Page last updated: 2024-11-11

muscalure

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

Description

muscalure: sex sttractant pheromone of housefly with formula C24H48, alkene hydrocarbon; RN given refers to cpd with unspecified stereochemistry; structure [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID5365075
CHEMBL ID1894305
CHEBI ID194482
MeSH IDM0044712

Synonyms (43)

Synonym
9-tricosene, (z)-
(z)-9-tricosene
(z)-9-tricosene, 97%
NCGC00163763-01
brn 1841622
einecs 248-505-7
caswell no. 883c
ai3-35349
muscalure
9-tricosene, (9z)-
muscamone
ent 35349
epa pesticide chemical code 103201
cis-tricos-9-ene
cis-9-tricosene ,
27519-02-4
z-9-tricosene
T1242
CHEBI:194482
(z)-tricos-9-ene
9z-tricosene
LMFA11000117
A819098
unii-6bsp6hfw73
6bsp6hfw73 ,
AM84868
tricosene, z-9-
muscalure [mi]
(9z)-9-tricosene
(9z)-9-tricosene #
CHEMBL1894305
(9z)-tricosene
(9z)-tricos-9-ene
AKOS024462408
DTXSID0032653
muscalure, pestanal(r), analytical standard
J-016797
AS-14813
Q135445
9z-tricosene cas 27519-02-4
PD057642
HY-W009165
CS-W009881
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Drug Classes (1)

ClassDescription
tricoseneAn alkene that is tricosane carrying 1 double bond (the position of the double bond is unspecified).
[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
(Z)-9-tricosene biosynthesis010

Protein Targets (3)

Potency Measurements

ProteinTaxonomyMeasurementAverage (µ)Min (ref.)Avg (ref.)Max (ref.)Bioassay(s)
farnesoid X nuclear receptorHomo sapiens (human)Potency0.00100.375827.485161.6524AID588527
vitamin D (1,25- dihydroxyvitamin D3) receptorHomo sapiens (human)Potency0.00140.023723.228263.5986AID588543
thyroid hormone receptor beta isoform aHomo sapiens (human)Potency44.66840.010039.53711,122.0200AID588547
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (18)

TimeframeStudies, This Drug (%)All Drugs %
pre-19903 (16.67)18.7374
1990's6 (33.33)18.2507
2000's3 (16.67)29.6817
2010's6 (33.33)24.3611
2020's0 (0.00)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 35.09

According to the monthly volume, diversity, and competition of internet searches for this compound, as well the volume and growth of publications, there is estimated to be strong demand-to-supply ratio for research on this compound.

MetricThis Compound (vs All)
Research Demand Index35.09 (24.57)
Research Supply Index2.94 (2.92)
Research Growth Index4.67 (4.65)
Search Engine Demand Index43.31 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (35.09)

All Compounds (24.57)

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%
Other18 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]