Page last updated: 2024-11-06

seselin

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

Description

Seselin is a naturally occurring coumarin found in various plants, including angelica, parsley, and celery. It exhibits diverse biological activities, including anti-inflammatory, antioxidant, and antimicrobial properties. Research suggests that seselin might have potential therapeutic benefits in conditions like cancer, neurodegenerative diseases, and cardiovascular disorders. Its synthesis is often achieved through chemical modification of other coumarin derivatives. The study of seselin is driven by its potential pharmacological applications and its role in understanding the complex biological interactions of coumarins in plants and humans.'

seselin: structure in first source [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID68229
CHEMBL ID71358
CHEBI ID69040
SCHEMBL ID8993385
MeSH IDM0506248

Synonyms (33)

Synonym
8,8-dimethyl-2h,8h-pyrano[2,3-f]chromen-2-one
pyranocoumarin deriv.
3',4'-di-o-(-)-camphanoyl-(+)-cis-khellactone
8,8-dimethylpyrano[2,3-f]chromen-2-one
523-59-1
seselin
C09312
OPREA1_187929
AKOS000276897
chebi:69040 ,
sesalin
CHEMBL71358 ,
HMS1648A10
bdbm50361397
5634e8957p ,
8,8-dimethyl-2h,8h-benzo(1,2-b:3,4-b')dipyran-2-one
2h,8h-benzo(1,2-b:3,4-b')dipyran-2-one, 8,8-dimethyl-
unii-5634e8957p
SCHEMBL8993385
seseline
amyrolin
2h,8h-benzo[1,2-b:3,4-b']dipyran-2-one, 8,8-dimethyl-
2h-1-benzopyran-6-acrylic acid, 5-hydroxy-2,2-dimethyl-, .delta.-lactone
8,8-dimethyl-2h,8h-pyrano[2,3-f]chromen-2-one #
QUVCQYQEIOLHFZ-UHFFFAOYSA-N
DTXSID60200322
8,8-dimethyl-2h,8h-benzo[1,2-b:3,4-b']dipyran-2-one
8,8-dimethyl-2h,8h-benzo[1,2-b:3,4-b']dipyran-2-one, 9ci
2',2'-dimethyl-3-pyreno[6'5:7,8]coumarin
Q27104968
8,8-dimethylpyrano[2,3-h]chromen-2-one
CS-0591374
HY-W505771
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Roles (1)

RoleDescription
metaboliteAny intermediate or product resulting from metabolism. The term 'metabolite' subsumes the classes commonly known as primary and secondary metabolites.
[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
coumarins
[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]

Protein Targets (2)

Inhibition Measurements

ProteinTaxonomyMeasurementAverageMin (ref.)Avg (ref.)Max (ref.)Bioassay(s)
Glyceraldehyde-3-phosphate dehydrogenaseHomo sapiens (human)IC50 (µMol)123.02706.00007.33338.0000AID75720
Beta-secretase 1Homo sapiens (human)IC50 (µMol)500.00000.00061.619410.0000AID637774
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023]

Biological Processes (33)

