Page last updated: 2024-12-11

helichrysetin

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

Description

helichrysetin: isolated from Helichrysum odoratissimum; RN from CA Index Guide 1986; RN given refers to (E)-isomer; RN for cpd without isomeric designation not avail. 10/89 [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

FloraRankFlora DefinitionFamilyFamily Definition
HelichrysumgenusA plant genus of the family ASTERACEAE. Members contain CHALCONE, helichrysetin, arenarin, and flamin.[MeSH]AsteraceaeA large plant family of the order Asterales, subclass Asteridae, class Magnoliopsida. The family is also known as Compositae. Flower petals are joined near the base and stamens alternate with the corolla lobes. The common name of daisy refers to several genera of this family including Aster; CHRYSANTHEMUM; RUDBECKIA; TANACETUM.[MeSH]

Cross-References

ID SourceID
PubMed CID6253344
CHEMBL ID507998
CHEBI ID178332
SCHEMBL ID2126372
MeSH IDM0169289

Synonyms (24)

Synonym
CHEBI:178332
62014-87-3
(e)-1-(2,4-dihydroxy-6-methoxyphenyl)-3-(4-hydroxyphenyl)prop-2-en-1-one
2-propen-1-one, 1-(2,4-dihydroxy-6-methoxyphenyl)-3-(4-hydroxyphenyl)-, (2e)-
helichrysetin
(e)-1-(2,4-dihydroxy-6-methoxy-phenyl)-3-(4-hydroxyphenyl)prop-2-en-1-one
LMPK12120300
4,2',4'-trihydroxy-6'-methoxychalcone
CHEMBL507998
helichysetin
SCHEMBL2126372
mj0kmg7aw4 ,
2-propen-1-one, 1-(2,4-dihydroxy-6-methoxyphenyl)-3-(4-hydroxyphenyl)-
unii-mj0kmg7aw4
1-(2,4-dihydroxy-6-methoxyphenyl)-3-(4-hydroxyphenyl)-2-propen-1-one
1-(2,4-dihydroxy-6-methoxy-phenyl)-3-(4-hydroxy-phenyl)-propenone
mfcd12546716
AKOS032948840
HY-N4058
CS-0024563
(2e)-1-(2,4-dihydroxy-6-methoxyphenyl)-3-(4-hydroxyphenyl)-2-propen-1-one
MS-24082
(2e)-1-(2,4-dihydroxy-6-methoxyphenyl)-3-(4-hydroxyphenyl)prop-2-en-1-one
DTXSID001317482
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Drug Classes (1)

ClassDescription
chalconesA ketone that is 1,3-diphenylpropenone (benzylideneacetophenone), ArCH=CH(=O)Ar, and its derivatives formed by substitution.
[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 (16)

