TCS PrP Inhibitor 13
CAS No. 34320-83-7
TCS PrP Inhibitor 13( 5-(4-Nitrophenyl)-2-Phenyl-4H-Pyrazol-3-One )
Catalog No. M27727 CAS No. 34320-83-7
TCS PrP Inhibitor 13 is an antiprion agent inhibiting protease-resistant prion protein (PrP-res) accumulation.
Purity : >98% (HPLC)
Size | Price / USD | Stock | Quantity |
2MG | 46 | Get Quote |
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5MG | 72 | Get Quote |
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10MG | 115 | Get Quote |
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25MG | 260 | Get Quote |
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50MG | 410 | Get Quote |
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100MG | 605 | Get Quote |
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500MG | 1287 | Get Quote |
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1G | Get Quote | Get Quote |
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Biological Information
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Product NameTCS PrP Inhibitor 13
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NoteResearch use only, not for human use.
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Brief DescriptionTCS PrP Inhibitor 13 is an antiprion agent inhibiting protease-resistant prion protein (PrP-res) accumulation.
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DescriptionTCS PrP Inhibitor 13 is an antiprion agent inhibiting protease-resistant prion protein (PrP-res) accumulation.(In Vitro):In Schwannoma cells, administration of 0-500 μM TCS PrP Inhibitor 13 reduces levels of total ERK1/2, pAKT, total FAK, Cyclin D1, PrPC and increases expression of cleaved caspase-3 significantly. TCS PrP Inhibitor 13 also significantly reduces the number of proliferating, Ki67-positive cells and total cell number in Schwannoma cells.
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In VitroTCS PrP Inhibitor 13 (0~500 μM; Schwannoma cells) significantly reduces levels of total ERK1/2, pAKT, total FAK, Cyclin D1, PrPC and significantly increases expression of cleaved caspase-3. TCS PrP Inhibitor 13 (Schwannoma cells) significantly reduces the number of proliferating, Ki67-positive cells and total cell number.
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In Vivo——
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Synonyms5-(4-Nitrophenyl)-2-Phenyl-4H-Pyrazol-3-One
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PathwayOthers
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TargetOther Targets
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Recptor——
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Research Area——
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Indication——
Chemical Information
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CAS Number34320-83-7
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Formula Weight281.271
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Molecular FormulaC15H11N3O3
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Purity>98% (HPLC)
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SolubilityIn Vitro:?DMSO : 100 mg/mL (355.53 mM)
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SMILES[O-][N+](=O)c1ccc(cc1)C1=NN(C(=O)C1)c1ccccc1
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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
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Calcitonin (8-32), s...
Calcitonin (8-32), salmon is a highly selective amylin receptor antagonist.Calcitonin is a hormone known to participate in calcium and phosphorus metabolism. In mammals, the major source of calcitonin is from the parafollicular or C cells in the thyroid gland. Calcitonin is a 32 amino acid peptide cleaved from a larger prohormone.
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2'-Deoxyguanosine mo...
Deoxyguanosine is a nucleoside consisting of the base guanine and the sugar deoxyribose. It is like guanosine but with one oxygen atom removed. It is a nucleoside component of DNA. Deoxyguanosine can be converted to 8-hydroxy-deoxyguanosine (8-OHdG) due to hydroxyl radical attack at the C8 of guanine.
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WRW4 TFA(878557-55-2...
Selective antagonist of formyl peptide receptor 2 (FPR2) signaling. Inhibits WKYMVm binding to FPR2 (IC50 = 0.23 μM) and inhibits intracellular calcium release induced by WKYMVm, MMK 1, amyloid β42, and F peptide. Also inhibits FPR2-mediated signaling in human neutrophils; blocks chemotactic migration and superoxide generation by amyloid β42 peptide.