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Home >> Signaling Pathways >> Tyrosine Kinase

Tyrosine Kinase

Products for  Tyrosine Kinase

  1. Cat.No. Product Name Information
  2. GC41183 α-Carotene

    α-Carotene is a precursor of vitamin A that has been found in various fruits and vegetables.

     α-Carotene Chemical Structure
  3. GC41653 (±)16(17)-DiHDPA (±)16(17)-DiHDPA is produced from cytochrome P450 epoxygenase action on docosahexaenoic acid. (±)16(17)-DiHDPA Chemical Structure
  4. GC41656 (±)2-(14,15-Epoxyeicosatrienoyl) Glycerol 2-Arachidonoyl glycerol (2-AG) is an endogenous central cannabinoid (CB1) receptor agonist that is present at relatively high levels in the central nervous system. (±)2-(14,15-Epoxyeicosatrienoyl) Glycerol Chemical Structure
  5. GC13944 (5Z)-7-Oxozeaenol

    TAK1 mitogen-activated protein kinase kinase kinase (MAPKKK) inhibitor

     (5Z)-7-Oxozeaenol Chemical Structure
  6. GC17800 (E)-FeCP-oxindole VEGFR-2 inhibitor (E)-FeCP-oxindole Chemical Structure
  7. GC61807 (E/Z)-AG490 (E/Z)-AG490 Chemical Structure
  8. GC63864 (E/Z)-Zotiraciclib hydrochloride (E/Z)-Zotiraciclib hydrochloride Chemical Structure
  9. GC14729 (R)-Crizotinib C-MET/ALK inhibitor,potent and ATP-competitve (R)-Crizotinib Chemical Structure
  10. GC19012 (R)-GNE-140

     A TRK kinase (TKI) inhibitor

     (R)-GNE-140 Chemical Structure
  11. GC13136 (S)-Crizotinib Potent MTH1 inhibitor (S)-Crizotinib Chemical Structure
  12. GC63797 (S)-Sunvozertinib (S)-Sunvozertinib Chemical Structure
  13. GC13344 (Z)-FeCP-oxindole VEGFR-2 inhibitor (Z)-FeCP-oxindole Chemical Structure
  14. GC62291 (Z)-Orantinib (Z)-Orantinib Chemical Structure
  15. GC12172 1-Naphthyl PP1 Src family kinases inhibitor 1-Naphthyl PP1 Chemical Structure
  16. GC34119 1-Naphthyl PP1 hydrochloride (1-NA-PP 1 hydrochloride) 1-Naphthyl PP1 hydrochloride (1-NA-PP 1 hydrochloride) Chemical Structure
  17. GC11696 1-NM-PP1 Pp60c-src inhibitor 1-NM-PP1 Chemical Structure
  18. GC42026 1-Palmitoyl-2-hydroxy-sn-glycero-3-PC 1-Palmitoyl-2-hydroxy-sn-glycero-3-PC is the ubiquitous lipid species generated following phospholipase A2 (PLA2) hydrolysis of phosphatidylcholine. 1-Palmitoyl-2-hydroxy-sn-glycero-3-PC Chemical Structure
  19. GC33087 2,4-Pyrimidinediamine with linker 2,4-Pyrimidinediamine with linker Chemical Structure
  20. GC33519 2,5-Dihydroxybenzoic acid 2,5-Dihydroxybenzoic acid Chemical Structure
  21. GC10408 2-D08 Sumoylation inhibitor 2-D08 Chemical Structure
  22. GC33319 2-Keto Crizotinib (PF-06260182) 2-Keto Crizotinib (PF-06260182) Chemical Structure
  23. GC35095 2-Phospho-L-ascorbic acid trisodium salt 2-Phospho-L-ascorbic acid trisodium salt Chemical Structure
  24. GC39689 3-Hydroxy Midostaurin 3-Hydroxy Midostaurin Chemical Structure
  25. GC12818 4-methyl Erlotinib EGFR inhibitor 4-methyl Erlotinib Chemical Structure
  26. GC63805 4SC-203 4SC-203 Chemical Structure
  27. GC11205 5'-Fluoroindirubinoxime FMS-like receptor tyrosine kinase-3 (FLT3) inhibitor 5'-Fluoroindirubinoxime Chemical Structure
  28. GC50157 6bK Insulin degrading enzyme (IDE) inhibitor 6bK Chemical Structure
  29. GC16853 7,8-Dihydroxyflavone Tyrosine kinase receptor B (TrkB) agonist 7,8-Dihydroxyflavone Chemical Structure
  30. GC32992 7-Hydroxy-4-chromone (7-Hydroxychromone) 7-Hydroxy-4-chromone (7-Hydroxychromone) Chemical Structure
  31. GC42616 7-oxo Staurosporine

