Page last updated: 2024-11-11

geiparvarin

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Description

geiparvarin: from Geijera parviflora; structure given in first source [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

FloraRankFlora DefinitionFamilyFamily Definition
Geijeragenus[no description available]RutaceaeA plant family in the order Sapindales that grows in warmer regions and has conspicuous flowers.[MeSH]

Cross-References

ID SourceID
PubMed CID5910585
CHEMBL ID56918
SCHEMBL ID2532495
MeSH IDM0162982

Synonyms (15)

Synonym
nsc 142227
2h-1-benzopyran-2-one, 7-((3-(4,5-dihydro-5,5-dimethyl-4-oxo-2-furanyl)-2-butenyl)oxy)-, (e)-
o0m5jb2l95 ,
unii-o0m5jb2l95
mls002920544 ,
36413-91-9
geiparvarin
nsc-142227
CHEMBL56918
7-[(e)-3-(5,5-dimethyl-4-oxofuran-2-yl)but-2-enoxy]chromen-2-one
7-(((2e)-3-(5,5-dimethyl-4-oxo-4,5-dihydrofuran-2-yl)but-2-en-1-yl)oxy)-2h-chromen-2-one
bdbm50421583
SCHEMBL2532495
Q5530160
DTXSID201026772

Research Excerpts

Overview

Geiparvarin is an antiproliferative compound isolated from the leaves of Geijera parviflora. It may represent a new drug which targets tubulin.

ExcerptReferenceRelevance
"Geiparvarin (GN) is a natural compound isolated from the leaves of Geijera parviflora and exhibits anticancer activity. "( Geiparvarin Inhibits the Progression of Osteosarcoma by Down-regulating COX2 Expression.
Chen, S; Du, J; Huang, P; Wang, B; Zhang, Z; Zou, H, 2023
)
3.8
"Geiparvarin is an antiproliferative compound whose mechanism of action has not yet been identified. "( Interaction of geiparvarin and related compounds with purified microtubular protein.
Bisi, A; Bocca, C; Da Re, P; Gabriel, L; Gadoni, E; Miglietta, A; Rampa, A; Valenti, P, 1996
)
2.09
"Geiparvarin is an antiproliferative compound isolated from the leaves of Geijera parviflora, and may represent a new drug which targets tubulin. "( Antimicrotubular and cytotoxic activity of geiparvarin analogues, alone and in combination with paclitaxel.
Bisi, A; Bocca, C; Gabriel, L; Miglietta, A; Rampa, A; Valenti, P, 2001
)
2.02
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Protein Targets (8)

Inhibition Measurements

ProteinTaxonomyMeasurementAverageMin (ref.)Avg (ref.)Max (ref.)Bioassay(s)
Carbonic anhydrase 12Homo sapiens (human)Ki0.83000.00021.10439.9000AID729559
Carbonic anhydrase 1Homo sapiens (human)Ki9.75000.00001.372610.0000AID729563
Carbonic anhydrase 2Homo sapiens (human)Ki100.00000.00000.72369.9200AID729562
Amine oxidase [flavin-containing] AHomo sapiens (human)IC50 (µMol)26.91540.00002.37899.7700AID126361
Amine oxidase [flavin-containing] BHomo sapiens (human)IC50 (µMol)0.14450.00001.89149.5700AID127195
Carbonic anhydrase 7Homo sapiens (human)Ki7.82000.00021.37379.9000AID729561
Carbonic anhydrase 9Homo sapiens (human)Ki0.60000.00010.78749.9000AID729560
Carbonic anhydrase 13Homo sapiens (human)Ki9.62000.00031.23099.8000AID729558
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023]

Biological Processes (31)

Processvia Protein(s)Taxonomy
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)
biogenic amine metabolic processAmine oxidase [flavin-containing] AHomo sapiens (human)
positive regulation of signal transductionAmine oxidase [flavin-containing] AHomo sapiens (human)
dopamine catabolic processAmine oxidase [flavin-containing] AHomo sapiens (human)
response to xenobiotic stimulusAmine oxidase [flavin-containing] BHomo sapiens (human)
response to toxic substanceAmine oxidase [flavin-containing] BHomo sapiens (human)
response to aluminum ionAmine oxidase [flavin-containing] BHomo sapiens (human)
response to selenium ionAmine oxidase [flavin-containing] BHomo sapiens (human)
negative regulation of serotonin secretionAmine oxidase [flavin-containing] BHomo sapiens (human)
phenylethylamine catabolic processAmine oxidase [flavin-containing] BHomo sapiens (human)
substantia nigra developmentAmine oxidase [flavin-containing] BHomo sapiens (human)
response to lipopolysaccharideAmine oxidase [flavin-containing] BHomo sapiens (human)
dopamine catabolic processAmine oxidase [flavin-containing] BHomo sapiens (human)
response to ethanolAmine oxidase [flavin-containing] BHomo sapiens (human)
positive regulation of dopamine metabolic processAmine oxidase [flavin-containing] BHomo sapiens (human)
hydrogen peroxide biosynthetic processAmine oxidase [flavin-containing] BHomo sapiens (human)
response to corticosteroneAmine oxidase [flavin-containing] BHomo 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)
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 13Homo sapiens (human)
[Information is prepared from geneontology information from the June-17-2024 release]