Processvia Protein(s)Taxonomy
microtubule cytoskeleton organizationGlyceraldehyde-3-phosphate dehydrogenaseHomo sapiens (human)
positive regulation of cytokine productionGlyceraldehyde-3-phosphate dehydrogenaseHomo sapiens (human)
glucose metabolic processGlyceraldehyde-3-phosphate dehydrogenaseHomo sapiens (human)
glycolytic processGlyceraldehyde-3-phosphate dehydrogenaseHomo sapiens (human)
negative regulation of endopeptidase activityGlyceraldehyde-3-phosphate dehydrogenaseHomo sapiens (human)
regulation of macroautophagyGlyceraldehyde-3-phosphate dehydrogenaseHomo sapiens (human)
negative regulation of translationGlyceraldehyde-3-phosphate dehydrogenaseHomo sapiens (human)
killing of cells of another organismGlyceraldehyde-3-phosphate dehydrogenaseHomo sapiens (human)
positive regulation of type I interferon productionGlyceraldehyde-3-phosphate dehydrogenaseHomo sapiens (human)
peptidyl-cysteine S-trans-nitrosylationGlyceraldehyde-3-phosphate dehydrogenaseHomo sapiens (human)
positive regulation of canonical NF-kappaB signal transductionGlyceraldehyde-3-phosphate dehydrogenaseHomo sapiens (human)
protein stabilizationGlyceraldehyde-3-phosphate dehydrogenaseHomo sapiens (human)
defense response to fungusGlyceraldehyde-3-phosphate dehydrogenaseHomo sapiens (human)
neuron apoptotic processGlyceraldehyde-3-phosphate dehydrogenaseHomo sapiens (human)
killing by host of symbiont cellsGlyceraldehyde-3-phosphate dehydrogenaseHomo sapiens (human)
antimicrobial humoral immune response mediated by antimicrobial peptideGlyceraldehyde-3-phosphate dehydrogenaseHomo sapiens (human)
cellular response to type II interferonGlyceraldehyde-3-phosphate dehydrogenaseHomo sapiens (human)
proteolysisBeta-secretase 1Homo sapiens (human)
membrane protein ectodomain proteolysisBeta-secretase 1Homo sapiens (human)
response to lead ionBeta-secretase 1Homo sapiens (human)
protein processingBeta-secretase 1Homo sapiens (human)
amyloid-beta formationBeta-secretase 1Homo sapiens (human)
amyloid precursor protein catabolic processBeta-secretase 1Homo sapiens (human)
positive regulation of neuron apoptotic processBeta-secretase 1Homo sapiens (human)
amyloid-beta metabolic processBeta-secretase 1Homo sapiens (human)
detection of mechanical stimulus involved in sensory perception of painBeta-secretase 1Homo sapiens (human)
prepulse inhibitionBeta-secretase 1Homo sapiens (human)
cellular response to copper ionBeta-secretase 1Homo sapiens (human)
cellular response to manganese ionBeta-secretase 1Homo sapiens (human)
presynaptic modulation of chemical synaptic transmissionBeta-secretase 1Homo sapiens (human)
signaling receptor ligand precursor processingBeta-secretase 1Homo sapiens (human)
cellular response to amyloid-betaBeta-secretase 1Homo sapiens (human)
amyloid fibril formationBeta-secretase 1Homo sapiens (human)
[Information is prepared from geneontology information from the June-17-2024 release]

Molecular Functions (16)

Processvia Protein(s)Taxonomy
glyceraldehyde-3-phosphate dehydrogenase (NAD+) (phosphorylating) activityGlyceraldehyde-3-phosphate dehydrogenaseHomo sapiens (human)
protein bindingGlyceraldehyde-3-phosphate dehydrogenaseHomo sapiens (human)
microtubule bindingGlyceraldehyde-3-phosphate dehydrogenaseHomo sapiens (human)
aspartic-type endopeptidase inhibitor activityGlyceraldehyde-3-phosphate dehydrogenaseHomo sapiens (human)
peptidyl-cysteine S-nitrosylase activityGlyceraldehyde-3-phosphate dehydrogenaseHomo sapiens (human)
identical protein bindingGlyceraldehyde-3-phosphate dehydrogenaseHomo sapiens (human)
NADP bindingGlyceraldehyde-3-phosphate dehydrogenaseHomo sapiens (human)
NAD bindingGlyceraldehyde-3-phosphate dehydrogenaseHomo sapiens (human)
disordered domain specific bindingGlyceraldehyde-3-phosphate dehydrogenaseHomo sapiens (human)
amyloid-beta bindingBeta-secretase 1Homo sapiens (human)
endopeptidase activityBeta-secretase 1Homo sapiens (human)
aspartic-type endopeptidase activityBeta-secretase 1Homo sapiens (human)
protein bindingBeta-secretase 1Homo sapiens (human)
peptidase activityBeta-secretase 1Homo sapiens (human)
beta-aspartyl-peptidase activityBeta-secretase 1Homo sapiens (human)
enzyme bindingBeta-secretase 1Homo sapiens (human)
protein serine/threonine kinase bindingBeta-secretase 1Homo sapiens (human)
[Information is prepared from geneontology information from the June-17-2024 release]

Ceullar Components (32)

