(2R)-5-Hydroxy-7,2',3'-trimethoxyflavanone

Details

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Internal ID 971496eb-bcdd-4431-8433-209548ff4cb8
Taxonomy Phenylpropanoids and polyketides > Flavonoids > O-methylated flavonoids > 7-O-methylated flavonoids
IUPAC Name (2R)-2-(2,3-dimethoxyphenyl)-5-hydroxy-7-methoxy-2,3-dihydrochromen-4-one
SMILES (Canonical) COC1=CC=CC(=C1OC)C2CC(=O)C3=C(C=C(C=C3O2)OC)O
SMILES (Isomeric) COC1=CC=CC(=C1OC)[C@H]2CC(=O)C3=C(C=C(C=C3O2)OC)O
InChI InChI=1S/C18H18O6/c1-21-10-7-12(19)17-13(20)9-15(24-16(17)8-10)11-5-4-6-14(22-2)18(11)23-3/h4-8,15,19H,9H2,1-3H3/t15-/m1/s1
InChI Key PWHHFNGLEOMEAA-OAHLLOKOSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C18H18O6
Molecular Weight 330.30 g/mol
Exact Mass 330.11033829 g/mol
Topological Polar Surface Area (TPSA) 74.20 Ų
XlogP 3.00
Atomic LogP (AlogP) 3.12
H-Bond Acceptor 6
H-Bond Donor 1
Rotatable Bonds 4

Synonyms

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LMPK12140130

2D Structure

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2D Structure of (2R)-5-Hydroxy-7,2',3'-trimethoxyflavanone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9659 96.59%
Caco-2 + 0.9006 90.06%
Blood Brain Barrier - 0.7000 70.00%
Human oral bioavailability - 0.6571 65.71%
Subcellular localzation Mitochondria 0.7780 77.80%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9451 94.51%
OATP1B3 inhibitior + 0.9840 98.40%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.4917 49.17%
P-glycoprotein inhibitior - 0.5598 55.98%
P-glycoprotein substrate - 0.8831 88.31%
CYP3A4 substrate + 0.6222 62.22%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7429 74.29%
CYP3A4 inhibition - 0.5738 57.38%
CYP2C9 inhibition - 0.7114 71.14%
CYP2C19 inhibition + 0.7224 72.24%
CYP2D6 inhibition - 0.7681 76.81%
CYP1A2 inhibition + 0.8124 81.24%
CYP2C8 inhibition + 0.5604 56.04%
CYP inhibitory promiscuity + 0.5729 57.29%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.5609 56.09%
Eye corrosion - 0.9863 98.63%
Eye irritation - 0.5694 56.94%
Skin irritation - 0.7459 74.59%
Skin corrosion - 0.9761 97.61%
Ames mutagenesis + 0.5800 58.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5848 58.48%
Micronuclear + 0.7759 77.59%
Hepatotoxicity - 0.5559 55.59%
skin sensitisation - 0.9412 94.12%
Respiratory toxicity + 0.5222 52.22%
Reproductive toxicity + 0.9333 93.33%
Mitochondrial toxicity + 0.7875 78.75%
Nephrotoxicity + 0.5753 57.53%
Acute Oral Toxicity (c) III 0.3955 39.55%
Estrogen receptor binding + 0.6064 60.64%
Androgen receptor binding - 0.5071 50.71%
Thyroid receptor binding + 0.5982 59.82%
Glucocorticoid receptor binding + 0.5792 57.92%
Aromatase binding - 0.6791 67.91%
PPAR gamma - 0.5085 50.85%
Honey bee toxicity - 0.8347 83.47%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity + 0.5200 52.00%
Fish aquatic toxicity + 0.8058 80.58%

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 98.36% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 96.19% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.64% 96.09%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 94.46% 99.15%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 94.29% 85.14%
CHEMBL2535 P11166 Glucose transporter 93.71% 98.75%
CHEMBL1293249 Q13887 Kruppel-like factor 5 92.08% 86.33%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 92.06% 99.23%
CHEMBL2581 P07339 Cathepsin D 91.25% 98.95%
CHEMBL1806 P11388 DNA topoisomerase II alpha 89.56% 89.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 89.09% 94.45%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 88.19% 94.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.63% 99.17%
CHEMBL5608 Q16288 NT-3 growth factor receptor 87.13% 95.89%
CHEMBL3192 Q9BY41 Histone deacetylase 8 86.84% 93.99%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 86.23% 97.14%
CHEMBL3137262 O60341 LSD1/CoREST complex 84.48% 97.09%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 83.60% 92.62%
CHEMBL4355 O14976 Serine/threonine-protein kinase GAK 81.95% 89.32%
CHEMBL4208 P20618 Proteasome component C5 81.06% 90.00%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 80.49% 91.07%

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.
Andrographis stenophylla
Andrographis viscosula

Cross-Links

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PubChem 9996718
NPASS NPC286594
LOTUS LTS0185142
wikiData Q76414940