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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- CAS No.: 3343-38-2
- Formule: C15H16O3
- Masse moléculaire:244.29
-
Stockage:
Please store the product under the recommended conditions in the Certificate of Analysis.
Activité biologique
Description
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] |
In Vitro
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.
Chemical Information
-
CAS No. 3343-38-2
-
Masse moléculaire 244.29
-
Formule C15H16O3
-
SMILES
O=C1C(O)=C(CCC(C)C)C(C2=C1C=CC=C2)=O
-
Livraison
Room temperature in continental US; may vary elsewhere.
-
Stockage
Please store the product under the recommended conditions in the Certificate of Analysis.
Pureté et documentation
Références
Calculators
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)