Page last updated: 2024-11-12

glutinol

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

Description

glutinol: from a medicinal lichen, Usnea longissima; structure in first source [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

glutinol : A pentacyclic triterpenoid that is picene which has been fully hydrogenated except for a double bond between the 4a and 5 positions and is substituted by methyl groups at the 4, 4, 6bbeta, 8abeta, 11, 11, 12balpha and 14bbeta positions, and by a hydroxy group at the 3beta position. [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 CID9932254
CHEMBL ID452242
CHEBI ID63462
SCHEMBL ID3132609
MeSH IDM0493248

Synonyms (23)

Synonym
bdbm50242217
glut-5-en-3-ol
chebi:63462 ,
glutinol
CHEMBL452242 ,
glut-5-en-3beta-ol
3beta-hydroxy-5-glutinene
545-24-4
d:b-friedoolean-5-en-3beta-ol
epi-alnusenol
C20188
glutin-5-en-3beta-ol
3beta-hydroxyglutin-5-ene
(3s,6as,6br,8ar,12ar,12bs,14ar,14bs)-4,4,6b,8a,11,11,12b,14a-octamethyl-1,2,3,4,6,6a,6b,7,8,8a,9,10,11,12,12a,12b,13,14,14a,14b-icosahydropicen-3-ol
3beta-hydroxy-d:b-friedoolean-5-ene
SCHEMBL3132609
5-glutinen-3-ol
DTXSID60202902
AKOS032948410
Q27132635
(3s,6as,6as,6br,8ar,12ar,14ar,14bs)-4,4,6a,6b,8a,11,11,14a-octamethyl-1,2,3,6,6a,7,8,9,10,12,12a,13,14,14b-tetradecahydropicen-3-ol
d:b-friedoolean-5-en-3-ol, (3)-; d:b-friedoolean-5-en-3-ol ; glutin-5-en-3-ol
FS-10002
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Drug Classes (2)

ClassDescription
pentacyclic triterpenoid
secondary alcoholA secondary alcohol is a compound in which a hydroxy group, -OH, is attached to a saturated carbon atom which has two other carbon atoms attached to it.
[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
pentacyclic triterpene biosynthesis210
pentacyclic triterpene biosynthesis1411

Protein Targets (1)

Inhibition Measurements

ProteinTaxonomyMeasurementAverageMin (ref.)Avg (ref.)Max (ref.)Bioassay(s)
Nitric oxide synthase, inducibleMus musculus (house mouse)IC50 (µMol)50.00000.00103.39119.6000AID344829
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023]

Bioassays (23)

