Magnolioside

Details

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Internal ID eb72642e-ef25-460b-a0b4-b28a3d0629a9
Taxonomy Phenylpropanoids and polyketides > Coumarins and derivatives > Coumarin glycosides
IUPAC Name 7-methoxy-6-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-2-one
SMILES (Canonical) COC1=C(C=C2C=CC(=O)OC2=C1)OC3C(C(C(C(O3)CO)O)O)O
SMILES (Isomeric) COC1=C(C=C2C=CC(=O)OC2=C1)O[C@H]3[C@@H]([C@H]([C@@H]([C@H](O3)CO)O)O)O
InChI InChI=1S/C16H18O9/c1-22-9-5-8-7(2-3-12(18)23-8)4-10(9)24-16-15(21)14(20)13(19)11(6-17)25-16/h2-5,11,13-17,19-21H,6H2,1H3/t11-,13-,14+,15-,16-/m1/s1
InChI Key WBAVLTNIRYDCPM-YMILTQATSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C16H18O9
Molecular Weight 354.31 g/mol
Exact Mass 354.09508215 g/mol
Topological Polar Surface Area (TPSA) 135.00 Ų
XlogP -1.10
Atomic LogP (AlogP) -1.02
H-Bond Acceptor 9
H-Bond Donor 4
Rotatable Bonds 4

Synonyms

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Methylesculin
20186-29-2
Esculin methyl ether
2H-1-Benzopyran-2-one, 6-(beta-D-glucopyranosyloxy)-7-methoxy-
IQ1QJO54R6
7-methoxy-6-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-2-one
ISOSCOPOLIN
7-METHYLESCULIN
UNII-IQ1QJO54R6
AESCULIN METHYL ETHER
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Magnolioside

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.5647 56.47%
Caco-2 - 0.7254 72.54%
Blood Brain Barrier - 0.8000 80.00%
Human oral bioavailability - 0.5714 57.14%
Subcellular localzation Mitochondria 0.5367 53.67%
OATP2B1 inhibitior - 0.8522 85.22%
OATP1B1 inhibitior + 0.8846 88.46%
OATP1B3 inhibitior + 0.9769 97.69%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.6474 64.74%
P-glycoprotein inhibitior - 0.8757 87.57%
P-glycoprotein substrate - 0.8168 81.68%
CYP3A4 substrate - 0.5201 52.01%
CYP2C9 substrate - 0.8306 83.06%
CYP2D6 substrate - 0.8491 84.91%
CYP3A4 inhibition - 0.9107 91.07%
CYP2C9 inhibition - 0.9346 93.46%
CYP2C19 inhibition - 0.9158 91.58%
CYP2D6 inhibition - 0.9306 93.06%
CYP1A2 inhibition - 0.8772 87.72%
CYP2C8 inhibition - 0.7234 72.34%
CYP inhibitory promiscuity - 0.8094 80.94%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 1.0000 100.00%
Carcinogenicity (trinary) Non-required 0.6881 68.81%
Eye corrosion - 0.9890 98.90%
Eye irritation - 0.9545 95.45%
Skin irritation - 0.8111 81.11%
Skin corrosion - 0.9624 96.24%
Ames mutagenesis - 0.7400 74.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6221 62.21%
Micronuclear + 0.6133 61.33%
Hepatotoxicity - 0.7476 74.76%
skin sensitisation - 0.9164 91.64%
Respiratory toxicity - 0.5556 55.56%
Reproductive toxicity + 0.7333 73.33%
Mitochondrial toxicity - 0.5750 57.50%
Nephrotoxicity - 0.7485 74.85%
Acute Oral Toxicity (c) III 0.7058 70.58%
Estrogen receptor binding - 0.4776 47.76%
Androgen receptor binding - 0.5304 53.04%
Thyroid receptor binding - 0.5830 58.30%
Glucocorticoid receptor binding + 0.7784 77.84%
Aromatase binding + 0.5927 59.27%
PPAR gamma + 0.5605 56.05%
Honey bee toxicity - 0.8771 87.71%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity - 0.6949 69.49%
Fish aquatic toxicity + 0.6492 64.92%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
CHEMBL3242 O43570 Carbonic anhydrase XII 780 nM
Ki
via Super-PRED

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL220 P22303 Acetylcholinesterase 98.58% 94.45%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.17% 91.11%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 93.88% 94.00%
CHEMBL2581 P07339 Cathepsin D 92.87% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.06% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.73% 99.17%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 85.65% 96.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.06% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.71% 86.33%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 84.67% 85.14%
CHEMBL3401 O75469 Pregnane X receptor 84.10% 94.73%
CHEMBL4306 P22460 Voltage-gated potassium channel subunit Kv1.5 82.81% 94.03%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 82.62% 86.92%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 80.03% 89.62%

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.
Artemisia capillaris
Corydalis decumbens
Erodium stephanianum
Griselinia littoralis
Helichrysum arenarium
Micromelum hirsutum
Olea capensis
Prunus domestica

Cross-Links

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PubChem 3084335
NPASS NPC41918
LOTUS LTS0074578
wikiData Q82919209