Processvia Protein(s)Taxonomy
nucleusGlyceraldehyde-3-phosphate dehydrogenaseHomo sapiens (human)
cytoplasmGlyceraldehyde-3-phosphate dehydrogenaseHomo sapiens (human)
lipid dropletGlyceraldehyde-3-phosphate dehydrogenaseHomo sapiens (human)
cytosolGlyceraldehyde-3-phosphate dehydrogenaseHomo sapiens (human)
plasma membraneGlyceraldehyde-3-phosphate dehydrogenaseHomo sapiens (human)
microtubule cytoskeletonGlyceraldehyde-3-phosphate dehydrogenaseHomo sapiens (human)
membraneGlyceraldehyde-3-phosphate dehydrogenaseHomo sapiens (human)
nuclear membraneGlyceraldehyde-3-phosphate dehydrogenaseHomo sapiens (human)
vesicleGlyceraldehyde-3-phosphate dehydrogenaseHomo sapiens (human)
intracellular membrane-bounded organelleGlyceraldehyde-3-phosphate dehydrogenaseHomo sapiens (human)
perinuclear region of cytoplasmGlyceraldehyde-3-phosphate dehydrogenaseHomo sapiens (human)
extracellular exosomeGlyceraldehyde-3-phosphate dehydrogenaseHomo sapiens (human)
GAIT complexGlyceraldehyde-3-phosphate dehydrogenaseHomo sapiens (human)
ribonucleoprotein complexGlyceraldehyde-3-phosphate dehydrogenaseHomo sapiens (human)
cytosolGlyceraldehyde-3-phosphate dehydrogenaseHomo sapiens (human)
lysosomeBeta-secretase 1Homo sapiens (human)
endosomeBeta-secretase 1Homo sapiens (human)
early endosomeBeta-secretase 1Homo sapiens (human)
late endosomeBeta-secretase 1Homo sapiens (human)
multivesicular bodyBeta-secretase 1Homo sapiens (human)
endoplasmic reticulum lumenBeta-secretase 1Homo sapiens (human)
Golgi apparatusBeta-secretase 1Homo sapiens (human)
trans-Golgi networkBeta-secretase 1Homo sapiens (human)
plasma membraneBeta-secretase 1Homo sapiens (human)
synaptic vesicleBeta-secretase 1Homo sapiens (human)
cell surfaceBeta-secretase 1Homo sapiens (human)
endosome membraneBeta-secretase 1Homo sapiens (human)
membraneBeta-secretase 1Homo sapiens (human)
axonBeta-secretase 1Homo sapiens (human)
dendriteBeta-secretase 1Homo sapiens (human)
neuronal cell bodyBeta-secretase 1Homo sapiens (human)
membrane raftBeta-secretase 1Homo sapiens (human)
recycling endosomeBeta-secretase 1Homo sapiens (human)
Golgi-associated vesicle lumenBeta-secretase 1Homo sapiens (human)
hippocampal mossy fiber to CA3 synapseBeta-secretase 1Homo sapiens (human)
endosomeBeta-secretase 1Homo sapiens (human)
plasma membraneBeta-secretase 1Homo sapiens (human)
trans-Golgi networkBeta-secretase 1Homo sapiens (human)
[Information is prepared from geneontology information from the June-17-2024 release]

Bioassays (34)

