Pestalotiopyrone K

Details

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Internal ID 5153304a-5cc6-4cdb-a26e-1ab479343de1
Taxonomy Organoheterocyclic compounds > Pyrans > Pyranones and derivatives
IUPAC Name [(2R,3R)-4-acetyloxy-2,3-dihydroxybutyl] (E)-3-(4-methoxy-6-oxopyran-2-yl)but-2-enoate
SMILES (Canonical) CC(=CC(=O)OCC(C(COC(=O)C)O)O)C1=CC(=CC(=O)O1)OC
SMILES (Isomeric) C/C(=C\C(=O)OC[C@H]([C@@H](COC(=O)C)O)O)/C1=CC(=CC(=O)O1)OC
InChI InChI=1S/C16H20O9/c1-9(14-5-11(22-3)6-16(21)25-14)4-15(20)24-8-13(19)12(18)7-23-10(2)17/h4-6,12-13,18-19H,7-8H2,1-3H3/b9-4+/t12-,13-/m1/s1
InChI Key BQIDYCAZPCUFST-BDFMHNHWSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C16H20O9
Molecular Weight 356.32 g/mol
Exact Mass 356.11073221 g/mol
Topological Polar Surface Area (TPSA) 129.00 Ų
XlogP 0.00
Atomic LogP (AlogP) -0.12
H-Bond Acceptor 9
H-Bond Donor 2
Rotatable Bonds 8

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Pestalotiopyrone K

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8840 88.40%
Caco-2 - 0.7267 72.67%
Blood Brain Barrier - 0.6250 62.50%
Human oral bioavailability - 0.6857 68.57%
Subcellular localzation Mitochondria 0.7768 77.68%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8824 88.24%
OATP1B3 inhibitior + 0.9348 93.48%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior + 0.6287 62.87%
P-glycoprotein inhibitior - 0.7374 73.74%
P-glycoprotein substrate - 0.8325 83.25%
CYP3A4 substrate - 0.5000 50.00%
CYP2C9 substrate - 0.8080 80.80%
CYP2D6 substrate - 0.8779 87.79%
CYP3A4 inhibition - 0.8762 87.62%
CYP2C9 inhibition - 0.9097 90.97%
CYP2C19 inhibition - 0.7853 78.53%
CYP2D6 inhibition - 0.8896 88.96%
CYP1A2 inhibition - 0.8207 82.07%
CYP2C8 inhibition - 0.8085 80.85%
CYP inhibitory promiscuity - 0.9582 95.82%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.6642 66.42%
Eye corrosion - 0.9837 98.37%
Eye irritation - 0.9603 96.03%
Skin irritation - 0.7996 79.96%
Skin corrosion - 0.9534 95.34%
Ames mutagenesis - 0.6770 67.70%
Human Ether-a-go-go-Related Gene inhibition - 0.5463 54.63%
Micronuclear - 0.5986 59.86%
Hepatotoxicity - 0.6724 67.24%
skin sensitisation - 0.7695 76.95%
Respiratory toxicity - 0.5667 56.67%
Reproductive toxicity + 0.7222 72.22%
Mitochondrial toxicity - 0.5875 58.75%
Nephrotoxicity - 0.7043 70.43%
Acute Oral Toxicity (c) III 0.6217 62.17%
Estrogen receptor binding + 0.6730 67.30%
Androgen receptor binding + 0.6939 69.39%
Thyroid receptor binding - 0.5075 50.75%
Glucocorticoid receptor binding + 0.7425 74.25%
Aromatase binding + 0.5942 59.42%
PPAR gamma - 0.6119 61.19%
Honey bee toxicity - 0.8694 86.94%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity - 0.6700 67.00%
Fish aquatic toxicity + 0.8804 88.04%

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
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 97.22% 85.14%
CHEMBL4040 P28482 MAP kinase ERK2 96.82% 83.82%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.34% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 95.80% 94.45%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.11% 96.09%
CHEMBL2581 P07339 Cathepsin D 93.26% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 92.55% 99.17%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 91.08% 95.50%
CHEMBL3401 O75469 Pregnane X receptor 88.93% 94.73%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 88.85% 91.07%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.03% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.53% 95.56%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 86.29% 96.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 84.52% 94.00%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 83.42% 92.62%

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.
Garcinia brasiliensis
Hypericum sampsonii
Hypericum scabrum

Cross-Links

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PubChem 71733427
LOTUS LTS0138127
wikiData Q105156889