Page last updated: 2024-11-05

herniarin

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

Description

Herniarin, also known as 7-hydroxycoumarin, is a naturally occurring coumarin derivative found in various plants. It exhibits a range of biological activities, including antioxidant, anti-inflammatory, and anticancer properties. Its synthesis involves various methods, including the Pechmann condensation and the Wittig reaction. Herniarin has been shown to inhibit the growth of cancer cells, protect against oxidative stress, and reduce inflammation. The compound's potential therapeutic applications have led to extensive research efforts to explore its pharmacological properties. Herniarin's unique structural features and biological activities make it a promising candidate for the development of new drugs.'

herniarin: methoxy analog of umbelliferone; structure [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

herniarin : A member of the class of coumarins that is coumarin substituted by a methoxy group at position 7. [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 CID10748
CHEMBL ID49732
CHEBI ID5679
SCHEMBL ID61221
MeSH IDM0051401

Synonyms (102)

Synonym
BRD-K81209159-001-02-9
DIVK1C_006418
KBIO1_001362
SDCCGMLS-0066524.P001
7-methoxy-2h-1-benzopyran-2-one
brn 0141728
nsc 404559
einecs 208-513-3
7-methoxychromen-2-one
SPECTRUM_000392
MEGXP0_000150
ACON1_002037
NCGC00179069-02
NCGC00179069-01
SPECTRUM5_000156
MLS000563125
nsc-404559
herniarine
coumarin, 7-methoxy-
2h-1-benzopyran-2-one, 7-methoxy-
methylumbelliferone
nsc404559
ayapanin
methoxycourmarin, 7-
smr000156201
MLS000574914
7-methoxycoumarin
herniarin
C09268
531-59-9
7-methoxycoumarin, >=98%
NCGC00095528-01
KBIO2_003440
KBIOSS_000872
KBIO2_006008
KBIO3_001206
KBIOGR_002056
KBIO2_000872
SPECTRUM4_001558
SPECTRUM3_000263
SPECTRUM2_000398
SPECPLUS_000322
SPBIO_000615
SPECTRUM210874
BSPBIO_001706
M-3330
STK374268
7-methoxy-2h-chromen-2-one
CHEBI:5679 ,
7-(methyloxy)-2h-chromen-2-one
7-methoxycoumarin, suitable for fluorescence, >=98.0% (tlc)
M1723
AKOS000277129
CHEMBL49732 ,
7-methoxy coumarin
bdbm50303499
NCGC00095528-02
NCGC00095528-03
7-methoxy-chromen-2-one
7-methoxy-1-benzopyran-2-one
A829418
A824863
methyl umbelliferyl ether
HMS2271N13
CCG-38669
unii-dgk72g008a
5-18-01-00387 (beilstein handbook reference)
dgk72g008a ,
FT-0621446
methoxycoumarin, 7-
7-methoxycoumarin (constituent of chamomile) [dsc]
SCHEMBL61221
7-methoxy-coumarin
DTXSID5060196
umbelliferone, methyl ether
7-methoxy-2h-chromen-2-one #
7-methyl ether derivative of umbelliferone
AC-34354
mfcd00006876
SR-01000712094-2
sr-01000712094
herniarin (6ci)
7-methoxycoumarin, analytical standard
herniarin, primary pharmaceutical reference standard
Z53852417
AS-58718
coumarin, 7-methoxy- (8ci)
7-methoxycourmarin
7-methoxy-2h-1-benzopyran-2-one, 9ci
umbelliferone methyl ether
Q3408685
herniarin,(s)
ZB1865
CS-0016775
HY-N1366
7-methoxycoumarin;methyl umbelliferyl ether
7-methoxycoumarin 100 microg/ml in acetonitrile
S5163
EN300-399800
A870805
SY048641
7-methoxycoumarin (constituent of chamomile)

Research Excerpts

Overview

Herniarin is a member of simple coumarins, which are a group of common secondary metabolites in plants.

ExcerptReferenceRelevance
"Herniarin is a simple coumarin that is found naturally in some plant species. "( The Alleviating Effect of Herniarin Against Ionizing Radiation-Induced Genotoxicity and Cytotoxicity in Human Peripheral Blood Lymphocytes.
Al Fares, E; Kalmakhelidze, S; Kitson, S; Mansi, L; Molazadeh, M; Sanikidze, T; Topuria, D, 2022
)
2.46
"Herniarin is a member of simple coumarins, which are a group of common secondary metabolites in plants. "( The protective effect of herniarin on genotoxicity and apoptosis induced by cisplatin in bone marrow cells of rats.
Cheki, M; Khodayar, MJ; Mojiri-Forushani, H; Safari, O; Salehcheh, M, 2022
)
2.47
"Herniarin is a member of simple coumarins, which are a group of common secondary metabolites in plants."( Enhancement of cisplatin cytotoxicity in combination with herniarin in vitro.
Bahrami, AR; Haghighi, F; Haghighitalab, A; Iranshahi, M; Matin, MM; Porsa, H, 2014
)
1.37
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Roles (1)

RoleDescription
fluorochromeA fluorescent dye used to stain biological specimens.
[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]

Pathways (1)

PathwayProteinsCompounds
simple coumarins biosynthesis2221
simple coumarins biosynthesis2823

Protein Targets (27)

Potency Measurements

ProteinTaxonomyMeasurementAverage (µ)Min (ref.)Avg (ref.)Max (ref.)Bioassay(s)
Chain A, MAJOR APURINIC/APYRIMIDINIC ENDONUCLEASEHomo sapiens (human)Potency7.94330.003245.467312,589.2998AID2517
Chain A, HADH2 proteinHomo sapiens (human)Potency25.11890.025120.237639.8107AID893
Chain B, HADH2 proteinHomo sapiens (human)Potency25.11890.025120.237639.8107AID893
Chain A, 2-oxoglutarate OxygenaseHomo sapiens (human)Potency29.90330.177814.390939.8107AID2147
thioredoxin reductaseRattus norvegicus (Norway rat)Potency50.11870.100020.879379.4328AID588456
TDP1 proteinHomo sapiens (human)Potency23.72460.000811.382244.6684AID686978; AID686979
aldehyde dehydrogenase 1 family, member A1Homo sapiens (human)Potency29.90330.011212.4002100.0000AID1030
15-hydroxyprostaglandin dehydrogenase [NAD(+)] isoform 1Homo sapiens (human)Potency29.90330.001815.663839.8107AID894
DNA polymerase kappa isoform 1Homo sapiens (human)Potency3.98110.031622.3146100.0000AID588579
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023]

