(4aR,6R,8aR)-6-hydroxy-4,8a-dimethyl-6-prop-1-en-2-yl-4a,5,7,8-tetrahydro-1H-naphthalen-2-one

Details

Top
Internal ID 18599764-4d3b-446b-92c0-15bbb4c86298
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids > Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
IUPAC Name (4aR,6R,8aR)-6-hydroxy-4,8a-dimethyl-6-prop-1-en-2-yl-4a,5,7,8-tetrahydro-1H-naphthalen-2-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H22O2/c1-10(2)15(17)6-5-14(4)8-12(16)7-11(3)13(14)9-15/h7,13,17H,1,5-6,8-9H2,2-4H3/t13-,14+,15+/m0/s1
InChI Key SAJFRLDIWQUNCQ-RRFJBIMHSA-N
Popularity 2 references in papers

Physical and Chemical Properties

Top
Molecular Formula C15H22O2
Molecular Weight 234.33 g/mol
Exact Mass 234.161979940 g/mol
Topological Polar Surface Area (TPSA) 37.30 Ų
XlogP 2.20
Atomic LogP (AlogP) 3.02
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of (4aR,6R,8aR)-6-hydroxy-4,8a-dimethyl-6-prop-1-en-2-yl-4a,5,7,8-tetrahydro-1H-naphthalen-2-one

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 1.0000 100.00%
Caco-2 + 0.8672 86.72%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability + 0.6429 64.29%
Subcellular localzation Mitochondria 0.5870 58.70%
OATP2B1 inhibitior - 0.8540 85.40%
OATP1B1 inhibitior + 0.9222 92.22%
OATP1B3 inhibitior + 0.9336 93.36%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior + 0.5750 57.50%
BSEP inhibitior - 0.8650 86.50%
P-glycoprotein inhibitior - 0.9588 95.88%
P-glycoprotein substrate - 0.7712 77.12%
CYP3A4 substrate + 0.5706 57.06%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8953 89.53%
CYP3A4 inhibition - 0.5863 58.63%
CYP2C9 inhibition - 0.8100 81.00%
CYP2C19 inhibition - 0.7765 77.65%
CYP2D6 inhibition - 0.9449 94.49%
CYP1A2 inhibition - 0.8554 85.54%
CYP2C8 inhibition - 0.9504 95.04%
CYP inhibitory promiscuity - 0.9455 94.55%
UGT catelyzed + 0.6362 63.62%
Carcinogenicity (binary) - 0.9300 93.00%
Carcinogenicity (trinary) Non-required 0.5215 52.15%
Eye corrosion - 0.9852 98.52%
Eye irritation + 0.6411 64.11%
Skin irritation + 0.5462 54.62%
Skin corrosion - 0.9698 96.98%
Ames mutagenesis - 0.7470 74.70%
Human Ether-a-go-go-Related Gene inhibition - 0.4396 43.96%
Micronuclear - 0.9600 96.00%
Hepatotoxicity - 0.5109 51.09%
skin sensitisation + 0.6720 67.20%
Respiratory toxicity + 0.6000 60.00%
Reproductive toxicity + 0.7556 75.56%
Mitochondrial toxicity + 0.7625 76.25%
Nephrotoxicity + 0.5696 56.96%
Acute Oral Toxicity (c) III 0.7901 79.01%
Estrogen receptor binding - 0.7911 79.11%
Androgen receptor binding - 0.6766 67.66%
Thyroid receptor binding - 0.6232 62.32%
Glucocorticoid receptor binding - 0.6359 63.59%
Aromatase binding - 0.5674 56.74%
PPAR gamma - 0.7911 79.11%
Honey bee toxicity - 0.8854 88.54%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity - 0.5100 51.00%
Fish aquatic toxicity + 0.9818 98.18%

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
CHEMBL253 P34972 Cannabinoid CB2 receptor 93.88% 97.25%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.60% 91.11%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 91.02% 82.69%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.03% 96.09%
CHEMBL1937 Q92769 Histone deacetylase 2 87.87% 94.75%
CHEMBL1994 P08235 Mineralocorticoid receptor 87.86% 100.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.93% 95.56%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 85.24% 99.23%
CHEMBL2581 P07339 Cathepsin D 84.84% 98.95%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 84.77% 85.14%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 83.62% 94.45%
CHEMBL1871 P10275 Androgen Receptor 83.10% 96.43%
CHEMBL4208 P20618 Proteasome component C5 81.69% 90.00%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 81.30% 93.04%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 80.78% 93.03%
CHEMBL3746 P80365 11-beta-hydroxysteroid dehydrogenase 2 80.35% 94.78%
CHEMBL1806 P11388 DNA topoisomerase II alpha 80.01% 89.00%

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.
Teucrium heterophyllum

Cross-Links

Top
PubChem 162961713
LOTUS LTS0090603
wikiData Q105248903