3b-Hydroxy-6b-methoxy-7(11)-eremophilen-12,8a-olide

Details

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Internal ID 3f872e2f-87a3-48db-8fc8-1423e17fee50
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Terpene lactones
IUPAC Name 6-hydroxy-4-methoxy-3,4a,5-trimethyl-4,5,6,7,8,8a,9,9a-octahydrobenzo[f][1]benzofuran-2-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C16H24O4/c1-8-13-12(20-15(8)18)7-10-5-6-11(17)9(2)16(10,3)14(13)19-4/h9-12,14,17H,5-7H2,1-4H3
InChI Key OBOOZVIHEDVWHF-UHFFFAOYSA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C16H24O4
Molecular Weight 280.36 g/mol
Exact Mass 280.16745924 g/mol
Topological Polar Surface Area (TPSA) 55.80 Ų
XlogP 1.60
Atomic LogP (AlogP) 2.06
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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CHEBI:174674
6-hydroxy-4-methoxy-3,4a,5-trimethyl-4,5,6,7,8,8a,9,9a-octahydrobenzo[][1]benzouran-2-one

2D Structure

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2D Structure of 3b-Hydroxy-6b-methoxy-7(11)-eremophilen-12,8a-olide

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9950 99.50%
Caco-2 + 0.8133 81.33%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Mitochondria 0.7290 72.90%
OATP2B1 inhibitior - 0.8558 85.58%
OATP1B1 inhibitior + 0.8946 89.46%
OATP1B3 inhibitior + 0.9499 94.99%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.6500 65.00%
BSEP inhibitior - 0.8876 88.76%
P-glycoprotein inhibitior - 0.8298 82.98%
P-glycoprotein substrate - 0.7399 73.99%
CYP3A4 substrate + 0.6523 65.23%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8747 87.47%
CYP3A4 inhibition - 0.6675 66.75%
CYP2C9 inhibition - 0.8551 85.51%
CYP2C19 inhibition - 0.8972 89.72%
CYP2D6 inhibition - 0.9486 94.86%
CYP1A2 inhibition - 0.6831 68.31%
CYP2C8 inhibition - 0.8137 81.37%
CYP inhibitory promiscuity - 0.8836 88.36%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.4810 48.10%
Eye corrosion - 0.9861 98.61%
Eye irritation - 0.9625 96.25%
Skin irritation - 0.5205 52.05%
Skin corrosion - 0.9104 91.04%
Ames mutagenesis - 0.6064 60.64%
Human Ether-a-go-go-Related Gene inhibition - 0.5278 52.78%
Micronuclear - 0.7100 71.00%
Hepatotoxicity + 0.6462 64.62%
skin sensitisation - 0.8086 80.86%
Respiratory toxicity + 0.6111 61.11%
Reproductive toxicity + 0.9778 97.78%
Mitochondrial toxicity + 0.8375 83.75%
Nephrotoxicity + 0.5077 50.77%
Acute Oral Toxicity (c) III 0.3236 32.36%
Estrogen receptor binding + 0.8487 84.87%
Androgen receptor binding + 0.5699 56.99%
Thyroid receptor binding + 0.6064 60.64%
Glucocorticoid receptor binding + 0.6226 62.26%
Aromatase binding - 0.6809 68.09%
PPAR gamma + 0.5782 57.82%
Honey bee toxicity - 0.7556 75.56%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.6000 60.00%
Fish aquatic toxicity + 0.9340 93.40%

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 95.24% 91.11%
CHEMBL3137262 O60341 LSD1/CoREST complex 92.39% 97.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.84% 95.56%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 90.80% 85.14%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 87.40% 99.23%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 84.47% 97.14%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 84.43% 96.09%
CHEMBL241 Q14432 Phosphodiesterase 3A 84.25% 92.94%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 84.12% 94.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.04% 86.33%
CHEMBL1994 P08235 Mineralocorticoid receptor 81.26% 100.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.67% 95.89%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 80.45% 91.07%
CHEMBL3045 P05771 Protein kinase C beta 80.40% 97.63%

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 131752927
LOTUS LTS0055248
wikiData Q105189098