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A Small Dibromotyrosine Derivative Purified From Pseudoceratina Sp. Suppresses TGF-β Responsiveness by Inhibiting TGF-β Type I Receptor Serine/Threonine Kinase Activity.Astaxanthin and Docosahexaenoic Acid Reverse the Toxicity of the Maxi-K (BK) Channel Antagonist Mycotoxin Penitrem AMicroindolinone A, a Novel 4,5,6,7-Tetrahydroindole, from the Deep-Sea-Derived Actinomycete Microbacterium sp. MCCC 1A11207.Recent Advances in the Isolation, Synthesis and Biological Activity of Marine Guanidine Alkaloids.Cobalt-catalysed reductive C-H alkylation of indoles using carboxylic acids and molecular hydrogen.Synthesis of annulated bis-indoles through Au(i)/Brønsted acid-catalyzed reactions of (1H-indol-3-yl)(aryl)methanols with 2-(arylethynyl)-1H-indoles.Safety evaluation of an oat grain alkaloid gramine by genotoxicity assays.The synthesis of polysubstituted indoles from 3-bromo-2-indolyl phosphates.Exploiting the Distal Reactivity of Indolyl Methylenemalononitriles: An Asymmetric Organocatalyzed [4+2] Cycloaddition with Enals Enables the Assembly of Elusive Dihydrocarbazoles.Development of the Regiodivergent Asymmetric Prenylation of 3-Substituted Oxindoles.Pd-Catalyzed Enantioselective [6+4] Cycloaddition of Vinyl Oxetanes with Azadienes to Access Ten-Membered Heterocycles.Enantiospecific Three-Component Alkylation of Furan and Indole.Bismuth nitrate-promoted disproportionative condensation of indoles with cyclohexanone: a new-type azafulvenium reactivity of indoleKororamides, Convolutamines, and Indole Derivatives as Possible Tau and Dual-Specificity Kinase Inhibitors for Alzheimer's Disease: A Computational Study
P2860
Q36010942-2055759A-045A-4D01-9700-A6E055C9228BQ37453638-331293CE-3C4B-4948-B67A-6826ED35A969Q38654921-4DE2EED7-35B9-4011-8D32-EA3AFAE3ABA9Q43612858-E8B3A3EF-340A-49DA-ABC6-6A40EBE859CAQ45784235-7E3010F6-7CFA-4F1D-B0F3-F885ADB1E854Q48121125-9D32CEF4-BB55-4007-B468-C4B5B0AC6CAAQ48122215-8E47CF46-7E69-4C72-94E4-EB9DA91511DFQ48135073-AD36C34D-90B1-4F35-ACE5-09199A51A13CQ48184621-A0AF3AB0-5AED-4C18-906D-61A5DB00C90FQ48292992-ECDA9C24-6DB0-4FEE-9F7D-50B02C64787FQ48370410-FDA242F3-437B-4449-A8AE-D16D08B373D0Q50143520-FBF628F9-6700-4B48-B93F-F7184157E63AQ57816636-5CAAFF01-DBCD-44BF-9745-E525719C2C93Q58557345-61041CC3-182C-4A0E-9376-C07928BB8A9F
P2860
description
2015 nî lūn-bûn
@nan
2015 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
@hyw
2015 թվականի օգոստոսին հրատարակված գիտական հոդված
@hy
2015年の論文
@ja
2015年論文
@yue
2015年論文
@zh-hant
2015年論文
@zh-hk
2015年論文
@zh-mo
2015年論文
@zh-tw
2015年论文
@wuu
name
Marine Indole Alkaloids
@ast
Marine Indole Alkaloids
@en
Marine Indole Alkaloids
@nl
type
label
Marine Indole Alkaloids
@ast
Marine Indole Alkaloids
@en
Marine Indole Alkaloids
@nl
prefLabel
Marine Indole Alkaloids
@ast
Marine Indole Alkaloids
@en
Marine Indole Alkaloids
@nl
P2860
P356
P1433
P1476
Marine Indole Alkaloids
@en
P2093
Natalie Netz
Till Opatz
P2860
P304
P356
10.3390/MD13084814
P407
P577
2015-08-01T00:00:00Z
2015-08-06T00:00:00Z