Schumanniofioside A

Details

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Internal ID 9a5323a5-27f0-42ea-b4fc-b34cdb42faf9
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbohydrates and carbohydrate conjugates > Glycosyl compounds > Phenolic glycosides
IUPAC Name 7-hydroxy-2-methyl-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C16H18O9/c1-6-2-8(19)12-9(23-6)3-7(18)4-10(12)24-16-15(22)14(21)13(20)11(5-17)25-16/h2-4,11,13-18,20-22H,5H2,1H3/t11-,13-,14+,15-,16-/m1/s1
InChI Key MSNMNLUHZBFJDF-YMILTQATSA-N
Popularity 4 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) 146.00 Ų
XlogP -0.60
Atomic LogP (AlogP) -1.01
H-Bond Acceptor 9
H-Bond Donor 5
Rotatable Bonds 3

Synonyms

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128396-15-6
5-(beta-D-Glucopyranosyloxy)-7-hydroxy-2-methyl-4H-1-benzopyran-4-one
7-hydroxy-2-methyl-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one
2-Methyl-5,7-dihydroxychromone 5-O-beta-glycopyranoside
DTXSID10155873
XS163685
4H-1-Benzopyran-4-one, 5-(beta-D-glucopyranosyloxy)-7-hydroxy-2-methyl-
5-(|A-D-Glucopyranosyloxy)-7-hydroxy-2-methyl-4H-1-benzopyran-4-one

2D Structure

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2D Structure of Schumanniofioside A

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.5998 59.98%
Caco-2 - 0.8508 85.08%
Blood Brain Barrier - 0.7000 70.00%
Human oral bioavailability - 0.7429 74.29%
Subcellular localzation Mitochondria 0.6483 64.83%
OATP2B1 inhibitior - 0.5668 56.68%
OATP1B1 inhibitior + 0.9037 90.37%
OATP1B3 inhibitior + 0.9671 96.71%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.9399 93.99%
P-glycoprotein inhibitior - 0.9027 90.27%
P-glycoprotein substrate - 0.8704 87.04%
CYP3A4 substrate + 0.5584 55.84%
CYP2C9 substrate - 0.8427 84.27%
CYP2D6 substrate - 0.8591 85.91%
CYP3A4 inhibition - 0.9417 94.17%
CYP2C9 inhibition - 0.9552 95.52%
CYP2C19 inhibition - 0.9427 94.27%
CYP2D6 inhibition - 0.9493 94.93%
CYP1A2 inhibition - 0.9020 90.20%
CYP2C8 inhibition - 0.7058 70.58%
CYP inhibitory promiscuity - 0.8183 81.83%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 1.0000 100.00%
Carcinogenicity (trinary) Non-required 0.6495 64.95%
Eye corrosion - 0.9920 99.20%
Eye irritation - 0.8751 87.51%
Skin irritation - 0.8214 82.14%
Skin corrosion - 0.9690 96.90%
Ames mutagenesis + 0.5600 56.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5267 52.67%
Micronuclear + 0.5633 56.33%
Hepatotoxicity - 0.7125 71.25%
skin sensitisation - 0.9235 92.35%
Respiratory toxicity - 0.6111 61.11%
Reproductive toxicity + 0.6444 64.44%
Mitochondrial toxicity - 0.5750 57.50%
Nephrotoxicity + 0.4682 46.82%
Acute Oral Toxicity (c) III 0.6607 66.07%
Estrogen receptor binding + 0.5854 58.54%
Androgen receptor binding + 0.5527 55.27%
Thyroid receptor binding - 0.5371 53.71%
Glucocorticoid receptor binding + 0.6580 65.80%
Aromatase binding + 0.5498 54.98%
PPAR gamma + 0.5659 56.59%
Honey bee toxicity - 0.8265 82.65%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity - 0.7750 77.50%
Fish aquatic toxicity + 0.7355 73.55%

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 97.11% 91.11%
CHEMBL3401 O75469 Pregnane X receptor 95.74% 94.73%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 92.96% 94.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 92.89% 89.00%
CHEMBL2581 P07339 Cathepsin D 92.45% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.57% 95.56%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 89.67% 96.21%
CHEMBL3060 Q9Y345 Glycine transporter 2 88.19% 99.17%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 87.19% 86.92%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.72% 86.33%
CHEMBL220 P22303 Acetylcholinesterase 85.49% 94.45%
CHEMBL3714130 P46095 G-protein coupled receptor 6 83.16% 97.36%
CHEMBL3194 P02766 Transthyretin 80.52% 90.71%

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.
Dysoxylum acutangulum
Schumanniophyton magnificum

Cross-Links

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PubChem 5486897
LOTUS LTS0064902
wikiData Q83023861