14 Results for "

fgf21+inhibitor

" in MedChemExpress (MCE) Product Catalog:
Products (14)

14 Results for "fgf21+inhibitor" in MCE Product Catalog:

1
1 Cited Publications
Cat. No.: HY-156019
CAS No.: 2426769-76-6
Purity:  98.92%
Target:  

FGFR

Research Areas:  

Cancer

FGFR1 inhibitor-10 (Compound 4i) is an FGFR1 inhibitor (IC50: 28 nM). FGFR1 inhibitor-10 inhibits the phosphorylation of FGFR1. FGFR1 inhibitor-10 has anti-angiogenic, anti-invasion activity, and anti-tumor effect .
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Cat. No.: HY-15813
CAS No.: 1256152-35-8
Purity:  99.11%
Synonyms: fgfR irreversible inhibitor-1
Target:  

FGFR

Research Areas:  

Cancer

FIIN-1 is a potent, irreversible, selective FGFR inhibitor. FIIN-1 binds to FGFR1/2/3/4 and Flt1/4 with Kds of 2.8/6.9/5.4/120 nM and 32/120 nM respectively. The biochemical IC50s of FIIN-1 are 9.2, 6.2, 11.9, and 189 nM against FGFR1/2/3/4, respectively .
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Cat. No.: HY-139376
CAS No.: 2410612-08-5
Target:  

FGFR

Research Areas:  

Cancer

FGFR1 inhibitor-2 is a FGFR1 inhibitor (IC50 is 4.55 μM in MDA-MB-231 cells). FGFR1 inhibitor-2 can be used for the research of metastatic triple-negative breast cancer .
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Cat. No.: HY-143272
Target:  

FGFR

Research Areas:  

Cancer

FGFR1 inhibitor-6 is a potent FGFR1 inhibitor with an IC50 value of 16.31 nM. FGFR1 inhibitor-6 shows cytotoxic activities. FGFR1 inhibitor-6 induces apoptosis and cell cycle arrest at pre-G1 and G2/M phase .
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Cat. No.: HY-149487
Target:  

FGFR

Research Areas:  

Cancer

FGFR1 inhibitor-8 (Compound 9) is a FGFR1 inhibitor (IC50s: 0.5 nM). FGFR1 inhibitor-8 binds to the ATP-binding pocket of FGFR1. FGFR1 inhibitor-8 has anticancer activity .
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Cat. No.: HY-149488
Target:  

FGFR

Research Areas:  

Cancer

FGFR1 inhibitor-9 (Compound 7) is an FGFR1 inhibitor (IC50s: 0.85 nM). FGFR1 inhibitor-9 binds to the ATP-binding pocket of FGFR1. FGFR1 inhibitor-9 has anticancer activity .
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Cat. No.: HY-158098
CAS No.: 2157482-40-9
Target:  

FGFR

Research Areas:  

Metabolic Disease

FGFR1 inhibitor-11 (compound 5g) binds to FGFR1, inactivation of its downstream ERK1/2 and IκBα/NF-κB signaling inhibited RANKL-induced osteoclastogenesis. FGFR1 inhibitor-11 has oral bioactivity .
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Cat. No.: HY-169710
CAS No.: 606958-57-0
Target:  

FGFR

Research Areas:  

Cancer

FGFR1 inhibitor-16 (Compound 89) is an FGFR1 inhibitor. FGFR1 inhibitor-16 exhibits an inhibitory rate of 53.00% against FGFR1 at a concentration of 50 μM and 24.95% at 10 μM. FGFR1 inhibitor-16 can be used in the study of cancer .
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Cat. No.: HY-172618
Target:  

FGFR

Research Areas:  

Cancer

FGFR1 inhibitor-18 (compound 16) is a potent FGFR1 inhibitor with an IC50 value of 1.31 nM. FGFR1 inhibitor-18 can occupy within the ATP-binding pocket of the target FGFR1 .
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Cat. No.: HY-W261325
CAS No.: 459137-97-4
Target:  

FGFR

Research Areas:  

Cancer

FGFR1 inhibitor-15 (Compound 23) is an FGFR1 inhibitor with an IC50 of 27 μM. FGFR1 inhibitor-15 can be used in the study of cancer .
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Cat. No.: HY-W801893
CAS No.: 670266-26-9
Target:  

FGFR

Research Areas:  

Cancer

FGFR1 inhibitor-13 (compound 1) is an FGFR1 inhibitor with an IC50 of 4.2 μM .
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Cat. No.: HY-149486
Target:  

FGFR

Research Areas:  

Cancer

FGFR1 inhibitor 7 (compound 5) is an inhibitor of FGFR1 Tyrosine Kinase with IC50 value of 0.33 nM. FGFR1 inhibitor 7 shows broad-spectrum cytotoxicity agasinst human cancer cell lines, and inhibits MOLT3 cells with IC50 of 2.1 μM .
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Cat. No.: HY-169623
CAS No.: 442534-83-0
Target:  

FGFR

Research Areas:  

Cancer

FGFR1 inhibitor-14 (compound 28) is a FGFR1 inhibitor, which can be used in anti-cancer research .
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Cat. No.: HY-169669
CAS No.: 308298-51-3
Target:  

FGFR

Research Areas:  

Cancer

FGFR1 inhibitor-17 (Compound 92) is a potent FGFR1 inhibitor. FGFR1 inhibitor-17 is promising for research of cancers .
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