Saccharomone A

Details

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Internal ID 189a3865-d18e-4dd1-9861-7dc505c68b52
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthones
IUPAC Name methyl (1S,2R)-6-formyl-2,8-dihydroxy-9-oxo-1,2-dihydroxanthene-1-carboxylate
SMILES (Canonical) COC(=O)C1C(C=CC2=C1C(=O)C3=C(C=C(C=C3O2)C=O)O)O
SMILES (Isomeric) COC(=O)[C@@H]1[C@@H](C=CC2=C1C(=O)C3=C(C=C(C=C3O2)C=O)O)O
InChI InChI=1S/C16H12O7/c1-22-16(21)13-8(18)2-3-10-14(13)15(20)12-9(19)4-7(6-17)5-11(12)23-10/h2-6,8,13,18-19H,1H3/t8-,13-/m1/s1
InChI Key CDKBGLWDBROJHO-AMIZOPFISA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C16H12O7
Molecular Weight 316.26 g/mol
Exact Mass 316.05830272 g/mol
Topological Polar Surface Area (TPSA) 110.00 Ų
XlogP 1.30
Atomic LogP (AlogP) 0.96
H-Bond Acceptor 7
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 Saccharomone A

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9701 97.01%
Caco-2 - 0.7089 70.89%
Blood Brain Barrier - 0.9000 90.00%
Human oral bioavailability + 0.5571 55.71%
Subcellular localzation Mitochondria 0.7638 76.38%
OATP2B1 inhibitior - 0.7168 71.68%
OATP1B1 inhibitior + 0.8539 85.39%
OATP1B3 inhibitior + 0.9889 98.89%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.7853 78.53%
P-glycoprotein inhibitior - 0.5764 57.64%
P-glycoprotein substrate - 0.6582 65.82%
CYP3A4 substrate + 0.6231 62.31%
CYP2C9 substrate + 0.6083 60.83%
CYP2D6 substrate - 0.8668 86.68%
CYP3A4 inhibition - 0.7926 79.26%
CYP2C9 inhibition + 0.6801 68.01%
CYP2C19 inhibition - 0.6260 62.60%
CYP2D6 inhibition - 0.9009 90.09%
CYP1A2 inhibition + 0.6551 65.51%
CYP2C8 inhibition + 0.4737 47.37%
CYP inhibitory promiscuity - 0.5374 53.74%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9513 95.13%
Carcinogenicity (trinary) Danger 0.4561 45.61%
Eye corrosion - 0.9797 97.97%
Eye irritation - 0.6243 62.43%
Skin irritation - 0.6361 63.61%
Skin corrosion - 0.9579 95.79%
Ames mutagenesis + 0.6736 67.36%
Human Ether-a-go-go-Related Gene inhibition - 0.8207 82.07%
Micronuclear + 0.9300 93.00%
Hepatotoxicity + 0.6500 65.00%
skin sensitisation - 0.9318 93.18%
Respiratory toxicity + 0.6556 65.56%
Reproductive toxicity + 0.7889 78.89%
Mitochondrial toxicity + 0.6500 65.00%
Nephrotoxicity + 0.5420 54.20%
Acute Oral Toxicity (c) III 0.5048 50.48%
Estrogen receptor binding + 0.7860 78.60%
Androgen receptor binding + 0.6805 68.05%
Thyroid receptor binding - 0.7133 71.33%
Glucocorticoid receptor binding + 0.6511 65.11%
Aromatase binding + 0.5326 53.26%
PPAR gamma + 0.5177 51.77%
Honey bee toxicity - 0.7939 79.39%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity + 0.5400 54.00%
Fish aquatic toxicity + 0.9783 97.83%

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 99.23% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.58% 95.56%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 95.44% 94.45%
CHEMBL1806 P11388 DNA topoisomerase II alpha 90.21% 89.00%
CHEMBL1163101 O75460 Serine/threonine-protein kinase/endoribonuclease IRE1 87.64% 98.11%
CHEMBL3194 P02766 Transthyretin 87.60% 90.71%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 86.96% 85.14%
CHEMBL3401 O75469 Pregnane X receptor 86.89% 94.73%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.69% 86.33%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 84.45% 99.23%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 82.96% 89.34%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.78% 99.17%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 81.13% 90.71%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 81.00% 94.00%
CHEMBL2581 P07339 Cathepsin D 80.63% 98.95%
CHEMBL4208 P20618 Proteasome component C5 80.09% 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 146682260
LOTUS LTS0227968
wikiData Q104954551