Methyl hydrogen 3-phenyl-2,2'-iminodipropionate

Details

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Internal ID a5d254c1-4e1f-4aa5-ab04-853210b0256c
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Amino acids, peptides, and analogues > Alpha amino acids and derivatives > Phenylalanine and derivatives
IUPAC Name 2-[(1-methoxy-1-oxo-3-phenylpropan-2-yl)amino]propanoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C13H17NO4/c1-9(12(15)16)14-11(13(17)18-2)8-10-6-4-3-5-7-10/h3-7,9,11,14H,8H2,1-2H3,(H,15,16)
InChI Key RZMXVCJQDSLRSR-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C13H17NO4
Molecular Weight 251.28 g/mol
Exact Mass 251.11575802 g/mol
Topological Polar Surface Area (TPSA) 75.60 Ų
XlogP -0.60
Atomic LogP (AlogP) 0.83
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 6

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Methyl hydrogen 3-phenyl-2,2'-iminodipropionate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9222 92.22%
Caco-2 + 0.5322 53.22%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability + 0.6143 61.43%
Subcellular localzation Mitochondria 0.6267 62.67%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9358 93.58%
OATP1B3 inhibitior + 0.9453 94.53%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.7122 71.22%
P-glycoprotein inhibitior - 0.9620 96.20%
P-glycoprotein substrate - 0.8696 86.96%
CYP3A4 substrate - 0.5827 58.27%
CYP2C9 substrate + 0.5963 59.63%
CYP2D6 substrate - 0.7619 76.19%
CYP3A4 inhibition - 0.9662 96.62%
CYP2C9 inhibition - 0.9231 92.31%
CYP2C19 inhibition - 0.9648 96.48%
CYP2D6 inhibition - 0.9013 90.13%
CYP1A2 inhibition - 0.8824 88.24%
CYP2C8 inhibition - 0.9392 93.92%
CYP inhibitory promiscuity - 0.9819 98.19%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7141 71.41%
Carcinogenicity (trinary) Non-required 0.7536 75.36%
Eye corrosion - 0.9958 99.58%
Eye irritation - 0.9931 99.31%
Skin irritation - 0.8712 87.12%
Skin corrosion - 0.9481 94.81%
Ames mutagenesis - 0.6900 69.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5726 57.26%
Micronuclear + 0.6000 60.00%
Hepatotoxicity + 0.6552 65.52%
skin sensitisation - 0.9275 92.75%
Respiratory toxicity + 0.6000 60.00%
Reproductive toxicity - 0.5111 51.11%
Mitochondrial toxicity - 0.5375 53.75%
Nephrotoxicity - 0.7150 71.50%
Acute Oral Toxicity (c) III 0.7365 73.65%
Estrogen receptor binding - 0.8159 81.59%
Androgen receptor binding - 0.6125 61.25%
Thyroid receptor binding - 0.8665 86.65%
Glucocorticoid receptor binding - 0.7700 77.00%
Aromatase binding + 0.5304 53.04%
PPAR gamma - 0.7265 72.65%
Honey bee toxicity - 0.9114 91.14%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.7000 70.00%
Fish aquatic toxicity + 0.6644 66.44%

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 99.25% 90.17%
CHEMBL2581 P07339 Cathepsin D 97.84% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.64% 96.09%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 90.24% 100.00%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 89.02% 95.50%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.98% 95.56%
CHEMBL1255126 O15151 Protein Mdm4 87.48% 90.20%
CHEMBL3060 Q9Y345 Glycine transporter 2 86.60% 99.17%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 81.76% 94.45%
CHEMBL5028 O14672 ADAM10 81.59% 97.50%

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 13320406
LOTUS LTS0151358
wikiData Q105248458