cyclo(DL-Ala-DL-xiThr-Gly-DL-xiThr-DL-Phe-DL-Leu-DL-xiIle)

Details

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Internal ID 77c314f8-ec6e-4d07-b702-4a39fb4255bd
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Amino acids, peptides, and analogues > Peptides > Oligopeptides
IUPAC Name 15-benzyl-9-butan-2-yl-3,18-bis(1-hydroxyethyl)-6-methyl-12-(2-methylpropyl)-1,4,7,10,13,16,19-heptazacyclohenicosane-2,5,8,11,14,17,20-heptone
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C34H53N7O9/c1-8-18(4)26-33(49)36-19(5)29(45)41-27(20(6)42)32(48)35-16-25(44)39-28(21(7)43)34(50)38-24(15-22-12-10-9-11-13-22)30(46)37-23(14-17(2)3)31(47)40-26/h9-13,17-21,23-24,26-28,42-43H,8,14-16H2,1-7H3,(H,35,48)(H,36,49)(H,37,46)(H,38,50)(H,39,44)(H,40,47)(H,41,45)
InChI Key LZVXYGLCVNPQDY-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C34H53N7O9
Molecular Weight 703.80 g/mol
Exact Mass 703.39047629 g/mol
Topological Polar Surface Area (TPSA) 244.00 Ų
XlogP 1.90
Atomic LogP (AlogP) -1.86
H-Bond Acceptor 9
H-Bond Donor 9
Rotatable Bonds 8

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of cyclo(DL-Ala-DL-xiThr-Gly-DL-xiThr-DL-Phe-DL-Leu-DL-xiIle)

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8612 86.12%
Caco-2 - 0.8636 86.36%
Blood Brain Barrier - 0.6750 67.50%
Human oral bioavailability + 0.6143 61.43%
Subcellular localzation Mitochondria 0.7150 71.50%
OATP2B1 inhibitior - 0.5786 57.86%
OATP1B1 inhibitior + 0.8662 86.62%
OATP1B3 inhibitior + 0.9110 91.10%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior + 0.7723 77.23%
P-glycoprotein inhibitior + 0.7125 71.25%
P-glycoprotein substrate + 0.8437 84.37%
CYP3A4 substrate + 0.6007 60.07%
CYP2C9 substrate - 0.6017 60.17%
CYP2D6 substrate - 0.8029 80.29%
CYP3A4 inhibition - 0.8735 87.35%
CYP2C9 inhibition - 0.9401 94.01%
CYP2C19 inhibition - 0.9084 90.84%
CYP2D6 inhibition - 0.9431 94.31%
CYP1A2 inhibition - 0.9267 92.67%
CYP2C8 inhibition - 0.6332 63.32%
CYP inhibitory promiscuity - 0.9854 98.54%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.7000 70.00%
Carcinogenicity (trinary) Non-required 0.6791 67.91%
Eye corrosion - 0.9919 99.19%
Eye irritation - 0.9247 92.47%
Skin irritation - 0.7976 79.76%
Skin corrosion - 0.9419 94.19%
Ames mutagenesis - 0.7245 72.45%
Human Ether-a-go-go-Related Gene inhibition - 0.4114 41.14%
Micronuclear + 0.7500 75.00%
Hepatotoxicity - 0.5020 50.20%
skin sensitisation - 0.8802 88.02%
Respiratory toxicity + 0.7333 73.33%
Reproductive toxicity + 0.8444 84.44%
Mitochondrial toxicity + 0.8500 85.00%
Nephrotoxicity - 0.6596 65.96%
Acute Oral Toxicity (c) III 0.6811 68.11%
Estrogen receptor binding + 0.7305 73.05%
Androgen receptor binding + 0.5738 57.38%
Thyroid receptor binding + 0.5571 55.71%
Glucocorticoid receptor binding + 0.6744 67.44%
Aromatase binding + 0.5963 59.63%
PPAR gamma + 0.7294 72.94%
Honey bee toxicity - 0.8369 83.69%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.6200 62.00%
Fish aquatic toxicity - 0.7816 78.16%

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 99.56% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.16% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.22% 91.11%
CHEMBL221 P23219 Cyclooxygenase-1 92.48% 90.17%
CHEMBL2693 Q9UIQ6 Cystinyl aminopeptidase 92.23% 97.64%
CHEMBL4071 P08311 Cathepsin G 90.96% 94.64%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.45% 95.56%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 89.55% 85.14%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.30% 86.33%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 85.61% 97.14%
CHEMBL5966 P55899 IgG receptor FcRn large subunit p51 84.80% 90.93%
CHEMBL253 P34972 Cannabinoid CB2 receptor 84.75% 97.25%
CHEMBL3137262 O60341 LSD1/CoREST complex 83.61% 97.09%
CHEMBL1949 P62937 Cyclophilin A 83.13% 98.57%
CHEMBL5103 Q969S8 Histone deacetylase 10 82.85% 90.08%
CHEMBL3401 O75469 Pregnane X receptor 81.84% 94.73%
CHEMBL4040 P28482 MAP kinase ERK2 81.80% 83.82%
CHEMBL3713062 P10646 Tissue factor pathway inhibitor 80.77% 97.33%
CHEMBL1937 Q92769 Histone deacetylase 2 80.51% 94.75%

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 85632468
LOTUS LTS0055428
wikiData Q105160168