Azanthromicin A

Details

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Internal ID c5d1b597-094f-4fa0-b260-ff141cb496ab
Taxonomy Benzenoids > Naphthalenes
IUPAC Name (5S)-5,9-dihydroxy-1,3,5,8-tetramethylbenzo[g]isoquinolin-10-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C17H17NO3/c1-8-5-6-11-14(15(8)19)16(20)13-10(3)18-9(2)7-12(13)17(11,4)21/h5-7,19,21H,1-4H3/t17-/m1/s1
InChI Key GTLFRJKAROJZPU-QGZVFWFLSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C17H17NO3
Molecular Weight 283.32 g/mol
Exact Mass 283.12084340 g/mol
Topological Polar Surface Area (TPSA) 70.40 Ų
XlogP 2.70
Atomic LogP (AlogP) 2.51
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Azanthromicin A

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9951 99.51%
Caco-2 + 0.8024 80.24%
Blood Brain Barrier - 0.5750 57.50%
Human oral bioavailability + 0.6000 60.00%
Subcellular localzation Mitochondria 0.8343 83.43%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8757 87.57%
OATP1B3 inhibitior + 0.9679 96.79%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.5737 57.37%
P-glycoprotein inhibitior - 0.8724 87.24%
P-glycoprotein substrate - 0.8502 85.02%
CYP3A4 substrate + 0.5210 52.10%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8644 86.44%
CYP3A4 inhibition - 0.8133 81.33%
CYP2C9 inhibition - 0.8754 87.54%
CYP2C19 inhibition + 0.6052 60.52%
CYP2D6 inhibition - 0.8841 88.41%
CYP1A2 inhibition + 0.8318 83.18%
CYP2C8 inhibition - 0.6538 65.38%
CYP inhibitory promiscuity - 0.6448 64.48%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9200 92.00%
Carcinogenicity (trinary) Non-required 0.5604 56.04%
Eye corrosion - 0.9951 99.51%
Eye irritation - 0.4945 49.45%
Skin irritation - 0.7963 79.63%
Skin corrosion - 0.9739 97.39%
Ames mutagenesis + 0.5700 57.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5999 59.99%
Micronuclear + 0.6100 61.00%
Hepatotoxicity + 0.6427 64.27%
skin sensitisation - 0.8627 86.27%
Respiratory toxicity + 0.5889 58.89%
Reproductive toxicity + 0.5556 55.56%
Mitochondrial toxicity - 0.5625 56.25%
Nephrotoxicity - 0.5849 58.49%
Acute Oral Toxicity (c) III 0.6031 60.31%
Estrogen receptor binding + 0.6573 65.73%
Androgen receptor binding + 0.6681 66.81%
Thyroid receptor binding + 0.6573 65.73%
Glucocorticoid receptor binding + 0.7150 71.50%
Aromatase binding + 0.7953 79.53%
PPAR gamma + 0.5265 52.65%
Honey bee toxicity - 0.9571 95.71%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity + 0.5500 55.00%
Fish aquatic toxicity + 0.6448 64.48%

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 97.08% 91.11%
CHEMBL1951 P21397 Monoamine oxidase A 94.01% 91.49%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.38% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.31% 86.33%
CHEMBL3401 O75469 Pregnane X receptor 91.06% 94.73%
CHEMBL2581 P07339 Cathepsin D 88.65% 98.95%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 87.99% 99.23%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 87.51% 96.67%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 85.51% 93.65%
CHEMBL1937 Q92769 Histone deacetylase 2 85.27% 94.75%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 84.39% 94.42%
CHEMBL215 P09917 Arachidonate 5-lipoxygenase 84.02% 92.68%
CHEMBL230 P35354 Cyclooxygenase-2 84.02% 89.63%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 83.64% 85.14%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 82.03% 99.15%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 81.48% 93.03%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 81.45% 100.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 81.16% 94.00%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 81.09% 93.40%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 80.67% 96.00%
CHEMBL3524 P56524 Histone deacetylase 4 80.59% 92.97%

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 146683962
LOTUS LTS0104334
wikiData Q105018972