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SCD1 inhibitor-3
CAS No. 1282606-48-7
SCD1 inhibitor-3( —— )
Catalog No. M35059 CAS No. 1282606-48-7
SCD1 inhibitor-3 (ML-270) is a highly effective and orally available compound that inhibits SCD1 with remarkable safety.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 2MG | 128 | Get Quote |
|
| 5MG | 187 | Get Quote |
|
| 10MG | 297 | Get Quote |
|
| 25MG | 490 | Get Quote |
|
| 50MG | 707 | Get Quote |
|
| 100MG | 972 | Get Quote |
|
| 500MG | Get Quote | Get Quote |
|
| 1G | Get Quote | Get Quote |
|
Biological Information
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Product NameSCD1 inhibitor-3
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NoteResearch use only, not for human use.
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Brief DescriptionSCD1 inhibitor-3 (ML-270) is a highly effective and orally available compound that inhibits SCD1 with remarkable safety.
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DescriptionSCD1 inhibitor-3 is a safe, potent and orally active SCD1 inhibitor. SCD1 inhibitor-3 can be used for the research of metabolic diseases such as obesity, type II diabetes and dyslipidemia, as well as skin diseases, acne and cancer.
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In Vitro——
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In VivoSCD1 inhibitor-3 (compound 17a) (5 mg/kg; p.o.; 4 hours) reduces the plasma C16:1/C16:0 triglycerides desaturation index by 54 %.SCD1 inhibitor-3 (2~10 mg/kg; p.o.; 4 hours) makes a dose-responsive reduction of plasma triglycerides desaturation index.Animal Model:Lewis rats Dosage:5 mg/kg Administration:P.o.; 4 hours Result:Reduced the plasma C16:1/C16:0 triglycerides desaturation index by 54 %.Animal Model:Lewis rats Dosage:2~10 mg/kg Administration:P.o.; 4 hours Result:A dose-responsive reduction of plasma triglycerides desaturation index.
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Synonyms——
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PathwayMetabolic Enzyme/Protease
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TargetDehydrogenase
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RecptorDehydrogenase
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Research Area——
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Indication——
Chemical Information
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CAS Number1282606-48-7
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Formula Weight393.37
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Molecular FormulaC19H16FN7O2
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Purity>98% (HPLC)
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SolubilityIn Vitro:?DMSO : ≥ 125 mg/mL (317.77 mM)
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SMILESFc1ccc(Cn2ncn(-c3cc(n[nH]3)C(=O)NCc3cccnc3)c2=O)cc1
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Chemical Name——
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
1. Sun S, et al. Discovery of triazolone derivatives as novel, potent stearoyl-CoA desaturase-1 (SCD1) inhibitors. Bioorg Med Chem. 2015;23(3):455-465.?
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