9 Results for "

mouse FGFR3

" in MedChemExpress (MCE) Product Catalog:
Products (9)

9 Results for "mouse FGFR3" in MCE Product Catalog:

  • Targets Recommended:
Cat. No.: HY-P991106
Synonyms: LY-3076226 antibody

Target:  

FGFR ADC Antibodies

Research Areas:  

Cancer

IMC-D11 (LY-3076226 antibody) is an anti-FGFR3 IgG1 monoclonal antibody with an EC50 of approximately 0.1 nM against hFGFR3b and hFGFR3c. IMC-D11 inhibits the growth of FGFR3-dependent lung adenocarcinoma in mouse models and shows no effect on tumors that do not express FGFR3. IMC-D11 can serve as an ADC Antibody for ADC synthesis, such as LY3076226. IMC-D11 is applicable to research related to urothelial carcinoma, multiple myeloma, lung adenocarcinoma, as well as advanced or metastatic cancers .
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Cat. No.: HY-RS04919
Research Areas:  

Others

Fgfr3 Mouse Pre-designed siRNA Set A contains three designed siRNAs for Fgfr3 gene (Mouse), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-176547
CAS No.: 3069945-78-1
Target:  

FGFR Cytochrome P450

Research Areas:  

Endocrinology

FGFR2/3-IN-3 is a dual-target FGFR2/3 inhibitor with IC50s of 2.7 nM (TEL-FGFR2) and 3.9 nM (TEL-FGFR3), respectively. FGFR2/3-IN-3 has effective activity against both wild-type and mutant FGFR3. FGFR2/3-IN-3 has low CYP3A4 inhibitory effect and hERG toxicity. FGFR2/3-IN-3 improves the imbalance between chondrocyte proliferation and differentiation and promotes bone growth by inhibiting the signaling pathway mediated by mutant FGFR3. FGFR2/3-IN-3 shows a growth-promoting effect in a dwarfism mouse model and has the potential to study bone development disorder-related diseases such as achondroplasia (ACH) .
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Cat. No.: HY-178059
Target:  

FGFR p38 MAPK Akt ERK Apoptosis

Research Areas:  

Cancer

FGFR-IN-23 (Compound 9p) is a covalent pan FGFR inhibitor with IC50s of 14, 4.2, 5 and 220 nM for FGFR1, FGFR2, FGFR3 and FGFR4, respectively. FGFR-IN-23 also has potent inhibitory activity against gatekeeper mutants, such as FGFR1 V561M and FGFR3 V555M. FGFR-IN-23 suppresses the activation of FGFR-mediated signaling and induces apoptosis. FGFR-IN-23 shows significant antitumor efficacy in RT112 xenograft mouse models. FGFR-IN-23 can be used for cancers and its drug resistance research .
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Cat. No.: HY-181152
Target:  

FGFR

Research Areas:  

Cancer

FGFR3-IN-11(compound B11) is a Fibroblast growth factor receptor 3 (FGFR3) inhibitor with a Ka value of 4.8 μM. FGFR3-IN-11 induces apoptosis, suppresses colony formation, and causes dose-dependent G0/G1 cell cycle arrest in cancer cells. FGFR3-IN-11 exerts anticancer activity against cancer cells with minimal toxicity toward normal hepatocytes and demonstrates tumor growth suppression in xenograft mouse models. FGFR3-IN-11 can be used for the research of hepatocellular carcinoma .
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Cat. No.: HY-P77662
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: ACH; CD333; CEK; CEK2; EC 2.7.10; FGF R3; FGFR3; HSFGFR3EX; JTK4
Species:  
Source:  
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Cat. No.: HY-P703984
Purity:  ≥ 95%, as determined by Bis-Tris PAGE.
Synonyms: ACH; CD333; CEK; CEK2; EC 2.7.10; FGF R3; FGFR3; HSFGFR3EX; JTK4
Species:  
Source:  
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Cat. No.: HY-P73056
Purity:  ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: Fibroblast growth factor receptor 3; FGFR-3; CD333; JTK4
Species:  
Source:  
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Cat. No.: HY-P74153
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: Fibroblast growth factor receptor 3; FGFR-3; CD333; Mfr3; Sam3
Species:  
Source:  
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