Tremorgenic and nontremorgenic 2,3-fused indole diterpenoids (Q35573809)

8 August 2017

title

Tremorgenic and nontremorgenic 2,3-fused indole diterpenoids (English)

1 reference

8 August 2017

Heather Sings

1

1 reference

8 August 2017

Sheo Singh

series ordinal

2

1 reference

8 August 2017

language of work or name

English

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=14593856

27 March 2024

publication date

1 January 2003

1 reference

The alkaloids. Chemistry and biology

8 August 2017

published in

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8 August 2017

volume

60

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8 August 2017

page(s)

51-163

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Endophytes: a rich source of functional metabolites

8 August 2017

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0099-9598%2803%2960002-7

7 January 2021

Fungal tremorgens: the mechanism of action of single nitrogen containing toxins--a hypothesis

1 reference

https://api.crossref.org/works/10.1016%2FS0099-9598%2803%2960002-7

7 January 2021

High-performance liquid chromatographic determination of profiles of mycotoxins and other secondary metabolites

1 reference

https://api.crossref.org/works/10.1016%2FS0099-9598%2803%2960002-7

7 January 2021

Paspaline and paspalicine, two indole-mevalonate metabolites from

1 reference

https://api.crossref.org/works/10.1016%2FS0099-9598%2803%2960002-7

7 January 2021

Paspalum staggers: isolation and identification of tremorgenic metabolites from sclerotia of Claviceps paspali

1 reference

https://api.crossref.org/works/10.1016%2FS0099-9598%2803%2960002-7

7 January 2021

Isolation and structures of indoloditerpenes, possible biosynthetic intermediates to the tremorgenic mycotoxin, paxilline, from Emericella striata

1 reference

https://api.crossref.org/works/10.1016%2FS0099-9598%2803%2960002-7

7 January 2021

Isolation of paspaline B, an indole-diterpenoid from Penicilium paxilli

1 reference

https://api.crossref.org/works/10.1016%2FS0099-9598%2803%2960002-7

7 January 2021

Terpendoles, novel ACAT inhibitors produced by Albophoma yamanashiensis. I. Production, isolation and biological properties.

1 reference

https://api.crossref.org/works/10.1016%2FS0099-9598%2803%2960002-7

7 January 2021

Terpendole M, a Novel Indole−Diterpenoid Isolated fromLoliumperenneInfected with the Endophytic FungusNeotyphodiumlolii

1 reference

https://api.crossref.org/works/10.1016%2FS0099-9598%2803%2960002-7

7 January 2021

Isokotanins A-C: new bicoumarins from the sclerotia of Aspergillus alliaceus.

1 reference

https://api.crossref.org/works/10.1016%2FS0099-9598%2803%2960002-7

7 January 2021

Aflavarin and β-Aflatrem: New Anti-Insectan Metabolites from the Sclerotia of Aspergillus flavus

1 reference

https://api.crossref.org/works/10.1016%2FS0099-9598%2803%2960002-7

7 January 2021

Isolation and determination of paspalitrem-type tremorgenic mycotoxins using liquid chromatography with diode-array detection

1 reference

https://api.crossref.org/works/10.1016%2FS0099-9598%2803%2960002-7

7 January 2021

Indole metabolites from a strain of Aspergillus flavus

1 reference

https://api.crossref.org/works/10.1016%2FS0099-9598%2803%2960002-7

7 January 2021

Antiinsectan alkaloids: Shearinines A-C and a new paxilline derivative from the ascostromata of Eupenicillium shearii

1 reference

https://api.crossref.org/works/10.1016%2FS0099-9598%2803%2960002-7

7 January 2021

A new tremorgenic metabolite from Penicillium paxilli

1 reference

https://api.crossref.org/works/10.1016%2FS0099-9598%2803%2960002-7

7 January 2021

The structure of paxilline, a tremorgenic metabolite of bainier

1 reference

https://api.crossref.org/works/10.1016%2FS0099-9598%2803%2960002-7

7 January 2021

Paxilline biosynthesis by Acremonium loliae; a step towards defining the origin of lolitrem neurotoxins

