5,6-Dimethoxy-7-(sulfooxy)-2h-1-benzopyran-2-one

Details

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Internal ID 8324e175-a179-40da-a438-286e8c92f5a5
Taxonomy Phenylpropanoids and polyketides > Coumarins and derivatives
IUPAC Name (5,6-dimethoxy-2-oxochromen-7-yl) hydrogen sulfate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C11H10O8S/c1-16-10-6-3-4-9(12)18-7(6)5-8(11(10)17-2)19-20(13,14)15/h3-5H,1-2H3,(H,13,14,15)
InChI Key MGMZLQXLGGSINI-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C11H10O8S
Molecular Weight 302.26 g/mol
Exact Mass 302.00963845 g/mol
Topological Polar Surface Area (TPSA) 117.00 Ų
XlogP 0.90
Atomic LogP (AlogP) 0.99
H-Bond Acceptor 7
H-Bond Donor 1
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 5,6-Dimethoxy-7-(sulfooxy)-2h-1-benzopyran-2-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8798 87.98%
Caco-2 - 0.6120 61.20%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability + 0.7714 77.14%
Subcellular localzation Mitochondria 0.4266 42.66%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9411 94.11%
OATP1B3 inhibitior + 0.9430 94.30%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.7753 77.53%
P-glycoprotein inhibitior - 0.8186 81.86%
P-glycoprotein substrate - 0.7757 77.57%
CYP3A4 substrate - 0.5538 55.38%
CYP2C9 substrate - 0.8405 84.05%
CYP2D6 substrate - 0.8468 84.68%
CYP3A4 inhibition - 0.9126 91.26%
CYP2C9 inhibition - 0.8901 89.01%
CYP2C19 inhibition - 0.8952 89.52%
CYP2D6 inhibition - 0.9178 91.78%
CYP1A2 inhibition + 0.6550 65.50%
CYP2C8 inhibition - 0.7742 77.42%
CYP inhibitory promiscuity - 0.8906 89.06%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.5255 52.55%
Carcinogenicity (trinary) Non-required 0.6369 63.69%
Eye corrosion - 0.9084 90.84%
Eye irritation - 0.5122 51.22%
Skin irritation - 0.8000 80.00%
Skin corrosion - 0.9170 91.70%
Ames mutagenesis - 0.5500 55.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7082 70.82%
Micronuclear + 0.8659 86.59%
Hepatotoxicity - 0.5000 50.00%
skin sensitisation - 0.8642 86.42%
Respiratory toxicity - 0.5222 52.22%
Reproductive toxicity + 0.7000 70.00%
Mitochondrial toxicity + 0.5500 55.00%
Nephrotoxicity - 0.7964 79.64%
Acute Oral Toxicity (c) III 0.5874 58.74%
Estrogen receptor binding + 0.7181 71.81%
Androgen receptor binding + 0.7712 77.12%
Thyroid receptor binding - 0.8001 80.01%
Glucocorticoid receptor binding - 0.7188 71.88%
Aromatase binding - 0.5515 55.15%
PPAR gamma + 0.5356 53.56%
Honey bee toxicity - 0.8812 88.12%
Biodegradation - 0.5250 52.50%
Crustacea aquatic toxicity + 0.5100 51.00%
Fish aquatic toxicity + 0.9836 98.36%

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
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.77% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.02% 91.11%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 92.75% 94.00%
CHEMBL2581 P07339 Cathepsin D 90.17% 98.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 88.99% 94.45%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 87.89% 96.00%
CHEMBL4306 P22460 Voltage-gated potassium channel subunit Kv1.5 85.98% 94.03%
CHEMBL1806 P11388 DNA topoisomerase II alpha 85.29% 89.00%
CHEMBL3401 O75469 Pregnane X receptor 84.37% 94.73%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 80.46% 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.
Pelargonium sidoides

Cross-Links

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PubChem 85779359
LOTUS LTS0128544
wikiData Q105163447