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UK-5099(PF-1005023)
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。
UK-5099(PF-1005023)图片
CAS NO:56396-35-1
规格:≥98%
包装与价格:
包装价格(元)
5mg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) 288.30
Formula C18H12N2O2
CAS No. 56396-35-1
Storage-20℃ for 3 years in powder form
-80℃ for 2 years in solvent
Solubility (In vitro)DMSO: 57 mg/mL (197.7 mM)
Water: <1 mg/mL
Ethanol: <1 mg/mL
Chemical Name 2-cyano-3-(1-phenyl-1H-indol-3-yl)-2-propenoic acid
Synonyms UK-5099, UK 5099, UK5099, PF1005023, PF-1005023, PF 1005023
SMILES Code O=C(O)/C(C#N)=C/C1=CN(C2=CC=CC=C2)C3=C1C=CC=C3
实验参考方法
In Vitro

In vitro activity: UK-5099 is a potent and specific inhibitor of the mitochondrial pyruvate carrier (MPC), it acts by inhibiting pyruvate transport across the plasma membrane of trypanosomes with Ki value of 49 μM. UK-5099 inhibits pyruvate-dependent O2 consumption with an IC50 of 50 nM. Cells treated with UK5099 showed significantly higher proportion of side population (SP) fraction and expressed higher levels of stemness markers Oct3/4 and Nanog. Meanwhile, chemosensitivity examinations revealed that the UK5099 treated cells became more resistant to chemotherapy compared to the non-treated cells.


Cell Assay: Cell viability is measured using CellTiter Blue. The assay is based on cellular reduction of resazurin to resorufin. Appearance of resorufin is monitored by fluorescence emission at 585 nm using a Spectramax M5 microplate reader with excitation at 555 nm. For UK5099-treated cells, cells are allowed to recover for 1 h before measuring cell viability. Data are expressed as -fold relative to no treatment or siCtrl.

In VivoUK-5099 suppresses the growth of patient-derived xenograft (PDX) tumors in mice without severe loss of animal body weight.
Animal model Female C.B-17-Icr-scid-scidJcl mice implanted subcutaneously with patient-derived grafts
Formulation & Dosage Dissolved in 0.5% methylcellulose; 10 or 100 mg/kg/day; oral
References Oncotarget. 2015 Nov 10;6(35):37758-69; EBioMedicine. 2017 May;19:31-38. doi