(1R,6R,8aR)-4,8a-dimethyl-6-prop-1-en-2-yl-2,3,5,6,7,8-hexahydro-1H-naphthalen-1-ol

Details

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Internal ID dd1bd45d-9bae-4b27-b973-bd2d4ca4298d
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids > Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
IUPAC Name (1R,6R,8aR)-4,8a-dimethyl-6-prop-1-en-2-yl-2,3,5,6,7,8-hexahydro-1H-naphthalen-1-ol
SMILES (Canonical) CC1=C2CC(CCC2(C(CC1)O)C)C(=C)C
SMILES (Isomeric) CC1=C2C[C@@H](CC[C@]2([C@@H](CC1)O)C)C(=C)C
InChI InChI=1S/C15H24O/c1-10(2)12-7-8-15(4)13(9-12)11(3)5-6-14(15)16/h12,14,16H,1,5-9H2,2-4H3/t12-,14-,15-/m1/s1
InChI Key FNPFLRZHHDQZCG-BPLDGKMQSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H24O
Molecular Weight 220.35 g/mol
Exact Mass 220.182715385 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 3.40
Atomic LogP (AlogP) 3.84
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,6R,8aR)-4,8a-dimethyl-6-prop-1-en-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 + 0.9968 99.68%
Caco-2 + 0.8438 84.38%
Blood Brain Barrier - 0.5750 57.50%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Lysosomes 0.5237 52.37%
OATP2B1 inhibitior - 0.8479 84.79%
OATP1B1 inhibitior + 0.9277 92.77%
OATP1B3 inhibitior + 0.9155 91.55%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.5250 52.50%
BSEP inhibitior - 0.8336 83.36%
P-glycoprotein inhibitior - 0.9283 92.83%
P-glycoprotein substrate - 0.8722 87.22%
CYP3A4 substrate + 0.5543 55.43%
CYP2C9 substrate - 0.6499 64.99%
CYP2D6 substrate - 0.6843 68.43%
CYP3A4 inhibition - 0.7847 78.47%
CYP2C9 inhibition - 0.7275 72.75%
CYP2C19 inhibition - 0.5964 59.64%
CYP2D6 inhibition - 0.9384 93.84%
CYP1A2 inhibition - 0.8085 80.85%
CYP2C8 inhibition - 0.8382 83.82%
CYP inhibitory promiscuity - 0.8476 84.76%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9000 90.00%
Carcinogenicity (trinary) Non-required 0.5504 55.04%
Eye corrosion - 0.9850 98.50%
Eye irritation + 0.8226 82.26%
Skin irritation + 0.6376 63.76%
Skin corrosion - 0.9380 93.80%
Ames mutagenesis - 0.8900 89.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3742 37.42%
Micronuclear - 0.9800 98.00%
Hepatotoxicity + 0.5375 53.75%
skin sensitisation + 0.5496 54.96%
Respiratory toxicity - 0.6222 62.22%
Reproductive toxicity + 0.8889 88.89%
Mitochondrial toxicity + 0.7375 73.75%
Nephrotoxicity + 0.5816 58.16%
Acute Oral Toxicity (c) III 0.8426 84.26%
Estrogen receptor binding - 0.8627 86.27%
Androgen receptor binding - 0.6273 62.73%
Thyroid receptor binding - 0.6117 61.17%
Glucocorticoid receptor binding - 0.7683 76.83%
Aromatase binding - 0.6346 63.46%
PPAR gamma - 0.7760 77.60%
Honey bee toxicity - 0.8918 89.18%
Biodegradation - 0.5250 52.50%
Crustacea aquatic toxicity - 0.5500 55.00%
Fish aquatic toxicity + 0.9917 99.17%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 91.87% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.01% 96.09%
CHEMBL1994 P08235 Mineralocorticoid receptor 87.09% 100.00%
CHEMBL2581 P07339 Cathepsin D 85.98% 98.95%
CHEMBL1871 P10275 Androgen Receptor 85.76% 96.43%
CHEMBL241 Q14432 Phosphodiesterase 3A 84.16% 92.94%
CHEMBL5608 Q16288 NT-3 growth factor receptor 83.34% 95.89%
CHEMBL221 P23219 Cyclooxygenase-1 82.52% 90.17%
CHEMBL253 P34972 Cannabinoid CB2 receptor 82.42% 97.25%
CHEMBL3975 P09467 Fructose-1,6-bisphosphatase 81.93% 92.95%
CHEMBL3137262 O60341 LSD1/CoREST complex 80.29% 97.09%

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.
Ligularia cyathiceps

Cross-Links

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PubChem 163049933
LOTUS LTS0213965
wikiData Q104998427