Assay IDTitleYearJournalArticle
AID383191Antioxidant activity assessed as trolox equivalent at 0.1 to 1 uM by ORAC-fluorescein assay2008Bioorganic & medicinal chemistry, Apr-15, Volume: 16, Issue:8
Natural and non-natural prenylated chalcones: synthesis, cytotoxicity and anti-oxidative activity.
AID358853Antiproliferative activity against human HT1080 cells by MTT assay2001Journal of natural products, Mar, Volume: 64, Issue:3
Six new diarylheptanoids from the seeds of Alpinia blepharocalyx.
AID358852Antiproliferative activity against mouse Colon 26-L5 cells by MTT assay2001Journal of natural products, Mar, Volume: 64, Issue:3
Six new diarylheptanoids from the seeds of Alpinia blepharocalyx.
AID1199603Cytotoxicity against human HepG2 cells assessed as inhibition of cell proliferation after 72 hrs by MTT assay2015Journal of medicinal chemistry, Feb-26, Volume: 58, Issue:4
Synthesis of xanthohumol analogues and discovery of potent thioredoxin reductase inhibitor as potential anticancer agent.
AID452945Antileishmanial activity against Leishmania amazonensis MHOM/BR/76/LTB-012 amastigotes infected in mouse macrophage by MTT assay2010Bioorganic & medicinal chemistry letters, Jan-01, Volume: 20, Issue:1
In vitro and in vivo anti-Leishmania activity of polysubstituted synthetic chalcones.
AID1199602Cytotoxicity against human HeLa cells assessed as inhibition of cell proliferation after 72 hrs by MTT assay2015Journal of medicinal chemistry, Feb-26, Volume: 58, Issue:4
Synthesis of xanthohumol analogues and discovery of potent thioredoxin reductase inhibitor as potential anticancer agent.
AID1537254Inhibition of TNFalpha/IL-1beta-induced NFkB p65 translocation from cytosol to nucleus in mouse MIN6 cells at 50 uM after 30 mins by immunofluorescence based high content imaging analysis2019Journal of natural products, 02-22, Volume: 82, Issue:2
Amides and Flavonoids from the Fruit and Leaf Extracts of Melodorum siamensis.
AID399390Antiplatelet activity in human whole blood assessed as inhibition of ristocetin-induced platelet aggregation at 100 ug/mL relative to control1998Journal of natural products, Jan, Volume: 61, Issue:1
A new antiplatelet diarylheptanoid from Alpinia blepharocalyx.
AID399389Antiplatelet activity in human whole blood assessed as inhibition of arachidonic acid-induced platelet aggregation at 100 ug/mL relative to control1998Journal of natural products, Jan, Volume: 61, Issue:1
A new antiplatelet diarylheptanoid from Alpinia blepharocalyx.
AID452949Selectivity index, ratio of IC50 for BALB/c macrophages to IC50 for Leishmania amazonensis (MHOM/BR/76/LTB-012)2010Bioorganic & medicinal chemistry letters, Jan-01, Volume: 20, Issue:1
In vitro and in vivo anti-Leishmania activity of polysubstituted synthetic chalcones.
AID399388Antiplatelet activity in human whole blood assessed as inhibition of ADP-induced platelet aggregation at 100 ug/mL relative to control1998Journal of natural products, Jan, Volume: 61, Issue:1
A new antiplatelet diarylheptanoid from Alpinia blepharocalyx.
AID383188Cytotoxicity against human HeLa cells by MTT assay2008Bioorganic & medicinal chemistry, Apr-15, Volume: 16, Issue:8
Natural and non-natural prenylated chalcones: synthesis, cytotoxicity and anti-oxidative activity.
AID1100871Antifeedant activity against Spodoptera litura in compound treated cork borer from fresh sweet potato leaves by Choice Leaf-Disk Bioassay2000Journal of agricultural and food chemistry, May, Volume: 48, Issue:5
Insect antifeedant flavonoids from Gnaphalium affine D. Don.
AID452948Toxicity against BALB/c mouse macrophage by MTT assay2010Bioorganic & medicinal chemistry letters, Jan-01, Volume: 20, Issue:1
In vitro and in vivo anti-Leishmania activity of polysubstituted synthetic chalcones.
AID399387Antiplatelet activity in human whole blood assessed as inhibition of collagen-induced platelet aggregation at 100 ug/mL relative to control1998Journal of natural products, Jan, Volume: 61, Issue:1
A new antiplatelet diarylheptanoid from Alpinia blepharocalyx.
AID1199601Cytotoxicity against human A549 cells assessed as inhibition of cell proliferation after 72 hrs by MTT assay2015Journal of medicinal chemistry, Feb-26, Volume: 58, Issue:4
Synthesis of xanthohumol analogues and discovery of potent thioredoxin reductase inhibitor as potential anticancer agent.
[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's1 (7.69)18.2507
2000's4 (30.77)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: 19.78

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 Index19.78 (24.57)
Research Supply Index2.71 (2.92)
Research Growth Index4.86 (4.65)
Search Engine Demand Index15.26 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (19.78)

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%
Other14 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]