Milletenone

Details

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Internal ID cbdf7927-b562-4a2b-a9c2-549e93989501
Taxonomy Phenylpropanoids and polyketides > Cinnamic acids and derivatives
IUPAC Name (Z)-3-(1,3-benzodioxol-5-yl)-1-(2,4-dimethoxyphenyl)-3-hydroxyprop-2-en-1-one
SMILES (Canonical) COC1=CC(=C(C=C1)C(=O)C=C(C2=CC3=C(C=C2)OCO3)O)OC
SMILES (Isomeric) COC1=CC(=C(C=C1)C(=O)/C=C(/C2=CC3=C(C=C2)OCO3)\O)OC
InChI InChI=1S/C18H16O6/c1-21-12-4-5-13(17(8-12)22-2)15(20)9-14(19)11-3-6-16-18(7-11)24-10-23-16/h3-9,19H,10H2,1-2H3/b14-9-
InChI Key MFEZQKKSZCXUBX-ZROIWOOFSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C18H16O6
Molecular Weight 328.30 g/mol
Exact Mass 328.09468823 g/mol
Topological Polar Surface Area (TPSA) 74.20 Ų
XlogP 3.40
Atomic LogP (AlogP) 3.21
H-Bond Acceptor 6
H-Bond Donor 1
Rotatable Bonds 5

Synonyms

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LMPK12120401

2D Structure

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2D Structure of Milletenone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9935 99.35%
Caco-2 + 0.9363 93.63%
Blood Brain Barrier - 0.5500 55.00%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Mitochondria 0.7651 76.51%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9469 94.69%
OATP1B3 inhibitior + 0.9470 94.70%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior + 0.6158 61.58%
P-glycoprotein inhibitior + 0.6758 67.58%
P-glycoprotein substrate - 0.9426 94.26%
CYP3A4 substrate - 0.5464 54.64%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8498 84.98%
CYP3A4 inhibition + 0.9197 91.97%
CYP2C9 inhibition + 0.8631 86.31%
CYP2C19 inhibition + 0.9386 93.86%
CYP2D6 inhibition + 0.8147 81.47%
CYP1A2 inhibition - 0.6029 60.29%
CYP2C8 inhibition - 0.6243 62.43%
CYP inhibitory promiscuity + 0.9138 91.38%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Danger 0.4073 40.73%
Eye corrosion - 0.9848 98.48%
Eye irritation - 0.6173 61.73%
Skin irritation - 0.7138 71.38%
Skin corrosion - 0.9688 96.88%
Ames mutagenesis - 0.5900 59.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6865 68.65%
Micronuclear + 0.8474 84.74%
Hepatotoxicity - 0.5685 56.85%
skin sensitisation - 0.5325 53.25%
Respiratory toxicity - 0.6444 64.44%
Reproductive toxicity + 0.7444 74.44%
Mitochondrial toxicity + 0.5625 56.25%
Nephrotoxicity + 0.5317 53.17%
Acute Oral Toxicity (c) II 0.4208 42.08%
Estrogen receptor binding + 0.9178 91.78%
Androgen receptor binding + 0.8690 86.90%
Thyroid receptor binding + 0.7683 76.83%
Glucocorticoid receptor binding + 0.7774 77.74%
Aromatase binding + 0.6112 61.12%
PPAR gamma + 0.8219 82.19%
Honey bee toxicity - 0.9399 93.99%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.7500 75.00%
Fish aquatic toxicity + 0.9845 98.45%

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 97.10% 96.77%
CHEMBL4208 P20618 Proteasome component C5 96.70% 90.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.69% 91.11%
CHEMBL1293249 Q13887 Kruppel-like factor 5 95.78% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.79% 95.56%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 91.96% 94.80%
CHEMBL3714130 P46095 G-protein coupled receptor 6 90.89% 97.36%
CHEMBL3060 Q9Y345 Glycine transporter 2 90.40% 99.17%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 90.09% 92.62%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.89% 96.09%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 87.63% 95.50%
CHEMBL2535 P11166 Glucose transporter 86.32% 98.75%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 84.16% 96.00%
CHEMBL340 P08684 Cytochrome P450 3A4 82.90% 91.19%
CHEMBL3492 P49721 Proteasome Macropain subunit 82.88% 90.24%
CHEMBL1293294 P51151 Ras-related protein Rab-9A 81.88% 87.67%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 81.44% 94.45%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 80.77% 97.14%
CHEMBL3401 O75469 Pregnane X receptor 80.30% 94.73%

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.
Derris ovalifolia
Millettia erythrocalyx
Millettia laurentii
Millettia peguensis
Pongamia pinnata

Cross-Links

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PubChem 42607652
NPASS NPC312609
LOTUS LTS0143075
wikiData Q76535076