(4aS,10aS)-8-ethyl-1,1,4a,7-tetramethyl-4,9,10,10a-tetrahydrophenanthrene

Details

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Internal ID e52d394c-2909-44ab-b51c-804679c07e73
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids
IUPAC Name (4aS,10aS)-8-ethyl-1,1,4a,7-tetramethyl-4,9,10,10a-tetrahydrophenanthrene
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C20H28/c1-6-15-14(2)8-10-17-16(15)9-11-18-19(3,4)12-7-13-20(17,18)5/h7-8,10,12,18H,6,9,11,13H2,1-5H3/t18-,20+/m0/s1
InChI Key ZXQNKMAHWBGRNM-AZUAARDMSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C20H28
Molecular Weight 268.40 g/mol
Exact Mass 268.219100893 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 6.50
Atomic LogP (AlogP) 5.36
H-Bond Acceptor 0
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,10aS)-8-ethyl-1,1,4a,7-tetramethyl-4,9,10,10a-tetrahydrophenanthrene

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 + 0.8890 88.90%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Lysosomes 0.3868 38.68%
OATP2B1 inhibitior - 0.8614 86.14%
OATP1B1 inhibitior + 0.8974 89.74%
OATP1B3 inhibitior + 0.9383 93.83%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior + 0.6430 64.30%
P-glycoprotein inhibitior - 0.8540 85.40%
P-glycoprotein substrate - 0.6871 68.71%
CYP3A4 substrate + 0.5476 54.76%
CYP2C9 substrate - 0.6141 61.41%
CYP2D6 substrate - 0.6865 68.65%
CYP3A4 inhibition - 0.8678 86.78%
CYP2C9 inhibition - 0.7612 76.12%
CYP2C19 inhibition + 0.5081 50.81%
CYP2D6 inhibition - 0.8830 88.30%
CYP1A2 inhibition - 0.6209 62.09%
CYP2C8 inhibition + 0.5058 50.58%
CYP inhibitory promiscuity + 0.7806 78.06%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7300 73.00%
Carcinogenicity (trinary) Non-required 0.5651 56.51%
Eye corrosion - 0.9376 93.76%
Eye irritation - 0.8986 89.86%
Skin irritation - 0.7432 74.32%
Skin corrosion - 0.9728 97.28%
Ames mutagenesis - 0.5900 59.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8523 85.23%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.5750 57.50%
skin sensitisation + 0.7229 72.29%
Respiratory toxicity + 0.6556 65.56%
Reproductive toxicity - 0.6026 60.26%
Mitochondrial toxicity + 0.5250 52.50%
Nephrotoxicity - 0.8974 89.74%
Acute Oral Toxicity (c) IV 0.4762 47.62%
Estrogen receptor binding + 0.5313 53.13%
Androgen receptor binding + 0.5482 54.82%
Thyroid receptor binding + 0.7813 78.13%
Glucocorticoid receptor binding - 0.6140 61.40%
Aromatase binding - 0.6358 63.58%
PPAR gamma + 0.5698 56.98%
Honey bee toxicity - 0.9387 93.87%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity + 0.5900 59.00%
Fish aquatic toxicity + 1.0000 100.00%

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 96.05% 89.76%
CHEMBL3137262 O60341 LSD1/CoREST complex 92.15% 97.09%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.53% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 90.44% 91.11%
CHEMBL2581 P07339 Cathepsin D 89.62% 98.95%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 87.76% 89.62%
CHEMBL1994 P08235 Mineralocorticoid receptor 87.73% 100.00%
CHEMBL3155 P34969 Serotonin 7 (5-HT7) receptor 87.59% 90.71%
CHEMBL221 P23219 Cyclooxygenase-1 84.65% 90.17%
CHEMBL5608 Q16288 NT-3 growth factor receptor 84.54% 95.89%
CHEMBL3192 Q9BY41 Histone deacetylase 8 84.21% 93.99%
CHEMBL2996 Q05655 Protein kinase C delta 80.35% 97.79%

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 162820604
LOTUS LTS0038647
wikiData Q105385714