4-Amino-3-methoxyphenol

Details

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Internal ID c1caea5b-a85e-42d3-8285-847928a96790
Taxonomy Benzenoids > Phenols > Methoxyphenols
IUPAC Name 4-amino-3-methoxyphenol
SMILES (Canonical) COC1=C(C=CC(=C1)O)N
SMILES (Isomeric) COC1=C(C=CC(=C1)O)N
InChI InChI=1S/C7H9NO2/c1-10-7-4-5(9)2-3-6(7)8/h2-4,9H,8H2,1H3
InChI Key SXJQUUPSLJTKKT-UHFFFAOYSA-N
Popularity 1 reference 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 0.90
Atomic LogP (AlogP) 0.98
H-Bond Acceptor 3
H-Bond Donor 2
Rotatable Bonds 1

Synonyms

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61638-01-5
Phenol, 4-amino-3-methoxy-
MFCD00272194
SCHEMBL282092
DTXSID00600281
SXJQUUPSLJTKKT-UHFFFAOYSA-N
AKOS005263973
MB01122
AS-31544
SY006410
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 4-Amino-3-methoxyphenol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9923 99.23%
Caco-2 + 0.8359 83.59%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability + 0.5286 52.86%
Subcellular localzation Mitochondria 0.4778 47.78%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9187 91.87%
OATP1B3 inhibitior + 0.9724 97.24%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.9570 95.70%
P-glycoprotein inhibitior - 0.9790 97.90%
P-glycoprotein substrate - 0.7543 75.43%
CYP3A4 substrate - 0.6786 67.86%
CYP2C9 substrate - 0.8019 80.19%
CYP2D6 substrate + 0.5261 52.61%
CYP3A4 inhibition - 0.8602 86.02%
CYP2C9 inhibition - 0.8812 88.12%
CYP2C19 inhibition - 0.6471 64.71%
CYP2D6 inhibition - 0.9594 95.94%
CYP1A2 inhibition - 0.6659 66.59%
CYP2C8 inhibition - 0.6771 67.71%
CYP inhibitory promiscuity - 0.6666 66.66%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.6590 65.90%
Carcinogenicity (trinary) Non-required 0.6233 62.33%
Eye corrosion - 0.9548 95.48%
Eye irritation + 1.0000 100.00%
Skin irritation - 0.8619 86.19%
Skin corrosion - 0.9081 90.81%
Ames mutagenesis + 0.7200 72.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6672 66.72%
Micronuclear + 0.5100 51.00%
Hepatotoxicity - 0.6125 61.25%
skin sensitisation - 0.5920 59.20%
Respiratory toxicity - 0.8889 88.89%
Reproductive toxicity + 0.6556 65.56%
Mitochondrial toxicity - 0.6875 68.75%
Nephrotoxicity + 0.5513 55.13%
Acute Oral Toxicity (c) II 0.4869 48.69%
Estrogen receptor binding - 0.7503 75.03%
Androgen receptor binding - 0.7135 71.35%
Thyroid receptor binding - 0.7362 73.62%
Glucocorticoid receptor binding - 0.8952 89.52%
Aromatase binding - 0.8130 81.30%
PPAR gamma - 0.6650 66.50%
Honey bee toxicity - 0.9369 93.69%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity + 0.5451 54.51%
Fish aquatic toxicity - 0.6884 68.84%

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 95.92% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.89% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.43% 86.33%
CHEMBL4040 P28482 MAP kinase ERK2 91.02% 83.82%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 89.63% 94.45%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 86.40% 89.62%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.86% 95.56%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.23% 99.17%
CHEMBL2535 P11166 Glucose transporter 84.10% 98.75%
CHEMBL4208 P20618 Proteasome component C5 83.82% 90.00%
CHEMBL1255126 O15151 Protein Mdm4 83.24% 90.20%
CHEMBL5608 Q16288 NT-3 growth factor receptor 81.24% 95.89%
CHEMBL241 Q14432 Phosphodiesterase 3A 80.41% 92.94%

Cross-Links

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PubChem 19818056
NPASS NPC136633
LOTUS LTS0266152
wikiData Q72438792