Eremofukinone

Details

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Internal ID 85fc0a55-9951-40ed-8845-7b1436797c83
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids > Eremophilane, 8,9-secoeremophilane and furoeremophilane sesquiterpenoids
IUPAC Name 4,4a-dimethyl-6-prop-1-en-2-yl-2,3,4,5,6,7,8,8a-octahydronaphthalen-1-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H24O/c1-10(2)12-6-7-13-14(16)8-5-11(3)15(13,4)9-12/h11-13H,1,5-9H2,2-4H3
InChI Key YHPOLTFUARNADB-UHFFFAOYSA-N
Popularity 6 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) 17.10 Ų
XlogP 4.30
Atomic LogP (AlogP) 3.98
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Eremofukinone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9971 99.71%
Caco-2 + 0.8584 85.84%
Blood Brain Barrier + 0.7750 77.50%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Mitochondria 0.4409 44.09%
OATP2B1 inhibitior - 0.8437 84.37%
OATP1B1 inhibitior + 0.9428 94.28%
OATP1B3 inhibitior + 0.8250 82.50%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.5500 55.00%
BSEP inhibitior - 0.7387 73.87%
P-glycoprotein inhibitior - 0.9092 90.92%
P-glycoprotein substrate - 0.8920 89.20%
CYP3A4 substrate + 0.5187 51.87%
CYP2C9 substrate - 0.8039 80.39%
CYP2D6 substrate - 0.7758 77.58%
CYP3A4 inhibition - 0.7280 72.80%
CYP2C9 inhibition - 0.8583 85.83%
CYP2C19 inhibition - 0.6154 61.54%
CYP2D6 inhibition - 0.9578 95.78%
CYP1A2 inhibition - 0.7452 74.52%
CYP2C8 inhibition - 0.9618 96.18%
CYP inhibitory promiscuity - 0.8420 84.20%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9100 91.00%
Carcinogenicity (trinary) Non-required 0.4825 48.25%
Eye corrosion - 0.9780 97.80%
Eye irritation + 0.6966 69.66%
Skin irritation + 0.6100 61.00%
Skin corrosion - 0.9732 97.32%
Ames mutagenesis - 0.8828 88.28%
Human Ether-a-go-go-Related Gene inhibition - 0.6798 67.98%
Micronuclear - 0.9500 95.00%
Hepatotoxicity + 0.5375 53.75%
skin sensitisation + 0.8188 81.88%
Respiratory toxicity - 0.6111 61.11%
Reproductive toxicity + 0.7667 76.67%
Mitochondrial toxicity - 0.5125 51.25%
Nephrotoxicity - 0.5881 58.81%
Acute Oral Toxicity (c) III 0.8106 81.06%
Estrogen receptor binding - 0.6957 69.57%
Androgen receptor binding - 0.6649 66.49%
Thyroid receptor binding - 0.7393 73.93%
Glucocorticoid receptor binding - 0.5597 55.97%
Aromatase binding - 0.5730 57.30%
PPAR gamma - 0.7716 77.16%
Honey bee toxicity - 0.8096 80.96%
Biodegradation + 0.6500 65.00%
Crustacea aquatic toxicity + 0.5300 53.00%
Fish aquatic toxicity + 0.9939 99.39%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.75% 91.11%
CHEMBL253 P34972 Cannabinoid CB2 receptor 93.96% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.36% 96.09%
CHEMBL1994 P08235 Mineralocorticoid receptor 88.01% 100.00%
CHEMBL241 Q14432 Phosphodiesterase 3A 86.82% 92.94%
CHEMBL2581 P07339 Cathepsin D 86.07% 98.95%
CHEMBL1871 P10275 Androgen Receptor 86.03% 96.43%
CHEMBL3137262 O60341 LSD1/CoREST complex 84.28% 97.09%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 82.65% 82.69%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 81.99% 95.56%
CHEMBL1806 P11388 DNA topoisomerase II alpha 81.90% 89.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 81.79% 95.89%
CHEMBL1902 P62942 FK506-binding protein 1A 80.56% 97.05%

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.
Petasites japonicus

Cross-Links

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PubChem 101417485
LOTUS LTS0063907
wikiData Q105348552