Phe-Asp

Details

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Internal ID 295d5ad7-b8c5-4d53-bddc-650e5bee1288
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Amino acids, peptides, and analogues > Peptides > Dipeptides
IUPAC Name (2S)-2-[[(2S)-2-amino-3-phenylpropanoyl]amino]butanedioic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C13H16N2O5/c14-9(6-8-4-2-1-3-5-8)12(18)15-10(13(19)20)7-11(16)17/h1-5,9-10H,6-7,14H2,(H,15,18)(H,16,17)(H,19,20)/t9-,10-/m0/s1
InChI Key HWMGTNOVUDIKRE-UWVGGRQHSA-N
Popularity 8 references in papers

Physical and Chemical Properties

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Molecular Formula C13H16N2O5
Molecular Weight 280.28 g/mol
Exact Mass 280.10592162 g/mol
Topological Polar Surface Area (TPSA) 130.00 Ų
XlogP -3.50
Atomic LogP (AlogP) -0.40
H-Bond Acceptor 4
H-Bond Donor 4
Rotatable Bonds 7

Synonyms

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Phe-Asp
22828-05-3
phenylalanylaspartic acid
Phenylalanyl-aspartic acid
L-phenylalanyl-L-aspartic acid
CHEBI:73631
(S)-2-((S)-2-Amino-3-phenylPropanamido)succinic acid
FD dipeptide
F-D Dipeptide
Phenylalanylaspartate
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Phe-Asp

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.6301 63.01%
Caco-2 - 0.7780 77.80%
Blood Brain Barrier + 0.6750 67.50%
Human oral bioavailability + 0.5571 55.71%
Subcellular localzation Mitochondria 0.6238 62.38%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9512 95.12%
OATP1B3 inhibitior + 0.9488 94.88%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.9388 93.88%
P-glycoprotein inhibitior - 0.9737 97.37%
P-glycoprotein substrate - 0.8729 87.29%
CYP3A4 substrate - 0.6381 63.81%
CYP2C9 substrate - 0.6276 62.76%
CYP2D6 substrate - 0.7609 76.09%
CYP3A4 inhibition - 0.9532 95.32%
CYP2C9 inhibition - 0.9715 97.15%
CYP2C19 inhibition - 0.9763 97.63%
CYP2D6 inhibition - 0.9458 94.58%
CYP1A2 inhibition - 0.9670 96.70%
CYP2C8 inhibition - 0.9223 92.23%
CYP inhibitory promiscuity - 0.9922 99.22%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7911 79.11%
Carcinogenicity (trinary) Non-required 0.7609 76.09%
Eye corrosion - 0.9961 99.61%
Eye irritation - 0.9949 99.49%
Skin irritation - 0.8471 84.71%
Skin corrosion - 0.9842 98.42%
Ames mutagenesis - 0.7600 76.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7031 70.31%
Micronuclear + 0.7300 73.00%
Hepatotoxicity - 0.5766 57.66%
skin sensitisation - 0.9182 91.82%
Respiratory toxicity + 0.6667 66.67%
Reproductive toxicity + 0.6667 66.67%
Mitochondrial toxicity + 0.5875 58.75%
Nephrotoxicity - 0.6586 65.86%
Acute Oral Toxicity (c) IV 0.5526 55.26%
Estrogen receptor binding - 0.6080 60.80%
Androgen receptor binding - 0.6327 63.27%
Thyroid receptor binding - 0.8312 83.12%
Glucocorticoid receptor binding + 0.7093 70.93%
Aromatase binding - 0.5428 54.28%
PPAR gamma - 0.7653 76.53%
Honey bee toxicity - 0.9287 92.87%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.7400 74.00%
Fish aquatic toxicity - 0.6980 69.80%

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
CHEMBL2581 P07339 Cathepsin D 98.74% 98.95%
CHEMBL221 P23219 Cyclooxygenase-1 98.45% 90.17%
CHEMBL1255126 O15151 Protein Mdm4 97.45% 90.20%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.25% 96.09%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 90.31% 95.50%
CHEMBL3060 Q9Y345 Glycine transporter 2 89.97% 99.17%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 89.13% 97.21%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 89.09% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.36% 95.56%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 85.09% 100.00%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 84.99% 94.62%
CHEMBL1795139 Q8IU80 Transmembrane protease serine 6 84.67% 98.33%
CHEMBL3359 P21462 Formyl peptide receptor 1 82.67% 93.56%
CHEMBL3776 Q14790 Caspase-8 82.20% 97.06%
CHEMBL2327 P21452 Neurokinin 2 receptor 82.16% 98.89%
CHEMBL3976 Q9UHL4 Dipeptidyl peptidase II 80.90% 92.29%
CHEMBL216 P11229 Muscarinic acetylcholine receptor M1 80.61% 94.23%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 80.20% 96.95%
CHEMBL3308 P55212 Caspase-6 80.07% 97.56%

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 6992643
LOTUS LTS0015365
wikiData Q27142130