1',2'-Epoxy-3',4'-didehydro-penicillide

Details

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Internal ID 529d98cb-2332-4b6f-b26c-665e736cc462
Taxonomy Organic oxygen compounds > Organooxygen compounds > Ethers > Diarylethers
IUPAC Name 6-hydroxy-1-methoxy-8-methyl-2-[(2R,3R)-3-prop-1-en-2-yloxiran-2-yl]-10H-benzo[b][1,5]benzodioxocin-12-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C21H20O6/c1-10(2)17-20(27-17)13-5-6-15-16(19(13)24-4)21(23)25-9-12-7-11(3)8-14(22)18(12)26-15/h5-8,17,20,22H,1,9H2,2-4H3/t17-,20-/m1/s1
InChI Key BLJNAQWNZHOUNA-YLJYHZDGSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C21H20O6
Molecular Weight 368.40 g/mol
Exact Mass 368.12598835 g/mol
Topological Polar Surface Area (TPSA) 77.50 Ų
XlogP 3.60
Atomic LogP (AlogP) 4.19
H-Bond Acceptor 6
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 1',2'-Epoxy-3',4'-didehydro-penicillide

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9717 97.17%
Caco-2 + 0.5297 52.97%
Blood Brain Barrier - 0.5750 57.50%
Human oral bioavailability - 0.7143 71.43%
Subcellular localzation Mitochondria 0.7239 72.39%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9150 91.50%
OATP1B3 inhibitior + 0.9216 92.16%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior + 0.7418 74.18%
P-glycoprotein inhibitior - 0.4816 48.16%
P-glycoprotein substrate - 0.7376 73.76%
CYP3A4 substrate + 0.6134 61.34%
CYP2C9 substrate - 0.8074 80.74%
CYP2D6 substrate - 0.8254 82.54%
CYP3A4 inhibition + 0.5437 54.37%
CYP2C9 inhibition + 0.5000 50.00%
CYP2C19 inhibition + 0.6959 69.59%
CYP2D6 inhibition - 0.8878 88.78%
CYP1A2 inhibition - 0.6339 63.39%
CYP2C8 inhibition + 0.5294 52.94%
CYP inhibitory promiscuity + 0.7334 73.34%
UGT catelyzed - 0.6638 66.38%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.5731 57.31%
Eye corrosion - 0.9865 98.65%
Eye irritation - 0.7182 71.82%
Skin irritation - 0.7536 75.36%
Skin corrosion - 0.9615 96.15%
Ames mutagenesis + 0.6100 61.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5803 58.03%
Micronuclear + 0.7000 70.00%
Hepatotoxicity + 0.6625 66.25%
skin sensitisation - 0.7397 73.97%
Respiratory toxicity + 0.7333 73.33%
Reproductive toxicity + 0.8000 80.00%
Mitochondrial toxicity + 0.5750 57.50%
Nephrotoxicity - 0.6084 60.84%
Acute Oral Toxicity (c) II 0.3668 36.68%
Estrogen receptor binding + 0.7441 74.41%
Androgen receptor binding + 0.7240 72.40%
Thyroid receptor binding + 0.6800 68.00%
Glucocorticoid receptor binding + 0.6772 67.72%
Aromatase binding - 0.5940 59.40%
PPAR gamma + 0.7807 78.07%
Honey bee toxicity - 0.7910 79.10%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.5000 50.00%
Fish aquatic toxicity + 0.9940 99.40%

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 99.40% 91.11%
CHEMBL1951 P21397 Monoamine oxidase A 98.32% 91.49%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 97.05% 95.56%
CHEMBL2581 P07339 Cathepsin D 96.19% 98.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 94.89% 94.45%
CHEMBL3401 O75469 Pregnane X receptor 94.67% 94.73%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 94.32% 85.14%
CHEMBL1293249 Q13887 Kruppel-like factor 5 94.28% 86.33%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.11% 96.09%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 93.56% 99.23%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 92.39% 94.80%
CHEMBL1806 P11388 DNA topoisomerase II alpha 89.26% 89.00%
CHEMBL240 Q12809 HERG 88.88% 89.76%
CHEMBL340 P08684 Cytochrome P450 3A4 86.42% 91.19%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 85.37% 94.00%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 84.78% 96.95%
CHEMBL3231 Q13464 Rho-associated protein kinase 1 84.51% 95.55%
CHEMBL2535 P11166 Glucose transporter 82.55% 98.75%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.35% 99.17%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 81.28% 95.89%
CHEMBL2056 P21728 Dopamine D1 receptor 80.28% 91.00%

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 139588489
LOTUS LTS0247293
wikiData Q105100847