3-(2-Hydroxypropan-2-yl)-5,8-dimethylnaphthalen-2-ol

Details

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Internal ID 31fabaf1-3cc6-4ca8-944c-8f1d24b4b4f5
Taxonomy Benzenoids > Naphthalenes > Naphthols and derivatives
IUPAC Name 3-(2-hydroxypropan-2-yl)-5,8-dimethylnaphthalen-2-ol
SMILES (Canonical) CC1=C2C=C(C(=CC2=C(C=C1)C)O)C(C)(C)O
SMILES (Isomeric) CC1=C2C=C(C(=CC2=C(C=C1)C)O)C(C)(C)O
InChI InChI=1S/C15H18O2/c1-9-5-6-10(2)12-8-14(16)13(7-11(9)12)15(3,4)17/h5-8,16-17H,1-4H3
InChI Key YKSYPXGCQRATJS-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H18O2
Molecular Weight 230.30 g/mol
Exact Mass 230.130679813 g/mol
Topological Polar Surface Area (TPSA) 40.50 Ų
XlogP 3.80
Atomic LogP (AlogP) 3.39
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 3-(2-Hydroxypropan-2-yl)-5,8-dimethylnaphthalen-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 + 0.9952 99.52%
Caco-2 + 0.8598 85.98%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability + 0.5857 58.57%
Subcellular localzation Mitochondria 0.6863 68.63%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9636 96.36%
OATP1B3 inhibitior + 0.9275 92.75%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.5000 50.00%
P-glycoprotein inhibitior - 0.9387 93.87%
P-glycoprotein substrate - 0.9321 93.21%
CYP3A4 substrate - 0.6410 64.10%
CYP2C9 substrate - 0.7698 76.98%
CYP2D6 substrate + 0.3486 34.86%
CYP3A4 inhibition - 0.9064 90.64%
CYP2C9 inhibition + 0.6294 62.94%
CYP2C19 inhibition + 0.5874 58.74%
CYP2D6 inhibition - 0.8341 83.41%
CYP1A2 inhibition + 0.9458 94.58%
CYP2C8 inhibition - 0.7521 75.21%
CYP inhibitory promiscuity + 0.6893 68.93%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.8111 81.11%
Carcinogenicity (trinary) Non-required 0.6493 64.93%
Eye corrosion - 0.9646 96.46%
Eye irritation + 0.9584 95.84%
Skin irritation - 0.6818 68.18%
Skin corrosion - 0.7631 76.31%
Ames mutagenesis - 0.5900 59.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5515 55.15%
Micronuclear - 0.6241 62.41%
Hepatotoxicity + 0.6375 63.75%
skin sensitisation + 0.5738 57.38%
Respiratory toxicity - 0.7556 75.56%
Reproductive toxicity - 0.7444 74.44%
Mitochondrial toxicity - 0.6375 63.75%
Nephrotoxicity - 0.7666 76.66%
Acute Oral Toxicity (c) III 0.7455 74.55%
Estrogen receptor binding + 0.8821 88.21%
Androgen receptor binding - 0.6521 65.21%
Thyroid receptor binding + 0.7199 71.99%
Glucocorticoid receptor binding + 0.7972 79.72%
Aromatase binding + 0.6032 60.32%
PPAR gamma + 0.6905 69.05%
Honey bee toxicity - 0.9761 97.61%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity + 0.6800 68.00%
Fish aquatic toxicity + 0.9712 97.12%

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 96.70% 91.11%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 93.17% 93.65%
CHEMBL3401 O75469 Pregnane X receptor 90.90% 94.73%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.30% 95.56%
CHEMBL5966 P55899 IgG receptor FcRn large subunit p51 88.98% 90.93%
CHEMBL1951 P21397 Monoamine oxidase A 88.17% 91.49%
CHEMBL2581 P07339 Cathepsin D 88.16% 98.95%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 84.48% 89.62%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 83.53% 99.15%
CHEMBL1293249 Q13887 Kruppel-like factor 5 82.54% 86.33%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 80.75% 100.00%

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.
Ajuga reptans
Emmotum nitens

Cross-Links

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PubChem 90474100
LOTUS LTS0114449
wikiData Q105021310