GLPG-0187

CAS No. 1320346-97-1

GLPG-0187( GLPG 0187 | GLPG0187 )

Catalog No. M11294 CAS No. 1320346-97-1

GLPG-0187 (GLPG0187) is a highly potent, broad spectrum integrin receptor antagonist.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
5MG 95 In Stock
10MG 140 In Stock
25MG 237 In Stock
50MG 350 In Stock
100MG 521 In Stock
500MG 1134 In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    GLPG-0187
  • Note
    Research use only, not for human use.
  • Brief Description
    GLPG-0187 (GLPG0187) is a highly potent, broad spectrum integrin receptor antagonist.
  • Description
    GLPG-0187 (GLPG0187) is a highly potent, broad spectrum integrin receptor antagonist with IC50 of 1-10 nM for αvβ1, αvβ3, αvβ5, αvβ6, αvβ8 and α5β1; significantly inhibits angiogenesis both in vivo and in vitro, osteoclastogenesis in vitro, and bone loss in vivo; inhibits de novo formation and progression of bone and visceral metastases in prostate cancer and breast cancer mice models.Solid Tumors Phase 1 Clinical(In Vitro):In a solid-phase assay, GLPG0187 shows selectivity for several RGD integrin receptors with IC50s of 1.3, 3.7, 2.0, 1.4, 1.2, 7.7 nM for αvβ1, αvβ3, αvβ5, αvβ6,αvβ8, and α5β1. GLPG0187 is a potent inhibitor of osteoclastic bone resorption and angiogenesis. Treatment with GLPG0187 dose-dependently increases the E-cadherin/vimentin ratio, rendering the cells a more epithelial, sessile phenotype. GLPG0187 dose-dependently diminishes the size of the aldehyde dehydrogenase high subpopulation of prostate cancer cells. GLPG0187 treatment results in cell rounding and clumping. GLPG0187 demonstrates a dose-dependent significant reduction in tumour cell migration. GLPG0187 at all concentrations significantly reduces cell proliferation.(In Vivo):Blocking αv-integrins by GLPG0187 markedly reduces their metastatic tumor growth. Bone tumor burden is significantly lower and the number of bone metastases/mouse is significantly inhibited. The progression of bone metastases and the formation of new bone metastases during the treatment period is significantly inhibited.
  • In Vitro
    ——
  • In Vivo
    ——
  • Synonyms
    GLPG 0187 | GLPG0187
  • Pathway
    Cell Cycle/DNA Damage
  • Target
    Integrin
  • Recptor
    αvβ1integrin
  • Research Area
    Cancer
  • Indication
    Solid Tumors

Chemical Information

  • CAS Number
    1320346-97-1
  • Formula Weight
    595.713
  • Molecular Formula
    C29H37N7O5S
  • Purity
    >98% (HPLC)
  • Solubility
    DMSO: 15 mg/mL
  • SMILES
    O=C(O)[C@H](CNC1=NC(C)=NC(N2CCC(C3=NC4=C(CCCN4)C=C3)CC2)=C1C)NS(=O)(C5=CC=C(OC)C=C5)=O
  • Chemical Name
    L-Alanine, 3-[[2,5-dimethyl-6-[4-(5,6,7,8-tetrahydro-1,8-naphthyridin-2-yl)-1-piperidinyl]-4-pyrimidinyl]amino]-N-[(4-methoxyphenyl)sulfonyl]-

Shipping & Storage Information

  • Storage
    (-20℃)
  • Shipping
    With Ice Pack
  • Stability
    ≥ 2 years

Reference

1. Pujuguet P, et al. Eur J Cancer. 2011;47:S28. doi: 10.1016/S0959-8049(11)72695-8. 2. Cirkel GA, et al. Invest New Drugs. 2016 Apr;34(2):184-92. 3. van der Horst G, et al. Neoplasia. 2011 Jun;13(6):516-25. 4. Reeves KJ, et al. Int J Cancer. 2015 Apr 1;136(7):1731-40.
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