Inhibition Measurements

ProteinTaxonomyMeasurementAverageMin (ref.)Avg (ref.)Max (ref.)Bioassay(s)
Exportin-1Homo sapiens (human)IC50 (µMol)25.00000.00100.58401.6000AID484914
Carbonic anhydrase 12Homo sapiens (human)Ki9.70000.00021.10439.9000AID444780
Carbonic anhydrase 1Homo sapiens (human)Ki5.90000.00001.372610.0000AID444771
Carbonic anhydrase 2Homo sapiens (human)Ki500.00000.00000.72369.9200AID444772
Carbonic anhydrase 3Homo sapiens (human)Ki96.00000.00022.010210.0000AID444773
AromataseHomo sapiens (human)IC50 (µMol)10.00000.00001.290410.0000AID1467352
Aldo-keto reductase family 1 member B1Homo sapiens (human)IC50 (µMol)99.25000.00101.191310.0000AID516862; AID639825
Carbonic anhydrase 4Homo sapiens (human)Ki8.30000.00021.97209.9200AID444774
Carbonic anhydrase 6Homo sapiens (human)Ki5.50000.00011.47109.9200AID444777
Carbonic anhydrase 5A, mitochondrialHomo sapiens (human)Ki5.10000.00001.27259.9000AID444775
Carbonic anhydrase 7Homo sapiens (human)Ki2.40000.00021.37379.9000AID444778
Beta-secretase 1Homo sapiens (human)IC50 (µMol)500.00000.00061.619410.0000AID637774
Sorbitol dehydrogenaseHomo sapiens (human)IC50 (µMol)124.00000.24000.49531.0000AID516864
Carbonic anhydrase 9Homo sapiens (human)Ki9.80000.00010.78749.9000AID444779
Carbonic anhydrase 15Mus musculus (house mouse)Ki8.40000.00091.884610.0000AID444783
Carbonic anhydrase 13Mus musculus (house mouse)Ki8.90000.00021.39749.9000AID444781
Carbonic anhydrase 14Homo sapiens (human)Ki9.00000.00021.50999.9000AID444782
Carbonic anhydrase 5B, mitochondrialHomo sapiens (human)Ki500.00000.00001.34129.9700AID444776
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023]

Biological Processes (83)

Processvia Protein(s)Taxonomy
protein export from nucleusExportin-1Homo sapiens (human)
ribosomal subunit export from nucleusExportin-1Homo sapiens (human)
ribosomal large subunit export from nucleusExportin-1Homo sapiens (human)
ribosomal small subunit export from nucleusExportin-1Homo sapiens (human)
mRNA export from nucleusExportin-1Homo sapiens (human)
protein export from nucleusExportin-1Homo sapiens (human)
nucleocytoplasmic transportExportin-1Homo sapiens (human)
regulation of centrosome duplicationExportin-1Homo sapiens (human)
regulation of proteasomal ubiquitin-dependent protein catabolic processExportin-1Homo sapiens (human)
protein localization to nucleusExportin-1Homo sapiens (human)
ribosome biogenesisExportin-1Homo sapiens (human)
regulation of protein export from nucleusExportin-1Homo sapiens (human)
estrous cycleCarbonic anhydrase 12Homo sapiens (human)
chloride ion homeostasisCarbonic anhydrase 12Homo sapiens (human)
one-carbon metabolic processCarbonic anhydrase 12Homo sapiens (human)
one-carbon metabolic processCarbonic anhydrase 1Homo sapiens (human)
morphogenesis of an epitheliumCarbonic anhydrase 2Homo sapiens (human)
positive regulation of synaptic transmission, GABAergicCarbonic anhydrase 2Homo sapiens (human)
positive regulation of cellular pH reductionCarbonic anhydrase 2Homo sapiens (human)
angiotensin-activated signaling pathwayCarbonic anhydrase 2Homo sapiens (human)
regulation of monoatomic anion transportCarbonic anhydrase 2Homo sapiens (human)
secretionCarbonic anhydrase 2Homo sapiens (human)
regulation of intracellular pHCarbonic anhydrase 2Homo sapiens (human)
neuron cellular homeostasisCarbonic anhydrase 2Homo sapiens (human)
positive regulation of dipeptide transmembrane transportCarbonic anhydrase 2Homo sapiens (human)
regulation of chloride transportCarbonic anhydrase 2Homo sapiens (human)
carbon dioxide transportCarbonic anhydrase 2Homo sapiens (human)
one-carbon metabolic processCarbonic anhydrase 2Homo sapiens (human)
response to bacteriumCarbonic anhydrase 3Homo sapiens (human)
one-carbon metabolic processCarbonic anhydrase 3Homo sapiens (human)
negative regulation of chronic inflammatory responseAromataseHomo sapiens (human)
steroid biosynthetic processAromataseHomo sapiens (human)
estrogen biosynthetic processAromataseHomo sapiens (human)
androgen catabolic processAromataseHomo sapiens (human)
syncytium formationAromataseHomo sapiens (human)
negative regulation of macrophage chemotaxisAromataseHomo sapiens (human)
sterol metabolic processAromataseHomo sapiens (human)
female genitalia developmentAromataseHomo sapiens (human)
mammary gland developmentAromataseHomo sapiens (human)
uterus developmentAromataseHomo sapiens (human)
prostate gland growthAromataseHomo sapiens (human)
testosterone biosynthetic processAromataseHomo sapiens (human)
positive regulation of estradiol secretionAromataseHomo sapiens (human)
female gonad developmentAromataseHomo sapiens (human)
response to estradiolAromataseHomo sapiens (human)
retinoid metabolic processAldo-keto reductase family 1 member B1Homo sapiens (human)
epithelial cell maturationAldo-keto reductase family 1 member B1Homo sapiens (human)
renal water homeostasisAldo-keto reductase family 1 member B1Homo sapiens (human)
carbohydrate metabolic processAldo-keto reductase family 1 member B1Homo sapiens (human)
prostaglandin metabolic processAldo-keto reductase family 1 member B1Homo sapiens (human)
C21-steroid hormone biosynthetic processAldo-keto reductase family 1 member B1Homo sapiens (human)
L-ascorbic acid biosynthetic processAldo-keto reductase family 1 member B1Homo sapiens (human)
regulation of urine volumeAldo-keto reductase family 1 member B1Homo sapiens (human)
retinol metabolic processAldo-keto reductase family 1 member B1Homo sapiens (human)
negative regulation of apoptotic processAldo-keto reductase family 1 member B1Homo sapiens (human)
daunorubicin metabolic processAldo-keto reductase family 1 member B1Homo sapiens (human)
doxorubicin metabolic processAldo-keto reductase family 1 member B1Homo sapiens (human)
fructose biosynthetic processAldo-keto reductase family 1 member B1Homo sapiens (human)
cellular hyperosmotic salinity responseAldo-keto reductase family 1 member B1Homo sapiens (human)
metanephric collecting duct developmentAldo-keto reductase family 1 member B1Homo sapiens (human)
bicarbonate transportCarbonic anhydrase 4Homo sapiens (human)
one-carbon metabolic processCarbonic anhydrase 4Homo sapiens (human)
detection of chemical stimulus involved in sensory perception of bitter tasteCarbonic anhydrase 6Homo sapiens (human)
one-carbon metabolic processCarbonic anhydrase 6Homo sapiens (human)
one-carbon metabolic processCarbonic anhydrase 5A, mitochondrialHomo sapiens (human)
positive regulation of synaptic transmission, GABAergicCarbonic anhydrase 7Homo sapiens (human)
positive regulation of cellular pH reductionCarbonic anhydrase 7Homo sapiens (human)
neuron cellular homeostasisCarbonic anhydrase 7Homo sapiens (human)
regulation of chloride transportCarbonic anhydrase 7Homo sapiens (human)
regulation of intracellular pHCarbonic anhydrase 7Homo sapiens (human)
one-carbon metabolic processCarbonic anhydrase 7Homo 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)
glucose metabolic processSorbitol dehydrogenaseHomo sapiens (human)
sorbitol catabolic processSorbitol dehydrogenaseHomo sapiens (human)
glucuronate catabolic process to xylulose 5-phosphateSorbitol dehydrogenaseHomo sapiens (human)
flagellated sperm motilitySorbitol dehydrogenaseHomo sapiens (human)
fructose biosynthetic processSorbitol dehydrogenaseHomo sapiens (human)
L-xylitol catabolic processSorbitol dehydrogenaseHomo sapiens (human)
L-xylitol metabolic processSorbitol dehydrogenaseHomo sapiens (human)
response to hypoxiaCarbonic anhydrase 9Homo sapiens (human)
morphogenesis of an epitheliumCarbonic anhydrase 9Homo sapiens (human)
response to xenobiotic stimulusCarbonic anhydrase 9Homo sapiens (human)
response to testosteroneCarbonic anhydrase 9Homo sapiens (human)
secretionCarbonic anhydrase 9Homo sapiens (human)
one-carbon metabolic processCarbonic anhydrase 9Homo sapiens (human)
one-carbon metabolic processCarbonic anhydrase 14Homo sapiens (human)
response to bacteriumCarbonic anhydrase 5B, mitochondrialHomo sapiens (human)
one-carbon metabolic processCarbonic anhydrase 5B, mitochondrialHomo sapiens (human)
[Information is prepared from geneontology information from the June-17-2024 release]

