4-Hydroxy-3-methoxy-4-(3-phenylprop-2-enyl)cyclohex-2-en-1-one

Details

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Internal ID 2d6387c4-602b-4554-b755-c2a2558e72ce
Taxonomy Benzenoids > Benzene and substituted derivatives > Styrenes
IUPAC Name 4-hydroxy-3-methoxy-4-(3-phenylprop-2-enyl)cyclohex-2-en-1-one
SMILES (Canonical) COC1=CC(=O)CCC1(CC=CC2=CC=CC=C2)O
SMILES (Isomeric) COC1=CC(=O)CCC1(CC=CC2=CC=CC=C2)O
InChI InChI=1S/C16H18O3/c1-19-15-12-14(17)9-11-16(15,18)10-5-8-13-6-3-2-4-7-13/h2-8,12,18H,9-11H2,1H3
InChI Key UMSXFHQOERKWAU-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C16H18O3
Molecular Weight 258.31 g/mol
Exact Mass 258.125594432 g/mol
Topological Polar Surface Area (TPSA) 46.50 Ų
XlogP 1.90
Atomic LogP (AlogP) 2.71
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 4-Hydroxy-3-methoxy-4-(3-phenylprop-2-enyl)cyclohex-2-en-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 + 0.9952 99.52%
Caco-2 + 0.8130 81.30%
Blood Brain Barrier + 0.5500 55.00%
Human oral bioavailability + 0.5286 52.86%
Subcellular localzation Mitochondria 0.8884 88.84%
OATP2B1 inhibitior - 0.8579 85.79%
OATP1B1 inhibitior + 0.8316 83.16%
OATP1B3 inhibitior + 0.9598 95.98%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior + 0.6204 62.04%
P-glycoprotein inhibitior - 0.8948 89.48%
P-glycoprotein substrate - 0.9460 94.60%
CYP3A4 substrate - 0.5000 50.00%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8153 81.53%
CYP3A4 inhibition - 0.8866 88.66%
CYP2C9 inhibition - 0.7944 79.44%
CYP2C19 inhibition - 0.5769 57.69%
CYP2D6 inhibition - 0.9383 93.83%
CYP1A2 inhibition - 0.8453 84.53%
CYP2C8 inhibition - 0.8112 81.12%
CYP inhibitory promiscuity - 0.8057 80.57%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.8271 82.71%
Carcinogenicity (trinary) Non-required 0.5549 55.49%
Eye corrosion - 0.9796 97.96%
Eye irritation - 0.6323 63.23%
Skin irritation - 0.6209 62.09%
Skin corrosion - 0.9604 96.04%
Ames mutagenesis - 0.6754 67.54%
Human Ether-a-go-go-Related Gene inhibition - 0.4387 43.87%
Micronuclear - 0.8141 81.41%
Hepatotoxicity - 0.5641 56.41%
skin sensitisation - 0.6433 64.33%
Respiratory toxicity + 0.8222 82.22%
Reproductive toxicity + 0.6444 64.44%
Mitochondrial toxicity - 0.6000 60.00%
Nephrotoxicity + 0.5119 51.19%
Acute Oral Toxicity (c) III 0.5538 55.38%
Estrogen receptor binding + 0.7664 76.64%
Androgen receptor binding + 0.6558 65.58%
Thyroid receptor binding - 0.6255 62.55%
Glucocorticoid receptor binding + 0.5707 57.07%
Aromatase binding + 0.5446 54.46%
PPAR gamma + 0.5987 59.87%
Honey bee toxicity - 0.9322 93.22%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity + 0.5200 52.00%
Fish aquatic toxicity + 0.8258 82.58%

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 98.42% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 97.71% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 95.31% 86.33%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.37% 96.09%
CHEMBL1821 P08173 Muscarinic acetylcholine receptor M4 93.35% 94.08%
CHEMBL2581 P07339 Cathepsin D 93.16% 98.95%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 91.32% 96.00%
CHEMBL3192 Q9BY41 Histone deacetylase 8 87.64% 93.99%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 86.30% 94.62%
CHEMBL221 P23219 Cyclooxygenase-1 84.40% 90.17%
CHEMBL4208 P20618 Proteasome component C5 84.20% 90.00%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 84.14% 91.71%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 82.69% 95.50%
CHEMBL216 P11229 Muscarinic acetylcholine receptor M1 82.45% 94.23%
CHEMBL5028 O14672 ADAM10 81.88% 97.50%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 81.10% 93.00%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 80.78% 85.14%

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 sissoo

Cross-Links

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PubChem 72805767
LOTUS LTS0144767
wikiData Q105275725