1beta,8alpha-Dihydroxyeremophila-7(11),9-dien-12,8-olide

Details

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Internal ID 428c3c10-f43e-487c-b7dd-e14bf9bc4291
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Terpene lactones
IUPAC Name (4aR,5S,8R,9aR)-8,9a-dihydroxy-3,4a,5-trimethyl-5,6,7,8-tetrahydro-4H-benzo[f][1]benzofuran-2-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H20O4/c1-8-4-5-12(16)11-7-15(18)10(6-14(8,11)3)9(2)13(17)19-15/h7-8,12,16,18H,4-6H2,1-3H3/t8-,12+,14+,15+/m0/s1
InChI Key ILDMSNFGPQLCNL-AZEZGGBOSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C15H20O4
Molecular Weight 264.32 g/mol
Exact Mass 264.13615911 g/mol
Topological Polar Surface Area (TPSA) 66.80 Ų
XlogP 0.90
Atomic LogP (AlogP) 1.68
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 1beta,8alpha-Dihydroxyeremophila-7(11),9-dien-12,8-olide

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9938 99.38%
Caco-2 + 0.7988 79.88%
Blood Brain Barrier + 0.5250 52.50%
Human oral bioavailability + 0.5571 55.71%
Subcellular localzation Mitochondria 0.7371 73.71%
OATP2B1 inhibitior - 0.8544 85.44%
OATP1B1 inhibitior + 0.9383 93.83%
OATP1B3 inhibitior + 0.9296 92.96%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.5321 53.21%
BSEP inhibitior - 0.9091 90.91%
P-glycoprotein inhibitior - 0.9431 94.31%
P-glycoprotein substrate - 0.8471 84.71%
CYP3A4 substrate + 0.6175 61.75%
CYP2C9 substrate - 0.7943 79.43%
CYP2D6 substrate - 0.8686 86.86%
CYP3A4 inhibition - 0.6314 63.14%
CYP2C9 inhibition - 0.9074 90.74%
CYP2C19 inhibition - 0.9135 91.35%
CYP2D6 inhibition - 0.9583 95.83%
CYP1A2 inhibition - 0.6469 64.69%
CYP2C8 inhibition - 0.8885 88.85%
CYP inhibitory promiscuity - 0.9152 91.52%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 1.0000 100.00%
Carcinogenicity (trinary) Non-required 0.4418 44.18%
Eye corrosion - 0.9928 99.28%
Eye irritation - 0.9543 95.43%
Skin irritation + 0.7082 70.82%
Skin corrosion - 0.9170 91.70%
Ames mutagenesis - 0.6470 64.70%
Human Ether-a-go-go-Related Gene inhibition - 0.5887 58.87%
Micronuclear - 0.8300 83.00%
Hepatotoxicity - 0.6425 64.25%
skin sensitisation - 0.8043 80.43%
Respiratory toxicity + 0.6444 64.44%
Reproductive toxicity + 0.9778 97.78%
Mitochondrial toxicity + 0.9750 97.50%
Nephrotoxicity + 0.6800 68.00%
Acute Oral Toxicity (c) I 0.5041 50.41%
Estrogen receptor binding - 0.7959 79.59%
Androgen receptor binding - 0.5220 52.20%
Thyroid receptor binding + 0.5590 55.90%
Glucocorticoid receptor binding + 0.5725 57.25%
Aromatase binding - 0.5169 51.69%
PPAR gamma - 0.6980 69.80%
Honey bee toxicity - 0.9118 91.18%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.5100 51.00%
Fish aquatic toxicity + 0.9910 99.10%

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 95.21% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.06% 95.56%
CHEMBL2581 P07339 Cathepsin D 91.39% 98.95%
CHEMBL1806 P11388 DNA topoisomerase II alpha 88.48% 89.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 85.81% 97.09%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 84.89% 99.23%
CHEMBL1871 P10275 Androgen Receptor 84.48% 96.43%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 80.36% 82.69%
CHEMBL1994 P08235 Mineralocorticoid receptor 80.06% 100.00%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 11357536
LOTUS LTS0167384
wikiData Q105115104