2,6,6-Trimethyl-9-methylidenecycloundeca-1,4-diene

Details

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Internal ID bdce72f6-2719-42aa-81f0-1a3d674f9208
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name 2,6,6-trimethyl-9-methylidenecycloundeca-1,4-diene
SMILES (Canonical) CC1=CCCC(=C)CCC(C=CC1)(C)C
SMILES (Isomeric) CC1=CCCC(=C)CCC(C=CC1)(C)C
InChI InChI=1S/C15H24/c1-13-7-5-8-14(2)10-12-15(3,4)11-6-9-13/h6-7,11H,2,5,8-10,12H2,1,3-4H3
InChI Key DYZCESKLDGNPIY-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H24
Molecular Weight 204.35 g/mol
Exact Mass 204.187800766 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 4.80
Atomic LogP (AlogP) 5.04
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2,6,6-Trimethyl-9-methylidenecycloundeca-1,4-diene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9886 98.86%
Caco-2 + 0.9558 95.58%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability + 0.6857 68.57%
Subcellular localzation Lysosomes 0.6135 61.35%
OATP2B1 inhibitior - 0.8514 85.14%
OATP1B1 inhibitior + 0.9421 94.21%
OATP1B3 inhibitior + 0.9265 92.65%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior - 0.7503 75.03%
P-glycoprotein inhibitior - 0.9601 96.01%
P-glycoprotein substrate - 0.9411 94.11%
CYP3A4 substrate - 0.5173 51.73%
CYP2C9 substrate - 0.8038 80.38%
CYP2D6 substrate - 0.7848 78.48%
CYP3A4 inhibition - 0.8953 89.53%
CYP2C9 inhibition - 0.7430 74.30%
CYP2C19 inhibition - 0.7356 73.56%
CYP2D6 inhibition - 0.9386 93.86%
CYP1A2 inhibition - 0.7590 75.90%
CYP2C8 inhibition - 0.8297 82.97%
CYP inhibitory promiscuity - 0.7893 78.93%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6500 65.00%
Carcinogenicity (trinary) Warning 0.5069 50.69%
Eye corrosion - 0.6668 66.68%
Eye irritation + 0.8979 89.79%
Skin irritation + 0.6623 66.23%
Skin corrosion - 0.9847 98.47%
Ames mutagenesis - 0.7795 77.95%
Human Ether-a-go-go-Related Gene inhibition + 0.7138 71.38%
Micronuclear - 0.9900 99.00%
Hepatotoxicity + 0.6594 65.94%
skin sensitisation + 0.8828 88.28%
Respiratory toxicity - 0.6444 64.44%
Reproductive toxicity - 0.7778 77.78%
Mitochondrial toxicity - 0.5375 53.75%
Nephrotoxicity + 0.4942 49.42%
Acute Oral Toxicity (c) III 0.7989 79.89%
Estrogen receptor binding - 0.9546 95.46%
Androgen receptor binding - 0.8856 88.56%
Thyroid receptor binding - 0.7897 78.97%
Glucocorticoid receptor binding - 0.7726 77.26%
Aromatase binding - 0.7370 73.70%
PPAR gamma - 0.7958 79.58%
Honey bee toxicity - 0.9129 91.29%
Biodegradation - 0.5000 50.00%
Crustacea aquatic toxicity + 0.7000 70.00%
Fish aquatic toxicity + 0.9972 99.72%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 86.26% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.74% 95.56%
CHEMBL230 P35354 Cyclooxygenase-2 84.36% 89.63%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 82.89% 94.45%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 82.33% 96.09%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 81.79% 85.30%

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.
Mentha aquatica

Cross-Links

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PubChem 162909931
LOTUS LTS0173222
wikiData Q104991659