KT5720
KT5720
Names
IUPAC name
(5R ,6S ,8S )-Hexyl 6-hydroxy-5-methyl-13-oxo-6,7,8,13,14,15-hexahydro-5H -16-oxa-4b,8a,14-triaza-5,8-methanodibenzo[b ,h ]cycloocta[jkl ]cyclopenta[e ]-as-indacene-6-carboxylate
Other names
KT 5720
Identifiers
ChEBI
ChemSpider
ECHA InfoCard
100.238.838
UNII
InChI=1S/C32H31N3O5/c1-3-4-5-10-15-39-30(37)32(38)16-23-34-21-13-8-6-11-18(21)25-26-20(17-33-29(26)36)24-19-12-7-9-14-22(19)35(28(24)27(25)34)31(32,2)40-23/h6-9,11-14,23,38H,3-5,10,15-17H2,1-2H3,(H,33,36)/t23-,31+,32+/m0/s1
N Key: ZHEHVZXPFVXKEY-RUAOOFDTSA-N
N InChI=1/C32H31N3O5/c1-3-4-5-10-15-39-30(37)32(38)16-23-34-21-13-8-6-11-18(21)25-26-20(17-33-29(26)36)24-19-12-7-9-14-22(19)35(28(24)27(25)34)31(32,2)40-23/h6-9,11-14,23,38H,3-5,10,15-17H2,1-2H3,(H,33,36)/t23-,31+,32+/m0/s1
Key: ZHEHVZXPFVXKEY-RUAOOFDTBS
CCCCCCOC(=O)[C@@]1(C[C@H]2N3C4=CC=CC=C4C5=C6C(=C7C8=CC=CC=C8N(C7=C53)[C@@]1(O2)C)CNC6=O)O
Properties
C 32 H 31 N 3 O 5
Molar mass
537.616 g·mol−1
Except where otherwise noted, data are given for materials in their
standard state (at 25 °C [77 °F], 100 kPa).
Chemical compound
KT5720 is a kinase inhibitor with specificity towards protein kinase A .[ 1] It is a semi-synthetic derivative of K252a [ 2] and analog of staurosporine .
References
^ Makarevich, A. V.; Sirotkin, A. V.; Rafay, J. (2010). "Comparison of Effects of Protein Kinase A, Mitogen-activated Protein Kinase, and Cyclin-dependent Kinase Blockers on Rabbit Ovarian Granulosa Cell Functions". Hormone and Metabolic Research . 42 (13): 936– 43. doi :10.1055/s-0030-1267226 . PMID 20972940 .
^ CID 3844 from PubChem