Tripropeptin aiC

Details

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Internal ID 3b0384f1-beb2-4871-9599-b2b1c3061c88
Taxonomy Organic acids and derivatives > Peptidomimetics > Depsipeptides > Cyclic depsipeptides
IUPAC Name (2R)-2-[(1R,7S,10S,13R,16S,21S,22S,25S,28R,32R)-25-[(S)-carboxy(hydroxy)methyl]-10-[3-(diaminomethylideneamino)propyl]-21-hydroxy-32-[(1R)-1-hydroxyethyl]-16-(hydroxymethyl)-28-(9-methylundecyl)-2,8,11,14,17,23,26,30,33-nonaoxo-27-oxa-3,9,12,15,18,24,31,34-octazatetracyclo[32.3.0.03,7.018,22]heptatriacontan-13-yl]-2-hydroxyacetic acid
SMILES (Canonical) CCC(C)CCCCCCCCC1CC(=O)NC(C(=O)N2CCCC2C(=O)N3CCCC3C(=O)NC(C(=O)NC(C(=O)NC(C(=O)N4CCC(C4C(=O)NC(C(=O)O1)C(C(=O)O)O)O)CO)C(C(=O)O)O)CCCN=C(N)N)C(C)O
SMILES (Isomeric) CCC(C)CCCCCCCC[C@@H]1CC(=O)N[C@@H](C(=O)N2CCC[C@@H]2C(=O)N3CCC[C@H]3C(=O)N[C@H](C(=O)N[C@@H](C(=O)N[C@H](C(=O)N4CC[C@@H]([C@H]4C(=O)N[C@H](C(=O)O1)[C@@H](C(=O)O)O)O)CO)[C@H](C(=O)O)O)CCCN=C(N)N)[C@@H](C)O
InChI InChI=1S/C51H83N11O19/c1-4-26(2)14-9-7-5-6-8-10-15-28-24-34(66)57-35(27(3)64)47(75)61-22-13-18-32(61)46(74)60-21-12-17-31(60)42(70)55-29(16-11-20-54-51(52)53)41(69)58-36(39(67)48(76)77)43(71)56-30(25-63)45(73)62-23-19-33(65)38(62)44(72)59-37(50(80)81-28)40(68)49(78)79/h26-33,35-40,63-65,67-68H,4-25H2,1-3H3,(H,55,70)(H,56,71)(H,57,66)(H,58,69)(H,59,72)(H,76,77)(H,78,79)(H4,52,53,54)/t26?,27-,28-,29+,30+,31+,32-,33+,35-,36-,37+,38+,39-,40+/m1/s1
InChI Key WSVZUQYMNNHNBK-AGAWFILRSA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C51H83N11O19
Molecular Weight 1154.30 g/mol
Exact Mass 1153.58666946 g/mol
Topological Polar Surface Area (TPSA) 473.00 Ų
XlogP 0.10
Atomic LogP (AlogP) -4.85
H-Bond Acceptor 18
H-Bond Donor 14
Rotatable Bonds 20

