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

Details

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Internal ID f3a62f42-754e-49d1-b593-a26a86dc3a73
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name 2-methyl-6-(4-methylcyclohex-3-en-1-yl)hept-6-ene-2,3-diol
SMILES (Canonical) CC1=CCC(CC1)C(=C)CCC(C(C)(C)O)O
SMILES (Isomeric) CC1=CCC(CC1)C(=C)CCC(C(C)(C)O)O
InChI InChI=1S/C15H26O2/c1-11-5-8-13(9-6-11)12(2)7-10-14(16)15(3,4)17/h5,13-14,16-17H,2,6-10H2,1,3-4H3
InChI Key ICHZVZARHVXZEH-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 2.90
Atomic LogP (AlogP) 3.20
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 5

Synonyms

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DTXSID60702836
2-Methyl-6-(4-methylcyclohex-3-en-1-yl)hept-6-ene-2,3-diol

2D Structure

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

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9847 98.47%
Caco-2 - 0.5377 53.77%
Blood Brain Barrier + 0.7750 77.50%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Mitochondria 0.5497 54.97%
OATP2B1 inhibitior - 0.8509 85.09%
OATP1B1 inhibitior + 0.9405 94.05%
OATP1B3 inhibitior + 0.9490 94.90%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior - 0.8572 85.72%
P-glycoprotein inhibitior - 0.9406 94.06%
P-glycoprotein substrate - 0.7963 79.63%
CYP3A4 substrate - 0.5000 50.00%
CYP2C9 substrate - 0.6063 60.63%
CYP2D6 substrate - 0.7644 76.44%
CYP3A4 inhibition - 0.7235 72.35%
CYP2C9 inhibition - 0.7381 73.81%
CYP2C19 inhibition - 0.6802 68.02%
CYP2D6 inhibition - 0.9116 91.16%
CYP1A2 inhibition - 0.7770 77.70%
CYP2C8 inhibition - 0.7963 79.63%
CYP inhibitory promiscuity - 0.8233 82.33%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.8300 83.00%
Carcinogenicity (trinary) Non-required 0.6875 68.75%
Eye corrosion - 0.9480 94.80%
Eye irritation - 0.7350 73.50%
Skin irritation - 0.5672 56.72%
Skin corrosion - 0.9694 96.94%
Ames mutagenesis - 0.8400 84.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4264 42.64%
Micronuclear - 0.9700 97.00%
Hepatotoxicity + 0.5195 51.95%
skin sensitisation + 0.7983 79.83%
Respiratory toxicity - 0.6333 63.33%
Reproductive toxicity - 0.7000 70.00%
Mitochondrial toxicity - 0.6875 68.75%
Nephrotoxicity - 0.7185 71.85%
Acute Oral Toxicity (c) III 0.8477 84.77%
Estrogen receptor binding - 0.6826 68.26%
Androgen receptor binding - 0.7478 74.78%
Thyroid receptor binding - 0.6645 66.45%
Glucocorticoid receptor binding + 0.6603 66.03%
Aromatase binding - 0.6590 65.90%
PPAR gamma - 0.6028 60.28%
Honey bee toxicity - 0.9295 92.95%
Biodegradation + 0.6000 60.00%
Crustacea aquatic toxicity - 0.5800 58.00%
Fish aquatic toxicity + 0.9693 96.93%

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 98.77% 97.25%
CHEMBL2581 P07339 Cathepsin D 95.42% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.65% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.80% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 87.08% 97.09%
CHEMBL3359 P21462 Formyl peptide receptor 1 85.66% 93.56%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 85.49% 95.89%
CHEMBL4581 P52732 Kinesin-like protein 1 85.17% 93.18%
CHEMBL3401 O75469 Pregnane X receptor 83.05% 94.73%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 80.22% 97.21%

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.
Acritopappus confertus

Cross-Links

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PubChem 53440826
LOTUS LTS0034522
wikiData Q82634845