5-Methylcoumarin-4-cellobioside

Details

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Internal ID bc5f7779-5b0f-4687-915b-3e182d4132fb
Taxonomy Phenylpropanoids and polyketides > Coumarins and derivatives > Coumarin glycosides
IUPAC Name 4-[(2S,3R,4R,5S,6R)-3,4-dihydroxy-6-(hydroxymethyl)-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-5-methylchromen-2-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C22H28O13/c1-8-3-2-4-9-14(8)10(5-13(25)31-9)32-21-19(30)17(28)20(12(7-24)34-21)35-22-18(29)16(27)15(26)11(6-23)33-22/h2-5,11-12,15-24,26-30H,6-7H2,1H3/t11-,12-,15-,16+,17-,18-,19-,20-,21-,22+/m1/s1
InChI Key HKXDQRBBOHHCKP-KGGQWWQZSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C22H28O13
Molecular Weight 500.40 g/mol
Exact Mass 500.15299094 g/mol
Topological Polar Surface Area (TPSA) 205.00 Ų
XlogP -2.30
Atomic LogP (AlogP) -2.90
H-Bond Acceptor 13
H-Bond Donor 7
Rotatable Bonds 6

Synonyms

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5-Methylcoumarin-4-cellobioside
109974-31-4
DTXSID60149085
RefChem:103180
DTXCID2071576
4-[(2S,3R,4R,5S,6R)-3,4-dihydroxy-6-(hydroxymethyl)-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-5-methylchromen-2-one

2D Structure

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2D Structure of 5-Methylcoumarin-4-cellobioside

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.6673 66.73%
Caco-2 - 0.8724 87.24%
Blood Brain Barrier - 0.6750 67.50%
Human oral bioavailability - 0.8714 87.14%
Subcellular localzation Mitochondria 0.6320 63.20%
OATP2B1 inhibitior - 0.8453 84.53%
OATP1B1 inhibitior + 0.9112 91.12%
OATP1B3 inhibitior + 0.9717 97.17%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.4838 48.38%
P-glycoprotein inhibitior - 0.7041 70.41%
P-glycoprotein substrate - 0.7992 79.92%
CYP3A4 substrate + 0.5767 57.67%
CYP2C9 substrate - 0.8232 82.32%
CYP2D6 substrate - 0.8681 86.81%
CYP3A4 inhibition - 0.9604 96.04%
CYP2C9 inhibition - 0.9542 95.42%
CYP2C19 inhibition - 0.9251 92.51%
CYP2D6 inhibition - 0.9462 94.62%
CYP1A2 inhibition - 0.9100 91.00%
CYP2C8 inhibition - 0.6658 66.58%
CYP inhibitory promiscuity - 0.8072 80.72%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 1.0000 100.00%
Carcinogenicity (trinary) Non-required 0.6171 61.71%
Eye corrosion - 0.9923 99.23%
Eye irritation - 0.9489 94.89%
Skin irritation - 0.8389 83.89%
Skin corrosion - 0.9692 96.92%
Ames mutagenesis + 0.5246 52.46%
Human Ether-a-go-go-Related Gene inhibition - 0.4734 47.34%
Micronuclear + 0.5433 54.33%
Hepatotoxicity - 0.7171 71.71%
skin sensitisation - 0.9230 92.30%
Respiratory toxicity + 0.5222 52.22%
Reproductive toxicity + 0.6222 62.22%
Mitochondrial toxicity - 0.5375 53.75%
Nephrotoxicity - 0.8428 84.28%
Acute Oral Toxicity (c) III 0.6211 62.11%
Estrogen receptor binding + 0.7903 79.03%
Androgen receptor binding + 0.6042 60.42%
Thyroid receptor binding + 0.5345 53.45%
Glucocorticoid receptor binding + 0.5628 56.28%
Aromatase binding + 0.7094 70.94%
PPAR gamma + 0.7184 71.84%
Honey bee toxicity - 0.7725 77.25%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.5800 58.00%
Fish aquatic toxicity + 0.7000 70.00%

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
CHEMBL220 P22303 Acetylcholinesterase 99.51% 94.45%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.89% 91.11%
CHEMBL2581 P07339 Cathepsin D 95.99% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 95.60% 94.73%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 94.45% 94.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.43% 95.56%
CHEMBL1806 P11388 DNA topoisomerase II alpha 92.29% 89.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.31% 86.33%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 91.29% 96.21%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 85.27% 94.45%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 83.80% 96.09%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 83.45% 96.00%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 83.13% 93.65%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.33% 95.89%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 81.95% 99.23%

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.
Coptis chinensis
Leibnitzia anandria

Cross-Links

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PubChem 196631
NPASS NPC79977