1,4a-Dimethyl-7-propan-2-yl-2,3,4,5-tetrahydronaphthalen-1-ol

Details

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Internal ID f5e50d7a-9be5-4150-9f9b-b975202b1827
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name 1,4a-dimethyl-7-propan-2-yl-2,3,4,5-tetrahydronaphthalen-1-ol
SMILES (Canonical) CC(C)C1=CCC2(CCCC(C2=C1)(C)O)C
SMILES (Isomeric) CC(C)C1=CCC2(CCCC(C2=C1)(C)O)C
InChI InChI=1S/C15H24O/c1-11(2)12-6-9-14(3)7-5-8-15(4,16)13(14)10-12/h6,10-11,16H,5,7-9H2,1-4H3
InChI Key LGUGFZKFDQBVJK-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 3.10
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 1,4a-Dimethyl-7-propan-2-yl-2,3,4,5-tetrahydronaphthalen-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 + 1.0000 100.00%
Caco-2 + 0.7539 75.39%
Blood Brain Barrier + 0.5250 52.50%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Mitochondria 0.4916 49.16%
OATP2B1 inhibitior - 0.8505 85.05%
OATP1B1 inhibitior + 0.9408 94.08%
OATP1B3 inhibitior + 0.9707 97.07%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.6250 62.50%
BSEP inhibitior - 0.8770 87.70%
P-glycoprotein inhibitior - 0.9377 93.77%
P-glycoprotein substrate - 0.8297 82.97%
CYP3A4 substrate - 0.5493 54.93%
CYP2C9 substrate - 0.5751 57.51%
CYP2D6 substrate - 0.7890 78.90%
CYP3A4 inhibition - 0.8938 89.38%
CYP2C9 inhibition - 0.6800 68.00%
CYP2C19 inhibition - 0.5822 58.22%
CYP2D6 inhibition - 0.9281 92.81%
CYP1A2 inhibition - 0.8433 84.33%
CYP2C8 inhibition - 0.9148 91.48%
CYP inhibitory promiscuity - 0.8281 82.81%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9100 91.00%
Carcinogenicity (trinary) Non-required 0.5747 57.47%
Eye corrosion - 0.9803 98.03%
Eye irritation + 0.8733 87.33%
Skin irritation + 0.6295 62.95%
Skin corrosion - 0.9473 94.73%
Ames mutagenesis - 0.7000 70.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7169 71.69%
Micronuclear - 0.9800 98.00%
Hepatotoxicity - 0.5832 58.32%
skin sensitisation + 0.6615 66.15%
Respiratory toxicity + 0.5778 57.78%
Reproductive toxicity + 0.7444 74.44%
Mitochondrial toxicity + 0.7250 72.50%
Nephrotoxicity - 0.7559 75.59%
Acute Oral Toxicity (c) III 0.8227 82.27%
Estrogen receptor binding - 0.7528 75.28%
Androgen receptor binding - 0.6222 62.22%
Thyroid receptor binding + 0.6453 64.53%
Glucocorticoid receptor binding - 0.6962 69.62%
Aromatase binding - 0.7704 77.04%
PPAR gamma - 0.7341 73.41%
Honey bee toxicity - 0.9502 95.02%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.6400 64.00%
Fish aquatic toxicity + 0.9772 97.72%

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 96.15% 91.11%
CHEMBL253 P34972 Cannabinoid CB2 receptor 95.32% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.05% 96.09%
CHEMBL2581 P07339 Cathepsin D 89.36% 98.95%
CHEMBL1937 Q92769 Histone deacetylase 2 88.40% 94.75%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 87.22% 94.45%
CHEMBL221 P23219 Cyclooxygenase-1 83.80% 90.17%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 81.58% 85.30%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 81.02% 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.
Guarea guidonia

Cross-Links

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PubChem 527224
LOTUS LTS0037318
wikiData Q105151583