Description
3-Tert-butyl-5-methoxy-catechol exhibits anticancer activity, inhibiting proliferation of leukemia cells. This compound may also induce cellular differentiation in vitro.
| Product Unit Size | Cost | Quantity | Stock |
|---|
3-Tert-butyl-5-methoxy-catechol exhibits anticancer activity, inhibiting proliferation of leukemia cells. This compound may also induce cellular differentiation in vitro.
| Cas No. | 80284-15-7 |
|---|---|
| Purity | ≥95% |
| Formula | C11H16O3 |
| Formula Wt. | 196.25 |
| Chemical Name | 3-tert-butyl-5-methoxybenzene-1,2-diol |
| IUPAC Name | 3-tert-butyl-5-methoxybenzene-1,2-diol |
| Synonym | 3-(1,1-Dimethylethyl)-5-methoxy-1,2-benzenediol, 3-tert-Butyl-4,5-dihydroxyanisole |
| Melting Point | 95-96°C |
| Solubility | Partly soluble in water. |
| Appearance | White/Off-white Crystalline Solid |
| Store Temp | -20°C |
|---|---|
| Ship Temp | Ambient |
| MSDS | |
|---|---|
| Info Sheet |
Tsuchiya T, Ishida A, Miyata N, et al. Effects of 3-tert-Butyl-4-hydroxyanisole and its hydroquinone and quinone metabolites on rat and human embryonic cells in culture. Toxicol In Vitro. 1988;2(4):291-6. PMID: 20837439.
Lam LK, Garg PK, Swanson SM, et al. Evaluation of the cytotoxic potential of catechols and quinones structurally related to butylated hydroxyanisole. J Pharm Sci. 1988 May;77(5):393-5. PMID: 3411459.
Mast cell destabilizer; potential TRP antagonis...
Nitroimidazole, binds DNA; nucleic acid synthes...
Endogenous calcitonin-family peptide frgament, ...
Neutrophil elastase inhibitor.
Recombinant HIV glycoprotein antigen fragment.<...
Synthetic antifungal.
Nitroimidazole; DNA synthesis inhibitor.
SIRT1/2 inhibitor.
Isoflavone found in Pueraria; 5-HT2C and GABA-A...
Endogenous vitamin D prodrug.
SERCA inhibitor.
Furanocoumarin found in Psoralea coryfolia, DNA...
Selective Cannabinoid receptor 2(CB2) inverse a...
Phenol found in Zingiber; 5-HT3 antagonist.
Triterpene saponin found in species of Panax.
α1-adrenergic antagonist.
Endogenous peptide, involved in stress signalin...
BACE1 inhibitor
ATR inhibitor.
p38 MAPK inhibitor.