Pseudomonol

Details

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Internal ID 790657f1-f514-4d01-b0a9-6afa5bf0cc4c
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Polyterpenoids
IUPAC Name 4-amino-3-[(2E,6E)-11,15,19,23,27,31,35-heptahydroxy-3,7,11,15,19,23,27,31,35-nonamethylhexatriaconta-2,6-dienyl]benzoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C52H93NO9/c1-40(19-11-20-41(2)22-23-42-39-43(45(54)55)24-25-44(42)53)21-12-27-47(5,57)29-14-31-49(7,59)33-16-35-51(9,61)37-18-38-52(10,62)36-17-34-50(8,60)32-15-30-48(6,58)28-13-26-46(3,4)56/h19,22,24-25,39,56-62H,11-18,20-21,23,26-38,53H2,1-10H3,(H,54,55)/b40-19+,41-22+
InChI Key MPSCWAUCNYKYOU-HLOLQSLYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C52H93NO9
Molecular Weight 876.30 g/mol
Exact Mass 875.68503354 g/mol
Topological Polar Surface Area (TPSA) 205.00 Ų
XlogP 8.90
Atomic LogP (AlogP) 10.65
H-Bond Acceptor 9
H-Bond Donor 9
Rotatable Bonds 34

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Pseudomonol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9803 98.03%
Caco-2 - 0.8474 84.74%
Blood Brain Barrier - 0.5750 57.50%
Human oral bioavailability + 0.6000 60.00%
Subcellular localzation Mitochondria 0.6262 62.62%
OATP2B1 inhibitior - 0.5749 57.49%
OATP1B1 inhibitior + 0.8810 88.10%
OATP1B3 inhibitior + 0.9191 91.91%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior + 0.8996 89.96%
P-glycoprotein inhibitior + 0.7281 72.81%
P-glycoprotein substrate - 0.5829 58.29%
CYP3A4 substrate + 0.5059 50.59%
CYP2C9 substrate - 0.8086 80.86%
CYP2D6 substrate - 0.8148 81.48%
CYP3A4 inhibition - 0.6785 67.85%
CYP2C9 inhibition - 0.7198 71.98%
CYP2C19 inhibition - 0.7204 72.04%
CYP2D6 inhibition - 0.8800 88.00%
CYP1A2 inhibition - 0.6869 68.69%
CYP2C8 inhibition + 0.5615 56.15%
CYP inhibitory promiscuity - 0.6602 66.02%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.7055 70.55%
Carcinogenicity (trinary) Non-required 0.6561 65.61%
Eye corrosion - 0.9921 99.21%
Eye irritation - 0.8985 89.85%
Skin irritation - 0.7433 74.33%
Skin corrosion - 0.9599 95.99%
Ames mutagenesis - 0.6200 62.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4202 42.02%
Micronuclear + 0.5300 53.00%
Hepatotoxicity - 0.6125 61.25%
skin sensitisation - 0.7222 72.22%
Respiratory toxicity - 0.5667 56.67%
Reproductive toxicity + 0.6802 68.02%
Mitochondrial toxicity + 0.6750 67.50%
Nephrotoxicity - 0.7613 76.13%
Acute Oral Toxicity (c) III 0.6181 61.81%
Estrogen receptor binding + 0.7354 73.54%
Androgen receptor binding + 0.6636 66.36%
Thyroid receptor binding + 0.5507 55.07%
Glucocorticoid receptor binding + 0.6446 64.46%
Aromatase binding + 0.6287 62.87%
PPAR gamma + 0.6894 68.94%
Honey bee toxicity - 0.9044 90.44%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.6852 68.52%
Fish aquatic toxicity + 0.9961 99.61%

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
CHEMBL4040 P28482 MAP kinase ERK2 97.56% 83.82%
CHEMBL1293249 Q13887 Kruppel-like factor 5 94.55% 86.33%
CHEMBL3401 O75469 Pregnane X receptor 94.24% 94.73%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.97% 91.11%
CHEMBL3060 Q9Y345 Glycine transporter 2 92.25% 99.17%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 92.06% 92.08%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.99% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.75% 95.56%
CHEMBL2581 P07339 Cathepsin D 88.14% 98.95%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 86.07% 96.95%
CHEMBL2039 P27338 Monoamine oxidase B 85.83% 92.51%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 82.59% 94.42%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 80.97% 96.00%

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 146684638
LOTUS LTS0148563
wikiData Q105169705