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Angiogenesis

Angiogenesis

Angiogenesis inhibitors are compounds that interfere with the formation of new blood vessels, a process critical in cancer growth and metastasis. By inhibiting angiogenesis, these compounds can restrict the blood supply to tumors, slowing or halting their growth. Angiogenesis inhibitors are essential in cancer research and therapeutic development, providing insights into the mechanisms of tumor progression and offering potential treatments for cancer and other angiogenesis-related diseases. At CymitQuimica, we offer a wide range of high-quality angiogenesis inhibitors to support your research in oncology and vascular biology.

Subcategories of "Angiogenesis"

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Found 1522 products of "Angiogenesis"

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  • Peficitinib hydrobromide
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    Peficitinib hydrobromide

    CAS:
    <p>Peficitinib hydrobromide is used in the treatment of Psoriasis and Rheumatoid Arthritis.</p>
    Formula:C18H23BrN4O2
    Color and Shape:Solid
    Molecular weight:407.312

    Ref: TM-T33905

  • JS25
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    JS25

    CAS:
    <p>JS25, a selective BTK inhibitor, inactivates it with a 5.8 nM IC50, halts cancer cell growth, induces death, and aids against lymphoma.</p>
    Formula:C29H24N4O4S
    Color and Shape:Solid
    Molecular weight:524.59

    Ref: TM-T69646

  • Lck-IN-1
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    Lck-IN-1

    CAS:
    <p>Lck-IN-1 is a potent inhibitor of lymphocyte protein tyrosine kinase (Lck) [1].</p>
    Formula:C14H15N5
    Color and Shape:Solid
    Molecular weight:253.3

    Ref: TM-T8888

  • CAY10717
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    CAY10717

    CAS:
    <p>CAY10717 inhibits 34/104 kinases at 100 nM, targets EGFR/ABL/B-Raf mutations, kills various cancer cells, and blocks HUVEC growth.</p>
    Formula:C29H25F3N6O3
    Color and Shape:Solid
    Molecular weight:562.54

    Ref: TM-T36193

  • AGL 2043
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    AGL 2043

    CAS:
    <p>AGL 2043 is a potent, reversible, ATP-competitive inhibitor of type III receptor tyrosine kinases.</p>
    Formula:C15H12N4S
    Color and Shape:Solid
    Molecular weight:280.35

    Ref: TM-T26576

  • α7 nAchR-JAK2-STAT3 agonist 1
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    α7 nAchR-JAK2-STAT3 agonist 1

    CAS:
    <p>α7 nAchR-JAK2-STAT3 agonist 1 is a potent inhibitor of the α7 nAchR-JAK2-STAT3 pathway that acts on nitric oxide (NO) (IC50: 0.32 μM).</p>
    Formula:C25H30O6
    Color and Shape:Solid
    Molecular weight:426.5

    Ref: TM-T62317

  • Mutated EGFR-IN-2
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    Mutated EGFR-IN-2

    CAS:
    Mutated EGFR-IN-2 is an inhibitor of mutant-selective EGFR.
    Formula:C29H35FN8O3
    Purity:98%
    Color and Shape:Solid
    Molecular weight:562.64

    Ref: TM-T12130

  • HP1328
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    HP1328

    CAS:
    <p>HP1328: potent FLT3/ITD inhibitor, reduces leukemia, extends survival in mice, belongs to benzoimidazole family.</p>
    Formula:C23H23N3O3
    Color and Shape:Solid
    Molecular weight:389.45

    Ref: TM-T61758

  • BCR-ABL-IN-5
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    BCR-ABL-IN-5

    CAS:
    BCR-ABL-IN-5: Bcr-Abl kinase inhibitor, IC50: Bcr-AblWT 0.014 μM, Bcr-AblT315I 0.45 μM; anti-leukemia cell growth.
    Formula:C25H21Cl2N5O2
    Color and Shape:Solid
    Molecular weight:494.37