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Tripropeptin aiC

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.4582 45.82%
Caco-2 - 0.8584 85.84%
Blood Brain Barrier - 0.8000 80.00%
Human oral bioavailability - 0.6857 68.57%
Subcellular localzation Lysosomes 0.6114 61.14%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8325 83.25%
OATP1B3 inhibitior + 0.9311 93.11%
MATE1 inhibitior - 0.8000 80.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior + 0.9006 90.06%
P-glycoprotein inhibitior + 0.7425 74.25%
P-glycoprotein substrate + 0.8527 85.27%
CYP3A4 substrate + 0.7200 72.00%
CYP2C9 substrate - 0.6038 60.38%
CYP2D6 substrate - 0.8413 84.13%
CYP3A4 inhibition - 0.9345 93.45%
CYP2C9 inhibition - 0.8934 89.34%
CYP2C19 inhibition - 0.8819 88.19%
CYP2D6 inhibition - 0.8972 89.72%
CYP1A2 inhibition - 0.8801 88.01%
CYP2C8 inhibition + 0.6825 68.25%
CYP inhibitory promiscuity - 0.9943 99.43%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.8700 87.00%
Carcinogenicity (trinary) Non-required 0.5586 55.86%
Eye corrosion - 0.9840 98.40%
Eye irritation - 0.8976 89.76%
Skin irritation - 0.7631 76.31%
Skin corrosion - 0.9199 91.99%
Ames mutagenesis - 0.5700 57.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3956 39.56%
Micronuclear + 0.8400 84.00%
Hepatotoxicity + 0.6250 62.50%
skin sensitisation - 0.8399 83.99%
Respiratory toxicity + 0.7333 73.33%
Reproductive toxicity + 0.8444 84.44%
Mitochondrial toxicity + 0.8125 81.25%
Nephrotoxicity + 0.7318 73.18%
Acute Oral Toxicity (c) III 0.5864 58.64%
Estrogen receptor binding + 0.7582 75.82%
Androgen receptor binding + 0.7160 71.60%
Thyroid receptor binding + 0.5680 56.80%
Glucocorticoid receptor binding + 0.6087 60.87%
Aromatase binding + 0.6514 65.14%
PPAR gamma + 0.7292 72.92%
Honey bee toxicity - 0.7664 76.64%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.6937 69.37%
Fish aquatic toxicity - 0.5793 57.93%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 99.55% 96.09%
CHEMBL2581 P07339 Cathepsin D 99.41% 98.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 97.63% 94.45%
CHEMBL4040 P28482 MAP kinase ERK2 96.58% 83.82%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.32% 91.11%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 94.72% 90.71%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 94.23% 100.00%
CHEMBL2069156 Q14145 Kelch-like ECH-associated protein 1 93.76% 82.38%
CHEMBL204 P00734 Thrombin 93.64% 96.01%
CHEMBL3137262 O60341 LSD1/CoREST complex 93.44% 97.09%
CHEMBL2443 P49862 Kallikrein 7 92.50% 94.00%
CHEMBL1902 P62942 FK506-binding protein 1A 92.25% 97.05%
CHEMBL5608 Q16288 NT-3 growth factor receptor 92.03% 95.89%
CHEMBL2693 Q9UIQ6 Cystinyl aminopeptidase 91.68% 97.64%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.85% 95.56%
CHEMBL3359 P21462 Formyl peptide receptor 1 90.69% 93.56%
CHEMBL5103 Q969S8 Histone deacetylase 10 90.67% 90.08%
CHEMBL4685 P14902 Indoleamine 2,3-dioxygenase 90.07% 96.38%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 89.69% 95.50%
CHEMBL4588 P22894 Matrix metalloproteinase 8 89.27% 94.66%
CHEMBL3060 Q9Y345 Glycine transporter 2 89.07% 99.17%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 88.83% 93.00%
CHEMBL3837 P07711 Cathepsin L 87.17% 96.61%
CHEMBL2514 O95665 Neurotensin receptor 2 86.36% 100.00%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 86.21% 93.03%
CHEMBL3524 P56524 Histone deacetylase 4 85.48% 92.97%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 85.45% 85.14%
CHEMBL3392948 Q9NP59 Solute carrier family 40 member 1 84.96% 95.00%
CHEMBL1907605 P24864 Cyclin-dependent kinase 2/cyclin E1 84.92% 92.88%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 84.59% 99.23%
CHEMBL274 P51681 C-C chemokine receptor type 5 84.16% 98.77%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 83.93% 96.47%
CHEMBL1293249 Q13887 Kruppel-like factor 5 82.62% 86.33%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 82.54% 91.81%
CHEMBL1795139 Q8IU80 Transmembrane protease serine 6 82.51% 98.33%
CHEMBL4581 P52732 Kinesin-like protein 1 82.13% 93.18%
CHEMBL4227 P25090 Lipoxin A4 receptor 80.60% 100.00%
CHEMBL4296 Q15858 Sodium channel protein type IX alpha subunit 80.47% 96.11%
CHEMBL3310 Q96DB2 Histone deacetylase 11 80.16% 88.56%
CHEMBL1801 P00747 Plasminogen 80.08% 92.44%
CHEMBL4394 Q9NYA1 Sphingosine kinase 1 80.02% 96.03%

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 139588453
LOTUS LTS0253816
wikiData Q105312171