[3,4,5-Triacetyloxy-6-[4-[6-(4-acetyloxy-3,5-dimethoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-3-yl]-2,6-dimethoxyphenoxy]oxan-2-yl]methyl acetate

Details

Top
Internal ID 1d2c250c-f790-449e-90c6-cb3a15b62e1d
Taxonomy Lignans, neolignans and related compounds > Lignan glycosides
IUPAC Name [3,4,5-triacetyloxy-6-[4-[6-(4-acetyloxy-3,5-dimethoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-3-yl]-2,6-dimethoxyphenoxy]oxan-2-yl]methyl acetate
SMILES (Canonical) CC(=O)OCC1C(C(C(C(O1)OC2=C(C=C(C=C2OC)C3C4COC(C4CO3)C5=CC(=C(C(=C5)OC)OC(=O)C)OC)OC)OC(=O)C)OC(=O)C)OC(=O)C
SMILES (Isomeric) CC(=O)OCC1C(C(C(C(O1)OC2=C(C=C(C=C2OC)C3C4COC(C4CO3)C5=CC(=C(C(=C5)OC)OC(=O)C)OC)OC)OC(=O)C)OC(=O)C)OC(=O)C
InChI InChI=1S/C38H46O18/c1-17(39)48-16-30-35(52-19(3)41)36(53-20(4)42)37(54-21(5)43)38(55-30)56-34-28(46-8)12-23(13-29(34)47-9)32-25-15-49-31(24(25)14-50-32)22-10-26(44-6)33(51-18(2)40)27(11-22)45-7/h10-13,24-25,30-32,35-38H,14-16H2,1-9H3
InChI Key BKLUEPLPMYEHOD-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C38H46O18
Molecular Weight 790.80 g/mol
Exact Mass 790.26841461 g/mol
Topological Polar Surface Area (TPSA) 205.00 Ų
XlogP 2.30
Atomic LogP (AlogP) 3.18
H-Bond Acceptor 18
H-Bond Donor 0
Rotatable Bonds 14

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of [3,4,5-Triacetyloxy-6-[4-[6-(4-acetyloxy-3,5-dimethoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-3-yl]-2,6-dimethoxyphenoxy]oxan-2-yl]methyl acetate

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9818 98.18%
Caco-2 - 0.8256 82.56%
Blood Brain Barrier + 0.7000 70.00%
Human oral bioavailability - 0.6000 60.00%
Subcellular localzation Mitochondria 0.8159 81.59%
OATP2B1 inhibitior + 0.5751 57.51%
OATP1B1 inhibitior + 0.8597 85.97%
OATP1B3 inhibitior + 0.9226 92.26%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior + 0.9583 95.83%
P-glycoprotein inhibitior + 0.8373 83.73%
P-glycoprotein substrate - 0.7977 79.77%
CYP3A4 substrate + 0.6370 63.70%
CYP2C9 substrate - 0.8022 80.22%
CYP2D6 substrate - 0.8625 86.25%
CYP3A4 inhibition - 0.7065 70.65%
CYP2C9 inhibition - 0.6785 67.85%
CYP2C19 inhibition + 0.6125 61.25%
CYP2D6 inhibition - 0.9355 93.55%
CYP1A2 inhibition - 0.7949 79.49%
CYP2C8 inhibition + 0.5384 53.84%
CYP inhibitory promiscuity + 0.6496 64.96%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.6112 61.12%
Eye corrosion - 0.9868 98.68%
Eye irritation - 0.9012 90.12%
Skin irritation - 0.8828 88.28%
Skin corrosion - 0.9698 96.98%
Ames mutagenesis - 0.6200 62.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7893 78.93%
Micronuclear - 0.5000 50.00%
Hepatotoxicity - 0.7875 78.75%
skin sensitisation - 0.7691 76.91%
Respiratory toxicity + 0.5667 56.67%
Reproductive toxicity + 0.8333 83.33%
Mitochondrial toxicity - 0.5250 52.50%
Nephrotoxicity - 0.8924 89.24%
Acute Oral Toxicity (c) III 0.6175 61.75%
Estrogen receptor binding + 0.8327 83.27%
Androgen receptor binding + 0.7091 70.91%
Thyroid receptor binding + 0.5523 55.23%
Glucocorticoid receptor binding + 0.8227 82.27%
Aromatase binding + 0.6643 66.43%
PPAR gamma + 0.7606 76.06%
Honey bee toxicity - 0.7499 74.99%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity - 0.5600 56.00%
Fish aquatic toxicity + 0.9896 98.96%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 99.20% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.19% 91.11%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 95.51% 85.14%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.04% 86.33%
CHEMBL3060 Q9Y345 Glycine transporter 2 89.98% 99.17%
CHEMBL253 P34972 Cannabinoid CB2 receptor 88.63% 97.25%
CHEMBL1806 P11388 DNA topoisomerase II alpha 88.02% 89.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 87.58% 94.00%
CHEMBL2581 P07339 Cathepsin D 86.94% 98.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 86.17% 94.45%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 84.94% 92.62%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 84.59% 95.89%
CHEMBL4208 P20618 Proteasome component C5 83.66% 90.00%
CHEMBL3401 O75469 Pregnane X receptor 83.45% 94.73%
CHEMBL5255 O00206 Toll-like receptor 4 83.43% 92.50%
CHEMBL3137262 O60341 LSD1/CoREST complex 83.33% 97.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 81.63% 95.56%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 81.06% 96.00%

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.
Arum italicum

Cross-Links

Top
PubChem 14827965
LOTUS LTS0047679
wikiData Q104937678