Yicathin C

Details

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Internal ID c71a3b30-4137-4f30-993c-7104d25e92a4
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthones
IUPAC Name 8-hydroxy-1-methoxy-6-methyl-9-oxoxanthene-3-carboxylic acid
SMILES (Canonical) CC1=CC(=C2C(=C1)OC3=C(C2=O)C(=CC(=C3)C(=O)O)OC)O
SMILES (Isomeric) CC1=CC(=C2C(=C1)OC3=C(C2=O)C(=CC(=C3)C(=O)O)OC)O
InChI InChI=1S/C16H12O6/c1-7-3-9(17)13-11(4-7)22-12-6-8(16(19)20)5-10(21-2)14(12)15(13)18/h3-6,17H,1-2H3,(H,19,20)
InChI Key CDOFUOUENPZVAF-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C16H12O6
Molecular Weight 300.26 g/mol
Exact Mass 300.06338810 g/mol
Topological Polar Surface Area (TPSA) 93.10 Ų
XlogP 3.00
Atomic LogP (AlogP) 2.67
H-Bond Acceptor 5
H-Bond Donor 2
Rotatable Bonds 2

Synonyms

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8-Hydroxy-1-methoxy-6-methyl-9-oxo-9H-xanthene-3-carboxylic acid
1416961-91-5

2D Structure

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2D Structure of Yicathin C

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9439 94.39%
Caco-2 + 0.7952 79.52%
Blood Brain Barrier - 0.9250 92.50%
Human oral bioavailability + 0.6429 64.29%
Subcellular localzation Mitochondria 0.7394 73.94%
OATP2B1 inhibitior - 0.5741 57.41%
OATP1B1 inhibitior + 0.9343 93.43%
OATP1B3 inhibitior + 0.9512 95.12%
MATE1 inhibitior - 0.7200 72.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.7050 70.50%
P-glycoprotein inhibitior - 0.7652 76.52%
P-glycoprotein substrate - 0.8930 89.30%
CYP3A4 substrate - 0.5201 52.01%
CYP2C9 substrate - 0.5940 59.40%
CYP2D6 substrate - 0.8985 89.85%
CYP3A4 inhibition - 0.7970 79.70%
CYP2C9 inhibition - 0.6776 67.76%
CYP2C19 inhibition - 0.9126 91.26%
CYP2D6 inhibition - 0.8478 84.78%
CYP1A2 inhibition - 0.5585 55.85%
CYP2C8 inhibition + 0.4852 48.52%
CYP inhibitory promiscuity - 0.7984 79.84%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9213 92.13%
Carcinogenicity (trinary) Non-required 0.5820 58.20%
Eye corrosion - 0.9591 95.91%
Eye irritation + 0.8836 88.36%
Skin irritation - 0.7635 76.35%
Skin corrosion - 0.9784 97.84%
Ames mutagenesis + 0.6036 60.36%
Human Ether-a-go-go-Related Gene inhibition - 0.6645 66.45%
Micronuclear + 0.9000 90.00%
Hepatotoxicity + 0.6284 62.84%
skin sensitisation - 0.9715 97.15%
Respiratory toxicity + 0.5667 56.67%
Reproductive toxicity + 0.7111 71.11%
Mitochondrial toxicity + 0.5625 56.25%
Nephrotoxicity - 0.6096 60.96%
Acute Oral Toxicity (c) III 0.6619 66.19%
Estrogen receptor binding + 0.7509 75.09%
Androgen receptor binding + 0.7287 72.87%
Thyroid receptor binding - 0.6120 61.20%
Glucocorticoid receptor binding + 0.6453 64.53%
Aromatase binding + 0.5350 53.50%
PPAR gamma + 0.7536 75.36%
Honey bee toxicity - 0.9186 91.86%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.7800 78.00%
Fish aquatic toxicity + 0.8997 89.97%

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 93.87% 95.56%
CHEMBL3194 P02766 Transthyretin 93.74% 90.71%
CHEMBL1293249 Q13887 Kruppel-like factor 5 93.24% 86.33%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 90.31% 81.11%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 90.14% 99.23%
CHEMBL1806 P11388 DNA topoisomerase II alpha 89.55% 89.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 88.72% 91.11%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.44% 99.17%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 87.12% 94.42%
CHEMBL2535 P11166 Glucose transporter 86.13% 98.75%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 86.11% 94.00%
CHEMBL340 P08684 Cytochrome P450 3A4 85.60% 91.19%
CHEMBL1293294 P51151 Ras-related protein Rab-9A 85.49% 87.67%
CHEMBL2581 P07339 Cathepsin D 83.72% 98.95%
CHEMBL1811 P34995 Prostanoid EP1 receptor 82.32% 95.71%
CHEMBL4208 P20618 Proteasome component C5 81.92% 90.00%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 81.56% 96.95%

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 102191487
LOTUS LTS0173534
wikiData Q77311062