5-Hydroxy-7-methoxy-6-methyl-4-oxo-2-phenyl-2,3-dihydrochromene-8-carbaldehyde

Details

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Internal ID f5cb24c3-fcea-4afb-b76c-94502f35da65
Taxonomy Phenylpropanoids and polyketides > Flavonoids > O-methylated flavonoids > 7-O-methylated flavonoids
IUPAC Name 5-hydroxy-7-methoxy-6-methyl-4-oxo-2-phenyl-2,3-dihydrochromene-8-carbaldehyde
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C18H16O5/c1-10-16(21)15-13(20)8-14(11-6-4-3-5-7-11)23-18(15)12(9-19)17(10)22-2/h3-7,9,14,21H,8H2,1-2H3
InChI Key QJQJKEWQUOORFC-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C18H16O5
Molecular Weight 312.30 g/mol
Exact Mass 312.09977361 g/mol
Topological Polar Surface Area (TPSA) 72.80 Ų
XlogP 2.90
Atomic LogP (AlogP) 3.23
H-Bond Acceptor 5
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 5-Hydroxy-7-methoxy-6-methyl-4-oxo-2-phenyl-2,3-dihydrochromene-8-carbaldehyde

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9689 96.89%
Caco-2 + 0.6341 63.41%
Blood Brain Barrier - 0.7250 72.50%
Human oral bioavailability - 0.6429 64.29%
Subcellular localzation Mitochondria 0.8299 82.99%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.7909 79.09%
OATP1B3 inhibitior + 0.9934 99.34%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.6244 62.44%
P-glycoprotein inhibitior - 0.5830 58.30%
P-glycoprotein substrate - 0.9025 90.25%
CYP3A4 substrate + 0.5401 54.01%
CYP2C9 substrate - 0.7977 79.77%
CYP2D6 substrate - 0.7847 78.47%
CYP3A4 inhibition - 0.5502 55.02%
CYP2C9 inhibition + 0.8047 80.47%
CYP2C19 inhibition + 0.6828 68.28%
CYP2D6 inhibition - 0.7213 72.13%
CYP1A2 inhibition + 0.8055 80.55%
CYP2C8 inhibition + 0.5199 51.99%
CYP inhibitory promiscuity + 0.5000 50.00%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9313 93.13%
Carcinogenicity (trinary) Non-required 0.6180 61.80%
Eye corrosion - 0.9890 98.90%
Eye irritation - 0.6308 63.08%
Skin irritation - 0.7591 75.91%
Skin corrosion - 0.9650 96.50%
Ames mutagenesis + 0.5700 57.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4203 42.03%
Micronuclear + 0.8059 80.59%
Hepatotoxicity + 0.6250 62.50%
skin sensitisation - 0.9602 96.02%
Respiratory toxicity + 0.6444 64.44%
Reproductive toxicity + 0.9556 95.56%
Mitochondrial toxicity + 0.8000 80.00%
Nephrotoxicity - 0.6676 66.76%
Acute Oral Toxicity (c) II 0.3631 36.31%
Estrogen receptor binding + 0.6637 66.37%
Androgen receptor binding - 0.5241 52.41%
Thyroid receptor binding - 0.5695 56.95%
Glucocorticoid receptor binding + 0.7280 72.80%
Aromatase binding + 0.5978 59.78%
PPAR gamma + 0.6559 65.59%
Honey bee toxicity - 0.8812 88.12%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.5700 57.00%
Fish aquatic toxicity + 0.8868 88.68%

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 98.80% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.85% 91.11%
CHEMBL1163101 O75460 Serine/threonine-protein kinase/endoribonuclease IRE1 93.34% 98.11%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 92.11% 99.23%
CHEMBL2581 P07339 Cathepsin D 91.54% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.43% 86.33%
CHEMBL1806 P11388 DNA topoisomerase II alpha 84.15% 89.00%
CHEMBL1951 P21397 Monoamine oxidase A 82.39% 91.49%
CHEMBL3401 O75469 Pregnane X receptor 82.39% 94.73%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 81.14% 96.09%
CHEMBL3359 P21462 Formyl peptide receptor 1 80.24% 93.56%

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.
Syzygium nervosum

Cross-Links

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PubChem 85435141
LOTUS LTS0220101
wikiData Q105222819