Molecular Functions (13)

Processvia Protein(s)Taxonomy
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)
protein bindingAmine oxidase [flavin-containing] AHomo sapiens (human)
primary amine oxidase activityAmine oxidase [flavin-containing] AHomo sapiens (human)
aliphatic amine oxidase activityAmine oxidase [flavin-containing] AHomo sapiens (human)
monoamine oxidase activityAmine oxidase [flavin-containing] AHomo sapiens (human)
flavin adenine dinucleotide bindingAmine oxidase [flavin-containing] AHomo sapiens (human)
protein bindingAmine oxidase [flavin-containing] BHomo sapiens (human)
primary amine oxidase activityAmine oxidase [flavin-containing] BHomo sapiens (human)
electron transfer activityAmine oxidase [flavin-containing] BHomo sapiens (human)
identical protein bindingAmine oxidase [flavin-containing] BHomo sapiens (human)
aliphatic amine oxidase activityAmine oxidase [flavin-containing] BHomo sapiens (human)
monoamine oxidase activityAmine oxidase [flavin-containing] BHomo sapiens (human)
flavin adenine dinucleotide bindingAmine oxidase [flavin-containing] BHomo sapiens (human)
zinc ion bindingCarbonic anhydrase 7Homo sapiens (human)
carbonate dehydratase activityCarbonic anhydrase 7Homo 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)
protein bindingCarbonic anhydrase 13Homo sapiens (human)
zinc ion bindingCarbonic anhydrase 13Homo sapiens (human)
carbonate dehydratase activityCarbonic anhydrase 13Homo sapiens (human)
[Information is prepared from geneontology information from the June-17-2024 release]

Ceullar Components (17)

Processvia Protein(s)Taxonomy
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)
mitochondrionAmine oxidase [flavin-containing] AHomo sapiens (human)
mitochondrial outer membraneAmine oxidase [flavin-containing] AHomo sapiens (human)
cytosolAmine oxidase [flavin-containing] AHomo sapiens (human)
mitochondrionAmine oxidase [flavin-containing] AHomo sapiens (human)
mitochondrionAmine oxidase [flavin-containing] BHomo sapiens (human)
mitochondrial envelopeAmine oxidase [flavin-containing] BHomo sapiens (human)
mitochondrial outer membraneAmine oxidase [flavin-containing] BHomo sapiens (human)
dendriteAmine oxidase [flavin-containing] BHomo sapiens (human)
neuronal cell bodyAmine oxidase [flavin-containing] BHomo sapiens (human)
mitochondrionAmine oxidase [flavin-containing] BHomo sapiens (human)
cytosolCarbonic anhydrase 7Homo sapiens (human)
cytoplasmCarbonic anhydrase 7Homo 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)
cytosolCarbonic anhydrase 13Homo sapiens (human)
myelin sheathCarbonic anhydrase 13Homo sapiens (human)
intracellular membrane-bounded organelleCarbonic anhydrase 13Homo sapiens (human)
cytoplasmCarbonic anhydrase 13Homo sapiens (human)
cytosolCarbonic anhydrase 13Homo sapiens (human)
[Information is prepared from geneontology information from the June-17-2024 release]

Bioassays (44)

