Eremolactone

Details

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Internal ID d5080ecf-fbc7-4237-8a3a-cfb10c4b1924
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Terpene lactones > Diterpene lactones
IUPAC Name (5Z)-3-methyl-5-[[(4S)-4,8,8-trimethyl-9-tricyclo[5.2.2.01,5]undec-5-enyl]methylidene]furan-2-one
SMILES (Canonical) CC1CCC23C1=CC(CC2)C(C3C=C4C=C(C(=O)O4)C)(C)C
SMILES (Isomeric) C[C@H]1CCC23C1=CC(CC2)C(C3/C=C\4/C=C(C(=O)O4)C)(C)C
InChI InChI=1S/C20H26O2/c1-12-5-7-20-8-6-14(10-16(12)20)19(3,4)17(20)11-15-9-13(2)18(21)22-15/h9-12,14,17H,5-8H2,1-4H3/b15-11-/t12-,14?,17?,20?/m0/s1
InChI Key XDOSSDQISIQOLI-MJNPNCJRSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C20H26O2
Molecular Weight 298.40 g/mol
Exact Mass 298.193280068 g/mol
Topological Polar Surface Area (TPSA) 26.30 Ų
XlogP 4.90
Atomic LogP (AlogP) 4.78
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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LMPR0104440001

2D Structure

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2D Structure of Eremolactone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 1.0000 100.00%
Caco-2 + 0.7743 77.43%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability + 0.6714 67.14%
Subcellular localzation Mitochondria 0.5693 56.93%
OATP2B1 inhibitior - 0.8618 86.18%
OATP1B1 inhibitior + 0.8432 84.32%
OATP1B3 inhibitior + 0.9503 95.03%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.5500 55.00%
BSEP inhibitior - 0.7588 75.88%
P-glycoprotein inhibitior - 0.7093 70.93%
P-glycoprotein substrate - 0.8302 83.02%
CYP3A4 substrate + 0.6257 62.57%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8558 85.58%
CYP3A4 inhibition - 0.7408 74.08%
CYP2C9 inhibition - 0.8773 87.73%
CYP2C19 inhibition + 0.6982 69.82%
CYP2D6 inhibition - 0.9249 92.49%
CYP1A2 inhibition + 0.5944 59.44%
CYP2C8 inhibition - 0.6194 61.94%
CYP inhibitory promiscuity - 0.6449 64.49%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.4974 49.74%
Eye corrosion - 0.9855 98.55%
Eye irritation - 0.9658 96.58%
Skin irritation - 0.5146 51.46%
Skin corrosion - 0.9523 95.23%
Ames mutagenesis - 0.6600 66.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7622 76.22%
Micronuclear - 0.8800 88.00%
Hepatotoxicity - 0.5019 50.19%
skin sensitisation + 0.5805 58.05%
Respiratory toxicity + 0.6889 68.89%
Reproductive toxicity + 0.6778 67.78%
Mitochondrial toxicity + 0.7375 73.75%
Nephrotoxicity - 0.6470 64.70%
Acute Oral Toxicity (c) III 0.7499 74.99%
Estrogen receptor binding + 0.6708 67.08%
Androgen receptor binding + 0.5554 55.54%
Thyroid receptor binding + 0.6297 62.97%
Glucocorticoid receptor binding + 0.6355 63.55%
Aromatase binding + 0.5494 54.94%
PPAR gamma + 0.7646 76.46%
Honey bee toxicity - 0.8586 85.86%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity + 0.6500 65.00%
Fish aquatic toxicity + 0.9971 99.71%

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 96.98% 91.11%
CHEMBL2581 P07339 Cathepsin D 95.60% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.41% 95.56%
CHEMBL325 Q13547 Histone deacetylase 1 93.44% 95.92%
CHEMBL1937 Q92769 Histone deacetylase 2 89.14% 94.75%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 87.69% 99.23%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.92% 86.33%
CHEMBL5203 P33316 dUTP pyrophosphatase 85.60% 99.18%
CHEMBL5608 Q16288 NT-3 growth factor receptor 85.01% 95.89%
CHEMBL1806 P11388 DNA topoisomerase II alpha 83.97% 89.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 82.04% 97.09%
CHEMBL1994 P08235 Mineralocorticoid receptor 80.69% 100.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 80.54% 96.09%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 80.22% 97.14%
CHEMBL1902 P62942 FK506-binding protein 1A 80.16% 97.05%
CHEMBL241 Q14432 Phosphodiesterase 3A 80.05% 92.94%

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.
Eremophila fraseri

Cross-Links

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PubChem 42608258
LOTUS LTS0050212
wikiData Q105325972