(2E,6E)-9-(furan-3-yl)-2,6-dimethylnona-2,6-dien-1-ol

Details

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Internal ID 565731c1-e360-4efb-a2ed-982e07e82579
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Monoterpenoids > Aromatic monoterpenoids
IUPAC Name (2E,6E)-9-(furan-3-yl)-2,6-dimethylnona-2,6-dien-1-ol
SMILES (Canonical) CC(=CCCC1=COC=C1)CCC=C(C)CO
SMILES (Isomeric) C/C(=C\CCC1=COC=C1)/CC/C=C(\C)/CO
InChI InChI=1S/C15H22O2/c1-13(5-3-7-14(2)11-16)6-4-8-15-9-10-17-12-15/h6-7,9-10,12,16H,3-5,8,11H2,1-2H3/b13-6+,14-7+
InChI Key AAVGOORHZRJMPA-AANLELRNSA-N
Popularity 1 reference 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) 33.40 Ų
XlogP 3.80
Atomic LogP (AlogP) 3.88
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 7

Synonyms

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1786-16-9
9-(3-Furyl)-2,6-dimethylnona-2,6-dien-1-ol
(2E,6E)-9-(furan-3-yl)-2,6-dimethylnona-2,6-dien-1-ol

2D Structure

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2D Structure of (2E,6E)-9-(furan-3-yl)-2,6-dimethylnona-2,6-dien-1-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9892 98.92%
Caco-2 + 0.9028 90.28%
Blood Brain Barrier + 0.8000 80.00%
Human oral bioavailability - 0.7286 72.86%
Subcellular localzation Lysosomes 0.4666 46.66%
OATP2B1 inhibitior - 0.8558 85.58%
OATP1B1 inhibitior + 0.7880 78.80%
OATP1B3 inhibitior + 0.9408 94.08%
MATE1 inhibitior - 0.9212 92.12%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior + 0.5629 56.29%
P-glycoprotein inhibitior - 0.9389 93.89%
P-glycoprotein substrate - 0.8696 86.96%
CYP3A4 substrate - 0.5416 54.16%
CYP2C9 substrate - 0.6219 62.19%
CYP2D6 substrate - 0.7173 71.73%
CYP3A4 inhibition - 0.6944 69.44%
CYP2C9 inhibition - 0.7643 76.43%
CYP2C19 inhibition - 0.6704 67.04%
CYP2D6 inhibition - 0.8447 84.47%
CYP1A2 inhibition - 0.6174 61.74%
CYP2C8 inhibition - 0.7383 73.83%
CYP inhibitory promiscuity - 0.6115 61.15%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.8328 83.28%
Carcinogenicity (trinary) Non-required 0.5029 50.29%
Eye corrosion - 0.8197 81.97%
Eye irritation + 0.5362 53.62%
Skin irritation - 0.5485 54.85%
Skin corrosion - 0.9483 94.83%
Ames mutagenesis - 0.7400 74.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6947 69.47%
Micronuclear - 0.9300 93.00%
Hepatotoxicity - 0.5875 58.75%
skin sensitisation + 0.6020 60.20%
Respiratory toxicity - 0.5111 51.11%
Reproductive toxicity + 0.5101 51.01%
Mitochondrial toxicity - 0.7000 70.00%
Nephrotoxicity - 0.5703 57.03%
Acute Oral Toxicity (c) III 0.8624 86.24%
Estrogen receptor binding - 0.6777 67.77%
Androgen receptor binding - 0.7171 71.71%
Thyroid receptor binding - 0.7046 70.46%
Glucocorticoid receptor binding - 0.5651 56.51%
Aromatase binding - 0.5789 57.89%
PPAR gamma + 0.7164 71.64%
Honey bee toxicity - 0.9384 93.84%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity + 0.5832 58.32%
Fish aquatic toxicity + 0.9623 96.23%

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
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 94.13% 92.08%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.96% 91.11%
CHEMBL2581 P07339 Cathepsin D 91.72% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 91.58% 94.73%
CHEMBL2039 P27338 Monoamine oxidase B 88.64% 92.51%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.64% 99.17%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 86.36% 94.45%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.83% 86.33%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 83.26% 96.09%

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.
Torreya nucifera

Cross-Links

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PubChem 12444395
NPASS NPC257500
LOTUS LTS0038447
wikiData Q104908382