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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 2526 products for "Angiogenesis".

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  • Dasatinib monohydrate

    CAS:
    Dasatinib monohydrate, an oral SRC-kinase inhibitor, counters imatinib-resistant chronic myeloid leukemia.
    Formula:C22H28ClN7O3S
    Purity:99.68% - >99.99%
    Color and Shape:White Solid
    Molecular weight:506.03
  • Naluzotan hydrochloride

    CAS:
    Naluzotan hydrochloride, a hERG K+ blocker (IC50: 3800 nM) and potent 5-HT1A agonist (IC50: ~20 nM, Ki: ~5.1 nM), is used in anxiety and depression studies.
    Formula:C23H39ClN4O3S
    Purity:99.96%
    Color and Shape:Solid
    Molecular weight:487.1
  • Ibuprofen

    CAS:
    Ibuprofen, an NSAID, reduces pain, inflammation, and fever by limiting prostaglandin production.
    Formula:C13H18O2
    Purity:99.7% - 99.96%
    Color and Shape:Colorless Solid Crystalline
    Molecular weight:206.2808
  • Lidocaine Hydrochloride hydrate

    CAS:
    Lidocaine Hydrochloride hydrate is an amide local anesthetic, has anti-inflammatory property.
    Formula:C14H22N2O·HCl·H2O
    Purity:99.95%
    Color and Shape:Solid
    Molecular weight:288.82
  • LDN-193189 2HCl

    CAS:
    LDN-193189 2HCl inhibits BMP signaling (ALK1/2/3/6), IC50: 0.8-16.7 nM; selective over TGF-β by 200-fold in C2C12 cells.
    Formula:C25H24Cl2N6
    Purity:99.87%
    Color and Shape:Solid
    Molecular weight:479.404
  • Formononetin

    CAS:
    Formononetin (Flavosil) is an O-methylated isoflavone and a phytoestrogen from the root of Astragalus membranaceus.
    Formula:C16H12O4
    Purity:97.39% - 99.94%
    Color and Shape:Solid
    Molecular weight:268.2641
  • Imatinib Mesylate

    CAS:
    Imatinib Mesylate (STI-571) is a tyrosine kinase receptor inhibitor with antineoplastic activity (IC50s: 0.6 μM, 0.1 μM and 0.1 μM for v-Abl, c-Kit and PDGFR,
    Formula:C29H31N7O·CH4SO3
    Purity:98% - >99.99%
    Color and Shape:White Solid
    Molecular weight:589.71
  • Lenvatinib

    CAS:
    Lenvatinib (E7080) is a multi-target receptor tyrosine kinase inhibitor that inhibits VEGFR1-3, FGFR1-4, KIT, PDGFR, and RET, and has oral activity.
    Formula:C21H19ClN4O4
    Purity:98.46% - 99.96%
    Color and Shape:White Solid
    Molecular weight:426.85
  • Gefitinib

    CAS:
    Gefitinib (ZD1839) is an EGFR first-generation inhibitor with oral activity that inhibits the EGFR 19 Del and L858R mutations.
    Formula:C22H24ClFN4O3
    Purity:99.89% - >99.99%
    Color and Shape:White Solid
    Molecular weight:446.902
  • Nimucitinib

    CAS:
    Nimucitinib is a Janus kinase (JAK) inhibitor that can be used to treat dry eye and promote tear production.
    Formula:C25H26F2N6O2
    Purity:99.58%
    Color and Shape:Yellow Solid
    Molecular weight:480.5097
  • Acalabrutinib enantiomer

    CAS:
    R-Acalabrutinib, a BTK inhibitor,enantiomer, is researched for cancer, autoimmune diseases, and inflammation.
    Formula:C26H23N7O2
    Purity:99.20%
    Color and Shape:Solid
    Molecular weight:465.5065
  • FGFR1/DDR2 inhibitor 1

    CAS:
    FGFR1/DDR2 inhibitor 1 is an inhibitor of discoindin domain receptor 2 (DDR2) and fibroblast growth factor receptor 1 (FGFR1), with IC50 values of 31.1 nM, 108
    Formula:C28H22F3N5O
    Purity:99.43%
    Color and Shape:White Solid
    Molecular weight:501.5024
  • Pemigatinib

    CAS:
    Pemigatinib (INCB054828) is an orally active, selective inhibitor of FGFR(IC50s of 0.4 nM, 0.5 nM, 1.2 nM, 30 nM for FGFR1, FGFR2, FGFR3, FGFR4, respectively).
    Formula:C24H27F2N5O4
    Purity:99.57% - 99.95%
    Color and Shape:White Solid
    Molecular weight:487.4991
  • Imatinib impurities3

    CAS:
    Imatinib impurities3 is a protein kinases inhibitor with IC50 values of 6.95uM, 0.245uM, 0.139uM for ABL1 wt, KIT wt, PDGFRR wt, respectively.
    Formula:C24H20ClN5O
    Purity:98.63%
    Color and Shape:Solid
    Molecular weight:429.902
  • Pumecitinib

    CAS:
    Pumecitinib is a Janus kinase (JAK) inhibitor. Pumecitinib exhibits anti-inflammatory activity.
    Formula:C17H20N8O2S
    Purity:99.93%
    Color and Shape:Soild
    Molecular weight:400.458
  • LC-MB12

    CAS:
    LC-MB12 is a PROTAC FGFR2 compound that degrades FGFR2 and can be used to study gastric cancer.
    Formula:C43H44Cl2N10O8
    Purity:99.16%
    Color and Shape:Solid
    Molecular weight:899.78
  • Edicotinib

    CAS:
    Edicotinib (JNJ-527) is a blood-brain permeable, selective CSF-1R inhibitor, with lesser inhibitory effects on KIT and FLT3.Cost-effective and quality-assured.
    Formula:C27H35N5O2
    Purity:98.58% - 99.72%
    Color and Shape:Solid
    Molecular weight:461.5991
  • Ilginatinib maleate

    CAS:
    Ilginatinib maleate (NS-018 maleate) is a highly active and orally bioavailable inhibitor of JAK2.
    Formula:C25H24FN7O4
    Purity:99.74% - 99.82%
    Color and Shape:Solid
    Molecular weight:505.501
  • Hexylresorcinol

    CAS:
    Hexylresorcinol (4-Hexylresorcinol) is a substituted dihydroxybenzene used topically as an antiseptic for the treatment of minor skin infections.
    Formula:C12H18O2
    Purity:99.26% - 99.51%
    Color and Shape:White Solid
    Molecular weight:194.2701
  • LXH254

    CAS:
    LXH254 is a B/C RAF inhibitor with IC50 values of 0.2 nM and 0.07 nM for inhibiting BRAF and CRAF.Cost-effective and quality-assured.
    Formula:C25H25F3N4O4
    Purity:98.30% - 99.92%
    Color and Shape:White Solid
    Molecular weight:502.4856