about
Ursolic acid and its derivative inhibit protein tyrosine phosphatase 1B, enhancing insulin receptor phosphorylation and stimulating glucose uptake.Frenolicins C-G, pyranonaphthoquinones from Streptomyces sp. RM-4-15Ruthmycin, a new tetracyclic polyketide from Streptomyces sp. RM-4-15.Terfestatins B and C, New p-Terphenyl Glycosides Produced by Streptomyces sp. RM-5-8FRET detection of lymphocyte function-associated antigen-1 conformational extension.Real-time analysis of the inside-out regulation of lymphocyte function-associated antigen-1 revealed similarities to and differences from very late antigen-4.Tertiary Amine Pyrazolones and Their Salts as Inhibitors of Mutant Superoxide Dismutase 1-Dependent Protein Aggregation for the Treatment of Amyotrophic Lateral Sclerosis.A divergent enantioselective strategy for the synthesis of griseusins.A novel synthesis of 1-aryl-3-piperidone derivativesArylazanylpyrazolone derivatives as inhibitors of mutant superoxide dismutase 1 dependent protein aggregation for the treatment of amyotrophic lateral sclerosis.A diastereoselective oxa-Pictet-Spengler-based strategy for (+)-frenolicin B and epi-(+)-frenolicin B synthesis.Bi- and Tetracyclic Spirotetronates from the Coal Mine Fire Isolate Streptomyces sp. LC-6-2.Catalytic enantioselective conjugate addition of fluorobis(phenylsulfonyl)methane to enals: synthesis of chiral monofluoromethyl compounds.Lindenane sesquiterpene dimers from Chloranthus fortunei.Triterpene saponins from Gynostemma cardiospermumInterplay of direct stereocontrol and dynamic kinetic resolution in a bifunctional amine thiourea catalyzed highly enantioselective cascade Michael-Michael reactionTotal synthesis of griseusins and elucidation of the griseusin mechanism of actionThermo-Promoted Reactions of Anthranils with Carboxylic Acids, Amines, Phenols, and Malononitrile under Catalyst-Free ConditionsBaraphenazines A-G, Divergent Fused Phenazine-Based Metabolites from a Himalayan StreptomycesInsecticidal Endostemonines A-J Produced by Endophytic Streptomyces from Stemona sessilifoliaDiastereo- and enantioselective organocatalytic direct conjugate addition of gamma-butenolide to chalcones
P50
Q33249371-6F267212-0B1C-4208-BE73-F432575F5978Q34363959-987469C4-6D91-4385-99E4-891FD6979E0DQ34392079-254047E4-5258-43FA-88F4-722B92050FA9Q34475922-1A58620A-D34B-4962-A761-98DDAB69A7BDQ34786041-E0F1F2D5-8DE3-4315-B474-BE3398089BADQ35063491-825A829F-1227-4CBC-B233-CCAADFF8431BQ35956262-E7AE41CB-B1CE-492C-BDC7-9AC9AF5C068CQ36047988-501AF301-6A0A-4E26-8D14-B06D88067EEBQ36523188-1F57A3CE-0D92-43B4-A933-4621A189EFC6Q36768705-8CEC3DC8-D268-4C84-8CF8-18C07B6C8E10Q37424878-1DB26741-41EA-4F00-9BD0-3D5D0786A9C3Q38867568-09E0958D-18AB-415C-8A01-C84F7C8461AFQ43299039-311F8D48-4E30-4AB6-9E99-D16B3E989DC6Q53548267-9C869C5C-1D09-486F-B8BC-485CC2C9C01DQ79304941-45849117-E394-4190-8819-28BF11B86EC5Q83174427-7CC8EAD2-495C-47A0-A9CB-3ED0AAA89281Q90470037-3A31A6F2-7D08-44B6-A99E-F8DC42BCCBDCQ91074294-D7D888F9-B03C-497C-B7B6-C76E177B8D0EQ92221310-C7E02400-D204-4D28-9F0A-87212EFA591FQ93023032-064BD291-3D24-4C36-993A-97FC73C1140CQ94998264-B364480B-C982-469F-BDCA-C282FA88E299
P50
description
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Yinan Zhang
@ast
Yinan Zhang
@en
Yinan Zhang
@es
Yinan Zhang
@nl
Yinan Zhang
@sl
type
label
Yinan Zhang
@ast
Yinan Zhang
@en
Yinan Zhang
@es
Yinan Zhang
@nl
Yinan Zhang
@sl
altLabel
张毅楠 Yi-Nan Zhang
@en
prefLabel
Yinan Zhang
@ast
Yinan Zhang
@en
Yinan Zhang
@es
Yinan Zhang
@nl
Yinan Zhang
@sl
P1053
D-5769-2016
P106
P31
P3829
P496
0000-0002-0362-1473