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Ser/Thr Kinase Inhibitors

  • 1-Norokadaone
    Shown to exhibit inhibitory effects on Serine/Threonine Phosphatases and potential use as an okadaic acid negative control.
    Katalog #CAS NummerSummenformelMenge
    sc-287172131204-29-0C43H66O1150 µg/100 µg
  • 8-MA-cAMP
    A selective cAMP-dependent protein kinase (PKA) activator and a site selective cyclic AMP analog with a similar affinity to site B of both protein kinase A type I and II. A priming analog which acts synergistically together with analogs showing site A preference. Together with e.g. 8-piperidino cAMP, selective stimulation of type I can be achieved
    Katalog #CAS NummerSummenformelMenge
    sc-25701733823-18-6C11H14N6O6PNa1 vial
  • 8-PIP-cAMP
    A selective cAMP-dependent protein kinase (PKA) activator which is a site selective cyclic AMP analog with high selectivity for the site A of protein kinase A type I and site B of type II. Acts synergistically together with analog having opposite site-selectivity.
    Katalog #CAS NummerSummenformelMenge
    sc-25702131357-06-9C15H20N6O6PNa1 vial
  • AD 198
    A PKC-delta activator. Phospholipid scramblase 3 (PLS3) is an enzyme which plays a crucial role in mitochondrial morphology, functions, and apoptotic response. During apoptosis, activated protein kinase C-delta (PKC-delta) translocates to mitochondria and phosphorylates PLS3. Used to show that PLS3 is a critical downstream effector of PKC-delta in AD 198-induced apoptosis.
    Katalog #CAS NummerSummenformelMenge
    sc-25235198983-21-2C39H43NO121 mg
  • Akt1/2 kinase inhibitor
    An Isozyme selective Akt1/2 kinase inhibitor.
    Katalog #CAS NummerSummenformelMenge
    sc-300173n.n.C36H32F3N7O45 mg
  • CGP-74514A hydrochloride
    CGP-74514A is a Cdk inhibitor selective for Cyclin-dependent kinase-1 (Cdk1).
    Katalog #CAS NummerSummenformelMenge
    sc-3003441173021-98-1C19H24ClN7•HCl5 mg/25 mg
  • CKI-7 dihydrochloride
    A CK1 inhibitor which also inhibits SGK, S6K1 and MSK1. Inhibits SGK as potently as CK1.
    Katalog #CAS NummerSummenformelMenge
    sc-2526211177141-67-1C11H12ClN3O2S•2HCl5 mg
  • DCP-LA
    A selective PKC-epsilon (PKC- ) activator. In the in situ PKC assay with a reversed phase high-performance liquid chromatography, DCP-LA significantly activates PKC in PC-12 cells in a concentration (10 nM-100 µM)-dependent manner, with the maximal effect at 100 nM. Maintains a 7-fold greater potency for activation of PKC- over other PKC isozymes.
    Katalog #CAS NummerSummenformelMenge
    sc-25506828399-31-7C20H36O21 mg
  • Guanosine 3',5'-cyclic monophosphorothioate, Rp Isomer triethylammonium salt
    cGMPS-dependent protein kinase Iå inhibitor.
    Katalog #CAS NummerSummenformelMenge
    sc-25286786562-09-6C16H27N6O6PS1 mg
  • H-9 dihydrochloride
    H-9 is a potent and competitive inhibitor of protein kinase C, cAMP-dependent protein kinase, cGRP cGMP and has been used in ligand affinity protein kinase purification.
    Katalog #CAS NummerSummenformelMenge
    sc-200553116970-50-4C11H13N3O2S ·2HCl10 mg/50 mg
  • K-252a
    At high concentrations it is an ATP-competitive inhibitor of cyclic nucleotide-dependent protien kinases. At very low concentrations, has been found to prolong the survival of septal, hippocampal, and cortical neurons
    Katalog #CAS NummerSummenformelMenge
    sc-20051799533-80-9C27H21N3O5100 µg/250 µg/1 mg
  • K-252b
    A metabolite of Nocardiopsis sp. that acts as an antibiotic and a strong inhibitor of protein kinase C (PKC).