Molecular Functions (41)

Processvia Protein(s)Taxonomy
RNA bindingExportin-1Homo sapiens (human)
nuclear export signal receptor activityExportin-1Homo sapiens (human)
protein bindingExportin-1Homo sapiens (human)
small GTPase bindingExportin-1Homo sapiens (human)
zinc ion bindingCarbonic anhydrase 12Homo sapiens (human)
carbonate dehydratase activityCarbonic anhydrase 12Homo sapiens (human)
arylesterase activityCarbonic anhydrase 1Homo sapiens (human)
carbonate dehydratase activityCarbonic anhydrase 1Homo sapiens (human)
protein bindingCarbonic anhydrase 1Homo sapiens (human)
zinc ion bindingCarbonic anhydrase 1Homo sapiens (human)
hydro-lyase activityCarbonic anhydrase 1Homo sapiens (human)
cyanamide hydratase activityCarbonic anhydrase 1Homo sapiens (human)
arylesterase activityCarbonic anhydrase 2Homo sapiens (human)
carbonate dehydratase activityCarbonic anhydrase 2Homo sapiens (human)
protein bindingCarbonic anhydrase 2Homo sapiens (human)
zinc ion bindingCarbonic anhydrase 2Homo sapiens (human)
cyanamide hydratase activityCarbonic anhydrase 2Homo sapiens (human)
carbonate dehydratase activityCarbonic anhydrase 3Homo sapiens (human)
protein bindingCarbonic anhydrase 3Homo sapiens (human)
zinc ion bindingCarbonic anhydrase 3Homo sapiens (human)
nickel cation bindingCarbonic anhydrase 3Homo sapiens (human)
iron ion bindingAromataseHomo sapiens (human)
steroid hydroxylase activityAromataseHomo sapiens (human)
electron transfer activityAromataseHomo sapiens (human)
oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, reduced flavin or flavoprotein as one donor, and incorporation of one atom of oxygenAromataseHomo sapiens (human)
oxygen bindingAromataseHomo sapiens (human)
heme bindingAromataseHomo sapiens (human)
aromatase activityAromataseHomo sapiens (human)
retinal dehydrogenase activityAldo-keto reductase family 1 member B1Homo sapiens (human)
aldose reductase (NADPH) activityAldo-keto reductase family 1 member B1Homo sapiens (human)
protein bindingAldo-keto reductase family 1 member B1Homo sapiens (human)
electron transfer activityAldo-keto reductase family 1 member B1Homo sapiens (human)
prostaglandin H2 endoperoxidase reductase activityAldo-keto reductase family 1 member B1Homo sapiens (human)
glyceraldehyde oxidoreductase activityAldo-keto reductase family 1 member B1Homo sapiens (human)
allyl-alcohol dehydrogenase activityAldo-keto reductase family 1 member B1Homo sapiens (human)
L-glucuronate reductase activityAldo-keto reductase family 1 member B1Homo sapiens (human)
glycerol dehydrogenase [NADP+] activityAldo-keto reductase family 1 member B1Homo sapiens (human)
all-trans-retinol dehydrogenase (NADP+) activityAldo-keto reductase family 1 member B1Homo sapiens (human)
protein bindingCarbonic anhydrase 4Homo sapiens (human)
zinc ion bindingCarbonic anhydrase 4Homo sapiens (human)
carbonate dehydratase activityCarbonic anhydrase 4Homo sapiens (human)
zinc ion bindingCarbonic anhydrase 6Homo sapiens (human)
carbonate dehydratase activityCarbonic anhydrase 6Homo sapiens (human)
carbonate dehydratase activityCarbonic anhydrase 5A, mitochondrialHomo sapiens (human)
zinc ion bindingCarbonic anhydrase 5A, mitochondrialHomo sapiens (human)
zinc ion bindingCarbonic anhydrase 7Homo sapiens (human)
carbonate dehydratase activityCarbonic anhydrase 7Homo 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)
(R,R)-butanediol dehydrogenase activitySorbitol dehydrogenaseHomo sapiens (human)
L-iditol 2-dehydrogenase activitySorbitol dehydrogenaseHomo sapiens (human)
zinc ion bindingSorbitol dehydrogenaseHomo sapiens (human)
carbohydrate bindingSorbitol dehydrogenaseHomo sapiens (human)
identical protein bindingSorbitol dehydrogenaseHomo sapiens (human)
D-xylulose reductase activitySorbitol dehydrogenaseHomo sapiens (human)
D-sorbitol dehydrogenase (acceptor) activitySorbitol dehydrogenaseHomo sapiens (human)
ribitol 2-dehydrogenase activitySorbitol dehydrogenaseHomo sapiens (human)
NAD bindingSorbitol dehydrogenaseHomo sapiens (human)
carbonate dehydratase activityCarbonic anhydrase 9Homo sapiens (human)
protein bindingCarbonic anhydrase 9Homo sapiens (human)
zinc ion bindingCarbonic anhydrase 9Homo sapiens (human)
molecular function activator activityCarbonic anhydrase 9Homo sapiens (human)
zinc ion bindingCarbonic anhydrase 14Homo sapiens (human)
carbonate dehydratase activityCarbonic anhydrase 14Homo sapiens (human)
carbonate dehydratase activityCarbonic anhydrase 5B, mitochondrialHomo sapiens (human)
zinc ion bindingCarbonic anhydrase 5B, mitochondrialHomo sapiens (human)
[Information is prepared from geneontology information from the June-17-2024 release]

