1,5,5,8-Tetramethyl-3,7-cycloundecadien-1-ol

Details

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Internal ID c0c1e65b-0703-4af9-bd84-3b5e05903edf
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name (3E,7Z)-1,5,5,8-tetramethylcycloundeca-3,7-dien-1-ol
SMILES (Canonical) CC1=CCC(C=CCC(CCC1)(C)O)(C)C
SMILES (Isomeric) C/C/1=C/CC(/C=C/CC(CCC1)(C)O)(C)C
InChI InChI=1S/C15H26O/c1-13-7-5-10-15(4,16)11-6-9-14(2,3)12-8-13/h6,8-9,16H,5,7,10-12H2,1-4H3/b9-6+,13-8-
InChI Key ZLMAVMBYWKVCLV-QYKINMCYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H26O
Molecular Weight 222.37 g/mol
Exact Mass 222.198365449 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 3.80
Atomic LogP (AlogP) 4.23
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 0

Synonyms

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SCHEMBL10748823
ZLMAVMBYWKVCLV-QYKINMCYSA-N
1,5,5,8-Tetramethyl-3,7-cycloundecadien-1-ol #

2D Structure

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2D Structure of 1,5,5,8-Tetramethyl-3,7-cycloundecadien-1-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9955 99.55%
Caco-2 + 0.9390 93.90%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability + 0.5857 58.57%
Subcellular localzation Mitochondria 0.4277 42.77%
OATP2B1 inhibitior - 0.8492 84.92%
OATP1B1 inhibitior + 0.9295 92.95%
OATP1B3 inhibitior + 0.9655 96.55%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior - 0.7162 71.62%
P-glycoprotein inhibitior - 0.9653 96.53%
P-glycoprotein substrate - 0.9355 93.55%
CYP3A4 substrate - 0.5383 53.83%
CYP2C9 substrate - 0.7795 77.95%
CYP2D6 substrate - 0.7954 79.54%
CYP3A4 inhibition - 0.8700 87.00%
CYP2C9 inhibition - 0.7162 71.62%
CYP2C19 inhibition - 0.7231 72.31%
CYP2D6 inhibition - 0.9398 93.98%
CYP1A2 inhibition - 0.7191 71.91%
CYP2C8 inhibition - 0.9220 92.20%
CYP inhibitory promiscuity - 0.8773 87.73%
UGT catelyzed - 0.7000 70.00%
Carcinogenicity (binary) - 0.8228 82.28%
Carcinogenicity (trinary) Non-required 0.5939 59.39%
Eye corrosion - 0.9150 91.50%
Eye irritation + 0.8819 88.19%
Skin irritation + 0.7873 78.73%
Skin corrosion - 0.9461 94.61%
Ames mutagenesis - 0.7070 70.70%
Human Ether-a-go-go-Related Gene inhibition - 0.4945 49.45%
Micronuclear - 0.9900 99.00%
Hepatotoxicity + 0.7221 72.21%
skin sensitisation + 0.7894 78.94%
Respiratory toxicity - 0.5889 58.89%
Reproductive toxicity - 0.6222 62.22%
Mitochondrial toxicity - 0.6500 65.00%
Nephrotoxicity - 0.6055 60.55%
Acute Oral Toxicity (c) III 0.7917 79.17%
Estrogen receptor binding - 0.8723 87.23%
Androgen receptor binding - 0.8875 88.75%
Thyroid receptor binding - 0.6456 64.56%
Glucocorticoid receptor binding - 0.5801 58.01%
Aromatase binding - 0.7401 74.01%
PPAR gamma - 0.7589 75.89%
Honey bee toxicity - 0.9659 96.59%
Biodegradation + 0.5250 52.50%
Crustacea aquatic toxicity + 0.5500 55.00%
Fish aquatic toxicity + 0.9106 91.06%

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 91.58% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.88% 96.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 85.24% 94.45%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.19% 95.56%
CHEMBL4208 P20618 Proteasome component C5 81.95% 90.00%
CHEMBL1871 P10275 Androgen Receptor 80.35% 96.43%
CHEMBL1293249 Q13887 Kruppel-like factor 5 80.14% 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.
Mentha arvensis
Mentha canadensis

Cross-Links

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PubChem 5367678
NPASS NPC78872