Page last updated: 2024-12-08

5-heptadecylresorcinol

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

Description

5-heptadecylresorcinol : A 5-alkylresorcinol that is resorcinol which is substituted by a heptadecyl group at position 5. It is found in wheat bran. [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 CID181700
CHEMBL ID497530
CHEBI ID145967
SCHEMBL ID1914183

Synonyms (25)

Synonym
5-heptadecylbenzene-1,3-diol
CHEMBL497530
1,3-dihydroxy-5-n-heptadecylbenzene
CHEBI:145967
5-heptadecyl-1,3-dihydroxybenzene
5-heptadecyl-1,3-benzenediol
41442-57-3
5-n-heptadecylresorcinol
5-heptadecylresorcinol
unii-mxe8zpj5xe
mxe8zpj5xe ,
1,3-benzenediol, 5-heptadecyl-
SCHEMBL1914183
AKOS022184647
LMPK15030003
5-heptadecylresorcinol, analytical standard
DTXSID50920522
FS-9410
1,3-dihydroxy-5-heptadecylbenzene
AMY37952
5-heptadecyl-1,3-benzenediol; 1,3-dihydroxy-5-heptadecylbenzene; 5-heptadecylresorcinol
1,3-dihydroxy-5-heptadecylbenzen;
A873058
CS-0023110
HY-N2673

Research Excerpts

Bioavailability

ExcerptReferenceRelevance
" However, the low bioavailability of AR-C17 due to its low water solubility restricts its application."( Quercetin Enhances the Availability of 5-Heptadecylresorcinol by Inhibiting the Expression of P-gp.
Fan, M; Jiang, L; Li, Y; Pan, W; Qian, H; Wang, L; Zhang, K, 2023
)
1.18
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Roles (2)

RoleDescription
antineoplastic agentA substance that inhibits or prevents the proliferation of neoplasms.
plant metaboliteAny eukaryotic metabolite produced during a metabolic reaction in plants, the kingdom that include flowering plants, conifers and other gymnosperms.
[role 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]

Drug Classes (1)

ClassDescription
5-alkylresorcinolA resorcinol compound having an alkyl substituent at the 5-position.
[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 (6)

Assay IDTitleYearJournalArticle
AID376620Antimicrobial activity against Candida albicans ATCC 90028 by broth dilution method2006Journal of natural products, Apr, Volume: 69, Issue:4
5-alkylresorcinols from Merulius incarnatus.
AID604333Growth inhibition of human HCT116 cells after 48 hrs by MTT assay2011Bioorganic & medicinal chemistry, Jul-01, Volume: 19, Issue:13
5-alk(en)ylresorcinols as the major active components in wheat bran inhibit human colon cancer cell growth.
AID376623Antimicrobial activity against Aspergillus fumigatus ATCC 90906 by broth dilution method2006Journal of natural products, Apr, Volume: 69, Issue:4
5-alkylresorcinols from Merulius incarnatus.
AID376621Antimicrobial activity against Candida glabrata ATCC 90030 by broth dilution method2006Journal of natural products, Apr, Volume: 69, Issue:4
5-alkylresorcinols from Merulius incarnatus.
AID376622Antimicrobial activity against Candida krusei ATCC 6258 by broth dilution method2006Journal of natural products, Apr, Volume: 69, Issue:4
5-alkylresorcinols from Merulius incarnatus.
AID604334Growth inhibition of human HT-29 cells after 48 hrs by MTT assay2011Bioorganic & medicinal chemistry, Jul-01, Volume: 19, Issue:13
5-alk(en)ylresorcinols as the major active components in wheat bran inhibit human colon cancer cell growth.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (10)

TimeframeStudies, This Drug (%)All Drugs %
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's1 (10.00)29.6817
2010's1 (10.00)24.3611
2020's8 (80.00)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 13.00

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 Index13.00 (24.57)
Research Supply Index2.40 (2.92)
Research Growth Index5.40 (4.65)
Search Engine Demand Index0.00 (26.88)
Search Engine Supply Index0.00 (0.95)

This Compound (13.00)

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%
Other10 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]