Assay IDTitleYearJournalArticle
AID540299A screen for compounds that inhibit the MenB enzyme of Mycobacterium tuberculosis2010Bioorganic & medicinal chemistry letters, Nov-01, Volume: 20, Issue:21
Synthesis and SAR studies of 1,4-benzoxazine MenB inhibitors: novel antibacterial agents against Mycobacterium tuberculosis.
AID588519A screen for compounds that inhibit viral RNA polymerase binding and polymerization activities2011Antiviral research, Sep, Volume: 91, Issue:3
High-throughput screening identification of poliovirus RNA-dependent RNA polymerase inhibitors.
AID636823Antiplasmodial activity against chloroquine-resistant Plasmodium falciparum FcB1/Colombia infected in human A+ve erythrocytes assessed as inhibition of [G-3H]hypoxanthine uptake preincubated for 24 hrs prior to [G-3H]hypoxanthine addition measured after 12011Journal of natural products, Oct-28, Volume: 74, Issue:10
Structure and in vitro antiparasitic activity of constituents of Citropsis articulata root bark.
AID376059Antimutagenic activity in Salmonella Typhimurium TA100 assessed as protection against benzo[a]pyrene-induced mutation at 16 ug/plate after 2 days by modified Ames test1999Journal of natural products, Oct, Volume: 62, Issue:10
Umbelliferone analogues and their potential to inhibit Benzo(a)pyrene- and hydrogen peroxide-induced mutations.
AID376064Antimutagenic activity in Salmonella Typhimurium TA102 assessed as protection against hydrogen peroxide-induced mutation at 4 ug/plate after 2 days by modified Ames test1999Journal of natural products, Oct, Volume: 62, Issue:10
Umbelliferone analogues and their potential to inhibit Benzo(a)pyrene- and hydrogen peroxide-induced mutations.
AID377035Antimicrobial activity against Klebsiella pneumoniae ATCC 13883 after 24 hrs by disk diffusion assay2005Journal of natural products, Jan, Volume: 68, Issue:1
Natural and synthetic 2,2-dimethylpyranocoumarins with antibacterial activity.
AID636826Cytotoxicity against african green monkey Vero cells2011Journal of natural products, Oct-28, Volume: 74, Issue:10
Structure and in vitro antiparasitic activity of constituents of Citropsis articulata root bark.
AID332445DNA damaging activity against DNA repair-proficient yeast RAD+ assessed as drug level required to produce 12 mm zone of inhibition1994Journal of natural products, Apr, Volume: 57, Issue:4
Biological activity of some coumarins from Sri Lankan Rutaceae.
AID1355970Cytotoxicity against human A549 cells by MTT assay2018Journal of natural products, 07-27, Volume: 81, Issue:7
Bioactive Phenolic Components from the Twigs of Atalantia buxifolia.
AID377032Antimicrobial activity against Enterobacter cloacae ATCC 13047 after 24 hrs by disk diffusion assay2005Journal of natural products, Jan, Volume: 68, Issue:1
Natural and synthetic 2,2-dimethylpyranocoumarins with antibacterial activity.
AID637774Inhibition of recombinant human BACE1 using Rh-EVNLDAEFK as substrate after 60 mins by fluorescence quenching assay2012Bioorganic & medicinal chemistry, Jan-15, Volume: 20, Issue:2
Structure-activity relationships for naturally occurring coumarins as β-secretase inhibitor.
AID332444DNA damaging activity against DNA repair-deficient yeast rad 6 assessed as drug level required to produce 12 mm zone of inhibition1994Journal of natural products, Apr, Volume: 57, Issue:4
Biological activity of some coumarins from Sri Lankan Rutaceae.
AID1355971Antiinflammatory activity in human neutrophils assessed as inhibition of fMLP/CB-induced superoxide anion generation preincubated for 5 mins followed by cytochalasin B/fMLP addition for 3 mins by superoxide dismutase inhibitable reduction of ferricytochro2018Journal of natural products, 07-27, Volume: 81, Issue:7
Bioactive Phenolic Components from the Twigs of Atalantia buxifolia.
AID332442DNA damaging activity against DNA repair-deficient yeast rad 52 assessed as drug level required to produce 12 mm zone of inhibition1994Journal of natural products, Apr, Volume: 57, Issue:4
Biological activity of some coumarins from Sri Lankan Rutaceae.
AID332446Cytotoxicity against african green monkey Vero cells after 7 days by XTT assay1994Journal of natural products, Apr, Volume: 57, Issue:4
Biological activity of some coumarins from Sri Lankan Rutaceae.
AID75720Inhibitory concentration against glyceraldehyde-3-phosphate dehydrogenase was determined as log 1/IC502004Bioorganic & medicinal chemistry letters, May-03, Volume: 14, Issue:9
Structure-activity relationships of novel inhibitors of glyceraldehyde-3-phosphate dehydrogenase.
AID636824Antileishmanial activity against Leishmania donovani MHOM/ET/L82/LV9 promastigotes after 3 days by MTT assay2011Journal of natural products, Oct-28, Volume: 74, Issue:10
Structure and in vitro antiparasitic activity of constituents of Citropsis articulata root bark.
AID1355969Cytotoxicity against human MDA-MB-231 cells by MTT assay2018Journal of natural products, 07-27, Volume: 81, Issue:7
Bioactive Phenolic Components from the Twigs of Atalantia buxifolia.
