13-(Furan-3-yl)-2,6,10-trimethyltrideca-2,6,10-trien-4-one

Details

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Internal ID 875b525f-2a86-479c-9d58-9338f211181e
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name 13-(furan-3-yl)-2,6,10-trimethyltrideca-2,6,10-trien-4-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C20H28O2/c1-16(2)13-20(21)14-18(4)9-5-7-17(3)8-6-10-19-11-12-22-15-19/h8-9,11-13,15H,5-7,10,14H2,1-4H3
InChI Key YMGPQWFLZKKFAH-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C20H28O2
Molecular Weight 300.40 g/mol
Exact Mass 300.208930132 g/mol
Topological Polar Surface Area (TPSA) 30.20 Ų
XlogP 5.80
Atomic LogP (AlogP) 5.81
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 9

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 13-(Furan-3-yl)-2,6,10-trimethyltrideca-2,6,10-trien-4-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9960 99.60%
Caco-2 + 0.8215 82.15%
Blood Brain Barrier + 0.8000 80.00%
Human oral bioavailability - 0.6571 65.71%
Subcellular localzation Mitochondria 0.3842 38.42%
OATP2B1 inhibitior - 0.8580 85.80%
OATP1B1 inhibitior + 0.8050 80.50%
OATP1B3 inhibitior + 0.9356 93.56%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior + 0.6898 68.98%
P-glycoprotein inhibitior - 0.5666 56.66%
P-glycoprotein substrate - 0.7616 76.16%
CYP3A4 substrate + 0.5274 52.74%
CYP2C9 substrate - 0.7891 78.91%
CYP2D6 substrate - 0.8447 84.47%
CYP3A4 inhibition - 0.8238 82.38%
CYP2C9 inhibition - 0.7270 72.70%
CYP2C19 inhibition - 0.5323 53.23%
CYP2D6 inhibition - 0.9021 90.21%
CYP1A2 inhibition + 0.6096 60.96%
CYP2C8 inhibition - 0.7380 73.80%
CYP inhibitory promiscuity - 0.5122 51.22%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7800 78.00%
Carcinogenicity (trinary) Non-required 0.5404 54.04%
Eye corrosion - 0.8511 85.11%
Eye irritation - 0.6783 67.83%
Skin irritation + 0.5826 58.26%
Skin corrosion - 0.9517 95.17%
Ames mutagenesis - 0.6500 65.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8741 87.41%
Micronuclear - 0.9000 90.00%
Hepatotoxicity - 0.5000 50.00%
skin sensitisation + 0.7302 73.02%
Respiratory toxicity + 0.5444 54.44%
Reproductive toxicity - 0.5730 57.30%
Mitochondrial toxicity - 0.7750 77.50%
Nephrotoxicity - 0.5526 55.26%
Acute Oral Toxicity (c) III 0.7947 79.47%
Estrogen receptor binding - 0.4948 49.48%
Androgen receptor binding - 0.6159 61.59%
Thyroid receptor binding - 0.5214 52.14%
Glucocorticoid receptor binding - 0.4647 46.47%
Aromatase binding - 0.5122 51.22%
PPAR gamma + 0.8250 82.50%
Honey bee toxicity - 0.9156 91.56%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity + 0.5800 58.00%
Fish aquatic toxicity + 0.9570 95.70%

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 94.90% 94.73%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.28% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 94.01% 94.45%
CHEMBL3060 Q9Y345 Glycine transporter 2 91.47% 99.17%
CHEMBL2581 P07339 Cathepsin D 91.33% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.45% 96.09%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 89.28% 92.08%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 86.01% 90.71%
CHEMBL1806 P11388 DNA topoisomerase II alpha 82.99% 89.00%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 74052480
LOTUS LTS0065073
wikiData Q105350518