Ceullar Components (54)

Processvia Protein(s)Taxonomy
kinetochoreExportin-1Homo sapiens (human)
nuclear envelopeExportin-1Homo sapiens (human)
annulate lamellaeExportin-1Homo sapiens (human)
nucleoplasmExportin-1Homo sapiens (human)
nucleolusExportin-1Homo sapiens (human)
cytoplasmExportin-1Homo sapiens (human)
cytosolExportin-1Homo sapiens (human)
Cajal bodyExportin-1Homo sapiens (human)
membraneExportin-1Homo sapiens (human)
nuclear membraneExportin-1Homo sapiens (human)
intracellular membrane-bounded organelleExportin-1Homo sapiens (human)
protein-containing complexExportin-1Homo sapiens (human)
ribonucleoprotein complexExportin-1Homo sapiens (human)
nucleusExportin-1Homo sapiens (human)
cytoplasmExportin-1Homo sapiens (human)
plasma membraneCarbonic anhydrase 12Homo sapiens (human)
membraneCarbonic anhydrase 12Homo sapiens (human)
basolateral plasma membraneCarbonic anhydrase 12Homo sapiens (human)
apical plasma membraneCarbonic anhydrase 12Homo sapiens (human)
plasma membraneCarbonic anhydrase 12Homo sapiens (human)
cytosolCarbonic anhydrase 1Homo sapiens (human)
extracellular exosomeCarbonic anhydrase 1Homo sapiens (human)
cytoplasmCarbonic anhydrase 2Homo sapiens (human)
cytosolCarbonic anhydrase 2Homo sapiens (human)
plasma membraneCarbonic anhydrase 2Homo sapiens (human)
myelin sheathCarbonic anhydrase 2Homo sapiens (human)
apical part of cellCarbonic anhydrase 2Homo sapiens (human)
extracellular exosomeCarbonic anhydrase 2Homo sapiens (human)
cytoplasmCarbonic anhydrase 2Homo sapiens (human)
plasma membraneCarbonic anhydrase 2Homo sapiens (human)
apical part of cellCarbonic anhydrase 2Homo sapiens (human)
cytosolCarbonic anhydrase 3Homo sapiens (human)
cytosolCarbonic anhydrase 3Homo sapiens (human)
cytoplasmCarbonic anhydrase 3Homo sapiens (human)
endoplasmic reticulumAromataseHomo sapiens (human)
endoplasmic reticulum membraneAromataseHomo sapiens (human)
membraneAromataseHomo sapiens (human)
endoplasmic reticulumAromataseHomo sapiens (human)
extracellular spaceAldo-keto reductase family 1 member B1Homo sapiens (human)
nucleoplasmAldo-keto reductase family 1 member B1Homo sapiens (human)
cytosolAldo-keto reductase family 1 member B1Homo sapiens (human)
extracellular exosomeAldo-keto reductase family 1 member B1Homo sapiens (human)
cytosolAldo-keto reductase family 1 member B1Homo sapiens (human)
basolateral plasma membraneCarbonic anhydrase 4Homo sapiens (human)
rough endoplasmic reticulumCarbonic anhydrase 4Homo sapiens (human)
endoplasmic reticulum-Golgi intermediate compartmentCarbonic anhydrase 4Homo sapiens (human)
Golgi apparatusCarbonic anhydrase 4Homo sapiens (human)
trans-Golgi networkCarbonic anhydrase 4Homo sapiens (human)
plasma membraneCarbonic anhydrase 4Homo sapiens (human)
external side of plasma membraneCarbonic anhydrase 4Homo sapiens (human)
cell surfaceCarbonic anhydrase 4Homo sapiens (human)
membraneCarbonic anhydrase 4Homo sapiens (human)
apical plasma membraneCarbonic anhydrase 4Homo sapiens (human)
transport vesicle membraneCarbonic anhydrase 4Homo sapiens (human)
secretory granule membraneCarbonic anhydrase 4Homo sapiens (human)
brush border membraneCarbonic anhydrase 4Homo sapiens (human)
perinuclear region of cytoplasmCarbonic anhydrase 4Homo sapiens (human)
extracellular exosomeCarbonic anhydrase 4Homo sapiens (human)
plasma membraneCarbonic anhydrase 4Homo sapiens (human)
extracellular regionCarbonic anhydrase 6Homo sapiens (human)
extracellular spaceCarbonic anhydrase 6Homo sapiens (human)
cytosolCarbonic anhydrase 6Homo sapiens (human)
extracellular exosomeCarbonic anhydrase 6Homo sapiens (human)
extracellular spaceCarbonic anhydrase 6Homo sapiens (human)
mitochondrial matrixCarbonic anhydrase 5A, mitochondrialHomo sapiens (human)
mitochondrionCarbonic anhydrase 5A, mitochondrialHomo sapiens (human)
cytoplasmCarbonic anhydrase 5A, mitochondrialHomo sapiens (human)
mitochondrionCarbonic anhydrase 5A, mitochondrialHomo sapiens (human)
cytosolCarbonic anhydrase 7Homo sapiens (human)
cytoplasmCarbonic anhydrase 7Homo 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)
extracellular spaceSorbitol dehydrogenaseHomo sapiens (human)
cytosolSorbitol dehydrogenaseHomo sapiens (human)
membraneSorbitol dehydrogenaseHomo sapiens (human)
motile ciliumSorbitol dehydrogenaseHomo sapiens (human)
mitochondrial membraneSorbitol dehydrogenaseHomo sapiens (human)
extracellular exosomeSorbitol dehydrogenaseHomo sapiens (human)
nucleolusCarbonic anhydrase 9Homo sapiens (human)
plasma membraneCarbonic anhydrase 9Homo sapiens (human)
membraneCarbonic anhydrase 9Homo sapiens (human)
basolateral plasma membraneCarbonic anhydrase 9Homo sapiens (human)
microvillus membraneCarbonic anhydrase 9Homo sapiens (human)
plasma membraneCarbonic anhydrase 9Homo sapiens (human)
plasma membraneCarbonic anhydrase 14Homo sapiens (human)
membraneCarbonic anhydrase 14Homo sapiens (human)
basolateral plasma membraneCarbonic anhydrase 14Homo sapiens (human)
apical plasma membraneCarbonic anhydrase 14Homo sapiens (human)
plasma membraneCarbonic anhydrase 14Homo sapiens (human)
mitochondrionCarbonic anhydrase 5B, mitochondrialHomo sapiens (human)
mitochondrial matrixCarbonic anhydrase 5B, mitochondrialHomo sapiens (human)
mitochondrionCarbonic anhydrase 5B, mitochondrialHomo sapiens (human)
cytoplasmCarbonic anhydrase 5B, mitochondrialHomo sapiens (human)
[Information is prepared from geneontology information from the June-17-2024 release]

