GLPBio

Angiogenesis

Research Areas

Products Related to Angiogenesis(378)

  • GC10048 structure
    GC10048MNS
    CAS: 1485-00-3
    Purity: >98%

    Inhibitor of Src/Syk tyrosine kinases

  • GC10140 structure
    GC10140Thrombin Receptor Agonist Peptide
    CAS: 137339-65-2
    Purity: >98%

    Thrombin Receptor Agonist Peptide is a synthetic thrombin receptor agonist peptide.

  • GC11230 structure
    GC11230RN486
    CAS: 1242156-23-5
    Purity: >99.50%

    Btk inhibitor,potent and selective

  • GC11662 structure
    GC11662TRAP-6
    CAS: 141136-83-6
    Purity: >99.50%

    TRAP-6 is a selective protease-activated receptor 1 (PAR1) agonist composed of six amino acids.

  • GC11727 structure
    GC11727VKGILS-NH2
    CAS: 942413-05-0
    Purity: >99.50%

    control peptide for SLIGKV-NH2, PAR1 agonist

  • GC11951 structure
    GC11951PAR 4 (1-6)
    CAS: 225779-44-2
    Purity: >98%

    PAR4 agonist

  • GC13227 structure
    GC13227LRGILS-NH2
    CAS: 245329-01-5
    Purity: >98%

    Protease-activated receptor agonist

  • GC13559 structure
    GC13559Cilengitide
    CAS: 188968-51-6
    Purity: >99.00%

    Cilengitide, a cyclized pentapeptide, is a potent integrins antagonist with IC 50 values of 0.61nM, 8.4nM and 14.9nM for ανβ3, ανβ5, and α5β1, respectively.

  • GC14540 structure
    GC14540SLIGKV-NH2
    CAS: 190383-13-2
    Purity: >98.00%

    SLIGKV-NH2 (SLIGKV-NH2) is a highly potent protease-activated receptor-2 (PAR2) activating peptide.

  • GC14831 structure
    GC14831AC 264613
    CAS: 1051487-82-1
    Purity: >95.00%

    PAR2 agonist,potent and selective

  • GC15192 structure
    GC15192A 286982
    CAS: 280749-17-9
    Purity: >98.00%

    A 286982 is a potent, nonpeptide inhibitors of leukocyte function-associated antigen-1/ intracellular adhesion molecule-1 (LFA-1/ICAM-1) interaction, with IC 50 values of 44 and 35nM in LFA-1/ICAM-1 binding assay and LFA-1-mediated cellular adhesion assay, respectively.

  • GC15290 structure
    GC15290AC 55541
    CAS: 916170-19-9
    Purity: >98.50%

    PAR2 agonist,potent and selective

  • GC15557 structure
    GC15557A 205804
    CAS: 251992-66-2
    Purity: >98.00%

    A 205804 is a potent and selective lead inhibitor of E-selectin and ICAM-1 expression (E-selectin: IC 50 = 20nM; ICAM-1: IC 50 = 25nM).

  • GC15817 structure
    GC15817PAR-4 Agonist Peptide, amide (AY-NH2)
    CAS: 352017-71-1
    Purity: >98%

    PAR-4 Agonist Peptide, amide(AY-NH2) (PAR-4-AP; AY-NH2) is a proteinase-activated receptor-4 (PAR-4) agonist, which has no effect on either PAR-1 or PAR-2 and whose effects are blocked by a PAR-4 antagonist.

  • GC17368 structure
    GC173682-Furoyl-LIGRLO-amide
    CAS: 729589-58-6
    Purity: >99.50%

    Protease-activated receptor agonist

  • GC17444 structure
    GC17444TFLLR-NH2
    CAS: 197794-83-5
    Purity: >98%

    PAR1 selective agonist

  • GC17514 structure
    GC17514SLIGRL-NH2
    CAS: 171436-38-7
    Purity: >99.50%

    SLIGRL-NH2 is a specific protease-activated receptor 2 (PAR2) agonist with an EC 50 value of approximately 10μM. SLIGRL-NH2 does not activate PAR1.

  • GC17560 structure
    GC17560BIO 1211
    CAS: 187735-94-0
    Purity: >98.00%

    BIO 1211 is an α4β1 (VLA-4) integrin inhibitor, which inhibits α4β1 (IC₅₀=4nM) and α4β7 (IC₅₀=2μM) .

  • GC17991 structure
    GC17991RLLFT-NH2
    CAS: 447408-68-6
    Purity: >98%

    Protease-activated receptor agonist

  • GA21303 structure
    GA21303Cyclo(Arg-Gly-Asp-D-Phe-Cys)
    CAS: 862772-11-0
    Purity: >99.00%

    Cyclo(Arg-Gly-Asp-D-Phe-Cys), commonly abbreviated as cRGDfC, is a cyclic RGD peptide that shows high affinity and selectivity for the integrin αvβ3 .

  • GA23350 structure
    GA23350PAR-3 (1-6) amide (human)
    CAS: 1872435-09-0
    Purity: >98%

    PAR-3 (1-6) amide (human) is a proteinase-activated receptor (PAR-3) agonist peptide.

  • GC10046 structure
    GC10046Molidustat (BAY85-3934)
    CAS: 1154028-82-6
    Purity: >99.00%

    Molidustat (BAY85-3934) (BAY 85-3934) is a novel inhibitor of hypoxia-inducible factor prolyl hydroxylase (HIF-PH) with mean IC50 values of 480 nM for PHD1, 280 nM for PHD2, and 450 nM for PHD3.

  • GC10235 structure
    GC10235Plinabulin (NPI-2358)
    CAS: 714272-27-2
    Purity: >98.00%

    Plinabulin (NPI-2358) (NPI-2358) is a vascular disrupting agen (VDA) against tubulin-depolymerizing with an IC50 of 9.8 nM against HT-29 cells. Plinabulin (NPI-2358) binds the colchicine binding site of β-tubulin preventing polymerization and has potent inhibitory to tumor cells.

  • GC10291 structure
    GC10291SCH 79797 dihydrochloride
    CAS: 1216720-69-2
    Purity: >98.00%

    SCH 79797 dihydrochloride is an efficient and selective non-peptide proteinase-activated receptor 1 (PAR1) antagonist, with an IC 50 of 70nM and a Ki of 35nM.