2-Naphthaleneethanol, 1,2,3,4,4a,5,6,7-octahydro-4a,8-dimethyl-beta-methylene-, (2R,4aR)-

Details

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Internal ID 1f67c67d-1023-40f8-98d2-e1155dda4e70
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids > Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
IUPAC Name 2-[(2R,4aR)-4a,8-dimethyl-2,3,4,5,6,7-hexahydro-1H-naphthalen-2-yl]prop-2-en-1-ol
SMILES (Canonical) CC1=C2CC(CCC2(CCC1)C)C(=C)CO
SMILES (Isomeric) CC1=C2C[C@@H](CC[C@]2(CCC1)C)C(=C)CO
InChI InChI=1S/C15H24O/c1-11-5-4-7-15(3)8-6-13(9-14(11)15)12(2)10-16/h13,16H,2,4-10H2,1,3H3/t13-,15-/m1/s1
InChI Key ITRHZWKEZJYJQO-UKRRQHHQSA-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 3.70
Atomic LogP (AlogP) 3.84
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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.gamma.-Costol
(+)-.gamma.-Costol
ITRHZWKEZJYJQO-UKRRQHHQSA-N
2-((2R,4aR)-4a,8-Dimethyl-1,2,3,4,4a,5,6,7-octahydronaphthalen-2-yl)prop-2-en-1-ol
2-Naphthaleneethanol, 1,2,3,4,4a,5,6,7-octahydro-4a,8-dimethyl-.beta.-methylene-, (2R,4aR)-
2-Naphthaleneethanol, 1,2,3,4,4a,5,6,7-octahydro-4a,8-dimethyl-.beta.-methylene-, (2R-cis)-
65018-14-6

2D Structure

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2D Structure of 2-Naphthaleneethanol, 1,2,3,4,4a,5,6,7-octahydro-4a,8-dimethyl-beta-methylene-, (2R,4aR)-

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9890 98.90%
Caco-2 + 0.8730 87.30%
Blood Brain Barrier + 0.8500 85.00%
Human oral bioavailability + 0.5714 57.14%
Subcellular localzation Lysosomes 0.7547 75.47%
OATP2B1 inhibitior - 0.8501 85.01%
OATP1B1 inhibitior + 0.8506 85.06%
OATP1B3 inhibitior + 0.8875 88.75%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.5750 57.50%
BSEP inhibitior - 0.7598 75.98%
P-glycoprotein inhibitior - 0.9156 91.56%
P-glycoprotein substrate - 0.9150 91.50%
CYP3A4 substrate + 0.5541 55.41%
CYP2C9 substrate - 0.7664 76.64%
CYP2D6 substrate - 0.7388 73.88%
CYP3A4 inhibition - 0.7263 72.63%
CYP2C9 inhibition - 0.5668 56.68%
CYP2C19 inhibition - 0.5541 55.41%
CYP2D6 inhibition - 0.8708 87.08%
CYP1A2 inhibition - 0.7398 73.98%
CYP2C8 inhibition - 0.7377 73.77%
CYP inhibitory promiscuity - 0.6091 60.91%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.8900 89.00%
Carcinogenicity (trinary) Non-required 0.6324 63.24%
Eye corrosion - 0.9394 93.94%
Eye irritation + 0.6198 61.98%
Skin irritation - 0.7587 75.87%
Skin corrosion - 0.9674 96.74%
Ames mutagenesis - 0.7079 70.79%
Human Ether-a-go-go-Related Gene inhibition - 0.4638 46.38%
Micronuclear - 0.9400 94.00%
Hepatotoxicity - 0.6271 62.71%
skin sensitisation + 0.6465 64.65%
Respiratory toxicity + 0.5222 52.22%
Reproductive toxicity - 0.5111 51.11%
Mitochondrial toxicity + 0.5500 55.00%
Nephrotoxicity + 0.5862 58.62%
Acute Oral Toxicity (c) III 0.6960 69.60%
Estrogen receptor binding - 0.8555 85.55%
Androgen receptor binding - 0.5286 52.86%
Thyroid receptor binding - 0.5660 56.60%
Glucocorticoid receptor binding - 0.7124 71.24%
Aromatase binding - 0.6716 67.16%
PPAR gamma - 0.8046 80.46%
Honey bee toxicity - 0.9369 93.69%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity + 0.5300 53.00%
Fish aquatic toxicity + 0.9949 99.49%

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 93.88% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.69% 91.11%
CHEMBL253 P34972 Cannabinoid CB2 receptor 92.11% 97.25%
CHEMBL5608 Q16288 NT-3 growth factor receptor 89.54% 95.89%
CHEMBL3137262 O60341 LSD1/CoREST complex 87.25% 97.09%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 85.96% 95.50%
CHEMBL206 P03372 Estrogen receptor alpha 83.82% 97.64%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 83.63% 93.03%
CHEMBL1994 P08235 Mineralocorticoid receptor 83.04% 100.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 82.67% 95.56%
CHEMBL2581 P07339 Cathepsin D 82.08% 98.95%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 82.07% 86.00%
CHEMBL1937 Q92769 Histone deacetylase 2 82.04% 94.75%
CHEMBL4835 P00338 L-lactate dehydrogenase A chain 80.73% 95.34%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 80.00% 82.69%

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 capillaris
Aucklandia costus

Cross-Links

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PubChem 91730038
NPASS NPC291393
LOTUS LTS0158255
wikiData Q104403760