2-Ethenyl-2-methyl-3,5-bis(prop-1-en-2-yl)cyclohexan-1-ol

Details

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Internal ID aabcb8e0-4700-4f75-9f7e-db91d34ba629
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids > Elemane sesquiterpenoids
IUPAC Name 2-ethenyl-2-methyl-3,5-bis(prop-1-en-2-yl)cyclohexan-1-ol
SMILES (Canonical) CC(=C)C1CC(C(C(C1)O)(C)C=C)C(=C)C
SMILES (Isomeric) CC(=C)C1CC(C(C(C1)O)(C)C=C)C(=C)C
InChI InChI=1S/C15H24O/c1-7-15(6)13(11(4)5)8-12(10(2)3)9-14(15)16/h7,12-14,16H,1-2,4,8-9H2,3,5-6H3
InChI Key YFNGGCSSPZBZRN-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H24O
Molecular Weight 220.35 g/mol
Exact Mass 220.182715385 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 4.80
Atomic LogP (AlogP) 3.72
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2-Ethenyl-2-methyl-3,5-bis(prop-1-en-2-yl)cyclohexan-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 + 0.9925 99.25%
Caco-2 - 0.6782 67.82%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Lysosomes 0.5190 51.90%
OATP2B1 inhibitior - 0.8530 85.30%
OATP1B1 inhibitior + 0.9534 95.34%
OATP1B3 inhibitior + 0.9373 93.73%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.9607 96.07%
P-glycoprotein inhibitior - 0.9440 94.40%
P-glycoprotein substrate - 0.8242 82.42%
CYP3A4 substrate + 0.5188 51.88%
CYP2C9 substrate - 0.6284 62.84%
CYP2D6 substrate - 0.7263 72.63%
CYP3A4 inhibition - 0.8135 81.35%
CYP2C9 inhibition - 0.8651 86.51%
CYP2C19 inhibition - 0.6380 63.80%
CYP2D6 inhibition - 0.9396 93.96%
CYP1A2 inhibition - 0.8624 86.24%
CYP2C8 inhibition - 0.9275 92.75%
CYP inhibitory promiscuity - 0.8444 84.44%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.6852 68.52%
Carcinogenicity (trinary) Non-required 0.6773 67.73%
Eye corrosion - 0.8734 87.34%
Eye irritation + 0.7956 79.56%
Skin irritation + 0.7243 72.43%
Skin corrosion - 0.8173 81.73%
Ames mutagenesis - 0.6454 64.54%
Human Ether-a-go-go-Related Gene inhibition - 0.4170 41.70%
Micronuclear - 0.9200 92.00%
Hepatotoxicity + 0.6500 65.00%
skin sensitisation + 0.7782 77.82%
Respiratory toxicity - 0.7333 73.33%
Reproductive toxicity - 0.6000 60.00%
Mitochondrial toxicity - 0.7000 70.00%
Nephrotoxicity + 0.7421 74.21%
Acute Oral Toxicity (c) III 0.8202 82.02%
Estrogen receptor binding - 0.7036 70.36%
Androgen receptor binding - 0.6633 66.33%
Thyroid receptor binding - 0.7099 70.99%
Glucocorticoid receptor binding - 0.7133 71.33%
Aromatase binding - 0.7320 73.20%
PPAR gamma - 0.6290 62.90%
Honey bee toxicity - 0.5904 59.04%
Biodegradation - 0.5500 55.00%
Crustacea aquatic toxicity - 0.5100 51.00%
Fish aquatic toxicity + 0.9147 91.47%

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
CHEMBL4040 P28482 MAP kinase ERK2 95.76% 83.82%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.52% 91.11%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 93.78% 85.14%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.56% 96.09%
CHEMBL240 Q12809 HERG 89.45% 89.76%
CHEMBL1951 P21397 Monoamine oxidase A 87.98% 91.49%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 87.77% 96.95%
CHEMBL241 Q14432 Phosphodiesterase 3A 83.77% 92.94%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 82.52% 97.21%
CHEMBL1994 P08235 Mineralocorticoid receptor 82.30% 100.00%
CHEMBL218 P21554 Cannabinoid CB1 receptor 80.70% 96.61%

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.
Achillea ageratum

Cross-Links

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PubChem 162884291
LOTUS LTS0208624
wikiData Q105347688