Eupenicillin A

Details

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Internal ID aa8200e2-c235-4302-9a2c-9c0360beeeb9
Taxonomy Organoheterocyclic compounds > Benzopyrans > 2-benzopyrans
IUPAC Name (3S)-6-hydroxy-3-(hydroxymethyl)-8-methoxy-3,4-dihydroisochromen-1-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C11H12O5/c1-15-9-4-7(13)2-6-3-8(5-12)16-11(14)10(6)9/h2,4,8,12-13H,3,5H2,1H3/t8-/m0/s1
InChI Key VAKHZMSIZBDNJR-QMMMGPOBSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C11H12O5
Molecular Weight 224.21 g/mol
Exact Mass 224.06847348 g/mol
Topological Polar Surface Area (TPSA) 76.00 Ų
XlogP 0.80
Atomic LogP (AlogP) 0.47
H-Bond Acceptor 5
H-Bond Donor 2
Rotatable Bonds 2

Synonyms

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DTXSID501133958
1H-2-Benzopyran-1-one, 3,4-dihydro-6-hydroxy-3-(hydroxymethyl)-8-methoxy-, (3S)-
2334434-59-0

2D Structure

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2D Structure of Eupenicillin A

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9010 90.10%
Caco-2 + 0.5779 57.79%
Blood Brain Barrier - 0.8250 82.50%
Human oral bioavailability - 0.6143 61.43%
Subcellular localzation Mitochondria 0.7145 71.45%
OATP2B1 inhibitior - 0.8529 85.29%
OATP1B1 inhibitior + 0.9013 90.13%
OATP1B3 inhibitior + 0.9553 95.53%
MATE1 inhibitior - 0.7600 76.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.9663 96.63%
P-glycoprotein inhibitior - 0.9681 96.81%
P-glycoprotein substrate - 0.8993 89.93%
CYP3A4 substrate + 0.5052 50.52%
CYP2C9 substrate - 0.5759 57.59%
CYP2D6 substrate - 0.7870 78.70%
CYP3A4 inhibition - 0.8930 89.30%
CYP2C9 inhibition - 0.6117 61.17%
CYP2C19 inhibition - 0.6084 60.84%
CYP2D6 inhibition - 0.8483 84.83%
CYP1A2 inhibition - 0.5080 50.80%
CYP2C8 inhibition - 0.7360 73.60%
CYP inhibitory promiscuity - 0.5959 59.59%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.6383 63.83%
Eye corrosion - 0.9738 97.38%
Eye irritation + 0.6979 69.79%
Skin irritation - 0.7781 77.81%
Skin corrosion - 0.9662 96.62%
Ames mutagenesis - 0.6624 66.24%
Human Ether-a-go-go-Related Gene inhibition - 0.7232 72.32%
Micronuclear + 0.5233 52.33%
Hepatotoxicity - 0.5198 51.98%
skin sensitisation - 0.8948 89.48%
Respiratory toxicity + 0.6000 60.00%
Reproductive toxicity + 0.7889 78.89%
Mitochondrial toxicity + 0.5625 56.25%
Nephrotoxicity + 0.7654 76.54%
Acute Oral Toxicity (c) III 0.6799 67.99%
Estrogen receptor binding - 0.6100 61.00%
Androgen receptor binding + 0.5314 53.14%
Thyroid receptor binding - 0.6076 60.76%
Glucocorticoid receptor binding - 0.5535 55.35%
Aromatase binding - 0.7666 76.66%
PPAR gamma - 0.5353 53.53%
Honey bee toxicity - 0.7744 77.44%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity - 0.5549 55.49%
Fish aquatic toxicity - 0.6096 60.96%

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 98.09% 91.11%
CHEMBL1293249 Q13887 Kruppel-like factor 5 94.16% 86.33%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.25% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.64% 95.56%
CHEMBL2581 P07339 Cathepsin D 90.79% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 90.65% 99.17%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 89.57% 94.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 88.36% 95.89%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 87.36% 95.89%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 86.67% 96.95%
CHEMBL3137262 O60341 LSD1/CoREST complex 86.23% 97.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 85.40% 94.45%
CHEMBL4208 P20618 Proteasome component C5 84.93% 90.00%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 84.74% 91.07%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 81.84% 97.14%
CHEMBL3401 O75469 Pregnane X receptor 81.15% 94.73%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 81.12% 86.92%

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 139591271
LOTUS LTS0001096
wikiData Q105282801