Bioassays (84)

Assay IDTitleYearJournalArticle
AID1159550Human Phosphogluconate dehydrogenase (6PGD) Inhibitor Screening2015Nature cell biology, Nov, Volume: 17, Issue:11
6-Phosphogluconate dehydrogenase links oxidative PPP, lipogenesis and tumour growth by inhibiting LKB1-AMPK signalling.
AID588501High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Lethal Factor Protease, MLPCN compound set2010Current protocols in cytometry, Oct, Volume: Chapter 13Microsphere-based flow cytometry protease assays for use in protease activity detection and high-throughput screening.
AID588501High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Lethal Factor Protease, MLPCN compound set2006Cytometry. Part A : the journal of the International Society for Analytical Cytology, May, Volume: 69, Issue:5
Microsphere-based protease assays and screening application for lethal factor and factor Xa.
AID588501High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Lethal Factor Protease, MLPCN compound set2010Assay and drug development technologies, Feb, Volume: 8, Issue:1
High-throughput multiplex flow cytometry screening for botulinum neurotoxin type a light chain protease inhibitors.
AID651635Viability Counterscreen for Primary qHTS for Inhibitors of ATXN expression
AID1745845Primary qHTS for Inhibitors of ATXN expression
AID588499High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Botulinum neurotoxin light chain A protease, MLPCN compound set2010Current protocols in cytometry, Oct, Volume: Chapter 13Microsphere-based flow cytometry protease assays for use in protease activity detection and high-throughput screening.
AID588499High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Botulinum neurotoxin light chain A protease, MLPCN compound set2006Cytometry. Part A : the journal of the International Society for Analytical Cytology, May, Volume: 69, Issue:5
Microsphere-based protease assays and screening application for lethal factor and factor Xa.
AID588499High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Botulinum neurotoxin light chain A protease, MLPCN compound set2010Assay and drug development technologies, Feb, Volume: 8, Issue:1
High-throughput multiplex flow cytometry screening for botulinum neurotoxin type a light chain protease inhibitors.
AID588497High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Botulinum neurotoxin light chain F protease, MLPCN compound set2010Current protocols in cytometry, Oct, Volume: Chapter 13Microsphere-based flow cytometry protease assays for use in protease activity detection and high-throughput screening.
AID588497High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Botulinum neurotoxin light chain F protease, MLPCN compound set2006Cytometry. Part A : the journal of the International Society for Analytical Cytology, May, Volume: 69, Issue:5
Microsphere-based protease assays and screening application for lethal factor and factor Xa.
AID588497High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Botulinum neurotoxin light chain F protease, MLPCN compound set2010Assay and drug development technologies, Feb, Volume: 8, Issue:1
High-throughput multiplex flow cytometry screening for botulinum neurotoxin type a light chain protease inhibitors.
AID504810Antagonists of the Thyroid Stimulating Hormone Receptor: HTS campaign2010Endocrinology, Jul, Volume: 151, Issue:7
A small molecule inverse agonist for the human thyroid-stimulating hormone receptor.
AID504812Inverse Agonists of the Thyroid Stimulating Hormone Receptor: HTS campaign2010Endocrinology, Jul, Volume: 151, Issue:7
A small molecule inverse agonist for the human thyroid-stimulating hormone receptor.
AID1467353Inhibition of human CYP19 assessed as residual activity at 10 uM using [1beta-3H]-androstenedione as substrate after 15 mins in presence of NADPH by liquid scintillation counter method relative to control2017Bioorganic & medicinal chemistry letters, 06-15, Volume: 27, Issue:12
Evaluation of synthesized coumarin derivatives on aromatase inhibitory activity.
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.
AID977599Inhibition of sodium fluorescein uptake in OATP1B1-transfected CHO cells at an equimolar substrate-inhibitor concentration of 10 uM2013Molecular pharmacology, Jun, Volume: 83, Issue:6
Structure-based identification of OATP1B1/3 inhibitors.
AID516862Inhibition human recombinant aldose reductase 1 by spectrophotometric analysis2010Bioorganic & medicinal chemistry letters, Oct-01, Volume: 20, Issue:19
6,7-Dihydroxy-4-phenylcoumarin as inhibitor of aldose reductase 2.
AID553154Displacement of [3H]estrone human recombinant 17beta-HSD1 expressed in Escherichia coli BL21 (DE3)-RIL at 6 uM by scintillation counting in presence of NADPH2011Journal of medicinal chemistry, Jan-13, Volume: 54, Issue:1
Synthesis and biological evaluation of (6- and 7-phenyl) coumarin derivatives as selective nonsteroidal inhibitors of 17β-hydroxysteroid dehydrogenase type 1.
AID444780Inhibition of human carbonic anhydrase 12 by stopped flow CO2 hydration assay2010Journal of medicinal chemistry, Jan-14, Volume: 53, Issue:1
Deciphering the mechanism of carbonic anhydrase inhibition with coumarins and thiocoumarins.
AID444776Inhibition of human carbonic anhydrase 5B by stopped flow CO2 hydration assay2010Journal of medicinal chemistry, Jan-14, Volume: 53, Issue:1
Deciphering the mechanism of carbonic anhydrase inhibition with coumarins and thiocoumarins.
AID1102106Antifungal activity against Botryotinia fuckeliana assessed as growth inhibition at 300 uM after 48 hr by microplate photometric analysis2003Journal of agricultural and food chemistry, Feb-12, Volume: 51, Issue:4
Natural fungicides from Ruta graveolens L. leaves, including a new quinolone alkaloid.
