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Synonyms: YC001, YC 001


| Pack Size | Price | USA Stock | Global Stock | Quantity |
|---|---|---|---|---|
| 1 mg | $32 | - | In Stock | |
| 5 mg | $73 | - | In Stock | |
| 10 mg | $118 | - | In Stock | |
| 25 mg | $193 | - | In Stock | |
| 50 mg | $286 | - | In Stock | |
| 100 mg | $423 | - | In Stock | |
| 1 mL x 10 mM (in DMSO) | $80 | - | In Stock |
| Description | YC-001 is an inverse agonist and antagonist targeting rod opsin. YC-001 binds reversibly to rod opsin, thereby stabilizing its structure and protecting mice from bright light-induced retinal degeneration, showing potential for research on retinal degenerative diseases. |
| Targets & IC50 | rod opsin:0.98 μM (EC₅₀) |
| In vitro | Methods: In vitro assays were performed using gradient concentrations of YC-001 (0–100 μM). Results: The potency of YC-001 was 8.7 μM, with an efficacy range of 150–310%. Methods: Samples were treated with gradient concentrations of YC-001 (0.5, 1, 5, 10, 20, 40 μM). Results: YC-001 improved the glycosylation profile of the P23H rhodopsin mutant. Methods: Binding assays were conducted using gradient concentrations of YC-001 (0–1.5 μM). Results: YC-001 bound reversibly to rod opsin, with an EC50 of 0.98 μM. Methods: NIH3T3 cells were treated with gradient concentrations of YC-001 (0.313, 0.625, 1.25, 2.5, 5, 10, 20, 80 μM). Results: YC-001 dose-dependently increased intracellular cAMP levels in NIH3T3 cells. |
| In vivo | Methods: Abca4⁻/⁻Rdh8⁻/⁻ mice were intraperitoneally injected with YC-001 (50, 200 mg/kg). Results: YC-001 protected Abca4⁻/⁻Rdh8⁻/⁻ mice against bright light–induced retinal degeneration. Methods: Mice were administered YC-001 systemically via intraperitoneal injection (200 mg/kg). Results: YC-001 could penetrate into mouse eyes after systemic administration but could not be retained for a long time. Methods: Mice were intraperitoneally injected with YC-001 (100 mg/kg, 200 mg/kg) once daily for 24 consecutive days. Results: YC-001 showed almost no acute toxicity[1]. |
| Synonyms | YC001, YC 001 |
| Molecular Weight | 282.77 |
| Formula | C12H7ClO2S2 |
| Cas No. | 748778-73-6 |
| Smiles | O=C1OCC(C=2SC(Cl)=CC2)=C1C=3SC=CC3 |
| Storage | Store at low temperature Powder: -20°C for 3 years | In solvent: -80°C for 1 year Shipping with blue ice/Shipping at ambient temperature. | |||||||||||||||||||||||||||||||||||
| Solubility Information | DMSO: 80 mg/mL (282.92 mM), Sonication is recommended. | |||||||||||||||||||||||||||||||||||
Solution Preparation Table | ||||||||||||||||||||||||||||||||||||
DMSO
Note : The dilution table applies only to solid products. For liquid products, please calculate the stock solution based on the stated concentration and/or density. | ||||||||||||||||||||||||||||||||||||
Dissolve 2 mg of the compound in 100 μL DMSO
to obtain a stock solution at a concentration of 20 mg/mL . If the required concentration exceeds the compound's known solubility, please contact us for technical support before proceeding.
1) Add 100 μL of the DMSO
stock solution to 400 μL PEG300
and mix thoroughly until the solution becomes clear.
2) Add 50 μL Tween 80 and mix well until fully clarified.
3) Add 450 μL Saline,PBS or ddH2O
and mix thoroughly until a homogeneous solution is obtained.
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