GLPBio

GTPase

Products Related to GTPase(30)

  • GC17852 structure
    GC17852Gue 1654
    CAS: 397290-30-1
    Purity: >98%

    Oxoeicosanoid receptor 1 (OXE-R) modulator

  • GC11483 structure
    GC114838-CPT-2Me-cAMP, sodium salt
    CAS: 634207-53-7
    Purity: >99.50%

    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.

  • GC11880 structure
    GC11880OctMAB
    CAS: 1120-02-1
    Purity: >98%

    Dynamin inhibitor

  • GC13243 structure
    GC13243MitMAB
    CAS: 1119-97-7
    Purity: >98.00%

    MitMAB, an organic building block, is a cationic surfactant with asymmetrical structure.

  • GC14179 structure
    GC14179Dynole 34-2
    CAS: 1128165-88-7
    Purity: >98%

    Dynamin I inhibitor

  • GC15722 structure
    GC15722HJC 0350
    CAS: 885434-70-8
    Purity: >98%

    EPAC2 antagonist, potent and selective

  • GC16199 structure
    GC161998-pCPT-2-O-Me-cAMP-AM
    CAS: 1152197-23-3
    Purity: >97.00%

    Epac activator

  • GC18260 structure
    GC18260FTase Inhibitor I
    CAS: 149759-96-6
    Purity: >95.00%

    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).

  • GC18426 structure
    GC184268-Nitroguanine
    CAS: 168701-80-2
    Purity: >98%

    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.

  • GC18445 structure
    GC18445N-Deacetylcolchicine
    CAS: 3476-50-4
    Purity: >98%

    An inhibitor of microtubule polymerization

  • GC20107 structure
    GC20107Fendiline hydrochloride
    CAS: 13636-18-5
    Purity: >98.00%

    Fendiline hydrochloride is a nonselective calcium channel blocker.

  • GC39810 structure
    GC39810CID44216842
    CAS: 1222513-26-9
    Purity: >99.50%

    CID44216842 (Cdc42-IN-1) is a potent Cdc42-selective guanine nucleotide binding lead inhibitor. The EC50s for Cdc42 WT and Cdc42Q61L mutant are 1.0 and 1.2 μM in GTP binding assay, respectively. The EC50s for Cdc42 WT and Cdc42Q61L mutant are 0.3 and 0.5 μM in GDP binding assay, respectively. Use as a molecular probe.

  • GC40452 structure
    GC4045215(S)-HETE MaxSpec® Standard
    CAS: 54845-95-3
    Purity: >98.00%

    15(S)-HETE is a major arachidonic acid metabolite from the 15-lipoxygenase pathway.

  • GC43306 structure
    GC43306Compound C108
    CAS: 15533-09-2
    Purity: >98.00%

    Compound C108 is an inhibitor of the GTPase-activating protein (SH3 domain)-binding protein 2 (G3BP2), which is involved in breast tumor initiation.

  • GC44020 structure
    GC44020L-681,217
    Purity: >95.00%

    L-681,217 is an antibiotic originally isolated from S.

  • GC44506 structure
    GC44506Oligomycin D
    CAS: 1404-59-7
    Purity: >95.00%

    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.

  • GC44763 structure
    GC44763PtdIns-(4,5)-P2 (1,2-dioctanoyl) (sodium salt)
    Purity: >97.00%

    The phosphatidylinositol (PtdIns) represent a small percentage of total membrane phospholipids.

  • GC47477 structure
    GC47477JKE-1674
    CAS: 2421119-60-8
    Purity: >98.00%

    A GPX4 inhibitor and active metabolite of ML-210

  • GC47478 structure
    GC47478JKE-1716
    CAS: 2421118-05-8
    Purity: >98.00%

    A GPX4 inhibitor

  • GC47601 structure
    GC47601Mastoparan (trifluoroacetate salt)
    Purity: >95.00%

    A neuropeptide with diverse biological activities

  • GC48094 structure
    GC48094Spiro-Oxanthromicin A
    CAS: 1616622-10-6
    Purity: >95.00%

    A polyketide

  • GC49033 structure
  • GC49089 structure
    GC49089FR900359
    CAS: 107530-18-7

    FR900359 is an inhibitor of G proteins Gα q , Gα 11 , and Gα 14 with IC 50 values of 13.18, 10.47, and 10nM, respectively and is isolated from the leaves of the ornamental plant Ardisia crenata

  • GC49703 structure
    GC49703Guanosine 5’-[γ-thio]triphosphate (lithium salt)
    CAS: 94825-44-2
    Purity: >75.00%

    A hydrolysis-resistant analog of GTP