about
Redox-directed cancer therapeutics: molecular mechanisms and opportunitiesInspirations, discoveries, and future perspectives in total synthesisCapturing Biological Activity in Natural Product Fragments by Chemical SynthesisStructure and Catalytic Mechanism of the Thioesterase CalE7 in Enediyne BiosynthesisTandem mass spectrometry for characterization of covalent adducts of DNA with anticancer therapeuticsReversible Bergman cyclization by atomic manipulationDNA sequence recognition by the indolocarbazole antitumor antibiotic AT2433-B1 and its diastereoisomer.Intracellular DNA damage by lysine-acetylene conjugatesAminobenzoates as building blocks for natural product assembly lines.From nature to the laboratory and into the clinicFine-tuning alkyne cycloadditions: Insights into photochemistry responsible for the double-strand DNA cleavage via structural perturbations in diaryl alkyne conjugatesA continuous assay for DNA cleavage: the application of "break lights" to enediynes, iron-dependent agents, and nucleasesOrganic synthesis and cell biology: partners in controlling gene expression.Specific inhibition of formation of transcription complexes by a calicheamicin oligosaccharide: a paradigm for the development of transcriptional antagonists.Direct comparison of solution and gas-phase reactions of the three distonic isomers of the pyridine radical cation with methanol.Engineered production of cancer targeting peptide (CTP)-containing C-1027 in Streptomyces globisporus and biological evaluationConstructing molecular complexity and diversity: total synthesis of natural products of biological and medicinal importance.Recent Advances in the Development of Antineoplastic Agents Derived from Natural ProductsTotal synthesis of sporolide B.Natural glycoconjugates with antitumor activity.Recent developments in enediyne chemistry.In vivo biotransformations of antibody-drug conjugates.(Hetero)aromatics from dienynes, enediynes and enyne-allenes.The Enzymology of Organic Transformations: A Survey of Name Reactions in Biological Systems.A novel application of radiomimetic compounds as antibiotic drugs.Heteroatom-Heteroatom Bond Formation in Natural Product Biosynthesis.Internalization and cell cycle-dependent killing of leukemic cells by Gemtuzumab Ozogamicin: rationale for efficacy in CD33-negative malignancies with endocytic capacity.The oxide anion accelerated retro-diels-alder reaction.A novel sulfonamide non-classical carbenoid: a mechanistic study for the synthesis of enediynes.Opening Enediyne Scissors Wider: pH-Dependent DNA Photocleavage by meta-Diyne Lysine Conjugates.The design of selectively-activated anti-cancer prodrugs for use in antibody-directed and gene-directed enzyme-prodrug therapies.Designed metalloenediyne warheads damage DNA and outpace DNA polymerase.Organic synthesis: the art and science of replicating the molecules of living nature and creating others like them in the laboratory.Insight into Pd-catalyzed branching cyclizations of enediyne-imides towards furo[2,3-b]pyridines: a DFT study.A phosphine-mediated stereocontrolled synthesis of Z-enediynes by a vicinal dialkynylation of ethynylphosphonium salts.Practical Synthesis of p- and o-Amino- and Methoxyphenolic Anthraquinones.Draft Genome Sequence of Micromonospora sp. Strain WMMA1996, a Marine Sponge-Associated Bacterium.YOU MAKE IT, I BREAK IT
P2860
Q24645584-E5D06D7F-2599-4D75-9959-3F0B266E7A62Q24655539-A60B83FC-013F-4C54-ADE2-F916F7072C5CQ26772873-27D0760B-E5DE-4D71-8AC9-1BBFBBBF982EQ27654596-032A2531-CBBC-4D36-97EF-C8949DE6B350Q28486298-F4C808D0-924C-4AE5-A52B-AA7C58FA0575Q29302518-2B265452-84D5-47DF-8FAF-2C88BAF2C1DFQ33827012-F40763F6-CE04-439F-9E3C-B50E315A7435Q34092697-3890FA0D-F0AA-418A-84CB-EE604CDDD327Q34230699-6AD28824-CDA6-4FD7-9F19-199D6C91CDFDQ34657694-DD64D4FE-E3AA-4974-A214-A708428AF771Q35101868-B6F4FB56-F449-4DDA-854E-627C12B31912Q35567329-ED8F4456-B87E-43DE-B8B5-7470ECD5D9F1Q35771242-937B9D3F-59A5-4DFF-8D6B-D83B6AFBD07BQ35771896-D2FE356E-AD33-4CBD-A8AA-EEF74E3F1DD2Q35927092-469C4FF0-9880-46FE-B9C6-CDA968DE36B5Q35994054-8498324F-E473-4B0B-AF1B-CA45A993C539Q36186718-7BE4BF6A-FA5A-4B66-BEA3-589B73429653Q36273796-23E4E9E7-4487-4218-A103-389A6FCC8F6FQ37172692-0CA9DC1E-1B11-48F4-972B-D7B539ACE00DQ37814157-C06C4D73-79AD-4939-91CB-E0D88931708FQ37994131-A78075E3-8F35-479B-878B-B90D10C87AB5Q38557525-E7FD3839-94A1-4AEC-A83F-161B11014BAFQ38855399-A0B3E22A-3520-4955-8F54-958A1CE338AAQ38922927-D9660388-4FB4-44D2-AC75-A2274BAC222BQ39013337-85A8C554-DB87-4EF5-A086-262B44601AECQ39218600-1A24FDF5-4532-4BD3-A5AB-D3B6E07BF07FQ40616812-56320E11-1669-4485-8D7A-BECC346C65EDQ46150614-052CD3EA-A582-4C70-A726-34D37A6CE3E8Q46258130-4EA6DECA-027F-4B1D-BBEB-875D22102DF2Q46793141-53ECA875-5A90-40F0-8C0A-A1A198029632Q47978690-4428DFEB-F2CE-469A-9D6C-4722B6E731D6Q48160064-D9428330-E0F7-40BB-B5BC-C59CFD8293D7Q51103557-EE7991C2-D929-4639-A2B0-87680B2356A6Q51687906-29595F73-F777-4C0E-A126-D9D39297A298Q53271421-A900B78E-C5A9-4D64-995C-2815D1633EA3Q53821823-71816771-1A9D-4F2F-A9CE-CCACD6929D94Q55109360-0E6A59D0-2D71-4B78-A767-3357356CC3F5Q57764036-1DB4FD19-1E53-4897-8DAA-AB156F89A16E
P2860
description
1993 nî lūn-bûn
@nan
1993 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
1993 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
1993年の論文
@ja
1993年論文
@yue
1993年論文
@zh-hant
1993年論文
@zh-hk
1993年論文
@zh-mo
1993年論文
@zh-tw
1993年论文
@wuu
name
Chemistry and biology of natural and designed enediynes
@ast
Chemistry and biology of natural and designed enediynes
@en
Chemistry and biology of natural and designed enediynes
@nl
type
label
Chemistry and biology of natural and designed enediynes
@ast
Chemistry and biology of natural and designed enediynes
@en
Chemistry and biology of natural and designed enediynes
@nl
prefLabel
Chemistry and biology of natural and designed enediynes
@ast
Chemistry and biology of natural and designed enediynes
@en
Chemistry and biology of natural and designed enediynes
@nl
P2093
P2860
P356
P1476
Chemistry and biology of natural and designed enediynes
@en
P2093
P2860
P304
P356
10.1073/PNAS.90.13.5881
P407
P577
1993-07-01T00:00:00Z