2-Methyl-6-(4-methylcyclohex-3-en-1-yl)hept-2-ene-1,6-diol

Details

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Internal ID a49c0fab-706d-4714-a2cf-d6d868f9c890
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name 2-methyl-6-(4-methylcyclohex-3-en-1-yl)hept-2-ene-1,6-diol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H26O2/c1-12-6-8-14(9-7-12)15(3,17)10-4-5-13(2)11-16/h5-6,14,16-17H,4,7-11H2,1-3H3
InChI Key DRUPYWVNTITDJV-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H26O2
Molecular Weight 238.37 g/mol
Exact Mass 238.193280068 g/mol
Topological Polar Surface Area (TPSA) 40.50 Ų
XlogP 2.50
Atomic LogP (AlogP) 3.20
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 5

Synonyms

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DTXSID70773936
2-Methyl-6-(4-methylcyclohex-3-en-1-yl)hept-2-ene-1,6-diol

2D Structure

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2D Structure of 2-Methyl-6-(4-methylcyclohex-3-en-1-yl)hept-2-ene-1,6-diol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9906 99.06%
Caco-2 + 0.8114 81.14%
Blood Brain Barrier + 0.8250 82.50%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Lysosomes 0.4887 48.87%
OATP2B1 inhibitior - 0.8507 85.07%
OATP1B1 inhibitior + 0.9308 93.08%
OATP1B3 inhibitior + 0.9418 94.18%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.7093 70.93%
BSEP inhibitior - 0.7105 71.05%
P-glycoprotein inhibitior - 0.9659 96.59%
P-glycoprotein substrate - 0.7900 79.00%
CYP3A4 substrate + 0.5247 52.47%
CYP2C9 substrate - 0.7836 78.36%
CYP2D6 substrate - 0.7868 78.68%
CYP3A4 inhibition - 0.5384 53.84%
CYP2C9 inhibition - 0.7894 78.94%
CYP2C19 inhibition - 0.8353 83.53%
CYP2D6 inhibition - 0.8790 87.90%
CYP1A2 inhibition - 0.7940 79.40%
CYP2C8 inhibition - 0.6704 67.04%
CYP inhibitory promiscuity - 0.7385 73.85%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.8528 85.28%
Carcinogenicity (trinary) Non-required 0.6447 64.47%
Eye corrosion - 0.9430 94.30%
Eye irritation - 0.6613 66.13%
Skin irritation - 0.7648 76.48%
Skin corrosion - 0.9883 98.83%
Ames mutagenesis - 0.7700 77.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5391 53.91%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.6324 63.24%
skin sensitisation + 0.7078 70.78%
Respiratory toxicity - 0.6333 63.33%
Reproductive toxicity - 0.6333 63.33%
Mitochondrial toxicity - 0.7250 72.50%
Nephrotoxicity - 0.5751 57.51%
Acute Oral Toxicity (c) III 0.8715 87.15%
Estrogen receptor binding - 0.7835 78.35%
Androgen receptor binding - 0.8087 80.87%
Thyroid receptor binding + 0.5939 59.39%
Glucocorticoid receptor binding - 0.4707 47.07%
Aromatase binding - 0.6906 69.06%
PPAR gamma + 0.6362 63.62%
Honey bee toxicity - 0.9147 91.47%
Biodegradation - 0.5250 52.50%
Crustacea aquatic toxicity - 0.6100 61.00%
Fish aquatic toxicity + 0.8394 83.94%

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
CHEMBL253 P34972 Cannabinoid CB2 receptor 95.63% 97.25%
CHEMBL2581 P07339 Cathepsin D 92.33% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 91.45% 91.11%
CHEMBL3137262 O60341 LSD1/CoREST complex 87.11% 97.09%
CHEMBL3401 O75469 Pregnane X receptor 86.94% 94.73%
CHEMBL1994 P08235 Mineralocorticoid receptor 85.64% 100.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 84.81% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.98% 95.56%
CHEMBL3359 P21462 Formyl peptide receptor 1 81.11% 93.56%
CHEMBL3192 Q9BY41 Histone deacetylase 8 80.57% 93.99%

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.
Santalum austrocaledonicum

Cross-Links

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PubChem 71348024
LOTUS LTS0230814
wikiData Q82734912