1 reference

https://api.crossref.org/works/10.1016%2FS0099-9598%2803%2960002-7

7 January 2021

Isolation of a new tremorgenic indoloditerpene, 1'-O-acetylpaxilline, from Emericella striata and distribution of paxilline in Emericella spp

1 reference

https://api.crossref.org/works/10.1016%2FS0099-9598%2803%2960002-7

7 January 2021

Studies on fungal products. Part 10. Isolation and structures of novel bicoumarins, desertorins A, B, and C, from Emericella desertorum

1 reference

https://api.crossref.org/works/10.1016%2FS0099-9598%2803%2960002-7

7 January 2021

Studies on fungal products. IX. Dethiosecoemestrin, a new metabolite related to emestrin, from Emericella striata

1 reference

https://api.crossref.org/works/10.1016%2FS0099-9598%2803%2960002-7

7 January 2021

High Levels of Ergonovine and Lysergic Acid Amide in ToxicAchnatherum inebriansAccompany Infection by anAcremonium-like Endophytic Fungus

1 reference

https://api.crossref.org/works/10.1016%2FS0099-9598%2803%2960002-7

7 January 2021

Oxidative transformation of paxilline in sheep bile.

1 reference

https://api.crossref.org/works/10.1016%2FS0099-9598%2803%2960002-7

7 January 2021

Tremorgenic indole alkaloids potently inhibit smooth muscle high-conductance calcium-activated potassium channels

1 reference

https://api.crossref.org/works/10.1016%2FS0099-9598%2803%2960002-7

7 January 2021

Paxilline inhibition of the alpha-subunit of the high-conductance calcium-activated potassium channel.

1 reference

https://api.crossref.org/works/10.1016%2FS0099-9598%2803%2960002-7

7 January 2021

Effects of paxilline on K+ channels in rat mesenteric arterial cells

1 reference

https://api.crossref.org/works/10.1016%2FS0099-9598%2803%2960002-7

7 January 2021

Effects of the K+ channel blockers paspalitrem-C and paxilline on mammalian smooth muscle

1 reference

https://api.crossref.org/works/10.1016%2FS0099-9598%2803%2960002-7

7 January 2021

The mycotoxin paxilline inhibits the cerebellar inositol 1,4, 5-trisphosphate receptor

1 reference

https://api.crossref.org/works/10.1016%2FS0099-9598%2803%2960002-7

7 January 2021

Biosynthesis and transformation of tremorgenic indolediterpenoids by Penicillium paxilli and Acremonium lolii

1 reference

https://api.crossref.org/works/10.1016%2FS0099-9598%2803%2960002-7

7 January 2021

Studies on fungal products. Part XXXIII. Structures of new indoloditerpenes, possible biosynthetic precursors of the tremorgenic mycotoxins, penitrems, from Penicillium crustosum.

1 reference

https://api.crossref.org/works/10.1016%2FS0099-9598%2803%2960002-7

7 January 2021

Immunochemical techniques in natural products chemistry: Isolation and structure determination of a novel indole-diterpenoid aided by TLC-ELISAgram

1 reference

https://api.crossref.org/works/10.1016%2FS0099-9598%2803%2960002-7

7 January 2021

New paspalinine derivatives with antiinsectan activity from the sclerotia of Aspergillus nomius

1 reference

https://api.crossref.org/works/10.1016%2FS0099-9598%2803%2960002-7

7 January 2021

Terpendoles, novel ACAT inhibitors produced by Albophoma yamanashiensis. II. Structure elucidation of terpendoles A, B, C and D

1 reference

https://api.crossref.org/works/10.1016%2FS0099-9598%2803%2960002-7

7 January 2021

Terpendoles, Novel ACAT Inhibitors Produced by Albophoma yamanashiensis. III. Production, Isolation and Structure Elucidation of New Components

1 reference

https://api.crossref.org/works/10.1016%2FS0099-9598%2803%2960002-7

7 January 2021

Thiersinines A and B: novel antiinsectan indole diterpenoids from a new fungicolous Penicillium species (NRRL 28147).

