Aeruginosin NOL1

Details

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Internal ID 8523a8ad-c063-4fed-94c1-b230470aab60
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Amino acids, peptides, and analogues > N-acyl-alpha amino acids and derivatives
IUPAC Name (2S,3aS,7aS)-1-[(2S)-2-acetamido-3-(4-hydroxyphenyl)propanoyl]-N-[5-(diaminomethylideneamino)-1-hydroxypentan-2-yl]-6-hydroxy-2,3,3a,4,5,6,7,7a-octahydroindole-2-carboxamide
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C26H40N6O6/c1-15(34)30-21(11-16-4-7-19(35)8-5-16)25(38)32-22-13-20(36)9-6-17(22)12-23(32)24(37)31-18(14-33)3-2-10-29-26(27)28/h4-5,7-8,17-18,20-23,33,35-36H,2-3,6,9-14H2,1H3,(H,30,34)(H,31,37)(H4,27,28,29)/t17-,18?,20?,21-,22-,23-/m0/s1
InChI Key KOYXPKZSNNFPER-CUTKURBCSA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C26H40N6O6
Molecular Weight 532.60 g/mol
Exact Mass 532.30093302 g/mol
Topological Polar Surface Area (TPSA) 204.00 Ų
XlogP -0.70
Atomic LogP (AlogP) -0.90
H-Bond Acceptor 7
H-Bond Donor 7
Rotatable Bonds 11

Synonyms

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DTXSID201046279

2D Structure

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2D Structure of Aeruginosin NOL1

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9408 94.08%
Caco-2 - 0.8776 87.76%
Blood Brain Barrier - 0.5750 57.50%
Human oral bioavailability - 0.7857 78.57%
Subcellular localzation Mitochondria 0.6808 68.08%
OATP2B1 inhibitior - 0.8580 85.80%
OATP1B1 inhibitior + 0.8819 88.19%
OATP1B3 inhibitior + 0.9418 94.18%
MATE1 inhibitior - 0.7800 78.00%
OCT2 inhibitior - 0.5250 52.50%
BSEP inhibitior + 0.7949 79.49%
P-glycoprotein inhibitior + 0.5911 59.11%
P-glycoprotein substrate + 0.8941 89.41%
CYP3A4 substrate + 0.7260 72.60%
CYP2C9 substrate - 0.6150 61.50%
CYP2D6 substrate - 0.7649 76.49%
CYP3A4 inhibition - 0.6452 64.52%
CYP2C9 inhibition - 0.8586 85.86%
CYP2C19 inhibition - 0.8161 81.61%
CYP2D6 inhibition - 0.9104 91.04%
CYP1A2 inhibition - 0.8890 88.90%
CYP2C8 inhibition - 0.6200 62.00%
CYP inhibitory promiscuity - 0.9437 94.37%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.8900 89.00%
Carcinogenicity (trinary) Non-required 0.6110 61.10%
Eye corrosion - 0.9889 98.89%
Eye irritation - 0.9685 96.85%
Skin irritation - 0.7741 77.41%
Skin corrosion - 0.9270 92.70%
Ames mutagenesis + 0.5430 54.30%
Human Ether-a-go-go-Related Gene inhibition - 0.5000 50.00%
Micronuclear + 0.8800 88.00%
Hepatotoxicity - 0.5821 58.21%
skin sensitisation - 0.8650 86.50%
Respiratory toxicity + 0.8778 87.78%
Reproductive toxicity + 0.9444 94.44%
Mitochondrial toxicity + 0.9125 91.25%
Nephrotoxicity + 0.5189 51.89%
Acute Oral Toxicity (c) III 0.6385 63.85%
Estrogen receptor binding + 0.6470 64.70%
Androgen receptor binding + 0.6155 61.55%
Thyroid receptor binding - 0.5765 57.65%
Glucocorticoid receptor binding + 0.6481 64.81%
Aromatase binding + 0.5874 58.74%
PPAR gamma + 0.6119 61.19%
Honey bee toxicity - 0.8091 80.91%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.6549 65.49%
Fish aquatic toxicity - 0.4526 45.26%

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 99.21% 96.09%
CHEMBL2581 P07339 Cathepsin D 98.98% 98.95%
CHEMBL4040 P28482 MAP kinase ERK2 98.36% 83.82%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.18% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 95.73% 94.45%
CHEMBL3137262 O60341 LSD1/CoREST complex 94.40% 97.09%
CHEMBL259 P32245 Melanocortin receptor 4 94.02% 95.38%
CHEMBL2107 P61073 C-X-C chemokine receptor type 4 93.52% 93.10%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 93.21% 97.21%
CHEMBL340 P08684 Cytochrome P450 3A4 93.14% 91.19%
CHEMBL3837 P07711 Cathepsin L 92.21% 96.61%
CHEMBL2514 O95665 Neurotensin receptor 2 92.06% 100.00%
CHEMBL249 P25103 Neurokinin 1 receptor 91.86% 99.17%
CHEMBL3060 Q9Y345 Glycine transporter 2 91.33% 99.17%
CHEMBL5608 Q16288 NT-3 growth factor receptor 91.31% 95.89%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 90.31% 95.89%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 89.08% 90.71%
CHEMBL1255126 O15151 Protein Mdm4 88.35% 90.20%
CHEMBL4777 P25929 Neuropeptide Y receptor type 1 88.26% 96.67%
CHEMBL2693 Q9UIQ6 Cystinyl aminopeptidase 87.22% 97.64%
CHEMBL4227 P25090 Lipoxin A4 receptor 87.14% 100.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.20% 95.56%
CHEMBL1795139 Q8IU80 Transmembrane protease serine 6 86.16% 98.33%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 84.71% 100.00%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 83.92% 93.00%
CHEMBL301 P24941 Cyclin-dependent kinase 2 83.30% 91.23%
CHEMBL4123 P30989 Neurotensin receptor 1 81.37% 96.67%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 81.10% 91.81%
CHEMBL2535 P11166 Glucose transporter 80.63% 98.75%

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 146683739
LOTUS LTS0119928
wikiData Q104203019