2-Naphthol

Details

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Internal ID d06392d9-bff2-4592-872e-1a4e61fa2900
Taxonomy Benzenoids > Naphthalenes > Naphthols and derivatives
IUPAC Name naphthalen-2-ol
SMILES (Canonical) C1=CC=C2C=C(C=CC2=C1)O
SMILES (Isomeric) C1=CC=C2C=C(C=CC2=C1)O
InChI InChI=1S/C10H8O/c11-10-6-5-8-3-1-2-4-9(8)7-10/h1-7,11H
InChI Key JWAZRIHNYRIHIV-UHFFFAOYSA-N
Popularity 4,201 references in papers

Physical and Chemical Properties

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Molecular Formula C10H8O
Molecular Weight 144.17 g/mol
Exact Mass 144.057514874 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 2.70
Atomic LogP (AlogP) 2.55
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 0

Synonyms

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naphthalen-2-ol
135-19-3
beta-naphthol
2-Naphthalenol
Betanaphthol
2-Hydroxynaphthalene
Isonaphthol
Developer BN
Naphthol B
2-Naphtol
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 2-Naphthol

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 + 0.9608 96.08%
Blood Brain Barrier + 0.5500 55.00%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Mitochondria 0.4551 45.51%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8832 88.32%
OATP1B3 inhibitior + 0.9539 95.39%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.8656 86.56%
P-glycoprotein inhibitior - 0.9814 98.14%
P-glycoprotein substrate - 0.9897 98.97%
CYP3A4 substrate - 0.7544 75.44%
CYP2C9 substrate - 0.8333 83.33%
CYP2D6 substrate + 0.3949 39.49%
CYP3A4 inhibition - 0.9377 93.77%
CYP2C9 inhibition - 0.8050 80.50%
CYP2C19 inhibition - 0.6429 64.29%
CYP2D6 inhibition - 0.9245 92.45%
CYP1A2 inhibition + 0.9600 96.00%
CYP2C8 inhibition - 0.6705 67.05%
CYP inhibitory promiscuity - 0.6796 67.96%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.7071 70.71%
Carcinogenicity (trinary) Warning 0.4595 45.95%
Eye corrosion - 0.8863 88.63%
Eye irritation + 1.0000 100.00%
Skin irritation + 0.7297 72.97%
Skin corrosion - 0.9640 96.40%
Ames mutagenesis - 0.8000 80.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7722 77.22%
Micronuclear - 0.6909 69.09%
Hepatotoxicity + 0.7178 71.78%
skin sensitisation + 0.9333 93.33%
Respiratory toxicity - 0.7556 75.56%
Reproductive toxicity - 0.6444 64.44%
Mitochondrial toxicity - 0.7875 78.75%
Nephrotoxicity + 0.5164 51.64%
Acute Oral Toxicity (c) III 0.8093 80.93%
Estrogen receptor binding + 0.5666 56.66%
Androgen receptor binding + 0.8262 82.62%
Thyroid receptor binding - 0.6479 64.79%
Glucocorticoid receptor binding - 0.7496 74.96%
Aromatase binding - 0.7155 71.55%
PPAR gamma + 0.5462 54.62%
Honey bee toxicity - 0.9521 95.21%
Biodegradation + 0.7250 72.50%
Crustacea aquatic toxicity + 0.7000 70.00%
Fish aquatic toxicity + 0.9206 92.06%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
CHEMBL3356 P05177 Cytochrome P450 1A2 17000 nM
IC50
PMID: 15916432

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.97% 91.11%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 86.37% 99.15%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 85.14% 94.62%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.12% 95.56%
CHEMBL4208 P20618 Proteasome component C5 83.03% 90.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 82.57% 86.33%
CHEMBL4296013 Q5VWK5 Interleukin-23 receptor 82.06% 88.00%
CHEMBL2535 P11166 Glucose transporter 81.91% 98.75%
CHEMBL4531 P17931 Galectin-3 80.37% 96.90%

Plants that contains it

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Cross-Links

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PubChem 8663
NPASS NPC32674
ChEMBL CHEMBL14126