4,4,8-Trimethyl-7-oxocycloundeca-1,5,8-triene-1-carboxylic acid

Details

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Internal ID bae0304a-bdd7-4455-a1d4-db273d50d9c6
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name 4,4,8-trimethyl-7-oxocycloundeca-1,5,8-triene-1-carboxylic acid
SMILES (Canonical) CC1=CCCC(=CCC(C=CC1=O)(C)C)C(=O)O
SMILES (Isomeric) CC1=CCCC(=CCC(C=CC1=O)(C)C)C(=O)O
InChI InChI=1S/C15H20O3/c1-11-5-4-6-12(14(17)18)7-9-15(2,3)10-8-13(11)16/h5,7-8,10H,4,6,9H2,1-3H3,(H,17,18)
InChI Key BPPXABXKJZPLPR-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H20O3
Molecular Weight 248.32 g/mol
Exact Mass 248.14124450 g/mol
Topological Polar Surface Area (TPSA) 54.40 Ų
XlogP 3.30
Atomic LogP (AlogP) 3.28
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 4,4,8-Trimethyl-7-oxocycloundeca-1,5,8-triene-1-carboxylic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9923 99.23%
Caco-2 + 0.8609 86.09%
Blood Brain Barrier - 0.5500 55.00%
Human oral bioavailability + 0.6000 60.00%
Subcellular localzation Mitochondria 0.8544 85.44%
OATP2B1 inhibitior - 0.8538 85.38%
OATP1B1 inhibitior + 0.9551 95.51%
OATP1B3 inhibitior + 0.8744 87.44%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.5000 50.00%
BSEP inhibitior - 0.4695 46.95%
P-glycoprotein inhibitior - 0.9603 96.03%
P-glycoprotein substrate - 0.9491 94.91%
CYP3A4 substrate - 0.5167 51.67%
CYP2C9 substrate - 0.7717 77.17%
CYP2D6 substrate - 0.9113 91.13%
CYP3A4 inhibition - 0.8058 80.58%
CYP2C9 inhibition - 0.7222 72.22%
CYP2C19 inhibition - 0.8019 80.19%
CYP2D6 inhibition - 0.9143 91.43%
CYP1A2 inhibition - 0.7430 74.30%
CYP2C8 inhibition - 0.9348 93.48%
CYP inhibitory promiscuity - 0.9347 93.47%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9028 90.28%
Carcinogenicity (trinary) Non-required 0.6200 62.00%
Eye corrosion - 0.9760 97.60%
Eye irritation + 0.8059 80.59%
Skin irritation + 0.6168 61.68%
Skin corrosion - 0.9664 96.64%
Ames mutagenesis - 0.6400 64.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6612 66.12%
Micronuclear - 0.8700 87.00%
Hepatotoxicity + 0.8463 84.63%
skin sensitisation + 0.7180 71.80%
Respiratory toxicity + 0.5111 51.11%
Reproductive toxicity + 0.5333 53.33%
Mitochondrial toxicity + 0.6625 66.25%
Nephrotoxicity + 0.7696 76.96%
Acute Oral Toxicity (c) III 0.6005 60.05%
Estrogen receptor binding - 0.6612 66.12%
Androgen receptor binding - 0.8155 81.55%
Thyroid receptor binding - 0.7783 77.83%
Glucocorticoid receptor binding - 0.7439 74.39%
Aromatase binding - 0.7149 71.49%
PPAR gamma - 0.5754 57.54%
Honey bee toxicity - 0.9660 96.60%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity - 0.7900 79.00%
Fish aquatic toxicity + 0.9964 99.64%

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
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.26% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 89.76% 91.11%
CHEMBL4040 P28482 MAP kinase ERK2 88.16% 83.82%
CHEMBL2581 P07339 Cathepsin D 86.47% 98.95%
CHEMBL4208 P20618 Proteasome component C5 85.58% 90.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 83.88% 99.23%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 82.90% 93.00%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 81.70% 85.14%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 80.90% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 80.08% 86.33%

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
Asteriscus intermedius

Cross-Links

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PubChem 162942647
LOTUS LTS0252085
wikiData Q104943462