1 reference

https://api.crossref.org/works/10.1016%2FS0099-9598%2803%2960002-7

7 January 2021

TOXIN FROM ASPERGILLUS FLAVUS: PRODUCTION ON FOOD MATERIALS OF A SUBSTANCE CAUSING TREMORS IN MICE

1 reference

https://api.crossref.org/works/10.1016%2FS0099-9598%2803%2960002-7

7 January 2021

Aflatrem, the tremorgenic mycotoxin from aspergillus flavus

1 reference

https://api.crossref.org/works/10.1016%2FS0099-9598%2803%2960002-7

7 January 2021

The potent tremorgenic neurotoxins lolitrem B and aflatrem: a comparison of the tremor response in mice

1 reference

https://api.crossref.org/works/10.1016%2FS0099-9598%2803%2960002-7

7 January 2021

Aflatrem: a tremorgenic mycotoxin with acute neurotoxic effects

1 reference

https://api.crossref.org/works/10.1016%2FS0099-9598%2803%2960002-7

7 January 2021

Action of tremorgenic mycotoxins on GABAA receptor

1 reference

https://api.crossref.org/works/10.1016%2FS0099-9598%2803%2960002-7

7 January 2021

Tremorgenic mycotoxins, paspalitrem A and C, from a tropical Phomopsis

1 reference

https://api.crossref.org/works/10.1016%2FS0099-9598%2803%2960002-7

7 January 2021

Paspalitrem C, a new metabolite from sclerotia of Claviceps paspali

1 reference

https://api.crossref.org/works/10.1016%2FS0099-9598%2803%2960002-7

7 January 2021

Sulpinines A-C and secopenitrem B: new antiinsectan metabolites from the sclerotia of Aspergillus sulphureus

1 reference

https://api.crossref.org/works/10.1016%2FS0099-9598%2803%2960002-7

7 January 2021

Tremorgenic Toxin from Penicillium cyclopium grown on Food Materials

1 reference

https://api.crossref.org/works/10.1016%2FS0099-9598%2803%2960002-7

7 January 2021

Tremorgenic toxins from penicillia. II. A new tremorgenic toxin, tremortin B, from Penicillium palitans

1 reference

https://api.crossref.org/works/10.1016%2FS0099-9598%2803%2960002-7

7 January 2021

Tremorgenic mycotoxins from Penicillium crustosum: isolation of penitrems A–F and the structure elucidation and absolute configuration of penitrem A

1 reference

https://api.crossref.org/works/10.1016%2FS0099-9598%2803%2960002-7

7 January 2021

Tremorgenic mycotoxins from Penicillium crustosum. Biosynthesis of penitrem A

1 reference

https://api.crossref.org/works/10.1016%2FS0099-9598%2803%2960002-7

7 January 2021

Actions of tremorgenic fungal toxins on neurotransmitter release

1 reference

https://api.crossref.org/works/10.1016%2FS0099-9598%2803%2960002-7

7 January 2021

The effects of the tremorgenic mycotoxin penitrem A on the rat cerebellum

1 reference

https://api.crossref.org/works/10.1016%2FS0099-9598%2803%2960002-7

7 January 2021

Brain neurotoxicity of Penitrem A: electrophysiological, behavioral and histopathological study

1 reference

https://api.crossref.org/works/10.1016%2FS0099-9598%2803%2960002-7

7 January 2021

Toxicity of selected tremorgenic mycotoxins and related compounds to Spodoptera frugiperda and Heliothis zea.

