Aspergicin

Details

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Internal ID b70d4067-5c42-4bd9-a9d0-744028aae881
Taxonomy Organoheterocyclic compounds > Diazanaphthalenes > Benzodiazines > Quinazolines
IUPAC Name 12-methoxy-17-[(2S)-pyrrolidin-2-yl]-9-oxa-1,16-diazatetracyclo[8.7.1.02,7.014,18]octadeca-2,4,6,10,12,14(18),16-heptaene-8,15-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C20H17N3O4/c1-26-11-9-13-17-16(10-11)27-20(25)12-5-2-3-7-15(12)23(17)18(22-19(13)24)14-6-4-8-21-14/h2-3,5,7,9-10,14,21H,4,6,8H2,1H3/t14-/m0/s1
InChI Key CNJSVNCVRSJABJ-AWEZNQCLSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C20H17N3O4
Molecular Weight 363.40 g/mol
Exact Mass 363.12190603 g/mol
Topological Polar Surface Area (TPSA) 80.20 Ų
XlogP 2.00
Atomic LogP (AlogP) 2.39
H-Bond Acceptor 7
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Aspergicin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9812 98.12%
Caco-2 - 0.5791 57.91%
Blood Brain Barrier + 0.8250 82.50%
Human oral bioavailability + 0.6429 64.29%
Subcellular localzation Lysosomes 0.4181 41.81%
OATP2B1 inhibitior - 0.8587 85.87%
OATP1B1 inhibitior + 0.9246 92.46%
OATP1B3 inhibitior + 0.9385 93.85%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.6571 65.71%
BSEP inhibitior + 0.7643 76.43%
P-glycoprotein inhibitior + 0.8316 83.16%
P-glycoprotein substrate - 0.5788 57.88%
CYP3A4 substrate + 0.6501 65.01%
CYP2C9 substrate - 0.7953 79.53%
CYP2D6 substrate - 0.8035 80.35%
CYP3A4 inhibition - 0.5119 51.19%
CYP2C9 inhibition - 0.5935 59.35%
CYP2C19 inhibition - 0.5874 58.74%
CYP2D6 inhibition - 0.7957 79.57%
CYP1A2 inhibition + 0.6379 63.79%
CYP2C8 inhibition - 0.5959 59.59%
CYP inhibitory promiscuity + 0.6273 62.73%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.6643 66.43%
Eye corrosion - 0.9875 98.75%
Eye irritation - 0.9670 96.70%
Skin irritation - 0.8050 80.50%
Skin corrosion - 0.9415 94.15%
Ames mutagenesis + 0.6200 62.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6596 65.96%
Micronuclear + 0.8300 83.00%
Hepatotoxicity + 0.5803 58.03%
skin sensitisation - 0.8922 89.22%
Respiratory toxicity + 0.7333 73.33%
Reproductive toxicity + 0.9556 95.56%
Mitochondrial toxicity + 0.8625 86.25%
Nephrotoxicity - 0.7972 79.72%
Acute Oral Toxicity (c) III 0.6068 60.68%
Estrogen receptor binding + 0.6080 60.80%
Androgen receptor binding + 0.7983 79.83%
Thyroid receptor binding + 0.5818 58.18%
Glucocorticoid receptor binding + 0.8115 81.15%
Aromatase binding + 0.7311 73.11%
PPAR gamma + 0.7513 75.13%
Honey bee toxicity - 0.8890 88.90%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity + 0.6300 63.00%
Fish aquatic toxicity - 0.5379 53.79%

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
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 97.19% 95.56%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 96.42% 99.23%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 96.42% 85.14%
CHEMBL3192 Q9BY41 Histone deacetylase 8 95.89% 93.99%
CHEMBL3137262 O60341 LSD1/CoREST complex 95.51% 97.09%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 95.47% 94.00%
CHEMBL2581 P07339 Cathepsin D 94.97% 98.95%
CHEMBL3524 P56524 Histone deacetylase 4 94.71% 92.97%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.61% 91.11%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 89.82% 92.62%
CHEMBL4145 Q9UKV0 Histone deacetylase 9 89.79% 85.49%
CHEMBL2095226 P05556 Integrin alpha-5/beta-1 87.45% 96.39%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 87.04% 99.15%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 86.88% 93.65%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 85.42% 96.67%
CHEMBL1806 P11388 DNA topoisomerase II alpha 84.87% 89.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.56% 86.33%
CHEMBL3476 O15111 Inhibitor of nuclear factor kappa B kinase alpha subunit 84.25% 95.83%
CHEMBL253 P34972 Cannabinoid CB2 receptor 83.27% 97.25%
CHEMBL2535 P11166 Glucose transporter 83.09% 98.75%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 82.96% 96.09%
CHEMBL5203 P33316 dUTP pyrophosphatase 81.94% 99.18%
CHEMBL2095172 P14867 GABA-A receptor; alpha-1/beta-2/gamma-2 81.26% 92.67%
CHEMBL4051 P13569 Cystic fibrosis transmembrane conductance regulator 80.77% 95.71%
CHEMBL228 P31645 Serotonin transporter 80.76% 95.51%
CHEMBL3706 P78536 ADAM17 80.08% 90.71%

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 56949729
LOTUS LTS0150441
wikiData Q77563750