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Angiogenèse

Angiogenèse

Les inhibiteurs de l'angiogenèse sont des composés qui interfèrent avec la formation de nouveaux vaisseaux sanguins, un processus crucial dans la croissance et la métastase des cancers. En inhibant l'angiogenèse, ces composés peuvent restreindre l'apport sanguin aux tumeurs, ralentissant ou arrêtant leur croissance. Les inhibiteurs de l'angiogenèse sont essentiels dans la recherche sur le cancer et le développement thérapeutique, offrant des informations sur les mécanismes de progression tumorale et proposant des traitements potentiels pour le cancer et d'autres maladies liées à l'angiogenèse. Chez CymitQuimica, nous offrons une large gamme d'inhibiteurs de l'angiogenèse de haute qualité pour soutenir vos recherches en oncologie et biologie vasculaire.

Sous-catégories appartenant à la catégorie "Angiogenèse"

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2330 produits trouvés pour "Angiogenèse"

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  • Protein kinase inhibitor 11

    CAS :
    Protein kinase inhibitor 11 (Compound I-96) is an agent that inhibits the activity of PIM-1, CDK-2, GSK-3, and SRC. It shows potential for research in cancer, autoimmune diseases, and neurodegenerative disorders.
    Formule :C21H18FN5O2S
    Couleur et forme :Solid
    Masse moléculaire :423.463

    Ref: TM-T205016

    10mg
    À demander
    50mg
    À demander
  • Pred17


    Pred17 is an effective EGFR inhibitor with potential applications in lung cancer research.
    Formule :C27H22BN3O
    Couleur et forme :Solid
    Masse moléculaire :415.29

    Ref: TM-T201786

    10mg
    À demander
    50mg
    À demander
  • VEGFR-2-IN-15


    VEGFR-2-IN-15 (Compound 14b) is a potent inhibitor of VEGFR-2. VEGFR-2-IN-15 inhibits the growth of HepG2 cells in the Pre-G1 phase and induces apoptosis.
    Formule :C23H18ClN3O4S
    Couleur et forme :Solid
    Masse moléculaire :467.92

    Ref: TM-T63002

    25mg
    1.369,00€
    50mg
    1.783,00€
    100mg
    2.250,00€
  • JP-153

    CAS :
    JP-153 is an inhibitor of Src-FAK-Paxillin signaling. It suppresses Src-dependent phosphorylation of paxillin (Y118) and subsequent activation of Akt (S473). JP-153 reduces VEGF-induced migration and proliferation of retinal endothelial cells and is applicable in the study of neovascular eye diseases.
    Formule :C21H19NO5
    Couleur et forme :Solid
    Masse moléculaire :365.379

    Ref: TM-T206442

    10mg
    À demander
    50mg
    À demander
  • JAK1/TYK2-IN-3


    JAK1/TYK2-IN-3, orally active, selectively inhibits TYK2 (IC50: 6 nM), JAK1 (37 nM), JAK2 (140 nM), JAK3 (362 nM), and has anti-inflammatory effects.
    Couleur et forme :Solid

    Ref: TM-T64265

    25mg
    1.369,00€
    50mg
    1.783,00€
    100mg
    2.250,00€
  • Dual Cathepsin L/JAK-IN-1

    CAS :
    DualCathepsinL/JAK-IN-1 (Compound A8) serves as a dual inhibitor of Cathepsin L (CTSL) and JAK, exhibiting IC50 values of 0.68 μM for CTSL and 337.1 nM, 5.251 nM, 27.29 nM, and 172.6 nM for JAK1/2/3 and TYK2, respectively. This compound effectively prevents the activation of MAPK, NF-κB, and JAK/STAT signaling pathways, leading to significant anti-inflammatory therapeutic effects. DualCathepsinL/JAK-IN-1 is applicable in research on acute lung injury (ALI).
    Formule :C19H18ClN5
    Couleur et forme :Solid
    Masse moléculaire :351.833

    Ref: TM-T205041

    10mg
    À demander
    50mg
    À demander
  • EGFR/HER2-IN-7


    EGFR/HER2-IN-7: Potent, selective dual inhibitor for MCF-7 cancer; IC50: EGFR 0.18μM, HER2 0.146μM, DHFR 0.907μM.
    Formule :C19H21N3O2S
    Couleur et forme :Solid
    Masse moléculaire :355.45

    Ref: TM-T61272

    25mg
    1.369,00€
    50mg
    1.783,00€
    100mg
    2.250,00€
  • Pimicotinib hydrochloride

    CAS :
    Pimicotinib hydrochloride is an inhibitor of CSF1R, displaying antitumor activity.
    Formule :C22H25ClN6O3
    Couleur et forme :Solid
    Masse moléculaire :456.925

    Ref: TM-T204920

    10mg
    À demander
    50mg
    À demander
  • UBX-382

    CAS :
    UBX-382 is an orally administered proteolysis-targeting chimera (PROTAC) designed to target BTK and disrupt B-cell receptor signaling. It demonstrates enhanced degradation of both wild-type and mutant BTK proteins, exhibiting anti-cancer effects in murine xenograft models using TMD-8 cells [1].
    Formule :C42H44N10O4
    Couleur et forme :Solid
    Masse moléculaire :752.86

