Eupenicilazaphilone A

Details

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Internal ID 5a0bea76-4e26-4a6c-94a0-3af73d455537
Taxonomy Organoheterocyclic compounds > Azaphilones
IUPAC Name (7R,8R,8aS)-5-chloro-3-[(E,3S,4R,5S)-3,4-dihydroxy-3,5-dimethylhept-1-enyl]-7,8-dihydroxy-7-methyl-8,8a-dihydro-1H-isochromen-6-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C19H27ClO6/c1-5-10(2)15(21)18(3,24)7-6-11-8-12-13(9-26-11)16(22)19(4,25)17(23)14(12)20/h6-8,10,13,15-16,21-22,24-25H,5,9H2,1-4H3/b7-6+/t10-,13+,15+,16+,18-,19+/m0/s1
InChI Key CPMFRQHRPWPNMP-JRMQMFIBSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C19H27ClO6
Molecular Weight 386.90 g/mol
Exact Mass 386.1496163 g/mol
Topological Polar Surface Area (TPSA) 107.00 Ų
XlogP 1.00
Atomic LogP (AlogP) 1.42
H-Bond Acceptor 6
H-Bond Donor 4
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Eupenicilazaphilone A

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9760 97.60%
Caco-2 - 0.7582 75.82%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Mitochondria 0.6856 68.56%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8652 86.52%
OATP1B3 inhibitior + 0.9135 91.35%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.5569 55.69%
P-glycoprotein inhibitior - 0.8241 82.41%
P-glycoprotein substrate - 0.5748 57.48%
CYP3A4 substrate + 0.6252 62.52%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8585 85.85%
CYP3A4 inhibition - 0.7995 79.95%
CYP2C9 inhibition - 0.6774 67.74%
CYP2C19 inhibition - 0.6542 65.42%
CYP2D6 inhibition - 0.8515 85.15%
CYP1A2 inhibition - 0.6639 66.39%
CYP2C8 inhibition - 0.7774 77.74%
CYP inhibitory promiscuity - 0.5679 56.79%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9100 91.00%
Carcinogenicity (trinary) Non-required 0.5273 52.73%
Eye corrosion - 0.9855 98.55%
Eye irritation - 0.9690 96.90%
Skin irritation - 0.6412 64.12%
Skin corrosion - 0.9208 92.08%
Ames mutagenesis - 0.5400 54.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3700 37.00%
Micronuclear - 0.6941 69.41%
Hepatotoxicity + 0.6303 63.03%
skin sensitisation - 0.7962 79.62%
Respiratory toxicity + 0.7444 74.44%
Reproductive toxicity + 0.7889 78.89%
Mitochondrial toxicity + 0.5750 57.50%
Nephrotoxicity + 0.4603 46.03%
Acute Oral Toxicity (c) III 0.5714 57.14%
Estrogen receptor binding + 0.7164 71.64%
Androgen receptor binding + 0.6559 65.59%
Thyroid receptor binding + 0.6746 67.46%
Glucocorticoid receptor binding + 0.6707 67.07%
Aromatase binding + 0.6077 60.77%
PPAR gamma + 0.6448 64.48%
Honey bee toxicity - 0.7924 79.24%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.5300 53.00%
Fish aquatic toxicity + 0.9772 97.72%

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
CHEMBL253 P34972 Cannabinoid CB2 receptor 99.30% 97.25%
CHEMBL2581 P07339 Cathepsin D 98.44% 98.95%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 97.20% 85.14%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 96.58% 89.34%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 95.01% 94.45%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.62% 96.09%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 93.28% 96.77%
CHEMBL3137262 O60341 LSD1/CoREST complex 92.95% 97.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 92.72% 86.33%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 91.97% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.28% 95.56%
CHEMBL3401 O75469 Pregnane X receptor 88.10% 94.73%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 86.64% 100.00%
CHEMBL1994 P08235 Mineralocorticoid receptor 85.90% 100.00%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 84.84% 86.92%
CHEMBL1907605 P24864 Cyclin-dependent kinase 2/cyclin E1 84.59% 92.88%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 84.05% 92.86%
CHEMBL226 P30542 Adenosine A1 receptor 83.54% 95.93%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 82.81% 96.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.67% 95.89%
CHEMBL1806 P11388 DNA topoisomerase II alpha 82.06% 89.00%
CHEMBL5163 Q9NY46 Sodium channel protein type III alpha subunit 80.61% 96.90%

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 139591268
LOTUS LTS0095815
wikiData Q104967645