Pyranonaphthoquinone lactones: a new class of AKT selective kinase inhibitors alkylate a regulatory loop cysteine.
about
Akt inhibitors in cancer treatment: The long journey from drug discovery to clinical use (Review)Accumulation of a bioactive benzoisochromanequinone compound kalafungin by a wild type antitumor-medermycin-producing streptomycete strainPhenylalanine-Based Inactivator of AKT Kinase: Design, Synthesis, and Biological Evaluation.Akt Cys-310-targeted inhibition by hydroxylated benzene derivatives is tightly linked to their immunosuppressive effectsFrenolicins C-G, pyranonaphthoquinones from Streptomyces sp. RM-4-15Ruthmycin, a new tetracyclic polyketide from Streptomyces sp. RM-4-15.Functional Characterization of a Ketoreductase-Encoding Gene med-ORF12 Involved in the Formation of a Stereospecific Pyran Ring during the Biosynthesis of an Antitumor Antibiotic Medermycin.Exploitation of the ability of γ-tocopherol to facilitate membrane co-localization of Akt and PHLPP1 to develop PHLPP1-targeted Akt inhibitorsA diastereoselective oxa-Pictet-Spengler-based strategy for (+)-frenolicin B and epi-(+)-frenolicin B synthesis.Recent development of anticancer therapeutics targeting Akt.Xiakemycin A, a novel pyranonaphthoquinone antibiotic, produced by the Streptomyces sp. CC8-201 from the soil of a karst cave.Pyranonaphthoquinones - isolation, biology and synthesis: an update.Expression, Crystallization and Preliminary X-ray Diffraction Analyses of Med-ORF10 in the Biosynthetic Pathway of an Antitumor Antibiotic Medermycin.The binding landscape of a partially-selective isopeptidase inhibitor with potent pro-death activity, based on the bis(arylidene)cyclohexanone scaffold.Exploring O-stannyl ketyl and acyl radical cyclizations for the synthesis of γ-lactone-fused benzopyrans and benzofurans.The value of pyrans as anticancer scaffolds in medicinal chemistry
P2860
Q28080599-EE750FA5-A3A7-4121-8110-45806E798BCAQ28543530-251CAE56-ACEF-486E-9223-E05A33986378Q33636467-AB4AC5B4-8499-43F3-9980-3F5657076DB2Q33744734-04591DA2-0711-4477-A5A4-23C096BE399DQ34363959-A2851705-1FA1-4C85-A5C8-E6B6583817FAQ34392079-121F1365-7A52-4921-97F9-6C79C149DAEEQ35688287-8CE24690-A6A6-4C92-8602-A02BD3FEE42EQ36482696-25968265-D5B5-4CBE-AC25-DFEAD8A9785BQ37424878-0863456B-437F-4F5C-8C05-FF1E87227BD4Q37812658-6C3A4360-B04E-47FC-935E-335C56595EC7Q38860756-4D7DE398-37CD-458A-A468-4F37D5B2882BQ38985163-47679594-FEB2-471E-BDE8-5B7CD8B50B25Q40351891-B3D14703-21F9-423D-8C28-119A2DFFE520Q50130103-98FABDB0-1EE7-405F-B70B-AD5A5E613894Q54577285-484A3812-53D2-46A8-B840-A1FA79CB6751Q58862089-339C9736-835C-4506-B483-304663E450EA
P2860
Pyranonaphthoquinone lactones: a new class of AKT selective kinase inhibitors alkylate a regulatory loop cysteine.
description
2009 nî lūn-bûn
@nan
2009年の論文
@ja
2009年論文
@yue
2009年論文
@zh-hant
2009年論文
@zh-hk
2009年論文
@zh-mo
2009年論文
@zh-tw
2009年论文
@wuu
2009年论文
@zh
2009年论文
@zh-cn
name
Pyranonaphthoquinone lactones: ...... te a regulatory loop cysteine.
@en
Pyranonaphthoquinone lactones: ...... te a regulatory loop cysteine.
@nl
type
label
Pyranonaphthoquinone lactones: ...... te a regulatory loop cysteine.
@en
Pyranonaphthoquinone lactones: ...... te a regulatory loop cysteine.
@nl
prefLabel
Pyranonaphthoquinone lactones: ...... te a regulatory loop cysteine.
@en
Pyranonaphthoquinone lactones: ...... te a regulatory loop cysteine.
@nl
P2093
P356
P1476
Pyranonaphthoquinone lactones: ...... te a regulatory loop cysteine.
@en
P2093
Ayako Yamashita
Bernard Johnson
Cilien Hanna
Dennis Powell
Edward J Salaski
Erick Honores
Girija Krishnamurthy
Jaechul Shim
Jeremy I Levin
P304
P356
10.1021/JM900075G
P407
P577
2009-04-01T00:00:00Z