6-(2-Hydroxy-4-methylphenyl)-2-methylheptan-3-one

Details

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Internal ID a2f0fa34-cada-4d8a-a061-97d27771a784
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name 6-(2-hydroxy-4-methylphenyl)-2-methylheptan-3-one
SMILES (Canonical) CC1=CC(=C(C=C1)C(C)CCC(=O)C(C)C)O
SMILES (Isomeric) CC1=CC(=C(C=C1)C(C)CCC(=O)C(C)C)O
InChI InChI=1S/C15H22O2/c1-10(2)14(16)8-6-12(4)13-7-5-11(3)9-15(13)17/h5,7,9-10,12,17H,6,8H2,1-4H3
InChI Key NJCAREDQTSPWPA-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H22O2
Molecular Weight 234.33 g/mol
Exact Mass 234.161979940 g/mol
Topological Polar Surface Area (TPSA) 37.30 Ų
XlogP 3.80
Atomic LogP (AlogP) 3.81
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 6-(2-Hydroxy-4-methylphenyl)-2-methylheptan-3-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9968 99.68%
Caco-2 + 0.9507 95.07%
Blood Brain Barrier + 0.7000 70.00%
Human oral bioavailability + 0.7429 74.29%
Subcellular localzation Mitochondria 0.9032 90.32%
OATP2B1 inhibitior - 0.8570 85.70%
OATP1B1 inhibitior + 0.9403 94.03%
OATP1B3 inhibitior + 0.9530 95.30%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.6494 64.94%
P-glycoprotein inhibitior - 0.9506 95.06%
P-glycoprotein substrate - 0.9307 93.07%
CYP3A4 substrate - 0.6418 64.18%
CYP2C9 substrate + 0.6168 61.68%
CYP2D6 substrate - 0.6944 69.44%
CYP3A4 inhibition - 0.8286 82.86%
CYP2C9 inhibition - 0.7313 73.13%
CYP2C19 inhibition - 0.7683 76.83%
CYP2D6 inhibition - 0.7707 77.07%
CYP1A2 inhibition + 0.8701 87.01%
CYP2C8 inhibition - 0.9493 94.93%
CYP inhibitory promiscuity - 0.7556 75.56%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.6822 68.22%
Carcinogenicity (trinary) Non-required 0.7111 71.11%
Eye corrosion - 0.7402 74.02%
Eye irritation - 0.5251 52.51%
Skin irritation + 0.6131 61.31%
Skin corrosion + 0.5163 51.63%
Ames mutagenesis - 0.8200 82.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3703 37.03%
Micronuclear - 0.9800 98.00%
Hepatotoxicity + 0.5750 57.50%
skin sensitisation + 0.8177 81.77%
Respiratory toxicity - 0.6222 62.22%
Reproductive toxicity - 0.6444 64.44%
Mitochondrial toxicity - 0.7375 73.75%
Nephrotoxicity - 0.6834 68.34%
Acute Oral Toxicity (c) III 0.8252 82.52%
Estrogen receptor binding - 0.8025 80.25%
Androgen receptor binding - 0.6138 61.38%
Thyroid receptor binding - 0.5668 56.68%
Glucocorticoid receptor binding - 0.7357 73.57%
Aromatase binding - 0.6863 68.63%
PPAR gamma - 0.7850 78.50%
Honey bee toxicity - 0.9695 96.95%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity - 0.6800 68.00%
Fish aquatic toxicity + 0.9413 94.13%

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 95.90% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.65% 91.11%
CHEMBL3401 O75469 Pregnane X receptor 92.17% 94.73%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.97% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.79% 95.56%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 90.58% 90.71%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 86.26% 99.15%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.40% 99.17%
CHEMBL4581 P52732 Kinesin-like protein 1 82.68% 93.18%
CHEMBL3359 P21462 Formyl peptide receptor 1 80.78% 93.56%

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.
Juniperus chinensis
Juniperus formosana
Pilocarpus riedelianus

Cross-Links

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PubChem 11128247
LOTUS LTS0044791
wikiData Q104172552