(2R,3R,4aS,8aS)-3-(2-hydroxypropan-2-yl)-8a-methyl-5-methylidene-2,3,4,6,7,8-hexahydro-1H-naphthalene-2,4a-diol

Details

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Internal ID 8b6336d7-4975-4ec3-9d8e-279c9fa8f19a
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids > Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
IUPAC Name (2R,3R,4aS,8aS)-3-(2-hydroxypropan-2-yl)-8a-methyl-5-methylidene-2,3,4,6,7,8-hexahydro-1H-naphthalene-2,4a-diol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H26O3/c1-10-6-5-7-14(4)9-12(16)11(13(2,3)17)8-15(10,14)18/h11-12,16-18H,1,5-9H2,2-4H3/t11-,12-,14+,15+/m1/s1
InChI Key XGPONYNKAOFSGR-UXOAXIEHSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C15H26O3
Molecular Weight 254.36 g/mol
Exact Mass 254.18819469 g/mol
Topological Polar Surface Area (TPSA) 60.70 Ų
XlogP 1.90
Atomic LogP (AlogP) 2.01
H-Bond Acceptor 3
H-Bond Donor 3
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (2R,3R,4aS,8aS)-3-(2-hydroxypropan-2-yl)-8a-methyl-5-methylidene-2,3,4,6,7,8-hexahydro-1H-naphthalene-2,4a-diol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9923 99.23%
Caco-2 + 0.7307 73.07%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability + 0.6286 62.86%
Subcellular localzation Mitochondria 0.4670 46.70%
OATP2B1 inhibitior - 0.8477 84.77%
OATP1B1 inhibitior + 0.9310 93.10%
OATP1B3 inhibitior + 0.8176 81.76%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior - 0.7474 74.74%
P-glycoprotein inhibitior - 0.9469 94.69%
P-glycoprotein substrate - 0.8596 85.96%
CYP3A4 substrate + 0.5272 52.72%
CYP2C9 substrate - 0.5811 58.11%
CYP2D6 substrate - 0.7340 73.40%
CYP3A4 inhibition - 0.7273 72.73%
CYP2C9 inhibition - 0.7835 78.35%
CYP2C19 inhibition - 0.7261 72.61%
CYP2D6 inhibition - 0.9412 94.12%
CYP1A2 inhibition - 0.8450 84.50%
CYP2C8 inhibition - 0.8570 85.70%
CYP inhibitory promiscuity - 0.7883 78.83%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9200 92.00%
Carcinogenicity (trinary) Non-required 0.5946 59.46%
Eye corrosion - 0.9891 98.91%
Eye irritation - 0.6954 69.54%
Skin irritation + 0.5122 51.22%
Skin corrosion - 0.9399 93.99%
Ames mutagenesis - 0.8100 81.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7589 75.89%
Micronuclear - 0.9700 97.00%
Hepatotoxicity + 0.5734 57.34%
skin sensitisation - 0.5330 53.30%
Respiratory toxicity + 0.5556 55.56%
Reproductive toxicity + 0.8778 87.78%
Mitochondrial toxicity + 0.8000 80.00%
Nephrotoxicity - 0.8023 80.23%
Acute Oral Toxicity (c) I 0.7675 76.75%
Estrogen receptor binding - 0.5232 52.32%
Androgen receptor binding - 0.6350 63.50%
Thyroid receptor binding - 0.5165 51.65%
Glucocorticoid receptor binding + 0.6795 67.95%
Aromatase binding - 0.5788 57.88%
PPAR gamma - 0.7256 72.56%
Honey bee toxicity - 0.8997 89.97%
Biodegradation - 0.5750 57.50%
Crustacea aquatic toxicity - 0.5300 53.00%
Fish aquatic toxicity + 0.9920 99.20%

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 97.53% 97.25%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.58% 91.11%
CHEMBL2996 Q05655 Protein kinase C delta 90.14% 97.79%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.74% 96.09%
CHEMBL1994 P08235 Mineralocorticoid receptor 85.98% 100.00%
CHEMBL2581 P07339 Cathepsin D 84.58% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.58% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.32% 86.33%
CHEMBL5608 Q16288 NT-3 growth factor receptor 83.21% 95.89%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 82.78% 94.45%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 81.64% 82.69%
CHEMBL3137262 O60341 LSD1/CoREST complex 81.56% 97.09%
CHEMBL259 P32245 Melanocortin receptor 4 80.21% 95.38%

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.
Artemisia arbuscula subsp. longiloba

Cross-Links

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PubChem 12135225
LOTUS LTS0125485
wikiData Q105327749