
PF-05231023
CAS No. 1037589-69-7
PF-05231023( —— )
Catalog No. M22505 CAS No. 1037589-69-7
PF-05231023 is a long-acting fibroblast growth factor 21 (FGF21) analog and is an FGF21-receptor agonist. It is also suitable for development as a potential treatment for T2DM. PF-05231023 is a analog of long-acting fibroblast growth factor 21.
Purity : >98% (HPLC)






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Biological Information
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Product NamePF-05231023
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NoteResearch use only, not for human use.
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Brief DescriptionPF-05231023 is a long-acting fibroblast growth factor 21 (FGF21) analog and is an FGF21-receptor agonist. It is also suitable for development as a potential treatment for T2DM. PF-05231023 is a analog of long-acting fibroblast growth factor 21.
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DescriptionPF-05231023 is a long-acting fibroblast growth factor 21 (FGF21) analog and is an FGF21-receptor agonist. It is also suitable for development as a potential treatment for T2DM. PF-05231023 is a analog of long-acting fibroblast growth factor 21.PF-05231023 suppresses oxidative-stress-induced inflammation in photoreceptors. PF-05231023 decreases the variability of retinal NRF2 levels and displays a trend (non-significant) towards increased NRF2 levels in Akita mice. PF-05231023 decreases retinal IL-1β mRNA expression in Akita mice. PF-05231023 enhances cone-specific arrestin4 expression in Akita mice. PF-05231023 restores photoreceptor morphology in Akita mice. Administration of native FGF21 and PF-05231023 (3?mg/kg or 10?mg/kg; subcutaneously twice a week for two weeks) improves glucose tolerance and liver insulin sensitivity in Zucker rats. PF-05231023 (10 mg/kg; intraperitoneally injected) reduces retinal inflammation in diabetic mice.(In Vivo):Animal Model: Eight week old Zucker ratsDosage: 3?mg/kg and 10?mg/kg.Administration: Subcutaneously twice a week for two weeks.Result: There was no change of BW observed, and food intake was not changed in the treated groups compared to control. Caused a significant decrease of glucose excursion during the oral glucose tolerance test (OGTT) compared to control.
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In Vitro——
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In VivoAnimal Model:Eight week old Zucker rats Dosage:3?mg/kg and 10?mg/kg Administration:Subcutaneously twice a week for two weeksResult:There was no change of BW observed, and food intake was not changed in the treated groups compared to control. Caused a significant decrease of glucose excursion during the oral glucose tolerance test (OGTT) compared to control. Animal Model:7-to-8-month-old Akita mice with type 1 diabete model Dosage:10 mg/kg Administration:Intraperitoneally injected; twice a week; for four weeks Result:Administration improved retinal function in diabetic Akita mice.
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Synonyms——
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PathwayOthers
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TargetOther Targets
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RecptorFGF21-receptor
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Research Area——
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Indication——
Chemical Information
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CAS Number1037589-69-7
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Formula Weight528.55
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Molecular FormulaC26H32N4O8
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Purity>98% (HPLC)
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SolubilityDMSO:125 mg/mL (236.50 mM; Need ultrasonic)
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SMILESO=C(CCN1C(=O)C=CC1=O)NCCOCCOCCC(=O)Nc1ccc(CCC(=O)N2CCC2=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. Dong JQ, et al. Pharmacokinetics and pharmacodynamics of PF-05231023, a novel long-acting FGF21 mimetic, in a first-in-human study. Br J Clin Pharmacol. 2015 Nov;80(5):1051-63.
molnova catalog



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