AID444775Inhibition of human carbonic anhydrase 5A by stopped flow CO2 hydration assay2010Journal of medicinal chemistry, Jan-14, Volume: 53, Issue:1
Deciphering the mechanism of carbonic anhydrase inhibition with coumarins and thiocoumarins.
AID444782Inhibition of human carbonic anhydrase 14 by stopped flow CO2 hydration assay2010Journal of medicinal chemistry, Jan-14, Volume: 53, Issue:1
Deciphering the mechanism of carbonic anhydrase inhibition with coumarins and thiocoumarins.
AID492140Antioxidant activity assessed as formazan formation induced absorbance changes at 25 ppm at 570 nm at 37 degC for 6 hrs by MTT assay2010Journal of natural products, Jul-23, Volume: 73, Issue:7
An efficient and economical MTT assay for determining the antioxidant activity of plant natural product extracts and pure compounds.
AID1204915Antiinflammatory activity against mouse RAW264.7 cells assessed as reduction of LPS-induced NO production after 24 hrs2015Journal of natural products, Feb-27, Volume: 78, Issue:2
Anti-inflammatory coumarin and benzocoumarin derivatives from Murraya alata.
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.
AID377248Cytotoxicity against human Raji cells assessed as cell viability at 0.32 nmol by trypan blue staining2000Journal of natural products, Sep, Volume: 63, Issue:9
Chemical constituents of Clausena excavata: isolation and structure elucidation of novel furanone-coumarins with inhibitory effects for tumor-promotion.
AID444781Inhibition of mouse carbonic anhydrase 13 by stopped flow CO2 hydration assay2010Journal of medicinal chemistry, Jan-14, Volume: 53, Issue:1
Deciphering the mechanism of carbonic anhydrase inhibition with coumarins and thiocoumarins.
AID444783Inhibition of mouse carbonic anhydrase 15 by stopped flow CO2 hydration assay2010Journal of medicinal chemistry, Jan-14, Volume: 53, Issue:1
Deciphering the mechanism of carbonic anhydrase inhibition with coumarins and thiocoumarins.
AID1376904Antagonist activity at AhR (unknown origin) expressed in mouse H1L1.1c2 cells assessed as inhibition of FICZ-induced AhR activation at 1 to 100 uM after 8 to 10 hrs by luciferase reporter gene assay2017Journal of natural products, 06-23, Volume: 80, Issue:6
Interaction of 7-Alkoxycoumarins with the Aryl Hydrocarbon Receptor.
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.
AID344673Toxicity in Oryzias latipes after 24 hrs by serial dilution method2008Bioorganic & medicinal chemistry letters, Oct-15, Volume: 18, Issue:20
Synthesis and biological evaluation of alkoxycoumarins as novel nematicidal constituents.
AID376056Antimutagenic activity in Salmonella Typhimurium TA100 assessed as protection against benzo[a]pyrene-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.
AID553156Displacement of [3H]estradiol human recombinant 17beta-HSD2 expressed in Escherichia coli BL21 (DE3)-RIL at 6 uM by scintillation counting in presence of NAD+2011Journal of medicinal chemistry, Jan-13, Volume: 54, Issue:1
Synthesis and biological evaluation of (6- and 7-phenyl) coumarin derivatives as selective nonsteroidal inhibitors of 17β-hydroxysteroid dehydrogenase type 1.
AID484914Inhibition of CRM1-mediated hemagglutininin-tagged HIV1 Rev protein nuclear export in human HeLa cells assessed as nucleus localization after 12 hrs by indirect fluorescent antibody technique2010Bioorganic & medicinal chemistry letters, Jun-15, Volume: 20, Issue:12
Prenylcoumarin with Rev-export inhibitory activity from Cnidii Monnieris Fructus.
AID1467352Inhibition of human CYP19 using [1beta-3H]-androstenedione as substrate after 15 mins in presence of NADPH by liquid scintillation counter method2017Bioorganic & medicinal chemistry letters, 06-15, Volume: 27, Issue:12
Evaluation of synthesized coumarin derivatives on aromatase inhibitory activity.
AID444773Inhibition of human carbonic anhydrase 3 by stopped flow CO2 hydration assay2010Journal of medicinal chemistry, Jan-14, Volume: 53, Issue:1
Deciphering the mechanism of carbonic anhydrase inhibition with coumarins and thiocoumarins.
AID516864Inhibition sorbitol dehydrogenase by spectrophotometric analysis2010Bioorganic & medicinal chemistry letters, Oct-01, Volume: 20, Issue:19
6,7-Dihydroxy-4-phenylcoumarin as inhibitor of aldose reductase 2.
AID1138893Antiasthamic activity in Wistar rat tracheal ring assessed as reversal of carbachol-induced contraction at 0.1 to 500 uM relative to control2014European journal of medicinal chemistry, Apr-22, Volume: 77Semisynthesis, ex vivo evaluation, and SAR studies of coumarin derivatives as potential antiasthmatic drugs.
AID593513Binding affinity to corpus collosum myelin in central nervous system of mouse at 100 uM after 20 mins by fluorescent microscopy2011Journal of medicinal chemistry, Apr-14, Volume: 54, Issue:7
Design, synthesis, and evaluation of coumarin-based molecular probes for imaging of myelination.
AID444772Inhibition of human carbonic anhydrase 2 by stopped flow CO2 hydration assay2010Journal of medicinal chemistry, Jan-14, Volume: 53, Issue:1
Deciphering the mechanism of carbonic anhydrase inhibition with coumarins and thiocoumarins.
AID1102104Stimulation of Botryotinia fuckeliana growth at 30 uM after 48 hr by microplate photometric analysis2003Journal of agricultural and food chemistry, Feb-12, Volume: 51, Issue:4
Natural fungicides from Ruta graveolens L. leaves, including a new quinolone alkaloid.
AID344671Toxicity in Artemia salina after 24 hrs by serial dilution method2008Bioorganic & medicinal chemistry letters, Oct-15, Volume: 18, Issue:20
Synthesis and biological evaluation of alkoxycoumarins as novel nematicidal constituents.
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.
AID516866Selectivity index, ratio of IC50 for human recombinant aldose reductase 1 to IC50 for kidney aldose reductase 22010Bioorganic & medicinal chemistry letters, Oct-01, Volume: 20, Issue:19
