Luotonin A

Details

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Internal ID 92251edd-6488-4e24-8a15-b1164b189404
Taxonomy Organoheterocyclic compounds > Diazanaphthalenes > Benzodiazines > Quinazolines
IUPAC Name 3,11,21-triazapentacyclo[11.8.0.02,11.04,9.015,20]henicosa-1(21),2,4,6,8,13,15,17,19-nonaen-10-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C18H11N3O/c22-18-13-6-2-4-8-15(13)20-17-16-12(10-21(17)18)9-11-5-1-3-7-14(11)19-16/h1-9H,10H2
InChI Key LUMDXNLBIYLTER-UHFFFAOYSA-N
Popularity 116 references in papers

Physical and Chemical Properties

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Molecular Formula C18H11N3O
Molecular Weight 285.30 g/mol
Exact Mass 285.090211983 g/mol
Topological Polar Surface Area (TPSA) 45.60 Ų
XlogP 2.70
Atomic LogP (AlogP) 2.97
H-Bond Acceptor 4
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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Luotonine A
205989-12-4
3,11,21-triazapentacyclo[11.8.0.02,11.04,9.015,20]henicosa-1(21),2,4,6,8,13,15,17,19-nonaen-10-one
CHEMBL19163
CHEBI:172341
DTXSID501347723
BDBM50223906
HY-119458
CS-0068434
3,11,21-triazapentacyclo[11.8.0.0?,??.0?,?.0??,??]henicosa-1(21),2,4,6,8,13,15,17,19-nonaen-10-one
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Luotonin A

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9971 99.71%
Caco-2 + 0.9093 90.93%
Blood Brain Barrier + 0.8750 87.50%
Human oral bioavailability + 0.6429 64.29%
Subcellular localzation Mitochondria 0.7825 78.25%
OATP2B1 inhibitior - 0.8576 85.76%
OATP1B1 inhibitior + 0.9494 94.94%
OATP1B3 inhibitior + 0.9485 94.85%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.7066 70.66%
BSEP inhibitior + 0.7476 74.76%
P-glycoprotein inhibitior - 0.7640 76.40%
P-glycoprotein substrate - 0.9464 94.64%
CYP3A4 substrate + 0.5368 53.68%
CYP2C9 substrate - 0.6166 61.66%
CYP2D6 substrate - 0.8786 87.86%
CYP3A4 inhibition - 0.7002 70.02%
CYP2C9 inhibition - 0.9046 90.46%
CYP2C19 inhibition - 0.8092 80.92%
CYP2D6 inhibition - 0.9473 94.73%
CYP1A2 inhibition + 0.9591 95.91%
CYP2C8 inhibition - 0.6703 67.03%
CYP inhibitory promiscuity + 0.5919 59.19%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.6041 60.41%
Eye corrosion - 0.9777 97.77%
Eye irritation - 0.9190 91.90%
Skin irritation - 0.8212 82.12%
Skin corrosion - 0.9630 96.30%
Ames mutagenesis + 0.8800 88.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6550 65.50%
Micronuclear + 0.8500 85.00%
Hepatotoxicity + 0.6625 66.25%
skin sensitisation - 0.9231 92.31%
Respiratory toxicity + 0.7889 78.89%
Reproductive toxicity + 0.7667 76.67%
Mitochondrial toxicity + 0.5875 58.75%
Nephrotoxicity + 0.6457 64.57%
Acute Oral Toxicity (c) II 0.4970 49.70%
Estrogen receptor binding + 0.9041 90.41%
Androgen receptor binding + 0.6003 60.03%
Thyroid receptor binding + 0.7621 76.21%
Glucocorticoid receptor binding + 0.6757 67.57%
Aromatase binding + 0.8653 86.53%
PPAR gamma + 0.7721 77.21%
Honey bee toxicity - 0.9377 93.77%
Biodegradation - 0.9250 92.50%
Crustacea aquatic toxicity + 0.6500 65.00%
Fish aquatic toxicity - 0.6605 66.05%

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 95.33% 95.56%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 93.44% 85.14%
CHEMBL1293249 Q13887 Kruppel-like factor 5 92.24% 86.33%
CHEMBL2581 P07339 Cathepsin D 92.03% 98.95%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 91.77% 99.23%
CHEMBL220 P22303 Acetylcholinesterase 91.63% 94.45%
CHEMBL5805 Q9NR97 Toll-like receptor 8 90.54% 96.25%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 90.14% 93.40%
CHEMBL3192 Q9BY41 Histone deacetylase 8 89.74% 93.99%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 88.62% 94.00%
CHEMBL4302 P08183 P-glycoprotein 1 88.34% 92.98%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 86.98% 96.67%
CHEMBL1868 P17948 Vascular endothelial growth factor receptor 1 86.15% 96.47%
CHEMBL1781 P11387 DNA topoisomerase I 85.83% 97.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 84.49% 89.00%
CHEMBL1951 P21397 Monoamine oxidase A 82.62% 91.49%
CHEMBL1899 P46098 Serotonin 3a (5-HT3a) receptor 82.16% 100.00%
CHEMBL1741221 Q9Y4P1 Cysteine protease ATG4B 81.56% 87.50%
CHEMBL2535 P11166 Glucose transporter 80.11% 98.75%

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.
Peganum nigellastrum

Cross-Links

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PubChem 10334120
LOTUS LTS0205357
wikiData Q104251453