2-Amino-4-methoxyphenol

Details

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Internal ID e5482a98-c3b5-4c96-9cb3-8c2f28a1e316
Taxonomy Benzenoids > Phenols > Methoxyphenols
IUPAC Name 2-amino-4-methoxyphenol
SMILES (Canonical) COC1=CC(=C(C=C1)O)N
SMILES (Isomeric) COC1=CC(=C(C=C1)O)N
InChI InChI=1S/C7H9NO2/c1-10-5-2-3-7(9)6(8)4-5/h2-4,9H,8H2,1H3
InChI Key TUADYTFWZPZZTP-UHFFFAOYSA-N
Popularity 5 references in papers

Physical and Chemical Properties

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Molecular Formula C7H9NO2
Molecular Weight 139.15 g/mol
Exact Mass 139.063328530 g/mol
Topological Polar Surface Area (TPSA) 55.50 Ų
XlogP 1.20
Atomic LogP (AlogP) 0.98
H-Bond Acceptor 3
H-Bond Donor 2
Rotatable Bonds 1

Synonyms

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20734-76-3
2-Amino-4-methoxy-phenol
Phenol, 2-amino-4-methoxy-
4-methoxy-2-aminophenol
MFCD06616911
Asinex-Reag Bas 13015559
2-Hydroxy-5-methoxyaniline
2-azanyl-4-methoxy-phenol
2-amino-4-(methyloxy)phenol
SCHEMBL245052
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-Amino-4-methoxyphenol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9852 98.52%
Caco-2 + 0.8472 84.72%
Blood Brain Barrier - 0.6750 67.50%
Human oral bioavailability + 0.6429 64.29%
Subcellular localzation Mitochondria 0.6363 63.63%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9550 95.50%
OATP1B3 inhibitior + 0.9677 96.77%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.9429 94.29%
P-glycoprotein inhibitior - 0.9850 98.50%
P-glycoprotein substrate - 0.9554 95.54%
CYP3A4 substrate - 0.7134 71.34%
CYP2C9 substrate - 0.8019 80.19%
CYP2D6 substrate + 0.5261 52.61%
CYP3A4 inhibition - 0.8936 89.36%
CYP2C9 inhibition - 0.8178 81.78%
CYP2C19 inhibition - 0.8115 81.15%
CYP2D6 inhibition - 0.9549 95.49%
CYP1A2 inhibition - 0.7382 73.82%
CYP2C8 inhibition - 0.8620 86.20%
CYP inhibitory promiscuity - 0.7901 79.01%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.6900 69.00%
Carcinogenicity (trinary) Non-required 0.5424 54.24%
Eye corrosion - 0.9696 96.96%
Eye irritation + 0.9971 99.71%
Skin irritation - 0.8863 88.63%
Skin corrosion - 0.9397 93.97%
Ames mutagenesis + 0.7600 76.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7833 78.33%
Micronuclear - 0.5000 50.00%
Hepatotoxicity - 0.6810 68.10%
skin sensitisation + 0.4818 48.18%
Respiratory toxicity - 0.7889 78.89%
Reproductive toxicity + 0.6000 60.00%
Mitochondrial toxicity - 0.6625 66.25%
Nephrotoxicity - 0.5928 59.28%
Acute Oral Toxicity (c) III 0.8670 86.70%
Estrogen receptor binding - 0.7034 70.34%
Androgen receptor binding - 0.4826 48.26%
Thyroid receptor binding - 0.7904 79.04%
Glucocorticoid receptor binding - 0.7360 73.60%
Aromatase binding - 0.8783 87.83%
PPAR gamma - 0.7254 72.54%
Honey bee toxicity - 0.9458 94.58%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity + 0.6500 65.00%
Fish aquatic toxicity - 0.6197 61.97%

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 98.32% 91.11%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 94.46% 99.15%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.96% 96.09%
CHEMBL4208 P20618 Proteasome component C5 91.94% 90.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.04% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.26% 86.33%
CHEMBL3492 P49721 Proteasome Macropain subunit 84.45% 90.24%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 83.46% 94.00%
CHEMBL1907 P15144 Aminopeptidase N 81.11% 93.31%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 81.08% 94.45%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.07% 99.17%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.19% 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.
Lygodium japonicum

Cross-Links

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PubChem 1419108
NPASS NPC235041