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Hexahydrocurcumin

🥰Excellent
Catalog No. TQ0288Cas No. 36062-05-2

Hexahydrocurcumin is a selective, orally active COX-2 inhibitor and inactive against COX-1.

Hexahydrocurcumin

Hexahydrocurcumin

🥰Excellent
Purity: 99.77%
Catalog No. TQ0288Cas No. 36062-05-2
Hexahydrocurcumin is a selective, orally active COX-2 inhibitor and inactive against COX-1.
Pack SizePriceAvailabilityQuantity
1 mg$122In Stock
5 mg$297In Stock
10 mg$439In Stock
25 mg$728In Stock
50 mg$987In Stock
100 mg$1,390In Stock
500 mg$2,780In Stock
1 mL x 10 mM (in DMSO)$329In Stock
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Purity:99.77%
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Product Introduction

Bioactivity
Description
Hexahydrocurcumin is a selective, orally active COX-2 inhibitor and inactive against COX-1.
In vitro
Hexahydrocurcumin (0-25 μM; 24-48 hours; HT-29 cells) significantly decreased HT-29 colon cancer cell viability in a time- and concentration-dependent manner, with IC50 values of 77.05 μM at 24 hours and 56.95 μM at 48 hours. When combined with 5-fluorouracil (5-FU; 5 μM), Hexahydrocurcumin markedly reduced COX-2 expression without altering COX-1 levels [1]. Moreover, Hexahydrocurcumin (7-14 μM; 24 hours) attenuated LPS-induced prostaglandin E2 (PGE2) increase in murine macrophages (RAW 264.7) in a concentration-dependent manner [2].
In vivo
In colon cancer rats, Hexahydrocurcumin (50 mg/kg; oral administration; daily; for 16 weeks; male Wistar rats) treatment significantly reduces the numbers of aberrant crypt foci. Hexahydrocurcumin also markedly decreases COX-2 protein expression [3].
Cell Research
Cell Line: HT-29 cells. Concentration: 0 μM, 5 μM, 10 μM, 25 μM. Incubation Time: 24 hours or 48 hours [1]
Animal Research
Animal Model: Male Wistar rats (100-120 g) injected with dimethylhydrazine (DMH). Dosage: 50 mg/kg. Administration: Oral administration; daily; for 16 weeks [3]
Chemical Properties
Molecular Weight374.43
FormulaC21H26O6
Cas No.36062-05-2
SmilesCOc1cc(CCC(O)CC(=O)CCc2ccc(O)c(OC)c2)ccc1O
Relative Density.1.226 g/cm3
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
Solubility Information
DMSO: 45 mg/mL (120.18 mM), Sonication is recommended.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM2.6707 mL13.3536 mL26.7073 mL133.5363 mL
5 mM0.5341 mL2.6707 mL5.3415 mL26.7073 mL
10 mM0.2671 mL1.3354 mL2.6707 mL13.3536 mL
20 mM0.1335 mL0.6677 mL1.3354 mL6.6768 mL
50 mM0.0534 mL0.2671 mL0.5341 mL2.6707 mL
100 mM0.0267 mL0.1335 mL0.2671 mL1.3354 mL

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Please enter your animal experiment information in the following box and click Calculate to obtain the mother liquor preparation method and in vivo formula preparation method:
TargetMol | Animal experimentsFor example, your dosage is 10 mg/kg Each animal weighs 20 g, and the dosage volume is 100 μL . TargetMol | Animal experiments A total of 10 animals were administered, and the formula you used is 5% TargetMol | reagent DMSO+30% PEG300+5% Tween 80+60% ddH2O. So your working solution concentration is 2 mg/mL。
Mother liquor preparation method: 2 mg of drug dissolved in 50 μL DMSOTargetMol | reagent (mother liquor concentration of 40 mg/mL), if you need to configure a concentration that exceeds the solubility of the product, please contact us first.
Preparation method for in vivo formula: Take 50 μL DMSOTargetMol | reagent main solution, add 300 μLPEG300TargetMol | reagent mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLddH2OTargetMol | reagent mix well and clarify
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