Page last updated: 2024-11-07

cholesta-5,8-dien-3 beta-ol

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

Description

cholesta-5,8-dien-3 beta-ol: found in tissue of rats given AY 9944 [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID129846
CHEBI ID89982
SCHEMBL ID2106790
MeSH IDM0086639

Synonyms (29)

Synonym
cholesta-5,8-dien-3beta-ol
8-dehydrocholesterol
70741-38-7
cholesta-5,8-dien-3 beta-ol
LMST01010242
8-dhc
(3s,10s,13r,14r,17r)-10,13-dimethyl-17-[(2r)-6-methylheptan-2-yl]-2,3,4,7,11,12,14,15,16,17-decahydro-1h-cyclopenta[a]phenanthren-3-ol
unii-r85ba49sys
cholesta-5,8-dien-3-ol, (3beta)-
(3beta)-cholesta-5,8-dien-3-ol
r85ba49sys ,
cholesta-5,8-dien-3-ol,(3b)-
VUKORTMHZDZZFR-BXAZICILSA-N
cholesta-5,8-dien-3b-ol
SCHEMBL2106790
8(9)-dehydrocholesterol
CHEBI:89982
AKOS030255165
3b-cholesta-5,8-dien-3-ol
Q27162187
(3.beta.)-cholesta-5,8-dien-3-ol
cholesta-5,8-dien-3-ol, (3.beta.)-
CS-0059524
HY-113435
F82237
MS-26338
VCA74138
DTXSID801315054
PD086660
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Drug Classes (1)

ClassDescription
steroidAny of naturally occurring compounds and synthetic analogues, based on the cyclopenta[a]phenanthrene carbon skeleton, partially or completely hydrogenated; there are usually methyl groups at C-10 and C-13, and often an alkyl group at C-17. By extension, one or more bond scissions, ring expansions and/or ring contractions of the skeleton may have occurred. Natural steroids are derived biogenetically from squalene which is a triterpene.
[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 (24)

PathwayProteinsCompounds
Steroid Biosynthesis2142
Smith-Lemli-Opitz Syndrome (SLOS)2142
CHILD Syndrome2142
Desmosterolosis2142
Chondrodysplasia Punctata II, X-Linked Dominant (CDPX2)2142
Lysosomal Acid Lipase Deficiency (Wolman Disease)2142
Ibandronate Action Pathway2143
Simvastatin Action Pathway2143
Pravastatin Action Pathway2143
Rosuvastatin Action Pathway2143
Alendronate Action Pathway2143
Hypercholesterolemia2142
Lovastatin Action Pathway2143
Zoledronate Action Pathway2143
Cerivastatin Action Pathway2143
Risedronate Action Pathway2143
Pamidronate Action Pathway2143
Fluvastatin Action Pathway2143
Atorvastatin Action Pathway2143
Cholesteryl Ester Storage Disease2142
Hyper-IgD Syndrome2142
Mevalonic Aciduria2142
Wolman Disease2142
Cholesterol biosynthesis with skeletal dysplasias014

Research

Studies (34)

TimeframeStudies, This Drug (%)All Drugs %
pre-19901 (2.94)18.7374
1990's8 (23.53)18.2507
2000's16 (47.06)29.6817
2010's9 (26.47)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: 11.84

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 weak demand-to-supply ratio for research on this compound.

MetricThis Compound (vs All)
Research Demand Index11.84 (24.57)
Research Supply Index3.64 (2.92)
Research Growth Index5.48 (4.65)
Search Engine Demand Index0.00 (26.88)
Search Engine Supply Index0.00 (0.95)

This Compound (11.84)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials1 (2.78%)5.53%
Reviews3 (8.33%)6.00%
Case Studies10 (27.78%)4.05%
Observational0 (0.00%)0.25%
Other22 (61.11%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]