青霉素V

更新时间:2024-01-03 15:54:21

青霉素V结构式
青霉素V结构式
品牌特惠专场
常用名 青霉素V 英文名 Penicillin-V
CAS号 87-08-1 分子量 350.389
密度 1.5±0.1 g/cm3 沸点 681.4±55.0 °C at 760 mmHg
分子式 C16H18N2O5S 熔点 120 - 128ºC
MSDS N/A 闪点 365.9±31.5 °C

 青霉素V用途


青霉素V(苯氧甲基青霉素)是一种有效的口服抗生素。青霉素V对链球菌、艰难梭菌和金黄色葡萄球菌具有抗菌活性。青霉素V具有研究中耳炎、鼻窦炎、咽炎和扁桃体炎的潜力[1][2][3][4]。

 青霉素V名称

中文名 青霉素V
英文名 phenoxymethylpenicillin
中文别名 苯氧甲基青霉素 | 青黴素V
英文别名 更多

 青霉素V生物活性

描述 青霉素V(苯氧甲基青霉素)是一种有效的口服抗生素。青霉素V对链球菌、艰难梭菌和金黄色葡萄球菌具有抗菌活性。青霉素V具有研究中耳炎、鼻窦炎、咽炎和扁桃体炎的潜力[1][2][3][4]。
相关类别
体外研究 青霉素V(0.002-8.0mg/L)抑制链球菌的生长,最低抑制浓度(MIC)为0.004-0.008mg/L[2]。青霉素V(0.002-8.0 mg/L)对艰难梭菌具有抗菌活性,MIC50值为4.0 mg/L,MIC90值为8.0 g/L[3]。青霉素V(0.004-0.063 mg/L;18 h)抑制金黄色葡萄球菌的生长,MIC值为0.016 mg/L[4]。
体内研究 青霉素V(0.063-0.25mg/kg;s.c.)抑制小鼠大腿肌肉中金黄色葡萄球菌的生长[4]。青霉素V(2 mg/kg;s.c.)的血浆半衰期(61 min)和平均AUC(0.47 mg/L·h)[4]。青霉素V(100mg/kg;每天一次,持续5天)可避免大鼠急性化脓性中耳炎(AOM)的暴发性感染[5]。动物模型:无特异性病原体(SPF)雄性瑞士小鼠(20-25 g)接种金黄色葡萄球菌[4]剂量:0.063、0.13、0.25 mg/kg给药:S.c.结果:与对照组(3.5×107计数/mL)相比,0.25 g/kg剂量下的CFU数量(1.34×107计数/mL)减少。
参考文献

[1]. Sabath LD. Et, al. Phenoxymethylpenicillin (penicillin V) and phenethicillin. Med Clin North Am. 1970 Sep;54(5):1101-11.

[2]. Kamme C, et, al. In vitro effect on group A streptococci of loracarbef versus cefadroxil, cefaclor and penicillin V. Scand J Infect Dis. 1993;25(1):37-42.

[3]. Norén T, et, al. In vitro susceptibility to 17 antimicrobials of clinical Clostridium difficile isolates collected in 1993-2007 in Sweden. Clin Microbiol Infect. 2010 Aug;16(8):1104-10.

[4]. Overbosch D, et, al. Comparative pharmacodynamics and clinical pharmacokinetics of phenoxymethylpenicillin and pheneticillin. Br J Clin Pharmacol. 1985 May;19(5):657-68.

[5]. Hermansson A, et, al. Prevention of experimental acute otitis media with penicillin V. Acta Otolaryngol. Jan-Feb 1990;109(1-2):119-23.

[6]. Timm A, et al. Photolysis of four β‑lactam antibiotics under simulated environmental conditions: Degradation, transformation products and antibacterial activity. Sci Total Environ. 2019 Feb 15;651(Pt 1):1605-1612.

 青霉素V物理化学性质

密度 1.5±0.1 g/cm3
沸点 681.4±55.0 °C at 760 mmHg
熔点 120 - 128ºC
分子式 C16H18N2O5S
分子量 350.389
闪点 365.9±31.5 °C
精确质量 350.093628
PSA 121.24000
LogP 1.88
外观性状 白色至灰白色结晶粉末
蒸汽压 0.0±2.2 mmHg at 25°C
折射率 1.651
储存条件 −20°C
稳定性 Stable. Combustible. Incompatible with strong oxidizing agents.
水溶解性 Very slightly soluble in water, soluble in ethanol (96 per cent).

 青霉素V毒性和生态

 青霉素V安全信息

危害码 (欧洲) Xn
风险声明 (欧洲) R42/43
安全声明 (欧洲) 22-36
危险品运输编码 NONH for all modes of transport
RTECS号 RY4025000
海关编码 3003101300

 青霉素V合成线路

 青霉素V海关

海关编码 3003101300

 青霉素V文献29

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 青霉素V英文别名

penicillin-V
Oracillin
Pen-vee-oral
Fenospen
(2S,5R,6R)-3,3-Dimethyl-7-oxo-6-[(phenoxyacetyl)amino]-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid
Penicillin phenoxymethyl
(2S,5R,6R)-3,3-dimethyl-7-oxo-6-[(2-phenoxyacetyl)amino]-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid
PenicillinV
Phenocillin
Beromycin
(2S,5R,6R)-3,3-dimethyl-7-oxo-6-{[(phenyloxy)acetyl]amino}-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid
Phenopenicillin
Acipen-V
Phenomycilline
Phenospen
V-Cillin
[2S-(2a,5a,6b)]-3,3-Dimethyl-7-oxo-6-[(phenoxy acetyl)amino]-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic Acid
Orocillin
penicillin V
6-phenoxyacetamidopenicillanic acid
dowpen v-k
4-Thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid, 3,3-dimethyl-7-oxo-6-[(2-phenoxyacetyl)amino]-, (2S,5R,6R)-
4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid, 3,3-dimethyl-7-oxo-6-[(phenoxyacetyl)amino]-, (2S,5R,6R)-
penicillin VK
Phenoxymethylpenicillin