Ascotrichester A

Details

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Internal ID ef9a1a5f-e73d-4bfb-95dd-d73eb5e2d02e
Taxonomy Phenylpropanoids and polyketides > Isocoumarins and derivatives
IUPAC Name [(2R)-1-(6,8-dihydroxy-1-oxoisochromen-3-yl)propan-2-yl] 2,4-dihydroxy-6-[(2R)-2-[(3R)-3-hydroxybutanoyl]oxypropyl]benzoate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C26H28O11/c1-12(27)4-22(32)35-13(2)5-15-7-17(28)10-20(30)23(15)25(33)36-14(3)6-19-9-16-8-18(29)11-21(31)24(16)26(34)37-19/h7-14,27-31H,4-6H2,1-3H3/t12-,13-,14-/m1/s1
InChI Key CHOQHDNARHROTH-MGPQQGTHSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C26H28O11
Molecular Weight 516.50 g/mol
Exact Mass 516.16316171 g/mol
Topological Polar Surface Area (TPSA) 180.00 Ų
XlogP 4.10
Atomic LogP (AlogP) 2.65
H-Bond Acceptor 11
H-Bond Donor 5
Rotatable Bonds 9

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Ascotrichester A

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.7869 78.69%
Caco-2 - 0.7074 70.74%
Blood Brain Barrier - 0.5750 57.50%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Mitochondria 0.6385 63.85%
OATP2B1 inhibitior - 0.7169 71.69%
OATP1B1 inhibitior + 0.8584 85.84%
OATP1B3 inhibitior + 0.8832 88.32%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior + 0.7444 74.44%
P-glycoprotein inhibitior + 0.6642 66.42%
P-glycoprotein substrate - 0.5964 59.64%
CYP3A4 substrate + 0.6091 60.91%
CYP2C9 substrate + 0.8332 83.32%
CYP2D6 substrate - 0.8628 86.28%
CYP3A4 inhibition - 0.7337 73.37%
CYP2C9 inhibition - 0.7925 79.25%
CYP2C19 inhibition - 0.9000 90.00%
CYP2D6 inhibition - 0.8889 88.89%
CYP1A2 inhibition - 0.5868 58.68%
CYP2C8 inhibition + 0.5241 52.41%
CYP inhibitory promiscuity - 0.8001 80.01%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.6930 69.30%
Eye corrosion - 0.9920 99.20%
Eye irritation - 0.9083 90.83%
Skin irritation - 0.8113 81.13%
Skin corrosion - 0.9491 94.91%
Ames mutagenesis - 0.5300 53.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8511 85.11%
Micronuclear + 0.5500 55.00%
Hepatotoxicity + 0.6120 61.20%
skin sensitisation - 0.9100 91.00%
Respiratory toxicity + 0.6889 68.89%
Reproductive toxicity + 0.9667 96.67%
Mitochondrial toxicity + 0.8125 81.25%
Nephrotoxicity + 0.5000 50.00%
Acute Oral Toxicity (c) I 0.5771 57.71%
Estrogen receptor binding + 0.7314 73.14%
Androgen receptor binding + 0.8112 81.12%
Thyroid receptor binding - 0.5229 52.29%
Glucocorticoid receptor binding + 0.6992 69.92%
Aromatase binding + 0.5396 53.96%
PPAR gamma + 0.6310 63.10%
Honey bee toxicity - 0.7886 78.86%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.6000 60.00%
Fish aquatic toxicity + 0.9822 98.22%

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 97.91% 91.11%
CHEMBL2581 P07339 Cathepsin D 96.42% 98.95%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 92.83% 99.15%
CHEMBL3060 Q9Y345 Glycine transporter 2 89.81% 99.17%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 89.01% 90.71%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.94% 96.09%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 88.73% 94.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 88.64% 89.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 88.25% 94.45%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 88.18% 95.50%
CHEMBL3401 O75469 Pregnane X receptor 86.98% 94.73%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 86.85% 96.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.59% 86.33%
CHEMBL1929 P47989 Xanthine dehydrogenase 85.35% 96.12%
CHEMBL4208 P20618 Proteasome component C5 82.53% 90.00%
CHEMBL2535 P11166 Glucose transporter 82.23% 98.75%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 81.11% 99.23%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 80.75% 95.56%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 80.10% 93.65%

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 132544540
LOTUS LTS0010935
wikiData Q77369339