517 Results for "

FGFR

" in MedChemExpress (MCE) Product Catalog:
Products (517)

517 Results for "FGFR" in MCE Product Catalog:

  • Targets Recommended:
  • Recombinant Proteins Recommended:
101
101 Publications Verification
Cat. No.: HY-10981
CAS No.: 417716-92-8
Purity:  99.75%
Synonyms: E7080
Target:  

VEGFR FGFR PDGFR c-Kit RET

Research Areas:  

Cancer

Lenvatinib (E7080) is an oral, multi-targeted tyrosine kinase inhibitor that inhibits VEGFR1-3, FGFR1-4, PDGFR, KIT, and RET, shows potent antitumor activities .
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101
101 Publications Verification
Cat. No.: HY-10981A
CAS No.: 857890-39-2
Purity:  99.86%
Synonyms: E7080 mesylate
Target:  

VEGFR FGFR PDGFR RET c-Kit

Research Areas:  

Cancer

Lenvatinib mesylate (E7080 mesylate), an oral, multi-targeted tyrosine kinase inhibitor that inhibits VEGFR1-3, FGFR1-4, PDGFR, KIT, and RET, shows potent antitumor activities .
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74
74 Cited Publications
Cat. No.: HY-50904
CAS No.: 656247-17-5
Synonyms: BIBF 1120
Target:  

PDGFR VEGFR FGFR

Research Areas:  

Cancer

Nintedanib (BIBF 1120) is a potent triple angiokinase inhibitor for VEGFR1/2/3, FGFR1/2/3 and PDGFRα/β with IC50s of 34 nM/13 nM/13 nM, 69 nM/37 nM/108 nM and 59 nM/65 nM, respectively.
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74
74 Cited Publications
Cat. No.: HY-11106
CAS No.: 656247-18-6
Purity:  99.96%
Synonyms: BIBF 1120 esylate
Target:  

PDGFR VEGFR FGFR

Research Areas:  

Cancer

Nintedanib esylate (BIBF 1120 esylate) is a potent triple angiokinase inhibitor for VEGFR1/2/3, FGFR1/2/3 and PDGFRα/β with IC50s of 34 nM/13 nM/13 nM, 69 nM/37 nM/108 nM and 59 nM/65 nM, respectively.
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56
56 Cited Publications
Cat. No.: HY-12047
CAS No.: 943319-70-8
Purity:  99.67%
Synonyms: AP24534
Ponatinib (AP24534) is an orally active multi-targeted kinase inhibitor with IC50s of 0.37 nM, 1.1 nM, 1.5 nM, 2.2 nM, and 5.4 nM for Abl, PDGFRα, VEGFR2, FGFR1, and Src, respectively .
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56
56 Cited Publications
Cat. No.: HY-108766
CAS No.: 1114544-31-8
Purity:  99.76%
Synonyms: AP24534 hydrochloride
Research Areas:  

Infection Cancer

Ponatinib hydrochloride (AP24534 hydrochloride) is a hydrochloride of ponatinib. Ponatinib is an orally active multi-targeted kinase inhibitor with IC50s of 0.37 nM, 1.1 nM, 1.5 nM, 2.2 nM, and 5.4 nM for Abl, PDGFRα, VEGFR2, FGFR1, and Src, respectively .
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48
48 Cited Publications
Cat. No.: HY-13311A
CAS No.: 1310746-10-1
Purity:  99.59%
Synonyms: BGJ-398 phosphate; NVP-BGJ398 phosphate
Target:  

FGFR

Research Areas:  

Cancer

Infigratinib phosphate (BGJ-398 phosphate; NVP-BGJ398 phosphate) is a potent inhibitor of the FGFR family with IC50 of 0.9 nM, 1.4 nM, 1 nM, and 60 nM for FGFR1, FGFR2, FGFR3, and FGFR4, respectively.
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48
48 Cited Publications
Cat. No.: HY-13311
CAS No.: 872511-34-7
Purity:  99.82%
Synonyms: BGJ-398; NVP-BGJ398
Target:  

FGFR Apoptosis

Research Areas:  

Cancer

Infigratinib (BGJ-398; NVP-BGJ398) is a potent inhibitor of the FGFR family with IC50s of 0.9 nM, 1.4 nM, 1 nM, and 60 nM for FGFR1, FGFR2, FGFR3, and FGFR4, respectively.
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39
39 Cited Publications
Cat. No.: HY-18708
CAS No.: 1346242-81-6
Synonyms: JNJ-42756493
Target:  

FGFR Apoptosis

Research Areas:  

Cancer

Erdafitinib (JNJ-42756493) is a potent and orally available FGFR family inhibitor; inhibits FGFR1/2/3/4 with IC50s of 1.2, 2.5, 3.0 and 5.7 nM, respectively.
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36
36 Cited Publications
Cat. No.: HY-13330
CAS No.: 1035270-39-3
Purity:  99.85%
Synonyms: AZD4547; ADSK091
Target:  

