N-methoxy-1-phenylpropan-2-amine

Details

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Internal ID 95e2db59-c640-45c6-b51c-6ae60de6fbbc
Taxonomy Benzenoids > Benzene and substituted derivatives > Phenethylamines > Amphetamines and derivatives
IUPAC Name N-methoxy-1-phenylpropan-2-amine
SMILES (Canonical) CC(CC1=CC=CC=C1)NOC
SMILES (Isomeric) CC(CC1=CC=CC=C1)NOC
InChI InChI=1S/C10H15NO/c1-9(11-12-2)8-10-6-4-3-5-7-10/h3-7,9,11H,8H2,1-2H3
InChI Key REIPDEIPEOYEDO-UHFFFAOYSA-N
Popularity 48 references in papers

Physical and Chemical Properties

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Molecular Formula C10H15NO
Molecular Weight 165.23 g/mol
Exact Mass 165.115364102 g/mol
Topological Polar Surface Area (TPSA) 21.30 Ų
XlogP 2.10
Atomic LogP (AlogP) 1.77
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 4

Synonyms

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63-97-8
MFCD01708057
NIOSH/SH8109000
N-Methoxy-alpha-methylphenethylamine
N-Methoxy-N-(2-phenyl)isopropylamine
Phenethylamine, N-methoxy-alpha-methyl-
SH81090000
Hydroxylamine, O-methyl-N-(alpha-methylphenethyl)-
Methoxyamphetamine
NCIOpen2_006033
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of N-methoxy-1-phenylpropan-2-amine

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9930 99.30%
Caco-2 + 0.9135 91.35%
Blood Brain Barrier + 0.9000 90.00%
Human oral bioavailability + 0.8143 81.43%
Subcellular localzation Lysosomes 0.7022 70.22%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9496 94.96%
OATP1B3 inhibitior + 0.9466 94.66%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior - 0.9246 92.46%
P-glycoprotein inhibitior - 0.9823 98.23%
P-glycoprotein substrate - 0.7947 79.47%
CYP3A4 substrate - 0.6947 69.47%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate + 0.3742 37.42%
CYP3A4 inhibition - 0.9184 91.84%
CYP2C9 inhibition - 0.8502 85.02%
CYP2C19 inhibition - 0.7273 72.73%
CYP2D6 inhibition - 0.6178 61.78%
CYP1A2 inhibition - 0.5157 51.57%
CYP2C8 inhibition - 0.9210 92.10%
CYP inhibitory promiscuity - 0.8148 81.48%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.5389 53.89%
Carcinogenicity (trinary) Non-required 0.4600 46.00%
Eye corrosion - 0.9594 95.94%
Eye irritation - 0.9072 90.72%
Skin irritation - 0.5797 57.97%
Skin corrosion - 0.7149 71.49%
Ames mutagenesis - 0.8900 89.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6533 65.33%
Micronuclear + 0.6985 69.85%
Hepatotoxicity - 0.5312 53.12%
skin sensitisation - 0.6955 69.55%
Respiratory toxicity + 0.7889 78.89%
Reproductive toxicity - 0.5889 58.89%
Mitochondrial toxicity + 0.6500 65.00%
Nephrotoxicity - 0.6188 61.88%
Acute Oral Toxicity (c) III 0.6141 61.41%
Estrogen receptor binding - 0.9407 94.07%
Androgen receptor binding - 0.8191 81.91%
Thyroid receptor binding - 0.8855 88.55%
Glucocorticoid receptor binding - 0.8820 88.20%
Aromatase binding - 0.8542 85.42%
PPAR gamma - 0.9374 93.74%
Honey bee toxicity - 0.9190 91.90%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity + 0.6400 64.00%
Fish aquatic toxicity - 0.4440 44.40%

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
CHEMBL221 P23219 Cyclooxygenase-1 96.99% 90.17%
CHEMBL2581 P07339 Cathepsin D 96.85% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.08% 96.09%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 92.06% 95.50%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.94% 95.56%
CHEMBL3401 O75469 Pregnane X receptor 84.98% 94.73%
CHEMBL3492 P49721 Proteasome Macropain subunit 81.41% 90.24%
CHEMBL1255126 O15151 Protein Mdm4 80.27% 90.20%

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.
Thymus quinquecostatus

Cross-Links

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PubChem 199112
LOTUS LTS0229017
wikiData Q105234892