5-Methoxy-4-amino-1-azabenzanthrone

Details

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Internal ID 2a9937d6-ebf7-4746-88ef-3b1d6456ef36
Taxonomy Alkaloids and derivatives > Isoaporphines > Oxoisoaporphines
IUPAC Name 12-amino-11-methoxy-16-azatetracyclo[7.7.1.02,7.013,17]heptadeca-1(16),2,4,6,9,11,13(17),14-octaen-8-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C17H12N2O2/c1-21-13-8-12-14-11(15(13)18)6-7-19-16(14)9-4-2-3-5-10(9)17(12)20/h2-8H,18H2,1H3
InChI Key DVXISAIJCXZAQX-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C17H12N2O2
Molecular Weight 276.29 g/mol
Exact Mass 276.089877630 g/mol
Topological Polar Surface Area (TPSA) 65.20 Ų
XlogP 2.60
Atomic LogP (AlogP) 3.04
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 5-Methoxy-4-amino-1-azabenzanthrone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 1.0000 100.00%
Caco-2 + 0.6215 62.15%
Blood Brain Barrier + 0.8000 80.00%
Human oral bioavailability + 0.7143 71.43%
Subcellular localzation Mitochondria 0.4335 43.35%
OATP2B1 inhibitior - 0.8561 85.61%
OATP1B1 inhibitior + 0.9648 96.48%
OATP1B3 inhibitior + 0.9739 97.39%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior + 0.6115 61.15%
P-glycoprotein inhibitior - 0.6046 60.46%
P-glycoprotein substrate - 0.6380 63.80%
CYP3A4 substrate + 0.5323 53.23%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate + 0.3553 35.53%
CYP3A4 inhibition + 0.7195 71.95%
CYP2C9 inhibition + 0.7045 70.45%
CYP2C19 inhibition + 0.7023 70.23%
CYP2D6 inhibition - 0.8882 88.82%
CYP1A2 inhibition + 0.9399 93.99%
CYP2C8 inhibition + 0.6206 62.06%
CYP inhibitory promiscuity + 0.8298 82.98%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8910 89.10%
Carcinogenicity (trinary) Non-required 0.4222 42.22%
Eye corrosion - 0.9956 99.56%
Eye irritation - 0.6165 61.65%
Skin irritation - 0.8305 83.05%
Skin corrosion - 0.9514 95.14%
Ames mutagenesis + 0.8000 80.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5000 50.00%
Micronuclear + 0.7900 79.00%
Hepatotoxicity + 0.6540 65.40%
skin sensitisation - 0.9529 95.29%
Respiratory toxicity - 0.6222 62.22%
Reproductive toxicity + 0.7444 74.44%
Mitochondrial toxicity - 0.8125 81.25%
Nephrotoxicity - 0.5676 56.76%
Acute Oral Toxicity (c) III 0.7327 73.27%
Estrogen receptor binding + 0.9259 92.59%
Androgen receptor binding + 0.8294 82.94%
Thyroid receptor binding + 0.7776 77.76%
Glucocorticoid receptor binding + 0.9621 96.21%
Aromatase binding + 0.8817 88.17%
PPAR gamma + 0.7568 75.68%
Honey bee toxicity - 0.7297 72.97%
Biodegradation - 1.0000 100.00%
Crustacea aquatic toxicity - 0.5300 53.00%
Fish aquatic toxicity - 0.7123 71.23%

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
CHEMBL1951 P21397 Monoamine oxidase A 97.01% 91.49%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.98% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.64% 96.09%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 93.37% 96.67%
CHEMBL2535 P11166 Glucose transporter 93.21% 98.75%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 92.62% 96.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 92.59% 86.33%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.27% 91.11%
CHEMBL1806 P11388 DNA topoisomerase II alpha 91.36% 89.00%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 90.02% 85.14%
CHEMBL2581 P07339 Cathepsin D 89.95% 98.95%
CHEMBL1907 P15144 Aminopeptidase N 89.50% 93.31%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 88.91% 94.00%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 87.60% 89.62%
CHEMBL2094127 P06493 Cyclin-dependent kinase 1/cyclin B 85.23% 96.00%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 85.16% 100.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 84.56% 99.23%
CHEMBL4306 P22460 Voltage-gated potassium channel subunit Kv1.5 83.60% 94.03%
CHEMBL3401 O75469 Pregnane X receptor 82.01% 94.73%
CHEMBL1868 P17948 Vascular endothelial growth factor receptor 1 80.12% 96.47%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
To see more specific details click the taxa you are interested in.
Sciadotenia toxifera

Cross-Links

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PubChem 50901246
NPASS NPC470018
ChEMBL CHEMBL1651053