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

Details

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Internal ID 89b8e912-f5da-4cf0-9bb2-5b42797c2b4b
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name 2-(8,8a-dimethyl-5,6,7,8-tetrahydro-1H-naphthalen-1-yl)propan-2-ol
SMILES (Canonical) CC1CCCC2=CC=CC(C12C)C(C)(C)O
SMILES (Isomeric) CC1CCCC2=CC=CC(C12C)C(C)(C)O
InChI InChI=1S/C15H24O/c1-11-7-5-8-12-9-6-10-13(14(2,3)16)15(11,12)4/h6,9-11,13,16H,5,7-8H2,1-4H3
InChI Key NAMGLFWPKVHQKV-UHFFFAOYSA-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) 3.70
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-5,6,7,8-tetrahydro-1H-naphthalen-1-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 + 0.9964 99.64%
Caco-2 + 0.8437 84.37%
Blood Brain Barrier + 0.8000 80.00%
Human oral bioavailability + 0.5571 55.71%
Subcellular localzation Lysosomes 0.5332 53.32%
OATP2B1 inhibitior - 0.8526 85.26%
OATP1B1 inhibitior + 0.8993 89.93%
OATP1B3 inhibitior + 0.8488 84.88%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior - 0.9683 96.83%
P-glycoprotein inhibitior - 0.9534 95.34%
P-glycoprotein substrate - 0.8842 88.42%
CYP3A4 substrate + 0.5302 53.02%
CYP2C9 substrate - 0.5886 58.86%
CYP2D6 substrate - 0.8006 80.06%
CYP3A4 inhibition - 0.9116 91.16%
CYP2C9 inhibition - 0.7455 74.55%
CYP2C19 inhibition - 0.6163 61.63%
CYP2D6 inhibition - 0.9098 90.98%
CYP1A2 inhibition - 0.7963 79.63%
CYP2C8 inhibition - 0.6120 61.20%
CYP inhibitory promiscuity - 0.5676 56.76%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.7700 77.00%
Carcinogenicity (trinary) Non-required 0.6016 60.16%
Eye corrosion - 0.9852 98.52%
Eye irritation - 0.8921 89.21%
Skin irritation + 0.5529 55.29%
Skin corrosion - 0.9523 95.23%
Ames mutagenesis - 0.7500 75.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5250 52.50%
Micronuclear - 0.9600 96.00%
Hepatotoxicity + 0.7678 76.78%
skin sensitisation + 0.7881 78.81%
Respiratory toxicity - 0.5667 56.67%
Reproductive toxicity + 0.5778 57.78%
Mitochondrial toxicity - 0.5750 57.50%
Nephrotoxicity - 0.8050 80.50%
Acute Oral Toxicity (c) III 0.7480 74.80%
Estrogen receptor binding - 0.7131 71.31%
Androgen receptor binding - 0.6475 64.75%
Thyroid receptor binding - 0.6165 61.65%
Glucocorticoid receptor binding - 0.7482 74.82%
Aromatase binding - 0.6460 64.60%
PPAR gamma - 0.6640 66.40%
Honey bee toxicity - 0.9304 93.04%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity + 0.5500 55.00%
Fish aquatic toxicity + 0.9877 98.77%

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 97.77% 97.25%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.85% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.45% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 91.34% 97.09%
CHEMBL2581 P07339 Cathepsin D 88.38% 98.95%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 87.82% 93.04%
CHEMBL241 Q14432 Phosphodiesterase 3A 86.81% 92.94%
CHEMBL1994 P08235 Mineralocorticoid receptor 85.37% 100.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.40% 86.33%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 81.26% 100.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 81.25% 95.56%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.60% 95.89%

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.
Reboulia hemisphaerica

Cross-Links

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PubChem 163034802
LOTUS LTS0044224
wikiData Q104172227