Excavatin M

Details

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Internal ID 4696367d-b7bb-461d-b159-d3ae921e9911
Taxonomy Phenylpropanoids and polyketides > Coumarins and derivatives
IUPAC Name 7-[[3-[(4-hydroxy-4-methyl-5-oxooxolan-2-yl)methyl]-3-methyloxiran-2-yl]methoxy]chromen-2-one
SMILES (Canonical) CC1(CC(OC1=O)CC2(C(O2)COC3=CC4=C(C=C3)C=CC(=O)O4)C)O
SMILES (Isomeric) CC1(CC(OC1=O)CC2(C(O2)COC3=CC4=C(C=C3)C=CC(=O)O4)C)O
InChI InChI=1S/C19H20O7/c1-18(22)8-13(24-17(18)21)9-19(2)15(26-19)10-23-12-5-3-11-4-6-16(20)25-14(11)7-12/h3-7,13,15,22H,8-10H2,1-2H3
InChI Key UMYAEKVHXDURJS-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C19H20O7
Molecular Weight 360.40 g/mol
Exact Mass 360.12090297 g/mol
Topological Polar Surface Area (TPSA) 94.60 Ų
XlogP 1.80
Atomic LogP (AlogP) 1.79
H-Bond Acceptor 7
H-Bond Donor 1
Rotatable Bonds 5

Synonyms

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250293-31-3
7-[[3-[(4-hydroxy-4-methyl-5-oxooxolan-2-yl)methyl]-3-methyloxiran-2-yl]methoxy]chromen-2-one
clauslactone H
CHEMBL470442
AKOS032961616
FS-9656

2D Structure

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2D Structure of Excavatin M

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9526 95.26%
Caco-2 - 0.5595 55.95%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Mitochondria 0.7588 75.88%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8818 88.18%
OATP1B3 inhibitior + 0.8536 85.36%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior + 0.9232 92.32%
P-glycoprotein inhibitior - 0.5434 54.34%
P-glycoprotein substrate - 0.6609 66.09%
CYP3A4 substrate + 0.6102 61.02%
CYP2C9 substrate - 0.6340 63.40%
CYP2D6 substrate - 0.8235 82.35%
CYP3A4 inhibition + 0.6479 64.79%
CYP2C9 inhibition - 0.7736 77.36%
CYP2C19 inhibition - 0.7801 78.01%
CYP2D6 inhibition - 0.9243 92.43%
CYP1A2 inhibition - 0.8452 84.52%
CYP2C8 inhibition - 0.6209 62.09%
CYP inhibitory promiscuity - 0.8593 85.93%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.5298 52.98%
Eye corrosion - 0.9903 99.03%
Eye irritation - 0.9680 96.80%
Skin irritation - 0.7159 71.59%
Skin corrosion - 0.9424 94.24%
Ames mutagenesis - 0.6500 65.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4348 43.48%
Micronuclear - 0.5100 51.00%
Hepatotoxicity + 0.5177 51.77%
skin sensitisation - 0.8383 83.83%
Respiratory toxicity + 0.6333 63.33%
Reproductive toxicity + 0.8333 83.33%
Mitochondrial toxicity + 0.8500 85.00%
Nephrotoxicity - 0.6045 60.45%
Acute Oral Toxicity (c) I 0.5665 56.65%
Estrogen receptor binding + 0.8806 88.06%
Androgen receptor binding + 0.7792 77.92%
Thyroid receptor binding + 0.6978 69.78%
Glucocorticoid receptor binding + 0.8607 86.07%
Aromatase binding + 0.7898 78.98%
PPAR gamma + 0.7500 75.00%
Honey bee toxicity - 0.9001 90.01%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity - 0.5400 54.00%
Fish aquatic toxicity + 0.9932 99.32%

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
CHEMBL2039 P27338 Monoamine oxidase B 99.63% 92.51%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 98.09% 91.11%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 95.21% 94.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 94.69% 97.09%
CHEMBL1951 P21397 Monoamine oxidase A 93.02% 91.49%
CHEMBL4208 P20618 Proteasome component C5 92.52% 90.00%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 92.12% 85.14%
CHEMBL3060 Q9Y345 Glycine transporter 2 88.80% 99.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.98% 96.09%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 86.27% 99.23%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 85.61% 94.45%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.07% 95.56%
CHEMBL1806 P11388 DNA topoisomerase II alpha 82.22% 89.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 81.69% 95.89%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 81.28% 92.62%
CHEMBL2581 P07339 Cathepsin D 81.02% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 80.94% 86.33%
CHEMBL3401 O75469 Pregnane X receptor 80.28% 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.
Clausena excavata

Cross-Links

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PubChem 15871351
LOTUS LTS0204192
wikiData Q105275815