Mucorisocoumarin C

Details

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Internal ID cd652bec-ee2b-4f15-9289-5f9677e6a85f
Taxonomy Phenylpropanoids and polyketides > Isocoumarins and derivatives
IUPAC Name methyl 2-hydroxy-3-(8-hydroxy-6-methoxy-1-oxoisochromen-3-yl)propanoate
SMILES (Canonical) COC1=CC(=C2C(=C1)C=C(OC2=O)CC(C(=O)OC)O)O
SMILES (Isomeric) COC1=CC(=C2C(=C1)C=C(OC2=O)CC(C(=O)OC)O)O
InChI InChI=1S/C14H14O7/c1-19-8-3-7-4-9(6-11(16)13(17)20-2)21-14(18)12(7)10(15)5-8/h3-5,11,15-16H,6H2,1-2H3
InChI Key VUNARYPDGBWBAZ-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C14H14O7
Molecular Weight 294.26 g/mol
Exact Mass 294.07395278 g/mol
Topological Polar Surface Area (TPSA) 102.00 Ų
XlogP 1.60
Atomic LogP (AlogP) 0.58
H-Bond Acceptor 7
H-Bond Donor 2
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Mucorisocoumarin C

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9074 90.74%
Caco-2 + 0.6810 68.10%
Blood Brain Barrier - 0.8000 80.00%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Mitochondria 0.6468 64.68%
OATP2B1 inhibitior - 0.8602 86.02%
OATP1B1 inhibitior + 0.9012 90.12%
OATP1B3 inhibitior + 0.8323 83.23%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.7682 76.82%
P-glycoprotein inhibitior - 0.8372 83.72%
P-glycoprotein substrate - 0.8612 86.12%
CYP3A4 substrate - 0.5000 50.00%
CYP2C9 substrate + 0.6387 63.87%
CYP2D6 substrate - 0.8431 84.31%
CYP3A4 inhibition - 0.8604 86.04%
CYP2C9 inhibition - 0.8620 86.20%
CYP2C19 inhibition - 0.8932 89.32%
CYP2D6 inhibition - 0.8516 85.16%
CYP1A2 inhibition - 0.7511 75.11%
CYP2C8 inhibition - 0.7103 71.03%
CYP inhibitory promiscuity - 0.8460 84.60%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.5877 58.77%
Eye corrosion - 0.9719 97.19%
Eye irritation - 0.6150 61.50%
Skin irritation - 0.8208 82.08%
Skin corrosion - 0.9658 96.58%
Ames mutagenesis - 0.5600 56.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7372 73.72%
Micronuclear + 0.7459 74.59%
Hepatotoxicity - 0.6267 62.67%
skin sensitisation - 0.9231 92.31%
Respiratory toxicity + 0.6778 67.78%
Reproductive toxicity + 0.8444 84.44%
Mitochondrial toxicity + 0.6125 61.25%
Nephrotoxicity - 0.6685 66.85%
Acute Oral Toxicity (c) III 0.6887 68.87%
Estrogen receptor binding + 0.7165 71.65%
Androgen receptor binding + 0.7920 79.20%
Thyroid receptor binding - 0.5658 56.58%
Glucocorticoid receptor binding + 0.7092 70.92%
Aromatase binding + 0.6100 61.00%
PPAR gamma + 0.5911 59.11%
Honey bee toxicity - 0.9114 91.14%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.7200 72.00%
Fish aquatic toxicity + 0.7117 71.17%

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 98.76% 91.11%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 96.95% 85.14%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 94.27% 99.15%
CHEMBL3060 Q9Y345 Glycine transporter 2 93.78% 99.17%
CHEMBL2581 P07339 Cathepsin D 91.27% 98.95%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 88.93% 94.00%
CHEMBL3401 O75469 Pregnane X receptor 88.93% 94.73%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 88.53% 94.45%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.67% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.44% 96.09%
CHEMBL4208 P20618 Proteasome component C5 86.01% 90.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.53% 86.33%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 84.76% 96.00%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 84.51% 91.07%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 84.30% 95.50%
CHEMBL2535 P11166 Glucose transporter 84.27% 98.75%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 82.55% 90.71%
CHEMBL340 P08684 Cytochrome P450 3A4 80.89% 91.19%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 80.50% 99.23%

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 139584688
LOTUS LTS0252733
wikiData Q77374020