Assay IDTitleYearJournalArticle
AID344828Inhibition of NADPH oxidase in LPS-induced mouse BV2 cells assessed as NOX-dependent ROS production at 50 uM2008Bioorganic & medicinal chemistry, Nov-15, Volume: 16, Issue:22
New diterpenoids and the bioactivity of Erythrophleum fordii.
AID356090Cytotoxicity against human KATO III cells by MTT assay2003Journal of natural products, Jul, Volume: 66, Issue:7
Cytotoxic diterpenes from Scoparia dulcis.
AID344829Inhibition of iNOS-mediated NO production in LPS-induced mouse BV2 cells2008Bioorganic & medicinal chemistry, Nov-15, Volume: 16, Issue:22
New diterpenoids and the bioactivity of Erythrophleum fordii.
AID466797Growth inhibition of human SKOV3 cells by MTT assay2010Bioorganic & medicinal chemistry letters, Mar-01, Volume: 20, Issue:5
Triterpene compounds isolated from Acer mandshuricum and their anti-inflammatory activity.
AID356087Cytotoxicity against human SCL6 cells by MTT assay2003Journal of natural products, Jul, Volume: 66, Issue:7
Cytotoxic diterpenes from Scoparia dulcis.
AID375387Cytotoxicity against human MCF7 cells by MTT assay2009Bioorganic & medicinal chemistry letters, Jul-01, Volume: 19, Issue:13
The regulation of inflammatory cytokine secretion in macrophage cell line by the chemical constituents of Rhus sylvestris.
AID1696173Antibacterial activity against Streptococcus sobrinus 6715 assessed as reduction in bacterial growth incubated for 24 hrs by INT dye based broth dilution method2020Journal of natural products, 07-24, Volume: 83, Issue:7
Garcinoic Acids and a Benzophenone Derivative from the Seeds of
AID466796Growth inhibition of human HL60 cells by MTT assay2010Bioorganic & medicinal chemistry letters, Mar-01, Volume: 20, Issue:5
Triterpene compounds isolated from Acer mandshuricum and their anti-inflammatory activity.
AID466798Growth inhibition of human A549 cells by MTT assay2010Bioorganic & medicinal chemistry letters, Mar-01, Volume: 20, Issue:5
Triterpene compounds isolated from Acer mandshuricum and their anti-inflammatory activity.
AID1696171Antibacterial activity against Porphyromonas gingivalis ATCC 33277 assessed as reduction in bacterial growth incubated for 24 hrs by INT dye based broth dilution method2020Journal of natural products, 07-24, Volume: 83, Issue:7
Garcinoic Acids and a Benzophenone Derivative from the Seeds of
AID356091Cytotoxicity against human NUGC4 cells by MTT assay2003Journal of natural products, Jul, Volume: 66, Issue:7
Cytotoxic diterpenes from Scoparia dulcis.
AID375389Antiinflammatory activity in mouse RAW264.7 cells assessed as inhibition LPS-induced TNFalpha secretion at 0.01 uM after 12 hrs2009Bioorganic & medicinal chemistry letters, Jul-01, Volume: 19, Issue:13
The regulation of inflammatory cytokine secretion in macrophage cell line by the chemical constituents of Rhus sylvestris.
AID375391Antiinflammatory activity in mouse RAW264.7 cells assessed as inhibition LPS-induced IL6 secretion at 1 uM after 12 hrs2009Bioorganic & medicinal chemistry letters, Jul-01, Volume: 19, Issue:13
The regulation of inflammatory cytokine secretion in macrophage cell line by the chemical constituents of Rhus sylvestris.
AID1327077Neuroprotective activity in human SH-SY5Y cells assessed as reduction in 6-OHDA-induced cell death measured after 24 hrs by MTT assay2016Journal of natural products, 08-26, Volume: 79, Issue:8
Chemical Constituents Isolated from the Root Bark of Cudrania tricuspidata and Their Potential Neuroprotective Effects.
AID375388Cytotoxicity against human SK-MEL-1 cells by MTT assay2009Bioorganic & medicinal chemistry letters, Jul-01, Volume: 19, Issue:13
The regulation of inflammatory cytokine secretion in macrophage cell line by the chemical constituents of Rhus sylvestris.
AID466801Antiinflammatory activity in mouse RAW264.7 cells assessed as inhibition of LPS-stimulated TNFalpha production at 100 nM pretreated 1 hr before LPS challenge measured after 24 hrs by sandwich ELISA relative to control2010Bioorganic & medicinal chemistry letters, Mar-01, Volume: 20, Issue:5
Triterpene compounds isolated from Acer mandshuricum and their anti-inflammatory activity.
AID356089Cytotoxicity against human SCL9 cells by MTT assay2003Journal of natural products, Jul, Volume: 66, Issue:7
Cytotoxic diterpenes from Scoparia dulcis.
AID375386Cytotoxicity against human HeLa cells by MTT assay2009Bioorganic & medicinal chemistry letters, Jul-01, Volume: 19, Issue:13
The regulation of inflammatory cytokine secretion in macrophage cell line by the chemical constituents of Rhus sylvestris.
AID1696172Bactericidal activity against Porphyromonas gingivalis ATCC 33277 assessed as reduction in bacterial growth incubated for 48 hrs by INT dye based broth dilution method2020Journal of natural products, 07-24, Volume: 83, Issue:7
Garcinoic Acids and a Benzophenone Derivative from the Seeds of
AID466799Growth inhibition of human HT-29 cells by MTT assay2010Bioorganic & medicinal chemistry letters, Mar-01, Volume: 20, Issue:5
Triterpene compounds isolated from Acer mandshuricum and their anti-inflammatory activity.
AID1696174Bactericidal activity against Streptococcus sobrinus 6715 assessed as reduction in bacterial growth incubated for 48 hrs by INT dye based broth dilution method2020Journal of natural products, 07-24, Volume: 83, Issue:7
Garcinoic Acids and a Benzophenone Derivative from the Seeds of
AID356086Cytotoxicity against human SCL cells by MTT assay2003Journal of natural products, Jul, Volume: 66, Issue:7
Cytotoxic diterpenes from Scoparia dulcis.
AID356088Cytotoxicity against human SCL37'6 cells by MTT assay2003Journal of natural products, Jul, Volume: 66, Issue:7
Cytotoxic diterpenes from Scoparia dulcis.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (13)

TimeframeStudies, This Drug (%)All Drugs %
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's5 (38.46)29.6817
2010's5 (38.46)24.3611
2020's3 (23.08)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 29.05

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

MetricThis Compound (vs All)
Research Demand Index29.05 (24.57)
Research Supply Index2.64 (2.92)
Research Growth Index4.50 (4.65)
Search Engine Demand Index34.37 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (29.05)

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%
Other13 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]