KT5823
Code | Size | Price |
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TAR-T15670-1mg | 1mg | £2,641.00 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Overview
Regulatory Status: RUO
Shipping:
cool pack
Storage:
-20℃
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Further Information
Bioactivity:
KT5823 is a selective the cGMP-dependent protein kinase (PKG) inhibitor (Ki: 0.23 μM), it also inhibits PKA and PKC with Ki values of 10 μM and 4 μM, respectively.
CAS:
126643-37-6
Formula:
C29H25N3O5
Molecular Weight:
495.535
Purity:
0.98
SMILES:
[H][C@]12C[C@](OC)(C(=O)OC)[C@](C)(O1)n1c3ccccc3c3c4CN(C)C(=O)c4c4c5ccccc5n2c4c13
References
1. Gadbois DM, et al. Multiple kinase arrest points in the G1 phase of nontransformed mammalian cells are absent in transformed cells. Proc Natl Acad Sci U S A. 1992 Sep 15;89(18):8626-30.
2. Wyatt TA, et al. KT5823 activates human neutrophils and fails to inhibit cGMP-dependent protein kinase phosphorylation of vimentin. Res Commun Chem Pathol Pharmacol. 1991 Oct;74(1):3-14.
3. Chan SL, et al. Guanylyl cyclase inhibitors NS2028 and ODQ and protein kinase G (PKG) inhibitor KT5823 trigger apoptotic DNA fragmentation in immortalized uterine epithelial cells: anti-apoptotic effects of basal cGMP/PKG. Mol Hum Reprod. 2003 Dec;9(12):775-83.