(E,6R)-2-methyl-6-(4-methylphenyl)hept-3-en-2-ol

Details

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Internal ID 61263031-d143-4ecb-84e6-92abea866c90
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name (E,6R)-2-methyl-6-(4-methylphenyl)hept-3-en-2-ol
SMILES (Canonical) CC1=CC=C(C=C1)C(C)CC=CC(C)(C)O
SMILES (Isomeric) CC1=CC=C(C=C1)[C@H](C)C/C=C/C(C)(C)O
InChI InChI=1S/C15H22O/c1-12-7-9-14(10-8-12)13(2)6-5-11-15(3,4)16/h5,7-11,13,16H,6H2,1-4H3/b11-5+/t13-/m1/s1
InChI Key FCWODWIUPFWVDN-HQIZRNBFSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H22O
Molecular Weight 218.33 g/mol
Exact Mass 218.167065321 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 3.60
Atomic LogP (AlogP) 3.82
H-Bond Acceptor 1
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 (E,6R)-2-methyl-6-(4-methylphenyl)hept-3-en-2-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9852 98.52%
Caco-2 + 0.8481 84.81%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability + 0.7286 72.86%
Subcellular localzation Mitochondria 0.4802 48.02%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8837 88.37%
OATP1B3 inhibitior + 0.9394 93.94%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.5754 57.54%
P-glycoprotein inhibitior - 0.9692 96.92%
P-glycoprotein substrate - 0.9492 94.92%
CYP3A4 substrate - 0.6788 67.88%
CYP2C9 substrate - 0.6048 60.48%
CYP2D6 substrate - 0.7198 71.98%
CYP3A4 inhibition - 0.6446 64.46%
CYP2C9 inhibition - 0.6120 61.20%
CYP2C19 inhibition - 0.6449 64.49%
CYP2D6 inhibition - 0.8665 86.65%
CYP1A2 inhibition - 0.6422 64.22%
CYP2C8 inhibition - 0.9679 96.79%
CYP inhibitory promiscuity - 0.5132 51.32%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.5675 56.75%
Carcinogenicity (trinary) Non-required 0.6097 60.97%
Eye corrosion + 0.4705 47.05%
Eye irritation + 0.6313 63.13%
Skin irritation + 0.7506 75.06%
Skin corrosion - 0.6082 60.82%
Ames mutagenesis - 0.8300 83.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6800 68.00%
Micronuclear - 0.9900 99.00%
Hepatotoxicity + 0.6088 60.88%
skin sensitisation + 0.9153 91.53%
Respiratory toxicity - 0.5222 52.22%
Reproductive toxicity - 0.7222 72.22%
Mitochondrial toxicity - 0.7435 74.35%
Nephrotoxicity - 0.7389 73.89%
Acute Oral Toxicity (c) III 0.7870 78.70%
Estrogen receptor binding - 0.6813 68.13%
Androgen receptor binding - 0.8174 81.74%
Thyroid receptor binding + 0.5551 55.51%
Glucocorticoid receptor binding - 0.6786 67.86%
Aromatase binding - 0.5000 50.00%
PPAR gamma - 0.6655 66.55%
Honey bee toxicity - 0.9414 94.14%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity + 0.5200 52.00%
Fish aquatic toxicity + 0.9401 94.01%

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
CHEMBL3401 O75469 Pregnane X receptor 94.01% 94.73%
CHEMBL2581 P07339 Cathepsin D 93.49% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.21% 95.56%
CHEMBL5966 P55899 IgG receptor FcRn large subunit p51 88.00% 90.93%
CHEMBL3359 P21462 Formyl peptide receptor 1 87.53% 93.56%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 84.12% 100.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 84.07% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 83.85% 96.09%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 82.25% 93.65%

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.
Baccharis dracunculifolia

Cross-Links

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PubChem 162868571
LOTUS LTS0275817
wikiData Q104993404