158 Results for "

VEGFR-2/P-gp-IN-1

" in MedChemExpress (MCE) Product Catalog:
Products (158)

158 Results for "VEGFR-2/P-gp-IN-1" in MCE Product Catalog:

3
3 Cited Publications
Cat. No.: HY-132305
CAS No.: 2756668-73-0
Purity:  98.55%
Target:  

VEGFR

Research Areas:  

Cancer

VEGFR-3-IN-1 is a potent and selective VEGFR3 inhibitor with an IC50 of 110.4 nM. VEGFR-3-IN-1 significantly inhibits proliferation and migration of VEGF-C-induced human dermal lymphatic endothelial cells (HDLEC), MDA-MB-231, and MDA-MB-436 cells by inactivating the VEGFR3 signaling pathway, and also effectively inhibits breast cancer growth .
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2
2 Cited Publications
Cat. No.: HY-P81643
Synonyms: KDR; FLK1; VEGFR2; Vascular endothelial growth factor receptor 2; VEGFR-2; Fetal liver kinase 1; FLK-1; Kinase insert domain receptor; KDR; Protein-tyrosine kinase receptor flk-1; CD antigen CD309

Host:  

Rabbit

Application:  

WB, IHC-P, IHC-F, ICC/IF, ELISA

Reactivity:  

Human, Mouse

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1
1 Cited Publications
Cat. No.: HY-P70636
Purity:  ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: FLT1; Tyrosine-Protein Kinase FRT; Prev. FLT; FLT-1; Vascular Endothelial Growth Factor Receptor 1; Vascular Endothelial Growth Factor Receptor 1 Variant; VEGFR1; Platelet-Derived Growth Factor Receptor-Like Protein; Vascular Permeability Factor Receptor
Species:  
Human
Source:  
HEK293
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1
1 Cited Publications
Cat. No.: HY-P70552
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: KDR; Fetal Liver Kinase 1; Kinase Insert Domain Receptor; Vascular Endothelial Growth Factor Receptor 2 Variant; Vascular Endothelial Growth Factor Receptor 2; Tyrosine Kinase Growth Factor Receptor; VEGFR2; Receptor Protein-Tyrosine Kinase; FLK1; Fetal L
Species:  
Human
Source:  
HEK293
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1
1 Cited Publications
Cat. No.: HY-P9920A
CAS No.: 947687-13-0

Target:  

VEGFR

Research Areas:  

Cancer

Ramucirumab (anti-VEGFR) is a human VEGFR-2 antagonist for the treatment of solid tumors. Ramucirumab (anti-VEGFR) is a recombinant human immunoglobulin G1 monoclonal antibody that binds to the extracellular binding domain of VEGFR-2 and prevents the binding of VEGFR ligands: VEGF-A, VEGF-C, and VEGF-D. Ramucirumab (anti-VEGFR) is also an angiogenesis inhibitor .
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Cat. No.: HY-143293
CAS No.: 2874264-13-6
Target:  

VEGFR Apoptosis

Research Areas:  

Cancer

VEGFR-IN-3 (compound 3f) is a VEGFR inhibitor. VEGFR-IN-3 inhibits OVCAR-4 and MDA-MB-468 cancer cells growth with IC50s of 0.29 and 0.35 μM, respectively. VEGFR-IN-3 can be used for the research of cancer .
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Cat. No.: HY-149024
CAS No.: 2411174-53-1
Target:  

VEGFR Apoptosis MDM-2/p53

Research Areas:  

Cancer

VEGFR-2-IN-23 (compound 11b) is a potent and selective VEGFR-2 inhibitor with an IC50 value of 0.34 nM. VEGFR-2-IN-23 shows antitumor activity. VEGFR-2-IN-23 induces apoptosis and cell cycle arrest at G1 phase .
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Cat. No.: HY-147133
CAS No.: 737818-56-3
Purity:  99.64%
Target:  

VEGFR

Research Areas:  

Cancer

VEGFR2-IN-2 (compound 6e) is a potent and selective VEGFR2 inhibitor with an IC50 of 19.32 nM. VEGFR2-IN-2 can be used for researching
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Cat. No.: HY-18625A
CAS No.: 2700435-52-3
Target:  

VEGFR

Research Areas:  

Cancer

VEGFR-2-IN-5 hydrochloride is a VEGFR2 inhibitor extracted from patent WO2013055780A1, Page 69 .
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Cat. No.: HY-146236
CAS No.: 2439096-14-5
Target:  

