Acetyldiphyllin

Details

Top
Internal ID f9f3a3d7-bb8e-4815-9d57-83f45e7ebd92
Taxonomy Lignans, neolignans and related compounds > Arylnaphthalene lignans
IUPAC Name [9-(1,3-benzodioxol-5-yl)-6,7-dimethoxy-1-oxo-3H-benzo[f][2]benzofuran-4-yl] acetate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C23H18O8/c1-11(24)31-22-14-8-18(27-3)17(26-2)7-13(14)20(21-15(22)9-28-23(21)25)12-4-5-16-19(6-12)30-10-29-16/h4-8H,9-10H2,1-3H3
InChI Key KEGZEHANNYRNOK-UHFFFAOYSA-N
Popularity 5 references in papers

Physical and Chemical Properties

Top
Molecular Formula C23H18O8
Molecular Weight 422.40 g/mol
Exact Mass 422.10016753 g/mol
Topological Polar Surface Area (TPSA) 89.50 Ų
XlogP 3.70
Atomic LogP (AlogP) 3.85
H-Bond Acceptor 8
H-Bond Donor 0
Rotatable Bonds 4

Synonyms

Top
Oprea1_062356
25001-54-1
MLS001048953
CHEMBL1370024
SCHEMBL11954031
DTXSID001347142
HMS2268O19
AKOS002141699
CCG-202818
NCGC00161918-01
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

Top
2D Structure of Acetyldiphyllin

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9880 98.80%
Caco-2 + 0.7523 75.23%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability - 0.5714 57.14%
Subcellular localzation Mitochondria 0.7251 72.51%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9385 93.85%
OATP1B3 inhibitior + 0.9637 96.37%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior + 0.9306 93.06%
P-glycoprotein inhibitior + 0.8655 86.55%
P-glycoprotein substrate - 0.8293 82.93%
CYP3A4 substrate + 0.5729 57.29%
CYP2C9 substrate - 0.7936 79.36%
CYP2D6 substrate - 0.8819 88.19%
CYP3A4 inhibition + 0.7960 79.60%
CYP2C9 inhibition + 0.9168 91.68%
CYP2C19 inhibition + 0.8720 87.20%
CYP2D6 inhibition - 0.8513 85.13%
CYP1A2 inhibition - 0.7873 78.73%
CYP2C8 inhibition + 0.5503 55.03%
CYP inhibitory promiscuity + 0.8669 86.69%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9243 92.43%
Carcinogenicity (trinary) Non-required 0.4094 40.94%
Eye corrosion - 0.9847 98.47%
Eye irritation - 0.6774 67.74%
Skin irritation - 0.8444 84.44%
Skin corrosion - 0.9652 96.52%
Ames mutagenesis + 0.6500 65.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6930 69.30%
Micronuclear + 0.7874 78.74%
Hepatotoxicity + 0.6625 66.25%
skin sensitisation - 0.6432 64.32%
Respiratory toxicity + 0.6222 62.22%
Reproductive toxicity + 0.6111 61.11%
Mitochondrial toxicity + 0.5750 57.50%
Nephrotoxicity + 0.5881 58.81%
Acute Oral Toxicity (c) III 0.6673 66.73%
Estrogen receptor binding + 0.8912 89.12%
Androgen receptor binding + 0.7125 71.25%
Thyroid receptor binding + 0.6292 62.92%
Glucocorticoid receptor binding + 0.9179 91.79%
Aromatase binding - 0.5000 50.00%
PPAR gamma + 0.6245 62.45%
Honey bee toxicity - 0.7297 72.97%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity - 0.5749 57.49%
Fish aquatic toxicity + 0.9776 97.76%

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 98.37% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 98.15% 94.45%
CHEMBL1293249 Q13887 Kruppel-like factor 5 95.43% 86.33%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 94.47% 96.77%
CHEMBL1806 P11388 DNA topoisomerase II alpha 94.43% 89.00%
CHEMBL2581 P07339 Cathepsin D 94.41% 98.95%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 94.24% 85.14%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 93.32% 94.80%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 92.99% 92.62%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.97% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.17% 96.09%
CHEMBL2535 P11166 Glucose transporter 91.24% 98.75%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 87.47% 94.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.84% 99.17%
CHEMBL2002 P12268 Inosine-5'-monophosphate dehydrogenase 2 83.63% 98.21%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 82.82% 95.50%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 82.34% 96.00%
CHEMBL5925 P22413 Ectonucleotide pyrophosphatase/phosphodiesterase family member 1 82.17% 92.38%
CHEMBL4225 P49760 Dual specificity protein kinase CLK2 81.73% 80.96%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 81.43% 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.
Haplophyllum bucharicum

Cross-Links

Top
PubChem 1760987
LOTUS LTS0058986
wikiData Q105139960