Millettocalyxin A

Details

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Internal ID 22b384da-c7f7-4e56-8fe3-5578b1589436
Taxonomy Phenylpropanoids and polyketides > Flavonoids > O-methylated flavonoids > 7-O-methylated flavonoids
IUPAC Name 7-methoxy-2-(4-methoxy-1,3-benzodioxol-5-yl)chromen-4-one
SMILES (Canonical) COC1=CC2=C(C=C1)C(=O)C=C(O2)C3=C(C4=C(C=C3)OCO4)OC
SMILES (Isomeric) COC1=CC2=C(C=C1)C(=O)C=C(O2)C3=C(C4=C(C=C3)OCO4)OC
InChI InChI=1S/C18H14O6/c1-20-10-3-4-11-13(19)8-16(24-15(11)7-10)12-5-6-14-18(17(12)21-2)23-9-22-14/h3-8H,9H2,1-2H3
InChI Key WTLDVCUMPOWRCG-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C18H14O6
Molecular Weight 326.30 g/mol
Exact Mass 326.07903816 g/mol
Topological Polar Surface Area (TPSA) 63.20 Ų
XlogP 2.90
Atomic LogP (AlogP) 3.21
H-Bond Acceptor 6
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

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LMPK12110056

2D Structure

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2D Structure of Millettocalyxin A

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9881 98.81%
Caco-2 + 0.9000 90.00%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Mitochondria 0.7511 75.11%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9380 93.80%
OATP1B3 inhibitior + 0.9481 94.81%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.4601 46.01%
P-glycoprotein inhibitior + 0.9369 93.69%
P-glycoprotein substrate - 0.7162 71.62%
CYP3A4 substrate + 0.5696 56.96%
CYP2C9 substrate - 0.8423 84.23%
CYP2D6 substrate - 0.8020 80.20%
CYP3A4 inhibition + 0.9439 94.39%
CYP2C9 inhibition + 0.9157 91.57%
CYP2C19 inhibition + 0.9679 96.79%
CYP2D6 inhibition + 0.7312 73.12%
CYP1A2 inhibition + 0.5782 57.82%
CYP2C8 inhibition - 0.7087 70.87%
CYP inhibitory promiscuity + 0.9441 94.41%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.4840 48.40%
Eye corrosion - 0.9760 97.60%
Eye irritation - 0.5633 56.33%
Skin irritation - 0.7589 75.89%
Skin corrosion - 0.9669 96.69%
Ames mutagenesis - 0.5500 55.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4440 44.40%
Micronuclear + 0.7974 79.74%
Hepatotoxicity - 0.5810 58.10%
skin sensitisation - 0.7461 74.61%
Respiratory toxicity - 0.5222 52.22%
Reproductive toxicity + 0.7889 78.89%
Mitochondrial toxicity - 0.5000 50.00%
Nephrotoxicity - 0.6111 61.11%
Acute Oral Toxicity (c) III 0.6554 65.54%
Estrogen receptor binding + 0.9171 91.71%
Androgen receptor binding + 0.8916 89.16%
Thyroid receptor binding + 0.6652 66.52%
Glucocorticoid receptor binding + 0.9070 90.70%
Aromatase binding + 0.7459 74.59%
PPAR gamma + 0.7406 74.06%
Honey bee toxicity - 0.8081 80.81%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity + 0.5600 56.00%
Fish aquatic toxicity + 0.9459 94.59%

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
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 99.15% 96.77%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 98.77% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 97.25% 95.56%
CHEMBL2581 P07339 Cathepsin D 93.78% 98.95%
CHEMBL1907 P15144 Aminopeptidase N 92.80% 93.31%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 92.78% 94.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 90.59% 89.00%
CHEMBL5311 P37023 Serine/threonine-protein kinase receptor R3 88.40% 82.67%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 88.03% 92.62%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 88.02% 94.80%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.33% 86.33%
CHEMBL4208 P20618 Proteasome component C5 85.23% 90.00%
CHEMBL2039 P27338 Monoamine oxidase B 84.82% 92.51%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 83.74% 85.30%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 83.48% 99.15%
CHEMBL3137262 O60341 LSD1/CoREST complex 83.42% 97.09%
CHEMBL2535 P11166 Glucose transporter 82.69% 98.75%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 82.22% 96.00%
CHEMBL4940 P07195 L-lactate dehydrogenase B chain 81.91% 95.53%
CHEMBL4225 P49760 Dual specificity protein kinase CLK2 81.30% 80.96%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 81.18% 96.67%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 81.02% 93.40%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 80.78% 94.45%

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.
Millettia erythrocalyx

Cross-Links

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PubChem 44257581
NPASS NPC280439
LOTUS LTS0044383
wikiData Q105312631