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YC-001

(Synonyms: YC001, YC 001) Copy Product Info
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Synonyms: YC001, YC 001

Catalog No. T73476 Copy Product Info
Purity: 99.52%
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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.
YC-001
Cas No. 748778-73-6
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Pack SizePriceUSA StockGlobal StockQuantity
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
For In stock only · Estimated delivery: USA Stock (1-2 days) Global Stock (5-7 days)
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For research use only—not for human use. No sales to individuals. Use as intended only.
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Purity:99.52%
Appearance:Solid
Color:Yellow
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Product Introduction

Bioactivity
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].
SynonymsYC001, YC 001
Chemical Properties
Molecular Weight282.77
FormulaC12H7ClO2S2
Cas No.748778-73-6
SmilesO=C1OCC(C=2SC(Cl)=CC2)=C1C=3SC=CC3
Storage & Solubility Information
StorageStore 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
1mg5mg10mg50mg
1 mM3.5364 mL17.6822 mL35.3644 mL176.8222 mL
5 mM0.7073 mL3.5364 mL7.0729 mL35.3644 mL
10 mM0.3536 mL1.7682 mL3.5364 mL17.6822 mL
20 mM0.1768 mL0.8841 mL1.7682 mL8.8411 mL
50 mM0.0707 mL0.3536 mL0.7073 mL3.5364 mL
100 mM0.0354 mL0.1768 mL0.3536 mL1.7682 mL
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.

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In Vivo Formulation Calculator (Clear solution)

Please enter your animal experiment information in the following box and click Calculate to obtain the stock solution preparation method and in vivo formula preparation method:
TargetMol | Animal experiments For example, if the intended dosage is 10 mg/kg for animals weighing 20 g , with a dosing volume of 100 μL per animal, TargetMol | Animal experiments and a total of 10 animals are to be administered, using a formulation of TargetMol | reagent 10% DMSO+ 40% PEG300+ 5% Tween 80+ 45% Saline/PBS/ddH2O , the resulting working solution concentration would be 2 mg/mL.
Stock Solution Preparation:

Dissolve 2 mg of the compound in 100 μL DMSOTargetMol | reagent 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.

Preparation of the In Vivo Formulation:

1) Add 100 μL of the DMSOTargetMol | reagent stock solution to 400 μL PEG300TargetMol | reagent 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 ddH2OTargetMol | reagent and mix thoroughly until a homogeneous solution is obtained.

This example is provided solely to demonstrate the use of the In Vivo Formulation Calculator and does not constitute a recommended formulation for any specific compound. Please select an appropriate dissolution and formulation strategy based on your experimental model and route of administration.
All co-solvents required for this protocol, includingDMSO, PEG300/PEG400, Tween 80, SBE-β-CD, and Corn oil, are available for purchase on the TargetMol website.
1 Enter information below:
mg/kg
g
μL
2 Enter the in vivo formulation:
% DMSO
%
% Tween 80
% Saline/PBS/ddH2O

Dose Conversion

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Related Tags: YC-001 chemical structure | YC-001 in vivo | YC-001 in vitro | YC-001 formula | YC-001 molecular weight