Ac-DL-xiThr(1)-DL-Phe-DL-Leu-DL-Val-DL-Pro-DL-Pro-DL-Leu-DL-N(Me)Tyr-(1)

Details

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Internal ID 363d1127-fbd5-435e-b1fb-65f65c6f8c2a
Taxonomy Organic acids and derivatives > Peptidomimetics > Depsipeptides > Cyclic depsipeptides
IUPAC Name N-[15-benzyl-22-[(4-hydroxyphenyl)methyl]-19,23-dimethyl-12,25-bis(2-methylpropyl)-2,8,11,14,17,21,24,27-octaoxo-9-propan-2-yl-20-oxa-1,7,10,13,16,23,26-heptazatricyclo[26.3.0.03,7]hentriacontan-18-yl]acetamide
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C52H74N8O11/c1-29(2)25-37-46(64)57-43(31(5)6)51(69)60-24-14-18-41(60)50(68)59-23-13-17-40(59)47(65)56-39(26-30(3)4)49(67)58(9)42(28-35-19-21-36(62)22-20-35)52(70)71-32(7)44(53-33(8)61)48(66)55-38(45(63)54-37)27-34-15-11-10-12-16-34/h10-12,15-16,19-22,29-32,37-44,62H,13-14,17-18,23-28H2,1-9H3,(H,53,61)(H,54,63)(H,55,66)(H,56,65)(H,57,64)
InChI Key GPZKACUYSXLPFP-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C52H74N8O11
Molecular Weight 987.20 g/mol
Exact Mass 986.54770521 g/mol
Topological Polar Surface Area (TPSA) 253.00 Ų
XlogP 5.20
Atomic LogP (AlogP) 2.12
H-Bond Acceptor 11
H-Bond Donor 6
Rotatable Bonds 10

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Ac-DL-xiThr(1)-DL-Phe-DL-Leu-DL-Val-DL-Pro-DL-Pro-DL-Leu-DL-N(Me)Tyr-(1)

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.5992 59.92%
Caco-2 - 0.8643 86.43%
Blood Brain Barrier - 0.9750 97.50%
Human oral bioavailability - 0.7286 72.86%
Subcellular localzation Mitochondria 0.4174 41.74%
OATP2B1 inhibitior - 0.5705 57.05%
OATP1B1 inhibitior + 0.8227 82.27%
OATP1B3 inhibitior + 0.9126 91.26%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior + 0.9099 90.99%
P-glycoprotein inhibitior + 0.7594 75.94%
P-glycoprotein substrate + 0.9043 90.43%
CYP3A4 substrate + 0.7055 70.55%
CYP2C9 substrate - 0.6012 60.12%
CYP2D6 substrate - 0.8077 80.77%
CYP3A4 inhibition - 0.6246 62.46%
CYP2C9 inhibition - 0.8087 80.87%
CYP2C19 inhibition - 0.8494 84.94%
CYP2D6 inhibition - 0.8460 84.60%
CYP1A2 inhibition - 0.9672 96.72%
CYP2C8 inhibition + 0.6587 65.87%
CYP inhibitory promiscuity - 0.9465 94.65%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9100 91.00%
Carcinogenicity (trinary) Non-required 0.6216 62.16%
Eye corrosion - 0.9907 99.07%
Eye irritation - 0.9066 90.66%
Skin irritation - 0.7859 78.59%
Skin corrosion - 0.9358 93.58%
Ames mutagenesis - 0.6500 65.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6553 65.53%
Micronuclear + 0.8300 83.00%
Hepatotoxicity + 0.7000 70.00%
skin sensitisation - 0.8994 89.94%
Respiratory toxicity + 0.8667 86.67%
Reproductive toxicity + 0.9444 94.44%
Mitochondrial toxicity + 0.9500 95.00%
Nephrotoxicity - 0.7147 71.47%
Acute Oral Toxicity (c) III 0.6623 66.23%
Estrogen receptor binding + 0.8161 81.61%
Androgen receptor binding + 0.7401 74.01%
Thyroid receptor binding + 0.5939 59.39%
Glucocorticoid receptor binding + 0.6854 68.54%
Aromatase binding + 0.5709 57.09%
PPAR gamma + 0.8076 80.76%
Honey bee toxicity - 0.7588 75.88%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity + 0.5600 56.00%
Fish aquatic toxicity + 0.9830 98.30%

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 99.92% 98.95%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 99.63% 85.14%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.82% 96.09%
CHEMBL5103 Q969S8 Histone deacetylase 10 96.24% 90.08%
CHEMBL5966 P55899 IgG receptor FcRn large subunit p51 95.11% 90.93%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.97% 95.56%
CHEMBL2693 Q9UIQ6 Cystinyl aminopeptidase 94.57% 97.64%
CHEMBL3524 P56524 Histone deacetylase 4 93.39% 92.97%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 90.44% 91.11%
CHEMBL2069156 Q14145 Kelch-like ECH-associated protein 1 89.24% 82.38%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 89.21% 95.89%
CHEMBL2563 Q9UQL6 Histone deacetylase 5 88.76% 89.67%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 86.51% 93.00%
CHEMBL4072 P07858 Cathepsin B 85.67% 93.67%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.66% 86.33%
CHEMBL5608 Q16288 NT-3 growth factor receptor 85.43% 95.89%
CHEMBL1806 P11388 DNA topoisomerase II alpha 85.40% 89.00%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 85.04% 97.14%
CHEMBL3392948 Q9NP59 Solute carrier family 40 member 1 84.52% 95.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.06% 99.17%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 83.01% 94.45%
CHEMBL333 P08253 Matrix metalloproteinase-2 82.40% 96.31%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 81.88% 99.23%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 81.56% 93.03%
CHEMBL4531 P17931 Galectin-3 81.14% 96.90%
CHEMBL3359 P21462 Formyl peptide receptor 1 80.71% 93.56%
CHEMBL1902 P62942 FK506-binding protein 1A 80.70% 97.05%

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 162815573
LOTUS LTS0154113
wikiData Q104167376