Myrothelactone C

Details

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Internal ID dca8d13a-8fb9-43c2-a7ee-d8c9cb770c7a
Taxonomy Phenylpropanoids and polyketides > Isocoumarins and derivatives
IUPAC Name 8-hydroxy-4-(2-hydroxyacetyl)-6-methoxyisochromen-1-one
SMILES (Canonical) COC1=CC2=C(C(=C1)O)C(=O)OC=C2C(=O)CO
SMILES (Isomeric) COC1=CC2=C(C(=C1)O)C(=O)OC=C2C(=O)CO
InChI InChI=1S/C12H10O6/c1-17-6-2-7-8(10(15)4-13)5-18-12(16)11(7)9(14)3-6/h2-3,5,13-14H,4H2,1H3
InChI Key BYDWOSCLWYIICB-UHFFFAOYSA-N
Popularity 1 reference 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 0.80
Atomic LogP (AlogP) 0.68
H-Bond Acceptor 6
H-Bond Donor 2
Rotatable Bonds 3

Synonyms

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8-hydroxy-4-(2-hydroxyacetyl)-6-methoxyisochromen-1-one
RefChem:160480
CHEBI:214322

2D Structure

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2D Structure of Myrothelactone C

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9098 90.98%
Caco-2 - 0.6367 63.67%
Blood Brain Barrier - 0.9000 90.00%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Mitochondria 0.7204 72.04%
OATP2B1 inhibitior - 0.7143 71.43%
OATP1B1 inhibitior + 0.9172 91.72%
OATP1B3 inhibitior + 0.9162 91.62%
MATE1 inhibitior - 0.6800 68.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.7677 76.77%
P-glycoprotein inhibitior - 0.9006 90.06%
P-glycoprotein substrate - 0.8825 88.25%
CYP3A4 substrate - 0.5392 53.92%
CYP2C9 substrate + 0.6171 61.71%
CYP2D6 substrate - 0.8666 86.66%
CYP3A4 inhibition - 0.8874 88.74%
CYP2C9 inhibition - 0.6429 64.29%
CYP2C19 inhibition - 0.7829 78.29%
CYP2D6 inhibition - 0.9191 91.91%
CYP1A2 inhibition - 0.7598 75.98%
CYP2C8 inhibition - 0.6851 68.51%
CYP inhibitory promiscuity - 0.7360 73.60%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9500 95.00%
Carcinogenicity (trinary) Non-required 0.6023 60.23%
Eye corrosion - 0.9597 95.97%
Eye irritation + 0.9265 92.65%
Skin irritation - 0.8427 84.27%
Skin corrosion - 0.9712 97.12%
Ames mutagenesis - 0.5600 56.00%
Human Ether-a-go-go-Related Gene inhibition - 0.9351 93.51%
Micronuclear + 0.6533 65.33%
Hepatotoxicity + 0.5625 56.25%
skin sensitisation - 0.9284 92.84%
Respiratory toxicity - 0.5222 52.22%
Reproductive toxicity + 0.7111 71.11%
Mitochondrial toxicity + 0.5875 58.75%
Nephrotoxicity - 0.6301 63.01%
Acute Oral Toxicity (c) III 0.7377 73.77%
Estrogen receptor binding + 0.5557 55.57%
Androgen receptor binding + 0.6459 64.59%
Thyroid receptor binding - 0.6194 61.94%
Glucocorticoid receptor binding + 0.6884 68.84%
Aromatase binding + 0.5641 56.41%
PPAR gamma + 0.7519 75.19%
Honey bee toxicity - 0.8967 89.67%
Biodegradation - 0.5750 57.50%
Crustacea aquatic toxicity - 0.7300 73.00%
Fish aquatic toxicity - 0.4332 43.32%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 98.93% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 93.45% 94.45%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.45% 95.56%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 91.35% 94.00%
CHEMBL2581 P07339 Cathepsin D 90.34% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 89.76% 99.17%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 89.22% 99.15%
CHEMBL2535 P11166 Glucose transporter 85.53% 98.75%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.28% 86.33%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.27% 96.09%
CHEMBL3401 O75469 Pregnane X receptor 83.98% 94.73%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 83.49% 85.14%
CHEMBL1806 P11388 DNA topoisomerase II alpha 83.28% 89.00%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 82.67% 91.07%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 81.12% 94.42%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 81.09% 95.50%
CHEMBL4208 P20618 Proteasome component C5 80.99% 90.00%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 139590751
LOTUS LTS0035895
wikiData Q104086370