6-(2,6-Dihydroxy-4-methylphenyl)-2-methylheptan-3-one

Details

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Internal ID 12bcfc38-7a37-46c6-a04e-fc62bd800283
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name 6-(2,6-dihydroxy-4-methylphenyl)-2-methylheptan-3-one
SMILES (Canonical) CC1=CC(=C(C(=C1)O)C(C)CCC(=O)C(C)C)O
SMILES (Isomeric) CC1=CC(=C(C(=C1)O)C(C)CCC(=O)C(C)C)O
InChI InChI=1S/C15H22O3/c1-9(2)12(16)6-5-11(4)15-13(17)7-10(3)8-14(15)18/h7-9,11,17-18H,5-6H2,1-4H3
InChI Key USAFCWDUVGSTRI-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H22O3
Molecular Weight 250.33 g/mol
Exact Mass 250.15689456 g/mol
Topological Polar Surface Area (TPSA) 57.50 Ų
XlogP 3.20
Atomic LogP (AlogP) 3.52
H-Bond Acceptor 3
H-Bond Donor 2
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 6-(2,6-Dihydroxy-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 + 0.9856 98.56%
Caco-2 + 0.9027 90.27%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability + 0.6857 68.57%
Subcellular localzation Mitochondria 0.8748 87.48%
OATP2B1 inhibitior - 0.8537 85.37%
OATP1B1 inhibitior + 0.9119 91.19%
OATP1B3 inhibitior + 0.9617 96.17%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.6492 64.92%
P-glycoprotein inhibitior - 0.9229 92.29%
P-glycoprotein substrate - 0.9627 96.27%
CYP3A4 substrate - 0.6576 65.76%
CYP2C9 substrate + 0.6168 61.68%
CYP2D6 substrate - 0.6944 69.44%
CYP3A4 inhibition + 0.5747 57.47%
CYP2C9 inhibition + 0.6100 61.00%
CYP2C19 inhibition - 0.5000 50.00%
CYP2D6 inhibition - 0.7608 76.08%
CYP1A2 inhibition + 0.8161 81.61%
CYP2C8 inhibition - 0.9705 97.05%
CYP inhibitory promiscuity - 0.5800 58.00%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.7545 75.45%
Carcinogenicity (trinary) Non-required 0.7246 72.46%
Eye corrosion - 0.9201 92.01%
Eye irritation + 0.6415 64.15%
Skin irritation - 0.5114 51.14%
Skin corrosion - 0.7042 70.42%
Ames mutagenesis - 0.7570 75.70%
Human Ether-a-go-go-Related Gene inhibition + 0.6506 65.06%
Micronuclear - 0.9000 90.00%
Hepatotoxicity + 0.5500 55.00%
skin sensitisation + 0.7040 70.40%
Respiratory toxicity - 0.6778 67.78%
Reproductive toxicity - 0.5778 57.78%
Mitochondrial toxicity - 0.5125 51.25%
Nephrotoxicity - 0.6788 67.88%
Acute Oral Toxicity (c) III 0.7303 73.03%
Estrogen receptor binding - 0.7808 78.08%
Androgen receptor binding - 0.5182 51.82%
Thyroid receptor binding - 0.5111 51.11%
Glucocorticoid receptor binding - 0.6441 64.41%
Aromatase binding - 0.6699 66.99%
PPAR gamma - 0.5487 54.87%
Honey bee toxicity - 0.9627 96.27%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.7400 74.00%
Fish aquatic toxicity + 0.9490 94.90%

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 95.96% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.46% 91.11%
CHEMBL3401 O75469 Pregnane X receptor 92.43% 94.73%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.77% 96.09%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 90.55% 90.71%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 87.31% 99.15%
CHEMBL3060 Q9Y345 Glycine transporter 2 85.64% 99.17%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.13% 95.56%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 80.09% 96.95%

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.
Dysoxylum parasiticum

Cross-Links

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PubChem 86201326
LOTUS LTS0212921
wikiData Q105278093