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hapalindole u

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

Description

hapalindole U: structure in first source [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

hapalindole U : A hapalindole that is hapalindole H in which the octahydronaphthalene ring junction carbons both have S configuration instead of R. [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]

Cross-References

ID SourceID
PubMed CID16069589
CHEMBL ID2071364
CHEBI ID141613
MeSH IDM0508465

Synonyms (11)

Synonym
hapalindole u
106928-30-7
CHEBI:141613
(6as,9r,10r,10as)-10-isocyano-6,6,9-trimethyl-9-vinyl-2,6,6a,7,8,9,10,10a-octahydronaphtho[1,2,3-cd]indole
CHEMBL2071364
8p6 ,
C21973
DTXSID601316244
(-)-hapalindole u
[6as,(+)]-9alpha-ethenyl-2,6,6aalpha,7,8,9,10,10abeta-octahydro-10alpha-isocyano-6,6,9-trimethylnaphtho[1,2,3-cd]in
(2s,3r,4r,7s)-4-ethenyl-3-isocyano-4,8,8-trimethyl-14-azatetracyclo[7.6.1.02,7.013,16]hexadeca-1(15),9(16),10,12-tetraene
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Drug Classes (3)

ClassDescription
isocyanideThe isomer HN(+)#C(-) of hydrocyanic acid, HC#N, and its hydrocarbyl derivatives RNC (RN(+)#C(-)).
organic heterotetracyclic compound
hapalindoleAny member of large group of hapalindole-type alkaloids that are bioactive metabolites of the Subsection V (formerly order Stigonematales)in the phylum Cyanobacteria which have either a tetracyclic structure based on 10-isocyano-6,6,9-trimethyl-9-vinyl-2,6,6a,7,8,9,10,10a-octahydronaphtho[1,2,3-cd]indole, or a tricyclic structure resulting from the cleavage of the bond linking the indole ring to the dimethyl-substituted carbon.
[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]

Bioassays (5)

Assay IDTitleYearJournalArticle
AID677136Cytotoxicity against human SF268 cells incubated for 3 days by SRB assay2012Bioorganic & medicinal chemistry, Sep-01, Volume: 20, Issue:17
Indole alkaloids from two cultured cyanobacteria, Westiellopsis sp. and Fischerella muscicola.
AID677133Cytotoxicity against human HT-29 cells by CellTiter 96 Aqueous One solution cell proliferation assay2012Bioorganic & medicinal chemistry, Sep-01, Volume: 20, Issue:17
Indole alkaloids from two cultured cyanobacteria, Westiellopsis sp. and Fischerella muscicola.
AID677135Cytotoxicity against human NCI-H460 cells incubated for 3 days by SRB assay2012Bioorganic & medicinal chemistry, Sep-01, Volume: 20, Issue:17
Indole alkaloids from two cultured cyanobacteria, Westiellopsis sp. and Fischerella muscicola.
AID677137Cytotoxicity against human IMR90 cells incubated for 3 days by SRB assay2012Bioorganic & medicinal chemistry, Sep-01, Volume: 20, Issue:17
Indole alkaloids from two cultured cyanobacteria, Westiellopsis sp. and Fischerella muscicola.
AID677134Cytotoxicity against human MCF7 cells incubated for 3 days by SRB assay2012Bioorganic & medicinal chemistry, Sep-01, Volume: 20, Issue:17
Indole alkaloids from two cultured cyanobacteria, Westiellopsis sp. and Fischerella muscicola.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (6)

TimeframeStudies, This Drug (%)All Drugs %
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's1 (16.67)29.6817
2010's4 (66.67)24.3611
2020's1 (16.67)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%
Reviews0 (0.00%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other6 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]