Auropolin

Details

Top
Internal ID a2354663-26c5-4020-8d3b-796db157eb6a
Taxonomy Organoheterocyclic compounds > Oxepanes
IUPAC Name [(1S,2R,6R,7S,9S,11S,12S)-1-[(2S)-2-acetyloxy-2-(furan-3-yl)ethyl]-11-hydroxy-12-methyl-8-oxospiro[10-oxatricyclo[7.2.1.02,7]dodecane-6,2'-oxirane]-7-yl]methyl acetate
SMILES (Canonical) CC1C2C(=O)C3(C(C1(C(O2)O)CC(C4=COC=C4)OC(=O)C)CCCC35CO5)COC(=O)C
SMILES (Isomeric) C[C@@H]1[C@H]2C(=O)[C@@]3([C@@H]([C@@]1([C@H](O2)O)C[C@@H](C4=COC=C4)OC(=O)C)CCC[C@]35CO5)COC(=O)C
InChI InChI=1S/C24H30O9/c1-13-19-20(27)24(12-30-14(2)25)18(5-4-7-22(24)11-31-22)23(13,21(28)33-19)9-17(32-15(3)26)16-6-8-29-10-16/h6,8,10,13,17-19,21,28H,4-5,7,9,11-12H2,1-3H3/t13-,17+,18-,19+,21+,22+,23-,24+/m1/s1
InChI Key KIOYVCPFPAIZEA-QYVGYWIBSA-N
Popularity 3 references in papers

Physical and Chemical Properties

Top
Molecular Formula C24H30O9
Molecular Weight 462.50 g/mol
Exact Mass 462.18898253 g/mol
Topological Polar Surface Area (TPSA) 125.00 Ų
XlogP 1.20
Atomic LogP (AlogP) 2.31
H-Bond Acceptor 9
H-Bond Donor 1
Rotatable Bonds 6

Synonyms

Top
CHEMBL2269679

2D Structure

Top
2D Structure of Auropolin

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9421 94.21%
Caco-2 - 0.7168 71.68%
Blood Brain Barrier + 0.6750 67.50%
Human oral bioavailability - 0.7143 71.43%
Subcellular localzation Mitochondria 0.8074 80.74%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8124 81.24%
OATP1B3 inhibitior + 0.8652 86.52%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior + 0.8801 88.01%
P-glycoprotein inhibitior + 0.6209 62.09%
P-glycoprotein substrate - 0.5380 53.80%
CYP3A4 substrate + 0.6763 67.63%
CYP2C9 substrate - 0.8069 80.69%
CYP2D6 substrate - 0.8478 84.78%
CYP3A4 inhibition - 0.7449 74.49%
CYP2C9 inhibition - 0.6481 64.81%
CYP2C19 inhibition - 0.6022 60.22%
CYP2D6 inhibition - 0.9557 95.57%
CYP1A2 inhibition - 0.8529 85.29%
CYP2C8 inhibition - 0.5762 57.62%
CYP inhibitory promiscuity - 0.8925 89.25%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.5621 56.21%
Eye corrosion - 0.9895 98.95%
Eye irritation - 0.9484 94.84%
Skin irritation - 0.7399 73.99%
Skin corrosion - 0.9392 93.92%
Ames mutagenesis - 0.5340 53.40%
Human Ether-a-go-go-Related Gene inhibition - 0.3622 36.22%
Micronuclear - 0.7100 71.00%
Hepatotoxicity - 0.5542 55.42%
skin sensitisation - 0.8907 89.07%
Respiratory toxicity + 0.7000 70.00%
Reproductive toxicity + 0.7444 74.44%
Mitochondrial toxicity + 0.6375 63.75%
Nephrotoxicity + 0.4651 46.51%
Acute Oral Toxicity (c) I 0.3639 36.39%
Estrogen receptor binding + 0.8966 89.66%
Androgen receptor binding + 0.7374 73.74%
Thyroid receptor binding - 0.5324 53.24%
Glucocorticoid receptor binding + 0.8006 80.06%
Aromatase binding + 0.7377 73.77%
PPAR gamma + 0.5171 51.71%
Honey bee toxicity - 0.7576 75.76%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity + 0.5100 51.00%
Fish aquatic toxicity + 0.9791 97.91%

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
CHEMBL4040 P28482 MAP kinase ERK2 99.15% 83.82%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.69% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.03% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 96.41% 94.45%
CHEMBL2581 P07339 Cathepsin D 95.34% 98.95%
CHEMBL221 P23219 Cyclooxygenase-1 91.53% 90.17%
CHEMBL3137262 O60341 LSD1/CoREST complex 90.79% 97.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 90.77% 97.25%
CHEMBL1806 P11388 DNA topoisomerase II alpha 90.13% 89.00%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 88.81% 94.80%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.17% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.17% 95.56%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 86.24% 82.69%
CHEMBL226 P30542 Adenosine A1 receptor 83.52% 95.93%
CHEMBL5028 O14672 ADAM10 83.27% 97.50%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 82.77% 93.04%
CHEMBL4051 P13569 Cystic fibrosis transmembrane conductance regulator 81.24% 95.71%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 81.24% 91.07%
CHEMBL5608 Q16288 NT-3 growth factor receptor 81.09% 95.89%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 80.12% 99.23%

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.
Teucrium asiaticum
Teucrium polium

Cross-Links

Top
PubChem 13966163
LOTUS LTS0001739
wikiData Q105141627