Page last updated: 2024-12-05

lyngbyatoxin a

Description Research Excerpts Clinical Trials Roles Classes Pathways Study Profile Bioassays Related Drugs Related Conditions Protein Interactions Research Growth

Description

lyngbyatoxin A: indole alkaloid from blue-green alga Lyngbya majuscula Gomont; responsible for dermatitis known as swimmers' itch in Hawaii [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID91706
CHEMBL ID5172923
CHEBI ID192687
MeSH IDM0071927

Synonyms (25)

Synonym
teleocidin a
3h-pyrrolo(4,3,2-gh)-1,4-benzodiazonin-3-one, 1,2,4,5,6,8-hexahydro-9-(1-ethenyl-1,5-dimethyl-4-hexenyl)-5-(hydroxymethyl)-1-methyl-2-(1-methylethyl)-
teleocidin a 1
3h-pyrrolo(4,3,2-gh)-1,4-benzodiazonin-3-one, 9-(1-ethenyl-1,5-dimethyl-4-hexenyl)-1,2,4,5,6,8-hexahydro-5-(hydroxymethyl)-1-methyl-2-(1-methylethyl)-
ccris 4044
70497-14-2
lyngbyatoxin a
CHEBI:192687
unii-se69l721cs
se69l721cs ,
lyngbyatoxin-a
3h-pyrrolo(4,3,2-gh)-1,4-benzodiazonin-3-one, 9-((1r)-1-ethenyl-1,5-dimethyl-4-hexenyl)-1,2,4,5,6,8-hexahydro-5-(hydroxymethyl)-1-methyl-2-(1-methylethyl)-, (2s,5s)-
3h-pyrrolo(4,3,2-gh)-1,4-benzodiazonin-3-one, 9-(1-ethenyl-1,5-dimethyl-4-hexenyl)-1,2,4,5,6,8-hexahydro-5-(hydroxymethyl)-1-methyl-2-(1-methylethyl)-, (2s-(2r*,5r*,9(s*)))-
3h-pyrrolo(4,3,2-gh)-1,4-benzodiazonin-3-one, 9-((1r)-1-ethenyl-1,5-dimethyl-4-hexen-1-yl)-1,2,4,5,6,8-hexahydro-5-(hydroxymethyl)-1-methyl-2-(1-methylethyl)-, (2s,5s)-
teleocidin a-1
teleocidin a1
(2s,5s)-9-[(3r)-3,7-dimethylocta-1,6-dien-3-yl]-5-(hydroxymethyl)-1-methyl-2-(propan-2-yl)-1,2,4,5,6,8-hexahydro-3h-[1,4]diazonino[7,6,5-cd]indol-3-one
CHEMBL5172923
(2s,5s)-9-((r)-3,7-dimethylocta-1,6-dien-3-yl)-5-(hydroxymethyl)-2-isopropyl-1-methyl-4,5,6,8-tetrahydro-1h-[1,4]diazonino[7,6,5-cd]indol-3(2h)-one
DTXSID90880015
Q5934205
(10s,13s)-5-[(3r)-3,7-dimethylocta-1,6-dien-3-yl]-13-(hydroxymethyl)-9-methyl-10-propan-2-yl-3,9,12-triazatricyclo[6.6.1.04,15]pentadeca-1,4,6,8(15)-tetraen-11-one
HY-118834
CS-0068632
AKOS040752807

Research Excerpts

Dosage Studied

The epidermal surfaces were dosed with 26 micrograms lyngbyatoxin A/cm2 dissolved in 13 microliters dimethyl sulphoxide. The dose-response curves are virtually the same as the one previously described for [3H]12-O-tetradecanoylphorbol-13-acetate.

ExcerptRelevanceReference
" The epidermal surfaces were dosed with 26 micrograms lyngbyatoxin A/cm2 dissolved in 13 microliters dimethyl sulphoxide/cm2."( Comparison of the partition coefficient and skin penetration of a marine algal toxin (lyngbyatoxin A).
Kemppainen, BW; Mehta, M; Stafford, RG, 1992
)
0.28
" The dose-response curves for the binding of [3H]lyngbyatoxin A and [3H]debromoaplysiatoxin to a mouse epidermal particulate fraction are virtually the same as the one previously described for [3H]12-O-tetradecanoylphorbol-13-acetate ([3H]TPA)."( Binding studies of [3H]lyngbyatoxin A and [3H]debromoaplysiatoxin to the phorbol ester receptor in a mouse epidermal particulate fraction.
Entzeroth, M; Fujiki, H; Hakii, H; Moore, RE; Morimoto, H; Patterson, GM; Suganuma, M; Sugimura, T, 1986
)
0.27
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Drug Classes (1)

ClassDescription
indolesAny compound containing an indole skeleton.
[compound class information is derived from Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

Pathways (1)

PathwayProteinsCompounds
lyngbyatoxin biosynthesis418

Bioassays (4)

Assay IDTitleYearJournalArticle
AID1870485Inhibition of GLI in SAG induced mouse Sufu-KO-LIGHT cells assessed as residual Smo-independent Gli luciferase activity in starvation medium at 100 nM incubated for 30 hrs by dual luciferase assay2022ACS medicinal chemistry letters, Jul-14, Volume: 13, Issue:7
Indolactam Dipeptides as Nanomolar Gli Inhibitors.
AID1870480Inhibition of GLI in SAG induced mouse Shh Light II cells assessed as residual Smo-dependent Gli luciferase activity in starvation medium incubated for 30 hrs by dual luciferase assay2022ACS medicinal chemistry letters, Jul-14, Volume: 13, Issue:7
Indolactam Dipeptides as Nanomolar Gli Inhibitors.
AID1870484Inhibition of GLI in SAG induced mouse Sufu-KO-LIGHT cells assessed as residual Smo-independent Gli luciferase activity in starvation medium incubated for 30 hrs by dual luciferase assay2022ACS medicinal chemistry letters, Jul-14, Volume: 13, Issue:7
Indolactam Dipeptides as Nanomolar Gli Inhibitors.
AID1870481Inhibition of GLI in SAG induced mouse Shh Light II cells assessed as residual Smo-dependent Gli luciferase activity in starvation medium at 100 nM incubated for 30 hrs by dual luciferase assay2022ACS medicinal chemistry letters, Jul-14, Volume: 13, Issue:7
Indolactam Dipeptides as Nanomolar Gli Inhibitors.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (38)

TimeframeStudies, This Drug (%)All Drugs %
pre-199016 (42.11)18.7374
1990's6 (15.79)18.2507
2000's4 (10.53)29.6817
2010's9 (23.68)24.3611
2020's3 (7.89)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews3 (7.89%)6.00%
Case Studies1 (2.63%)4.05%
Observational0 (0.00%)0.25%
Other34 (89.47%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]