1 reference

https://api.crossref.org/works/10.1016%2FS0099-9598%2803%2960002-7

7 January 2021

Tremorgenic mycotoxins from Penicillium crustosum. Structure elucidation and absolute configuration of penitrems B–F

1 reference

https://api.crossref.org/works/10.1016%2FS0099-9598%2803%2960002-7

7 January 2021

Structure elucidation of janthitrem B, a tremorgenic metabolite of Penicillium janthinellum, and relative configuration of the A and B rings of janthitrems B, E, and F

1 reference

https://api.crossref.org/works/10.1016%2FS0099-9598%2803%2960002-7

7 January 2021

Thomitrems A and E, two indole-alkaloid isoprenoids from Penicillium crustosum Thom

1 reference

https://api.crossref.org/works/10.1016%2FS0099-9598%2803%2960002-7

7 January 2021

Pennigritrem, a naturally-occurring penitrem A analogue with novel cyclisation in the diterpenoid moiety

1 reference

https://api.crossref.org/works/10.1016%2FS0099-9598%2803%2960002-7

7 January 2021

A new penitrem analog with antiinsectan activity from the sclerotia of Aspergillus sulphureus

1 reference

https://api.crossref.org/works/10.1016%2FS0099-9598%2803%2960002-7

7 January 2021

Penitremones A–C, Penicillium metabolites containing an oxidised penitrem carbon skeleton giving insight into structure–tremorgenic relationships

1 reference

https://api.crossref.org/works/10.1016%2FS0099-9598%2803%2960002-7

7 January 2021

Janthitrems B and C, two principal indole-diterpenoids produced by Penicillium janthinellum

1 reference

https://api.crossref.org/works/10.1016%2FS0099-9598%2803%2960002-7

7 January 2021

Structure elucidation of the janthitrems, novel tremorgenic mycotoxins from Penicillium janthinellum

1 reference

https://api.crossref.org/works/10.1016%2FS0099-9598%2803%2960002-7

7 January 2021

Suspected tremorgenic mycotoxicosis (ryegrass staggers) in alpacas (Llama pacos) in the UK

1 reference

https://api.crossref.org/works/10.1016%2FS0099-9598%2803%2960002-7

7 January 2021

An association of a Lolium endophyte with ryegrass staggers

1 reference

https://api.crossref.org/works/10.1016%2FS0099-9598%2803%2960002-7

7 January 2021

Ryegrass staggers: isolation of potent neurotoxins lolitrem A and lolitrem B from staggers-producing pastures

1 reference

https://api.crossref.org/works/10.1016%2FS0099-9598%2803%2960002-7

7 January 2021

Tremorgenic neurotoxins from perennial ryegrass causing ryegrass staggers disorder of livestock: structure elucidation of lolitrem B

1 reference

https://api.crossref.org/works/10.1016%2FS0099-9598%2803%2960002-7

7 January 2021

Isolation of Lolicine A, Lolicine B, Lolitriol, and Lolitrem N from Lolium perenne Infected with Neotyphodium lolii and Evidence for the Natural Occurrence of 31-Epilolitrem N and 31-Epilolitrem F.

1 reference

https://api.crossref.org/works/10.1016%2FS0099-9598%2803%2960002-7

7 January 2021

Ryegrass staggers: the presence of lolitrem neurotoxins in perennial ryegrass seed

1 reference

https://api.crossref.org/works/10.1016%2FS0099-9598%2803%2960002-7

7 January 2021

Isolation and Structure Elucidation of Lolitrem A, a Tremorgenic Mycotoxin from Perennial Ryegrass Infected with Acremonium lolii

1 reference

https://api.crossref.org/works/10.1016%2FS0099-9598%2803%2960002-7

7 January 2021

Structure Elucidation of Lolitrem F, a Naturally Occurring Stereoisomer of the Tremorgenic Mycotoxin Lolitrem B, Isolated fromLolium perenneInfected withAcremonium lolii

1 reference

https://api.crossref.org/works/10.1016%2FS0099-9598%2803%2960002-7

7 January 2021

Large-Scale Isolation of Lolitrem B and Structure Determination of Lolitrem E

1 reference

https://api.crossref.org/works/10.1016%2FS0099-9598%2803%2960002-7

7 January 2021

Rapid determination of the neurotoxin lolitrem B in perennial ryegrass by high-performance liquid chromatography with fluorescence detection

