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製品番号: HY-183424

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Hydrolapachol

Hydrolapachol is a mitochondrial respiratory chain inhibitor that targets the site between cytochrome b and c₁, and inhibits succinate oxidation in rat liver mitochondria. Hydrolapachol can be used in studies related to mitochondrial respiration.

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研究用途以外に使用した場合、当社は一切の責任を負いかねます。

CAS 番号: 3343-38-2
分子式: C₁₅H₁₆O₃
分子量:244.29

保管条件:

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

Hydrolapachol 構造式

CAS 番号: 3343-38-2

価格（税別）

Amount: USD 0.00

* アイテムを追加する前、数量をご選択ください

Use of MCE Products

Strong Fluorescence Signal / Multi-Disciplinary Applications / High Fluorescence Specificity

生物活性

製品説明

Cellular Effect

Cell Line	Type	Value	Description	References
HCT-8	IC₅₀	20.46 μM Compound: 7	Cytotoxicity against human HCT8 cells after 72 hrs by MTT assay Cytotoxicity against human HCT8 cells after 72 hrs by MTT assay	[PMID: 21115213]
HL-60	IC₅₀	62.13 μM Compound: 13	Cytotoxicity against human promyelocytic leukemia HL60 cell line by MTT assay Cytotoxicity against human promyelocytic leukemia HL60 cell line by MTT assay	[PMID: 17249647]
HL-60	IC₅₀	20.46 μM Compound: 7	Cytotoxicity against human HL60 cells after 72 hrs by MTT assay Cytotoxicity against human HL60 cells after 72 hrs by MTT assay	[PMID: 21115213]
MDA-MB-435	IC₅₀	20.46 μM Compound: 7	Cytotoxicity against human MDA-MB-435 cells after 72 hrs by MTT assay Cytotoxicity against human MDA-MB-435 cells after 72 hrs by MTT assay	[PMID: 21115213]
PBMC	IC₅₀	20.46 μM Compound: 7	Cytotoxicity against human PBMC cells after 72 hrs by Alamar Blue assay Cytotoxicity against human PBMC cells after 72 hrs by Alamar Blue assay	[PMID: 21115213]
PBMC	IC₅₀	102.34 μM Compound: 3	Cytotoxicity against human PBMC after 72 hrs by Alamar blue assay Cytotoxicity against human PBMC after 72 hrs by Alamar blue assay	[PMID: 21820768]
SF-295	IC₅₀	20.46 μM Compound: 7	Cytotoxicity against human SF295 cells after 72 hrs by MTT assay Cytotoxicity against human SF295 cells after 72 hrs by MTT assay	[PMID: 21115213]

体外実験

Hydrolapachol inhibits succinate oxidation in intact rat liver mitochondria with an IC₅₀ of 1.6 μg per mg protein^[1].
Hydrolapachol exerts a stronger inhibitory effect on succinate oxidation in intact rat liver mitochondria at lower pH, and this inhibition is completely reversed by bovine serum albumin, CCCP (HY-100941) and 2,4-dibromophenol, and partially reversed by 2,4-dinitrophenol; at low inhibitor concentrations, phosphate (or arsenate) is required to achieve maximal inhibition of succinate oxidation in intact rat liver mitochondria^[1].
Hydrolapachol can be prepared by platinum oxide-platinum black-catalyzed hydrogenation of Isolapachol, and can also be obtained by hydrogenation of lapachol^[2].

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

化学情報

CAS 番号 3343-38-2
分子量 244.29
分子式 C₁₅H₁₆O₃
SMILES

O=C1C(O)=C(CCC(C)C)C(C2=C1C=CC=C2)=O
輸送条件

Room temperature in continental US; may vary elsewhere.
保管条件

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

純度とドキュメンテーション

取扱説明書 (2659 KB)

参考文献

[1]. Howland JL. Inhibition of mitochondrial succinate oxidation by alkyl hydroxy naphthoquinones. Biochim Biophys Acta. 1965 Aug 24;105(2):205-13. [Content Brief]

[2]. Hooker SC. Condensation of Aldehydes with β-Hydroxy-α-naphthoquinone. Synthesis of Hydrolapachol. J Am Chem Soc. 1936;58(7):1163-1167.

Calculators

モル濃度計算機

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

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濃度濃度

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分子量分子量

希釈計算機

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濃度 _(開始) 濃度 _(開始)

体積 _(開始) 体積 _(開始)

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Help & FAQs

How should lyophilized recombinant proteins be reconstituted and stored?

1. Before opening the cap, centrifuge the vial at 13000 rpm for 20-30 seconds. This step will ensure that any lyophilized powder that may have adhered to the cap or walls is collected at the bottom of the vial, minimizing the risk of product loss.

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MOQ

Minimum order quantity

100 mg

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