Cyclo-[L-Tyr-L-Leu-D-Pro]

Details

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Internal ID 6ab69f2c-7f08-4104-ab51-68b228dc7d0b
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Amino acids, peptides, and analogues > Peptides > Cyclic peptides
IUPAC Name (3S,6S,11aR)-3-[(4-hydroxyphenyl)methyl]-6-(2-methylpropyl)-2,3,5,6,9,10,11,11a-octahydropyrrolo[1,2-a][1,4,7]triazonine-1,4,7-trione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C20H27N3O4/c1-12(2)10-16-20(27)23-9-3-4-17(23)19(26)21-15(18(25)22-16)11-13-5-7-14(24)8-6-13/h5-8,12,15-17,24H,3-4,9-11H2,1-2H3,(H,21,26)(H,22,25)/t15-,16-,17+/m0/s1
InChI Key UWOBQRKCCVXFIG-YESZJQIVSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C20H27N3O4
Molecular Weight 373.40 g/mol
Exact Mass 373.20015635 g/mol
Topological Polar Surface Area (TPSA) 98.70 Ų
XlogP 2.10
Atomic LogP (AlogP) 0.95
H-Bond Acceptor 4
H-Bond Donor 3
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Cyclo-[L-Tyr-L-Leu-D-Pro]

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9191 91.91%
Caco-2 + 0.5270 52.70%
Blood Brain Barrier - 0.6750 67.50%
Human oral bioavailability - 0.6857 68.57%
Subcellular localzation Mitochondria 0.8205 82.05%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8861 88.61%
OATP1B3 inhibitior + 0.9380 93.80%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior + 0.6204 62.04%
P-glycoprotein inhibitior - 0.6313 63.13%
P-glycoprotein substrate + 0.7913 79.13%
CYP3A4 substrate + 0.5662 56.62%
CYP2C9 substrate - 0.6147 61.47%
CYP2D6 substrate - 0.7779 77.79%
CYP3A4 inhibition - 0.8618 86.18%
CYP2C9 inhibition - 0.8624 86.24%
CYP2C19 inhibition - 0.8011 80.11%
CYP2D6 inhibition - 0.9056 90.56%
CYP1A2 inhibition - 0.9407 94.07%
CYP2C8 inhibition - 0.7324 73.24%
CYP inhibitory promiscuity - 0.8928 89.28%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.8700 87.00%
Carcinogenicity (trinary) Non-required 0.7019 70.19%
Eye corrosion - 0.9922 99.22%
Eye irritation - 0.9899 98.99%
Skin irritation - 0.7763 77.63%
Skin corrosion - 0.9288 92.88%
Ames mutagenesis - 0.6891 68.91%
Human Ether-a-go-go-Related Gene inhibition - 0.6453 64.53%
Micronuclear + 0.8100 81.00%
Hepatotoxicity + 0.5875 58.75%
skin sensitisation - 0.8948 89.48%
Respiratory toxicity + 0.8111 81.11%
Reproductive toxicity + 0.9222 92.22%
Mitochondrial toxicity + 0.9250 92.50%
Nephrotoxicity - 0.6082 60.82%
Acute Oral Toxicity (c) III 0.6715 67.15%
Estrogen receptor binding + 0.5509 55.09%
Androgen receptor binding + 0.6028 60.28%
Thyroid receptor binding - 0.5787 57.87%
Glucocorticoid receptor binding - 0.5072 50.72%
Aromatase binding - 0.5594 55.94%
PPAR gamma - 0.6516 65.16%
Honey bee toxicity - 0.9221 92.21%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.5700 57.00%
Fish aquatic toxicity + 0.9037 90.37%

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 99.76% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.64% 96.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 96.38% 94.45%
CHEMBL5103 Q969S8 Histone deacetylase 10 95.93% 90.08%
CHEMBL5966 P55899 IgG receptor FcRn large subunit p51 95.37% 90.93%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 95.30% 85.14%
CHEMBL253 P34972 Cannabinoid CB2 receptor 94.37% 97.25%
CHEMBL3524 P56524 Histone deacetylase 4 93.48% 92.97%
CHEMBL5608 Q16288 NT-3 growth factor receptor 93.31% 95.89%
CHEMBL2069156 Q14145 Kelch-like ECH-associated protein 1 91.08% 82.38%
CHEMBL3137262 O60341 LSD1/CoREST complex 91.01% 97.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.87% 95.56%
CHEMBL1902 P62942 FK506-binding protein 1A 89.77% 97.05%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 89.65% 90.71%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 88.56% 91.11%
CHEMBL2693 Q9UIQ6 Cystinyl aminopeptidase 86.97% 97.64%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 85.35% 95.89%
CHEMBL5852 Q96P65 Pyroglutamylated RFamide peptide receptor 84.36% 85.00%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 83.33% 100.00%
CHEMBL1937 Q92769 Histone deacetylase 2 83.30% 94.75%
CHEMBL4616 Q92847 Ghrelin receptor 81.31% 92.00%
CHEMBL6175 Q9H3R0 Lysine-specific demethylase 4C 81.24% 96.69%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 81.24% 93.00%
CHEMBL217 P14416 Dopamine D2 receptor 80.89% 95.62%
CHEMBL3310 Q96DB2 Histone deacetylase 11 80.48% 88.56%
CHEMBL5203 P33316 dUTP pyrophosphatase 80.33% 99.18%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 80.07% 93.40%

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 146684321
LOTUS LTS0261568
wikiData Q105280469