(4aS,10aR)-8-ethyl-1,1,4a,7-tetramethyl-10,10a-dihydrophenanthrene-2,9-dione

Details

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Internal ID c57fbe07-325b-4f4e-8eb7-af317131d2a4
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids
IUPAC Name (4aS,10aR)-8-ethyl-1,1,4a,7-tetramethyl-10,10a-dihydrophenanthrene-2,9-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C20H24O2/c1-6-13-12(2)7-8-14-18(13)15(21)11-16-19(3,4)17(22)9-10-20(14,16)5/h7-10,16H,6,11H2,1-5H3/t16-,20+/m0/s1
InChI Key BEYNZZVKYQTAAE-OXJNMPFZSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C20H24O2
Molecular Weight 296.40 g/mol
Exact Mass 296.177630004 g/mol
Topological Polar Surface Area (TPSA) 34.10 Ų
XlogP 4.40
Atomic LogP (AlogP) 4.18
H-Bond Acceptor 2
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 (4aS,10aR)-8-ethyl-1,1,4a,7-tetramethyl-10,10a-dihydrophenanthrene-2,9-dione

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 + 0.7661 76.61%
Blood Brain Barrier + 0.8250 82.50%
Human oral bioavailability + 0.6857 68.57%
Subcellular localzation Mitochondria 0.7856 78.56%
OATP2B1 inhibitior - 0.8597 85.97%
OATP1B1 inhibitior + 0.8593 85.93%
OATP1B3 inhibitior + 0.9678 96.78%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior + 0.7109 71.09%
P-glycoprotein inhibitior - 0.7098 70.98%
P-glycoprotein substrate - 0.6952 69.52%
CYP3A4 substrate + 0.5589 55.89%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8669 86.69%
CYP3A4 inhibition - 0.7265 72.65%
CYP2C9 inhibition + 0.5000 50.00%
CYP2C19 inhibition + 0.6629 66.29%
CYP2D6 inhibition - 0.8378 83.78%
CYP1A2 inhibition - 0.5000 50.00%
CYP2C8 inhibition - 0.7057 70.57%
CYP inhibitory promiscuity + 0.6612 66.12%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8334 83.34%
Carcinogenicity (trinary) Non-required 0.6537 65.37%
Eye corrosion - 0.9762 97.62%
Eye irritation - 0.8163 81.63%
Skin irritation - 0.6906 69.06%
Skin corrosion - 0.9374 93.74%
Ames mutagenesis - 0.5400 54.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7526 75.26%
Micronuclear - 0.8200 82.00%
Hepatotoxicity + 0.5355 53.55%
skin sensitisation + 0.7989 79.89%
Respiratory toxicity + 0.5556 55.56%
Reproductive toxicity - 0.5333 53.33%
Mitochondrial toxicity + 0.5500 55.00%
Nephrotoxicity - 0.6968 69.68%
Acute Oral Toxicity (c) III 0.6132 61.32%
Estrogen receptor binding + 0.8079 80.79%
Androgen receptor binding + 0.5819 58.19%
Thyroid receptor binding + 0.6973 69.73%
Glucocorticoid receptor binding + 0.6692 66.92%
Aromatase binding + 0.5962 59.62%
PPAR gamma + 0.7536 75.36%
Honey bee toxicity - 0.9111 91.11%
Biodegradation - 0.9250 92.50%
Crustacea aquatic toxicity + 0.5300 53.00%
Fish aquatic toxicity + 0.9928 99.28%

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
CHEMBL2581 P07339 Cathepsin D 94.62% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.77% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.53% 95.56%
CHEMBL3137262 O60341 LSD1/CoREST complex 87.16% 97.09%
CHEMBL1994 P08235 Mineralocorticoid receptor 83.52% 100.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 80.61% 86.33%
CHEMBL4208 P20618 Proteasome component C5 80.31% 90.00%

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.
Vellozia piresiana

Cross-Links

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PubChem 162993914
LOTUS LTS0133958
wikiData Q104933769