別品名 |
SP 924, A 154475.0, KT 5555, CEP-701, (15S,16S,18R)-16-Hydroxy-16-(hydroxymethyl)-15-methyl-28-oxa-4,14,19-triazaoctacyclo[12.11.2.115,18.02,6.07,27.08,13.019,26.020,25]octacosa-1,6,8,10,12,20,22,24,26-nonaen-3-one
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別包装 |
あり
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純度 |
>=98%
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分子量 |
439.47
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CAS RN® |
111358-88-4
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化合物の概要 |
PRK1, JAK, FLT3 inhibitor.
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構造 |
C25H21N3O4
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溶媒 |
DMSO100mMethanol25mM
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参考文献 |
Chamberlain P, Delker S, Pagarigan B, et al. Crystal structures of PRK1 in complex with the clinical compounds lestaurtinib and tofacitinib reveal ligand induced conformational changes. PLoS One. 2014 Aug 11;9(8):e103638. PMID: 25111382. Tam CS, Verstovsek S. Investigational Janus kinase inhibitors. Expert Opin Investig Drugs. 2013 Jun;22(6):687-99. PMID: 23432430. Diaz T, Navarro A, Ferrer G, et al. Lestaurtinib inhibition of the Jak/STAT signaling pathway in hodgkin lymphoma inhibits proliferation and induces apoptosis. PLoS One. 2011 Apr 20;6(4):e18856. PMID: 21533094. Wiernik PH. FLT3 inhibitors for the treatment of acute myeloid leukemia. Clin Adv Hematol Oncol. 2010 Jun;8(6):429-36, 444. PMID: 20733555. Iyer R, Evans AE, Qi X, et al. Lestaurtinib enhances the antitumor efficacy of chemotherapy in murine xenograft models of neuroblastoma. Clin Cancer Res. 2010 Mar 1;16(5):1478-85. PMID: 20179224.
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メーカー |
品番 |
包装 |
LKT
|
L1875
|
1 MG
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※表示価格について
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