Cyclo(-D-Trp-Tyr)

Details

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Internal ID b7b70076-0bc8-482c-9cef-8c7ebd87e4d2
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Amino acids, peptides, and analogues > Alpha amino acids and derivatives
IUPAC Name 3-[(4-hydroxyphenyl)methyl]-6-(1H-indol-3-ylmethyl)piperazine-2,5-dione
SMILES (Canonical) C1=CC=C2C(=C1)C(=CN2)CC3C(=O)NC(C(=O)N3)CC4=CC=C(C=C4)O
SMILES (Isomeric) C1=CC=C2C(=C1)C(=CN2)CC3C(=O)NC(C(=O)N3)CC4=CC=C(C=C4)O
InChI InChI=1S/C20H19N3O3/c24-14-7-5-12(6-8-14)9-17-19(25)23-18(20(26)22-17)10-13-11-21-16-4-2-1-3-15(13)16/h1-8,11,17-18,21,24H,9-10H2,(H,22,26)(H,23,25)
InChI Key ZJDMXAAEAVGGSK-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C20H19N3O3
Molecular Weight 349.40 g/mol
Exact Mass 349.14264148 g/mol
Topological Polar Surface Area (TPSA) 94.20 Ų
XlogP 2.40
Atomic LogP (AlogP) 1.64
H-Bond Acceptor 3
H-Bond Donor 4
Rotatable Bonds 4

Synonyms

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20829-53-2
852955-00-1
DTXSID00875215
25Piperazinedione, indole derivative
FT-0772597
3-[(4-hydroxyphenyl)methyl]-6-(1h-indol-3-ylmethyl)piperazine-2,5-dione

2D Structure

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2D Structure of Cyclo(-D-Trp-Tyr)

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9760 97.60%
Caco-2 - 0.6182 61.82%
Blood Brain Barrier + 0.6750 67.50%
Human oral bioavailability + 0.5286 52.86%
Subcellular localzation Mitochondria 0.7723 77.23%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8922 89.22%
OATP1B3 inhibitior + 0.9516 95.16%
MATE1 inhibitior - 0.8000 80.00%
OCT2 inhibitior - 0.8716 87.16%
BSEP inhibitior + 0.9586 95.86%
P-glycoprotein inhibitior - 0.6538 65.38%
P-glycoprotein substrate - 0.6586 65.86%
CYP3A4 substrate + 0.5843 58.43%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7679 76.79%
CYP3A4 inhibition - 0.8689 86.89%
CYP2C9 inhibition - 0.7258 72.58%
CYP2C19 inhibition - 0.8362 83.62%
CYP2D6 inhibition - 0.6857 68.57%
CYP1A2 inhibition - 0.7052 70.52%
CYP2C8 inhibition + 0.5378 53.78%
CYP inhibitory promiscuity - 0.6920 69.20%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.8923 89.23%
Carcinogenicity (trinary) Non-required 0.6882 68.82%
Eye corrosion - 0.9948 99.48%
Eye irritation - 0.9755 97.55%
Skin irritation - 0.8219 82.19%
Skin corrosion - 0.9647 96.47%
Ames mutagenesis - 0.6154 61.54%
Human Ether-a-go-go-Related Gene inhibition + 0.8168 81.68%
Micronuclear + 0.8800 88.00%
Hepatotoxicity - 0.6966 69.66%
skin sensitisation - 0.9038 90.38%
Respiratory toxicity + 0.7000 70.00%
Reproductive toxicity + 0.9000 90.00%
Mitochondrial toxicity + 0.7875 78.75%
Nephrotoxicity - 0.6724 67.24%
Acute Oral Toxicity (c) III 0.5232 52.32%
Estrogen receptor binding + 0.6795 67.95%
Androgen receptor binding + 0.6990 69.90%
Thyroid receptor binding - 0.7031 70.31%
Glucocorticoid receptor binding + 0.6151 61.51%
Aromatase binding - 0.5459 54.59%
PPAR gamma + 0.6719 67.19%
Honey bee toxicity - 0.8441 84.41%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.5300 53.00%
Fish aquatic toxicity - 0.6190 61.90%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 99.27% 91.11%
CHEMBL4040 P28482 MAP kinase ERK2 95.72% 83.82%
CHEMBL2581 P07339 Cathepsin D 95.33% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.99% 95.56%
CHEMBL3310 Q96DB2 Histone deacetylase 11 93.38% 88.56%
CHEMBL5103 Q969S8 Histone deacetylase 10 92.55% 90.08%
CHEMBL1951 P21397 Monoamine oxidase A 92.53% 91.49%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 91.54% 94.62%
CHEMBL2693 Q9UIQ6 Cystinyl aminopeptidase 90.17% 97.64%
CHEMBL3830 Q2M2I8 Adaptor-associated kinase 89.77% 83.10%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 89.47% 92.62%
CHEMBL1937 Q92769 Histone deacetylase 2 88.98% 94.75%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.65% 96.09%
CHEMBL3192 Q9BY41 Histone deacetylase 8 87.64% 93.99%
CHEMBL2535 P11166 Glucose transporter 87.25% 98.75%
CHEMBL2095172 P14867 GABA-A receptor; alpha-1/beta-2/gamma-2 85.76% 92.67%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 85.21% 94.45%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 85.20% 94.00%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 84.90% 91.71%
CHEMBL5966 P55899 IgG receptor FcRn large subunit p51 83.49% 90.93%
CHEMBL1806 P11388 DNA topoisomerase II alpha 82.73% 89.00%
CHEMBL213 P08588 Beta-1 adrenergic receptor 82.68% 95.56%
CHEMBL1293287 P14735 Insulin-degrading enzyme 82.55% 88.10%
CHEMBL2563 Q9UQL6 Histone deacetylase 5 82.52% 89.67%
CHEMBL255 P29275 Adenosine A2b receptor 81.86% 98.59%
CHEMBL3137262 O60341 LSD1/CoREST complex 81.86% 97.09%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 80.14% 95.50%

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 9863179
LOTUS LTS0078807
wikiData Q82856562