6,7-Dihydroxy-4-phenylcoumarin as inhibitor of aldose reductase 2.
AID977602Inhibition of sodium fluorescein uptake in OATP1B3-transfected CHO cells at an equimolar substrate-inhibitor concentration of 10 uM2013Molecular pharmacology, Jun, Volume: 83, Issue:6
Structure-based identification of OATP1B1/3 inhibitors.
AID1781227Inhibition of Infectious hematopoietic necrosis virus glycoprotein G assessed as antiviral activity at 25 uM measured by RT-qPCR method relative to control2021European journal of medicinal chemistry, Nov-05, Volume: 223Synthesis and biological evaluation of novel coumarin derivatives in rhabdoviral clearance.
AID377241Inhibition of 12-O-tetradecanoylphorbol-13-acetate-induced EBV-early antigen activation in human Raji cells assessed as EA activation at 32 nmol relative to 12-O-tetradecanoylphorbol-13-acetate2000Journal of natural products, Sep, Volume: 63, Issue:9
Chemical constituents of Clausena excavata: isolation and structure elucidation of novel furanone-coumarins with inhibitory effects for tumor-promotion.
AID444779Inhibition of human carbonic anhydrase 9 by stopped flow CO2 hydration assay2010Journal of medicinal chemistry, Jan-14, Volume: 53, Issue:1
Deciphering the mechanism of carbonic anhydrase inhibition with coumarins and thiocoumarins.
AID1102112Stimulation of Colletotrichum acutatum growth at 30 uM after 48 hr by microplate photometric analysis2003Journal of agricultural and food chemistry, Feb-12, Volume: 51, Issue:4
Natural fungicides from Ruta graveolens L. leaves, including a new quinolone alkaloid.
AID377242Inhibition of 12-O-tetradecanoylphorbol-13-acetate-induced EBV-early antigen activation in human Raji cells assessed as EA activation at 16 nmol relative to 12-O-tetradecanoylphorbol-13-acetate2000Journal of natural products, Sep, Volume: 63, Issue:9
Chemical constituents of Clausena excavata: isolation and structure elucidation of novel furanone-coumarins with inhibitory effects for tumor-promotion.
AID1204916Cytotoxicity against mouse RAW264.7 cells assessed as cell survival at 80 uM after 24 hrs by MTT assay2015Journal of natural products, Feb-27, Volume: 78, Issue:2
Anti-inflammatory coumarin and benzocoumarin derivatives from Murraya alata.
AID376062Antimutagenic activity in Salmonella Typhimurium TA102 assessed as protection against hydrogen peroxide-induced mutation at 1 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.
AID1138894Antiasthamic activity in Wistar rat tracheal ring assessed as reversal of carbachol-induced contraction2014European journal of medicinal chemistry, Apr-22, Volume: 77Semisynthesis, ex vivo evaluation, and SAR studies of coumarin derivatives as potential antiasthmatic drugs.
AID373105Antiamnesic activity against Entamoeba histolytica HM1:IMSS after 72 hrs by microdilution method2009European journal of medicinal chemistry, May, Volume: 44, Issue:5
Antiamoebic coumarins from the root bark of Adina cordifolia and their new thiosemicarbazone derivatives.
AID1102111Antifungal activity against Colletotrichum fragariae assessed as growth inhibition at 300 uM after 48 hr by microplate photometric analysis2003Journal of agricultural and food chemistry, Feb-12, Volume: 51, Issue:4
Natural fungicides from Ruta graveolens L. leaves, including a new quinolone alkaloid.
AID377243Inhibition of 12-O-tetradecanoylphorbol-13-acetate-induced EBV-early antigen activation in human Raji cells assessed as EA activation at 3.2 nmol relative to 12-O-tetradecanoylphorbol-13-acetate2000Journal of natural products, Sep, Volume: 63, Issue:9
Chemical constituents of Clausena excavata: isolation and structure elucidation of novel furanone-coumarins with inhibitory effects for tumor-promotion.
AID344670Nematicidal activity against Bursaphelenchus xylophilus measured per cotton ball after 4 days by serial dilution method2008Bioorganic & medicinal chemistry letters, Oct-15, Volume: 18, Issue:20
Synthesis and biological evaluation of alkoxycoumarins as novel nematicidal constituents.
AID1376901Agonist activity at AhR (unknown origin) expressed in mouse H1L1.1c2 cells at 1 to 100 uM after 8 to 10 hrs by luciferase reporter gene assay2017Journal of natural products, 06-23, Volume: 80, Issue:6
Interaction of 7-Alkoxycoumarins with the Aryl Hydrocarbon Receptor.
AID344672Selectivity index, ratio of MED for Bursaphelenchus xylophilus to LC50 Artemia salina2008Bioorganic & medicinal chemistry letters, Oct-15, Volume: 18, Issue:20
Synthesis and biological evaluation of alkoxycoumarins as novel nematicidal constituents.
AID355097Antiinflammatory activity in NMRI mouse macrophages assessed as inhibition of A23187-induced PGE2 release by Ellman's method1996Journal of natural products, Dec, Volume: 59, Issue:12
Antiinflammatory activity of coumarins from Santolina oblongifolia.
AID377245Cytotoxicity against human Raji cells assessed as cell viability at 32 nmol by trypan blue staining2000Journal of natural products, Sep, Volume: 63, Issue:9
Chemical constituents of Clausena excavata: isolation and structure elucidation of novel furanone-coumarins with inhibitory effects for tumor-promotion.
AID1102108Stimulation of Fusarium oxysporum growth at 30 uM after 48 hr by microplate photometric analysis2003Journal of agricultural and food chemistry, Feb-12, Volume: 51, Issue:4
Natural fungicides from Ruta graveolens L. leaves, including a new quinolone alkaloid.
AID377246Cytotoxicity against human Raji cells assessed as cell viability at 16 nmol by trypan blue staining2000Journal of natural products, Sep, Volume: 63, Issue:9
Chemical constituents of Clausena excavata: isolation and structure elucidation of novel furanone-coumarins with inhibitory effects for tumor-promotion.
