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Buy high quality KT 5720 108068-98-0 from toronto research chemicals Inc. KT 5720 is prepared by a modificiation of K-252a (sc-200517), which is synthesized by the fungus Nocardiopsis sp. KT 5720 is a potent, specific and cell-permeable inhibitor of PKA (K i = 56 nM). This compound blocks PKA signaling through competitive inhibition. KT 5720; KT 5720. Catalog No. B9002.
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KT5720 is a kinase inhibitor with specificity towards protein kinase A. It is a semi-synthetic derivative of K252a and analog of staurosporine. Scientific background KT5720 is a semi-synthetic derivative of K525a. It is a cell-permeable, selective inhibitor of cAMP-dependent protein kinase (PKA; IC 50 = 56 nM). No significant effect on protein kinase C (PKC), protein kinase G (PKG) or myosin light chain kinase (MLCK), was observed. 1 KT5720 was used to examine the role of PKA in various cellular events such as cell adhesion, 2 neurite MW 537.61, Purity > 98%. Potent, selective protein kinase A (Ki = 60 nM) inhibitor. Reversibly arrests human skin fibroblasts in the G1 phase.
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Following the initial thaw, aliquot and freeze (20° KT 5720. Catalog # 1288. Citations (27).
chemBlink provides information about CAS # 108068-98-0, Antibiotic KT 5720, KT 5720, molecular formula: C32H31N3O5. 1995-01-01
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180000 Naantali kt. 40000. 40000 5720 k. Länsi-Suomen Voima Oy. Harjavalta.
These studies indicate that KT 5720 has
KT 5720, an anti-bacterial agent synthesized by the fungus Nocardiopsis sp, specificly blocks PKA signaling through competitive inhibition of ATP with a Ki value of 60 nM. Please be kindly noted products are not for therapeutic use.
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Size / Price. Qty. KT5720 is a hexylester derivative of K-252a and is a selective inhibitor of PKA (Ki =0.056 µM).
Cited in 27 publications. KT 5720 is a hexylester derivative of K-252a that is a potent and selective inhibitor of PKA.2 KT 5720 has been used in many studies to characterize the role of PKA in various cellular and physiological events.