(1S,2R,8aS)-1-ethyl-1,5,5-trimethyl-2,3,6,7,8,8a-hexahydronaphthalene-2-carboxylic acid

Details

Top
Internal ID e881b256-5a47-4436-8d7b-9ce3bb50b8fd
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Carboxylic acids
IUPAC Name (1S,2R,8aS)-1-ethyl-1,5,5-trimethyl-2,3,6,7,8,8a-hexahydronaphthalene-2-carboxylic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C16H26O2/c1-5-16(4)12-7-6-10-15(2,3)11(12)8-9-13(16)14(17)18/h8,12-13H,5-7,9-10H2,1-4H3,(H,17,18)/t12-,13+,16+/m1/s1
InChI Key SVWIWSHBOOWWND-WWGRRREGSA-N
Popularity 2 references in papers

Physical and Chemical Properties

Top
Molecular Formula C16H26O2
Molecular Weight 250.38 g/mol
Exact Mass 250.193280068 g/mol
Topological Polar Surface Area (TPSA) 37.30 Ų
XlogP 4.50
Atomic LogP (AlogP) 4.26
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of (1S,2R,8aS)-1-ethyl-1,5,5-trimethyl-2,3,6,7,8,8a-hexahydronaphthalene-2-carboxylic acid

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 1.0000 100.00%
Caco-2 + 0.8908 89.08%
Blood Brain Barrier + 0.7250 72.50%
Human oral bioavailability + 0.5571 55.71%
Subcellular localzation Mitochondria 0.4555 45.55%
OATP2B1 inhibitior - 0.8399 83.99%
OATP1B1 inhibitior + 0.8757 87.57%
OATP1B3 inhibitior - 0.2953 29.53%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.6000 60.00%
BSEP inhibitior - 0.7369 73.69%
P-glycoprotein inhibitior - 0.9221 92.21%
P-glycoprotein substrate - 0.9379 93.79%
CYP3A4 substrate - 0.5146 51.46%
CYP2C9 substrate - 0.5859 58.59%
CYP2D6 substrate - 0.8733 87.33%
CYP3A4 inhibition - 0.8323 83.23%
CYP2C9 inhibition + 0.5888 58.88%
CYP2C19 inhibition + 0.6014 60.14%
CYP2D6 inhibition - 0.9185 91.85%
CYP1A2 inhibition - 0.8251 82.51%
CYP2C8 inhibition - 0.8437 84.37%
CYP inhibitory promiscuity - 0.5266 52.66%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8800 88.00%
Carcinogenicity (trinary) Non-required 0.6246 62.46%
Eye corrosion - 0.9856 98.56%
Eye irritation - 0.6697 66.97%
Skin irritation - 0.7082 70.82%
Skin corrosion - 0.9803 98.03%
Ames mutagenesis - 0.7900 79.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6449 64.49%
Micronuclear - 0.9400 94.00%
Hepatotoxicity + 0.5203 52.03%
skin sensitisation + 0.7467 74.67%
Respiratory toxicity + 0.5111 51.11%
Reproductive toxicity + 0.7000 70.00%
Mitochondrial toxicity + 0.6375 63.75%
Nephrotoxicity - 0.6520 65.20%
Acute Oral Toxicity (c) IV 0.4744 47.44%
Estrogen receptor binding - 0.7145 71.45%
Androgen receptor binding - 0.5211 52.11%
Thyroid receptor binding + 0.5560 55.60%
Glucocorticoid receptor binding - 0.6521 65.21%
Aromatase binding - 0.5426 54.26%
PPAR gamma - 0.6259 62.59%
Honey bee toxicity - 0.9557 95.57%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity - 0.6200 62.00%
Fish aquatic toxicity + 1.0000 100.00%

Targets

Top

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 94.13% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 92.49% 97.25%
CHEMBL221 P23219 Cyclooxygenase-1 92.33% 90.17%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 90.06% 91.11%
CHEMBL3137262 O60341 LSD1/CoREST complex 88.34% 97.09%
CHEMBL2581 P07339 Cathepsin D 87.90% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.01% 95.56%
CHEMBL226 P30542 Adenosine A1 receptor 84.70% 95.93%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 83.84% 92.62%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 80.80% 94.45%
CHEMBL218 P21554 Cannabinoid CB1 receptor 80.48% 96.61%

Plants that contains it

Top
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

Top
PubChem 101922019
LOTUS LTS0275953
wikiData Q105262497