H-Ile-Ser-Thr-Ala-Ile-Ala(imidazol-2-yl)-Asn-Ser-Lys-OH

Details

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Internal ID 22f7084d-53d5-4b5c-8e05-e50782b2d563
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Amino acids, peptides, and analogues > Peptides
IUPAC Name (2S)-6-amino-2-[[(2S)-2-[[(2S)-4-amino-2-[[(2S)-2-[[(2S,3S)-2-[[(2S)-2-[[(2S,3R)-2-[[(2S)-2-[[(2S,3S)-2-amino-3-methylpentanoyl]amino]-3-hydroxypropanoyl]amino]-3-hydroxybutanoyl]amino]propanoyl]amino]-3-methylpentanoyl]amino]-3-(1H-imidazol-2-yl)propanoyl]amino]-4-oxobutanoyl]amino]-3-hydroxypropanoyl]amino]hexanoic acid
SMILES (Canonical) CCC(C)C(C(=O)NC(CO)C(=O)NC(C(C)O)C(=O)NC(C)C(=O)NC(C(C)CC)C(=O)NC(CC1=NC=CN1)C(=O)NC(CC(=O)N)C(=O)NC(CO)C(=O)NC(CCCCN)C(=O)O)N
SMILES (Isomeric) CC[C@H](C)[C@@H](C(=O)N[C@@H](CO)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](C)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CC1=NC=CN1)C(=O)N[C@@H](CC(=O)N)C(=O)N[C@@H](CO)C(=O)N[C@@H](CCCCN)C(=O)O)N
InChI InChI=1S/C41H71N13O14/c1-7-19(3)30(44)38(64)52-27(18-56)37(63)54-32(22(6)57)40(66)47-21(5)33(59)53-31(20(4)8-2)39(65)50-25(16-29-45-13-14-46-29)35(61)49-24(15-28(43)58)34(60)51-26(17-55)36(62)48-23(41(67)68)11-9-10-12-42/h13-14,19-27,30-32,55-57H,7-12,15-18,42,44H2,1-6H3,(H2,43,58)(H,45,46)(H,47,66)(H,48,62)(H,49,61)(H,50,65)(H,51,60)(H,52,64)(H,53,59)(H,54,63)(H,67,68)/t19-,20-,21-,22+,23-,24-,25-,26-,27-,30-,31-,32-/m0/s1
InChI Key WDBUEXYJQPAORL-DAELXKLDSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C41H71N13O14
Molecular Weight 970.10 g/mol
Exact Mass 969.52434399 g/mol
Topological Polar Surface Area (TPSA) 455.00 Ų
XlogP -7.10

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of H-Ile-Ser-Thr-Ala-Ile-Ala(imidazol-2-yl)-Asn-Ser-Lys-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
CHEMBL4040 P28482 MAP kinase ERK2 99.73% 83.82%
CHEMBL2581 P07339 Cathepsin D 99.25% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 99.20% 96.09%
CHEMBL1907594 P30926 Neuronal acetylcholine receptor; alpha3/beta4 98.80% 97.23%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 96.36% 100.00%
CHEMBL2107 P61073 C-X-C chemokine receptor type 4 95.84% 93.10%
CHEMBL3359 P21462 Formyl peptide receptor 1 95.76% 93.56%
CHEMBL2094135 Q96BI3 Gamma-secretase 95.43% 98.05%
CHEMBL2514 O95665 Neurotensin receptor 2 95.32% 100.00%
CHEMBL1255126 O15151 Protein Mdm4 95.22% 90.20%
CHEMBL3060 Q9Y345 Glycine transporter 2 94.89% 99.17%
CHEMBL1795139 Q8IU80 Transmembrane protease serine 6 94.26% 98.33%
CHEMBL2885 P07451 Carbonic anhydrase III 93.80% 87.45%
CHEMBL4018 P49146 Neuropeptide Y receptor type 2 92.52% 98.94%
CHEMBL221 P23219 Cyclooxygenase-1 92.22% 90.17%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 91.63% 96.00%
CHEMBL3776 Q14790 Caspase-8 90.82% 97.06%
CHEMBL3837 P07711 Cathepsin L 89.36% 96.61%
CHEMBL2492 P36544 Neuronal acetylcholine receptor protein alpha-7 subunit 88.69% 88.42%
CHEMBL4227 P25090 Lipoxin A4 receptor 88.31% 100.00%
CHEMBL3308 P55212 Caspase-6 87.01% 97.56%
CHEMBL3038469 P24941 CDK2/Cyclin A 86.96% 91.38%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 85.11% 90.71%
CHEMBL5163 Q9NY46 Sodium channel protein type III alpha subunit 84.63% 96.90%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 84.37% 93.00%
CHEMBL4581 P52732 Kinesin-like protein 1 83.90% 93.18%
CHEMBL4296013 Q5VWK5 Interleukin-23 receptor 83.70% 88.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 82.92% 95.56%
CHEMBL3401 O75469 Pregnane X receptor 82.16% 94.73%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 82.14% 95.50%
CHEMBL3392948 Q9NP59 Solute carrier family 40 member 1 81.03% 95.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 81.01% 91.11%
CHEMBL3286 P00749 Urokinase-type plasminogen activator 80.61% 97.88%

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.
Phytolacca americana

Cross-Links

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PubChem 163187101
LOTUS LTS0029578
wikiData Q105302218