Assay IDTitleYearJournalArticle
AID665498Induction of apoptosis in human A549 cells assessed as viable cells at 1 uM after 48 hrs by annexinV/propidium iodide staining-based flow cytometric analysis ( Rvb = 95.96%)2012European journal of medicinal chemistry, Jul, Volume: 53Convenient synthesis of novel geiparvarin analogs with potential anti-cancer activity via click chemistry.
AID665494Cytotoxicity against human QGY7701 cells by after 48 hrs by MTT assay2012European journal of medicinal chemistry, Jul, Volume: 53Convenient synthesis of novel geiparvarin analogs with potential anti-cancer activity via click chemistry.
AID729563Inhibition of human carbonic anhydrase 1 preincubated for 6 hrs by CO2 hydration stopped-flow assay2013Bioorganic & medicinal chemistry, Mar-15, Volume: 21, Issue:6
Natural product coumarins that inhibit human carbonic anhydrases.
AID729559Inhibition of human carbonic anhydrase 12 preincubated for 6 hrs by CO2 hydration stopped-flow assay2013Bioorganic & medicinal chemistry, Mar-15, Volume: 21, Issue:6
Natural product coumarins that inhibit human carbonic anhydrases.
AID225074Inhibitory effect on the proliferation of murine mammary carcinoma FM3A cells1992Journal of medicinal chemistry, May-15, Volume: 35, Issue:10
Geiparvarin analogues. 3. Synthesis and cytostatic activity of 3(2H)-furanone and 4,5-dihydro-3(2H)-furanone congeners of geiparvarin, containing a geraniol-like fragment in the side chain.
AID665511Induction of apoptosis in human A549 cells assessed as early apoptotic cells at 8 uM after 48 hrs by annexinV/propidium iodide staining-based flow cytometric analysis ( Rvb = 0.15%)2012European journal of medicinal chemistry, Jul, Volume: 53Convenient synthesis of novel geiparvarin analogs with potential anti-cancer activity via click chemistry.
AID729560Inhibition of human carbonic anhydrase 9 preincubated for 6 hrs by CO2 hydration stopped-flow assay2013Bioorganic & medicinal chemistry, Mar-15, Volume: 21, Issue:6
Natural product coumarins that inhibit human carbonic anhydrases.
AID665499Induction of apoptosis in human A549 cells assessed as early apoptotic cells at 1 uM after 48 hrs by annexinV/propidium iodide staining-based flow cytometric analysis ( Rvb = 0.15%)2012European journal of medicinal chemistry, Jul, Volume: 53Convenient synthesis of novel geiparvarin analogs with potential anti-cancer activity via click chemistry.
AID665495Cytotoxicity against human SW480 cells by after 48 hrs by MTT assay2012European journal of medicinal chemistry, Jul, Volume: 53Convenient synthesis of novel geiparvarin analogs with potential anti-cancer activity via click chemistry.
AID47468Ability to inhibit human CEM tumor cell proliferation by 50%1989Journal of medicinal chemistry, Feb, Volume: 32, Issue:2
Synthesis and cytostatic activity of geiparvarin analogues.
AID665491Cytotoxicity against human L02 cells by after 48 hrs by MTT assay2012European journal of medicinal chemistry, Jul, Volume: 53Convenient synthesis of novel geiparvarin analogs with potential anti-cancer activity via click chemistry.
AID665509Induction of apoptosis in human A549 cells assessed as viable cells at 4 uM after 48 hrs by annexinV/propidium iodide staining-based flow cytometric analysis (Rvb = 3.72%)2012European journal of medicinal chemistry, Jul, Volume: 53Convenient synthesis of novel geiparvarin analogs with potential anti-cancer activity via click chemistry.
AID221971Inhibitory effect on the proliferation of human T-lymphocyte MT-4 cells.1992Journal of medicinal chemistry, May-15, Volume: 35, Issue:10
Geiparvarin analogues. 3. Synthesis and cytostatic activity of 3(2H)-furanone and 4,5-dihydro-3(2H)-furanone congeners of geiparvarin, containing a geraniol-like fragment in the side chain.
AID665503Induction of apoptosis in human A549 cells assessed as early apoptotic cells at 2 uM after 48 hrs by annexinV/propidium iodide staining-based flow cytometric analysis ( Rvb = 0.15%)2012European journal of medicinal chemistry, Jul, Volume: 53Convenient synthesis of novel geiparvarin analogs with potential anti-cancer activity via click chemistry.
AID125492Ability to inhibit human Molt/4F tumor cell proliferation by 50%1989Journal of medicinal chemistry, Feb, Volume: 32, Issue:2
Synthesis and cytostatic activity of geiparvarin analogues.
