(24-Ethyl-3,7,28-trihydroxy-14-methoxy-25-methyl-5,26-dioxo-12,18,20-trioxa-25-azaheptacyclo[15.11.1.02,15.04,13.06,11.021,29.022,27]nonacosa-1(28),2(15),3,6(11),13,21(29),22(27),23-octaen-10-yl) acetate

Details

Top
Internal ID 56e26494-12d2-4398-8292-2037bf2e0f20
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthones
IUPAC Name (24-ethyl-3,7,28-trihydroxy-14-methoxy-25-methyl-5,26-dioxo-12,18,20-trioxa-25-azaheptacyclo[15.11.1.02,15.04,13.06,11.021,29.022,27]nonacosa-1(28),2(15),3,6(11),13,21(29),22(27),23-octaen-10-yl) acetate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C31H29NO11/c1-5-12-8-13-19(31(38)32(12)3)25(36)22-18-14(9-17-21(22)27(13)41-10-40-17)28(39-4)30-23(24(18)35)26(37)20-15(34)6-7-16(29(20)43-30)42-11(2)33/h8,15-17,34-36H,5-7,9-10H2,1-4H3
InChI Key MZBKOFOJDDZCQA-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C31H29NO11
Molecular Weight 591.60 g/mol
Exact Mass 591.17406074 g/mol
Topological Polar Surface Area (TPSA) 161.00 Ų
XlogP 2.90
Atomic LogP (AlogP) 3.69
H-Bond Acceptor 12
H-Bond Donor 3
Rotatable Bonds 3

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of (24-Ethyl-3,7,28-trihydroxy-14-methoxy-25-methyl-5,26-dioxo-12,18,20-trioxa-25-azaheptacyclo[15.11.1.02,15.04,13.06,11.021,29.022,27]nonacosa-1(28),2(15),3,6(11),13,21(29),22(27),23-octaen-10-yl) acetate

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.7008 70.08%
Caco-2 - 0.7883 78.83%
Blood Brain Barrier - 0.6250 62.50%
Human oral bioavailability - 0.6143 61.43%
Subcellular localzation Nucleus 0.4427 44.27%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8335 83.35%
OATP1B3 inhibitior + 0.9149 91.49%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior + 0.6230 62.30%
P-glycoprotein inhibitior + 0.7003 70.03%
P-glycoprotein substrate + 0.7814 78.14%
CYP3A4 substrate + 0.6962 69.62%
CYP2C9 substrate + 0.7932 79.32%
CYP2D6 substrate - 0.8616 86.16%
CYP3A4 inhibition + 0.6579 65.79%
CYP2C9 inhibition - 0.8011 80.11%
CYP2C19 inhibition - 0.7319 73.19%
CYP2D6 inhibition - 0.8990 89.90%
CYP1A2 inhibition - 0.6989 69.89%
CYP2C8 inhibition + 0.6886 68.86%
CYP inhibitory promiscuity - 0.6888 68.88%
UGT catelyzed - 0.7000 70.00%
Carcinogenicity (binary) - 0.9300 93.00%
Carcinogenicity (trinary) Non-required 0.5819 58.19%
Eye corrosion - 0.9894 98.94%
Eye irritation - 0.9231 92.31%
Skin irritation - 0.8181 81.81%
Skin corrosion - 0.9471 94.71%
Ames mutagenesis + 0.5928 59.28%
Human Ether-a-go-go-Related Gene inhibition - 0.5098 50.98%
Micronuclear + 0.6700 67.00%
Hepatotoxicity - 0.5218 52.18%
skin sensitisation - 0.8993 89.93%
Respiratory toxicity + 0.8111 81.11%
Reproductive toxicity + 0.8778 87.78%
Mitochondrial toxicity + 0.9000 90.00%
Nephrotoxicity - 0.9348 93.48%
Acute Oral Toxicity (c) III 0.6722 67.22%
Estrogen receptor binding + 0.8034 80.34%
Androgen receptor binding + 0.7389 73.89%
Thyroid receptor binding + 0.5476 54.76%
Glucocorticoid receptor binding + 0.7924 79.24%
Aromatase binding + 0.6632 66.32%
PPAR gamma + 0.6340 63.40%
Honey bee toxicity - 0.6956 69.56%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity + 0.5100 51.00%
Fish aquatic toxicity + 0.7666 76.66%

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 98.88% 91.11%
CHEMBL2581 P07339 Cathepsin D 98.56% 98.95%
CHEMBL1806 P11388 DNA topoisomerase II alpha 97.43% 89.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 97.34% 94.45%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.16% 96.09%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 95.22% 94.00%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 94.25% 92.62%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 92.45% 95.17%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 90.64% 96.77%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.84% 86.33%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 89.82% 85.14%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 89.18% 94.42%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.09% 95.56%
CHEMBL5608 Q16288 NT-3 growth factor receptor 84.83% 95.89%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.44% 99.17%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 81.90% 93.00%
CHEMBL4895 P30530 Tyrosine-protein kinase receptor UFO 80.89% 90.95%
CHEMBL2094127 P06493 Cyclin-dependent kinase 1/cyclin B 80.54% 96.00%
CHEMBL3713062 P10646 Tissue factor pathway inhibitor 80.38% 97.33%

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.
There are no matching plants.

Cross-Links

Top
PubChem 163054137
LOTUS LTS0224392
wikiData Q104172190