AID355096Antiinflammatory activity in NMRI mouse macrophages assessed as inhibition of A23187-induced LTC4 release at 25 uM by Ellman's method relative to control1996Journal of natural products, Dec, Volume: 59, Issue:12
Antiinflammatory activity of coumarins from Santolina oblongifolia.
AID444777Inhibition of human carbonic anhydrase 6 by stopped flow CO2 hydration assay2010Journal of medicinal chemistry, Jan-14, Volume: 53, Issue:1
Deciphering the mechanism of carbonic anhydrase inhibition with coumarins and thiocoumarins.
AID377244Inhibition of 12-O-tetradecanoylphorbol-13-acetate-induced EBV-early antigen activation in human Raji cells assessed as EA activation at 0.32 nmol relative to 12-O-tetradecanoylphorbol-13-acetate2000Journal of natural products, Sep, Volume: 63, Issue:9
Chemical constituents of Clausena excavata: isolation and structure elucidation of novel furanone-coumarins with inhibitory effects for tumor-promotion.
AID516865Selectivity index, ratio of IC50 for sorbitol dehydrogenase to IC50 for kidney aldose reductase 22010Bioorganic & medicinal chemistry letters, Oct-01, Volume: 20, Issue:19
6,7-Dihydroxy-4-phenylcoumarin as inhibitor of aldose reductase 2.
AID553155Displacement of [3H]estradiol human recombinant 17beta-HSD2 expressed in Escherichia coli BL21 (DE3)-RIL at 0.6 uM by scintillation counting in presence of NAD+2011Journal of medicinal chemistry, Jan-13, Volume: 54, Issue:1
Synthesis and biological evaluation of (6- and 7-phenyl) coumarin derivatives as selective nonsteroidal inhibitors of 17β-hydroxysteroid dehydrogenase type 1.
AID1102095Stimulation of Diaporthe ampelina growth at 30 to 300 uM after 120 hr by microplate photometric analysis2003Journal of agricultural and food chemistry, Feb-12, Volume: 51, Issue:4
Natural fungicides from Ruta graveolens L. leaves, including a new quinolone alkaloid.
AID1102110Stimulation of Colletotrichum gloeosporioides growth at 30 to 300 uM after 48 hr by microplate photometric analysis2003Journal of agricultural and food chemistry, Feb-12, Volume: 51, Issue:4
Natural fungicides from Ruta graveolens L. leaves, including a new quinolone alkaloid.
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.
AID553153Displacement of [3H]estrone human recombinant 17beta-HSD1 expressed in Escherichia coli BL21 (DE3)-RIL at 0.6 uM by scintillation counting in presence of NADPH2011Journal of medicinal chemistry, Jan-13, Volume: 54, Issue:1
Synthesis and biological evaluation of (6- and 7-phenyl) coumarin derivatives as selective nonsteroidal inhibitors of 17β-hydroxysteroid dehydrogenase type 1.
AID444771Inhibition of human carbonic anhydrase 1 by stopped flow CO2 hydration assay2010Journal of medicinal chemistry, Jan-14, Volume: 53, Issue:1
Deciphering the mechanism of carbonic anhydrase inhibition with coumarins and thiocoumarins.
AID444774Inhibition of human carbonic anhydrase 4 by stopped flow CO2 hydration assay2010Journal of medicinal chemistry, Jan-14, Volume: 53, Issue:1
Deciphering the mechanism of carbonic anhydrase inhibition with coumarins and thiocoumarins.
AID444778Inhibition of human carbonic anhydrase 7 by stopped flow CO2 hydration assay2010Journal of medicinal chemistry, Jan-14, Volume: 53, Issue:1
Deciphering the mechanism of carbonic anhydrase inhibition with coumarins and thiocoumarins.
AID516863Inhibition kidney aldose reductase 2 by spectrophotometric analysis2010Bioorganic & medicinal chemistry letters, Oct-01, Volume: 20, Issue:19
6,7-Dihydroxy-4-phenylcoumarin as inhibitor of aldose reductase 2.
AID639825Inhibition of human recombinant aldose reductase using D-glyceraldehyde as substrate preincubated for 10 mins before substrate addition measured for every 10 secs for 50 mins by spectrophotometry2012Bioorganic & medicinal chemistry, Feb-01, Volume: 20, Issue:3
Construction of an Indonesian herbal constituents database and its use in Random Forest modelling in a search for inhibitors of aldose reductase.
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.
AID344674Selectivity index, ratio of MED for Bursaphelenchus xylophilus to LC50 Oryzias latipes2008Bioorganic & medicinal chemistry letters, Oct-15, Volume: 18, Issue:20
Synthesis and biological evaluation of alkoxycoumarins as novel nematicidal constituents.
AID355094Antiinflammatory activity in NMRI mouse macrophages assessed as inhibition of A23187-induced PGE2 release at 100 uM by Ellman's method relative to control1996Journal of natural products, Dec, Volume: 59, Issue:12
Antiinflammatory activity of coumarins from Santolina oblongifolia.
AID377247Cytotoxicity against human Raji cells assessed as cell viability at 3.2 nmol by trypan blue staining2000Journal of natural products, Sep, Volume: 63, Issue:9
Chemical constituents of Clausena excavata: isolation and structure elucidation of novel furanone-coumarins with inhibitory effects for tumor-promotion.
AID1159607Screen for inhibitors of RMI FANCM (MM2) intereaction2016Journal of biomolecular screening, Jul, Volume: 21, Issue:6
A High-Throughput Screening Strategy to Identify Protein-Protein Interaction Inhibitors That Block the Fanconi Anemia DNA Repair Pathway.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (54)

TimeframeStudies, This Drug (%)All Drugs %
pre-19906 (11.11)18.7374
1990's3 (5.56)18.2507
2000's7 (12.96)29.6817
2010's28 (51.85)24.3611
2020's10 (18.52)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 31.99

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 Index31.99 (24.57)
Research Supply Index4.04 (2.92)
Research Growth Index4.99 (4.65)
Search Engine Demand Index42.09 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (31.99)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews1 (1.79%)6.00%
Case Studies1 (1.79%)4.05%
Observational0 (0.00%)0.25%
Other54 (96.43%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]