Pestaloficiol T

Details

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Internal ID 21dc8147-dc2b-4931-b630-1ed1b85608c6
Taxonomy Benzenoids > Benzene and substituted derivatives > Diphenylethers
IUPAC Name [(1S)-1-[3-(hydroxymethyl)-4-methoxy-6-oxopyran-2-yl]heptyl] 2-hydroxy-6-(2-hydroxy-4-methoxy-6-methoxycarbonylphenoxy)-4-methylbenzoate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C31H36O12/c1-6-7-8-9-10-23(29-20(16-32)24(39-4)15-26(35)43-29)42-31(37)27-21(33)11-17(2)12-25(27)41-28-19(30(36)40-5)13-18(38-3)14-22(28)34/h11-15,23,32-34H,6-10,16H2,1-5H3/t23-/m0/s1
InChI Key XCYKAMMGHWDGSQ-QHCPKHFHSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C31H36O12
Molecular Weight 600.60 g/mol
Exact Mass 600.22067658 g/mol
Topological Polar Surface Area (TPSA) 167.00 Ų
XlogP 5.00
Atomic LogP (AlogP) 5.32
H-Bond Acceptor 12
H-Bond Donor 3
Rotatable Bonds 14

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Pestaloficiol T

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8942 89.42%
Caco-2 - 0.7491 74.91%
Blood Brain Barrier - 0.5500 55.00%
Human oral bioavailability - 0.6000 60.00%
Subcellular localzation Mitochondria 0.8681 86.81%
OATP2B1 inhibitior - 0.8591 85.91%
OATP1B1 inhibitior + 0.7994 79.94%
OATP1B3 inhibitior + 0.8011 80.11%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.6250 62.50%
BSEP inhibitior + 0.9873 98.73%
P-glycoprotein inhibitior + 0.8632 86.32%
P-glycoprotein substrate + 0.6223 62.23%
CYP3A4 substrate + 0.6616 66.16%
CYP2C9 substrate + 0.6400 64.00%
CYP2D6 substrate - 0.8587 85.87%
CYP3A4 inhibition + 0.5705 57.05%
CYP2C9 inhibition - 0.8506 85.06%
CYP2C19 inhibition + 0.5708 57.08%
CYP2D6 inhibition - 0.9276 92.76%
CYP1A2 inhibition - 0.5488 54.88%
CYP2C8 inhibition + 0.8091 80.91%
CYP inhibitory promiscuity - 0.8190 81.90%
UGT catelyzed - 0.9000 90.00%
Carcinogenicity (binary) - 0.9000 90.00%
Carcinogenicity (trinary) Non-required 0.7579 75.79%
Eye corrosion - 0.9924 99.24%
Eye irritation - 0.9183 91.83%
Skin irritation - 0.8603 86.03%
Skin corrosion - 0.9677 96.77%
Ames mutagenesis - 0.7500 75.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7110 71.10%
Micronuclear - 0.8100 81.00%
Hepatotoxicity + 0.5214 52.14%
skin sensitisation - 0.9188 91.88%
Respiratory toxicity + 0.5667 56.67%
Reproductive toxicity + 0.5556 55.56%
Mitochondrial toxicity - 0.6375 63.75%
Nephrotoxicity + 0.5720 57.20%
Acute Oral Toxicity (c) III 0.6547 65.47%
Estrogen receptor binding + 0.7920 79.20%
Androgen receptor binding + 0.7423 74.23%
Thyroid receptor binding - 0.5109 51.09%
Glucocorticoid receptor binding + 0.8408 84.08%
Aromatase binding + 0.6141 61.41%
PPAR gamma + 0.6013 60.13%
Honey bee toxicity - 0.8321 83.21%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity + 0.6963 69.63%
Fish aquatic toxicity + 0.9837 98.37%

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
CHEMBL3060 Q9Y345 Glycine transporter 2 97.53% 99.17%
CHEMBL2581 P07339 Cathepsin D 96.91% 98.95%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 96.83% 95.17%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.70% 91.11%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 93.48% 95.50%
CHEMBL3401 O75469 Pregnane X receptor 92.31% 94.73%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.85% 96.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 91.72% 94.45%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 91.63% 96.95%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 89.82% 97.21%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 89.49% 92.08%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 88.68% 94.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.44% 95.56%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 87.32% 99.23%
CHEMBL2535 P11166 Glucose transporter 87.04% 98.75%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 86.99% 90.71%
CHEMBL340 P08684 Cytochrome P450 3A4 86.29% 91.19%
CHEMBL3976 Q9UHL4 Dipeptidyl peptidase II 85.31% 92.29%
CHEMBL3192 Q9BY41 Histone deacetylase 8 83.41% 93.99%
CHEMBL5979 P05186 Alkaline phosphatase, tissue-nonspecific isozyme 83.04% 85.40%
CHEMBL3359 P21462 Formyl peptide receptor 1 82.54% 93.56%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 81.99% 96.00%
CHEMBL5163 Q9NY46 Sodium channel protein type III alpha subunit 81.96% 96.90%
CHEMBL1293249 Q13887 Kruppel-like factor 5 81.52% 86.33%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 81.45% 91.07%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 81.02% 97.29%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 80.48% 99.15%

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 139585903
LOTUS LTS0125362
wikiData Q77494473