(E)-Eremophila-1(10),7(11)-dien-12-ol

Details

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Internal ID ba7b0991-faf9-4ea3-9e3e-8141e07bb266
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids > Eremophilane, 8,9-secoeremophilane and furoeremophilane sesquiterpenoids
IUPAC Name (2E)-2-[(8R,8aS)-8,8a-dimethyl-1,3,4,6,7,8-hexahydronaphthalen-2-ylidene]propan-1-ol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H24O/c1-11(10-16)13-7-8-14-6-4-5-12(2)15(14,3)9-13/h6,12,16H,4-5,7-10H2,1-3H3/b13-11+/t12-,15+/m1/s1
InChI Key FXWSXJNUPFBCMQ-GDULLBNJSA-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 3.20
Atomic LogP (AlogP) 3.84
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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SCHEMBL18289196

2D Structure

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2D Structure of (E)-Eremophila-1(10),7(11)-dien-12-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9916 99.16%
Caco-2 + 0.9332 93.32%
Blood Brain Barrier + 0.8500 85.00%
Human oral bioavailability - 0.6143 61.43%
Subcellular localzation Lysosomes 0.7244 72.44%
OATP2B1 inhibitior - 0.8506 85.06%
OATP1B1 inhibitior + 0.9069 90.69%
OATP1B3 inhibitior + 0.8247 82.47%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.5750 57.50%
BSEP inhibitior - 0.6183 61.83%
P-glycoprotein inhibitior - 0.9397 93.97%
P-glycoprotein substrate - 0.7919 79.19%
CYP3A4 substrate + 0.5214 52.14%
CYP2C9 substrate - 0.7664 76.64%
CYP2D6 substrate - 0.7388 73.88%
CYP3A4 inhibition - 0.7593 75.93%
CYP2C9 inhibition - 0.6241 62.41%
CYP2C19 inhibition - 0.5931 59.31%
CYP2D6 inhibition - 0.8922 89.22%
CYP1A2 inhibition - 0.7686 76.86%
CYP2C8 inhibition - 0.6834 68.34%
CYP inhibitory promiscuity + 0.5000 50.00%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.8800 88.00%
Carcinogenicity (trinary) Non-required 0.6149 61.49%
Eye corrosion - 0.9680 96.80%
Eye irritation - 0.8306 83.06%
Skin irritation - 0.6906 69.06%
Skin corrosion - 0.9659 96.59%
Ames mutagenesis - 0.8600 86.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6551 65.51%
Micronuclear - 0.9600 96.00%
Hepatotoxicity - 0.6197 61.97%
skin sensitisation + 0.5127 51.27%
Respiratory toxicity - 0.6000 60.00%
Reproductive toxicity + 0.5889 58.89%
Mitochondrial toxicity - 0.5125 51.25%
Nephrotoxicity + 0.4559 45.59%
Acute Oral Toxicity (c) III 0.6680 66.80%
Estrogen receptor binding - 0.8575 85.75%
Androgen receptor binding - 0.5744 57.44%
Thyroid receptor binding - 0.7059 70.59%
Glucocorticoid receptor binding - 0.6084 60.84%
Aromatase binding - 0.5679 56.79%
PPAR gamma - 0.7345 73.45%
Honey bee toxicity - 0.9318 93.18%
Biodegradation + 0.5750 57.50%
Crustacea aquatic toxicity - 0.6200 62.00%
Fish aquatic toxicity + 0.9936 99.36%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.53% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.53% 91.11%
CHEMBL253 P34972 Cannabinoid CB2 receptor 93.16% 97.25%
CHEMBL1994 P08235 Mineralocorticoid receptor 89.32% 100.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 88.93% 97.09%
CHEMBL2581 P07339 Cathepsin D 85.71% 98.95%
CHEMBL241 Q14432 Phosphodiesterase 3A 84.96% 92.94%
CHEMBL5608 Q16288 NT-3 growth factor receptor 83.21% 95.89%

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.
Cussonia bancoensis

Cross-Links

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PubChem 6428372
NPASS NPC288969