Notoamide O, a structurally unprecedented prenylated indole alkaloid, and notoamides P-R from a marine-derived fungus, Aspergillus sp.
about
Marine Indole AlkaloidsFungal origins of the bicyclo[2.2.2]diazaoctane ring system of prenylated indole alkaloidsStudies on the Biosynthesis of the Stephacidin and Notoamide Natural Products: A Stereochemical and Genetic ConundrumWaikialoid A suppresses hyphal morphogenesis and inhibits biofilm development in pathogenic Candida albicans.An update on 2,5-diketopiperazines from marine organisms.Biosynthetic studies of the notoamides: isotopic synthesis of stephacidin A and incorporation into notoamide B and sclerotiamide.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 spPhytochemical study of Caulerpa racemosa (Forsk.) J. Agarth, an invading alga in the habitat of La Maddalena Archipelago.Study on the biosynthesis of the notoamides: Pinacol-type rearrangement of the isoprenyl unit in deoxybrevianamide E and 6-hydroxydeoxybrevianamide E.Notoamide E: Biosynthetic incorporation into notoamides C and D in cultures of Aspergillus versicolor NRRL 35600.Synthesis and bioconversions of notoamide T: a biosynthetic precursor to stephacidin A and notoamide BTaichunamides: Prenylated Indole Alkaloids from Aspergillus taichungensis (IBT 19404).Secondary metabolites of fungi from marine habitats.Two novel cyclic hexapeptides from the genetically engineered Actinosynnema pretiosum.A new cyclic hexapeptide and a new isocoumarin derivative from the marine sponge-associated fungus Aspergillus similanensis KUFA 0013.Penicitroamide, an Antimicrobial Metabolite with High Carbonylization from the Endophytic Fungus Penicillium sp. (NO. 24).Biochemical characterization of NotB as an FAD-dependent oxidase in the biosynthesis of notoamide indole alkaloidsOrganocatalytic Asymmetric Domino Michael/Henry Reaction of Indolin-3-ones with o-Formyl-β-nitrostyrenes.Histone deacetylase inhibitors as a tool to up-regulate new fungal biosynthetic products: isolation of EGM-556, a cyclodepsipeptide, from Microascus sp.Enantioselective inhibitory abilities of enantiomers of notoamides against RANKL-induced formation of multinuclear osteoclasts.Bioinspired chemical synthesis of monomeric and dimeric stephacidin A congeners.Total Synthesis of Notoamides F, I, and R and Sclerotiamide.New diketopiperazine derivatives with cytotoxicity from Nocardiopsis sp. YIM M13066.Isolation of amoenamide A and five antipodal prenylated alkaloids from Aspergillus amoenus NRRL 35600.Simple indole alkaloids and those with a non-rearranged monoterpenoid unitStructural and stereochemical diversity in prenylated indole alkaloids containing the bicyclo[2.2.2]diazaoctane ring system from marine and terrestrial fungi
P2860
Q26796630-AB42F07A-99E0-4414-84E2-1BEF569EF36FQ27009360-7E14114A-52E9-49EA-9180-BAD3298F289AQ33351935-4F1C970D-44FA-42B5-B9CC-657B8D93A53FQ34188367-706DD0AA-7182-461E-910F-BD0C0A86849AQ34780658-C2D2F090-5722-4AF9-8974-537233F96425Q35136579-A28667F7-2268-4091-9B6A-1B2E5C7B57E9Q35141069-D9F751D7-91C6-4E9E-9F96-EF32DAE4BF6FQ35158442-F7E03A57-D66D-46C6-80CD-974A5C6AAFA0Q35222838-044B908D-3930-4A39-9433-F4038602650FQ35580559-3CA65837-1313-4F8E-993D-8F9DFF363934Q35580563-E4C14E55-B5DA-445E-BBDF-F8E0C1FB7BBBQ36547184-A893E622-947A-4679-9F39-54430C8709C8Q37126268-B2BB43A2-E824-4ADA-A708-FE83C191EE9FQ37828075-5ED1973F-1414-41CD-B049-D3FC3EB68C8FQ38727801-E22A07E6-1FC7-4816-A4FC-45B8B0305714Q38897600-E5C596AF-7D83-4E0D-9EA9-E653BA8F6648Q39227689-04C2FDBE-50D1-445D-9335-60FB5FE5F54AQ40964072-79744D49-B422-4553-A100-F310CEDE8820Q41587304-57F6F45B-3B93-4B87-825E-8BD36AC158CDQ42586901-C65DA80B-2587-4FC0-89D0-50F85D42196AQ47644802-4DB00A60-8AC9-44D3-ACA9-5A54B17175BDQ48095543-8D4DBE94-848B-4168-9595-B884799EAB46Q48148786-EDE4BDA4-B56C-4572-9E68-2EB7603913ECQ51218136-EAF62DB3-347D-4C46-A6AE-3E901BFCDD5EQ52603758-19F13885-C1C6-40DF-AA05-A66FCECEC3D5Q58221078-CDDDED16-318D-4042-B361-DF222D5AD474Q59140396-AD4D8E94-429E-4760-9EAB-E8BEFBF67ACB
P2860
Notoamide O, a structurally unprecedented prenylated indole alkaloid, and notoamides P-R from a marine-derived fungus, Aspergillus sp.
description
2010 nî lūn-bûn
@nan
2010 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի օգոստոսին հրատարակված գիտական հոդված
@hy
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
name
Notoamide O, a structurally un ...... erived fungus, Aspergillus sp.
@ast
Notoamide O, a structurally un ...... erived fungus, Aspergillus sp.
@en
Notoamide O, a structurally un ...... erived fungus, Aspergillus sp.
@nl
type
label
Notoamide O, a structurally un ...... erived fungus, Aspergillus sp.
@ast
Notoamide O, a structurally un ...... erived fungus, Aspergillus sp.
@en
Notoamide O, a structurally un ...... erived fungus, Aspergillus sp.
@nl
prefLabel
Notoamide O, a structurally un ...... erived fungus, Aspergillus sp.
@ast
Notoamide O, a structurally un ...... erived fungus, Aspergillus sp.
@en
Notoamide O, a structurally un ...... erived fungus, Aspergillus sp.
@nl
P2093
P356
P1476
Notoamide O, a structurally un ...... erived fungus, Aspergillus sp.
@en
P2093
Hideharu Umaoka
Hiroshi Hirota
Kohei Yoshikawa
Tsuyoshi Ikeda
P304
P356
10.1021/NP1002498
P577
2010-08-01T00:00:00Z