H-Trp-phe-OH

Details

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Internal ID 4405d872-1c31-43b8-9c62-616cb51d4450
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Amino acids, peptides, and analogues > Peptides > Dipeptides
IUPAC Name (2S)-2-[[(2S)-2-amino-3-(1H-indol-3-yl)propanoyl]amino]-3-phenylpropanoic acid
SMILES (Canonical) C1=CC=C(C=C1)CC(C(=O)O)NC(=O)C(CC2=CNC3=CC=CC=C32)N
SMILES (Isomeric) C1=CC=C(C=C1)C[C@@H](C(=O)O)NC(=O)[C@H](CC2=CNC3=CC=CC=C32)N
InChI InChI=1S/C20H21N3O3/c21-16(11-14-12-22-17-9-5-4-8-15(14)17)19(24)23-18(20(25)26)10-13-6-2-1-3-7-13/h1-9,12,16,18,22H,10-11,21H2,(H,23,24)(H,25,26)/t16-,18-/m0/s1
InChI Key IMMPMHKLUUZKAZ-WMZOPIPTSA-N
Popularity 15 references in papers

Physical and Chemical Properties

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Molecular Formula C20H21N3O3
Molecular Weight 351.40 g/mol
Exact Mass 351.15829154 g/mol
Topological Polar Surface Area (TPSA) 108.00 Ų
XlogP -0.80
Atomic LogP (AlogP) 1.85
H-Bond Acceptor 3
H-Bond Donor 4
Rotatable Bonds 7

Synonyms

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6686-02-8
Trp-Phe
(S)-2-((S)-2-Amino-3-(1H-indol-3-yl)propanamido)-3-phenylpropanoic acid
L-tryptophyl-L-phenylalanine
CHEBI:74874
(2S)-2-[[(2S)-2-amino-3-(1H-indol-3-yl)propanoyl]amino]-3-phenylpropanoic acid
Tryptophyl-Phenylalanine
Tryptophanyl-phenylalanine
L-Phenylalanine, L-tryptophyl-
L-Trp-L-Phe
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of H-Trp-phe-OH

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9723 97.23%
Caco-2 - 0.7925 79.25%
Blood Brain Barrier + 0.7000 70.00%
Human oral bioavailability + 0.6143 61.43%
Subcellular localzation Mitochondria 0.5186 51.86%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9418 94.18%
OATP1B3 inhibitior + 0.9489 94.89%
MATE1 inhibitior - 0.9609 96.09%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior + 0.8500 85.00%
P-glycoprotein inhibitior - 0.7777 77.77%
P-glycoprotein substrate - 0.7119 71.19%
CYP3A4 substrate + 0.5244 52.44%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7507 75.07%
CYP3A4 inhibition - 0.8868 88.68%
CYP2C9 inhibition - 0.8902 89.02%
CYP2C19 inhibition - 0.9214 92.14%
CYP2D6 inhibition - 0.8332 83.32%
CYP1A2 inhibition - 0.8685 86.85%
CYP2C8 inhibition - 0.7788 77.88%
CYP inhibitory promiscuity - 0.8737 87.37%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8200 82.00%
Carcinogenicity (trinary) Non-required 0.6766 67.66%
Eye corrosion - 0.9954 99.54%
Eye irritation - 0.9958 99.58%
Skin irritation - 0.8506 85.06%
Skin corrosion - 0.9691 96.91%
Ames mutagenesis - 0.8200 82.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7283 72.83%
Micronuclear + 0.8100 81.00%
Hepatotoxicity - 0.6518 65.18%
skin sensitisation - 0.9209 92.09%
Respiratory toxicity + 0.8111 81.11%
Reproductive toxicity + 0.9111 91.11%
Mitochondrial toxicity + 0.7500 75.00%
Nephrotoxicity - 0.8775 87.75%
Acute Oral Toxicity (c) III 0.5081 50.81%
Estrogen receptor binding + 0.6028 60.28%
Androgen receptor binding - 0.5000 50.00%
Thyroid receptor binding - 0.6698 66.98%
Glucocorticoid receptor binding + 0.7003 70.03%
Aromatase binding + 0.6012 60.12%
PPAR gamma - 0.5614 56.14%
Honey bee toxicity - 0.8941 89.41%
Biodegradation - 0.9250 92.50%
Crustacea aquatic toxicity - 0.7949 79.49%
Fish aquatic toxicity - 0.4185 41.85%

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
CHEMBL1255126 O15151 Protein Mdm4 98.73% 90.20%
CHEMBL2581 P07339 Cathepsin D 98.06% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.60% 91.11%
CHEMBL221 P23219 Cyclooxygenase-1 94.66% 90.17%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.70% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.75% 96.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 90.90% 94.45%
CHEMBL3830 Q2M2I8 Adaptor-associated kinase 89.30% 83.10%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 88.10% 95.50%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 87.88% 94.62%
CHEMBL1795139 Q8IU80 Transmembrane protease serine 6 87.57% 98.33%
CHEMBL3976 Q9UHL4 Dipeptidyl peptidase II 87.26% 92.29%
CHEMBL2535 P11166 Glucose transporter 86.57% 98.75%
CHEMBL3060 Q9Y345 Glycine transporter 2 86.32% 99.17%
CHEMBL4101 P17612 cAMP-dependent protein kinase alpha-catalytic subunit 85.95% 82.86%
CHEMBL2693 Q9UIQ6 Cystinyl aminopeptidase 85.75% 97.64%
CHEMBL1808 P12821 Angiotensin-converting enzyme 85.71% 93.39%
CHEMBL4816 Q9Y243 Serine/threonine-protein kinase AKT3 85.39% 96.28%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 84.36% 97.21%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 84.21% 96.95%
CHEMBL1287628 Q9Y5S8 NADPH oxidase 1 84.11% 95.48%
CHEMBL216 P11229 Muscarinic acetylcholine receptor M1 82.35% 94.23%
CHEMBL2431 P31751 Serine/threonine-protein kinase AKT2 82.08% 98.33%
CHEMBL3310 Q96DB2 Histone deacetylase 11 81.78% 88.56%
CHEMBL2327 P21452 Neurokinin 2 receptor 81.14% 98.89%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 80.05% 100.00%

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.
Arabidopsis thaliana

Cross-Links

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PubChem 6426942
LOTUS LTS0009610
wikiData Q27144985