(2E,6Z,10E)-6-(hydroxymethyl)-2,10-dimethyldodeca-2,6,10-triene-1,12-diol

Details

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Internal ID f9ead141-dbd0-4515-8338-652c695d34cc
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name (2E,6Z,10E)-6-(hydroxymethyl)-2,10-dimethyldodeca-2,6,10-triene-1,12-diol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H26O3/c1-13(9-10-16)5-3-7-15(12-18)8-4-6-14(2)11-17/h6-7,9,16-18H,3-5,8,10-12H2,1-2H3/b13-9+,14-6+,15-7-
InChI Key MOFGXPKHCUZJEB-TVVOFDSQSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C15H26O3
Molecular Weight 254.36 g/mol
Exact Mass 254.18819469 g/mol
Topological Polar Surface Area (TPSA) 60.70 Ų
XlogP 2.30
Atomic LogP (AlogP) 2.34
H-Bond Acceptor 3
H-Bond Donor 3
Rotatable Bonds 9

Synonyms

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SCHEMBL3078531

2D Structure

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2D Structure of (2E,6Z,10E)-6-(hydroxymethyl)-2,10-dimethyldodeca-2,6,10-triene-1,12-diol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9613 96.13%
Caco-2 + 0.8090 80.90%
Blood Brain Barrier + 0.6105 61.05%
Human oral bioavailability - 0.6000 60.00%
Subcellular localzation Lysosomes 0.4526 45.26%
OATP2B1 inhibitior - 0.8526 85.26%
OATP1B1 inhibitior + 0.9274 92.74%
OATP1B3 inhibitior + 0.9457 94.57%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.7893 78.93%
BSEP inhibitior - 0.6190 61.90%
P-glycoprotein inhibitior - 0.9333 93.33%
P-glycoprotein substrate - 0.9114 91.14%
CYP3A4 substrate - 0.5620 56.20%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7450 74.50%
CYP3A4 inhibition - 0.8266 82.66%
CYP2C9 inhibition - 0.8700 87.00%
CYP2C19 inhibition - 0.8977 89.77%
CYP2D6 inhibition - 0.8864 88.64%
CYP1A2 inhibition - 0.8273 82.73%
CYP2C8 inhibition - 0.9285 92.85%
CYP inhibitory promiscuity - 0.8397 83.97%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.7123 71.23%
Carcinogenicity (trinary) Non-required 0.6478 64.78%
Eye corrosion - 0.6175 61.75%
Eye irritation + 0.7453 74.53%
Skin irritation - 0.8122 81.22%
Skin corrosion - 0.9741 97.41%
Ames mutagenesis - 0.7100 71.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5656 56.56%
Micronuclear - 0.9800 98.00%
Hepatotoxicity - 0.8125 81.25%
skin sensitisation + 0.6357 63.57%
Respiratory toxicity - 0.8333 83.33%
Reproductive toxicity - 0.9479 94.79%
Mitochondrial toxicity - 0.8125 81.25%
Nephrotoxicity + 0.6230 62.30%
Acute Oral Toxicity (c) IV 0.6097 60.97%
Estrogen receptor binding - 0.6162 61.62%
Androgen receptor binding - 0.8140 81.40%
Thyroid receptor binding - 0.6265 62.65%
Glucocorticoid receptor binding - 0.5153 51.53%
Aromatase binding - 0.6008 60.08%
PPAR gamma + 0.7533 75.33%
Honey bee toxicity - 0.9251 92.51%
Biodegradation + 0.5250 52.50%
Crustacea aquatic toxicity - 0.6100 61.00%
Fish aquatic toxicity + 0.9481 94.81%

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 85.39% 92.08%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 84.05% 96.09%
CHEMBL2581 P07339 Cathepsin D 83.85% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 80.87% 91.11%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.75% 99.17%

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.
Arctotis venusta

Cross-Links

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PubChem 87477157
LOTUS LTS0104086
wikiData Q105168863