    7-oxo Staurosporine is an antibiotic originally isolated from S.

     7-oxo Staurosporine Chemical Structure
  32. GC35209 A 419259 A 419259 Chemical Structure
  33. GC17789 A 419259 trihydrochloride LCK inhibitor, orally available A 419259 trihydrochloride Chemical Structure
  34. GC35213 A-770041 A-770041 Chemical Structure
  35. GC10938 AAL-993 VEGF receptors inhibitor AAL-993 Chemical Structure
  36. GC13257 AC480 (BMS-599626) HER1/2 inhibitor,selective and efficacious AC480 (BMS-599626) Chemical Structure
  37. GC18167 AC710

    A potent and selective PDGFR family inhibitor

     AC710 Chemical Structure
  38. GC35225 AC710 Mesylate AC710 Mesylate Chemical Structure
  39. GC30242 Acrizanib Acrizanib Chemical Structure
  40. GC15801 ACTB-1003 FGFR1 inhibitor ACTB-1003 Chemical Structure
  41. GC32797 AD80 AD80 Chemical Structure
  42. GC15579 Adaphostin P210bcr/abl tyrosine kinase inhibitor Adaphostin Chemical Structure
  43. GC11892 AEE788 (NVP-AEE788) EGFR/HER-2/VEGFR inhibitor AEE788 (NVP-AEE788) Chemical Structure
  44. GC10707 Afatinib dimaleate

    EGFR inhibitor

     Afatinib dimaleate Chemical Structure
  45. GC60567 Afatinib impurity 11 Afatinib impurity 11 Chemical Structure
  46. GC13296 Afatinib(BIBW2992) Irreversible EGFR/HER2 inhibitor Afatinib(BIBW2992) Chemical Structure
  47. GC38645 AG 1295 AG 1295 Chemical Structure
  48. GC50013 AG 1478 hydrochloride Highly potent EGFR-kinase inhibitor AG 1478 hydrochloride Chemical Structure
  49. GC17489 AG 494 Potent EGFR-kinase inhibitor AG 494 Chemical Structure
  50. GC11744 AG 555 Potent EGFR-kinase inhibitor AG 555 Chemical Structure
  51. GC12233 AG 556 EGFR inhibitor AG 556 Chemical Structure
  52. GC13168 AG 825 Selective ErbB2 inhibitor AG 825 Chemical Structure
  53. GC14494 AG 99 EGFR inhibitor AG 99 Chemical Structure
  54. GC13697 AG-1024 Selective IGF-1R inhibitor AG-1024 Chemical Structure
  55. GC16235 AG-1295 potent and selective inhibitor of PDGF receptor kinase AG-1295 Chemical Structure
  56. GC35263 AG-13958 AG-13958 Chemical Structure
  57. GC17226 AG-1478 EGFR inhibitor,potent and selective AG-1478 Chemical Structure
  58. GC12864 AG-1557 inhibitor of epidermal growth factor receptor (EGFR) tyrosine kinase AG-1557 Chemical Structure
  59. GC17647 AG-18 EGFR/PDGFR inhibitor AG-18 Chemical Structure
  60. GC14890 AG-183

    inhibitor of epidermal growth factor (EGF) receptor kinase

     AG-183 Chemical Structure
  61. GC11024 AG-213 inhibitor of epidermal growth factor (EGF) receptor kinase AG-213 Chemical Structure
  62. GC11712 AG-370 PDGFR inhibitor AG-370 Chemical Structure
  63. GC13854 AG-490 (Tyrphostin B42)