AID79297Anti-HIV activity in acutely infected H9 lymphocytes.1994Journal of medicinal chemistry, Nov-11, Volume: 37, Issue:23
Anti-AIDS agents. 15. Synthesis and anti-HIV activity of dihydroseselins and related analogs.
AID1355972Antiinflammatory activity in human neutrophils assessed as inhibition of fMLP/CB-induced elastase release preincubated for 5 mins followed by fMLP/CB stimulation and measured for 10 mins using MeO-Suc-Ala-Ala-Pro-Val-p-nitroanilide as substrate2018Journal of natural products, 07-27, Volume: 81, Issue:7
Bioactive Phenolic Components from the Twigs of Atalantia buxifolia.
AID377031Antimicrobial activity against Pseudomonas aeruginosa ATCC 27853 after 24 hrs by disk diffusion assay2005Journal of natural products, Jan, Volume: 68, Issue:1
Natural and synthetic 2,2-dimethylpyranocoumarins with antibacterial activity.
AID332443DNA damaging activity against DNA repair-deficient yeast rad 52Y assessed as drug level required to produce 12 mm zone of inhibition1994Journal of natural products, Apr, Volume: 57, Issue:4
Biological activity of some coumarins from Sri Lankan Rutaceae.
AID79440Tested for in vitro therapeutic index as the ratio of IC50 to EC50 in acutely infected H9 Lymphocytes1994Journal of medicinal chemistry, Nov-11, Volume: 37, Issue:23
Anti-AIDS agents. 15. Synthesis and anti-HIV activity of dihydroseselins and related analogs.
AID377033Antimicrobial activity against Escherichia coli ATCC 25922 after 24 hrs by disk diffusion assay2005Journal of natural products, Jan, Volume: 68, Issue:1
Natural and synthetic 2,2-dimethylpyranocoumarins with antibacterial activity.
AID637775Inhibition of recombinant human BACE1 using Rh-EVNLDAEFK as substrate at 500 uM after 60 mins by fluorescence quenching assay2012Bioorganic & medicinal chemistry, Jan-15, Volume: 20, Issue:2
Structure-activity relationships for naturally occurring coumarins as β-secretase inhibitor.
AID377034Antimicrobial activity against Proteus mirabilis after 24 hrs by disk diffusion assay2005Journal of natural products, Jan, Volume: 68, Issue:1
Natural and synthetic 2,2-dimethylpyranocoumarins with antibacterial activity.
AID377030Antimicrobial activity against Staphylococcus epidermidis ATCC 12228 after 24 hrs by disk diffusion assay2005Journal of natural products, Jan, Volume: 68, Issue:1
Natural and synthetic 2,2-dimethylpyranocoumarins with antibacterial activity.
AID376063Antimutagenic activity in Salmonella Typhimurium TA102 assessed as protection against hydrogen peroxide-induced mutation at 2 ug/plate after 2 days by modified Ames test1999Journal of natural products, Oct, Volume: 62, Issue:10
Umbelliferone analogues and their potential to inhibit Benzo(a)pyrene- and hydrogen peroxide-induced mutations.
AID376065Antimutagenic activity in Salmonella Typhimurium TA102 assessed as protection against hydrogen peroxide-induced mutation at 8 ug/plate after 2 days by modified Ames test1999Journal of natural products, Oct, Volume: 62, Issue:10
Umbelliferone analogues and their potential to inhibit Benzo(a)pyrene- and hydrogen peroxide-induced mutations.
AID376058Antimutagenic activity in Salmonella Typhimurium TA100 assessed as protection against benzo[a]pyrene-induced mutation at 8 ug/plate after 2 days by modified Ames test1999Journal of natural products, Oct, Volume: 62, Issue:10
Umbelliferone analogues and their potential to inhibit Benzo(a)pyrene- and hydrogen peroxide-induced mutations.
AID376057Antimutagenic activity in Salmonella Typhimurium TA100 assessed as protection against benzo[a]pyrene-induced mutation at 4 ug/plate after 2 days by modified Ames test1999Journal of natural products, Oct, Volume: 62, Issue:10
Umbelliferone analogues and their potential to inhibit Benzo(a)pyrene- and hydrogen peroxide-induced mutations.
AID636825Antitrypanosomal activity against Trypanosoma brucei brucei2011Journal of natural products, Oct-28, Volume: 74, Issue:10
Structure and in vitro antiparasitic activity of constituents of Citropsis articulata root bark.
AID1355968Cytotoxicity against human HepG2 cells by MTT assay2018Journal of natural products, 07-27, Volume: 81, Issue:7
Bioactive Phenolic Components from the Twigs of Atalantia buxifolia.
AID377029Antimicrobial activity against Staphylococcus aureus ATCC 25923 after 24 hrs by disk diffusion assay2005Journal of natural products, Jan, Volume: 68, Issue:1
Natural and synthetic 2,2-dimethylpyranocoumarins with antibacterial activity.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (25)

TimeframeStudies, This Drug (%)All Drugs %
pre-19901 (4.00)18.7374
1990's3 (12.00)18.2507
2000's6 (24.00)29.6817
2010's12 (48.00)24.3611
2020's3 (12.00)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 27.63

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 Index27.63 (24.57)
Research Supply Index3.26 (2.92)
Research Growth Index5.10 (4.65)
Search Engine Demand Index31.58 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (27.63)

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%
Other25 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]