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camps-sp, triethylammonium

" in TargetMol Product Catalog
  • Inhibitors & Agonists
    10
    TargetMol | Activity
Rp-cAMPS
T2262173208-40-9
Rp-cAMPS competitively inhibits the cAMP-induced activation of cAMP-dependent protein kinase (PKA).
  • $418
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Rp-cAMPS triethylammonium salt
T12764151837-09-1
Rp-cAMPS triethylammonium salt is an analog of cAMP.It acts as a potent, competitive and cell-permeable antagonist of cAMP-induced activation of cAMP-dependent PKA I and II with Kis of 6.05 µM and 9.75 µM, respectively.
  • $398
35 days
Size
QTY
Sp-cAMPS triethylamine
T7370893602-66-5
Sp-cAMPS triethylamine, a cAMP analog, serves as a potent activator of cAMP-dependent PKA I and II, and acts as a competitive inhibitor of phosphodiesterase (PDE3A) with a K i of 47.6 µM. Additionally, it binds the PDE10 GAF domain with an EC 50 of 40 μM [1] [2] [3].
  • $493
35 days
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QTY
Sp-8-CPT-cAMPS
T38694129693-13-6
Sp-8-CPT-cAMPS is a powerful and specific cAMP analog that activates cAMP-dependent protein kinase A (PKA I and PKA II) selectively and effectively. It exhibits a 153-fold preference for site A of RI over site A of RII, and a 59-fold preference for site B of RII over site B of RI.
  • $970
Backorder
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Sp-cAMPS
T2861571774-13-5
Rp-cAMPS TEA salt is a cAMP-dependent protein kinase (PKA) activator.
  • $1,520
6-8 weeks
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Sp-2-Cl-cAMPS
T88786124854-63-3
Sp-2-Cl-cAMPS serves as an agonist for PKA, boasting enhanced membrane permeability and stability against phosphodiesterases. This compound exhibits antimalarial activity, inhibiting the proliferation of the malaria parasite Plasmodium falciparum with an EC50 of 4 µM. Furthermore, Sp-2-Cl-cAMPS binds to the purified regulatory subunit of PfPKA (PfPKAr) with a Ki of 1.3 µM.
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10-14 weeks
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Sp-cAMPS-AM
T88508152218-24-1
Sp-cAMPS-AM is an analog of cAMP that functions by penetrating cells and liberating its parent polar structure, Sp-cAMPS, thereby inducing PKA activation and CREB phosphorylation.
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10-14 weeks
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Sp-6-Phe-cAMPS
T88546169335-92-6
Sp-6-Phe-cAMPS is an effective activator of cAMP-dependent protein kinase (PKA) with site selectivity and membrane permeability. It does not activate the exchange factors directly stimulated by cAMP, making it suitable as a negative control for Epac. Sp-6-Phe-cAMPS can also be utilized in research on neurodegenerative diseases.
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10-14 weeks
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Sp-8-Cl-cAMPS
T88766142754-28-7
  • Inquiry Price
10-14 weeks
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Sp-8-Br-cAMPS
T88637127634-20-2
Sp-8-Br-cAMPS, an analog of cAMP, acts as an agonist for activating protein kinase A (PKA) with an EC50 of 360 nM. It inhibits T-cell proliferation and non-self responses in the hematocytes of Lepidopteran larvae.
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10-14 weeks
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