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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 1483 productos de "Angiogénesis"

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  • PROTAC EGFR degrader 2


    Potent PROTAC EGFR degrader 2; IC50: 4.0 nM, DC50: 36.51 nM; inhibits cell growth; for NTR-responsive synthesis.
    Fórmula:C58H72ClFN12O8S
    Forma y color:Solid
    Peso molecular:1151.78
  • MLK3-IN-1


    <p>MLK3-IN-1 (Compound 37) is a selective inhibitor of mixed-lineage kinase 3 (MLK3) with an IC50 of less than 1 nM. It also inhibits FAK with an IC50 of 15.5 μM. In both murine and human liver microsomes, MLK3-IN-1 demonstrates excellent metabolic stability.</p>
    Fórmula:C20H16F6N4O2S
    Forma y color:Solid
    Peso molecular:490.422
  • Apoptosis inducer 35


    <p>Apoptosisinducer 35 (Compound 6) is a multi-target inhibitor that reduces the expression of EGFR, AKT, ERK, and P38-MAPKα. It suppresses the proliferation of cancer cells A549 and Jurkat, induces cell cycle arrest at the S phase, and triggers apoptosis (cell death).</p>
    Fórmula:C23H21ClN8O2S2
    Forma y color:Solid
    Peso molecular:541.048
  • DD0-2363


    <p>DD0-2363 (Compound 32d) is a dual-target inhibitor of WDR5-MLL1/HDAC. It can suppress the proliferation of acute myeloid leukemia cells and induce apoptosis. With its antitumor properties, DD0-2363 is applicable for research on acute myeloid leukemia.</p>
    Fórmula:C36H36ClFN6O4
    Forma y color:Solid
    Peso molecular:671.16
  • 2-Keto Crizotinib

    CAS:
    <p>2-Keto Crizotinib is an active lactam metabolite of crizotinib.</p>
    Fórmula:C21H20Cl2FN5O2
    Pureza:98%
    Forma y color:Solid
    Peso molecular:464.32
  • Syk-IN-4


    <p>Syk-IN-4: potent, selective SYK inhibitor, orally bioavailable, IC50=0.31 nM, targets autoimmunity, cancers.</p>
    Forma y color:Solid
  • PROTAC FLT-3 degrader 1

    CAS:
    <p>PROTAC FLT-3 degrader 1 is a PROTAC FLT-3 degrader of internal tandem duplication (ITD)(IC50 0.6 nM),with anti-proliferative activity.</p>
    Fórmula:C52H61N9O9S2
    Pureza:98%
    Forma y color:Solid
    Peso molecular:1020.23
  • TL13-12

    CAS:
    <p>TL13-12 is a selective degrader of ALK-PROTAC and inhibits ALK activity (IC50: 0.69 nM).</p>
    Fórmula:C45H53ClN10O10S
    Pureza:98%
    Forma y color:Solid
    Peso molecular:961.49
  • BMS-599626 2HCL(714971-09-2 Free base)

    CAS:
    <p>BMS-599626 2HCL (AC480 2HCl) is a BMS-599626 derivative.</p>
    Fórmula:C27H29Cl2FN8O3
    Pureza:99.11%
    Forma y color:Odour Solid
    Peso molecular:603.47
  • JAK1/TYK2-IN-1

    CAS:
    <p>JAK1/TYK2-IN-1 is a dual inhibitor of TYK2 and JAK1 ( IC 50 = 29 and 41 nM respectively).</p>
    Fórmula:C18H20F3N7O
    Forma y color:Solid
    Peso molecular:407.401
  • MHES0488A


    <p>MHES0488A is a selective humanized antibody targeting HER2, with a KD value of 0.8 nM. It constitutes the antibody portion of DHES0815A. Upon cellular internalization, MHES0488A is transported to lysosomes, releasing PBD-monoamide into the nucleus, where it alkylates DNA, inducing DNA damage and apoptosis. It shows potential for research in cancers such as HER2-positive breast cancer and gastric cancer.</p>
    Forma y color:Odour Liquid
  • TL13-110

    CAS:
    <p>Negative control for TL 13-112 . Displays no degradation of ALK in cell lines. Highly potent ALK inhibitor (IC50 = 0.34 nM).</p>
    Fórmula:C49H62ClN9O9S
    Forma y color:Solid
    Peso molecular:988.59
  • FLT3-IN-20


    <p>FLT3-IN-20 (compound 34f) is a potent FLT3 inhibitor, demonstrating IC50 values of 1 nM for FLT3-D835Y and 4 nM for FLT3-ITD.</p>
    Fórmula:C28H33N7O2S
    Forma y color:Solid
    Peso molecular:531.67
  • EGFR/BRAFV600E-IN-3


    <p>EGFR/BRAFV600E-IN-3 is an inhibitor targeting EGFR, BRAFV600E, and EGFRT790M with IC50 values of 57 nM, 68 nM, and 9.70 nM, respectively.</p>
    Fórmula:C25H18N4O3
    Pureza:98%
    Forma y color:Solid
    Peso molecular:422.44
  • EGFR-IN-22

    CAS:
    <p>EGFR-IN-22: potent for EGFR (IC50: 4.91 nM) &amp; L858R/T790M/C797S mutation (IC50: 0.54 nM).</p>
    Fórmula:C38H47BrFN10O2P
    Forma y color:Solid
    Peso molecular:805.72
  • Angiogenesis related Compound Library


    <p>A unique collection of 1353 proangiogenic and antiangiogenic compounds for new targets identification, research in mechanisms of angiogenesis, and high</p>
    Forma y color:Odour Solid
  • AKN-028

    CAS:
    <p>AKN-028 is an orally active and potent FLT3 tyrosine kinase inhibitor ( IC 50 = 6 nM). AKN-028 causes dose-dependent inhibition of FLT3 autophosphorylation.</p>
    Fórmula:C17H14N6
    Pureza:99.88%
    Forma y color:Solid
    Peso molecular:302.33
  • SNIPER(ABL)-050


    <p>SNIPER(ABL)-050 is a chemical compound that combines Imatinib, an ABL inhibitor, with MV-1, an IAP ligand, using a linker.</p>
    Fórmula:C68H84N12O9
    Pureza:98%
    Forma y color:Solid
    Peso molecular:1213.47
  • Multi-target kinase inhibitor 2


    <p>Compound 5K (Multi-target kinase inhibitor 2) is a multi-targeted kinase inhibitor demonstrating activity against EGFR, Her2, VEGFR2, and CDK2 with IC50 values</p>
    Pureza:98%
    Forma y color:Odour Solid
  • Trastuzumab envedotin


    <p>Trastuzumab envedotin (DP303c) is an antibody-drug conjugate (ADC) targeting the human epidermal growth factor receptor 2 (HER2). It consists of the anti-HER2 antibody DP001 linked to the microtubule polymerization inhibitor MonomethylauristatinE (MMAE) through a cleavable linker. This compound is utilized in research involving HER2-positive solid tumors such as breast cancer, colorectal cancer, and gastric cancer.</p>
    Forma y color:Odour Liquid