Eremophyllene

Details

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Internal ID 739209af-0934-46f4-b333-531ac71ba961
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids > Eremophilane, 8,9-secoeremophilane and furoeremophilane sesquiterpenoids
IUPAC Name 8,8a-dimethyl-2-prop-1-en-2-yl-2,3,4,4a,5,6-hexahydro-1H-naphthalene
SMILES (Canonical) CC1=CCCC2C1(CC(CC2)C(=C)C)C
SMILES (Isomeric) CC1=CCCC2C1(CC(CC2)C(=C)C)C
InChI InChI=1S/C15H24/c1-11(2)13-8-9-14-7-5-6-12(3)15(14,4)10-13/h6,13-14H,1,5,7-10H2,2-4H3
InChI Key ZZPSOALECBMAMW-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C15H24
Molecular Weight 204.35 g/mol
Exact Mass 204.187800766 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 5.40
Atomic LogP (AlogP) 4.73
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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ZZPSOALECBMAMW-UHFFFAOYSA-N
Q67879873

2D Structure

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2D Structure of Eremophyllene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9928 99.28%
Caco-2 + 0.8726 87.26%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Lysosomes 0.7597 75.97%
OATP2B1 inhibitior - 0.8517 85.17%
OATP1B1 inhibitior + 0.9559 95.59%
OATP1B3 inhibitior + 0.8085 80.85%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.6500 65.00%
BSEP inhibitior - 0.7240 72.40%
P-glycoprotein inhibitior - 0.9355 93.55%
P-glycoprotein substrate - 0.8258 82.58%
CYP3A4 substrate + 0.5149 51.49%
CYP2C9 substrate - 0.7731 77.31%
CYP2D6 substrate - 0.7252 72.52%
CYP3A4 inhibition - 0.7327 73.27%
CYP2C9 inhibition - 0.7626 76.26%
CYP2C19 inhibition - 0.6178 61.78%
CYP2D6 inhibition - 0.9371 93.71%
CYP1A2 inhibition - 0.7867 78.67%
CYP2C8 inhibition - 0.7601 76.01%
CYP inhibitory promiscuity - 0.5629 56.29%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7800 78.00%
Carcinogenicity (trinary) Non-required 0.4642 46.42%
Eye corrosion - 0.9467 94.67%
Eye irritation + 0.6075 60.75%
Skin irritation - 0.6240 62.40%
Skin corrosion - 0.9634 96.34%
Ames mutagenesis - 0.8500 85.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5067 50.67%
Micronuclear - 0.9800 98.00%
Hepatotoxicity - 0.5500 55.00%
skin sensitisation + 0.8143 81.43%
Respiratory toxicity - 0.7333 73.33%
Reproductive toxicity - 0.5333 53.33%
Mitochondrial toxicity - 0.6000 60.00%
Nephrotoxicity - 0.5678 56.78%
Acute Oral Toxicity (c) III 0.7893 78.93%
Estrogen receptor binding - 0.7755 77.55%
Androgen receptor binding - 0.8204 82.04%
Thyroid receptor binding - 0.8301 83.01%
Glucocorticoid receptor binding - 0.5605 56.05%
Aromatase binding + 0.6422 64.22%
PPAR gamma - 0.8016 80.16%
Honey bee toxicity - 0.9192 91.92%
Biodegradation + 0.6500 65.00%
Crustacea aquatic toxicity - 0.5300 53.00%
Fish aquatic toxicity + 1.0000 100.00%

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 95.43% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.25% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 86.67% 97.09%
CHEMBL4208 P20618 Proteasome component C5 86.53% 90.00%
CHEMBL1994 P08235 Mineralocorticoid receptor 85.49% 100.00%
CHEMBL241 Q14432 Phosphodiesterase 3A 85.20% 92.94%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 83.60% 97.21%
CHEMBL4683 Q12884 Fibroblast activation protein alpha 83.59% 93.07%
CHEMBL4040 P28482 MAP kinase ERK2 81.63% 83.82%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.99% 95.89%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 80.00% 95.56%

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.
Helichrysum italicum subsp. picardii
Micromeria myrtifolia
Petasites albus

Cross-Links

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PubChem 6428416
LOTUS LTS0138743
wikiData Q67879873