H-Tyr-Gln-Val-Pro-OH

Details

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Internal ID 3515bc9a-3bba-4171-a728-bc6e52a38570
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Amino acids, peptides, and analogues > Peptides
IUPAC Name (2S)-1-[(2S)-2-[[(2S)-5-amino-2-[[(2S)-2-amino-3-(4-hydroxyphenyl)propanoyl]amino]-5-oxopentanoyl]amino]-3-methylbutanoyl]pyrrolidine-2-carboxylic acid
SMILES (Canonical) CC(C)C(C(=O)N1CCCC1C(=O)O)NC(=O)C(CCC(=O)N)NC(=O)C(CC2=CC=C(C=C2)O)N
SMILES (Isomeric) CC(C)[C@@H](C(=O)N1CCC[C@H]1C(=O)O)NC(=O)[C@H](CCC(=O)N)NC(=O)[C@H](CC2=CC=C(C=C2)O)N
InChI InChI=1S/C24H35N5O7/c1-13(2)20(23(34)29-11-3-4-18(29)24(35)36)28-22(33)17(9-10-19(26)31)27-21(32)16(25)12-14-5-7-15(30)8-6-14/h5-8,13,16-18,20,30H,3-4,9-12,25H2,1-2H3,(H2,26,31)(H,27,32)(H,28,33)(H,35,36)/t16-,17-,18-,20-/m0/s1
InChI Key OXDRUVUDFAXCKB-JPLJXNOCSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C24H35N5O7
Molecular Weight 505.60 g/mol
Exact Mass 505.25364847 g/mol
Topological Polar Surface Area (TPSA) 205.00 Ų
XlogP -4.10

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of H-Tyr-Gln-Val-Pro-OH

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 99.66% 98.95%
CHEMBL2514 O95665 Neurotensin receptor 2 97.45% 100.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.11% 96.09%
CHEMBL1795139 Q8IU80 Transmembrane protease serine 6 96.21% 98.33%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 95.49% 94.45%
CHEMBL2107 P61073 C-X-C chemokine receptor type 4 95.12% 93.10%
CHEMBL4394 Q9NYA1 Sphingosine kinase 1 94.96% 96.03%
CHEMBL3359 P21462 Formyl peptide receptor 1 93.70% 93.56%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 93.61% 93.00%
CHEMBL340 P08684 Cytochrome P450 3A4 92.46% 91.19%
CHEMBL5608 Q16288 NT-3 growth factor receptor 92.19% 95.89%
CHEMBL249 P25103 Neurokinin 1 receptor 91.49% 99.17%
CHEMBL4979 P13866 Sodium/glucose cotransporter 1 91.44% 98.24%
CHEMBL3437 Q16853 Amine oxidase, copper containing 90.11% 94.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 89.60% 97.09%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 88.92% 90.71%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 88.82% 100.00%
CHEMBL233 P35372 Mu opioid receptor 88.46% 97.93%
CHEMBL3060 Q9Y345 Glycine transporter 2 88.09% 99.17%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 87.37% 95.89%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 87.07% 91.11%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 86.30% 82.69%
CHEMBL1808 P12821 Angiotensin-converting enzyme 86.26% 93.39%
CHEMBL4227 P25090 Lipoxin A4 receptor 86.23% 100.00%
CHEMBL3837 P07711 Cathepsin L 85.88% 96.61%
CHEMBL221 P23219 Cyclooxygenase-1 85.61% 90.17%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 85.60% 100.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.59% 95.56%
CHEMBL1907594 P30926 Neuronal acetylcholine receptor; alpha3/beta4 85.50% 97.23%
CHEMBL4777 P25929 Neuropeptide Y receptor type 1 85.10% 96.67%
CHEMBL5852 Q96P65 Pyroglutamylated RFamide peptide receptor 84.13% 85.00%
CHEMBL2693 Q9UIQ6 Cystinyl aminopeptidase 83.39% 97.64%
CHEMBL4123 P30989 Neurotensin receptor 1 83.14% 96.67%
CHEMBL253 P34972 Cannabinoid CB2 receptor 82.49% 97.25%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 82.13% 97.21%
CHEMBL2073 P07947 Tyrosine-protein kinase YES 81.32% 83.14%
CHEMBL4040 P28482 MAP kinase ERK2 80.78% 83.82%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 80.16% 94.33%

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 146684322
LOTUS LTS0211008
wikiData Q105202539