(2R,3S,4S,5R,6S)-2-(hydroxymethyl)-6-(7-hydroxy-3,4,6-trimethoxyphenanthren-2-yl)oxyoxane-3,4,5-triol

Details

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Internal ID ee4ac89f-b2ef-414b-ba84-9e2a3daeebbb
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbohydrates and carbohydrate conjugates > Glycosyl compounds > Phenolic glycosides
IUPAC Name (2R,3S,4S,5R,6S)-2-(hydroxymethyl)-6-(7-hydroxy-3,4,6-trimethoxyphenanthren-2-yl)oxyoxane-3,4,5-triol
SMILES (Canonical) COC1=C(C=C2C=CC3=CC(=C(C(=C3C2=C1)OC)OC)OC4C(C(C(C(O4)CO)O)O)O)O
SMILES (Isomeric) COC1=C(C=C2C=CC3=CC(=C(C(=C3C2=C1)OC)OC)O[C@H]4[C@@H]([C@H]([C@@H]([C@H](O4)CO)O)O)O)O
InChI InChI=1S/C23H26O10/c1-29-14-8-12-10(6-13(14)25)4-5-11-7-15(21(30-2)22(31-3)17(11)12)32-23-20(28)19(27)18(26)16(9-24)33-23/h4-8,16,18-20,23-28H,9H2,1-3H3/t16-,18-,19+,20-,23-/m1/s1
InChI Key HNMHZSRVQJZGPQ-PUIBNRJISA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C23H26O10
Molecular Weight 462.40 g/mol
Exact Mass 462.15259702 g/mol
Topological Polar Surface Area (TPSA) 147.00 Ų
XlogP 1.80
Atomic LogP (AlogP) 0.90
H-Bond Acceptor 10
H-Bond Donor 5
Rotatable Bonds 6

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (2R,3S,4S,5R,6S)-2-(hydroxymethyl)-6-(7-hydroxy-3,4,6-trimethoxyphenanthren-2-yl)oxyoxane-3,4,5-triol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.6043 60.43%
Caco-2 - 0.7803 78.03%
Blood Brain Barrier - 0.7250 72.50%
Human oral bioavailability - 0.6429 64.29%
Subcellular localzation Mitochondria 0.4558 45.58%
OATP2B1 inhibitior - 0.5797 57.97%
OATP1B1 inhibitior + 0.8658 86.58%
OATP1B3 inhibitior + 0.9569 95.69%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior + 0.6454 64.54%
P-glycoprotein inhibitior - 0.6132 61.32%
P-glycoprotein substrate - 0.7516 75.16%
CYP3A4 substrate + 0.5393 53.93%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7747 77.47%
CYP3A4 inhibition - 0.9235 92.35%
CYP2C9 inhibition - 0.9180 91.80%
CYP2C19 inhibition - 0.8735 87.35%
CYP2D6 inhibition - 0.8894 88.94%
CYP1A2 inhibition - 0.6951 69.51%
CYP2C8 inhibition + 0.6497 64.97%
CYP inhibitory promiscuity - 0.7558 75.58%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.6882 68.82%
Eye corrosion - 0.9897 98.97%
Eye irritation - 0.9343 93.43%
Skin irritation - 0.8480 84.80%
Skin corrosion - 0.9633 96.33%
Ames mutagenesis + 0.6363 63.63%
Human Ether-a-go-go-Related Gene inhibition + 0.7244 72.44%
Micronuclear + 0.5659 56.59%
Hepatotoxicity - 0.7125 71.25%
skin sensitisation - 0.9192 91.92%
Respiratory toxicity + 0.5222 52.22%
Reproductive toxicity + 0.7000 70.00%
Mitochondrial toxicity - 0.5250 52.50%
Nephrotoxicity - 0.8808 88.08%
Acute Oral Toxicity (c) III 0.6762 67.62%
Estrogen receptor binding + 0.7111 71.11%
Androgen receptor binding - 0.5544 55.44%
Thyroid receptor binding + 0.6609 66.09%
Glucocorticoid receptor binding + 0.5827 58.27%
Aromatase binding + 0.6331 63.31%
PPAR gamma + 0.6703 67.03%
Honey bee toxicity - 0.8717 87.17%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.5449 54.49%
Fish aquatic toxicity + 0.6759 67.59%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 99.17% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.25% 96.09%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 94.11% 94.00%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 92.11% 89.62%
CHEMBL3060 Q9Y345 Glycine transporter 2 90.51% 99.17%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 89.05% 96.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.55% 86.33%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 87.04% 94.45%
CHEMBL241 Q14432 Phosphodiesterase 3A 86.85% 92.94%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 85.85% 92.62%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.25% 95.56%
CHEMBL1806 P11388 DNA topoisomerase II alpha 83.20% 89.00%
CHEMBL3476 O15111 Inhibitor of nuclear factor kappa B kinase alpha subunit 82.10% 95.83%
CHEMBL3401 O75469 Pregnane X receptor 80.74% 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.
Epimedium brevicornu
Epimedium koreanum

Cross-Links

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PubChem 5318401
NPASS NPC170324