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Formula | C21H26O3 |
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Molecular Weight | 326.43 | CAS No. | 55079-83-9 | |
Solubility (25°C)* | In vitro | DMSO | 20 mg/mL (61.26 mM) | |
Water | Insoluble | |||
Ethanol | Insoluble | |||
* <1 mg/ml means slightly soluble or insoluble. * Please note that Selleck tests the solubility of all compounds in-house, and the actual solubility may differ slightly from published values. This is normal and is due to slight batch-to-batch variations. * Room temperature shipping (Stability testing shows this product can be shipped without any cooling measures.) |
Description | Acitretin (Etretin, RO 10-1670) is a second generation retinoid used for psoriasis. |
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In vitro | Acitretin stimulates ADAM10 promoter activity with an EC(50) of 1.5 mM and leads to an increase of mature ADAM10 protein that results in a two- to three-fold increase of the ratio between alpha- and beta-secretase activity in neuroblastoma cells. [1] Acitretin (5-20 μM) impairs mitochondrial phosphorylation efficiency as demonstrated by the decrease in the state 3 respiration and ATP levels, and by the increase in the lag phase of ADP phosphorylation cycle, without affecting the membrane potential. Acitretin induces Ca(2+)-mediated mitochondrial permeability transition (MPT) and decreased the adenine nucleotide translocase (ANT) content. [2] Acitretin preferentially inhibits the growth of SCL-1 cells in a dose- and time-dependent manner, but not of non-malignant keratinocyte HaCaT cells. Acitretin increases the levels of CD95 (Fas), CD95-ligand and Fas-associated death domain. Acitretin is able to induce apoptosis in skin cancer cells possibly via death receptor CD95 apoptosis pathway without affecting the viability of normal keratinocyte. [3] |
In vivo | Acitretin undergoes alpha-oxidation, chain shortening O-demethylation, and glucuronidation in the perfused rat liver. [4] Acitretin rapidly appears in liver and muscle of rats, where it undergoes redistribution into skin and adipose tissue. [5] |
Data from [Data independently produced by , , Antimicrob Agents Chemother, 2016, 61(11). pii: e01368-17]
Data from [Data independently produced by , , Saudi Pharm J, 2017, 25(4):620-624]
Isolation of Reporter Cells That Respond to Vitamin A and/or D Using a piggyBac Transposon Promoter-Trapping Vector System [ Int J Mol Sci, 2022, 23(16)9366] | PubMed: 36012634 |
Acitretin mitigates uroporphyrin-induced bone defects in congenital erythropoietic porphyria models [ Sci Rep, 2021, 11(1):9601] | PubMed: 33953217 |
Evaluation of the Innate Immune Modulator Acitretin as a Strategy To Clear the HIV Reservoir. [Garcia-Vidal E, et al. Antimicrob Agents Chemother, 2017, 61(11). pii: e01368-17] | PubMed: 28874382 |
Acitretin modulates HaCaT cells proliferation through STAT1- and STAT3-dependent signaling. [Qin X, et al. Saudi Pharm J, 2017, 25(4):620-624] | PubMed: 28579901 |
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Selleck products are transported at room temperature. If you receive the product at room temperature, please rest assured, the Selleck Quality Inspection Department has conducted experiments to verify that the normal temperature placement of one month will not affect the biological activity of powder products. After collecting, please store the product according to the requirements described in the datasheet. Most Selleck products are stable under the recommended conditions.
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