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Omadacycline hydrochloride
本产品不向个人销售,仅用作科学研究,不用于任何人体实验及非科研性质的动物实验。
Omadacycline hydrochloride图片
CAS NO:1196800-39-1
包装与价格:
包装价格(元)
10 mM * 1 mL in DMSO电议
2mg电议
5mg电议
10mg电议
50mg电议
100mg电议
200mg电议

产品名称
PTK0796 hydrochloride
Amadacycline hydrochloride
产品介绍
Omadacycline (PTK 0796) hydrochloride,首创的具有口服活性的氨基甲基环素抗菌剂,是一种四环素类抗生素。Omadacycline hydrochloride 通过与 30S 核糖体亚基结合来抑制细菌蛋白质的合成。Omadacycline hydrochloride 对多种细菌表现出活性,包括好氧和厌氧革兰氏阳性细菌和革兰氏阴性细菌,非典型病原体。Omadacycline hydrochloride 可用于研究急性细菌性皮肤和皮肤结构感染,感染性肺炎和尿路感染。
生物活性

Omadacycline (PTK 0796) hydrochloride, a first-in-class orally active aminomethylcyclineantibacterial, is a member of thetetracyclineclass ofantibiotics. Omadacycline hydrochloride acts through the inhibition ofbacterialprotein synthesisby binding to the 30S ribosomal subunit. Omadacycline hydrochloride possesses broad-spectrum antibacterial activity against aerobic and anaerobic Gram-positive and Gram-negative bacteria, as well as atypical bacteria. Omadacycline hydrochloride can be used for the research of acutebacterialskin and skin-structure infections, community-acquired pneumonia, and urinary tract infections[1][2][3][4].

IC50& Target

Tetracycline

 

体外研究
(In Vitro)

Omadacycline displays activity against methicillin-resistantStaphylococcus aureus(MRSA), vancomycin-resistantEnterococcus(VRE), beta-hemolytic streptococci, penicillin-resistantStreptococcus pneumonia(PRSP) andHaemophilus influenzae (H. influenzae), with MIC90s of 1.0, 0.25, 0.5, 0.25 and 2.0 μg/mL respectively[2].
Omadacycline is active against strains expressing tetracycline and other antibiotics resistance by ribosomal protection and active tetracycline efflux[2].

体内研究
(In Vivo)

Omadacycline (0.11-18 mg/kg; a single i.v.) exhibits efficacy againstStreptococcus pneumonia,Escherichia coli, andStaphylococcus aureusin mice systemic infection model, with ED50s ranging from 0.30 mg/kg to 3.39 mg/kg[2].

Clinical Trial
分子量

593.11

性状

Solid

Formula

C29H40N4O7.HCl

CAS 号

1196800-39-1

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

-20°C, sealed storage, away from moisture

*In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture)

溶解性数据
In Vitro: 

DMSO : 105 mg/mL(177.03 mM;Need ultrasonic)

H2O : ≥ 50 mg/mL(84.30 mM)

*"≥" means soluble, but saturation unknown.

配制储备液
浓度溶剂体积质量1 mg5 mg10 mg
1 mM1.6860 mL8.4301 mL16.8603 mL
5 mM0.3372 mL1.6860 mL3.3721 mL
10 mM0.1686 mL0.8430 mL1.6860 mL
*

请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液;一旦配成溶液,请分装保存,避免反复冻融造成的产品失效
储备液的保存方式和期限:-80℃, 6 months; -20℃, 1 month (sealed storage, away from moisture)。-80℃ 储存时,请在 6 个月内使用,-20℃ 储存时,请在 1 个月内使用。

In Vivo:

请根据您的实验动物和给药方式选择适当的溶解方案。以下溶解方案都请先按照In Vitro方式配制澄清的储备液,再依次添加助溶剂:

——为保证实验结果的可靠性,澄清的储备液可以根据储存条件,适当保存;体内实验的工作液,建议您现用现配,当天使用; 以下溶剂前显示的百
分比是指该溶剂在您配制终溶液中的体积占比;如在配制过程中出现沉淀、析出现象,可以通过加热和/或超声的方式助溶

  • 1.

    请依序添加每种溶剂: PBS

    Solubility: 50 mg/mL (84.30 mM); Clear solution; Need ultrasonic

  • 2.

    请依序添加每种溶剂: 5% DMSO    95% (20%SBE-β-CDin saline)

    Solubility: ≥ 2.62 mg/mL (4.42 mM); Clear solution

*以上所有助溶剂都可在本网站选购。