5-Hydroxy-2-phenyl-4-chromanone

Details

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Internal ID 6231434b-a8a6-4917-988f-7c233186ef32
Taxonomy Phenylpropanoids and polyketides > Flavonoids > Flavans > Flavanones
IUPAC Name 5-hydroxy-2-phenyl-2,3-dihydrochromen-4-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H12O3/c16-11-7-4-8-13-15(11)12(17)9-14(18-13)10-5-2-1-3-6-10/h1-8,14,16H,9H2
InChI Key CRWQDRUCLPDWEK-UHFFFAOYSA-N
Popularity 36 references in papers

Physical and Chemical Properties

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Molecular Formula C15H12O3
Molecular Weight 240.25 g/mol
Exact Mass 240.078644241 g/mol
Topological Polar Surface Area (TPSA) 46.50 Ų
XlogP 3.10
Atomic LogP (AlogP) 3.10
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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5-Hydroxy-2-phenyl-4-chromanone
22701-17-3
5-hydroxy-2-phenyl-3,4-dihydro-2H-1-benzopyran-4-one
5-hydroxy-flavanone
5-hydroxy-2-phenyl-2,3-dihydrochromen-4-one
SCHEMBL10362225
5-Hydroxy-2-phenyl-2,3-dihydro-4H-chromen-4-one #

2D Structure

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2D Structure of 5-Hydroxy-2-phenyl-4-chromanone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9940 99.40%
Caco-2 - 0.5517 55.17%
Blood Brain Barrier - 0.7000 70.00%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Mitochondria 0.8014 80.14%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9487 94.87%
OATP1B3 inhibitior + 0.9912 99.12%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.7975 79.75%
P-glycoprotein inhibitior - 0.9192 91.92%
P-glycoprotein substrate - 0.9646 96.46%
CYP3A4 substrate - 0.5966 59.66%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7429 74.29%
CYP3A4 inhibition - 0.7489 74.89%
CYP2C9 inhibition + 0.8634 86.34%
CYP2C19 inhibition + 0.9058 90.58%
CYP2D6 inhibition - 0.8422 84.22%
CYP1A2 inhibition + 0.8753 87.53%
CYP2C8 inhibition - 0.7243 72.43%
CYP inhibitory promiscuity - 0.5811 58.11%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.9513 95.13%
Carcinogenicity (trinary) Non-required 0.4772 47.72%
Eye corrosion - 0.9871 98.71%
Eye irritation + 0.8950 89.50%
Skin irritation + 0.6217 62.17%
Skin corrosion - 0.9835 98.35%
Ames mutagenesis + 0.5700 57.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6508 65.08%
Micronuclear + 0.7118 71.18%
Hepatotoxicity + 0.5158 51.58%
skin sensitisation - 0.8266 82.66%
Respiratory toxicity + 0.6222 62.22%
Reproductive toxicity + 0.9000 90.00%
Mitochondrial toxicity + 0.6750 67.50%
Nephrotoxicity + 0.6272 62.72%
Acute Oral Toxicity (c) II 0.3619 36.19%
Estrogen receptor binding + 0.6218 62.18%
Androgen receptor binding - 0.4936 49.36%
Thyroid receptor binding - 0.5359 53.59%
Glucocorticoid receptor binding - 0.7826 78.26%
Aromatase binding + 0.6852 68.52%
PPAR gamma + 0.8246 82.46%
Honey bee toxicity - 0.9070 90.70%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity - 0.6400 64.00%
Fish aquatic toxicity + 0.7545 75.45%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
No proven targets yet!

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.51% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.40% 95.56%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 93.94% 99.23%
CHEMBL2581 P07339 Cathepsin D 92.13% 98.95%
CHEMBL3137262 O60341 LSD1/CoREST complex 85.03% 97.09%
CHEMBL1806 P11388 DNA topoisomerase II alpha 82.14% 89.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 80.64% 86.33%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 80.18% 99.15%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
To see more specific details click the taxa you are interested in.
Dalbergia cochinchinensis

Cross-Links

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PubChem 586090
LOTUS LTS0172109
wikiData Q105103137