2-Benzyloxyaniline

Details

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Internal ID faaa812f-1af8-4189-9a6a-820a86ebdd55
Taxonomy Benzenoids > Phenol ethers > Aminophenyl ethers
IUPAC Name 2-phenylmethoxyaniline
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C13H13NO/c14-12-8-4-5-9-13(12)15-10-11-6-2-1-3-7-11/h1-9H,10,14H2
InChI Key PLPVLSBYYOWFKM-UHFFFAOYSA-N
Popularity 10 references in papers

Physical and Chemical Properties

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Molecular Formula C13H13NO
Molecular Weight 199.25 g/mol
Exact Mass 199.099714038 g/mol
Topological Polar Surface Area (TPSA) 35.30 Ų
XlogP 2.70
Atomic LogP (AlogP) 2.85
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

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20012-63-9
DTXSID10286656
RefChem:85589
DTXCID50237804
628-010-6
PLPVLSBYYOWFKM-UHFFFAOYSA-N
2-(benzyloxy)aniline
2-phenylmethoxyaniline
Benzenamine, 2-(phenylmethoxy)-
MFCD03093873
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-Benzyloxyaniline

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 + 0.9034 90.34%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability + 0.6286 62.86%
Subcellular localzation Mitochondria 0.4960 49.60%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9694 96.94%
OATP1B3 inhibitior + 0.9514 95.14%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior - 0.7520 75.20%
P-glycoprotein inhibitior - 0.9764 97.64%
P-glycoprotein substrate - 0.8752 87.52%
CYP3A4 substrate - 0.6954 69.54%
CYP2C9 substrate - 0.7983 79.83%
CYP2D6 substrate + 0.5553 55.53%
CYP3A4 inhibition - 0.7528 75.28%
CYP2C9 inhibition + 0.6660 66.60%
CYP2C19 inhibition + 0.8847 88.47%
CYP2D6 inhibition - 0.6743 67.43%
CYP1A2 inhibition + 0.9541 95.41%
CYP2C8 inhibition + 0.5365 53.65%
CYP inhibitory promiscuity + 0.9437 94.37%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7108 71.08%
Carcinogenicity (trinary) Non-required 0.4997 49.97%
Eye corrosion - 0.9755 97.55%
Eye irritation + 0.9462 94.62%
Skin irritation - 0.8651 86.51%
Skin corrosion - 0.9405 94.05%
Ames mutagenesis + 0.5400 54.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4864 48.64%
Micronuclear + 0.6000 60.00%
Hepatotoxicity + 0.5931 59.31%
skin sensitisation - 0.7541 75.41%
Respiratory toxicity - 0.7444 74.44%
Reproductive toxicity - 0.5111 51.11%
Mitochondrial toxicity - 0.6500 65.00%
Nephrotoxicity + 0.6142 61.42%
Acute Oral Toxicity (c) III 0.9182 91.82%
Estrogen receptor binding + 0.7145 71.45%
Androgen receptor binding + 0.6734 67.34%
Thyroid receptor binding - 0.5902 59.02%
Glucocorticoid receptor binding - 0.7272 72.72%
Aromatase binding + 0.8733 87.33%
PPAR gamma + 0.6780 67.80%
Honey bee toxicity - 0.7840 78.40%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity + 0.5500 55.00%
Fish aquatic toxicity + 0.9103 91.03%

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
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 92.66% 94.62%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.98% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 90.27% 99.17%
CHEMBL221 P23219 Cyclooxygenase-1 88.71% 90.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.73% 86.33%
CHEMBL2319 P06870 Kallikrein 1 86.91% 90.95%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 86.81% 95.50%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.49% 95.56%
CHEMBL3891 P07384 Calpain 1 85.32% 93.04%
CHEMBL1287628 Q9Y5S8 NADPH oxidase 1 80.98% 95.48%
CHEMBL2581 P07339 Cathepsin D 80.00% 98.95%

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.
Atractylodes lancea

Cross-Links

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PubChem 240548
NPASS NPC292300