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Enduspeptide A

Table of Contents

Details
Physical and Chemical Properties
Synonyms
2D Structure
3D Structure
ADMET Properties
Targets (proven and/or predicted)
Plants that contains it
Cross-Links

Details

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Internal ID 6f9fa9c0-4d64-499c-8933-046be77f9d95
Taxonomy Organic acids and derivatives > Peptidomimetics > Depsipeptides > Cyclic depsipeptides
IUPAC Name N-[(3S,9S,12S,15S,18S,19S,22S,25S,28S)-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]propanamide
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C53H76N8O11/c1-10-43(63)57-45-33(8)72-53(71)42(29-35-20-22-36(62)23-21-35)59(9)50(68)39(27-31(4)5)56-48(66)40-18-14-24-60(40)51(69)41-19-15-25-61(41)52(70)44(32(6)7)58-47(65)37(26-30(2)3)54-46(64)38(55-49(45)67)28-34-16-12-11-13-17-34/h11-13,16-17,20-23,30-33,37-42,44-45,62H,10,14-15,18-19,24-29H2,1-9H3,(H,54,64)(H,55,67)(H,56,66)(H,57,63)(H,58,65)/t33-,37-,38-,39-,40-,41-,42-,44-,45-/m0/s1
InChI Key DWBRAORZZAUFMW-MUNNLIKUSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C53H76N8O11
Molecular Weight 1001.20 g/mol
Exact Mass 1000.56335527 g/mol
Topological Polar Surface Area (TPSA) 253.00 Ų
XlogP 5.60
Atomic LogP (AlogP) 2.51
H-Bond Acceptor 11
H-Bond Donor 6
Rotatable Bonds 11

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Enduspeptide A

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.6127 61.27%
Caco-2 - 0.8645 86.45%
Blood Brain Barrier - 0.9750 97.50%
Human oral bioavailability - 0.7429 74.29%
Subcellular localzation Mitochondria 0.4094 40.94%
OATP2B1 inhibitior - 0.5703 57.03%
OATP1B1 inhibitior + 0.8254 82.54%
OATP1B3 inhibitior + 0.9057 90.57%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior + 0.9297 92.97%
P-glycoprotein inhibitior + 0.7570 75.70%
P-glycoprotein substrate + 0.8939 89.39%
CYP3A4 substrate + 0.7066 70.66%
CYP2C9 substrate - 0.6012 60.12%
CYP2D6 substrate - 0.8077 80.77%
CYP3A4 inhibition - 0.6214 62.14%
CYP2C9 inhibition - 0.8623 86.23%
CYP2C19 inhibition - 0.8512 85.12%
CYP2D6 inhibition - 0.8477 84.77%
CYP1A2 inhibition - 0.9688 96.88%
CYP2C8 inhibition + 0.7211 72.11%
CYP inhibitory promiscuity - 0.9557 95.57%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.8800 88.00%
Carcinogenicity (trinary) Non-required 0.6088 60.88%
Eye corrosion - 0.9908 99.08%
Eye irritation - 0.9057 90.57%
Skin irritation - 0.7980 79.80%
Skin corrosion - 0.9327 93.27%
Ames mutagenesis - 0.6800 68.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6695 66.95%
Micronuclear + 0.8500 85.00%
Hepatotoxicity + 0.7125 71.25%
skin sensitisation - 0.9003 90.03%
Respiratory toxicity + 0.8667 86.67%
Reproductive toxicity + 0.9222 92.22%
Mitochondrial toxicity + 0.9250 92.50%
Nephrotoxicity - 0.7829 78.29%
Acute Oral Toxicity (c) III 0.6509 65.09%
Estrogen receptor binding + 0.8217 82.17%
Androgen receptor binding + 0.7400 74.00%
Thyroid receptor binding + 0.5923 59.23%
Glucocorticoid receptor binding + 0.6646 66.46%
Aromatase binding + 0.5801 58.01%
PPAR gamma + 0.8121 81.21%
Honey bee toxicity - 0.7647 76.47%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity + 0.5900 59.00%
Fish aquatic toxicity + 0.9778 97.78%

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 99.91% 98.95%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 97.61% 85.14%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.39% 96.09%
CHEMBL5966 P55899 IgG receptor FcRn large subunit p51 95.92% 90.93%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.49% 95.56%
CHEMBL5103 Q969S8 Histone deacetylase 10 95.11% 90.08%
CHEMBL2693 Q9UIQ6 Cystinyl aminopeptidase 94.31% 97.64%
CHEMBL2069156 Q14145 Kelch-like ECH-associated protein 1 92.96% 82.38%
CHEMBL4072 P07858 Cathepsin B 88.69% 93.67%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 87.21% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 86.15% 94.45%
CHEMBL5608 Q16288 NT-3 growth factor receptor 86.05% 95.89%
CHEMBL333 P08253 Matrix metalloproteinase-2 85.90% 96.31%
CHEMBL3060 Q9Y345 Glycine transporter 2 85.80% 99.17%
CHEMBL3524 P56524 Histone deacetylase 4 85.79% 92.97%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 85.57% 99.23%
CHEMBL1806 P11388 DNA topoisomerase II alpha 85.37% 89.00%
CHEMBL3392948 Q9NP59 Solute carrier family 40 member 1 85.24% 95.00%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 84.69% 93.00%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 83.97% 90.71%
CHEMBL226 P30542 Adenosine A1 receptor 83.71% 95.93%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 83.41% 97.14%
CHEMBL3137262 O60341 LSD1/CoREST complex 83.39% 97.09%
CHEMBL2535 P11166 Glucose transporter 82.99% 98.75%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 82.40% 95.89%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 81.41% 93.03%
CHEMBL1902 P62942 FK506-binding protein 1A 80.85% 97.05%

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.
There are no matching plants.

Cross-Links

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PubChem 139590177
LOTUS LTS0231011
wikiData Q104990474