Microminutin

Details

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Internal ID 0d31031c-2386-4c78-8d39-bf8d84f69a69
Taxonomy Phenylpropanoids and polyketides > Coumarins and derivatives
IUPAC Name 7-methoxy-8-(3-methyl-5-oxo-2H-furan-4-yl)chromen-2-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H12O5/c1-8-7-19-15(17)12(8)13-10(18-2)5-3-9-4-6-11(16)20-14(9)13/h3-6H,7H2,1-2H3
InChI Key AZYVCLJYWIHOAD-UHFFFAOYSA-N
Popularity 7 references in papers

Physical and Chemical Properties

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Molecular Formula C15H12O5
Molecular Weight 272.25 g/mol
Exact Mass 272.06847348 g/mol
Topological Polar Surface Area (TPSA) 61.80 Ų
XlogP 1.70
Atomic LogP (AlogP) 2.13
H-Bond Acceptor 5
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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84041-46-3
7-methoxy-8-(3-methyl-5-oxo-2H-furan-4-yl)chromen-2-one
CHEMBL156967
CHEBI:181852
DTXSID501346101
AKOS040734259
7-methoxy-8-(3-methyl-5-oxo-2H-uran-4-yl)chromen-2-one
7-Methoxy-8-(4-methyl-2-oxo-2,5-dihydrofuran-3-yl)-2H-chromen-2-one

2D Structure

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2D Structure of Microminutin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9947 99.47%
Caco-2 + 0.7751 77.51%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability + 0.5429 54.29%
Subcellular localzation Mitochondria 0.7924 79.24%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9553 95.53%
OATP1B3 inhibitior + 0.9548 95.48%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior + 0.7104 71.04%
P-glycoprotein inhibitior - 0.7071 70.71%
P-glycoprotein substrate - 0.8692 86.92%
CYP3A4 substrate - 0.5452 54.52%
CYP2C9 substrate - 0.6506 65.06%
CYP2D6 substrate - 0.8717 87.17%
CYP3A4 inhibition + 0.7090 70.90%
CYP2C9 inhibition + 0.9353 93.53%
CYP2C19 inhibition + 0.9159 91.59%
CYP2D6 inhibition - 0.7790 77.90%
CYP1A2 inhibition + 0.7616 76.16%
CYP2C8 inhibition - 0.7304 73.04%
CYP inhibitory promiscuity + 0.9230 92.30%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.5003 50.03%
Eye corrosion - 0.9828 98.28%
Eye irritation - 0.5682 56.82%
Skin irritation - 0.7977 79.77%
Skin corrosion - 0.9615 96.15%
Ames mutagenesis + 0.6100 61.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6264 62.64%
Micronuclear + 0.7274 72.74%
Hepatotoxicity + 0.7625 76.25%
skin sensitisation - 0.7047 70.47%
Respiratory toxicity - 0.5556 55.56%
Reproductive toxicity + 0.7333 73.33%
Mitochondrial toxicity - 0.5125 51.25%
Nephrotoxicity + 0.5000 50.00%
Acute Oral Toxicity (c) III 0.3940 39.40%
Estrogen receptor binding + 0.6258 62.58%
Androgen receptor binding + 0.8194 81.94%
Thyroid receptor binding - 0.7583 75.83%
Glucocorticoid receptor binding + 0.6866 68.66%
Aromatase binding + 0.7695 76.95%
PPAR gamma + 0.5404 54.04%
Honey bee toxicity - 0.8833 88.33%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.5400 54.00%
Fish aquatic toxicity + 0.9964 99.64%

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 94.84% 95.56%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 92.89% 94.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 87.93% 99.23%
CHEMBL4306 P22460 Voltage-gated potassium channel subunit Kv1.5 87.17% 94.03%
CHEMBL2581 P07339 Cathepsin D 86.29% 98.95%
CHEMBL2535 P11166 Glucose transporter 85.56% 98.75%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.07% 86.33%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 82.57% 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.
Micromelum minutum
Murraya paniculata

Cross-Links

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PubChem 5319827
LOTUS LTS0162313
wikiData Q104394142