1 reference

https://api.crossref.org/works/10.1016%2FS0099-9598%2803%2960002-7

7 January 2021

Nodulisporic acid: its chemistry and biology

1 reference

https://api.crossref.org/works/10.1016%2FS0099-9598%2803%2960002-7

7 January 2021

Nodulisporic Acid A, a Novel and Potent Insecticide from aNodulisporiumSp. Isolation, Structure Determination, and Chemical Transformations

1 reference

https://api.crossref.org/works/10.1016%2FS0099-9598%2803%2960002-7

7 January 2021

Isolation and structure of nodulisporic acid A1 and A2, novel insecticides from a Nodulisporium sp.

1 reference

https://api.crossref.org/works/10.1016%2FS0099-9598%2803%2960002-7

7 January 2021

Nodulisporic acid B, B1, and B2: a series of 1'-deoxy-nodulisporic acids from Nodulisporium sp.

1 reference

https://api.crossref.org/works/10.1016%2FS0099-9598%2803%2960002-7

7 January 2021

Nodulisporic acids C, C1, and C2: a series of D-ring-opened nodulisporic acids from the fungus Nodulisporium sp

1 reference

https://api.crossref.org/works/10.1016%2FS0099-9598%2803%2960002-7

7 January 2021

Synthesis of side chain truncated 3"-aldehyde, 3"-carboxylic acid, and 1"-aldehyde from nodulisporic acid A.

1 reference

https://api.crossref.org/works/10.1016%2FS0099-9598%2803%2960002-7

7 January 2021

Nodulisporic acid side-chain modifications: access to the 2", 3", 4", and 6" registers.

1 reference

https://api.crossref.org/works/10.1016%2FS0099-9598%2803%2960002-7

7 January 2021

Side-chain homologation of nodulisporic acid: synthesis of potent new dienyl derivatives

1 reference

https://api.crossref.org/works/10.1016%2FS0099-9598%2803%2960002-7

7 January 2021

Synthesis of nodulisporic acid 2' '-oxazoles and 2' '-thiazoles.

1 reference

https://api.crossref.org/works/10.1016%2FS0099-9598%2803%2960002-7

7 January 2021

Chemical modification of nodulisporic acid A: preliminary structure-activity relationships.

1 reference

https://api.crossref.org/works/10.1016%2FS0099-9598%2803%2960002-7

7 January 2021

Nodulisporic acid opens insect glutamate-gated chloride channels: identification of a new high affinity modulator.

1 reference

https://api.crossref.org/works/10.1016%2FS0099-9598%2803%2960002-7

7 January 2021

Drug-resistant Drosophila indicate glutamate-gated chloride channels are targets for the antiparasitics nodulisporic acid and ivermectin.

1 reference

https://api.crossref.org/works/10.1016%2FS0099-9598%2803%2960002-7

7 January 2021

Ivermectin and nodulisporic acid receptors in Drosophila melanogaster contain both gamma-aminobutyric acid-gated Rdl and glutamate-gated GluCl alpha chloride channel subunits

1 reference

https://api.crossref.org/works/10.1016%2FS0099-9598%2803%2960002-7

7 January 2021

Comparison of nodulisporic acid analogs in a Lucilia sericata in vitro assay and a Ctenocephalides felis membrane feeding system.

1 reference

https://api.crossref.org/works/10.1016%2FS0099-9598%2803%2960002-7

7 January 2021

Systemic efficacy of nodulisporamides against fleas on dogs.

