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Angiogénesis

Angiogénesis

Los inhibidores de la angiogénesis son compuestos que interfieren con la formación de nuevos vasos sanguíneos, un proceso crucial en el crecimiento y la metástasis del cáncer. Al inhibir la angiogénesis, estos compuestos pueden restringir el suministro de sangre a los tumores, ralentizando o deteniendo su crecimiento. Los inhibidores de la angiogénesis son esenciales en la investigación del cáncer y en el desarrollo terapéutico, proporcionando información sobre los mecanismos de progresión tumoral y ofreciendo posibles tratamientos para el cáncer y otras enfermedades relacionadas con la angiogénesis. En CymitQuimica, ofrecemos una amplia gama de inhibidores de la angiogénesis de alta calidad para apoyar su investigación en oncología y biología vascular.

Subcategorías de "Angiogénesis"

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Se han encontrado 1884 productos de "Angiogénesis"

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  • MBM-55S
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    MBM-55S

    CAS:
    MBM-55S, a Nek2 inhibitor with 1 nM IC50, induces cell cycle arrest and apoptosis, suppressing tumor growth.
    Fórmula:C36H39FN6O10
    Pureza:99.37% - 99.89%
    Forma y color:Solid
    Peso molecular:734.73

    Ref: TM-T11961

  • CGI560
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    CGI560

    CAS:
    CGI560 is a potent BTK inhibitor with IC50 = 400 nM for BTK.
    Fórmula:C29H27N5O
    Forma y color:Solid
    Peso molecular:461.56

    Ref: TM-T68584

  • FLT3-IN-6
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    FLT3-IN-6

    CAS:
    FLT3-IN-6 is a potent and selective inhibitor of FLT3-ITD (FLT3 mutation) with an IC50 of 1.336 nM.
    Fórmula:C23H25N5O3
    Forma y color:Solid
    Peso molecular:419.48

    Ref: TM-T11300

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

    CAS:
    Mutated EGFR-IN-2 is an inhibitor of mutant-selective EGFR.
    Fórmula:C29H35FN8O3
    Pureza:98%
    Forma y color:Solid
    Peso molecular:562.64

    Ref: TM-T12130

  • Y 11
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    Y 11

    CAS:
    focal adhesion kinase (FAK) inhibitor
    Fórmula:C8H17BrN4O
    Pureza:98%
    Forma y color:Solid
    Peso molecular:265.15

    Ref: TM-T23539

  • EGFR-IN-46
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    EGFR-IN-46

    CAS:
    EGFR-IN-46: Potent EGFR/FAK inhibitor (IC50: 20.17 & 14.25 nM), curbs cancer cell growth, triggers apoptosis.
    Fórmula:C27H32F3N3O3
    Forma y color:Solid
    Peso molecular:503.56

    Ref: TM-T63431

  • JTV-519 free base
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    JTV-519 free base

    CAS:
    JTV-519 free base (K201 free base), recognized for its antiarrhythmic and cardioprotective properties, functions as a Ca2+-dependent blocker of sarcoplasmic
    Fórmula:C25H32N2O2S
    Pureza:98%
    Forma y color:Solid
    Peso molecular:424.6

    Ref: TM-T11731

  • PP2 Analog
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    PP2 Analog

    CAS:
    PP2 Analog is an analog of PP2. It also acts as a protein trafficking modulator.
    Fórmula:C16H17ClN4
    Pureza:98%
    Forma y color:Solid
    Peso molecular:300.79

    Ref: TM-T6266L

  • Cyt-PTPε Inhibitor-1
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    Cyt-PTPε Inhibitor-1

    CAS:
    Cyt-PTPε Inhibitor-1 (A Inhibitor-1) is an inhibitor of cytosolic protein tyrosine phosphatase ε.
    Fórmula:C19H20N4O2S
    Pureza:99.55% - 99.82%
    Forma y color:Solid
    Peso molecular:368.45