    Ref: TM-T87590

    10mg
    À demander
    50mg
    À demander
  • GNE-431

    CAS :
    GNE-431: potent, selective noncovalent Btk inhibitor, IC50=3.2 nM; effective against C481R, T474I, T474M mutants, may counter ibrutinib resistance.
    Formule :C30H32N10O2
    Couleur et forme :Solid
    Masse moléculaire :564.64

    Ref: TM-T70668

    25mg
    2.043,00€
    50mg
    2.682,00€
    100mg
    3.600,00€
  • Vatalanib hydrochloride

    CAS :
    Vatalanib hydrochloride (PTK787 hydrochloride) is an orally available and highly potent tyrosine kinase (VEGF) inhibitor that reduces the number and size of Aβ plaques in the cortex of 5xFAD mice, which may be useful in the study of Alzheimer's disease and cancer.
    Formule :C20H16Cl2N4
    Degré de pureté :99.7%
    Couleur et forme :Solid
    Masse moléculaire :383.27

    Ref: TM-T87609

    1mg
    133,00€
    5mg
    318,00€
    10mg
    475,00€
    25mg
    767,00€
    50mg
    1.054,00€
    100mg
    1.423,00€
    200mg
    1.918,00€
  • NDI-034858

    CAS :
    NDI-034858 (TAK-279) is a tyrosine kinase 2 (TYK2) inhibitor (Kd<200 pM) that targets the JH2 structural domain of Tyk2 for the treatment of autoimmune diseases
    Formule :C23H24N8O3
    Degré de pureté :>99.99%
    Couleur et forme :Solid
    Masse moléculaire :460.49

    Ref: TM-T62902

    1mg
    236,00€
    5mg
    710,00€
    10mg
    1.134,00€
    25mg
    1.684,00€
    50mg
    2.277,00€
    100mg
    3.052,00€
  • XMD-17-51 Trifluoroacetate

    CAS :
    XMD-17-51 Trifluoroacetate is a pyrimido-diazepinone compound that regulates protein kinases.
    Formule :C23H25F3N8O3
    Degré de pureté :99.65%
    Couleur et forme :Solid
    Masse moléculaire :518.49

    Ref: TM-T9191

    1mg
    71,00€
    5mg
    152,00€
    10mg
    236,00€
    25mg
    401,00€
    50mg
    580,00€
    100mg
    797,00€
    1mL*10mM (DMSO)
    168,00€
  • JAK2-IN-7

    CAS :
    JAK2-IN-7 selectively inhibits JAK2 (IC50: 3 nM), shows 14-fold selectivity over JAK1/3, FLT3, induces G0/G1 arrest, apoptosis, and has antitumor effects.
    Formule :C26H33N7O
    Degré de pureté :99.54%
    Couleur et forme :Solid
    Masse moléculaire :459.59

    Ref: TM-T35900

    1mg
    145,00€
    5mg
    354,00€
    10mg
    630,00€
    25mg
    1.301,00€
    50mg
    1.738,00€
    100mg
    2.357,00€
    1mL*10mM (DMSO)
    358,00€
  • JDTic

    CAS :
    JDTic, a 4-phenylpiperidine derivative distantly related to analgesics like meperidine and ketobemidone and more closely to the mu opioid antagonist alvimopan, exhibits a notably long duration of action, maintaining effects in animals for weeks following a single dose. This duration is not due to irreversible binding to the kappa opioid receptor but rather to altered activity of c-Jun N-terminal kinases. As a highly selective antagonist for the κ-opioid receptor, without influencing the μ- or δ-opioid receptors, JDTic has shown potential in animal studies for producing antidepressant and anxiolytic effects. It also demonstrates promise in treating addiction to substances such as cocaine and morphine, distinguishing itself structurally from other kappa antagonists like norbinaltorphimine.
    Formule :C28H39N3O3
    Couleur et forme :Solid
    Masse moléculaire :465.63

    Ref: TM-T11721

    5mg
    1.735,00€
    50mg
    3.509,00€
    100mg
    4.803,00€
  • Ibrutinib Racemate

    CAS :
    Ibrutinib is a selective, irreversible Btk inhibitor (IC50: 0.5 nM). Ibrutinib Racemate is the racemate of Ibrutinib.
    Formule :C25H24N6O2
    Degré de pureté :98%
    Couleur et forme :Solid
    Masse moléculaire :440.5

    Ref: TM-T16440

    Produit arrêté
  • Dihydrodiol-Ibrutinib

    CAS :
    PCI 45227 is an active metabolite of the Bruton's tyrosine kinase inhibitor ibrutinib .1PCI 45227 is formed from ibrutinib by the cytochrome P450 (CYP) isoform CYP3A. 1.Veeraraghavan, S., Viswanadha, S., Thappali, S., et al.Simultaneous quantification of lenalidomide, ibrutinib and its active metabolite PCI-45227 in rat plasma by LC-MS/MS: Application to a pharmacokinetic studyJ. Pharm. Biomed. Anal.107151-158(2015)
    Formule :C25H26N6O4
    Couleur et forme :Solid
    Masse moléculaire :474.521

    Ref: TM-T36429

    Produit arrêté
  • HMBD-001


    HMBD-001 is a humanized IgG1 monoclonal antibody inhibitor that targets HER3. By inhibiting the dimerization of HER3, HMBD-001 suppresses the growth and proliferation of tumor cells. It holds potential for research in cancer treatments, specifically for pancreatic cancer and non-small cell lung cancer.

