Xyl(b1-6)Glc(b)-O-Ph(2-Ac)

Details

Top
Internal ID 5a3ea598-e378-433b-8c91-4f403ae69423
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbohydrates and carbohydrate conjugates > Glycosyl compounds > Phenolic glycosides
IUPAC Name 1-[2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxymethyl]oxan-2-yl]oxyphenyl]ethanone
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C19H26O11/c1-8(20)9-4-2-3-5-11(9)29-19-17(26)15(24)14(23)12(30-19)7-28-18-16(25)13(22)10(21)6-27-18/h2-5,10,12-19,21-26H,6-7H2,1H3/t10-,12-,13+,14-,15+,16-,17-,18+,19-/m1/s1
InChI Key VBRTUQGIOMQJIE-HWNZEACOSA-N
Popularity 2 references in papers

Physical and Chemical Properties

Top
Molecular Formula C19H26O11
Molecular Weight 430.40 g/mol
Exact Mass 430.14751164 g/mol
Topological Polar Surface Area (TPSA) 175.00 Ų
XlogP -2.60
Atomic LogP (AlogP) -2.47
H-Bond Acceptor 11
H-Bond Donor 6
Rotatable Bonds 6

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of Xyl(b1-6)Glc(b)-O-Ph(2-Ac)

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.7092 70.92%
Caco-2 - 0.8505 85.05%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability - 0.7714 77.14%
Subcellular localzation Mitochondria 0.7582 75.82%
OATP2B1 inhibitior - 0.8584 85.84%
OATP1B1 inhibitior + 0.9292 92.92%
OATP1B3 inhibitior + 0.9225 92.25%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.6857 68.57%
P-glycoprotein inhibitior - 0.8329 83.29%
P-glycoprotein substrate - 0.8081 80.81%
CYP3A4 substrate + 0.5705 57.05%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8525 85.25%
CYP3A4 inhibition - 0.9297 92.97%
CYP2C9 inhibition - 0.9464 94.64%
CYP2C19 inhibition - 0.9492 94.92%
CYP2D6 inhibition - 0.9288 92.88%
CYP1A2 inhibition - 0.9059 90.59%
CYP2C8 inhibition - 0.7115 71.15%
CYP inhibitory promiscuity - 0.9044 90.44%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.7050 70.50%
Eye corrosion - 0.9930 99.30%
Eye irritation - 0.9603 96.03%
Skin irritation - 0.8333 83.33%
Skin corrosion - 0.9624 96.24%
Ames mutagenesis + 0.5700 57.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5085 50.85%
Micronuclear - 0.5893 58.93%
Hepatotoxicity - 0.7628 76.28%
skin sensitisation - 0.8560 85.60%
Respiratory toxicity - 0.5333 53.33%
Reproductive toxicity + 0.5667 56.67%
Mitochondrial toxicity - 0.5625 56.25%
Nephrotoxicity - 0.6523 65.23%
Acute Oral Toxicity (c) III 0.7521 75.21%
Estrogen receptor binding + 0.7180 71.80%
Androgen receptor binding - 0.7762 77.62%
Thyroid receptor binding + 0.5621 56.21%
Glucocorticoid receptor binding - 0.6397 63.97%
Aromatase binding + 0.6105 61.05%
PPAR gamma + 0.7192 71.92%
Honey bee toxicity - 0.8590 85.90%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity - 0.7555 75.55%
Fish aquatic toxicity + 0.7362 73.62%

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 98.19% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.43% 96.09%
CHEMBL2581 P07339 Cathepsin D 92.72% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.32% 86.33%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 86.43% 95.50%
CHEMBL3401 O75469 Pregnane X receptor 86.20% 94.73%
CHEMBL253 P34972 Cannabinoid CB2 receptor 84.82% 97.25%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 84.67% 89.62%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.96% 95.56%
CHEMBL220 P22303 Acetylcholinesterase 83.73% 94.45%
CHEMBL5028 O14672 ADAM10 83.07% 97.50%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 81.86% 94.00%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 80.48% 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.
There are no matching plants.

Cross-Links

Top
PubChem 9980113
LOTUS LTS0235705
wikiData Q105283459