2-(8,8a-dimethyl-2,3,5,6,7,8-hexahydro-1H-naphthalen-2-yl)propan-2-ol

Details

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Internal ID 0ebe9708-86bb-4d38-9f14-26004c070a81
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids > Eremophilane, 8,9-secoeremophilane and furoeremophilane sesquiterpenoids
IUPAC Name 2-(8,8a-dimethyl-2,3,5,6,7,8-hexahydro-1H-naphthalen-2-yl)propan-2-ol
SMILES (Canonical) CC1CCCC2=CCC(CC12C)C(C)(C)O
SMILES (Isomeric) CC1CCCC2=CCC(CC12C)C(C)(C)O
InChI InChI=1S/C15H26O/c1-11-6-5-7-12-8-9-13(14(2,3)16)10-15(11,12)4/h8,11,13,16H,5-7,9-10H2,1-4H3
InChI Key KEBVXBNFLKYWDP-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H26O
Molecular Weight 222.37 g/mol
Exact Mass 222.198365449 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 3.70
Atomic LogP (AlogP) 3.92
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 2-(8,8a-dimethyl-2,3,5,6,7,8-hexahydro-1H-naphthalen-2-yl)propan-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 + 0.9972 99.72%
Caco-2 + 0.9139 91.39%
Blood Brain Barrier + 0.8250 82.50%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Mitochondria 0.4026 40.26%
OATP2B1 inhibitior - 0.8492 84.92%
OATP1B1 inhibitior + 0.9294 92.94%
OATP1B3 inhibitior + 0.8452 84.52%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior - 0.9185 91.85%
P-glycoprotein inhibitior - 0.9549 95.49%
P-glycoprotein substrate - 0.8693 86.93%
CYP3A4 substrate + 0.5243 52.43%
CYP2C9 substrate + 0.5024 50.24%
CYP2D6 substrate - 0.7533 75.33%
CYP3A4 inhibition - 0.8452 84.52%
CYP2C9 inhibition - 0.6266 62.66%
CYP2C19 inhibition - 0.6204 62.04%
CYP2D6 inhibition - 0.9309 93.09%
CYP1A2 inhibition - 0.8238 82.38%
CYP2C8 inhibition - 0.6449 64.49%
CYP inhibitory promiscuity - 0.6132 61.32%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.8100 81.00%
Carcinogenicity (trinary) Non-required 0.5891 58.91%
Eye corrosion - 0.9818 98.18%
Eye irritation - 0.5665 56.65%
Skin irritation - 0.5707 57.07%
Skin corrosion - 0.9690 96.90%
Ames mutagenesis - 0.8900 89.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5142 51.42%
Micronuclear - 0.9600 96.00%
Hepatotoxicity - 0.5540 55.40%
skin sensitisation + 0.7826 78.26%
Respiratory toxicity - 0.6333 63.33%
Reproductive toxicity + 0.5333 53.33%
Mitochondrial toxicity - 0.5125 51.25%
Nephrotoxicity - 0.7132 71.32%
Acute Oral Toxicity (c) III 0.5623 56.23%
Estrogen receptor binding - 0.8654 86.54%
Androgen receptor binding - 0.8383 83.83%
Thyroid receptor binding - 0.5168 51.68%
Glucocorticoid receptor binding - 0.6638 66.38%
Aromatase binding - 0.5647 56.47%
PPAR gamma - 0.8823 88.23%
Honey bee toxicity - 0.9406 94.06%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity + 0.5300 53.00%
Fish aquatic toxicity + 0.9963 99.63%

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 98.67% 97.25%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.91% 91.11%
CHEMBL2581 P07339 Cathepsin D 90.99% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.87% 96.09%
CHEMBL1994 P08235 Mineralocorticoid receptor 88.74% 100.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 87.65% 97.09%
CHEMBL1871 P10275 Androgen Receptor 86.56% 96.43%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.98% 95.56%
CHEMBL5608 Q16288 NT-3 growth factor receptor 81.87% 95.89%
CHEMBL3192 Q9BY41 Histone deacetylase 8 81.12% 93.99%
CHEMBL3359 P21462 Formyl peptide receptor 1 80.58% 93.56%

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.
Alpinia japonica

Cross-Links

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PubChem 14355276
LOTUS LTS0243235
wikiData Q105139869