Nodulapeptin 851

Details

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Internal ID d9cc2429-34cc-405d-affa-b78e5b4bcb6f
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Amino acids, peptides, and analogues > Peptides > Cyclic peptides
IUPAC Name 3-methyl-2-[[7-methyl-3-(2-methylsulfanylethyl)-2,5,8,11,14-pentaoxo-6,9-bis(2-phenylethyl)-12-propan-2-yl-1,4,7,10,13-pentazacyclononadec-15-yl]carbamoylamino]pentanoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C44H65N7O8S/c1-7-29(4)37(43(57)58)50-44(59)48-32-20-14-15-26-45-38(52)33(25-27-60-6)46-40(54)35(24-22-31-18-12-9-13-19-31)51(5)42(56)34(23-21-30-16-10-8-11-17-30)47-41(55)36(28(2)3)49-39(32)53/h8-13,16-19,28-29,32-37H,7,14-15,20-27H2,1-6H3,(H,45,52)(H,46,54)(H,47,55)(H,49,53)(H,57,58)(H2,48,50,59)
InChI Key HZXYJCCVMAKAEX-UHFFFAOYSA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C44H65N7O8S
Molecular Weight 852.10 g/mol
Exact Mass 851.46153323 g/mol
Topological Polar Surface Area (TPSA) 240.00 Ų
XlogP 5.60
Atomic LogP (AlogP) 3.41
H-Bond Acceptor 8
H-Bond Donor 7
Rotatable Bonds 15

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Nodulapeptin 851

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.7371 73.71%
Caco-2 - 0.8662 86.62%
Blood Brain Barrier - 0.7750 77.50%
Human oral bioavailability - 0.6571 65.71%
Subcellular localzation Lysosomes 0.4915 49.15%
OATP2B1 inhibitior - 0.5707 57.07%
OATP1B1 inhibitior + 0.8246 82.46%
OATP1B3 inhibitior + 0.9278 92.78%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior + 0.9331 93.31%
P-glycoprotein inhibitior + 0.7661 76.61%
P-glycoprotein substrate + 0.8279 82.79%
CYP3A4 substrate + 0.6911 69.11%
CYP2C9 substrate + 0.6063 60.63%
CYP2D6 substrate - 0.8687 86.87%
CYP3A4 inhibition - 0.5085 50.85%
CYP2C9 inhibition - 0.6983 69.83%
CYP2C19 inhibition - 0.8304 83.04%
CYP2D6 inhibition - 0.9028 90.28%
CYP1A2 inhibition - 0.9265 92.65%
CYP2C8 inhibition + 0.6576 65.76%
CYP inhibitory promiscuity - 0.9581 95.81%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7900 79.00%
Carcinogenicity (trinary) Non-required 0.6474 64.74%
Eye corrosion - 0.9879 98.79%
Eye irritation - 0.9150 91.50%
Skin irritation - 0.7773 77.73%
Skin corrosion - 0.9373 93.73%
Ames mutagenesis - 0.7300 73.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3877 38.77%
Micronuclear + 0.8000 80.00%
Hepatotoxicity + 0.6054 60.54%
skin sensitisation - 0.8835 88.35%
Respiratory toxicity + 0.8333 83.33%
Reproductive toxicity + 0.7444 74.44%
Mitochondrial toxicity + 0.8250 82.50%
Nephrotoxicity - 0.8350 83.50%
Acute Oral Toxicity (c) III 0.6696 66.96%
Estrogen receptor binding + 0.8319 83.19%
Androgen receptor binding + 0.6785 67.85%
Thyroid receptor binding + 0.5974 59.74%
Glucocorticoid receptor binding + 0.6572 65.72%
Aromatase binding + 0.6166 61.66%
PPAR gamma + 0.7866 78.66%
Honey bee toxicity - 0.8078 80.78%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity - 0.5200 52.00%
Fish aquatic toxicity + 0.9796 97.96%

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 99.88% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 99.07% 96.09%
CHEMBL226 P30542 Adenosine A1 receptor 97.30% 95.93%
CHEMBL4072 P07858 Cathepsin B 92.75% 93.67%
CHEMBL3359 P21462 Formyl peptide receptor 1 92.18% 93.56%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 91.57% 85.14%
CHEMBL5103 Q969S8 Histone deacetylase 10 91.08% 90.08%
CHEMBL221 P23219 Cyclooxygenase-1 90.01% 90.17%
CHEMBL2492 P36544 Neuronal acetylcholine receptor protein alpha-7 subunit 89.59% 88.42%
CHEMBL268 P43235 Cathepsin K 89.37% 96.85%
CHEMBL2693 Q9UIQ6 Cystinyl aminopeptidase 89.37% 97.64%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 89.19% 93.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 89.18% 97.09%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 89.00% 93.03%
CHEMBL1795139 Q8IU80 Transmembrane protease serine 6 88.45% 98.33%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 88.03% 90.71%
CHEMBL3392948 Q9NP59 Solute carrier family 40 member 1 86.78% 95.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 86.67% 94.45%
CHEMBL3202 P48147 Prolyl endopeptidase 86.53% 90.65%
CHEMBL255 P29275 Adenosine A2b receptor 86.16% 98.59%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.26% 95.56%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 84.55% 94.62%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 83.55% 97.14%
CHEMBL4979 P13866 Sodium/glucose cotransporter 1 82.18% 98.24%
CHEMBL3155 P34969 Serotonin 7 (5-HT7) receptor 81.45% 90.71%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 81.21% 91.11%
CHEMBL1949 P62937 Cyclophilin A 80.02% 98.57%

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 146683782
LOTUS LTS0041925
wikiData Q104203254