About: Sachiko Tsukamoto

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About: Sachiko Tsukamoto Goto Sponge NotDistinct Permalink

An Entity of Type : wikibase:Item, within Data Space : wikidata.demo.openlinksw.com associated with source document(s)

researcher

Attributes	Values
rdf:type	Item
description	researcher (en) 연구원 (ko) গবেষক (bn) 研究者 (ja) дослідниця (uk) эрдэмтэн (mn) वैज्ञानिक (hi) باحت (ary) изилдөөчү (ky) 研究者 (zh) հետազոտող (hy) onderzoeker (nl) hulumtuese (sq)
rdfs:label	Sachiko Tsukamoto (en) Sachiko Tsukamoto (es) Sachiko Tsukamoto (nl) Sachiko Tsukamoto (sl) Sachiko Tsukamoto (ast)
skos:prefLabel	Sachiko Tsukamoto (en) Sachiko Tsukamoto (es) Sachiko Tsukamoto (nl) Sachiko Tsukamoto (sl) Sachiko Tsukamoto (ast)
name	Sachiko Tsukamoto (en) Sachiko Tsukamoto (es) Sachiko Tsukamoto (nl) Sachiko Tsukamoto (sl) Sachiko Tsukamoto (ast)
Scopus author ID	wds:Q46216379-E7FD66D7-DCDB-42AE-BE7A-CF0290F24AAB
Scopus author ID	7102089628
given name	wds:Q46216379-4AC142FB-9D5E-49B1-8084-7C33F863EAFD
given name	Sachiko
instance of	wds:Q46216379-E62ABABD-CA0F-42F6-94B3-442DEDA779BD
instance of	Homo sapiens
occupation	wds:Q46216379-6A874710-34E9-44D5-8973-8B1A0917C9CA
sex or gender	wds:Q46216379-3B704E47-E97C-4432-A6DA-04E7B5762918
date of birth	wds:Q46216379-AFDC88AF-45C5-4D10-8BB9-9754B03EBB87
family name	wds:Q46216379-3C1339B6-DF9A-4FE6-A5A3-BE79578CB789
occupation	researcher
sex or gender	female organism
date of birth	2000-01-01 00:00:00Z (xsd:dateTime)
family name	Tsukamoto
ORCID iD	wds:Q46216379-CB78DDD6-D4CC-4F24-A25A-1E3DF1DF4551
ORCID iD	https://orcid.org/0000-0002-7993-381X
ORCID iD	0000-0002-7993-381X
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q46216379
is author of	CYP3A4 Inhibitory Activity of New Bisalkaloids, Dipiperamides D and E, and Cognates from White Pepper Monodictyquinone A: a New Antimicrobial Anthraquinone from a Sea Urchin-Derived Fungus Monodictys sp Onionin A from Allium cepa inhibits macrophage activation Three New Cytotoxic Sesterterpenes from a Marine SpongeSpongiasp CYP3A4 inhibitors isolated from Licorice Anti-obesity compounds in green leaves of Eucommia ulmoides. Isolation of CYP3A4 Inhibitors from the Black Cohosh (Cimicifuga racemosa) Taichunamides: Prenylated Indole Alkaloids from Aspergillus taichungensis (IBT 19404). Notoamides A–D: Prenylated Indole Alkaloids Isolated from a Marine-Derived Fungus,Aspergillus sp Hyrtioreticulins A-E, indole alkaloids inhibiting the ubiquitin-activating enzyme, from the marine sponge Hyrtios reticulatus Manadosterols A and B, sulfonated sterol dimers inhibiting the Ubc13-Uev1A interaction, isolated from the marine sponge Lissodendryx fibrosa Stereochemical studies of hexylitaconic acid, an inhibitor of p53-HDM2 interaction. Hexylitaconic acid: a new inhibitor of p53-HDM2 interaction isolated from a marine-derived fungus, Arthrinium sp. Leucettamol A: A new inhibitor of Ubc13-Uev1A interaction isolated from a marine sponge, Leucetta aff. microrhaphis Himeic acid A: a new ubiquitin-activating enzyme inhibitor isolated from a marine-derived fungus, Aspergillus sp Isolation of salsolinol, a tetrahydroisoquinoline alkaloid, from the marine sponge Xestospongia cf. vansoesti as a proteasome inhibitor 7-hydroxy-3-(4-hydroxybenzyl)chroman and broussonin b: neurotrophic compounds, isolated from Anemarrhena asphodeloides BUNGE, function as proteasome inhibitors Hachijodines A−G: Seven New Cytotoxic 3-Alkylpyridine Alkaloids from Two Marine Sponges of the GeneraXestospongiaandAmphimedon1 Antibacterial and Antifungal Sulfated Alkane and Alkenes from the Hepatopancreas of the