FGFR

Research Areas:  

Cancer

Fexagratinib (AZD4547; ADSK091) is a potent inhibitor of the FGFR family with IC50s of 0.2 nM, 2.5 nM, 1.8 nM, and 165 nM for FGFR1, FGFR2, FGFR3, and FGFR4, respectively.
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25
25 Cited Publications
Cat. No.: HY-12009
CAS No.: 635702-64-6
Purity:  99.99%
Synonyms: GW786034 Hydrochloride
Research Areas:  

Cancer

Pazopanib Hydrochloride (GW786034 Hydrochloride) is a novel multi-target inhibitor of VEGFR1, VEGFR2, VEGFR3, PDGFRβ, c-Kit, FGFR1, and c-Fms with an IC50 of 10, 30, 47, 84, 74, 140 and 146 nM, respectively.
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25
25 Cited Publications
Cat. No.: HY-10208
CAS No.: 444731-52-6
Purity:  99.91%
Synonyms: GW786034
Research Areas:  

Cancer

Pazopanib (GW786034) is a novel multi-target inhibitor of VEGFR1, VEGFR2, VEGFR3, PDGFRβ, c-Kit, FGFR1, and c-Fms with IC50s of 10, 30, 47, 84, 74, 140 and 146 nM, respectively.
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24
24 Cited Publications
Cat. No.: HY-N0183
CAS No.: 485-72-3
Synonyms: Biochanin B; Flavosil; Formononetol
Formononetin is a potent FGFR2 inhibitor with an IC50 of ~4.31 μM. Formononetin potently inhibits angiogenesis and tumor growth .
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22
22 Cited Publications
Cat. No.: HY-109099
CAS No.: 1513857-77-6
Purity:  99.84%
Synonyms: INCB054828
Target:  

FGFR

Research Areas:  

Cancer

Pemigatinib (INCB054828) is an orally active, selective FGFR inhibitor with IC50s of 0.4 nM, 0.5 nM, 1.2 nM, 30 nM for FGFR1, FGFR2, FGFR3, FGFR4, respectively. Pemigatinib has the potential for cholangiocarcinoma .
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22
22 Cited Publications
Cat. No.: HY-10321
CAS No.: 219580-11-7
Purity:  99.86%
Target:  

FGFR VEGFR Apoptosis

Research Areas:  

Cancer

PD173074 is a potent FGFR1 inhibitor with an IC50 of 25 nM and also inhibits VEGFR2 with an IC50 of 100-200 nM, showing 1000-fold selectivity for FGFR1 over PDGFR and c-Src.
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19
19 Cited Publications
Cat. No.: HY-N0060
CAS No.: 1135-24-6
Synonyms: Coniferic acid
Ferulic acid is a novel fibroblast growth factor receptor 1 (FGFR1) inhibitor with IC50s of 3.78 and 12.5 μM for FGFR1 and FGFR2, respectively.
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19
19 Cited Publications
Cat. No.: HY-N0060A
CAS No.: 24276-84-4
Synonyms: Coniferic acid sodium
Ferulic acid sodium is a novel fibroblast growth factor receptor 1 (FGFR1) inhibitor with IC50s of 3.78 and 12.5 μM for FGFR1 and FGFR2, respectively.
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13
13 Cited Publications
Cat. No.: HY-10407
CAS No.: 215543-92-3
Purity:  99.86%
Target:  

VEGFR FGFR PDGFR

Research Areas:  

Cancer

SU 5402 is a potent multi-targeted receptor tyrosine kinase inhibitor with IC50 of 20 nM, 30 nM, and 510 nM for VEGFR2, FGFR1, and PDGFRβ, respectively.
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11
11 Cited Publications
Cat. No.: HY-50905
CAS No.: 405169-16-6
Synonyms: CHIR-258; TKI258
Target:  

FLT3 c-Kit FGFR VEGFR PDGFR c-Fms

Research Areas:  

Cancer

Dovitinib (CHIR-258) is an orally active, potent multi-targeted tyrosine kinase (RTK) inhibitor with IC50s of 1, 2, 36, 8/9, 10/13/8, 27/210 nM for FLT3, c-Kit, CSF-1R, FGFR1/FGFR3, VEGFR1/VEGFR2/VEGFR3 and PDGFRα/PDGFRβ, respectively. Dovitinib has potent antitumor activity .
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11
11 Cited Publications
Cat. No.: HY-101296
CAS No.: 192705-79-6
Purity:  99.75%
Target:  

FGFR Autophagy

Research Areas:  

Cancer

PD166866 is a selective FGFR1 tyrosine kinase inhibitor with an IC50 of 52.4 nM.
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