Oxypaeonidanin

Details

Top
Internal ID 99fe1b1c-150c-4ec9-a9de-595009fd1c08
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Terpene glycosides
IUPAC Name [(1R,3R,6S,8S,9S)-8-methoxy-6-methyl-4-oxo-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-7-oxatricyclo[4.3.0.03,9]nonan-9-yl]methyl 4-hydroxybenzoate
SMILES (Canonical) CC12CC(=O)C3CC1(C3(C(O2)OC)COC(=O)C4=CC=C(C=C4)O)OC5C(C(C(C(O5)CO)O)O)O
SMILES (Isomeric) C[C@]12CC(=O)[C@@H]3C[C@]1([C@@]3([C@H](O2)OC)COC(=O)C4=CC=C(C=C4)O)O[C@H]5[C@@H]([C@H]([C@@H]([C@H](O5)CO)O)O)O
InChI InChI=1S/C24H30O12/c1-22-8-14(27)13-7-24(22,35-20-18(30)17(29)16(28)15(9-25)34-20)23(13,21(32-2)36-22)10-33-19(31)11-3-5-12(26)6-4-11/h3-6,13,15-18,20-21,25-26,28-30H,7-10H2,1-2H3/t13-,15+,16+,17-,18+,20-,21-,22-,23-,24-/m0/s1
InChI Key WNFREEOKSZROFI-RIXLYZTQSA-N
Popularity 2 references in papers

Physical and Chemical Properties

Top
Molecular Formula C24H30O12
Molecular Weight 510.50 g/mol
Exact Mass 510.17372639 g/mol
Topological Polar Surface Area (TPSA) 181.00 Ų
XlogP -1.30
Atomic LogP (AlogP) -1.16
H-Bond Acceptor 12
H-Bond Donor 5
Rotatable Bonds 7

Synonyms

Top
CHEMBL2205282

2D Structure

Top
2D Structure of Oxypaeonidanin

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.6347 63.47%
Caco-2 - 0.8214 82.14%
Blood Brain Barrier - 0.5750 57.50%
Human oral bioavailability - 0.8429 84.29%
Subcellular localzation Mitochondria 0.6403 64.03%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8563 85.63%
OATP1B3 inhibitior + 0.9416 94.16%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.4874 48.74%
P-glycoprotein inhibitior - 0.5555 55.55%
P-glycoprotein substrate - 0.5935 59.35%
CYP3A4 substrate + 0.6839 68.39%
CYP2C9 substrate - 0.8028 80.28%
CYP2D6 substrate - 0.8713 87.13%
CYP3A4 inhibition - 0.7869 78.69%
CYP2C9 inhibition - 0.8820 88.20%
CYP2C19 inhibition - 0.7908 79.08%
CYP2D6 inhibition - 0.9345 93.45%
CYP1A2 inhibition - 0.8693 86.93%
CYP2C8 inhibition + 0.6710 67.10%
CYP inhibitory promiscuity - 0.9172 91.72%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.5944 59.44%
Eye corrosion - 0.9887 98.87%
Eye irritation - 0.9451 94.51%
Skin irritation - 0.7787 77.87%
Skin corrosion - 0.9385 93.85%
Ames mutagenesis - 0.7200 72.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5183 51.83%
Micronuclear - 0.6600 66.00%
Hepatotoxicity - 0.7272 72.72%
skin sensitisation - 0.8840 88.40%
Respiratory toxicity + 0.5778 57.78%
Reproductive toxicity + 0.8444 84.44%
Mitochondrial toxicity + 0.7125 71.25%
Nephrotoxicity - 0.5708 57.08%
Acute Oral Toxicity (c) III 0.3740 37.40%
Estrogen receptor binding + 0.7903 79.03%
Androgen receptor binding + 0.7721 77.21%
Thyroid receptor binding + 0.5428 54.28%
Glucocorticoid receptor binding + 0.6686 66.86%
Aromatase binding + 0.6826 68.26%
PPAR gamma + 0.6377 63.77%
Honey bee toxicity - 0.7597 75.97%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.7300 73.00%
Fish aquatic toxicity + 0.9670 96.70%

Targets

Top

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.51% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.44% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 94.58% 97.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 93.65% 86.33%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.51% 99.17%
CHEMBL5608 Q16288 NT-3 growth factor receptor 86.97% 95.89%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 86.67% 94.00%
CHEMBL3476 O15111 Inhibitor of nuclear factor kappa B kinase alpha subunit 86.29% 95.83%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.11% 95.56%
CHEMBL5852 Q96P65 Pyroglutamylated RFamide peptide receptor 86.05% 85.00%
CHEMBL5255 O00206 Toll-like receptor 4 85.93% 92.50%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 85.00% 94.45%
CHEMBL2581 P07339 Cathepsin D 84.82% 98.95%
CHEMBL2996 Q05655 Protein kinase C delta 84.35% 97.79%
CHEMBL1994 P08235 Mineralocorticoid receptor 84.08% 100.00%
CHEMBL3437 Q16853 Amine oxidase, copper containing 83.95% 94.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 82.29% 89.00%
CHEMBL4208 P20618 Proteasome component C5 82.22% 90.00%
CHEMBL3401 O75469 Pregnane X receptor 82.11% 94.73%
CHEMBL340 P08684 Cytochrome P450 3A4 80.18% 91.19%

Plants that contains it

Top
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 subelliptica
Paeonia suffruticosa

Cross-Links

Top
PubChem 71457653
LOTUS LTS0048775
wikiData Q104949011