    STAT3/EGFR/JAK2/JAK3 inhibitor

     AG-490 (Tyrphostin B42) Chemical Structure
  64. GC11845 AG-82 inhibitor of EGFR kinase AG-82 Chemical Structure
  65. GC11737 AG957 a tyrphostin that targets transforming Bcr-Abl fusion proteins AG957 Chemical Structure
  66. GC31371 AGL-2263 AGL-2263 Chemical Structure
  67. GC16228 AIM-100 Ack1 inhibitor AIM-100 Chemical Structure
  68. GC35280 Alectinib Hydrochloride Alectinib Hydrochloride Chemical Structure
  69. GC35287 ALK inhibitor 1 ALK inhibitor 1 Chemical Structure
  70. GC17376 ALK inhibitor 2 ALK inhibitor, novel and selective ALK inhibitor 2 Chemical Structure
  71. GC63387 ALK kinase inhibitor-1 ALK kinase inhibitor-1 Chemical Structure
  72. GC32127 Alofanib (RPT835) Alofanib (RPT835) Chemical Structure
  73. GC16604 Altiratinib c-MET/TIE-2/VEGFR inhibitor Altiratinib Chemical Structure
  74. GC11134 ALW-II-41-27 Eph receptor inhibitor ALW-II-41-27 Chemical Structure
  75. GC15655 AMG 337 MET inhibitor AMG 337 Chemical Structure
  76. GC14974 AMG 925 FLT3/CDK4 inhibitor,potent and selective AMG 925 Chemical Structure
  77. GC35315 AMG 925 HCl AMG 925 HCl Chemical Structure
  78. GC12600 AMG-208 C-Met inhibitor,potent and highly selective AMG-208 Chemical Structure
  79. GC11481 AMG-458 Potent c-Met inhibitor AMG-458 Chemical Structure
  80. GC17669 AMG-47A destabilizer of the KRAS oncoprotein AMG-47A Chemical Structure
  81. GC64015 AMP-945 AMP-945 Chemical Structure
  82. GC16391 Amuvatinib (MP-470, HPK 56)

    Tyrosine kinase inhibitor

     Amuvatinib (MP-470, HPK 56) Chemical Structure
  83. GC33362 Amuvatinib hydrochloride (MP470 hydrochloride) Amuvatinib hydrochloride (MP470 hydrochloride) Chemical Structure
  84. GC11486 ANA 12 TrkB receptor antagonist ANA 12 Chemical Structure
  85. GC17283 AP26113 Anaplastic lymphoma kinase (ALK) inhibitor AP26113 Chemical Structure
  86. GC14292 Apatinib Mesylate

    VEGFR2 inhibitor, orally bioavailable, selective

     Apatinib Mesylate Chemical Structure
  87. GC12478 ARRY-380 Tyrosine kinase HER2 and p95-HER2 inhibitor ARRY-380 Chemical Structure
  88. GC46013 AS-2444697 (hydrochloride) AS-2444697 (hydrochloride) Chemical Structure
  89. GC32703 Asciminib (ABL001) Asciminib (ABL001) Chemical Structure
  90. GC62402 ASK120067 ASK120067 Chemical Structure
  91. GC14446 ASP3026 ALK inhibitor,potent and selective ASP3026 Chemical Structure
  92. GC34476 ASP5878 ASP5878 Chemical Structure
  93. GC10914 AST 487 RET kinase inhibitor AST 487 Chemical Structure
  94. GC11691 AST-1306 EGFR/HER2 inhibitor AST-1306 Chemical Structure
  95. GC15669 AST-1306 TsOH ErbB2 and EGFR inhibitor AST-1306 TsOH Chemical Structure
  96. GC33096 AST2818 mesylate AST2818 mesylate Chemical Structure
  97. GC62481 AST5902 trimesylate AST5902 trimesylate Chemical Structure
  98. GC35413 Astragaloside VI Astragaloside VI Chemical Structure
  99. GC10638 AT9283 Aurora kinase/JAK inhibitor AT9283 Chemical Structure
  100. GC62499 ATH686 ATH686 Chemical Structure
  101. GC35435 AV-412 AV-412 Chemical Structure

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