FGIN-1-27
CAS No. 142720-24-9
FGIN-1-27( —— )
Catalog No. M27629 CAS No. 142720-24-9
FGIN-1-27 is a high-affinity agonist of the translocator protein and a specific peripheral benzodiazepine receptor (PBR) ligand(Ki = 5.0 nM).
Purity : >98% (HPLC)
Size | Price / USD | Stock | Quantity |
5MG | 35 | In Stock |
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10MG | 58 | In Stock |
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25MG | 115 | In Stock |
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50MG | 177 | In Stock |
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100MG | 295 | In Stock |
|
200MG | Get Quote | In Stock |
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500MG | Get Quote | In Stock |
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1G | Get Quote | In Stock |
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Biological Information
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Product NameFGIN-1-27
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NoteResearch use only, not for human use.
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Brief DescriptionFGIN-1-27 is a high-affinity agonist of the translocator protein and a specific peripheral benzodiazepine receptor (PBR) ligand(Ki = 5.0 nM).
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DescriptionFGIN-1-27 is a high-affinity agonist of the translocator protein and a specific peripheral benzodiazepine receptor (PBR) ligand(Ki = 5.0 nM). FGIN 1-27 can cross the blood-brain barrier.
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In Vitro——
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In Vivo——
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Synonyms——
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PathwayOthers
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TargetOther Targets
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RecptorBcl-2|Caspase|COX|gp120/CD4|GSK-3|IL Receptor|Nrf2|p53|PPAR|TNF-α|Wnt/β-catenin
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Research Area——
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Indication——
Chemical Information
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CAS Number142720-24-9
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Formula Weight436.615
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Molecular FormulaC28H37FN2O
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Purity>98% (HPLC)
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SolubilityIn Vitro:?DMSO : 100 mg/mL (229.04 mM)
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SMILESCCCCCCN(CCCCCC)C(=O)Cc1c([nH]c2ccccc12)-c1ccc(F)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
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ACTH (18-39), human
Adrenocorticotropic Hormone (ACTH) (18-39) is known as the Corticotropin-like Intermediate Lobe Peptide. It stimulates insulin secretion as well as amylase and protein secretion in a dose-dependent manner similar to those of secretin and carbamylcholine.
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Cephapirin Benzathin...
Cephapirin Benzathine is a semisynthetic broad-spectrum first-generation cephalosporin with antibacterial activity.
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2-Methylsuccinic aci...
Methylsuccinic acid is a normal metabolite found in human fluids. Increased urinary levels of Methylsuccinic acid (together with ethylmalonic acid) are the main biochemical measurable features in ethylmalonic encephalopathy a rare metabolic disorder with an autosomal recessive mode of inheritance that is clinically characterized by neuromotor delay hyperlactic acidemia recurrent petechiae orthostatic acrocyanosis and chronic diarrhea.