CBD-TSC1
CBD-TSC1 is a reversible mixed-type inhibitor of human and mushroom tyrosinase, with an IC50 of 27.72 μM against mushroom tyrosinase. CBD-TSC1 interacts with both the free enzyme and the enzyme-substrate complex. CBD-TSC1 reduces intracellular reactive oxygen species (ROS) levels under oxidative stress as well as melanin content in zebrafish larvae.
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- 화학식: C23H33N3O2S
- 분자량:415.59
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보관:
Please store the product under the recommended conditions in the Certificate of Analysis.
Biological Activity
제품 설명
IC50 & Target
[1]|
mushroom Tyrosinase 27.72 μM (IC50) |
In Vitro
CBD-TSC1 inhibits mushroom tyrosinase diphenolase with an IC50 of 27.72 μM, and as a reversible mixed-type inhibitor, it prolongs the lag phase of monophenolase by 5.5 min[1].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
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Cell Line:G361 human melanoma cells and HaCaT human keratinocytes
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Concentration:5 μM; 10 μM; 15 μM; 20 μM
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Incubation Time:8, 12, 24 h
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Result:At short-term exposure (up to 24 h), CBD-TSC1 was well tolerated in both cell lines, with viability remaining above 70% across all tested concentrations.
These findings indicate that CBD-TSC1 exhibited low acute cytotoxicity under the tested conditions and showed a comparable or slightly improved tolerability profile relative to CBD during the initial 12 h of exposure.
Chemical Information
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분자량 415.59
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화학식 C23H33N3O2S
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SMILES
CC1=C[C@@H](C2=C(O)C=C(CCCCC)C(/C=N/NC(N)=S)=C2O)[C@H](C(C)=C)CC1
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선적
Room temperature in continental US; may vary elsewhere.
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보관
Please store the product under the recommended conditions in the Certificate of Analysis.
순도&문서
References
Calculators
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)