Nodulapeptin 823

Details

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Internal ID 6bb0e72b-c629-4126-9505-743e07784a26
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Amino acids, peptides, and analogues > Peptides > Cyclic peptides
IUPAC Name 2-[[3-(hydroxymethyl)-6-[2-(4-hydroxyphenyl)ethyl]-7-methyl-2,5,8,11,14-pentaoxo-9-(2-phenylethyl)-12-propan-2-yl-1,4,7,10,13-pentazacyclononadec-15-yl]carbamoylamino]-3-methylpentanoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C42H61N7O10/c1-6-26(4)35(41(57)58)48-42(59)46-30-14-10-11-23-43-36(52)32(24-50)45-38(54)33(22-18-28-15-19-29(51)20-16-28)49(5)40(56)31(21-17-27-12-8-7-9-13-27)44-39(55)34(25(2)3)47-37(30)53/h7-9,12-13,15-16,19-20,25-26,30-35,50-51H,6,10-11,14,17-18,21-24H2,1-5H3,(H,43,52)(H,44,55)(H,45,54)(H,47,53)(H,57,58)(H2,46,48,59)
InChI Key UOBGMYUXNSKBFF-UHFFFAOYSA-N
Popularity 5 references in papers

Physical and Chemical Properties

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Molecular Formula C42H61N7O10
Molecular Weight 824.00 g/mol
Exact Mass 823.44799117 g/mol
Topological Polar Surface Area (TPSA) 256.00 Ų
XlogP 4.10
Atomic LogP (AlogP) 1.35
H-Bond Acceptor 9
H-Bond Donor 9
Rotatable Bonds 13

Synonyms

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DTXSID801334753

2D Structure

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2D Structure of Nodulapeptin 823

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.7634 76.34%
Caco-2 - 0.8745 87.45%
Blood Brain Barrier - 0.8500 85.00%
Human oral bioavailability - 0.7143 71.43%
Subcellular localzation Mitochondria 0.5394 53.94%
OATP2B1 inhibitior - 0.5741 57.41%
OATP1B1 inhibitior + 0.8191 81.91%
OATP1B3 inhibitior + 0.9189 91.89%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior + 0.8932 89.32%
P-glycoprotein inhibitior + 0.7452 74.52%
P-glycoprotein substrate + 0.8438 84.38%
CYP3A4 substrate + 0.6958 69.58%
CYP2C9 substrate + 0.6054 60.54%
CYP2D6 substrate - 0.8497 84.97%
CYP3A4 inhibition + 0.6967 69.67%
CYP2C9 inhibition - 0.7340 73.40%
CYP2C19 inhibition - 0.7922 79.22%
CYP2D6 inhibition - 0.8747 87.47%
CYP1A2 inhibition - 0.8993 89.93%
CYP2C8 inhibition + 0.6883 68.83%
CYP inhibitory promiscuity - 0.8793 87.93%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.8100 81.00%
Carcinogenicity (trinary) Non-required 0.6449 64.49%
Eye corrosion - 0.9868 98.68%
Eye irritation - 0.9132 91.32%
Skin irritation - 0.7775 77.75%
Skin corrosion - 0.9365 93.65%
Ames mutagenesis - 0.6900 69.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3922 39.22%
Micronuclear + 0.8600 86.00%
Hepatotoxicity + 0.5804 58.04%
skin sensitisation - 0.8765 87.65%
Respiratory toxicity + 0.8333 83.33%
Reproductive toxicity + 0.8333 83.33%
Mitochondrial toxicity + 0.7750 77.50%
Nephrotoxicity - 0.8525 85.25%
Acute Oral Toxicity (c) III 0.6668 66.68%
Estrogen receptor binding + 0.8295 82.95%
Androgen receptor binding + 0.7275 72.75%
Thyroid receptor binding + 0.5928 59.28%
Glucocorticoid receptor binding + 0.6137 61.37%
Aromatase binding + 0.5896 58.96%
PPAR gamma + 0.7705 77.05%
Honey bee toxicity - 0.8125 81.25%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.5700 57.00%
Fish aquatic toxicity + 0.9576 95.76%

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%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 98.81% 96.09%
CHEMBL268 P43235 Cathepsin K 97.20% 96.85%
CHEMBL226 P30542 Adenosine A1 receptor 96.53% 95.93%
CHEMBL4072 P07858 Cathepsin B 93.70% 93.67%
CHEMBL5103 Q969S8 Histone deacetylase 10 93.53% 90.08%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 92.72% 94.62%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 90.21% 94.45%
CHEMBL3359 P21462 Formyl peptide receptor 1 89.81% 93.56%
CHEMBL3137262 O60341 LSD1/CoREST complex 89.28% 97.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 88.73% 91.11%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 88.02% 93.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.74% 95.56%
CHEMBL2693 Q9UIQ6 Cystinyl aminopeptidase 87.06% 97.64%
CHEMBL2095172 P14867 GABA-A receptor; alpha-1/beta-2/gamma-2 86.99% 92.67%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 85.07% 90.71%
CHEMBL5608 Q16288 NT-3 growth factor receptor 83.81% 95.89%
CHEMBL3392948 Q9NP59 Solute carrier family 40 member 1 82.93% 95.00%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 82.05% 95.50%
CHEMBL1806 P11388 DNA topoisomerase II alpha 81.81% 89.00%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 81.67% 100.00%
CHEMBL218 P21554 Cannabinoid CB1 receptor 81.14% 96.61%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 81.12% 97.14%
CHEMBL253 P34972 Cannabinoid CB2 receptor 81.10% 97.25%
CHEMBL1949 P62937 Cyclophilin A 80.85% 98.57%
CHEMBL2514 O95665 Neurotensin receptor 2 80.40% 100.00%
CHEMBL216 P11229 Muscarinic acetylcholine receptor M1 80.15% 94.23%

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 146684902
LOTUS LTS0059153
wikiData Q104246157