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Synonyms:
(S,S)-SARM1-IN-9
| Pack Size | Price | USA Stock | Global Stock | Quantity |
|---|---|---|---|---|
| 10 mg | Inquiry | 10-14 weeks | 10-14 weeks | |
| 50 mg | Inquiry | 10-14 weeks | 10-14 weeks |
| Description | (S,S)-SARM1-IN-9 (Compound MY-13A) is a stereoselective SARM1 inhibitor with covalent binding properties. It covalently modifies cysteine-311 within the auto-regulatory ARM domain of wild-type SARM1, thereby blocking NADase activity without inhibiting SARM1C311A or SARM1C311S mutants. This compound also prevents axonal degeneration in primary rodent dorsal root ganglion neurons induced by vacor and vincristine. (S,S)-SARM1-IN-9 is applicable for the study of axon degeneration-dependent neurological diseases, including chemotherapy-induced peripheral neuropathy. |
| Molecular Weight | 427.45 |
| Formula | C25H21N3O4 |
| Cas No. | 3020765-70-9 |
| Smiles | C(C=C)(=O)N1[C@H](C2=C(C=3C(N2)=CC=CC3)C[C@H]1C(NCC#C)=O)C=4C=C5C(=CC4)OCO5 |
| Storage | Powder: -20°C for 3 years | In solvent: -80°C for 1 year Shipping with blue ice/Shipping at ambient temperature. |
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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