(2S)-5,7-dimethyl-2-phenyl-2,3-dihydrochromen-4-one

Details

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Internal ID 4b57659a-29b4-4154-a7eb-0b524a9ca6a7
Taxonomy Phenylpropanoids and polyketides > Flavonoids > Flavans > Flavanones
IUPAC Name (2S)-5,7-dimethyl-2-phenyl-2,3-dihydrochromen-4-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C17H16O2/c1-11-8-12(2)17-14(18)10-15(19-16(17)9-11)13-6-4-3-5-7-13/h3-9,15H,10H2,1-2H3/t15-/m0/s1
InChI Key FGUBFGWYEYFGRK-HNNXBMFYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C17H16O2
Molecular Weight 252.31 g/mol
Exact Mass 252.115029749 g/mol
Topological Polar Surface Area (TPSA) 26.30 Ų
XlogP 3.60
Atomic LogP (AlogP) 4.01
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (2S)-5,7-dimethyl-2-phenyl-2,3-dihydrochromen-4-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 1.0000 100.00%
Caco-2 + 0.9349 93.49%
Blood Brain Barrier + 0.6750 67.50%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Mitochondria 0.7250 72.50%
OATP2B1 inhibitior - 0.8633 86.33%
OATP1B1 inhibitior + 0.9538 95.38%
OATP1B3 inhibitior + 0.9861 98.61%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior + 0.6352 63.52%
P-glycoprotein inhibitior - 0.8262 82.62%
P-glycoprotein substrate - 0.9589 95.89%
CYP3A4 substrate - 0.5815 58.15%
CYP2C9 substrate - 0.8074 80.74%
CYP2D6 substrate - 0.7466 74.66%
CYP3A4 inhibition - 0.6920 69.20%
CYP2C9 inhibition + 0.7187 71.87%
CYP2C19 inhibition + 0.8412 84.12%
CYP2D6 inhibition - 0.9619 96.19%
CYP1A2 inhibition + 0.9525 95.25%
CYP2C8 inhibition - 0.7291 72.91%
CYP inhibitory promiscuity + 0.5899 58.99%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9413 94.13%
Carcinogenicity (trinary) Non-required 0.5459 54.59%
Eye corrosion - 0.9671 96.71%
Eye irritation - 0.6906 69.06%
Skin irritation - 0.6487 64.87%
Skin corrosion - 0.9752 97.52%
Ames mutagenesis - 0.5200 52.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3716 37.16%
Micronuclear + 0.5959 59.59%
Hepatotoxicity + 0.5875 58.75%
skin sensitisation - 0.6807 68.07%
Respiratory toxicity + 0.5333 53.33%
Reproductive toxicity + 0.7556 75.56%
Mitochondrial toxicity - 0.7000 70.00%
Nephrotoxicity + 0.5588 55.88%
Acute Oral Toxicity (c) III 0.8057 80.57%
Estrogen receptor binding + 0.6965 69.65%
Androgen receptor binding + 0.5602 56.02%
Thyroid receptor binding - 0.5396 53.96%
Glucocorticoid receptor binding - 0.5995 59.95%
Aromatase binding + 0.5917 59.17%
PPAR gamma - 0.5881 58.81%
Honey bee toxicity - 0.9149 91.49%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity + 0.6300 63.00%
Fish aquatic toxicity + 0.7866 78.66%

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
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 96.53% 95.56%
CHEMBL2581 P07339 Cathepsin D 94.89% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.09% 91.11%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 89.99% 85.14%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 89.51% 99.23%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.51% 86.33%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 87.97% 94.80%
CHEMBL1806 P11388 DNA topoisomerase II alpha 87.31% 89.00%
CHEMBL3401 O75469 Pregnane X receptor 87.19% 94.73%
CHEMBL5805 Q9NR97 Toll-like receptor 8 85.81% 96.25%

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.
Cryptocarya chinensis

Cross-Links

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PubChem 162937491
LOTUS LTS0051721
wikiData Q104995065