AID729558Inhibition of human carbonic anhydrase 13 preincubated for 6 hrs by CO2 hydration stopped-flow assay2013Bioorganic & medicinal chemistry, Mar-15, Volume: 21, Issue:6
Natural product coumarins that inhibit human carbonic anhydrases.
AID665500Induction of apoptosis in human A549 cells assessed as late apoptotic cells at 1 uM after 48 hrs by annexinV/propidium iodide staining-based flow cytometric analysis (Rvb = 0.16%)2012European journal of medicinal chemistry, Jul, Volume: 53Convenient synthesis of novel geiparvarin analogs with potential anti-cancer activity via click chemistry.
AID665502Induction of apoptosis in human A549 cells assessed as viable cells at 2 uM after 48 hrs by annexinV/propidium iodide staining-based flow cytometric analysis ( Rvb = 95.96%)2012European journal of medicinal chemistry, Jul, Volume: 53Convenient synthesis of novel geiparvarin analogs with potential anti-cancer activity via click chemistry.
AID665504Induction of apoptosis in human A549 cells assessed as late apoptotic cells at 2 uM after 48 hrs by annexinV/propidium iodide staining-based flow cytometric analysis (Rvb = 0.16%)2012European journal of medicinal chemistry, Jul, Volume: 53Convenient synthesis of novel geiparvarin analogs with potential anti-cancer activity via click chemistry.
AID729562Inhibition of human carbonic anhydrase 2 preincubated for 6 hrs by CO2 hydration stopped-flow assay2013Bioorganic & medicinal chemistry, Mar-15, Volume: 21, Issue:6
Natural product coumarins that inhibit human carbonic anhydrases.
AID165914Ability to inhibit human Raji tumor cell proliferation by 50%1989Journal of medicinal chemistry, Feb, Volume: 32, Issue:2
Synthesis and cytostatic activity of geiparvarin analogues.
AID15873Partition coefficient of compound was determined2002Bioorganic & medicinal chemistry letters, Dec-16, Volume: 12, Issue:24
Natural and synthetic geiparvarins are strong and selective MAO-B inhibitors. Synthesis and SAR studies.
AID665497Cytotoxicity against human MDA-MB-231 cells by after 48 hrs by MTT assay2012European journal of medicinal chemistry, Jul, Volume: 53Convenient synthesis of novel geiparvarin analogs with potential anti-cancer activity via click chemistry.
AID221801Inhibitory effect on the proliferation of human B-lymphoblast Raji cells.1992Journal of medicinal chemistry, May-15, Volume: 35, Issue:10
Geiparvarin analogues. 3. Synthesis and cytostatic activity of 3(2H)-furanone and 4,5-dihydro-3(2H)-furanone congeners of geiparvarin, containing a geraniol-like fragment in the side chain.
AID72034Ability to inhibit murine FM3A tumor cell proliferation by 50%1989Journal of medicinal chemistry, Feb, Volume: 32, Issue:2
Synthesis and cytostatic activity of geiparvarin analogues.
AID79135Ability to inhibit human H9 tumor cell proliferation by 50%1989Journal of medicinal chemistry, Feb, Volume: 32, Issue:2
Synthesis and cytostatic activity of geiparvarin analogues.
AID665501Induction of apoptosis in human A549 cells assessed as viable cells at 1 uM after 48 hrs by annexinV/propidium iodide staining-based flow cytometric analysis (Rvb = 3.72%)2012European journal of medicinal chemistry, Jul, Volume: 53Convenient synthesis of novel geiparvarin analogs with potential anti-cancer activity via click chemistry.
AID665512Induction of apoptosis in human A549 cells assessed as late apoptotic cells at 8 uM after 48 hrs by annexinV/propidium iodide staining-based flow cytometric analysis (Rvb = 0.16%)2012European journal of medicinal chemistry, Jul, Volume: 53Convenient synthesis of novel geiparvarin analogs with potential anti-cancer activity via click chemistry.
AID225051Inhibitory effect on the proliferation of murine leukemia L1210 cells.1992Journal of medicinal chemistry, May-15, Volume: 35, Issue:10
Geiparvarin analogues. 3. Synthesis and cytostatic activity of 3(2H)-furanone and 4,5-dihydro-3(2H)-furanone congeners of geiparvarin, containing a geraniol-like fragment in the side chain.
AID98701Ability to inhibit murine L1210 tumor cell proliferation by 50%1989Journal of medicinal chemistry, Feb, Volume: 32, Issue:2
Synthesis and cytostatic activity of geiparvarin analogues.
AID665508Induction of apoptosis in human A549 cells assessed as late apoptotic cells at 4 uM after 48 hrs by annexinV/propidium iodide staining-based flow cytometric analysis (Rvb = 0.16%)2012European journal of medicinal chemistry, Jul, Volume: 53Convenient synthesis of novel geiparvarin analogs with potential anti-cancer activity via click chemistry.
