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  3. Chlorhexidine-d8

Chlorhexidine-d8  (Synonyms: 氯己定-d8)

目录号: HY-W738281
产品使用指南 技术支持

Chlorhexidine-d8 是氘代标记的 Chlorhexidine (HY-B1248)。Chlorhexidine 是一种口服有效、靶向微生物细胞膜的阳离子抗菌剂。Chlorhexidine 通过与细胞膜磷脂非特异性结合,破坏膜结构并诱导细胞内容物泄漏,对革兰氏阳性/阴性菌均具广谱杀菌活性。Chlorhexidine 可干扰膜通透性、导致蛋白质沉淀及能量代谢障碍,如快速抑制微生物生长并诱导细胞死亡 (坏死 (necroptosis) 或凋亡 (apoptosis))。

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Chlorhexidine-d<sub>8</sub> Chemical Structure

Chlorhexidine-d8 Chemical Structure

CAS No. : 1246816-96-5

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Chlorhexidine-d8 的其他形式现货产品:

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Other Forms of Chlorhexidine-d8:

  • 生物活性

  • 纯度 & 产品资料

  • 参考文献

生物活性

Chlorhexidine-d8 is deuterium-labeled Chlorhexidine (HY-B1248)[1]. Chlorhexidine is a orally active cationic antimicrobial agent that targets microbial cell membranes. Chlorhexidine binds to cell membrane phospholipids non-specifically, destroys membrane structure and induces leakage of cell contents. Chlorhexidine has broad-spectrum bactericidal activity against both Gram-positive and Gram-negative bacteria. Chlorhexidine can interfere with membrane permeability, cause protein precipitation and energy metabolism disorders, such as rapid inhibition of microbial growth and induction of cell death (necrosis or apoptosis)[1][2][3].

细胞效力
(Cellular Effect)
Cell Line Type Value Description References
Fibroblast CC50
6.32 μg/mL
Compound: Chlorohexidine
Cytotoxicity against human skin fibroblasts assessed as cell viability measured after 72 hrs by MTT assay
Cytotoxicity against human skin fibroblasts assessed as cell viability measured after 72 hrs by MTT assay
[PMID: 33385851]
HEK293 IC50
0.21 μM
Compound: chlorhexidine
Inhibition of human OCT1-mediated ASP+ uptake expressed in HEK293 cells after 3 mins by fluorescence assay
Inhibition of human OCT1-mediated ASP+ uptake expressed in HEK293 cells after 3 mins by fluorescence assay
[PMID: 23241029]
HEK293 IC50
0.4 μM
Compound: chlorhexidine
Inhibition of human OCT2-mediated ASP+ uptake expressed in HEK293 cells after 3 mins by fluorescence assay
Inhibition of human OCT2-mediated ASP+ uptake expressed in HEK293 cells after 3 mins by fluorescence assay
[PMID: 23241029]
HEK293 IC50
0.41 μM
Compound: chlorhexidine
Inhibition of human OCT3-mediated ASP+ uptake expressed in HEK293 cells after 3 mins by fluorescence assay
Inhibition of human OCT3-mediated ASP+ uptake expressed in HEK293 cells after 3 mins by fluorescence assay
[PMID: 23241029]
HEK293 IC50
0.5 μM
Compound: chlorhexidine
Inhibition of human MATE2K-mediated ASP+ uptake expressed in HEK293 cells after 1.5 mins by fluorescence assay
Inhibition of human MATE2K-mediated ASP+ uptake expressed in HEK293 cells after 1.5 mins by fluorescence assay
[PMID: 23241029]
HEK293 IC50
0.7 μM
Compound: chlorhexidine
Inhibition of human MATE1-mediated ASP+ uptake expressed in HEK293 cells after 1.5 mins by fluorescence assay
Inhibition of human MATE1-mediated ASP+ uptake expressed in HEK293 cells after 1.5 mins by fluorescence assay
[PMID: 23241029]
HEK293 CC50
7.28 μg/mL
Compound: Chlorohexidine
Cytotoxicity against human HEK293 cells assessed as cell viability measured after 72 hrs by MTT assay
Cytotoxicity against human HEK293 cells assessed as cell viability measured after 72 hrs by MTT assay
[PMID: 33385851]
HSF (VGS) CC50
5.48 μg/mL
Compound: Chlorhexidine
Cytotoxicity against human HSF cells assessed as reduction in cell viability incubated for 72 hrs by MTT assay
Cytotoxicity against human HSF cells assessed as reduction in cell viability incubated for 72 hrs by MTT assay
[PMID: 33310546]
HT-22 IC50
5.6 μM
Compound: 34
Cytotoxicity against mouse HT-22 cells assessed as reduction in cell viability incubated for 48 hrs by MTS assay
Cytotoxicity against mouse HT-22 cells assessed as reduction in cell viability incubated for 48 hrs by MTS assay
[PMID: 36876904]
体外研究
(In Vitro)

Stable heavy isotopes of hydrogen, carbon, and other elements have been incorporated into drug molecules, largely as tracers for quantitation during the drug development process. Deuteration has gained attention because of its potential to affect the pharmacokinetic and metabolic profiles of drugs[1].

MCE has not independently confirmed the accuracy of these methods. They are for reference only.

分子量

513.50

Formula

C22H22D8Cl2N10

CAS 号
非标记 CAS
运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

Please store the product under the recommended conditions in the Certificate of Analysis.

纯度 & 产品资料
参考文献
  • 摩尔计算器

  • 稀释计算器

The molarity calculator equation

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

质量   浓度   体积   分子量 *
= × ×

The dilution calculator equation

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

浓度 (start) × 体积 (start) = 浓度 (final) × 体积 (final)
× = ×
C1   V1   C2   V2
Help & FAQs
  • Do most proteins show cross-species activity?

    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

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