about
Isolation and identification of lateral bud growth inhibitor, indole-3-aldehyde, involved in apical dominance of pea seedlings.Comparative transcriptional profiling-based identification of raphanusanin-inducible genes.Neuroprotective effect of 3,5-di-O-caffeoylquinic acid on SH-SY5Y cells and senescence-accelerated-prone mice 8 through the up-regulation of phosphoglycerate kinase-1.Isolation of 5-(hydroxymethyl)furfural from Lycium chinense and its inhibitory effect on the chemical mediator release by basophilic cells.Bioactive taxoids from the Japanese yew Taxus cuspidata.3,4,5-tri-O-caffeoylquinic acid inhibits amyloid β-mediated cellular toxicity on SH-SY5Y cells through the upregulation of PGAM1 and G3PDH.Biological activity and chemistry of taxoids from the Japanese yew, Taxus cuspidata.Methanol and Butanol Extracts of Paeonia lutea Leaves Repress Metastasis of Squamous Cell Carcinoma.Hirseins A and B, daphnane diterpenoids from Thymelaea hirsuta that inhibit melanogenesis in B16 melanoma cells.Protective effects of caffeoylquinic acids on the aggregation and neurotoxicity of the 42-residue amyloid β-protein.Suffruyabiosides A and B, two new monoterpene diglycosides from moutan cortex.Structure-activity relationship of caffeoylquinic acids on the accelerating activity on ATP production.Inhibitory effect of acteoside isolated from Cistanche tubulosa on chemical mediator release and inflammatory cytokine production by RBL-2H3 and KU812 cells.Indoleacetic acid falcarindiol ester induces granulocytic differentiation of the human leukemia cell line HL-60.Inhibitory effect of tannins from galls of Carpinus tschonoskii on the degranulation of RBL-2H3 Cells.Effect of O-methylated and glucuronosylated flavonoids from Tamarix gallica on α-glucosidase inhibitory activity: structure-activity relationship and synergistic potential.Allelopathy and allelopathic substance in the moss Rhynchostegium pallidifolium.Hirseins inhibit melanogenesis by regulating the gene expressions of Mitf and melanogenesis enzymes.Raphanusanin-mediated resistance to pathogens is light dependent in radish and Arabidopsis thaliana.Inhibition of amyloid β aggregation by acteoside, a phenylethanoid glycoside.Palmaenones A and B, two new antimicrobial chlorinated cyclopentenones from discomycete Lachnum palmae.Lupenone from Erica multiflora leaf extract stimulates melanogenesis in B16 murine melanoma cells through the inhibition of ERK1/2 activation.Renealtins A and B, new diarylheptanoids with a tetrahydrofuran ring from the seeds of Renealmia exaltata.Subincanadines A-C, novel quaternary indole alkaloids from Aspidosperma subincanum.Pycnalin, a new α-glucosidase inhibitor from Acer pycnanthum.Naucleamides A-E, new monoterpene indole alkaloids from Nauclea latifolia.Induction of hepatocyte growth factor production in human dermal fibroblasts by caffeic acid derivatives.Plant-growth inhibitory activity of heliannuol derivatives.First total synthesis of 4-methylthio-3-butenyl glucosinolate.Cladionol A, a polyketide glycoside from marine-derived fungus Gliocladium species.Induction of beta-glucosidase activity in maize coleoptiles by blue light illumination.Hederyne A, a new antimicrobial