(1S,4aS,7R,8aS)-7-(2-hydroxypropan-2-yl)-1,4a-dimethyl-1,3,4,5,6,7,8,8a-octahydronaphthalen-2-one

Details

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Internal ID 13ff8837-6e5c-4c5f-ae45-f942c75717ee
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids > Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
IUPAC Name (1S,4aS,7R,8aS)-7-(2-hydroxypropan-2-yl)-1,4a-dimethyl-1,3,4,5,6,7,8,8a-octahydronaphthalen-2-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H26O2/c1-10-12-9-11(14(2,3)17)5-7-15(12,4)8-6-13(10)16/h10-12,17H,5-9H2,1-4H3/t10-,11+,12-,15-/m0/s1
InChI Key CUDHRTAOLMZZFB-OXIQGZBJSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C15H26O2
Molecular Weight 238.37 g/mol
Exact Mass 238.193280068 g/mol
Topological Polar Surface Area (TPSA) 37.30 Ų
XlogP 2.70
Atomic LogP (AlogP) 3.18
H-Bond Acceptor 2
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 (1S,4aS,7R,8aS)-7-(2-hydroxypropan-2-yl)-1,4a-dimethyl-1,3,4,5,6,7,8,8a-octahydronaphthalen-2-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9974 99.74%
Caco-2 + 0.6897 68.97%
Blood Brain Barrier + 0.8250 82.50%
Human oral bioavailability + 0.5857 58.57%
Subcellular localzation Mitochondria 0.8081 80.81%
OATP2B1 inhibitior - 0.8484 84.84%
OATP1B1 inhibitior + 0.9077 90.77%
OATP1B3 inhibitior + 0.9784 97.84%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior + 0.6500 65.00%
BSEP inhibitior - 0.7463 74.63%
P-glycoprotein inhibitior - 0.8769 87.69%
P-glycoprotein substrate - 0.9101 91.01%
CYP3A4 substrate + 0.5921 59.21%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7949 79.49%
CYP3A4 inhibition - 0.8332 83.32%
CYP2C9 inhibition - 0.7717 77.17%
CYP2C19 inhibition - 0.8561 85.61%
CYP2D6 inhibition - 0.9704 97.04%
CYP1A2 inhibition - 0.6276 62.76%
CYP2C8 inhibition - 0.8422 84.22%
CYP inhibitory promiscuity - 0.9595 95.95%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.9500 95.00%
Carcinogenicity (trinary) Non-required 0.6368 63.68%
Eye corrosion - 0.9720 97.20%
Eye irritation - 0.6581 65.81%
Skin irritation + 0.6196 61.96%
Skin corrosion - 0.9406 94.06%
Ames mutagenesis - 0.8500 85.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8246 82.46%
Micronuclear - 1.0000 100.00%
Hepatotoxicity + 0.5065 50.65%
skin sensitisation + 0.5723 57.23%
Respiratory toxicity + 0.5444 54.44%
Reproductive toxicity + 0.8111 81.11%
Mitochondrial toxicity - 0.6250 62.50%
Nephrotoxicity - 0.6584 65.84%
Acute Oral Toxicity (c) III 0.8478 84.78%
Estrogen receptor binding - 0.5000 50.00%
Androgen receptor binding - 0.6603 66.03%
Thyroid receptor binding - 0.5516 55.16%
Glucocorticoid receptor binding - 0.4732 47.32%
Aromatase binding - 0.7262 72.62%
PPAR gamma - 0.7112 71.12%
Honey bee toxicity - 0.8252 82.52%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity + 0.5800 58.00%
Fish aquatic toxicity + 0.9701 97.01%

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 99.39% 97.25%
CHEMBL1871 P10275 Androgen Receptor 93.68% 96.43%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 91.38% 91.11%
CHEMBL2996 Q05655 Protein kinase C delta 89.50% 97.79%
CHEMBL3137262 O60341 LSD1/CoREST complex 88.27% 97.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.30% 95.56%
CHEMBL1994 P08235 Mineralocorticoid receptor 87.12% 100.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.76% 96.09%
CHEMBL2581 P07339 Cathepsin D 85.87% 98.95%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 84.80% 93.04%
CHEMBL218 P21554 Cannabinoid CB1 receptor 84.67% 96.61%
CHEMBL1902 P62942 FK506-binding protein 1A 84.41% 97.05%
CHEMBL1937 Q92769 Histone deacetylase 2 84.37% 94.75%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 82.46% 96.77%
CHEMBL241 Q14432 Phosphodiesterase 3A 82.14% 92.94%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 81.92% 99.23%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 80.10% 85.14%

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.
Nicotiana undulata

Cross-Links

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PubChem 15601420
LOTUS LTS0074024
wikiData Q104970187