(4aS,10aR)-8-ethyl-1,1,4a,7-tetramethyl-3,4,10,10a-tetrahydrophenanthrene-2,9-dione

Details

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Internal ID d1345901-1fd3-4e94-979a-f39d91d1185b
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids
IUPAC Name (4aS,10aR)-8-ethyl-1,1,4a,7-tetramethyl-3,4,10,10a-tetrahydrophenanthrene-2,9-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C20H26O2/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/h7-8,16H,6,9-11H2,1-5H3/t16-,20+/m0/s1
InChI Key UXGFDGDPHNRIBO-OXJNMPFZSA-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) 34.10 Ų
XlogP 4.20
Atomic LogP (AlogP) 4.41
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-3,4,10,10a-tetrahydrophenanthrene-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 + 0.8330 83.30%
Blood Brain Barrier + 0.8750 87.50%
Human oral bioavailability + 0.6000 60.00%
Subcellular localzation Mitochondria 0.7764 77.64%
OATP2B1 inhibitior - 0.8621 86.21%
OATP1B1 inhibitior + 0.8851 88.51%
OATP1B3 inhibitior + 0.9768 97.68%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior + 0.6684 66.84%
P-glycoprotein inhibitior - 0.7213 72.13%
P-glycoprotein substrate - 0.8455 84.55%
CYP3A4 substrate + 0.5479 54.79%
CYP2C9 substrate - 0.8058 80.58%
CYP2D6 substrate - 0.8035 80.35%
CYP3A4 inhibition - 0.7909 79.09%
CYP2C9 inhibition - 0.6255 62.55%
CYP2C19 inhibition - 0.6470 64.70%
CYP2D6 inhibition - 0.9138 91.38%
CYP1A2 inhibition - 0.6332 63.32%
CYP2C8 inhibition - 0.6153 61.53%
CYP inhibitory promiscuity - 0.7332 73.32%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8600 86.00%
Carcinogenicity (trinary) Non-required 0.6753 67.53%
Eye corrosion - 0.9760 97.60%
Eye irritation - 0.7825 78.25%
Skin irritation - 0.7366 73.66%
Skin corrosion - 0.9608 96.08%
Ames mutagenesis - 0.5737 57.37%
Human Ether-a-go-go-Related Gene inhibition + 0.6418 64.18%
Micronuclear - 0.9900 99.00%
Hepatotoxicity - 0.5002 50.02%
skin sensitisation - 0.5622 56.22%
Respiratory toxicity + 0.6778 67.78%
Reproductive toxicity + 0.5725 57.25%
Mitochondrial toxicity + 0.5875 58.75%
Nephrotoxicity - 0.7507 75.07%
Acute Oral Toxicity (c) III 0.6457 64.57%
Estrogen receptor binding + 0.6135 61.35%
Androgen receptor binding + 0.6002 60.02%
Thyroid receptor binding + 0.6767 67.67%
Glucocorticoid receptor binding + 0.7031 70.31%
Aromatase binding - 0.6520 65.20%
PPAR gamma + 0.7714 77.14%
Honey bee toxicity - 0.8393 83.93%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.5200 52.00%
Fish aquatic toxicity + 0.9957 99.57%

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
CHEMBL240 Q12809 HERG 96.23% 89.76%
CHEMBL2581 P07339 Cathepsin D 94.41% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 90.63% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.76% 95.56%
CHEMBL3137262 O60341 LSD1/CoREST complex 85.95% 97.09%
CHEMBL1994 P08235 Mineralocorticoid receptor 85.79% 100.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.29% 86.33%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 83.46% 96.09%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 82.56% 99.23%

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 163049293
LOTUS LTS0014360
wikiData Q105280768