(E)-3-[(9R,10R)-9-hydroxy-10-(hydroxymethyl)-3,7-dimethoxy-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-9,10-dihydrophenanthren-2-yl]prop-2-enal

Details

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Internal ID ecbc63b8-f189-4f0f-b9d7-f95b2a77d556
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbohydrates and carbohydrate conjugates > Glycosyl compounds > Phenolic glycosides
IUPAC Name (E)-3-[(9R,10R)-9-hydroxy-10-(hydroxymethyl)-3,7-dimethoxy-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-9,10-dihydrophenanthren-2-yl]prop-2-enal
SMILES (Canonical) COC1=CC2=C(C=C1)C3=C(C=C(C(=C3OC4C(C(C(C(O4)CO)O)O)O)OC)C=CC=O)C(C2O)CO
SMILES (Isomeric) COC1=CC2=C(C=C1)C3=C(C=C(C(=C3O[C@H]4[C@@H]([C@H]([C@@H]([C@H](O4)CO)O)O)O)OC)/C=C/C=O)[C@@H]([C@H]2O)CO
InChI InChI=1S/C26H30O11/c1-34-13-5-6-14-16(9-13)20(30)17(10-28)15-8-12(4-3-7-27)24(35-2)25(19(14)15)37-26-23(33)22(32)21(31)18(11-29)36-26/h3-9,17-18,20-23,26,28-33H,10-11H2,1-2H3/b4-3+/t17-,18+,20-,21+,22-,23+,26-/m0/s1
InChI Key RYOIXTXQSJPJMG-LBHUKDJMSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C26H30O11
Molecular Weight 518.50 g/mol
Exact Mass 518.17881177 g/mol
Topological Polar Surface Area (TPSA) 175.00 Ų
XlogP 0.10
Atomic LogP (AlogP) -0.12
H-Bond Acceptor 11
H-Bond Donor 6
Rotatable Bonds 8

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (E)-3-[(9R,10R)-9-hydroxy-10-(hydroxymethyl)-3,7-dimethoxy-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-9,10-dihydrophenanthren-2-yl]prop-2-enal

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.5464 54.64%
Caco-2 - 0.8155 81.55%
Blood Brain Barrier - 0.7750 77.50%
Human oral bioavailability - 0.7571 75.71%
Subcellular localzation Mitochondria 0.4736 47.36%
OATP2B1 inhibitior - 0.8513 85.13%
OATP1B1 inhibitior + 0.8073 80.73%
OATP1B3 inhibitior + 0.9792 97.92%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior + 0.8063 80.63%
P-glycoprotein inhibitior - 0.5328 53.28%
P-glycoprotein substrate - 0.6375 63.75%
CYP3A4 substrate + 0.6586 65.86%
CYP2C9 substrate - 0.8031 80.31%
CYP2D6 substrate - 0.8406 84.06%
CYP3A4 inhibition - 0.8536 85.36%
CYP2C9 inhibition - 0.9125 91.25%
CYP2C19 inhibition - 0.8321 83.21%
CYP2D6 inhibition - 0.8722 87.22%
CYP1A2 inhibition - 0.7771 77.71%
CYP2C8 inhibition + 0.6127 61.27%
CYP inhibitory promiscuity - 0.6236 62.36%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 1.0000 100.00%
Carcinogenicity (trinary) Non-required 0.7153 71.53%
Eye corrosion - 0.9894 98.94%
Eye irritation - 0.9432 94.32%
Skin irritation - 0.8323 83.23%
Skin corrosion - 0.9581 95.81%
Ames mutagenesis + 0.5377 53.77%
Human Ether-a-go-go-Related Gene inhibition + 0.7539 75.39%
Micronuclear + 0.6033 60.33%
Hepatotoxicity - 0.6875 68.75%
skin sensitisation - 0.8697 86.97%
Respiratory toxicity - 0.5889 58.89%
Reproductive toxicity + 0.7556 75.56%
Mitochondrial toxicity + 0.5625 56.25%
Nephrotoxicity - 0.6037 60.37%
Acute Oral Toxicity (c) III 0.6542 65.42%
Estrogen receptor binding + 0.8571 85.71%
Androgen receptor binding + 0.6141 61.41%
Thyroid receptor binding + 0.5550 55.50%
Glucocorticoid receptor binding + 0.7142 71.42%
Aromatase binding + 0.5688 56.88%
PPAR gamma + 0.6687 66.87%
Honey bee toxicity - 0.7899 78.99%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity + 0.5100 51.00%
Fish aquatic toxicity + 0.8551 85.51%

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 99.15% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.33% 96.09%
CHEMBL226 P30542 Adenosine A1 receptor 97.31% 95.93%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 94.95% 96.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.63% 95.56%
CHEMBL2581 P07339 Cathepsin D 93.58% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 93.15% 99.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.05% 86.33%
CHEMBL4208 P20618 Proteasome component C5 90.30% 90.00%
CHEMBL3401 O75469 Pregnane X receptor 89.97% 94.73%
CHEMBL1907 P15144 Aminopeptidase N 86.07% 93.31%
CHEMBL1966 Q02127 Dihydroorotate dehydrogenase 85.71% 96.09%
CHEMBL1806 P11388 DNA topoisomerase II alpha 85.63% 89.00%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 85.52% 86.92%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 82.63% 95.89%
CHEMBL3137262 O60341 LSD1/CoREST complex 81.75% 97.09%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 80.22% 92.62%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 163187049
LOTUS LTS0033040
wikiData Q105247733