VEGFR

Research Areas:  

Cancer

VEGFR-2-IN-27 (compound 7a) is a highly potent VEGFR-2 inhibitor with an IC50 value of 14.8 nM. VEGFR-2-IN-27 can be used for researching anticancer .
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Cat. No.: HY-175019
Research Areas:  

Cancer

VEGFR-2-IN-70 is a potent VEGFR-2 inhibitor with an IC50 of 18.04 nM. VEGFR-2-IN-70 exhibits cytotoxicity against A549 and MCF-7 cancer cells with IC50 values of 0.43 μM and 3.8 μM, respectively. VEGFR-2-IN-70 induces G1 cell cycle arrest and apoptosis in lung cancer cells. VEGFR-2-IN-70 is useful in cancer research .
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Cat. No.: HY-178453
Target:  

VEGFR Apoptosis

Research Areas:  

Cancer

VEGFR-2-IN-74 (compound 55) is a potent VEGFR-2 inhibitor (IC50 = 0.035 µM). VEGFR-2-IN-74 exhibits good anti proliferative activity and can induce apoptosis in various cancer cells, such as A549 (IC50 = 2.67 µM) and HCT116 (IC50 = 10.87 µM) cells. VEGFR-2-IN-74 has low toxicity to normal cells. VEGFR-2-IN-74 shows significant anti angiogenic effects in chicken embryo models. VEGFR-2-IN-74 can be used in the research of cancer .
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Cat. No.: HY-112337
CAS No.: 288144-20-7
Target:  

VEGFR PDGFR

Research Areas:  

Cancer

VEGFR-2-IN-44 (compound 4b) is a selective VEGF-R2 (Flk-1) inhibitor with an IC50 value of 70 nM. VEGFR-2-IN-44 also inhibits PDGF-Rβ with an IC50 of 920 nM .
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Cat. No.: HY-18625
CAS No.: 1430089-64-7
Target:  

VEGFR

Research Areas:  

Cancer

VEGFR-2-IN-5 is a VEGFR2 inhibitor extracted from patent WO2013055780A1, Page 69 .
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Cat. No.: HY-131658
CAS No.: 444731-47-9
Purity:  99.89%
Target:  

VEGFR

Research Areas:  

Others

VEGFR-2-IN-6 (example 64) is a VEGFR2 inhibitor (angiogenesis modulator), which is extracted from patent WO 02/059110 .
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Cat. No.: HY-147779
CAS No.: 2404581-25-3
Target:  

VEGFR

Research Areas:  

Cancer

VEGFR-2-IN-20 (Compound 7) is a potent inhibitor of VEGFR. VEGFR-2-IN-20 has the potential for the research of cancer diseases .
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Cat. No.: HY-169626
CAS No.: 683235-34-9
Target:  

VEGFR

Research Areas:  

Cardiovascular Disease Cancer

VEGFR-IN-6 (Compound 3) is a vascular endothelial growth factor receptor (VEGFR) inhibitor. VEGFR-IN-6 can inhibit angiogenesis. VEGFR-IN-6 is promising for research of tumor diseases that rely on angiogenesis .
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Cat. No.: HY-169627
CAS No.: 683235-33-8
Target:  

VEGFR

Research Areas:  

Cardiovascular Disease

VEGFR-IN-7 (Compound 2) is a VEGFR inhibitor, showing inhibition of angiogenesis to a lesser extent. VEGFR-IN-7 is promising for research of cardiovascular diseases .
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Cat. No.: HY-162326
Target:  

VEGFR Apoptosis

Research Areas:  

Cancer

VEGFR-2 IN-41 (Compound 8) is a VEGFR-2 inhibitor with an IC50 of 0.0554 μM. VEGFR-2 IN-41 can induce apoptosis. VEGFR-2-IN-41 has antitumor activity .
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Cat. No.: HY-159565
Target:  

Bacterial VEGFR

Research Areas:  

Infection

VEGFR-2/InhA-IN-1 is a pyrazole-based dual inhibitor of InhA-VEGFR with anti-tuberculosis and anti-angiogenic activities. VEGFR-2/InhA-IN-1 has good antibacterial activity against Mycobacterium tuberculosis H37Rv strain (MIC=6.25 μg/mL) and significantly inhibits VEGFR-2 (IC50=15.27 nM) .
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