Synthesis enables identification of the cellular target of leucascandrolide A and neopeltolide.
about
Discovery of natural product anticancer agents from biodiverse organismsContemporary Strategies for the Synthesis of Tetrahydropyran Derivatives: Application to Total Synthesis of Neopeltolide, a Marine Macrolide Natural ProductMechanism of inhibition of human glucose transporter GLUT1 is conserved between cytochalasin B and phenylalanine amidesSocially responsive effects of brain oxidative metabolism on aggression.Naturally diverse: highlights in versatile synthetic methods enabling target- and diversity-oriented synthesis.Terpestacin inhibits tumor angiogenesis by targeting UQCRB of mitochondrial complex III and suppressing hypoxia-induced reactive oxygen species production and cellular oxygen sensing.A pairwise chemical genetic screen identifies new inhibitors of glucose transport.Total synthesis of neopeltolide and analogsExploring the role of mitochondrial UQCRB in angiogenesis using small molecules.Enantioselective Alcohol C-H Functionalization for Polyketide Construction: Unlocking Redox-Economy and Site-Selectivity for Ideal Chemical Synthesis.Programmed cell death induced by (-)-8,9-dehydroneopeltolide in human promyelocytic leukemia HL-60 cells under energy stress conditionsNatural products from the Lithistida: a review of the literature since 2000.Concise synthesis and biological assessment of (+)-neopeltolide and a 16-member stereoisomer library of 8,9-dehydroneopeltolide: identification of pharmacophoric elements.Identification of fumarate hydratase inhibitors with nutrient-dependent cytotoxicity.Total synthesis and biological evaluation of tyroscherin.Synthesis and biological evaluation of neopeltolide and analogsIdentification and Optimization of the First Highly Selective GLUT1 Inhibitor BAY-876.Studies for the enantiocontrolled preparation of substituted tetrahydropyrans: Applications for the synthesis of leucascandrolide A macrolactoneOxidative carbocation formation in macrocycles: synthesis of the neopeltolide macrocycle.Prins-type macrocyclizations as an efficient ring-closing strategy in natural product synthesis.The Lithistida: important sources of compounds useful in biomedical research.The medicinal potential of promising marine macrolides with anticancer activity.Design and synthesis of analogues of natural products.Strategies and Methods for the Synthesis of Anticancer Natural Product Neopeltolide and its AnalogsTotal synthesis and structure-activity investigation of the marine natural product neopeltolide.Synthesis of tetrahydropyran/tetrahydrofuran-containing macrolides by palladium-catalyzed alkoxycarbonylative macrolactonizationsA Synthetic Analogue of Neopeltolide, 8,9-Dehydroneopeltolide, Is a Potent Anti-Austerity Agent against Starved Tumor Cells.Enantioselective total synthesis of macrolide (+)-neopeltolide.Approach to the Synthesis of the C-C and C-C portion of Leucascandrolide A
P2860
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P2860
Synthesis enables identification of the cellular target of leucascandrolide A and neopeltolide.
description
2008 nî lūn-bûn
@nan
2008年の論文
@ja
2008年学术文章
@wuu
2008年学术文章
@zh-cn
2008年学术文章
@zh-hans
2008年学术文章
@zh-my
2008年学术文章
@zh-sg
2008年學術文章
@yue
2008年學術文章
@zh
2008年學術文章
@zh-hant
name
Synthesis enables identificati ...... candrolide A and neopeltolide.
@en
Synthesis enables identificati ...... candrolide A and neopeltolide.
@nl
type
label
Synthesis enables identificati ...... candrolide A and neopeltolide.
@en
Synthesis enables identificati ...... candrolide A and neopeltolide.
@nl
prefLabel
Synthesis enables identificati ...... candrolide A and neopeltolide.
@en
Synthesis enables identificati ...... candrolide A and neopeltolide.
@nl
P2093
P2860
P356
P1476
Synthesis enables identificati ...... candrolide A and neopeltolide.
@en
P2093
Jelena Janjic
Masato Suzuki
Olesya A Ulanovskaya
Paul T Schumacker
Sergey A Kozmin
Simran S Sabharwal
P2860
P2888
P304
P356
10.1038/NCHEMBIO.94
P577
2008-05-30T00:00:00Z