3-Methyl-6-(6-methylhept-5-en-2-yl)cyclohex-2-enol

Details

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Internal ID f5cfa069-3546-4c46-8f2d-80ed9e4ceb6c
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name 3-methyl-6-(6-methylhept-5-en-2-yl)cyclohex-2-en-1-ol
SMILES (Canonical) CC1=CC(C(CC1)C(C)CCC=C(C)C)O
SMILES (Isomeric) CC1=CC(C(CC1)C(C)CCC=C(C)C)O
InChI InChI=1S/C15H26O/c1-11(2)6-5-7-13(4)14-9-8-12(3)10-15(14)16/h6,10,13-16H,5,7-9H2,1-4H3
InChI Key ZOYAMQNIYAMHTE-UHFFFAOYSA-N
Popularity 1 reference 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 4.10
Atomic LogP (AlogP) 4.09
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 3-Methyl-6-(6-methylhept-5-en-2-yl)cyclohex-2-enol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9935 99.35%
Caco-2 + 0.9213 92.13%
Blood Brain Barrier + 0.7500 75.00%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Mitochondria 0.5890 58.90%
OATP2B1 inhibitior - 0.8518 85.18%
OATP1B1 inhibitior + 0.9195 91.95%
OATP1B3 inhibitior + 0.9206 92.06%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior - 0.8071 80.71%
P-glycoprotein inhibitior - 0.9541 95.41%
P-glycoprotein substrate - 0.8893 88.93%
CYP3A4 substrate - 0.5762 57.62%
CYP2C9 substrate - 0.8090 80.90%
CYP2D6 substrate - 0.7021 70.21%
CYP3A4 inhibition - 0.7551 75.51%
CYP2C9 inhibition - 0.7601 76.01%
CYP2C19 inhibition - 0.8038 80.38%
CYP2D6 inhibition - 0.8719 87.19%
CYP1A2 inhibition - 0.6922 69.22%
CYP2C8 inhibition - 0.9756 97.56%
CYP inhibitory promiscuity - 0.5766 57.66%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.8428 84.28%
Carcinogenicity (trinary) Non-required 0.6574 65.74%
Eye corrosion - 0.8185 81.85%
Eye irritation - 0.6568 65.68%
Skin irritation + 0.6392 63.92%
Skin corrosion - 0.8040 80.40%
Ames mutagenesis - 0.8400 84.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4448 44.48%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.6630 66.30%
skin sensitisation + 0.8836 88.36%
Respiratory toxicity - 0.5000 50.00%
Reproductive toxicity - 0.6111 61.11%
Mitochondrial toxicity - 0.7500 75.00%
Nephrotoxicity - 0.6391 63.91%
Acute Oral Toxicity (c) III 0.6573 65.73%
Estrogen receptor binding - 0.8987 89.87%
Androgen receptor binding - 0.6464 64.64%
Thyroid receptor binding - 0.5916 59.16%
Glucocorticoid receptor binding - 0.6715 67.15%
Aromatase binding - 0.9230 92.30%
PPAR gamma - 0.7077 70.77%
Honey bee toxicity - 0.9283 92.83%
Biodegradation - 0.5250 52.50%
Crustacea aquatic toxicity - 0.6300 63.00%
Fish aquatic toxicity + 0.9922 99.22%

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
CHEMBL2581 P07339 Cathepsin D 94.80% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 90.90% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.07% 96.09%
CHEMBL1994 P08235 Mineralocorticoid receptor 88.20% 100.00%
CHEMBL3359 P21462 Formyl peptide receptor 1 88.04% 93.56%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 86.20% 94.45%
CHEMBL5608 Q16288 NT-3 growth factor receptor 84.61% 95.89%
CHEMBL3137262 O60341 LSD1/CoREST complex 84.38% 97.09%
CHEMBL4005 P42336 PI3-kinase p110-alpha subunit 83.29% 97.47%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 81.18% 95.56%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 80.96% 96.47%

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.
Argyranthemum adauctum
Fitzroya cupressoides

Cross-Links

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PubChem 154732199
LOTUS LTS0025870
wikiData Q105380779