5,7-Dihydroxy-2-(1-hydroxy-2,6-dimethoxy-4-oxocyclohexyl)chromen-4-one

Details

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Internal ID 24c85330-195a-4457-9688-a25f2a76a1bb
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Chromones
IUPAC Name 5,7-dihydroxy-2-(1-hydroxy-2,6-dimethoxy-4-oxocyclohexyl)chromen-4-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C17H18O8/c1-23-13-5-9(19)6-14(24-2)17(13,22)15-7-11(21)16-10(20)3-8(18)4-12(16)25-15/h3-4,7,13-14,18,20,22H,5-6H2,1-2H3
InChI Key MZUPRMHPNSKUQZ-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C17H18O8
Molecular Weight 350.30 g/mol
Exact Mass 350.10016753 g/mol
Topological Polar Surface Area (TPSA) 123.00 Ų
XlogP -0.30
Atomic LogP (AlogP) 0.78
H-Bond Acceptor 8
H-Bond Donor 3
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 5,7-Dihydroxy-2-(1-hydroxy-2,6-dimethoxy-4-oxocyclohexyl)chromen-4-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9588 95.88%
Caco-2 - 0.5171 51.71%
Blood Brain Barrier - 0.7250 72.50%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Mitochondria 0.6764 67.64%
OATP2B1 inhibitior - 0.7094 70.94%
OATP1B1 inhibitior + 0.9374 93.74%
OATP1B3 inhibitior + 0.9478 94.78%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.9320 93.20%
P-glycoprotein inhibitior - 0.6086 60.86%
P-glycoprotein substrate - 0.6977 69.77%
CYP3A4 substrate + 0.5833 58.33%
CYP2C9 substrate + 0.6040 60.40%
CYP2D6 substrate - 0.8276 82.76%
CYP3A4 inhibition - 0.6693 66.93%
CYP2C9 inhibition - 0.8383 83.83%
CYP2C19 inhibition - 0.8081 80.81%
CYP2D6 inhibition - 0.8807 88.07%
CYP1A2 inhibition - 0.7801 78.01%
CYP2C8 inhibition - 0.5707 57.07%
CYP inhibitory promiscuity - 0.8579 85.79%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.6596 65.96%
Eye corrosion - 0.9883 98.83%
Eye irritation - 0.8219 82.19%
Skin irritation - 0.7628 76.28%
Skin corrosion - 0.9290 92.90%
Ames mutagenesis + 0.5600 56.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5249 52.49%
Micronuclear + 0.5600 56.00%
Hepatotoxicity - 0.6125 61.25%
skin sensitisation - 0.9114 91.14%
Respiratory toxicity + 0.5222 52.22%
Reproductive toxicity + 0.8000 80.00%
Mitochondrial toxicity + 0.7375 73.75%
Nephrotoxicity + 0.4630 46.30%
Acute Oral Toxicity (c) III 0.6150 61.50%
Estrogen receptor binding + 0.8479 84.79%
Androgen receptor binding + 0.7492 74.92%
Thyroid receptor binding + 0.5643 56.43%
Glucocorticoid receptor binding + 0.7471 74.71%
Aromatase binding + 0.7723 77.23%
PPAR gamma + 0.8506 85.06%
Honey bee toxicity - 0.7607 76.07%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.5700 57.00%
Fish aquatic toxicity + 0.9233 92.33%

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 99.29% 91.11%
CHEMBL1806 P11388 DNA topoisomerase II alpha 94.21% 89.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.71% 95.56%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 92.32% 94.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 92.27% 94.45%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.42% 96.09%
CHEMBL2581 P07339 Cathepsin D 88.36% 98.95%
CHEMBL3137262 O60341 LSD1/CoREST complex 87.29% 97.09%
CHEMBL3194 P02766 Transthyretin 86.17% 90.71%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.79% 86.33%
CHEMBL241 Q14432 Phosphodiesterase 3A 85.44% 92.94%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 84.77% 99.23%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 83.52% 90.71%
CHEMBL4208 P20618 Proteasome component C5 83.41% 90.00%
CHEMBL1937 Q92769 Histone deacetylase 2 83.36% 94.75%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.74% 95.89%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 82.65% 97.14%

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.
Macrothelypteris torresiana

Cross-Links

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PubChem 162877402
LOTUS LTS0220499
wikiData Q105176073