2,4]三氮杂-4-内盐




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比阿培南



英文别名
更多





?比阿培南生物活性












































描述
Biapenem是不经肠道的广谱碳青霉烯抗生素。
相关类别



溶解度

体外:

H 2 O:20 mg / mL(57.08 mM;需要超声波)


储备液

1 mM 2.8540 mL 14.2698 mL 28.5396 mL
5 mM 0.5708 mL 2.8540 mL 5.7079 mL
10 mM 0.2854 mL 1.4270 mL 2.8540 mL


存储

粉末 -20℃下 3年
4℃下 2年
在溶剂中 -80℃下 6个月
-20℃下 1个月


运输

室温;可能会有所不同
SMILES

O=C1N2C(C([O-])=O)=C(SC(C3)CN4[N+]3=CN=C4)[C@H](C)[C@]2([H])[C@@]1([H])[C@H](O)C
参考文献

[1]. Perry, C.M. and T. Ibbotson, Biapenem. Drugs, 2002. 62(15): p. 2221-34; discussion 2235.

[2]. Kasahara, S., et al., [Clinical effects of biapenem on febrile neutropenia in patients with hematological malignancy]. Jpn J Antibiot, 2008. 61(3): p. 115-21.


相关活性
小分子




嘌呤霉素盐酸盐



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G-418 硫酸盐



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衣霉素



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潮霉素B



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盐霉素



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阿维巴坦钠



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硫酸新霉素



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法硼巴坦



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甲氧西林钠



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利福平



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甲硝唑



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羧苄青霉素钠



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头孢他啶



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Eravacycline dihydrochloride



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头孢噻肟钠






?比阿培南物理化学性质































熔点 265-271°C (dec.)
分子式 C15H18N4O4S
分子量 350.393
精确质量 350.104889
PSA 127.67000
外观性状 白色至淡黄色粉末
折射率 1.651
储存条件 -20?C Freezer






?比阿培南安全信息

















危险品运输编码 NONH for all modes of transport










?比阿培南上下游产品











比阿培南上游产品? 2

比阿培南下游产品? 0













?比阿培南文献30

更多文献














Nationwide surveillance of bacterial respiratory pathogens conducted by the surveillance committee of Japanese Society of Chemotherapy, the Japanese Association for Infectious Diseases, and the Japanese Society for Clinical Microbiology in 2010: General view of the pathogens’ antibacterial susceptibility.

J. Infect. Chemother. 21 , 410-20, (2015)

The nationwide surveillance on antimicrobial susceptibility of bacterial respiratory pathogens from patients in Japan, was conducted by Japanese Society of Chemotherapy, Japanese Association for Infec…





Novel approach to optimize synergistic carbapenem-aminoglycoside combinations against carbapenem-resistant Acinetobacter baumannii.

Antimicrob. Agents Chemother. 59 , 2286-98, (2015)

Acinetobacter baumannii is among the most dangerous pathogens and emergence of resistance is highly problematic. Our objective was to identify and rationally optimize β-lactam-plus-aminoglycoside comb…





Biapenem inactivation by B2 metallo β-lactamases: energy landscape of the post-hydrolysis reactions.

PLoS ONE 7(1) , e30079, (2012)

The first line of defense by bacteria against β-lactam antibiotics is the expression of β-lactamases, which cleave the amide bond of the β-lactam ring. In the reaction of biapenem inactivation by B2 m…









?比阿培南英文别名



















































Biapenem (JAN/USAN)


EINECS 204-352-8


5H-Pyrazolo[1,2-a][1,2,4]triazol-4-ium, 6-[[(4R,5S,6S)-2-carboxy-6-[(1R)-1-hydroxyethyl]-4-methyl-7-oxo-1-azabicyclo[3.2.0]hept-2-en-3-yl]thio]-6,7-dihydro-, inner salt


BiapeneM Crude


Biapenem [USAN:INN]


(4R,5S,6S)-3-(6,7-Dihydro-5H-pyrazolo[1,2-a][1,2,4]triazol-4-ium-6-ylsulfanyl)-6-[(1R)-1-hydroxyethyl]-4-methyl-7-oxo-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylate


[4R-[4a,5b,6b(R*)]]-6-[[2-Carboxy-6-(1-hydroxyethyl)-4-methyl-7-oxo-1-azabicyclo[3.2.0]hept-2-en-3-yl]thio]-6,7-dihydro-5 H-pyrazolo[1,2-a][1,2,4]triazol-4-ium inner salt


LJ C10627


omegacin


MFCD00864863


Biapenem


LJ C10,627


Biapenern


L-627








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