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

Details

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Internal ID 40d3b5a2-809c-4aef-89d2-b0f7c9ee0531
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids > Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
IUPAC Name (2R,4aR,6S,8aS)-6-(3-hydroxyprop-1-en-2-yl)-4,8a-dimethyl-2,4a,5,6,7,8-hexahydro-1H-naphthalen-2-ol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H24O2/c1-10-6-13(17)8-15(3)5-4-12(7-14(10)15)11(2)9-16/h6,12-14,16-17H,2,4-5,7-9H2,1,3H3/t12-,13-,14-,15-/m0/s1
InChI Key JPHVROHPIMQMJI-AJNGGQMLSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C15H24O2
Molecular Weight 236.35 g/mol
Exact Mass 236.177630004 g/mol
Topological Polar Surface Area (TPSA) 40.50 Ų
XlogP 2.70
Atomic LogP (AlogP) 2.67
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (2R,4aR,6S,8aS)-6-(3-hydroxyprop-1-en-2-yl)-4,8a-dimethyl-2,4a,5,6,7,8-hexahydro-1H-naphthalen-2-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9936 99.36%
Caco-2 + 0.7385 73.85%
Blood Brain Barrier + 0.6750 67.50%
Human oral bioavailability + 0.5714 57.14%
Subcellular localzation Lysosomes 0.6312 63.12%
OATP2B1 inhibitior - 0.8519 85.19%
OATP1B1 inhibitior + 0.8926 89.26%
OATP1B3 inhibitior + 0.9649 96.49%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.5984 59.84%
BSEP inhibitior - 0.9209 92.09%
P-glycoprotein inhibitior - 0.9356 93.56%
P-glycoprotein substrate - 0.8319 83.19%
CYP3A4 substrate + 0.5809 58.09%
CYP2C9 substrate - 0.6284 62.84%
CYP2D6 substrate - 0.7222 72.22%
CYP3A4 inhibition - 0.5960 59.60%
CYP2C9 inhibition - 0.8576 85.76%
CYP2C19 inhibition - 0.7498 74.98%
CYP2D6 inhibition - 0.8805 88.05%
CYP1A2 inhibition - 0.7268 72.68%
CYP2C8 inhibition - 0.7582 75.82%
CYP inhibitory promiscuity - 0.7247 72.47%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.8800 88.00%
Carcinogenicity (trinary) Non-required 0.6482 64.82%
Eye corrosion - 0.9812 98.12%
Eye irritation - 0.8842 88.42%
Skin irritation - 0.6916 69.16%
Skin corrosion - 0.9662 96.62%
Ames mutagenesis - 0.8207 82.07%
Human Ether-a-go-go-Related Gene inhibition - 0.4364 43.64%
Micronuclear - 0.9600 96.00%
Hepatotoxicity - 0.6073 60.73%
skin sensitisation - 0.5313 53.13%
Respiratory toxicity - 0.5000 50.00%
Reproductive toxicity + 0.8222 82.22%
Mitochondrial toxicity + 0.7000 70.00%
Nephrotoxicity - 0.8048 80.48%
Acute Oral Toxicity (c) III 0.8687 86.87%
Estrogen receptor binding - 0.4902 49.02%
Androgen receptor binding - 0.6545 65.45%
Thyroid receptor binding - 0.5099 50.99%
Glucocorticoid receptor binding - 0.5056 50.56%
Aromatase binding - 0.5384 53.84%
PPAR gamma - 0.6861 68.61%
Honey bee toxicity - 0.9002 90.02%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity - 0.5000 50.00%
Fish aquatic toxicity + 0.9503 95.03%

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 95.49% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.89% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 93.50% 97.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.92% 91.11%
CHEMBL221 P23219 Cyclooxygenase-1 88.12% 90.17%
CHEMBL1994 P08235 Mineralocorticoid receptor 88.05% 100.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 84.05% 95.89%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 82.25% 94.45%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 82.04% 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.
There are no matching plants.

Cross-Links

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PubChem 163018768
LOTUS LTS0118952
wikiData Q105132766