| Size | Price | Stock |
|---|---|---|
| 41.60 mM * 100 μL in Ethanol | $90 | In-stock |
| We match the lowest price on market. | ||
We offer a substantial discount on larger orders, please inquire via [email protected]
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Inquiry for price and availability only. Please place your order via our email or fax.
| Cat. No. : | HY-120996 |
| M.Wt: | 240.38 |
| Formula: | C15H28O2 |
| Purity: | >98 % |
| Solubility: |
10 (E)-Pentadecenoic acid (trans-10-Pentadecenoic acid) is a melanin synthesis inhibitor. 10 (E)-Pentadecenoic acid inhibits nuclear translocation and reduces the protein level of phosphorylated microphthalmia-associated transcription factor (MITF), as well as decreases intracellular tyrosinase activity. 10 (E)-Pentadecenoic acid can be used in the research of skin pigmentation disorders[1].
In Vitro:10(E)-Pentadecenoic acid (1-60 μM; 10 min) exhibits dose-dependent copper ion reduction capacity, as measured by the CUPRAC assay, with the highest activity at 60 μM[1].
10(E)-Pentadecenoic acid (1-60 μM; 20 min) only slightly inhibits mushroom tyrosinase activity at 1 μM, with no significant inhibition at higher concentrations (5, 15, 60 μM)[1].
10(E)-Pentadecenoic acid (1-100 μM; 24 h) is non-cytotoxic to Hs68 human dermal fibroblast cells at concentrations up to 100 μM, but shows cytotoxicity to B16F10 murine melanoma cells at ≥50 μM and to HaCaT human keratinocyte cells at 100 μM[1].
10(E)-Pentadecenoic acid (1-15 μM; 1 h pre-incubation, followed by 6 days co-incubation with 500 nM α-MSH) dose-dependently reduces α-MSH-stimulated melanin production in B16F10 murine melanoma cells at concentrations of 1, 5, and 15 μM[1].
10(E)-Pentadecenoic acid (1-15 μM; 1 h pre-incubation, followed by 3 days co-incubation with 500 nM α-MSH) dose-dependently inhibits α-MSH-stimulated intracellular tyrosinase activity in B16F10 murine melanoma cells at concentrations of 1, 5, and 15 μM[1].
10(E)-Pentadecenoic acid (5-15 μM; 1 h pre-incubation, followed by 6 days co-incubation with 500 nM α-MSH) reduces α-MSH-stimulated mRNA expression of TRP-1, TRP-2, and tyrosinase in B16F10 murine melanoma cells at concentrations of 5 and 15 μM[1].
10(E)-Pentadecenoic acid (5-15 μM; 1 h pre-incubation, followed by 6 days co-incubation with 500 nM α-MSH) reduces α-MSH-stimulated protein expression of TRP-1, tyrosinase, and p-MITF (but not TRP-2) in B16F10 murine melanoma cells at concentrations of 5 and 15 μM[1].
10(E)-Pentadecenoic acid (5-15 μM; co-incubation with 500 nM α-MSH) inhibits α-MSH-stimulated nuclear translocation of MITF in B16F10 murine melanoma cells at concentrations of 5 and 15 μM[1].
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