    Ref: TM-T63332

  • Luxeptinib
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    Luxeptinib

    CAS:
    <p>Luxeptinib (CG-806) is an oral, non-covalent pan-FLT3/BTK inhibitor for acute myeloid leukemia.</p>
    Formula:C25H17F4N5O2
    Color and Shape:Solid
    Molecular weight:495.43

    Ref: TM-T37085

  • Thi-DPPY
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    Thi-DPPY

    CAS:
    <p>Thi-DPPY: Potent JAK3/BTK inhibitor (IC50: 1.38/62.4 nM), anti-proliferative, anti-inflammatory, potential in IPF research.</p>
    Formula:C28H28ClN5O4S
    Color and Shape:Solid
    Molecular weight:566.07

    Ref: TM-T64008

  • GDC-4379
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    GDC-4379

    CAS:
    <p>GDC-4379 is a JAK1 inhibitor that can be used to study asthma.</p>
    Formula:C21H18ClF2N7O3
    Color and Shape:Solid
    Molecular weight:489.86

    Ref: TM-T63280

  • TG53
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    TG53

    CAS:
    <p>TG53 is a tissue transglutaminase (TG2) and fibronectin (FN) protein-protein interaction inhibitor.</p>
    Formula:C21H22ClN5O2
    Purity:98%
    Color and Shape:Solid
    Molecular weight:411.88

    Ref: TM-T26265

  • GW837016X
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    GW837016X

    CAS:
    <p>GW837016X, also known as NEU-391, is a potent inhibitor of protozoan parasite proliferation.</p>
    Formula:C25H20ClFN4OS
    Color and Shape:Solid
    Molecular weight:478.97

    Ref: TM-T68611

  • PHA-680626
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    PHA-680626

    CAS:
    <p>PHA-680626 is a PLK inhibitor, effective on resistant leukemia cells, with IC50: Plk1 (0.53 μM), Plk2 (0.07 μM), Plk3 (1.61 μM).</p>
    Formula:C23H26N6O2S
    Color and Shape:Solid
    Molecular weight:450.56

    Ref: TM-T69296

  • Nuvenzepine
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    Nuvenzepine

    CAS:
    Nuvenzepine is an antagonist of mAChR. It has the potential for gastrospasm treatment.
    Formula:C19H20N4O2
    Purity:98%
    Color and Shape:Solid
    Molecular weight:336.39

    Ref: TM-T16362

  • FGFR-IN-9
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    FGFR-IN-9

    <p>FGFR-IN-9: oral FGFR inhibitor, IC50: 17.1 nM (FGFR4 WT), 29.6 (FGFR3), 30.7 (V550L), 46.7 (FGFR2), 64.3 nM (FGFR1).</p>
    Formula:C25H28N6O3S
    Color and Shape:Solid
    Molecular weight:492.59

    Ref: TM-T73316

  • EGFR-IN-63
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    EGFR-IN-63

    CAS:
    <p>EGFR- IN-63 is an EGFR inhibitor with an IC50 value of 0.096 μM. EGFR- IN-63 exhibited anticancer effects on MCF-7 cells (IC50: 2.49 μM).</p>
    Formula:C20H12BrN5S
    Color and Shape:Solid
    Molecular weight:434.31

    Ref: TM-T62446

  • AP 24149
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    AP 24149

    CAS:
    <p>AP 24149, a potent dual inhibitor targeting Src and Abl, exhibits IC50 values of 9.1 nM for Src and 3.6 nM for Abl, respectively.</p>
    Formula:C23H24N5OP
    Color and Shape:Solid
    Molecular weight:417.44

    Ref: TM-T73345

  • BTK-IN-22
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    BTK-IN-22

    CAS:
    <p>BTK-IN-22 is a selective BTK inhibitor with IC50 of 0.9 nM; also targets BLX, BMX (IC50s: 1.4, 1.2 nM); better selectivity than Ibrutinib.</p>
    Formula:C26H26N6O2
    Color and Shape:Solid
    Molecular weight:454.52

    Ref: TM-T73275