1 reference

https://api.crossref.org/works/10.1016%2FS0099-9598%2803%2960002-7

7 January 2021

Asymmetric synthesis of bicyclic intermediates of natural product chemistry

1 reference

https://api.crossref.org/works/10.1016%2FS0099-9598%2803%2960002-7

7 January 2021

Dipyridine-chromium(VI) oxide oxidation of alcohols in dichloromethane

1 reference

https://api.crossref.org/works/10.1016%2FS0099-9598%2803%2960002-7

7 January 2021

PERIODATE–PERMANGANATE OXIDATIONS: I. OXIDATION OF OLEFINS

1 reference

https://api.crossref.org/works/10.1016%2FS0099-9598%2803%2960002-7

7 January 2021

Sulfur trioxide in the oxidation of alcohols by dimethyl sulfoxide

1 reference

https://api.crossref.org/works/10.1016%2FS0099-9598%2803%2960002-7

7 January 2021

Organoselenium chemistry. A facile one-step synthesis of alkyl aryl selenides from alcohols

1 reference

https://api.crossref.org/works/10.1016%2FS0099-9598%2803%2960002-7

7 January 2021

Nodulisporic acid A synthetic studies. 1. Overall strategy and construction of a western hemisphere subtarget

1 reference

https://api.crossref.org/works/10.1016%2FS0099-9598%2803%2960002-7

7 January 2021

Nodulisporic acid A synthetic studies. 2. Construction of an eastern hemisphere subtarget

1 reference

https://api.crossref.org/works/10.1016%2FS0099-9598%2803%2960002-7

7 January 2021

Pyridine-derived triflating reagents: An improved preparation of vinyl triflates from metallo enolates

1 reference

https://api.crossref.org/works/10.1016%2FS0099-9598%2803%2960002-7

7 January 2021

Studies on fungal products. Part 19. Isolation and structure of a novel indoloditerpene, emindole SA, from Emericella striata

1 reference

https://api.crossref.org/works/10.1016%2FS0099-9598%2803%2960002-7

7 January 2021

Studies on fungal products. Part 17. Isolation and structures of novel indoloditerpenes, emindoles DA and DB, from Emericella desertorum: X-ray molecular structure of emindole DA acetate

1 reference

https://api.crossref.org/works/10.1016%2FS0099-9598%2803%2960002-7

7 January 2021

Paxilline-negative mutants of Penicillium paxilli generated by heterologous and homologous plasmid integration

1 reference

https://api.crossref.org/works/10.1016%2FS0099-9598%2803%2960002-7

7 January 2021

Molecular cloning and genetic analysis of an indole-diterpene gene cluster from Penicillium paxilli

1 reference

https://api.crossref.org/works/10.1016%2FS0099-9598%2803%2960002-7

7 January 2021

https://api.crossref.org/works/10.1016%2FS0099-9598%2803%2960002-7

1 reference

7 January 2021

Biosynthesis of nodulisporic acid A: precursor studies

1 reference

https://api.crossref.org/works/10.1016%2FS0099-9598%2803%2960002-7

7 January 2021

Molecular Pharmacology

49

35

319

Yao

1989

1 reference

https://api.crossref.org/works/10.1016/S0099-9598(03)60002-7

Structure and biosynthesis of the penitrems A–F, six novel tremorgenic mycotoxins from Penicillium crustosum

27 March 2024

series ordinal

57

1 reference

https://api.crossref.org/works/10.1016/S0099-9598(03)60002-7

27 March 2024

110

62

373

Robinson

1962

1 reference

https://api.crossref.org/works/10.1016/S0099-9598(03)60002-7

Journal of the Chemical Society

27 March 2024

113

1091

Kirk

1962

1 reference

https://api.crossref.org/works/10.1016/S0099-9598(03)60002-7

High-field FT NMR application of Mosher's method. The absolute configurations of marine terpenoids

27 March 2024

series ordinal

151

1 reference

https://api.crossref.org/works/10.1016/S0099-9598(03)60002-7

Journal of General Microbiology

27 March 2024

158

135

2679

Laws

1989

1 reference

https://api.crossref.org/works/10.1016/S0099-9598(03)60002-7

27 March 2024

Identifiers

1 reference

8 August 2017

1 reference