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FGFR1/VEGFR2-IN-1

Cat. No. M43552
FGFR1/VEGFR2-IN-1 Structure
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Biological Activity

FGFR1/VEGFR2-IN-1 is an FGFR1/VEGFR2 inhibitor.

Chemical Information
Molecular Weight 522.49
Formula C26H27N4O6P
Storage Powder          -20°C   3 years ;  4°C   2 years
In solvent       -80°C   6 months ;  -20°C   1 month
Conversion of different model animals based on BSA (PMID: 27057123)
Species Mouse Rat Rabbit Guinea pig Hamster Dog
Weight (kg) 0.02 0.15 1.8 0.4 0.08 10
Body Surface Area (m2) 0.007 0.025 0.15 0.05 0.02 0.5
Km factor 3 6 12 8 5 20
Animal A (mg/kg) = Animal B (mg/kg) multiplied by  Animal B Km
Animal A Km

For example, to modify the dose of Compound A used for a mouse (20 mg/kg) to a dose based on the BSA for a rat, multiply 20 mg/kg by the Km factor for a mouse and then divide by the Km factor for a rat. This calculation results in a rat equivalent dose for Compound A of 10 mg/kg.

References

[1] Fanxiang Yin et al. Acta Pharm Sin B. Novel dual inhibitor for targeting PIM1 and FGFR1 kinases inhibits colorectal cancer growth in vitro and patient-derived xenografts in vivo

[2] Xiaolong Zhu et al. Proc Natl Acad Sci U S A. FGFR1 SUMOylation coordinates endothelial angiogenic signaling in angiogenesis

[3] Alberto Servetto et al. Clin Cancer Res. Nuclear FGFR1 Regulates Gene Transcription and Promotes Antiestrogen Resistance in ER+ Breast Cancer

[4] Huiting Xiao et al. PeerJ. Evaluation of FGFR1 as a diagnostic biomarker for ovarian cancer using TCGA and GEO datasets

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  Catalog
Abmole Inhibitor Catalog




Keywords: FGFR1/VEGFR2-IN-1 supplier, VEGFR/PDGFR, inhibitors, activators


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