D-phenylalanine

Details

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Internal ID 20b39a68-af03-4670-9983-334e259bf9e7
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Amino acids, peptides, and analogues > Alpha amino acids and derivatives > Phenylalanine and derivatives
IUPAC Name (2R)-2-amino-3-phenylpropanoic acid
SMILES (Canonical) C1=CC=C(C=C1)CC(C(=O)O)N
SMILES (Isomeric) C1=CC=C(C=C1)C[C@H](C(=O)O)N
InChI InChI=1S/C9H11NO2/c10-8(9(11)12)6-7-4-2-1-3-5-7/h1-5,8H,6,10H2,(H,11,12)/t8-/m1/s1
InChI Key COLNVLDHVKWLRT-MRVPVSSYSA-N
Popularity 1,665 references in papers

Physical and Chemical Properties

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Molecular Formula C9H11NO2
Molecular Weight 165.19 g/mol
Exact Mass 165.078978594 g/mol
Topological Polar Surface Area (TPSA) 63.30 Ų
XlogP -1.50

Synonyms

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673-06-3
H-D-Phe-OH
(2R)-2-amino-3-phenylpropanoic acid
Phenylalanine D-form
Sabiden
D-Phe
(R)-2-AMINO-3-PHENYLPROPANOIC ACID
Alanine, phenyl-, D-
NCI-C60195
Phenylalanine,d-
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of D-phenylalanine

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
No predicted properties yet!

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 95.86% 98.95%
CHEMBL221 P23219 Cyclooxygenase-1 94.56% 90.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.15% 96.09%
CHEMBL1255126 O15151 Protein Mdm4 90.26% 90.20%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.61% 95.56%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 86.45% 95.50%
CHEMBL3060 Q9Y345 Glycine transporter 2 85.27% 99.17%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 85.18% 91.11%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 85.06% 94.62%
CHEMBL2327 P21452 Neurokinin 2 receptor 81.14% 98.89%

Cross-Links

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PubChem 71567
LOTUS LTS0048920
wikiData Q26841253