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7-hydroxy-4-phenyl-8-(1-piperidinylmethyl)-1-benzopyran-2-one

Description

7-hydroxy-4-phenyl-8-(1-piperidinylmethyl)-1-benzopyran-2-one : no description available [CHeBI]

Cross-References

ID SourceID
PubMed CID5360356
CHEMBL ID1312987
CHEBI ID116562

Synonyms (23)

Synonym
brn 1297095
7-hydroxy-4-phenyl-8-(piperidinomethyl)coumarin
coumarin, 7-hydroxy-4-phenyl-8-(piperidinomethyl)-
OPREA1_211574
smr000080082
7-hydroxy-4-phenyl-8-(1-piperidinylmethyl)-2h-chromen-2-one
MLS000065505
OPREA1_499950
CHEBI:116562
7-hydroxy-4-phenyl-8-(piperidin-1-ylmethyl)chromen-2-one
AKOS001629665
7-hydroxy-4-phenyl-8-(piperidin-1-ylmethyl)-2h-chromen-2-one
STK711897
5-20-03-00407 (beilstein handbook reference)
10549-67-4
HMS2392P23
CHEMBL1312987
Q27199449
7-hydroxy-4-phenyl-8-(1-piperidinylmethyl)-1-benzopyran-2-one
DTXSID50147156
SR-01000443028-1
sr-01000443028
mfcd01731752

Drug Classes (1)

ClassDescription
neoflavonoidAny 1-benzopyran with an aryl substituent at position 4. The term was originally restricted to natural products, but is now also used to describe semi-synthetic and fully synthetic compounds.

Protein Targets (15)

Potency Measurements

ProteinTaxonomyMeasurementAverage (mM)Bioassay(s)
Chain A, HADH2 proteinHomo sapiens (human)Potency31.6228AID893
Chain B, HADH2 proteinHomo sapiens (human)Potency31.6228AID893
Chain A, 2-oxoglutarate OxygenaseHomo sapiens (human)Potency35.4813AID2147
Chain A, Ferritin light chainEquus caballus (horse)Potency4.4668AID485281
Chain A, CruzipainTrypanosoma cruziPotency15.8489AID1476
acid sphingomyelinaseHomo sapiens (human)Potency15.8489AID504937
aldehyde dehydrogenase 1 family, member A1Homo sapiens (human)Potency39.8107AID1030
nonstructural protein 1Influenza A virus (A/WSN/1933(H1N1))Potency3.1623AID2326
15-hydroxyprostaglandin dehydrogenase [NAD(+)] isoform 1Homo sapiens (human)Potency15.8489AID894
importin subunit beta-1 isoform 1Homo sapiens (human)Potency7.0648AID540253; AID540263
snurportin-1Homo sapiens (human)Potency7.0648AID540253; AID540263
GTP-binding nuclear protein Ran isoform 1Homo sapiens (human)Potency2.9093AID540253
gemininHomo sapiens (human)Potency23.1093AID624296
caspase-1 isoform alpha precursorHomo sapiens (human)Potency3.1623AID900
Caspase-7Homo sapiens (human)Potency3.1623AID889

Bioassays (7)

Assay IDTitleYearJournalArticle
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 13ISSN: 1934-9300Microsphere-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
ISSN: 1552-4922
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
ISSN: 1557-8127
High-throughput multiplex flow cytometry screening for botulinum neurotoxin type a light chain protease inhibitors.
AID504812Inverse Agonists of the Thyroid Stimulating Hormone Receptor: HTS campaign2010Endocrinology, Jul, Volume: 151, Issue:7
ISSN: 1945-7170
A small molecule inverse agonist for the human thyroid-stimulating hormone receptor.
AID588501High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Lethal Factor Protease, MLPCN compound set2010Current protocols in cytometry, Oct, Volume: Chapter 13ISSN: 1934-9300Microsphere-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
ISSN: 1552-4922
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
ISSN: 1557-8127
High-throughput multiplex flow cytometry screening for botulinum neurotoxin type a light chain protease inhibitors.
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 13ISSN: 1934-9300Microsphere-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
ISSN: 1552-4922
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
ISSN: 1557-8127
High-throughput multiplex flow cytometry screening for botulinum neurotoxin type a light chain protease inhibitors.
AID651635Viability Counterscreen for Primary qHTS for Inhibitors of ATXN expression2022The Journal of biological chemistry, 08, Volume: 298, Issue:8
ISSN: 1083-351X
AID1745845Primary qHTS for Inhibitors of ATXN expression2022The Journal of biological chemistry, 08, Volume: 298, Issue:8
ISSN: 1083-351X
AID504810Antagonists of the Thyroid Stimulating Hormone Receptor: HTS campaign2010Endocrinology, Jul, Volume: 151, Issue:7
ISSN: 1945-7170
A small molecule inverse agonist for the human thyroid-stimulating hormone receptor.

Research

Studies (5)

TimeframeStudies, This Drug (%)All Drugs %
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's1 (20.00)29.6817
2010's3 (60.00)24.3611
2020's1 (20.00)2.80

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%
Other5 (100.00%)84.16%
SubstanceStudiesClassesRolesFirst YearLast YearAverage AgeRelationship StrengthTrialspre-19901990's2000's2010'spost-2020
LSM-26505neoflavonoid00low000000
7'-hydroxy-4'-(4-methoxyphenyl)-4,4,5'-trimethyl-2-spiro[1,3-diazinane-6,2'-3,4-dihydro-2H-1-benzopyran]thioneneoflavonoid00low000000
calophyllolidneoflavonoid00low000000
mammeisinneoflavonoidmetabolite00low000000
8-(diethylaminomethyl)-7-hydroxy-4-phenyl-1-benzopyran-2-oneneoflavonoid00low000000
8-[[butyl(ethyl)amino]methyl]-7-hydroxy-4-phenyl-1-benzopyran-2-oneneoflavonoid00low000000
serratinneoflavonoid00low000000
3'-Hydroxy-5,7,4'-trimethoxy-4-phenylcoumarinneoflavonoid00low000000
4-(4-Methoxyphenyl)-5,7-dihydroxychroman-2-oneneoflavonoid00low000000
crolibulinneoflavonoid00low000000
ConditionIndicatedStudiesFirst YearLast YearAverage AgeRelationship StrengthTrialspre-19901990's2000's2010'spost-2020
Inflammation02010201014.0high000100
Innate Inflammatory Response02010201014.0high000100