8-ethyl-1,1,4a,7-tetramethyl-4,9,10,10a-tetrahydro-3H-phenanthren-2-one

Details

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Internal ID c07ecdeb-1429-48e4-b264-164e77853a2a
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids
IUPAC Name 8-ethyl-1,1,4a,7-tetramethyl-4,9,10,10a-tetrahydro-3H-phenanthren-2-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C20H28O/c1-6-14-13(2)7-9-16-15(14)8-10-17-19(3,4)18(21)11-12-20(16,17)5/h7,9,17H,6,8,10-12H2,1-5H3
InChI Key RBAHQKBUVTZPPX-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C20H28O
Molecular Weight 284.40 g/mol
Exact Mass 284.214015512 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 5.30
Atomic LogP (AlogP) 4.77
H-Bond Acceptor 1
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 8-ethyl-1,1,4a,7-tetramethyl-4,9,10,10a-tetrahydro-3H-phenanthren-2-one

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 + 0.8794 87.94%
Blood Brain Barrier + 0.8750 87.50%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Mitochondria 0.6534 65.34%
OATP2B1 inhibitior - 0.8610 86.10%
OATP1B1 inhibitior + 0.8955 89.55%
OATP1B3 inhibitior + 0.9796 97.96%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior + 0.6781 67.81%
P-glycoprotein inhibitior - 0.6916 69.16%
P-glycoprotein substrate - 0.8544 85.44%
CYP3A4 substrate + 0.5771 57.71%
CYP2C9 substrate - 0.5623 56.23%
CYP2D6 substrate - 0.6878 68.78%
CYP3A4 inhibition - 0.8565 85.65%
CYP2C9 inhibition - 0.6898 68.98%
CYP2C19 inhibition - 0.6981 69.81%
CYP2D6 inhibition - 0.9281 92.81%
CYP1A2 inhibition - 0.5861 58.61%
CYP2C8 inhibition - 0.6105 61.05%
CYP inhibitory promiscuity - 0.6960 69.60%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8500 85.00%
Carcinogenicity (trinary) Non-required 0.6698 66.98%
Eye corrosion - 0.9575 95.75%
Eye irritation - 0.7934 79.34%
Skin irritation - 0.6706 67.06%
Skin corrosion - 0.9641 96.41%
Ames mutagenesis - 0.6237 62.37%
Human Ether-a-go-go-Related Gene inhibition + 0.7195 71.95%
Micronuclear - 0.9900 99.00%
Hepatotoxicity - 0.5948 59.48%
skin sensitisation + 0.6318 63.18%
Respiratory toxicity + 0.7333 73.33%
Reproductive toxicity + 0.5333 53.33%
Mitochondrial toxicity - 0.5250 52.50%
Nephrotoxicity - 0.8055 80.55%
Acute Oral Toxicity (c) III 0.5778 57.78%
Estrogen receptor binding + 0.6192 61.92%
Androgen receptor binding + 0.5792 57.92%
Thyroid receptor binding + 0.7739 77.39%
Glucocorticoid receptor binding + 0.5993 59.93%
Aromatase binding - 0.6322 63.22%
PPAR gamma + 0.6682 66.82%
Honey bee toxicity - 0.9100 91.00%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity + 0.5400 54.00%
Fish aquatic toxicity + 0.9950 99.50%

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 96.25% 89.76%
CHEMBL2581 P07339 Cathepsin D 92.87% 98.95%
CHEMBL3137262 O60341 LSD1/CoREST complex 90.67% 97.09%
CHEMBL1994 P08235 Mineralocorticoid receptor 88.24% 100.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.02% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 86.62% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.39% 96.09%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 85.32% 89.62%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 83.05% 85.30%
CHEMBL1907 P15144 Aminopeptidase N 82.47% 93.31%
CHEMBL1871 P10275 Androgen Receptor 81.86% 96.43%
CHEMBL1293249 Q13887 Kruppel-like factor 5 81.63% 86.33%
CHEMBL1914 P06276 Butyrylcholinesterase 80.63% 95.00%
CHEMBL3192 Q9BY41 Histone deacetylase 8 80.51% 93.99%

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 162820597
LOTUS LTS0252850
wikiData Q104196425