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SP-13786(UAMC1110,FAP-IN-1)
本产品不向个人销售,仅用作科学研究,不用于任何人体实验及非科研性质的动物实验。
SP-13786(UAMC1110,FAP-IN-1)图片
CAS NO:1448440-52-5
规格:≥98%
包装与价格:
包装价格(元)
5mg电议
10mg电议
25mg电议
50mg电议
100mg电议
250mg电议
500mg电议

产品介绍
理化性质和储存条件
Molecular Weight (MW) 344.32
Formula C17H14F2N4O2
CAS No. 1448440-52-5
Storage-20℃ for 3 years in powder form
-80℃ for 2 years in solvent
Solubility (In vitro)DMSO: 10 mM
Water: N/A
Ethanol: N/A
SMILES O=C(C1=CC=NC2=CC=CC=C12)NCC(N3[C@H](C#N)CC(F)(F)C3)=O
Synonyms SP-13786; SP13786; SP 13786; FAP-IN 1; FAP-IN-1; FAP IN 1; FAP IN-1; UAMC-1110; UAMC 1110; UAMC1110
实验参考方法
In Vitro

In vitro activity: SP-13786 (formerly known as FAP-IN-1) is a novel, potent and highly selective inhibitor of fibroblast activation protein (FAP) with IC50 of 3.2 nM; it also inhibits prolyl oligopeptidase (PREP) with an IC50 of 1.8 μM. Fibroblast activation protein (FAP) is a serine protease related to dipeptidyl peptidase IV (DPPIV). It has been convincingly linked to multiple disease states involving remodeling of the extracellular matrix. FAP inhibition is investigated as a therapeutic option for several of these diseases, with most attention so far devoted to oncology applications. The log D values, plasma stabilities, and microsomal stabilities of SP-13786 were found to be highly satisfactory. Pharmacokinetic evaluation in mice of SP-13786 demonstrated high oral bioavailability, plasma half-life, and the potential to selectively and completely inhibit FAP in vivo.


Kinase Assay: SP-13786 (formerly known as FAP-IN-1) is a novel, potent and highly selective inhibitor of fibroblast activation protein (FAP) with IC50 of 3.2 nM; it also inhibits prolyl oligopeptidase (PREP) with an IC50 of 1.8 μM.


Cell Assay: FAP-IN-1 is also found to have better FAP/PREP selectivity and a very proficient ligand efficiency of 0.34.

In Vivo FAP-IN-1 is the most extensive and prolonged inhibitior of FAP in the PK studies. No tight binding behavior is observed, and the inhibitor proves to bind reversibly to FAP. Pharmacokinetic evaluation in mice of FAP-IN-1 demonstrates high oral bioavailability, plasma half-life, and the potential to selectively and completely inhibit FAP in vivo
Animal model Rats: The PK parameters are determined for inhibitors 4, 5, 60 (FAP-IN-1), and 61 in rats. Six male rats are treated for each inhibitor tested, three of which received the compound via a single intravenous (iv) administration at 5 mg/kg. The other three animals are dosed per os (po) at 20 mg/kg. Blood samples are collected at 0.083, 0.25, 0.5, 1, 2, 4, 6, and 24 h after administration. Inhibitor concentrations are determined using UPLC–MS/MS, and pharmacokinetic parameters are calculated using standard algorithms
Formulation & Dosage 20 mg/kg; p.o.; 5 mg/kg. i.v.
References J Med Chem. 2014 Apr 10;57(7):3053-74