(1R,3R,5R,6S,8aR)-3,4,5,8a-tetramethyl-6-propan-2-yl-2,3,5,6,7,8-hexahydro-1H-naphthalen-1-ol

Details

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Internal ID 71d7d2e5-2207-4626-b2d3-4921a92c7920
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids > Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
IUPAC Name (1R,3R,5R,6S,8aR)-3,4,5,8a-tetramethyl-6-propan-2-yl-2,3,5,6,7,8-hexahydro-1H-naphthalen-1-ol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C17H30O/c1-10(2)14-7-8-17(6)15(18)9-11(3)12(4)16(17)13(14)5/h10-11,13-15,18H,7-9H2,1-6H3/t11-,13-,14+,15-,17+/m1/s1
InChI Key LJNXAYQGMHMWTR-AQFIFQLPSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C17H30O
Molecular Weight 250.40 g/mol
Exact Mass 250.229665576 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 4.10
Atomic LogP (AlogP) 4.41
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 (1R,3R,5R,6S,8aR)-3,4,5,8a-tetramethyl-6-propan-2-yl-2,3,5,6,7,8-hexahydro-1H-naphthalen-1-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 + 0.7847 78.47%
Blood Brain Barrier - 0.5750 57.50%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Mitochondria 0.5374 53.74%
OATP2B1 inhibitior - 0.8457 84.57%
OATP1B1 inhibitior + 0.9318 93.18%
OATP1B3 inhibitior + 0.9680 96.80%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.6500 65.00%
BSEP inhibitior - 0.9078 90.78%
P-glycoprotein inhibitior - 0.8134 81.34%
P-glycoprotein substrate - 0.8009 80.09%
CYP3A4 substrate + 0.5514 55.14%
CYP2C9 substrate - 0.6499 64.99%
CYP2D6 substrate - 0.6843 68.43%
CYP3A4 inhibition - 0.8699 86.99%
CYP2C9 inhibition - 0.7983 79.83%
CYP2C19 inhibition - 0.6636 66.36%
CYP2D6 inhibition - 0.9399 93.99%
CYP1A2 inhibition - 0.8575 85.75%
CYP2C8 inhibition - 0.8909 89.09%
CYP inhibitory promiscuity - 0.7882 78.82%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9200 92.00%
Carcinogenicity (trinary) Non-required 0.5745 57.45%
Eye corrosion - 0.9863 98.63%
Eye irritation - 0.6692 66.92%
Skin irritation + 0.6645 66.45%
Skin corrosion - 0.9471 94.71%
Ames mutagenesis - 0.8800 88.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4813 48.13%
Micronuclear - 0.9800 98.00%
Hepatotoxicity - 0.5729 57.29%
skin sensitisation + 0.6420 64.20%
Respiratory toxicity - 0.6000 60.00%
Reproductive toxicity + 0.8667 86.67%
Mitochondrial toxicity + 0.7500 75.00%
Nephrotoxicity - 0.8323 83.23%
Acute Oral Toxicity (c) III 0.8299 82.99%
Estrogen receptor binding - 0.6111 61.11%
Androgen receptor binding + 0.6177 61.77%
Thyroid receptor binding + 0.5821 58.21%
Glucocorticoid receptor binding - 0.6956 69.56%
Aromatase binding - 0.7393 73.93%
PPAR gamma - 0.7996 79.96%
Honey bee toxicity - 0.8646 86.46%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity + 0.5400 54.00%
Fish aquatic toxicity + 0.9875 98.75%

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 93.52% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 93.22% 97.25%
CHEMBL3137262 O60341 LSD1/CoREST complex 86.90% 97.09%
CHEMBL2581 P07339 Cathepsin D 86.08% 98.95%
CHEMBL1994 P08235 Mineralocorticoid receptor 85.35% 100.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 84.47% 95.89%
CHEMBL259 P32245 Melanocortin receptor 4 82.88% 95.38%
CHEMBL1871 P10275 Androgen Receptor 82.87% 96.43%
CHEMBL3359 P21462 Formyl peptide receptor 1 81.88% 93.56%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 81.04% 96.47%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 80.94% 91.11%
CHEMBL1951 P21397 Monoamine oxidase A 80.14% 91.49%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 80.07% 95.56%

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.
Teucrium polium

Cross-Links

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PubChem 163191014
LOTUS LTS0180105
wikiData Q105152682