    Couleur et forme :Odour Liquid
  • ENMD-2076 tartrate

    CAS :
    ENMD-2076 is an orally active kinase inhibitor. It also has antiangiogenic and antiproliferative mechanisms of action.
    Formule :C25H31N7O6
    Couleur et forme :Solid
    Masse moléculaire :525.56

    Ref: TM-T2358L

    Produit arrêté
  • Nimotuzumab (powder)

    CAS :

    Nimotuzumab (powder) is a humanized IgG1 monoclonal antibody that specifically targets the epidermal growth factor receptor (EGFR), possessing a dissociation constant (KD) of 0.21 nM. It blocks the binding to its ligand by targeting the extracellular domain of EGFR. Nimotuzumab exhibits strong antitumor activity by inducing both antibody-dependent cellular cytotoxicity (ADCC) and complement-dependent cytotoxicity (CDC), exerting cytolytic effects on target tumors.

    Couleur et forme :Liquid
  • Imbotolimod


    Imbotolimod, a humanized monoclonal antibody of the immunoglobulin G1-kappa class, exhibits both anti-ERBB2 and antineoplastic activities.
    Couleur et forme :Odour Liquid
  • XMU-MP-3

    CAS :
    XMU-MP-3 is a robust, non-covalent inhibitor of BTK, exhibiting exceptional potency with IC50 values of 10.7 nM and 17.0 nM for BTK WT and BTK C481S mutation, respectively, in the presence of 10 μM ATP. Moreover, XMU-MP-3 elicits apoptosis.
    Formule :C27H27F3N8O
    Couleur et forme :Solid
    Masse moléculaire :536.563

    Ref: TM-T39430

    Produit arrêté
  • PM-8002


    PM-8002 is a bispecific antibody that targets PD-L1 and VEGF-A. It is applicable for research on solid tumors.

    Couleur et forme :Odour Liquid
  • (3R,4S)-Tofacitinib

    CAS :
    (3R,4S)-Tofacitinib, the less active enantiomer of Tofacitinib, is a JAK3 inhibitor with an IC50 of 1 nM.
    Formule :C16H20N6O
    Degré de pureté :98%
    Couleur et forme :Solid
    Masse moléculaire :312.37

    Ref: TM-T13426

    Produit arrêté
  • TLC9995-0188

    CAS :
    Tyrosine-protein kinase ABL, IC50: 1500 nM
    Formule :C16H15N5
    Couleur et forme :Yellow Solid
    Masse moléculaire :277.331
  • Desidustat

    CAS :

    Desidustat is an inhibitor of HIF hydroxylase.

    Formule :C16H16N2O6
    Degré de pureté :98%
    Couleur et forme :Solid
    Masse moléculaire :332.31
  • Olmutinib

    CAS :
    Olmutinib (BI1482694) is a Novel Epidermal Growth Factor Receptor Tyrosine Kinase Inhibitor
    Formule :C26H26N6O2S
    Degré de pureté :99.14%
    Couleur et forme :Solid
    Masse moléculaire :486.59
  • Duligotuzumab

    CAS :

    Duligotuzumab (MEHD-7945A) is a bispecific humanised IgG-κ monoclonal antibody targeting HER3 and EGFR, solid tumours, head and neck cancer,colorectal cancer.

    Degré de pureté :95%
    Couleur et forme :Liquid
  • 3,3',4,4'-Tetrabromobiphenyl

    Produit contrôlé
    CAS :

    Applications 3,3',4,4'-Tetrabromobiphenyl is multi-persistent organic pollutants analyzed in breast milk of first time mothers. An environmental pollutant that affects copper and molybdenum metabolism in rats. Also, it is derived from 1-Bromo-2- nitrobenze (B686175), which is an organic building block used for the synthesis of various pharmaceutical compounds. It is an intermediate for the synthesis of novel Diarylamino-1,3,5-triazine derivatives as FAK inhibitors with anti-angiogenic activity.
    References Tlustos, C., et al.: Organohalogen Compd., 75, 1185-1188 (2013); Salman, K. N., et al.: Environ. Sci. Pollut. R., 21, 6400-6409 (2014); Dao, P., et al.: Bioorg. Med. Chem. Lett., 23, 4552 (2013);

    Formule :C12H6Br4
    Couleur et forme :Off-White To Light Brown
    Masse moléculaire :469.79

    Ref: TR-T291333

    Produit arrêté
  • VEGFR-IN-1

    CAS :
    VEGFR inhibitor
    Formule :C19H16ClN3O
    Degré de pureté :98%
    Couleur et forme :Solid
    Masse moléculaire :337.8