Myrothelactone D

Details

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Internal ID 259244f2-79f7-4090-834b-927f38ff66b9
Taxonomy Phenylpropanoids and polyketides > Isocoumarins and derivatives
IUPAC Name 8-hydroxy-6-methoxy-3-methyl-1-oxoisochromene-4-carboxylic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C12H10O6/c1-5-9(11(14)15)7-3-6(17-2)4-8(13)10(7)12(16)18-5/h3-4,13H,1-2H3,(H,14,15)
InChI Key ZDDOXLAUNUWIDW-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C12H10O6
Molecular Weight 250.20 g/mol
Exact Mass 250.04773803 g/mol
Topological Polar Surface Area (TPSA) 93.10 Ų
XlogP 1.70
Atomic LogP (AlogP) 1.51
H-Bond Acceptor 5
H-Bond Donor 2
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Myrothelactone D

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9386 93.86%
Caco-2 + 0.5744 57.44%
Blood Brain Barrier - 0.9250 92.50%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Mitochondria 0.7850 78.50%
OATP2B1 inhibitior - 0.8584 85.84%
OATP1B1 inhibitior + 0.9315 93.15%
OATP1B3 inhibitior + 0.9681 96.81%
MATE1 inhibitior - 0.7200 72.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.9138 91.38%
P-glycoprotein inhibitior - 0.8632 86.32%
P-glycoprotein substrate - 0.9337 93.37%
CYP3A4 substrate - 0.5663 56.63%
CYP2C9 substrate + 0.6328 63.28%
CYP2D6 substrate - 0.8980 89.80%
CYP3A4 inhibition - 0.9023 90.23%
CYP2C9 inhibition - 0.5608 56.08%
CYP2C19 inhibition - 0.8999 89.99%
CYP2D6 inhibition - 0.8731 87.31%
CYP1A2 inhibition + 0.6393 63.93%
CYP2C8 inhibition - 0.6427 64.27%
CYP inhibitory promiscuity - 0.7292 72.92%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9513 95.13%
Carcinogenicity (trinary) Non-required 0.6484 64.84%
Eye corrosion - 0.9792 97.92%
Eye irritation + 0.9017 90.17%
Skin irritation - 0.7269 72.69%
Skin corrosion - 0.9702 97.02%
Ames mutagenesis - 0.5200 52.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8267 82.67%
Micronuclear + 0.9200 92.00%
Hepatotoxicity + 0.5658 56.58%
skin sensitisation - 0.9660 96.60%
Respiratory toxicity + 0.5778 57.78%
Reproductive toxicity + 0.7778 77.78%
Mitochondrial toxicity + 0.6625 66.25%
Nephrotoxicity - 0.6462 64.62%
Acute Oral Toxicity (c) II 0.5724 57.24%
Estrogen receptor binding - 0.5000 50.00%
Androgen receptor binding + 0.5901 59.01%
Thyroid receptor binding - 0.6871 68.71%
Glucocorticoid receptor binding + 0.6364 63.64%
Aromatase binding - 0.5000 50.00%
PPAR gamma + 0.6168 61.68%
Honey bee toxicity - 0.9324 93.24%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity - 0.6800 68.00%
Fish aquatic toxicity + 0.9569 95.69%

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 98.07% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 96.10% 95.56%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 94.93% 99.15%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 90.91% 85.14%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 90.00% 94.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 89.35% 99.23%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 88.97% 94.42%
CHEMBL3194 P02766 Transthyretin 88.23% 90.71%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.61% 86.33%
CHEMBL3060 Q9Y345 Glycine transporter 2 86.00% 99.17%
CHEMBL3192 Q9BY41 Histone deacetylase 8 85.88% 93.99%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 85.15% 95.50%
CHEMBL1806 P11388 DNA topoisomerase II alpha 84.80% 89.00%
CHEMBL3401 O75469 Pregnane X receptor 84.20% 94.73%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 84.07% 94.45%
CHEMBL2581 P07339 Cathepsin D 83.04% 98.95%
CHEMBL1811 P34995 Prostanoid EP1 receptor 82.54% 95.71%
CHEMBL2535 P11166 Glucose transporter 81.55% 98.75%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 80.76% 96.00%
CHEMBL4208 P20618 Proteasome component C5 80.62% 90.00%

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.
There are no matching plants.

Cross-Links

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PubChem 139590752
LOTUS LTS0142820
wikiData Q104202302