Ascidian Halocynthia roretzi Isolation of notoamide E, a key precursor in the biosynthesis of prenylated indole alkaloids in a marine-derived fungus, Aspergillus sp Asymmetric total syntheses of (+)- and (-)-versicolamide B and biosynthetic implications Genome-based characterization of two prenylation steps in the assembly of the stephacidin and notoamide anticancer agents in a marine-derived Aspergillus sp Notoamide O, a structurally unprecedented prenylated indole alkaloid, and notoamides P-R from a marine-derived fungus, Aspergillus sp. Isolation of antipodal (-)-versicolamide B and notoamides L-N from a marine-derived Aspergillus sp. STUDIES ON THE BIOSYNTHESIS OF THE STEPHACIDINS AND NOTOAMIDES. TOTAL SYNTHESIS OF NOTOAMIDE S. Notoamides F-K, prenylated indole alkaloids isolated from a marine-derived Aspergillus sp. A Concise Total Synthesis of the Notoamides C and D A Concise, Biomimetic Total Synthesis of Stephacidin A and Notoamide B Acantholactam and pre-neo-kauluamine, manzamine-related alkaloids from the Indonesian marine sponge Acanthostrongylophora ingens Inhibition of the ubiquitin-proteasome system by natural products for cancer therapy Four New Bioactive Pyrrole-Derived Alkaloids from the Marine SpongeAxinellabrevistyla Naamidines H and I, cytotoxic imidazole alkaloids from the Indonesian marine sponge Leucetta chagosensis Tricholomalides A-C, new neurotrophic diterpenes from the mushroom Tricholoma sp. Spongiacidin C, a pyrrole alkaloid from the marine sponge Stylissa massa, functions as a USP7 inhibitor Paradisin C: a new CYP3A4 inhibitor from grapefruit juice Natural products inhibiting the ubiquitin-proteasome proteolytic pathway, a target for drug development Dipiperamides A, B, and C: bisalkaloids from the white pepper Piper nigrum inhibiting CYP3A4 activity Collective Synthesis and Biological Evaluation of Tryptophan-Based Dimeric Diketopiperazine Alkaloids. Targeting the proteasome pathway Stellettadine A: a new acylated bisguanidinium alkaloid which induces larval metamorphosis in ascidians from a marine sponge Stelletta sp Ceratinamine: An Unprecedented Antifouling Cyanoformamide from the Marine SpongePseudoceratina purpurea Natural Diels-Alderases: Elusive and Irresistable Lumichrome. A larval metamorphosis-inducing substance in the ascidian Halocynthia roretzi Urochordamines A and B: Larval settlement/metamorphosis-promoting, pteridine-containing physostigmine alkaloids from the tunicate Ciona savignyi Studies on the biosynthesis of the notoamides: synthesis of an isotopomer of 6-hydroxydeoxybrevianamide E and biosynthetic incorporation into notoamide J. Bioconversion of 6-epi-Notoamide T Produces Metabolites of Unprecedented Structures in a Marine-derived Aspergillus sp Study on the biosynthesis of the notoamides: Pinacol-type rearrangement of the isoprenyl unit in deoxybrevianamide E and 6-hydroxydeoxybrevianamide E. Isolation of notoamide S and enantiomeric 6-epi-stephacidin A from the fungus Aspergillus amoenus: biogenetic implications Comparative analysis of the biosynthetic systems for fungal bicyclo[2.2.2]diazaoctane indole alkaloids: the (+)/(-)-notoamide, paraherquamide and malbrancheamide pathways Isolation of amoenamide A and five antipodal prenylated alkaloids from Aspergillus amoenus NRRL 35600. Isolation of cytochrome P450 inhibitors from strawberry fruit, Fragaria ananassa Synthesis and bioconversions of notoamide T: a biosynthetic precursor to stephacidin A and notoamide B Manadodioxans A−E: polyketide endoperoxides from the marine sponge Plakortis bergquistae

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