8-Ethyl-1,1,4a,7-tetramethyl-2,3,4,9,10,10a-hexahydrophenanthren-2-ol

Details

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Internal ID fabaac06-c3a6-4f48-bd78-e17665b65c80
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids
IUPAC Name 8-ethyl-1,1,4a,7-tetramethyl-2,3,4,9,10,10a-hexahydrophenanthren-2-ol
SMILES (Canonical) CCC1=C(C=CC2=C1CCC3C2(CCC(C3(C)C)O)C)C
SMILES (Isomeric) CCC1=C(C=CC2=C1CCC3C2(CCC(C3(C)C)O)C)C
InChI InChI=1S/C20H30O/c1-6-14-13(2)7-9-16-15(14)8-10-17-19(3,4)18(21)11-12-20(16,17)5/h7,9,17-18,21H,6,8,10-12H2,1-5H3
InChI Key NUHBHAAXQHHOMG-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C20H30O
Molecular Weight 286.50 g/mol
Exact Mass 286.229665576 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 5.60
Atomic LogP (AlogP) 4.56
H-Bond Acceptor 1
H-Bond Donor 1
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-2,3,4,9,10,10a-hexahydrophenanthren-2-ol

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 + 0.8985 89.85%
Blood Brain Barrier + 0.8250 82.50%
Human oral bioavailability - 0.6000 60.00%
Subcellular localzation Mitochondria 0.6055 60.55%
OATP2B1 inhibitior - 0.8614 86.14%
OATP1B1 inhibitior + 0.8999 89.99%
OATP1B3 inhibitior + 0.9600 96.00%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior + 0.6492 64.92%
P-glycoprotein inhibitior - 0.8763 87.63%
P-glycoprotein substrate - 0.8454 84.54%
CYP3A4 substrate + 0.5776 57.76%
CYP2C9 substrate - 0.5581 55.81%
CYP2D6 substrate + 0.4478 44.78%
CYP3A4 inhibition - 0.7274 72.74%
CYP2C9 inhibition - 0.7617 76.17%
CYP2C19 inhibition - 0.7515 75.15%
CYP2D6 inhibition - 0.9194 91.94%
CYP1A2 inhibition - 0.5000 50.00%
CYP2C8 inhibition - 0.6262 62.62%
CYP inhibitory promiscuity - 0.6690 66.90%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.7511 75.11%
Carcinogenicity (trinary) Non-required 0.7024 70.24%
Eye corrosion - 0.9729 97.29%
Eye irritation - 0.9400 94.00%
Skin irritation - 0.6193 61.93%
Skin corrosion - 0.9099 90.99%
Ames mutagenesis - 0.7500 75.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3647 36.47%
Micronuclear - 0.9900 99.00%
Hepatotoxicity - 0.6875 68.75%
skin sensitisation + 0.5000 50.00%
Respiratory toxicity + 0.6111 61.11%
Reproductive toxicity + 0.7667 76.67%
Mitochondrial toxicity + 0.6625 66.25%
Nephrotoxicity - 0.9326 93.26%
Acute Oral Toxicity (c) III 0.7324 73.24%
Estrogen receptor binding + 0.5499 54.99%
Androgen receptor binding + 0.6006 60.06%
Thyroid receptor binding + 0.7358 73.58%
Glucocorticoid receptor binding - 0.4779 47.79%
Aromatase binding - 0.5729 57.29%
PPAR gamma + 0.5541 55.41%
Honey bee toxicity - 0.9277 92.77%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity + 0.5200 52.00%
Fish aquatic toxicity + 0.9930 99.30%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.57% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 91.67% 97.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 91.54% 91.11%
CHEMBL2581 P07339 Cathepsin D 91.01% 98.95%
CHEMBL221 P23219 Cyclooxygenase-1 90.24% 90.17%
CHEMBL240 Q12809 HERG 90.20% 89.76%
CHEMBL1994 P08235 Mineralocorticoid receptor 89.83% 100.00%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 88.82% 89.62%
CHEMBL1871 P10275 Androgen Receptor 85.12% 96.43%
CHEMBL2781 P19634 Sodium/hydrogen exchanger 1 83.74% 90.24%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.07% 95.89%
CHEMBL3192 Q9BY41 Histone deacetylase 8 80.81% 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 162820592
LOTUS LTS0044102
wikiData Q104180026