Stilbostemin B 3'-beta-d-glucopyranoside

Details

Top
Internal ID fb62d736-ede5-4327-b5cf-5f09869bac51
Taxonomy Phenylpropanoids and polyketides > Stilbenes > Stilbene glycosides
IUPAC Name (2R,3S,4S,5R,6S)-2-(hydroxymethyl)-6-[3-hydroxy-2-methyl-5-(2-phenylethyl)phenoxy]oxane-3,4,5-triol
SMILES (Canonical) CC1=C(C=C(C=C1OC2C(C(C(C(O2)CO)O)O)O)CCC3=CC=CC=C3)O
SMILES (Isomeric) CC1=C(C=C(C=C1O[C@H]2[C@@H]([C@H]([C@@H]([C@H](O2)CO)O)O)O)CCC3=CC=CC=C3)O
InChI InChI=1S/C21H26O7/c1-12-15(23)9-14(8-7-13-5-3-2-4-6-13)10-16(12)27-21-20(26)19(25)18(24)17(11-22)28-21/h2-6,9-10,17-26H,7-8,11H2,1H3/t17-,18-,19+,20-,21-/m1/s1
InChI Key WTRYYJMNPMGQFI-YMQHIKHWSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

Top
Molecular Formula C21H26O7
Molecular Weight 390.40 g/mol
Exact Mass 390.16785316 g/mol
Topological Polar Surface Area (TPSA) 120.00 Ų
XlogP 1.70
Atomic LogP (AlogP) 0.66
H-Bond Acceptor 7
H-Bond Donor 5
Rotatable Bonds 6

Synonyms

Top
CHEMBL495642
(2R,3S,4S,5R,6S)-2-(hydroxymethyl)-6-[3-hydroxy-2-methyl-5-(2-phenylethyl)phenoxy]oxane-3,4,5-triol

2D Structure

Top
2D Structure of Stilbostemin B 3'-beta-d-glucopyranoside

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.7954 79.54%
Caco-2 - 0.8412 84.12%
Blood Brain Barrier - 0.5500 55.00%
Human oral bioavailability - 0.7857 78.57%
Subcellular localzation Mitochondria 0.7906 79.06%
OATP2B1 inhibitior - 0.7060 70.60%
OATP1B1 inhibitior + 0.8802 88.02%
OATP1B3 inhibitior + 0.9412 94.12%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior - 0.6291 62.91%
P-glycoprotein inhibitior - 0.7428 74.28%
P-glycoprotein substrate - 0.8571 85.71%
CYP3A4 substrate + 0.5656 56.56%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8034 80.34%
CYP3A4 inhibition - 0.8897 88.97%
CYP2C9 inhibition - 0.5776 57.76%
CYP2C19 inhibition - 0.8190 81.90%
CYP2D6 inhibition - 0.9301 93.01%
CYP1A2 inhibition - 0.8479 84.79%
CYP2C8 inhibition + 0.6419 64.19%
CYP inhibitory promiscuity - 0.6765 67.65%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Non-required 0.7059 70.59%
Eye corrosion - 0.9917 99.17%
Eye irritation - 0.9501 95.01%
Skin irritation - 0.8257 82.57%
Skin corrosion - 0.9469 94.69%
Ames mutagenesis - 0.5570 55.70%
Human Ether-a-go-go-Related Gene inhibition - 0.5095 50.95%
Micronuclear - 0.6441 64.41%
Hepatotoxicity - 0.8319 83.19%
skin sensitisation - 0.8599 85.99%
Respiratory toxicity - 0.5000 50.00%
Reproductive toxicity + 0.5333 53.33%
Mitochondrial toxicity - 0.7500 75.00%
Nephrotoxicity - 0.7801 78.01%
Acute Oral Toxicity (c) III 0.7855 78.55%
Estrogen receptor binding + 0.6025 60.25%
Androgen receptor binding - 0.4871 48.71%
Thyroid receptor binding + 0.6748 67.48%
Glucocorticoid receptor binding - 0.6587 65.87%
Aromatase binding + 0.5934 59.34%
PPAR gamma + 0.7245 72.45%
Honey bee toxicity - 0.8368 83.68%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity + 0.5200 52.00%
Fish aquatic toxicity - 0.3695 36.95%

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 96.98% 91.11%
CHEMBL2581 P07339 Cathepsin D 96.74% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.38% 96.09%
CHEMBL3401 O75469 Pregnane X receptor 92.25% 94.73%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.44% 86.33%
CHEMBL3060 Q9Y345 Glycine transporter 2 89.37% 99.17%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.13% 95.56%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 87.70% 94.62%
CHEMBL5805 Q9NR97 Toll-like receptor 8 86.34% 96.25%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 84.28% 95.89%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 83.48% 96.95%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 82.40% 94.00%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 80.78% 95.50%

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.
Stemona tuberosa

Cross-Links

Top
PubChem 11560189
LOTUS LTS0274930
wikiData Q105312764