cyclo[Phe-Tyr-D-Ser-D-Val-D-Pro-D-Tyr-D-Pro-Pro]

Details

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Internal ID c373016e-5f7e-4848-a454-db7e18a2d7b7
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Amino acids, peptides, and analogues > Peptides > Cyclic peptides
IUPAC Name (3R,9R,12R,18R,21R,24S,27S,30S)-27-benzyl-21-(hydroxymethyl)-9,24-bis[(4-hydroxyphenyl)methyl]-18-propan-2-yl-1,7,10,16,19,22,25,28-octazatetracyclo[28.3.0.03,7.012,16]tritriacontane-2,8,11,17,20,23,26,29-octone
SMILES (Canonical) CC(C)C1C(=O)N2CCCC2C(=O)NC(C(=O)N3CCCC3C(=O)N4CCCC4C(=O)NC(C(=O)NC(C(=O)NC(C(=O)N1)CO)CC5=CC=C(C=C5)O)CC6=CC=CC=C6)CC7=CC=C(C=C7)O
SMILES (Isomeric) CC(C)[C@@H]1C(=O)N2CCC[C@@H]2C(=O)N[C@@H](C(=O)N3CCC[C@@H]3C(=O)N4CCC[C@H]4C(=O)N[C@H](C(=O)N[C@H](C(=O)N[C@@H](C(=O)N1)CO)CC5=CC=C(C=C5)O)CC6=CC=CC=C6)CC7=CC=C(C=C7)O
InChI InChI=1S/C50H62N8O11/c1-29(2)42-50(69)57-23-7-12-40(57)47(66)53-37(27-32-16-20-34(61)21-17-32)48(67)58-24-8-13-41(58)49(68)56-22-6-11-39(56)46(65)52-36(25-30-9-4-3-5-10-30)43(62)51-35(26-31-14-18-33(60)19-15-31)44(63)54-38(28-59)45(64)55-42/h3-5,9-10,14-21,29,35-42,59-61H,6-8,11-13,22-28H2,1-2H3,(H,51,62)(H,52,65)(H,53,66)(H,54,63)(H,55,64)/t35-,36-,37+,38+,39-,40+,41+,42+/m0/s1
InChI Key VGQVPZUFUDZAGA-JABIFFPESA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C50H62N8O11
Molecular Weight 951.10 g/mol
Exact Mass 950.45380482 g/mol
Topological Polar Surface Area (TPSA) 267.00 Ų
XlogP 3.40

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of cyclo[Phe-Tyr-D-Ser-D-Val-D-Pro-D-Tyr-D-Pro-Pro]

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 99.83% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.52% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.73% 95.56%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 95.35% 85.14%
CHEMBL5103 Q969S8 Histone deacetylase 10 94.89% 90.08%
CHEMBL5608 Q16288 NT-3 growth factor receptor 93.54% 95.89%
CHEMBL2693 Q9UIQ6 Cystinyl aminopeptidase 93.34% 97.64%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 93.05% 94.45%
CHEMBL3524 P56524 Histone deacetylase 4 92.54% 92.97%
CHEMBL5966 P55899 IgG receptor FcRn large subunit p51 90.19% 90.93%
CHEMBL3137262 O60341 LSD1/CoREST complex 89.52% 97.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 89.31% 91.11%
CHEMBL2069156 Q14145 Kelch-like ECH-associated protein 1 88.93% 82.38%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 84.30% 91.71%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 83.64% 95.89%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 83.40% 97.14%
CHEMBL1902 P62942 FK506-binding protein 1A 83.05% 97.05%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 82.70% 93.00%
CHEMBL3476 O15111 Inhibitor of nuclear factor kappa B kinase alpha subunit 82.18% 95.83%
CHEMBL226 P30542 Adenosine A1 receptor 82.09% 95.93%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 80.35% 90.71%

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.
Stellaria delavayi

Cross-Links

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PubChem 163188534
LOTUS LTS0135387
wikiData Q105285975