Methyl 4,4,8-trimethyl-7-oxocycloundeca-1,5,8-triene-1-carboxylate

Details

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Internal ID e95e7cc3-6c9f-4edc-a14d-5eeb0c61105f
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name methyl 4,4,8-trimethyl-7-oxocycloundeca-1,5,8-triene-1-carboxylate
SMILES (Canonical) CC1=CCCC(=CCC(C=CC1=O)(C)C)C(=O)OC
SMILES (Isomeric) CC1=CCCC(=CCC(C=CC1=O)(C)C)C(=O)OC
InChI InChI=1S/C16H22O3/c1-12-6-5-7-13(15(18)19-4)8-10-16(2,3)11-9-14(12)17/h6,8-9,11H,5,7,10H2,1-4H3
InChI Key OPNKSPPKQUMBSL-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C16H22O3
Molecular Weight 262.34 g/mol
Exact Mass 262.15689456 g/mol
Topological Polar Surface Area (TPSA) 43.40 Ų
XlogP 3.60
Atomic LogP (AlogP) 3.37
H-Bond Acceptor 3
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Methyl 4,4,8-trimethyl-7-oxocycloundeca-1,5,8-triene-1-carboxylate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9941 99.41%
Caco-2 + 0.9504 95.04%
Blood Brain Barrier + 0.6500 65.00%
Human oral bioavailability + 0.6857 68.57%
Subcellular localzation Mitochondria 0.8302 83.02%
OATP2B1 inhibitior - 0.8572 85.72%
OATP1B1 inhibitior + 0.9439 94.39%
OATP1B3 inhibitior + 0.9447 94.47%
MATE1 inhibitior - 0.7200 72.00%
OCT2 inhibitior - 0.5500 55.00%
BSEP inhibitior - 0.5944 59.44%
P-glycoprotein inhibitior - 0.9057 90.57%
P-glycoprotein substrate - 0.9068 90.68%
CYP3A4 substrate + 0.6096 60.96%
CYP2C9 substrate - 0.7974 79.74%
CYP2D6 substrate - 0.9074 90.74%
CYP3A4 inhibition - 0.8208 82.08%
CYP2C9 inhibition - 0.7598 75.98%
CYP2C19 inhibition - 0.7033 70.33%
CYP2D6 inhibition - 0.9409 94.09%
CYP1A2 inhibition - 0.7576 75.76%
CYP2C8 inhibition - 0.8082 80.82%
CYP inhibitory promiscuity - 0.9031 90.31%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7871 78.71%
Carcinogenicity (trinary) Non-required 0.5688 56.88%
Eye corrosion - 0.9671 96.71%
Eye irritation + 0.5401 54.01%
Skin irritation - 0.5502 55.02%
Skin corrosion - 0.9868 98.68%
Ames mutagenesis - 0.6300 63.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6812 68.12%
Micronuclear - 0.7700 77.00%
Hepatotoxicity + 0.7750 77.50%
skin sensitisation + 0.5907 59.07%
Respiratory toxicity - 0.5778 57.78%
Reproductive toxicity - 0.6275 62.75%
Mitochondrial toxicity - 0.6000 60.00%
Nephrotoxicity + 0.8099 80.99%
Acute Oral Toxicity (c) III 0.7086 70.86%
Estrogen receptor binding + 0.5325 53.25%
Androgen receptor binding - 0.8545 85.45%
Thyroid receptor binding - 0.7438 74.38%
Glucocorticoid receptor binding - 0.7655 76.55%
Aromatase binding - 0.6113 61.13%
PPAR gamma - 0.5526 55.26%
Honey bee toxicity - 0.9489 94.89%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity - 0.7300 73.00%
Fish aquatic toxicity + 0.9941 99.41%

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
CHEMBL4040 P28482 MAP kinase ERK2 96.32% 83.82%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.06% 91.11%
CHEMBL4208 P20618 Proteasome component C5 88.39% 90.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.86% 96.09%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 86.90% 85.14%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 86.28% 94.45%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.81% 95.56%
CHEMBL2581 P07339 Cathepsin D 85.56% 98.95%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 81.78% 99.23%
CHEMBL1871 P10275 Androgen Receptor 81.31% 96.43%
CHEMBL5966 P55899 IgG receptor FcRn large subunit p51 80.66% 90.93%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.23% 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.
Asteriscus daltonii subsp. vogelii
Asteriscus graveolens

Cross-Links

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PubChem 73831179
LOTUS LTS0053079
wikiData Q105196453