    Katalog #CAS NummerSummenformelMenge
    sc-20058599570-78-2C26H19N3O5100 µg/1 mg
  • KRIBB3
    An inhibitior of PKC-dependent phosphorylation of Hsp27 through its direct binding to Hsp27. Has antimigratory and anti-invasive activities in MDA-MB-231 cells. KRIBB3 blocked phorbol 12-myristate 13-acetate-induced phosphorylation of Hsp27 and tumor cell migration.
    Katalog #CAS NummerSummenformelMenge
    sc-252935129414-88-6C19H19NO45 mg
  • Methyl Okadaate
    Serine/Threonine protein phosphatase inhibitor
    Katalog #CAS NummerSummenformelMenge
    sc-29545478111-14-5C45H70O13100 µg
  • Okadaic Acid, Potassium Salt
    An inhibitor of PP1, PP2A, PP2B, PP2C and endogenous phosphatase smooth muscle myosin. Additionally used to study tumor promotion, nitric oxide metabolism, apoptosis, cell cycling and calcium signaling.
    Katalog #CAS NummerSummenformelMenge
    sc-202261155751-72-7C44H67KO1350 µg
  • PS-1145 dihydrochloride
    PS-1145 has been shown to be an IKB kinase (IKK) inhibitor.
    Katalog #CAS NummerSummenformelMenge
    sc-301621431898-65-6C17H11ClN4O•2HCl5 mg
  • SB 220025 trihydrochloride
    A potent, specific inhibitor of human p38 mitogen-activated protein (MAP) kinase.
    Katalog #CAS NummerSummenformelMenge
    sc-253537197446-75-6C18H19FN6··3HCl500 µg
  • SB 431542 hydrate
    A potent and selective inhibitor of transforming growth factor-β superfamily type I activin receptor-like kinase (ALK) receptors.
    Katalog #CAS NummerSummenformelMenge
    sc-255604301836-41-9 (anhydrous)C22H16N4O3•xH2O5 mg
  • SB-505124
    Katalog #CAS NummerSummenformelMenge
    sc-362794694433-59-5C20H21N3O210 mg/50 mg
  • SB-505124 hydrochloride hydrate
    An inhibitor of ALK-5, demonstrated to suppress the action of TGF-β.
    Katalog #CAS NummerSummenformelMenge
    sc-253542694433-59-5 (non-salt)C20H21N3O2 ·xHCl ·yH2O5 mg
  • SIS3 hydrochloride
    A specific inhibitor of Smad3 phosphorylation via inhibiting the effects of TGF-β1. Reestablishes myofibroblast differentiation of scleroderma fibroblasts via reducing expression of α-SMA.
    Katalog #CAS NummerSummenformelMenge
    sc-253565521984-48-5C28H27N3O3 ·HCl5 mg
  • SMER28
    A cell-permeable quinazoline compound which augments the cytostatic effects of Rapamycin in Saccharomyces cerevisiae and acts as an autophagy stimulator both in mammalian cultures in vitro and in a Drosophila melanogaster HD model in vivo. Although SMER28 and Rapamycin do exhibit additive effects on the clearance of cellular autophagy substrates, SMER28 functions independently of Rapamycin by presumably acting on celluar target(s) downstream of the Rapamycin/FKBP12 target, mTOR.
    Katalog #CAS NummerSummenformelMenge
    sc-222320307538-42-7C11H10BrN310 mg
  • Sp-8-pCPT-cAMPS
    Katalog #CAS NummerSummenformelMenge
    sc-253602129693-13-6 (non-salt)C16H14ClNaN5O5PS22.5 mg
  • Sp-Adenosine 3',5'-cyclic monophosphorothioate triethylammonium salt hydrate
    Sp-Diastereomer of adenosine 3',5'-cyclic monophosphorothioate is a potent, membrane-permeable activator of cAMP dependent protein kinase I and II that mimics the effects of cAMP as a second messenger in numerous systems while being resistant to cyclic nucleotide phosphodiesterases; exhibits greater specificity and affinity than forskolin and cAMP analogs such as dibutyryl-cAMP.
    Katalog #CAS NummerSummenformelMenge
    sc-25817693602-66-5 (anhydrous)C10H11N5O5PS•C6H16N•xH2O1 mg
  • Staurosporine
    Inhibits PKC and most other kinases, including tyrosine kinases; binds to ATP binding domain; inhibits topoisomerase II.
    Katalog #CAS NummerSummenformelMenge
    sc-351062996-74-1C28H26N4O3100 µg/1 mg