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Home >> Signaling Pathways >> Angiogenesis

Angiogenesis(血管生成)

  1. Cat.No. 产品名称 Information
  2. GC67940 BTK inhibitor 10
  3. GC67857 (R)-Elsubrutinib
  4. GC67708 PLN-1474
  5. GC65909 Bexotegrast
  6. GC65597 Abciximab
  7. GC65529 TRAP-6 amide A peptide PAR1 agonist
  8. GC65455 c(phg-isoDGR-(NMe)k)
  9. GC65439 GB-88
  10. GC65312 AZ8838
  11. GC64979 I-191 I-191 is a potent PAR2 antagonist that inhibits multiple PAR2-induced signaling pathways and functional responses. I-191 also inhibits ERK1/2 phosphorylation, RhoA activation, and inhibition of forskolin-stimulated cAMP accumulation induced by micromolar concentrations of biased ligand GB88.
  12. GC64932 αvβ5 integrin-IN-1
  13. GC64819 Elsubrutinib
  14. GC64571 Sibrafiban
  15. GC49882 Hemokinin 1 (human) (trifluoroacetate salt) A peptide agonist of NK1 receptors
  16. GC49873 Protectin D1 methyl ester An esterified form of protectin D1
  17. GC49808 12-methyl Tridecanoic Acid A methylated fatty acid
  18. GC49799 Apatinib-d8 An internal standard for the quantification of apatinib
  19. GC64360 BTK inhibitor 18
  20. GC64347 Vorapaxar sulfate A PAR1 antagonist
  21. GC64212 Valategrast hydrochloride
  22. GC64120 TAK-020
  23. GC63896 AS-1763
  24. GC63846 BIIB091
  25. GC63797 (S)-Sunvozertinib DZD9008 (Sunvozertinib) is an oral, potent, irreversible, wild type-selective EGFR inhibitor against EGFR or HER2 Exon20ins and other mutations with IC50 ranging from 0.4 nM to 2.1 nM for mutant EGFR.
  26. GC49716 Cyclo(RGDyK) (trifluoroacetate salt) A cyclic peptide ligand of αVβ3 integrin
  27. GC49713 SIKVAV (acetate) A laminin α1-derived peptide
  28. GC49686 N-desmethyl Regorafenib N-oxide An active metabolite of regorafenib
  29. GC49562 4-methoxy Estrone An active metabolite of estrone
  30. GC63658 Atopaxar Atopaxar(E5555,ER-172594-00) is a potent, orally active, selective and reversible thrombin receptor protease-activated receptor-1 (PAR-1) antagonist.
  31. GC63540 SCH79797 An antagonist of PAR1
  32. GC63490 Valategrast
  33. GC63232 Tolebrutinib Tolebrutinib (SAR442168, PRN2246, BTKi'168, BTKi('168)) is an oral, CNS-penetrant, irreversible inhibitor of Bruton's tyrosine kinase (BTK) with IC50s of 0.4 nM and 0.7 nM in Ramos B cells and in HMC microglia cells, respectively.
  34. GC63229 TL-895 TL-895 is a potent, orally active, ATP-competitive, and highly selective irreversible BTK inhibitor with IC50 and Ki of 1.5 nM and 11.9 nM, respectively.
  35. GC62872 BMS-587101
  36. GC49433 Capsiate A capsaicin analog with diverse biological activities
  37. GC49358 Sildenafil Chlorosulfonyl An intermediate in the synthesis of sildenafil
  38. GC49349 O-Desethyl Sildenafil A metabolite of sildenafil
  39. GC49221 QLT0267 An ILK inhibitor
  40. GC62614 SJF620 hydrochloride
  41. GC62566 αvβ1 integrin-IN-1 TFA
  42. GC62515 Pirtobrutinib A BTK inhibitor
  43. GC62498 BTK inhibitor 17
  44. GC62469 Protease-Activated Receptor-1, PAR-1 Agonist TFA
  45. GC62397 RO0270608
  46. GC62380 αvβ1 integrin-IN-1
  47. GC62255 N-piperidine Ibrutinib hydrochloride N-piperidine Ibrutinib hydrochloride, a reversible Ibrutinib derivative, is a potent BTK inhibitor with IC50s of 51.0 and 30.7 nM for WT BTK and C481S BTK, respectively.
  48. GC62182 Echistatin TFA
  49. GC62143 Carotegrast methyl
  50. GC62101 PAR-2-IN-1 IUN76750 is a PAR-2 signaling pathway inhibitor.
  51. GC61777 RWJ-56110 dihydrochloride

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