(1-Ethyl-1,5,5-trimethyl-2,3,6,7,8,8a-hexahydronaphthalen-2-yl)methanol

Details

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Internal ID 661a7677-44ac-4a28-82fb-234e27e58004
Taxonomy Organic oxygen compounds > Organooxygen compounds > Alcohols and polyols > Primary alcohols
IUPAC Name (1-ethyl-1,5,5-trimethyl-2,3,6,7,8,8a-hexahydronaphthalen-2-yl)methanol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C16H28O/c1-5-16(4)12(11-17)8-9-13-14(16)7-6-10-15(13,2)3/h9,12,14,17H,5-8,10-11H2,1-4H3
InChI Key FJTAPRWKOZSAMT-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C16H28O
Molecular Weight 236.39 g/mol
Exact Mass 236.214015512 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 4.60
Atomic LogP (AlogP) 4.17
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (1-Ethyl-1,5,5-trimethyl-2,3,6,7,8,8a-hexahydronaphthalen-2-yl)methanol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9963 99.63%
Caco-2 + 0.9031 90.31%
Blood Brain Barrier + 0.8500 85.00%
Human oral bioavailability + 0.5429 54.29%
Subcellular localzation Lysosomes 0.6413 64.13%
OATP2B1 inhibitior - 0.8402 84.02%
OATP1B1 inhibitior + 0.8782 87.82%
OATP1B3 inhibitior + 0.8389 83.89%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.6000 60.00%
BSEP inhibitior - 0.6414 64.14%
P-glycoprotein inhibitior - 0.9246 92.46%
P-glycoprotein substrate - 0.9098 90.98%
CYP3A4 substrate - 0.5316 53.16%
CYP2C9 substrate - 0.7664 76.64%
CYP2D6 substrate - 0.7388 73.88%
CYP3A4 inhibition - 0.7251 72.51%
CYP2C9 inhibition - 0.5311 53.11%
CYP2C19 inhibition - 0.5890 58.90%
CYP2D6 inhibition - 0.8701 87.01%
CYP1A2 inhibition - 0.8027 80.27%
CYP2C8 inhibition - 0.7920 79.20%
CYP inhibitory promiscuity + 0.6851 68.51%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9000 90.00%
Carcinogenicity (trinary) Non-required 0.6338 63.38%
Eye corrosion - 0.9712 97.12%
Eye irritation - 0.5955 59.55%
Skin irritation - 0.7724 77.24%
Skin corrosion - 0.9673 96.73%
Ames mutagenesis - 0.8000 80.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3961 39.61%
Micronuclear - 0.9700 97.00%
Hepatotoxicity + 0.5118 51.18%
skin sensitisation + 0.6017 60.17%
Respiratory toxicity - 0.5333 53.33%
Reproductive toxicity + 0.5333 53.33%
Mitochondrial toxicity + 0.5375 53.75%
Nephrotoxicity + 0.4564 45.64%
Acute Oral Toxicity (c) IV 0.5293 52.93%
Estrogen receptor binding - 0.8195 81.95%
Androgen receptor binding - 0.6181 61.81%
Thyroid receptor binding + 0.5549 55.49%
Glucocorticoid receptor binding - 0.6984 69.84%
Aromatase binding - 0.5958 59.58%
PPAR gamma - 0.7772 77.72%
Honey bee toxicity - 0.9397 93.97%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity - 0.6400 64.00%
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
CHEMBL253 P34972 Cannabinoid CB2 receptor 96.20% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.80% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 94.34% 97.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.16% 91.11%
CHEMBL226 P30542 Adenosine A1 receptor 89.59% 95.93%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 85.60% 92.62%
CHEMBL218 P21554 Cannabinoid CB1 receptor 84.92% 96.61%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 83.84% 95.50%
CHEMBL3192 Q9BY41 Histone deacetylase 8 83.71% 93.99%
CHEMBL2581 P07339 Cathepsin D 83.42% 98.95%
CHEMBL1937 Q92769 Histone deacetylase 2 82.97% 94.75%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 82.55% 94.45%
CHEMBL1994 P08235 Mineralocorticoid receptor 81.77% 100.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 81.73% 95.89%

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 squamata

Cross-Links

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PubChem 162967110
LOTUS LTS0103004
wikiData Q104996331