Pieristoxin J

Details

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Internal ID 49bbe82e-5a29-4756-acc4-f53ccd9d60f2
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids > Grayanoids
IUPAC Name [(1R,2S,3R,4R,6R,8S,9R,10S,11S,14R,15R,17R)-2,4,10,11,15,17-hexahydroxy-5,5,10,15-tetramethyl-7-oxapentacyclo[12.2.1.01,11.04,9.06,8]heptadecan-3-yl] acetate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C22H34O9/c1-9(23)30-16-14(25)20-8-18(4,26)10(13(20)24)6-7-21(20,28)19(5,27)12-11-15(31-11)17(2,3)22(12,16)29/h10-16,24-29H,6-8H2,1-5H3/t10-,11+,12+,13-,14-,15+,16-,18-,19+,20-,21-,22+/m1/s1
InChI Key XRCWCMXMUOHEKM-TYUXWFJVSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C22H34O9
Molecular Weight 442.50 g/mol
Exact Mass 442.22028266 g/mol
Topological Polar Surface Area (TPSA) 160.00 Ų
XlogP -1.80
Atomic LogP (AlogP) -1.16
H-Bond Acceptor 9
H-Bond Donor 6
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Pieristoxin J

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8190 81.90%
Caco-2 - 0.7830 78.30%
Blood Brain Barrier - 0.6750 67.50%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Mitochondria 0.6406 64.06%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8833 88.33%
OATP1B3 inhibitior + 0.9222 92.22%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.7821 78.21%
BSEP inhibitior - 0.9190 91.90%
P-glycoprotein inhibitior - 0.7299 72.99%
P-glycoprotein substrate - 0.7298 72.98%
CYP3A4 substrate + 0.7146 71.46%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8488 84.88%
CYP3A4 inhibition - 0.6786 67.86%
CYP2C9 inhibition - 0.7319 73.19%
CYP2C19 inhibition - 0.7485 74.85%
CYP2D6 inhibition - 0.9418 94.18%
CYP1A2 inhibition - 0.7159 71.59%
CYP2C8 inhibition - 0.7029 70.29%
CYP inhibitory promiscuity - 0.9772 97.72%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.7086 70.86%
Eye corrosion - 0.9891 98.91%
Eye irritation - 0.9446 94.46%
Skin irritation - 0.5825 58.25%
Skin corrosion - 0.9088 90.88%
Ames mutagenesis - 0.7200 72.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5123 51.23%
Micronuclear - 0.7100 71.00%
Hepatotoxicity - 0.5162 51.62%
skin sensitisation - 0.8439 84.39%
Respiratory toxicity + 0.6111 61.11%
Reproductive toxicity + 0.8000 80.00%
Mitochondrial toxicity + 0.8250 82.50%
Nephrotoxicity + 0.6098 60.98%
Acute Oral Toxicity (c) III 0.3806 38.06%
Estrogen receptor binding + 0.8533 85.33%
Androgen receptor binding + 0.7118 71.18%
Thyroid receptor binding + 0.6129 61.29%
Glucocorticoid receptor binding + 0.6302 63.02%
Aromatase binding + 0.7212 72.12%
PPAR gamma + 0.6171 61.71%
Honey bee toxicity - 0.7797 77.97%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.5455 54.55%
Fish aquatic toxicity + 0.9454 94.54%

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
CHEMBL253 P34972 Cannabinoid CB2 receptor 98.03% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.09% 96.09%
CHEMBL1994 P08235 Mineralocorticoid receptor 89.49% 100.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 86.59% 91.11%
CHEMBL4208 P20618 Proteasome component C5 85.59% 90.00%
CHEMBL4227 P25090 Lipoxin A4 receptor 85.42% 100.00%
CHEMBL2581 P07339 Cathepsin D 85.41% 98.95%
CHEMBL5608 Q16288 NT-3 growth factor receptor 83.57% 95.89%
CHEMBL5028 O14672 ADAM10 82.91% 97.50%
CHEMBL1806 P11388 DNA topoisomerase II alpha 82.38% 89.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 81.70% 94.45%
CHEMBL1293249 Q13887 Kruppel-like factor 5 80.97% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 80.84% 95.56%
CHEMBL2996 Q05655 Protein kinase C delta 80.80% 97.79%
CHEMBL340 P08684 Cytochrome P450 3A4 80.56% 91.19%
CHEMBL5646 Q6L5J4 FML2_HUMAN 80.51% 100.00%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 80.46% 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.
Pieris japonica

Cross-Links

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PubChem 101229269
LOTUS LTS0066541
wikiData Q105340377