polyacetylene from galls of Hedera rhombea Bean.Antimitotic activity of moroidin, a bicyclic peptide from the seeds of Celosia argenteaRaphanusanin-induced genes and the characterization of RsCSN3, a raphanusanin-induced gene in etiolated radish hypocotyls.An allelopathic substance in red pine needles (Pinus densiflora).Inhibitory Activities of Antioxidant Flavonoids from Tamarix gallica on Amyloid Aggregation Related to Alzheimer's and Type 2 Diabetes Diseases.l-Histidine Induces Resistance in Plants to the Bacterial Pathogen Ralstonia solanacearum Partially Through the Activation of Ethylene Signaling.Modulation of multidrug resistance in tumor cells by taxinine derivatives.Identification of dehydrocostus lactone and 4-hydroxy-β-thujone as auxin polar transport inhibitorsBioactive substances from L.G. Don and their biological activities
P50
Q33337915-36E3528C-3DD5-4687-9A32-A6BE8B863B6CQ33606231-F54291A1-D8D8-4EA3-BBC0-BF40BA240604Q33613383-A10456E0-9D04-413A-9D31-41AB743C4DFAQ33732701-E01D5147-E4FD-45BA-BBC9-D9B8AECBC7B6Q34587524-DFDDCAC4-9B0D-4D4F-915E-B0CE3EFF114DQ34827756-8A116B0D-2834-407F-90F1-B732DCD46D6AQ35676865-08E3D278-7A68-43B1-8D83-9963E8C2FDCFQ36949160-D870F9F9-76DC-453E-A6E7-98C5449CC89CQ39255837-3DB936CF-1ED4-45C8-8EEF-CCFB471E0D65Q39291419-54D91D18-D8A1-4BE8-9E00-67286586566CQ39355990-3BDD746F-0497-4D2E-8B03-4E0765FFA0B3Q39563968-93E3CA96-2D66-4C90-A3E9-857FDFF74926Q39720657-CC743B86-6DCC-4E9E-927F-828311886244Q39912631-190EC325-1840-416F-BC86-29E9A2D118F1Q42219915-4AA17447-7318-4707-B305-2189B2D0F8FDQ43029021-E32D308B-1329-4FB9-9E22-9530C9E33DB1Q43217025-D915DF6C-5C29-4562-B851-059D30DB03FEQ43274565-74DB1BD6-94B3-43A4-B263-7D4F2640188DQ43471069-CFE7A418-971F-414E-9947-6B0DCAADCFEAQ43483451-0680D4C9-6D52-4892-806A-886C2B009C2EQ43523517-3E89AC4B-B861-482A-94E7-28E6977631D7Q43827234-1F4AD812-8CE7-45D0-8646-0578B0762772Q43927721-CE860708-5A6F-440B-A3B9-DC4B59FB9009Q44118643-73416E8A-DF94-4C8C-BFCB-70484CDA357FQ44216619-DDFA648E-18B1-47F0-86E1-5C09ACBF301DQ44273433-957CDD69-F827-43B9-A615-895273E23398Q44327733-DC32909B-5AAD-4C1A-A739-EDCA49AB756FQ44961686-2CD52E32-2501-4869-997C-C10C3A5E1C6FQ46095667-0AEEE023-6468-4655-A6B7-38D1EBBC6E21Q46514572-BF39071E-716F-43D2-839C-440487BF8F01Q46940948-E46063E1-74AE-4504-AC54-7FBAE96B2870Q46988712-A61CAA31-1122-4C63-BFF5-EB9ACA17E52EQ46996066-C9CF2798-2D8D-4E5C-925C-EE220FF52F18Q50456535-33082B67-065F-420C-857A-EE5F03B3903BQ50636924-03CDA204-2CDA-4E31-97E4-2B5E10216D56Q51155438-5E12A3C0-FCEC-44F7-B78C-B79A1E10AB6AQ53780228-51F458A9-9E67-4851-8251-F96EBABDC1A6Q54102146-0C53F975-9DF9-4720-963B-31760030C764Q56958189-6CF95C47-7F16-4FAF-974B-74D2563B71E1Q57903215-FA54A657-05EF-4814-9AC1-A1FAFBF93C2C
P50
description
hulumtues
@sq
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Hideyuki Shigemori
@ast
Hideyuki Shigemori
@en
Hideyuki Shigemori
@es
Hideyuki Shigemori
@nl
Hideyuki Shigemori
@sl
type
label
Hideyuki Shigemori
@ast
Hideyuki Shigemori
@en
Hideyuki Shigemori
@es
Hideyuki Shigemori
@nl
Hideyuki Shigemori
@sl
prefLabel
Hideyuki Shigemori
@ast
Hideyuki Shigemori
@en
Hideyuki Shigemori
@es
Hideyuki Shigemori
@nl
Hideyuki Shigemori
@sl
P106
P1153
7005079197
P21
P31
P496
0000-0001-9778-8057
P569
2000-01-01T00:00:00Z