H-Lys(1)-Lys(Bz(2,3-diOH))(Bz(2,3-diOH))-D-Phe-OH.Bz(2,3-diOH)-Gly-(1)

Details

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Internal ID 35679714-2a40-451e-a6f6-462163ff697b
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Amino acids, peptides, and analogues > Peptides
IUPAC Name (2R)-2-[[(2S)-2-[[(2S)-2-amino-6-[[2-[(2,3-dihydroxybenzoyl)amino]acetyl]amino]hexanoyl]amino]-6-[(2,3-dihydroxybenzoyl)amino]hexanoyl]amino]-3-phenylpropanoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C37H46N6O11/c38-25(14-4-6-18-39-30(46)21-41-34(50)24-13-9-17-29(45)32(24)48)35(51)42-26(36(52)43-27(37(53)54)20-22-10-2-1-3-11-22)15-5-7-19-40-33(49)23-12-8-16-28(44)31(23)47/h1-3,8-13,16-17,25-27,44-45,47-48H,4-7,14-15,18-21,38H2,(H,39,46)(H,40,49)(H,41,50)(H,42,51)(H,43,52)(H,53,54)/t25-,26-,27+/m0/s1
InChI Key AQVANOYBWBHIEH-GMQQYTKMSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C37H46N6O11
Molecular Weight 750.80 g/mol
Exact Mass 750.32245630 g/mol
Topological Polar Surface Area (TPSA) 290.00 Ų
XlogP 0.50

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of H-Lys(1)-Lys(Bz(2,3-diOH))(Bz(2,3-diOH))-D-Phe-OH.Bz(2,3-diOH)-Gly-(1)

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 99.71% 98.95%
CHEMBL1255126 O15151 Protein Mdm4 99.00% 90.20%
CHEMBL221 P23219 Cyclooxygenase-1 98.84% 90.17%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.29% 91.11%
CHEMBL5701 Q9H2K8 Serine/threonine-protein kinase TAO3 95.84% 96.67%
CHEMBL5261 Q7L7X3 Serine/threonine-protein kinase TAO1 95.59% 89.33%
CHEMBL3359 P21462 Formyl peptide receptor 1 94.17% 93.56%
CHEMBL1795139 Q8IU80 Transmembrane protease serine 6 93.81% 98.33%
CHEMBL3891 P07384 Calpain 1 93.72% 93.04%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 93.68% 95.50%
CHEMBL2514 O95665 Neurotensin receptor 2 93.47% 100.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 93.40% 99.17%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 92.30% 100.00%
CHEMBL4101 P17612 cAMP-dependent protein kinase alpha-catalytic subunit 92.18% 82.86%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 90.14% 95.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.50% 96.09%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 89.38% 91.81%
CHEMBL4361 Q07820 Induced myeloid leukemia cell differentiation protein Mcl-1 89.06% 95.52%
CHEMBL2321614 Q9NPC2 Potassium channel subfamily K member 9 88.46% 80.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.25% 95.56%
CHEMBL2535 P11166 Glucose transporter 87.08% 98.75%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 86.94% 94.45%
CHEMBL1914 P06276 Butyrylcholinesterase 84.39% 95.00%
CHEMBL4227 P25090 Lipoxin A4 receptor 83.32% 100.00%
CHEMBL2096618 P11274 Bcr/Abl fusion protein 83.06% 85.83%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 82.26% 97.21%
CHEMBL3976 Q9UHL4 Dipeptidyl peptidase II 82.19% 92.29%
CHEMBL3230 O95977 Sphingosine 1-phosphate receptor Edg-6 82.18% 94.01%
CHEMBL340 P08684 Cytochrome P450 3A4 82.10% 91.19%
CHEMBL3401 O75469 Pregnane X receptor 81.81% 94.73%
CHEMBL2327 P21452 Neurokinin 2 receptor 81.60% 98.89%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 81.41% 99.15%
CHEMBL1907594 P30926 Neuronal acetylcholine receptor; alpha3/beta4 80.75% 97.23%

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 163041620
LOTUS LTS0061815
wikiData Q104917100