(2-(Methylamino)phenyl)methanol

Details

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Internal ID f794314f-a8ac-4fc8-b872-1158e27cda29
Taxonomy Benzenoids > Benzene and substituted derivatives > Benzyl alcohols
IUPAC Name [2-(methylamino)phenyl]methanol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C8H11NO/c1-9-8-5-3-2-4-7(8)6-10/h2-5,9-10H,6H2,1H3
InChI Key ZWIBBLPQTVLYKW-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C8H11NO
Molecular Weight 137.18 g/mol
Exact Mass 137.084063974 g/mol
Topological Polar Surface Area (TPSA) 32.30 Ų
XlogP 1.50
Atomic LogP (AlogP) 1.22
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 2

Synonyms

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29055-08-1
Benzenemethanol, 2-(methylamino)-
[2-(Methylamino)phenyl]methanol
(2-METHYLAMINO-PHENYL)-METHANOL
Benzyl alcohol, o-(methylamino)-
2-(Methylamino)benzenemethanol
o-(Methylamino)benzyl alcohol
NSC-165606
NSC165606
38SPE8SY6A
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-(Methylamino)phenyl)methanol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9278 92.78%
Caco-2 + 0.9588 95.88%
Blood Brain Barrier + 0.7000 70.00%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Mitochondria 0.4579 45.79%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9216 92.16%
OATP1B3 inhibitior + 0.9425 94.25%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.9275 92.75%
P-glycoprotein inhibitior - 0.9916 99.16%
P-glycoprotein substrate - 0.9175 91.75%
CYP3A4 substrate - 0.7093 70.93%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate + 0.4470 44.70%
CYP3A4 inhibition - 0.9804 98.04%
CYP2C9 inhibition - 0.7295 72.95%
CYP2C19 inhibition - 0.8377 83.77%
CYP2D6 inhibition - 0.9012 90.12%
CYP1A2 inhibition + 0.6590 65.90%
CYP2C8 inhibition - 0.9429 94.29%
CYP inhibitory promiscuity - 0.8244 82.44%
UGT catelyzed - 0.7000 70.00%
Carcinogenicity (binary) - 0.7310 73.10%
Carcinogenicity (trinary) Non-required 0.7290 72.90%
Eye corrosion - 0.8808 88.08%
Eye irritation + 0.9247 92.47%
Skin irritation - 0.7246 72.46%
Skin corrosion - 0.8683 86.83%
Ames mutagenesis + 0.5300 53.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7185 71.85%
Micronuclear - 0.5200 52.00%
Hepatotoxicity - 0.5351 53.51%
skin sensitisation + 0.5379 53.79%
Respiratory toxicity - 0.5556 55.56%
Reproductive toxicity - 0.5333 53.33%
Mitochondrial toxicity + 0.6625 66.25%
Nephrotoxicity + 0.5492 54.92%
Acute Oral Toxicity (c) III 0.8474 84.74%
Estrogen receptor binding - 0.8495 84.95%
Androgen receptor binding - 0.8537 85.37%
Thyroid receptor binding - 0.8075 80.75%
Glucocorticoid receptor binding - 0.8799 87.99%
Aromatase binding - 0.8020 80.20%
PPAR gamma - 0.7959 79.59%
Honey bee toxicity - 0.9501 95.01%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity - 0.5000 50.00%
Fish aquatic toxicity - 0.5270 52.70%

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 95.95% 91.11%
CHEMBL2581 P07339 Cathepsin D 91.66% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.72% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.03% 95.56%
CHEMBL3401 O75469 Pregnane X receptor 85.76% 94.73%

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 295953
LOTUS LTS0238550
wikiData Q82050286