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GTPase

Products for  GTPase

  1. Cat.No. Product Name Information
  2. GC11483 8-CPT-2Me-cAMP, sodium salt 8-CPT-2Me-cAMP, sodium salt is a selective activator of exchange proteins activated by cAMP (Epac), the cAMP sensitive guanine nucleotide exchange factors (GEFs) for the small GTPases Rap1 and Rap2. 8-CPT-2Me-cAMP, sodium salt  Chemical Structure
  3. GC18426 8-Nitroguanine 8-Nitroguanine is a nitrative guanine derivative formed by oxidative damage to the guanine base in DNA by reactive nitrogen species (RNS) during inflammation and in vitro by reaction of DNA with peroxynitrite and other RNS reagents. 8-Nitroguanine  Chemical Structure
  4. GC16199 8-pCPT-2-O-Me-cAMP-AM Epac activator 8-pCPT-2-O-Me-cAMP-AM  Chemical Structure
  5. GC43306 Compound C108 Compound C108 is an inhibitor of the GTPase-activating protein (SH3 domain)-binding protein 2 (G3BP2), which is involved in breast tumor initiation. Compound C108  Chemical Structure
  6. GC14179 Dynole 34-2 Dynamin I inhibitor Dynole 34-2  Chemical Structure
  7. GC49089 FR900359

    A cyclic depsipeptide and an inhibitor of Gαq, Gα11, and Gα14

    FR900359  Chemical Structure
  8. GC18260 FTase Inhibitor I FTase inhibitor I is a potent inhibitor of farnesyltransferase (FTase; IC50 = 21 nM) that is greater than 30-fold selective for FTase over geranylgeranyl transferase (GGTase; IC50 = 790 nM). FTase Inhibitor I  Chemical Structure
  9. GC52503 FTase Inhibitor II (trifluoroacetate salt) A potent, selective inhibitor of farnesyltransferase FTase Inhibitor II (trifluoroacetate salt)  Chemical Structure
  10. GC49033 Guanosine 5’-diphosphate (sodium salt hydrate) A purine nucleotide Guanosine 5’-diphosphate (sodium salt hydrate)  Chemical Structure
  11. GC49703 Guanosine 5’-[γ-thio]triphosphate (lithium salt) A hydrolysis-resistant analog of GTP Guanosine 5’-[γ-thio]triphosphate (lithium salt)  Chemical Structure
  12. GC17852 Gue 1654

    Oxoeicosanoid receptor 1 (OXE-R) modulator

    Gue 1654  Chemical Structure
  13. GC15722 HJC 0350 EPAC2 antagonist, potent and selective HJC 0350  Chemical Structure
  14. GC47477 JKE-1674 A GPX4 inhibitor and active metabolite of ML-210 JKE-1674  Chemical Structure
  15. GC47478 JKE-1716 A GPX4 inhibitor JKE-1716  Chemical Structure
  16. GC44020 L-681,217 L-681,217 is an antibiotic originally isolated from S. L-681,217  Chemical Structure
  17. GC52250 Mevalonate (lithium salt) An intermediate in the mevalonate pathway Mevalonate (lithium salt)  Chemical Structure
  18. GC13243 MitMAB MitMAB, an organic building block, is a cationic surfactant with asymmetrical structure. MitMAB  Chemical Structure
  19. GC18445 N-Deacetylcolchicine An inhibitor of microtubule polymerization N-Deacetylcolchicine  Chemical Structure
  20. GC11880 OctMAB Dynamin inhibitor OctMAB  Chemical Structure
  21. GC44506 Oligomycin D

    Oligomycin D is a macrolide antibiotic produced by several species of Streptomyces that inhibits the mitochondrial F1FO-ATPase and is used to uncouple oxidative phosphorylation from electron transport.

    Oligomycin D  Chemical Structure
  22. GC48094 Spiro-Oxanthromicin A A polyketide Spiro-Oxanthromicin A  Chemical Structure

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