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Angiogenesis/Protein Tyrosine Kinase

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Chemical Structure Cat. No. Product Name CAS No.
QLT0267 Chemical Structure
BCP25954 QLT0267 866409-68-9
QLT0267 is an ATP-competitive selective inhibitor of integrin-linked kinase (ILK).
Vedolizumab Chemical Structure
BCP26256 Vedolizumab 943609-66-3
Vedolizumab is a humanized monoclonal antibody that targets the α4β7 integrin for the treatment of ulcerative colitis and Crohn's disease.
ILK-IN-1 Chemical Structure
BCP23690 ILK-IN-1 1333146-24-9
OSU-T315 (1,5-regioisomer) is a potent and specific integrin-linked kinase (ILK) inhibitor.
ILK-IN-2 Chemical Structure
BCP30839 ILK-IN-2 2070015-22-2
ILK-IN-2 is a ILK inhibitor.
TR-14035 Chemical Structure
BCP30639 TR-14035 232271-19-1
TR-14035 is a a dual alpha4beta7(IC50=7 nM)/alpha4beta1 (IC50=87 nM) integrin antagonist .
Abciximab Chemical Structure
BCP30526 Abciximab 143653-53-6
Abciximab is a glycoprotein IIb/IIIa receptor antagonist and a platelet aggregation inhibitor mainly used during and after coronary artery procedures like angioplasty to prevent platelets from sticking together and causing thrombus (blood clot) formation within the coronary artery.
GSK3008348 Chemical Structure
BCP17153 GSK3008348 1629249-33-7
GSK3008348 is an Integrin alphaV inhibitor.
RGD (Arg-Gly-Asp) Peptides Chemical Structure
BCP12422 RGD (Arg-Gly-Asp) Peptides 99896-85-2
RGD Trifluoroacetate is a tripeptide that effectively triggers cell adhesion, addresses certain cell lines and elicits specific cell responses; binds to integrins. Sequence: Arg-Gly-Asp.
SB-273005 Chemical Structure
BCP14131 SB-273005 205678-31-5
SB-273005 is an inhibitor of integrin αvβ3.
Leukadherin 1 Chemical Structure
BCP18444 Leukadherin 1 344897-95-6
Leukadherin-1, also known as LA1, is a CD11b/CD18 agonist. Leukadherin-1 suppresses human innate inflammatory signalling. leukadherin-1 increases CD11b/CD18-dependent adhesion via membrane tethers.
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