4-(4-Hydroxy-3-methoxyphenyl)-2,3-dihydroinden-1-one

Details

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Internal ID f8a02b7a-3d34-4082-a651-0ad9f2f9ef4e
Taxonomy Benzenoids > Indanes > Indanones
IUPAC Name 4-(4-hydroxy-3-methoxyphenyl)-2,3-dihydroinden-1-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C16H14O3/c1-19-16-9-10(5-7-15(16)18)11-3-2-4-13-12(11)6-8-14(13)17/h2-5,7,9,18H,6,8H2,1H3
InChI Key KARVYYFAYWTLFR-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C16H14O3
Molecular Weight 254.28 g/mol
Exact Mass 254.094294304 g/mol
Topological Polar Surface Area (TPSA) 46.50 Ų
XlogP 2.90
Atomic LogP (AlogP) 3.20
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 4-(4-Hydroxy-3-methoxyphenyl)-2,3-dihydroinden-1-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 + 0.8485 84.85%
Blood Brain Barrier - 0.6250 62.50%
Human oral bioavailability + 0.6429 64.29%
Subcellular localzation Mitochondria 0.8795 87.95%
OATP2B1 inhibitior - 0.8587 85.87%
OATP1B1 inhibitior + 0.9622 96.22%
OATP1B3 inhibitior + 0.9705 97.05%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior + 0.5685 56.85%
P-glycoprotein inhibitior - 0.9335 93.35%
P-glycoprotein substrate - 0.8997 89.97%
CYP3A4 substrate + 0.5136 51.36%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.6901 69.01%
CYP3A4 inhibition - 0.7140 71.40%
CYP2C9 inhibition + 0.7472 74.72%
CYP2C19 inhibition + 0.7086 70.86%
CYP2D6 inhibition - 0.9370 93.70%
CYP1A2 inhibition + 0.8864 88.64%
CYP2C8 inhibition + 0.6389 63.89%
CYP inhibitory promiscuity - 0.6215 62.15%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.8720 87.20%
Carcinogenicity (trinary) Warning 0.4612 46.12%
Eye corrosion - 0.9819 98.19%
Eye irritation + 0.6179 61.79%
Skin irritation - 0.5711 57.11%
Skin corrosion - 0.9688 96.88%
Ames mutagenesis - 0.5082 50.82%
Human Ether-a-go-go-Related Gene inhibition - 0.6661 66.61%
Micronuclear - 0.5292 52.92%
Hepatotoxicity + 0.5250 52.50%
skin sensitisation - 0.8838 88.38%
Respiratory toxicity + 0.5333 53.33%
Reproductive toxicity + 0.7444 74.44%
Mitochondrial toxicity + 0.5250 52.50%
Nephrotoxicity + 0.4936 49.36%
Acute Oral Toxicity (c) III 0.6483 64.83%
Estrogen receptor binding + 0.8828 88.28%
Androgen receptor binding + 0.5750 57.50%
Thyroid receptor binding + 0.5710 57.10%
Glucocorticoid receptor binding + 0.9094 90.94%
Aromatase binding + 0.7777 77.77%
PPAR gamma + 0.7733 77.33%
Honey bee toxicity - 0.9008 90.08%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.5049 50.49%
Fish aquatic toxicity + 0.8781 87.81%

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
CHEMBL2581 P07339 Cathepsin D 98.23% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 96.12% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 95.36% 86.33%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.47% 91.11%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 94.12% 99.15%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.34% 96.09%
CHEMBL1907 P15144 Aminopeptidase N 92.58% 93.31%
CHEMBL2535 P11166 Glucose transporter 91.87% 98.75%
CHEMBL1951 P21397 Monoamine oxidase A 90.73% 91.49%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 89.23% 94.00%
CHEMBL2056 P21728 Dopamine D1 receptor 84.54% 91.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 84.29% 99.23%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 83.56% 93.03%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 82.38% 85.14%
CHEMBL2146302 O94925 Glutaminase kidney isoform, mitochondrial 82.08% 100.00%
CHEMBL1163101 O75460 Serine/threonine-protein kinase/endoribonuclease IRE1 81.91% 98.11%
CHEMBL5608 Q16288 NT-3 growth factor receptor 81.82% 95.89%
CHEMBL3438 Q05513 Protein kinase C zeta 81.70% 88.48%
CHEMBL1806 P11388 DNA topoisomerase II alpha 81.30% 89.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.61% 99.17%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 80.01% 95.50%

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.
Uvaria afzelii

Cross-Links

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PubChem 90995952
LOTUS LTS0178767
wikiData Q105137980