about
Inspirations, discoveries, and future perspectives in total synthesisStructural characterization of CalO2: A putative orsellinic acid P450 oxidase in the calicheamicin biosynthetic pathwayStructural characterization of CalO1: a putative orsellinic acid methyltransferase in the calicheamicin-biosynthetic pathwayRole of steric effects in protein-directed enediyne cycloaromatization of neocarzinostatin.Rapid PCR amplification of minimal enediyne polyketide synthase cassettes leads to a predictive familial classification model.From nature to the laboratory and into the clinicBiosynthesis of enediyne antitumor antibioticsSynthesis of the carboline disaccharide domain of shishijimicin A.DNA damage-site recognition by lysine conjugates.Generation and characterization of a distonic biradical anion formed from an enediynone prodrug in the gas phase.Two-photon photochemical generation of reactive enediyne.Characterization of the maduropeptin biosynthetic gene cluster from Actinomadura madurae ATCC 39144 supporting a unifying paradigm for enediyne biosynthesis.Recent developments in enediyne chemistry.Synthesis and anticancer activity of 13-membered cyclic enediynes.New synthetic enediynes and their conjugates may provide effective treatment for cancer.Triggering of the Bergman cyclization by photochemical ring contraction. Facile cycloaromatization of benzannulated cyclodeca-3,7-diene-1,5-diynesRecovering Genomics Clusters of Secondary Metabolites from Lakes Using Genome-Resolved Metagenomics.
P2860
Q24655539-BFB9A9AF-33C0-4427-AE0B-A8DEC06FDD7FQ27650879-8845EDD2-B6BE-4A15-9E22-C32CF9788E2CQ27667100-03D16F7B-BC59-466E-92C2-973021C73450Q33350520-5DB42E2D-FBB7-4D51-8338-D564CDB93491Q34267723-06217FCA-A21F-4B92-878E-DC7EDC25B698Q34657694-5D6F4A72-23C0-4BED-B99E-954C2329AE3EQ35024692-4EB2E8BF-A0AD-4B22-98F1-6031E4CA75AFQ35136566-AAA658E2-D24A-409F-817C-3B31F4273E16Q35928828-24A8617F-9E22-42AE-9909-47A49BBB8CA9Q36802842-F58A55D3-AFC3-4172-B02E-8E596E3E38D8Q36858892-A96D4620-EE43-41B9-80D7-07BF81B5D210Q36862015-205DB690-9214-49D4-B203-FAEF41F00CA4Q37994131-7847A729-44EC-4E92-8306-7ABF00A85C0FQ39480351-C1B5922D-0D9F-4C34-A747-5D3622D3B4AEQ39778374-91DF1F1D-25E7-47E9-AF54-1E4EAE97CF29Q42704334-D3040F3A-9AFE-4D7F-A463-2BA1C82A3BABQ51149027-035C4B39-52DD-4313-BF45-BC31182FDB45
P2860
description
2002 nî lūn-bûn
@nan
2002 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2002 թվականի հունվարին հրատարակված գիտական հոդված
@hy
2002年の論文
@ja
2002年論文
@yue
2002年論文
@zh-hant
2002年論文
@zh-hk
2002年論文
@zh-mo
2002年論文
@zh-tw
2002年论文
@wuu
name
Designed enediyne antitumor agents.
@ast
Designed enediyne antitumor agents.
@en
Designed enediyne antitumor agents.
@nl
type
label
Designed enediyne antitumor agents.
@ast
Designed enediyne antitumor agents.
@en
Designed enediyne antitumor agents.
@nl
prefLabel
Designed enediyne antitumor agents.
@ast
Designed enediyne antitumor agents.
@en
Designed enediyne antitumor agents.
@nl
P356
P1476
Designed enediyne antitumor agents.
@en
P2093
P304
P356
10.2174/1381612023392810
P577
2002-01-01T00:00:00Z