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Activity Type | Activity Value -log(M) | Mechanism of Action | Activity Reference | Publications (PubMed IDs) |
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SKU | Size | Availability | Price | Qty |
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S276482-5mg | 5mg | In stock | $124.90 | |
S276482-10mg | 10mg | In stock | $179.90 | |
S276482-25mg | 25mg | In stock | $405.90 | |
S276482-50mg | 50mg | In stock | $767.90 |
A\xa0selective Δ6 desaturase inhibitor
Synonyms | 2,2-Diphenyl-5-[4-[(E)-pyridin-3-ylmethylideneamino]piperazin-1-yl]pentanenitrile;a,a-diphenyl-4-[(3-pyridinylmethylene)amino]-1-piperazinepentanenitrile |
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Specifications & Purity | ≥98% |
Biochemical and Physiological Mechanisms | Selective Δ6 desaturase inhibitor (IC 50 =0.2 μM in vitro ). It displays selectivity over Δ5 and Δ9 desaturases (IC 50 values are >200 μM in vitro). Exhibits anti inflammatory properties in a mouse edema model. Eliminates CSCs from ovarian cancer cell lin |
Storage Temp | Protected from light,Store at -20°C |
Shipped In | Ice chest + Ice pads |
Note | Refer to SDS for further information. Need more advice on solubility, usage and handling? Please visit our frequently asked questions (FAQ) page for more details. |
Product Description | Product description: SC-26196 is a potent, orally active Delta6 desaturase (D6D, FADS2) inhibitor (IC50=0.2 µM in a rat liver microsomal assay). Antiinflammatory properties. Application: SC-26196 has been used as an inhibitor of delta6 (Δ6) fatty acid desaturase: in mouse inner medullary collecting duct (IMCD3) and human (female) embryonic kidney (HEK) 293 cell culture as Dulbecco′s modified eagle′s medium (DMEM) component in hepatic HepG2 cells in glioblastoma cell lines to test its effect post-radiation treatments |
Activity Type | Activity Value -log(M) | Mechanism of Action | Activity Reference | Publications (PubMed IDs) |
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IUPAC Name | 2,2-diphenyl-5-[4-[(E)-pyridin-3-ylmethylideneamino]piperazin-1-yl]pentanenitrile |
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INCHI | InChI=1S/C27H29N5/c28-23-27(25-10-3-1-4-11-25,26-12-5-2-6-13-26)14-8-16-31-17-19-32(20-18-31)30-22-24-9-7-15-29-21-24/h1-7,9-13,15,21-22H,8,14,16-20H2/b30-22+ |
InChi Key | QFYKXKMYVYOUNJ-JBASAIQMSA-N |
Canonical SMILES | C1CN(CCN1CCCC(C#N)(C2=CC=CC=C2)C3=CC=CC=C3)N=CC4=CN=CC=C4 |
Isomeric SMILES | C1CN(CCN1CCCC(C#N)(C2=CC=CC=C2)C3=CC=CC=C3)/N=C/C4=CN=CC=C4 |
PubChem CID | 9845201 |
Molecular Weight | 423.56 |
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Lot Number | Certificate Type | Date | Item |
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K2219127 | Certificate of Analysis | Sep 20, 2023 | S276482 |
K2219126 | Certificate of Analysis | Sep 15, 2023 | S276482 |
K2219128 | Certificate of Analysis | Sep 15, 2023 | S276482 |
K2219129 | Certificate of Analysis | Sep 07, 2022 | S276482 |
Solubility | Soluble in DMSO to 10\xa0mM |
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1. Obukowicz MG et al.. (1998) Novel, selective delta6 or delta5 fatty acid desaturase inhibitors as antiinflammatory agents in mice.. J Pharmacol Exp Ther, 287 (157-66). [PMID:9765335] |
2. Hansen-Petrik MB et al.. (2002) Selective inhibition of Delta-6 desaturase impedes intestinal tumorigenesis.. Cancer Lett, 175 (2): (157-63). [PMID:11741743] |