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D-Histidine

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纯度: 99.57%

货号 T9372Cas号 351-50-8

D-Histidine 是一种 L-histidine 的对映体。其中 L-histidine 是婴儿必需的氨基酸,是一种线粒体谷氨酰胺转运的抑制剂。

D-Histidine

D-Histidine

一键复制产品信息
Rating icon 很棒

纯度: 99.57%

货号 T9372Cas号 351-50-8

D-Histidine 是一种 L-histidine 的对映体。其中 L-histidine 是婴儿必需的氨基酸,是一种线粒体谷氨酰胺转运的抑制剂。

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1 g
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5 g
¥ 150
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产品介绍


生物活性
产品描述
D-Histidine is an enantiomer of L-histidine. L-Histidine is an inhibitor of mitochondrial glutamine transport and also an essential amino acid for infants.
化学信息
分子量155.15
分子式C6H9N3O2
CAS No.351-50-8
SmilesN[C@H](Cc1c[nH]cn1)C(O)=O
密度1.3092 g/cm3 (Estimated)
颜色White
物理性状solid
储存&溶解度
存储keep away from direct sunlight,store under nitrogen | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
溶解度信息
H2O: 31.2 mg/mL (201.1 mM), Sonication and heating are recommended.
DMSO: < 1.55 mg/mL (10 mM, insoluble or slightly soluble)
溶液配制表
DMSO/H2O
1mg5mg10mg50mg
1 mM6.4454 mL32.2269 mL64.4538 mL322.2688 mL
5 mM1.2891 mL6.4454 mL12.8908 mL64.4538 mL
10 mM0.6445 mL3.2227 mL6.4454 mL32.2269 mL
H2O
1mg5mg10mg50mg
20 mM0.3223 mL1.6113 mL3.2227 mL16.1134 mL
50 mM0.1289 mL0.6445 mL1.2891 mL6.4454 mL
100 mM0.0645 mL0.3223 mL0.6445 mL3.2227 mL

计算器

  • 摩尔浓度 计算器
  • 稀释 计算器
  • 配液 计算器
  • 分子量 计算器

体内实验配液计算器

请在以下方框中输入您的动物实验信息后点击计算,可以得到母液配置方法和体内配方的制备方法:
TargetMol | Animal experiments 比如您的给药剂量是10 mg/kg,每只动物体重20g,给药体积100 μLTargetMol | Animal experiments 一共给药动物10只,您使用的配方为5%TargetMol | reagent DMSO + 30%PEG300 + 5%Tween 80 + 60%Saline/PBS/ddH2O, 那么您的工作液浓度为2mg/mL
母液配置方法: 2 mg 药物溶于 50 μLDMSOTargetMol | reagent ( 母液浓度为 40 mg/mL ), 如您需要配置的浓度超过该产品的溶解度,请先与我们联系。
体内配方的制备方法:50μLDMSOTargetMol | reagent 母液,添加 300 μLPEG300TargetMol | reagent 混匀澄清,再加 50μLTween80, 混匀澄清,再加 600μLSaline/PBS/ddH2OTargetMol | reagent 混匀澄清

以上为“体内实验配液计算器”的使用方法举例,并不是具体某个化合物的推荐配制方式,请根据您的实验动物和给药方式选择适当的溶解方案。

方案所需的各类助溶剂如: DMSOPEG300 / PEG400Tween 80SBE-β-CD玉米油 等, 均可在TargetMol网站点击购买。
1 请输入动物实验的基本信息
mg/kg
g
μL
2 请输入动物体内配方组成,不同的产品配方组成不同,如有配方需求,可先联系我们提供正确的体内配方。
% DMSO
%
% Tween 80
% Saline/PBS/ddH2O

剂量转换

对于不同动物的给药剂量换算,您也可以参考 更多

TargetMol AI Summary
D-Histidine exhibits diverse bioactivities, notably in modulating carbonic anhydrase (CA) enzymes and exhibiting antiviral properties. It acts as a potent activator for several human CA isoforms, including CA1 with a KA value of 0.09 uM, CA5A with a KA value of 0.12 uM, and CA13 also with a KA value of 0.09 uM. Moderate activation was observed for CA3 (KA of 1.1 uM), CA7 (KA of 0.71 uM), and CA14 (KA of 2.4 uM), while lower affinities were noted for CA2 (KA of 43.0 uM), CA4 (KA of 12.3 uM), and CA5B (KA of 4.38 uM). The compound also shows inhibitory activity against human carbonic anhydrase 1 (KA of 0.09 uM) and CA2 (KA of 43.0 uM). Additionally, D-Histidine exhibits antiviral activity, particularly against SARS-CoV-2. It reduces virus-induced cytotoxicity in Vero-6 cells and demonstrates some degree of inhibition against the SARS-CoV-2 3CL-Pro protease. Furthermore, the compound shows inhibition of the human LAT1 transporter in TREx HEK293 cells with an IC50 value of 460000.0 nM and inhibition of the human HDAC6 enzyme with variable percentages depending on the substrate used. Overall, D-Histidine displays a broad spectrum of biological activities, making it a versatile candidate for therapeutic exploration..
Note: Summary generated by AI, AI may be wrong some times, we do not provide any medical advice and only sell our product to accredited institution, Please cross-check with other sources, data source: chembl
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