2-Methyl-1-naphthol

Details

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Internal ID 8991022e-9424-4dd4-a54e-50e30c98baba
Taxonomy Benzenoids > Naphthalenes > Naphthols and derivatives
IUPAC Name 2-methylnaphthalen-1-ol
SMILES (Canonical) CC1=C(C2=CC=CC=C2C=C1)O
SMILES (Isomeric) CC1=C(C2=CC=CC=C2C=C1)O
InChI InChI=1S/C11H10O/c1-8-6-7-9-4-2-3-5-10(9)11(8)12/h2-7,12H,1H3
InChI Key SRJCJJKWVSSELL-UHFFFAOYSA-N
Popularity 92 references in papers

Physical and Chemical Properties

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Molecular Formula C11H10O
Molecular Weight 158.20 g/mol
Exact Mass 158.073164938 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 3.20
Atomic LogP (AlogP) 2.85
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 0

Synonyms

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7469-77-4
1-Naphthol, 2-methyl-
COU5JQ433I
NSC-402211
DTXSID50225665
RefChem:474903
DTXCID80148156
231-265-2
2-methylnaphthalen-1-ol
1-Naphthalenol, 2-methyl-
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-Methyl-1-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 + 0.8620 86.20%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability + 0.6286 62.86%
Subcellular localzation Mitochondria 0.6801 68.01%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9207 92.07%
OATP1B3 inhibitior + 0.9698 96.98%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.7458 74.58%
P-glycoprotein inhibitior - 0.9795 97.95%
P-glycoprotein substrate - 0.9704 97.04%
CYP3A4 substrate - 0.6196 61.96%
CYP2C9 substrate - 0.7905 79.05%
CYP2D6 substrate + 0.3652 36.52%
CYP3A4 inhibition - 0.9274 92.74%
CYP2C9 inhibition + 0.6282 62.82%
CYP2C19 inhibition + 0.5426 54.26%
CYP2D6 inhibition - 0.9142 91.42%
CYP1A2 inhibition + 0.9800 98.00%
CYP2C8 inhibition - 0.7112 71.12%
CYP inhibitory promiscuity + 0.5000 50.00%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.7429 74.29%
Carcinogenicity (trinary) Non-required 0.4646 46.46%
Eye corrosion - 0.9209 92.09%
Eye irritation + 0.9943 99.43%
Skin irritation + 0.7230 72.30%
Skin corrosion - 0.8486 84.86%
Ames mutagenesis + 0.6300 63.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7968 79.68%
Micronuclear - 0.6809 68.09%
Hepatotoxicity + 0.7750 77.50%
skin sensitisation + 0.8820 88.20%
Respiratory toxicity - 0.8444 84.44%
Reproductive toxicity - 0.6222 62.22%
Mitochondrial toxicity - 0.7125 71.25%
Nephrotoxicity - 0.7933 79.33%
Acute Oral Toxicity (c) III 0.5563 55.63%
Estrogen receptor binding - 0.5644 56.44%
Androgen receptor binding - 0.5144 51.44%
Thyroid receptor binding - 0.6233 62.33%
Glucocorticoid receptor binding - 0.7433 74.33%
Aromatase binding - 0.7319 73.19%
PPAR gamma - 0.5314 53.14%
Honey bee toxicity - 0.9850 98.50%
Biodegradation - 0.5750 57.50%
Crustacea aquatic toxicity + 0.6900 69.00%
Fish aquatic toxicity + 0.9703 97.03%

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 95.65% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.01% 95.56%
CHEMBL3401 O75469 Pregnane X receptor 87.93% 94.73%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 87.17% 93.65%
CHEMBL2885 P07451 Carbonic anhydrase III 81.67% 87.45%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 24055
NPASS NPC238696
ChEMBL CHEMBL122451