Aspergiloid E

Details

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Internal ID 84dc95fc-8920-46b6-a443-9e1ce8d4a997
Taxonomy Organoheterocyclic compounds > Lactones > Gamma butyrolactones
IUPAC Name (1S,2S,5R,9S,10S)-5-ethenyl-9-hydroxy-5,11,11-trimethyl-16-oxatetracyclo[7.5.2.01,10.02,7]hexadec-6-ene-8,15-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C20H26O4/c1-5-18(4)10-7-13-12(11-18)14(21)20(23)15-17(2,3)8-6-9-19(13,15)16(22)24-20/h5,11,13,15,23H,1,6-10H2,2-4H3/t13-,15-,18-,19-,20+/m0/s1
InChI Key AHEAPTSGUOGOKK-XZWBYJIQSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C20H26O4
Molecular Weight 330.40 g/mol
Exact Mass 330.18310931 g/mol
Topological Polar Surface Area (TPSA) 63.60 Ų
XlogP 4.10
Atomic LogP (AlogP) 3.16
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Aspergiloid E

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9823 98.23%
Caco-2 + 0.6207 62.07%
Blood Brain Barrier + 0.7750 77.50%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Mitochondria 0.7177 71.77%
OATP2B1 inhibitior - 0.8583 85.83%
OATP1B1 inhibitior + 0.8925 89.25%
OATP1B3 inhibitior + 0.8547 85.47%
MATE1 inhibitior - 0.8000 80.00%
OCT2 inhibitior + 0.6250 62.50%
BSEP inhibitior - 0.4504 45.04%
P-glycoprotein inhibitior - 0.7828 78.28%
P-glycoprotein substrate - 0.9034 90.34%
CYP3A4 substrate + 0.6086 60.86%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8641 86.41%
CYP3A4 inhibition - 0.7417 74.17%
CYP2C9 inhibition - 0.7133 71.33%
CYP2C19 inhibition - 0.7875 78.75%
CYP2D6 inhibition - 0.9314 93.14%
CYP1A2 inhibition + 0.6477 64.77%
CYP2C8 inhibition - 0.6880 68.80%
CYP inhibitory promiscuity - 0.8948 89.48%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.5034 50.34%
Eye corrosion - 0.9874 98.74%
Eye irritation - 0.9136 91.36%
Skin irritation + 0.5678 56.78%
Skin corrosion - 0.9010 90.10%
Ames mutagenesis - 0.8453 84.53%
Human Ether-a-go-go-Related Gene inhibition - 0.5796 57.96%
Micronuclear - 0.7500 75.00%
Hepatotoxicity + 0.7041 70.41%
skin sensitisation - 0.7352 73.52%
Respiratory toxicity + 0.6667 66.67%
Reproductive toxicity + 0.8111 81.11%
Mitochondrial toxicity + 0.8750 87.50%
Nephrotoxicity + 0.5221 52.21%
Acute Oral Toxicity (c) III 0.5256 52.56%
Estrogen receptor binding + 0.7339 73.39%
Androgen receptor binding + 0.6765 67.65%
Thyroid receptor binding + 0.6270 62.70%
Glucocorticoid receptor binding + 0.6976 69.76%
Aromatase binding + 0.5731 57.31%
PPAR gamma + 0.6870 68.70%
Honey bee toxicity - 0.8983 89.83%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity + 0.5846 58.46%
Fish aquatic toxicity + 1.0000 100.00%

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 97.92% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.39% 95.56%
CHEMBL253 P34972 Cannabinoid CB2 receptor 91.23% 97.25%
CHEMBL2581 P07339 Cathepsin D 89.75% 98.95%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 88.85% 82.69%
CHEMBL1293255 P15428 15-hydroxyprostaglandin dehydrogenase [NAD+] 88.49% 83.57%
CHEMBL1937 Q92769 Histone deacetylase 2 87.92% 94.75%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.75% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 86.41% 97.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.04% 86.33%
CHEMBL1994 P08235 Mineralocorticoid receptor 85.78% 100.00%
CHEMBL3192 Q9BY41 Histone deacetylase 8 85.36% 93.99%
CHEMBL1806 P11388 DNA topoisomerase II alpha 84.67% 89.00%
CHEMBL1902 P62942 FK506-binding protein 1A 84.16% 97.05%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 83.98% 97.14%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 83.75% 93.03%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 83.12% 99.23%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 80.90% 94.80%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.07% 95.89%

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 102572825
LOTUS LTS0072599
wikiData Q77504188