    Ref: TM-T10927

  • ARQ 069
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    ARQ 069

    CAS:
    ARQ 069 inhibits FGFR2 phosphorylation concentration-dependently (IC50: 9.7 µM), without affecting β-actin. Preferentially binds inactive FGFR1/2.
    Fórmula:C18H15N3
    Pureza:98%
    Forma y color:Solid
    Peso molecular:273.33

    Ref: TM-T10372

  • Naphazoline
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    Naphazoline

    CAS:
    Naphazoline (Naphcon-a) is a sympathomimetic compound with marked alpha adrenergic activity.
    Fórmula:C14H14N2
    Pureza:99.79%
    Forma y color:White Crystalline Powder Solid
    Peso molecular:210.27

    Ref: TM-T21445

  • VA5 TG2 inhibitor
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    VA5 TG2 inhibitor

    CAS:
    VA5 inhibits transamidase and GTP-binding by locking protein in an open state, disabling GTPase.
    Fórmula:C31H34N4O8
    Pureza:98%
    Forma y color:Solid
    Peso molecular:590.62

    Ref: TM-T29086

  • TyK2-IN-2
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    TyK2-IN-2

    CAS:
    TyK2-IN-2 is a selective inhibitor of TYK2 (IC50s: 7 nM, 0.1 μM, and 0.05 μM for TYK2 JH2, IL-23, and IFNα).
    Fórmula:C16H18N6O
    Pureza:98%
    Forma y color:Solid
    Peso molecular:310.35

    Ref: TM-T13232

  • RET-IN-19
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    RET-IN-19

    CAS:
    <p>RET-IN-19, a potent RET inhibitor, anticancer: IC50 6.8 nM (RET-wt), 13.51 nM (RET V804M); for NSCLC research.</p>
    Fórmula:C28H28N6O4S
    Forma y color:Solid
    Peso molecular:544.62

    Ref: TM-T63837

  • DMPQ dihydrochloride
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    DMPQ dihydrochloride

    CAS:
    PDGFRβ inhibitor
    Fórmula:C16H16Cl2N2O2
    Pureza:99.51%
    Forma y color:Solid
    Peso molecular:339.22

    Ref: TM-T22740

  • MMPP
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    MMPP

    CAS:
    MMPP is a VEGFR2 inhibitor with anti-inflammatory activity, inhibits STAT3 , inhibits angiogenesis, and can be used to alleviate myocardial injury.
    Fórmula:C17H18O3
    Pureza:99.31% - 99.83%
    Forma y color:Solid
    Peso molecular:270.32

    Ref: TM-T28077

  • THS-044
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    THS-044

    CAS:
    THS-044 (N-[2-Nitro-4-(Trifluoromethyl)phenyl]morpholin-4-Amine) binding stabilizes the HIF2α PAS-B folded state with a kd of 2 μM and regulates HIF2 activity
    Fórmula:C11H12F3N3O3
    Pureza:99.89%
    Forma y color:Solid
    Peso molecular:291.23

    Ref: TM-T13925

  • FAK inhibitor 2
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    FAK inhibitor 2

    CAS:
    FAK inhibitor 2, antitumor and anti-angiogenesis activitiesis ,is a potent focal adhesion kinase (FAK) inhibitor with an IC50 of 0.07 nM .
    Fórmula:C29H33F3N8O2S2
    Forma y color:Solid
    Peso molecular:646.75

    Ref: TM-T11260

  • CGP60474
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    CGP60474

    CAS:
    CGP60474 is an inhibitor of VEGFR-2 (IC50 = 84 nM) and an inhibitor of ATP-competitive PKC.
    Fórmula:C18H18ClN5O
    Pureza:98.81%
    Forma y color:Solid
    Peso molecular:355.82

    Ref: TM-T14943

  • FGFR2-IN-1
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    FGFR2-IN-1

    CAS:
    FGFR2-IN-1 is an FGFR inhibitor that inhibits FGFR1, FGFR2, and FGFR3, and can be used to study FGFR2-associated cancers.
    Fórmula:C22H19N3O2
    Pureza:98.71%
    Forma y color:Solid
    Peso molecular:357.41

    Ref: TM-T61304