AID665513Induction of apoptosis in human A549 cells assessed as viable cells at 8 uM after 48 hrs by annexinV/propidium iodide staining-based flow cytometric analysis (Rvb = 3.72%)2012European journal of medicinal chemistry, Jul, Volume: 53Convenient synthesis of novel geiparvarin analogs with potential anti-cancer activity via click chemistry.
AID127195Inhibitory potency against Monoamine oxidase B2002Bioorganic & medicinal chemistry letters, Dec-16, Volume: 12, Issue:24
Natural and synthetic geiparvarins are strong and selective MAO-B inhibitors. Synthesis and SAR studies.
AID665510Induction of apoptosis in human A549 cells assessed as viable cells at 8 uM after 48 hrs by annexinV/propidium iodide staining-based flow cytometric analysis ( Rvb = 95.96%)2012European journal of medicinal chemistry, Jul, Volume: 53Convenient synthesis of novel geiparvarin analogs with potential anti-cancer activity via click chemistry.
AID210309Inhibitory effect on the proliferation of T-lymphoblast molt/4F cells.1992Journal of medicinal chemistry, May-15, Volume: 35, Issue:10
Geiparvarin analogues. 3. Synthesis and cytostatic activity of 3(2H)-furanone and 4,5-dihydro-3(2H)-furanone congeners of geiparvarin, containing a geraniol-like fragment in the side chain.
AID665496Cytotoxicity against human SGC7901 cells by after 48 hrs by MTT assay2012European journal of medicinal chemistry, Jul, Volume: 53Convenient synthesis of novel geiparvarin analogs with potential anti-cancer activity via click chemistry.
AID665492Cytotoxicity against human A549 cells by after 48 hrs by MTT assay2012European journal of medicinal chemistry, Jul, Volume: 53Convenient synthesis of novel geiparvarin analogs with potential anti-cancer activity via click chemistry.
AID729561Inhibition of human carbonic anhydrase 7 preincubated for 6 hrs by CO2 hydration stopped-flow assay2013Bioorganic & medicinal chemistry, Mar-15, Volume: 21, Issue:6
Natural product coumarins that inhibit human carbonic anhydrases.
AID105737Ability to inhibit human MT-4 tumor cell proliferation by 50%1989Journal of medicinal chemistry, Feb, Volume: 32, Issue:2
Synthesis and cytostatic activity of geiparvarin analogues.
AID665505Induction of apoptosis in human A549 cells assessed as viable cells at 2 uM after 48 hrs by annexinV/propidium iodide staining-based flow cytometric analysis (Rvb = 3.72%)2012European journal of medicinal chemistry, Jul, Volume: 53Convenient synthesis of novel geiparvarin analogs with potential anti-cancer activity via click chemistry.
AID665493Cytotoxicity against human HeLa cells by after 48 hrs by MTT assay2012European journal of medicinal chemistry, Jul, Volume: 53Convenient synthesis of novel geiparvarin analogs with potential anti-cancer activity via click chemistry.
AID665506Induction of apoptosis in human A549 cells assessed as viable cells at 4 uM after 48 hrs by annexinV/propidium iodide staining-based flow cytometric analysis ( Rvb = 95.96%)2012European journal of medicinal chemistry, Jul, Volume: 53Convenient synthesis of novel geiparvarin analogs with potential anti-cancer activity via click chemistry.
AID665507Induction of apoptosis in human A549 cells assessed as early apoptotic cells at 4 uM after 48 hrs by annexinV/propidium iodide staining-based flow cytometric analysis ( Rvb = 0.15%)2012European journal of medicinal chemistry, Jul, Volume: 53Convenient synthesis of novel geiparvarin analogs with potential anti-cancer activity via click chemistry.
AID126361Inhibitory potency against Monoamine oxidase A2002Bioorganic & medicinal chemistry letters, Dec-16, Volume: 12, Issue:24
Natural and synthetic geiparvarins are strong and selective MAO-B inhibitors. Synthesis and SAR studies.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (17)

TimeframeStudies, This Drug (%)All Drugs %
pre-19901 (5.88)18.7374
1990's8 (47.06)18.2507
2000's5 (29.41)29.6817
2010's2 (11.76)24.3611
2020's1 (5.88)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 20.01

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 Index20.01 (24.57)
Research Supply Index2.89 (2.92)
Research Growth Index5.27 (4.65)
Search Engine Demand Index15.26 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (20.01)

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%
Other17 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]