Dichotomoside E

Details

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Internal ID 805d21f2-35f0-4485-97fa-62c067feb12c
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbohydrates and carbohydrate conjugates > Glycosyl compounds > Phenolic glycosides
IUPAC Name butyl 3-[3-methoxy-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]propanoate
SMILES (Canonical) CCCCOC(=O)CCC1=CC(=C(C=C1)OC2C(C(C(C(O2)CO)O)O)O)OC
SMILES (Isomeric) CCCCOC(=O)CCC1=CC(=C(C=C1)O[C@H]2[C@@H]([C@H]([C@@H]([C@H](O2)CO)O)O)O)OC
InChI InChI=1S/C20H30O9/c1-3-4-9-27-16(22)8-6-12-5-7-13(14(10-12)26-2)28-20-19(25)18(24)17(23)15(11-21)29-20/h5,7,10,15,17-21,23-25H,3-4,6,8-9,11H2,1-2H3/t15-,17-,18+,19-,20-/m1/s1
InChI Key XTIIKSGREOOAOR-XIKSMUEASA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C20H30O9
Molecular Weight 414.40 g/mol
Exact Mass 414.18898253 g/mol
Topological Polar Surface Area (TPSA) 135.00 Ų
XlogP 0.30
Atomic LogP (AlogP) 0.15
H-Bond Acceptor 9
H-Bond Donor 4
Rotatable Bonds 10

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Dichotomoside E

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.6025 60.25%
Caco-2 - 0.6956 69.56%
Blood Brain Barrier - 0.5750 57.50%
Human oral bioavailability - 0.7571 75.71%
Subcellular localzation Mitochondria 0.8409 84.09%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8069 80.69%
OATP1B3 inhibitior + 0.9214 92.14%
MATE1 inhibitior - 0.9012 90.12%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior + 0.6696 66.96%
P-glycoprotein inhibitior - 0.7015 70.15%
P-glycoprotein substrate - 0.6030 60.30%
CYP3A4 substrate + 0.6483 64.83%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8595 85.95%
CYP3A4 inhibition - 0.6646 66.46%
CYP2C9 inhibition - 0.8065 80.65%
CYP2C19 inhibition - 0.7089 70.89%
CYP2D6 inhibition - 0.8864 88.64%
CYP1A2 inhibition - 0.6539 65.39%
CYP2C8 inhibition + 0.8576 85.76%
CYP inhibitory promiscuity - 0.8117 81.17%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9500 95.00%
Carcinogenicity (trinary) Non-required 0.7540 75.40%
Eye corrosion - 0.9910 99.10%
Eye irritation - 0.9458 94.58%
Skin irritation - 0.8349 83.49%
Skin corrosion - 0.9626 96.26%
Ames mutagenesis - 0.7800 78.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4613 46.13%
Micronuclear - 0.8900 89.00%
Hepatotoxicity - 0.8375 83.75%
skin sensitisation - 0.8469 84.69%
Respiratory toxicity - 0.6444 64.44%
Reproductive toxicity + 0.5556 55.56%
Mitochondrial toxicity - 0.6625 66.25%
Nephrotoxicity - 0.8276 82.76%
Acute Oral Toxicity (c) III 0.6873 68.73%
Estrogen receptor binding - 0.5223 52.23%
Androgen receptor binding - 0.6391 63.91%
Thyroid receptor binding - 0.6138 61.38%
Glucocorticoid receptor binding - 0.4922 49.22%
Aromatase binding - 0.6847 68.47%
PPAR gamma - 0.5898 58.98%
Honey bee toxicity - 0.8912 89.12%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity - 0.5152 51.52%
Fish aquatic toxicity + 0.9463 94.63%

Targets

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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 98.95% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 98.51% 99.17%
CHEMBL2581 P07339 Cathepsin D 96.26% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 94.09% 86.33%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.31% 91.11%
CHEMBL253 P34972 Cannabinoid CB2 receptor 91.78% 97.25%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 89.21% 92.08%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 86.73% 96.00%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 86.32% 92.62%
CHEMBL5608 Q16288 NT-3 growth factor receptor 84.41% 95.89%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 83.94% 90.71%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 83.91% 86.92%
CHEMBL241 Q14432 Phosphodiesterase 3A 83.59% 92.94%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 83.27% 100.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 83.09% 94.00%
CHEMBL3437 Q16853 Amine oxidase, copper containing 82.84% 94.00%
CHEMBL220 P22303 Acetylcholinesterase 82.60% 94.45%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 82.03% 95.89%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 81.99% 94.45%
CHEMBL5255 O00206 Toll-like receptor 4 81.92% 92.50%
CHEMBL3401 O75469 Pregnane X receptor 81.36% 94.73%

Plants that contains it

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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.
Stellaria dichotoma

Cross-Links

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PubChem 11327449
NPASS NPC280423
LOTUS LTS0227542
wikiData Q105341583