Eupolauridine

Details

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Internal ID 7c6a0e7e-8739-4835-b69e-776e7b241bdd
Taxonomy Organoheterocyclic compounds > Diazanaphthalenes > Naphthyridines
IUPAC Name 2,8-diazatetracyclo[7.6.1.05,16.010,15]hexadeca-1,3,5(16),6,8,10,12,14-octaene
SMILES (Canonical) C1=CC=C2C(=C1)C3=NC=CC4=C3C2=NC=C4
SMILES (Isomeric) C1=CC=C2C(=C1)C3=NC=CC4=C3C2=NC=C4
InChI InChI=1S/C14H8N2/c1-2-4-11-10(3-1)13-12-9(5-7-15-13)6-8-16-14(11)12/h1-8H
InChI Key KIVUUVOREYMMFE-UHFFFAOYSA-N
Popularity 16 references in papers

Physical and Chemical Properties

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Molecular Formula C14H8N2
Molecular Weight 204.23 g/mol
Exact Mass 204.068748264 g/mol
Topological Polar Surface Area (TPSA) 25.80 Ų
XlogP 2.40
Atomic LogP (AlogP) 3.28
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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Canangine
Indeno(1,2,3-ij)(2,7)naphthyridine
58786-39-3
CHEBI:67605
M3LXQ9G7MF
Indeno[1,2,3-ij][2,7]naphthyridine
2,8-diazatetracyclo[7.6.1.05,16.010,15]hexadeca-1,3,5(16),6,8,10,12,14-octaene
Eupolauridin
EL Base 1
1,6-Diazafluoranthene
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Eupolauridine

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9949 99.49%
Caco-2 + 0.5000 50.00%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.7571 75.71%
Subcellular localzation Mitochondria 0.6171 61.71%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9704 97.04%
OATP1B3 inhibitior + 0.9617 96.17%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior + 0.5560 55.60%
P-glycoprotein inhibitior - 0.9535 95.35%
P-glycoprotein substrate - 0.9597 95.97%
CYP3A4 substrate - 0.6846 68.46%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7482 74.82%
CYP3A4 inhibition + 0.5996 59.96%
CYP2C9 inhibition + 0.6068 60.68%
CYP2C19 inhibition + 0.5801 58.01%
CYP2D6 inhibition - 0.5415 54.15%
CYP1A2 inhibition + 0.9522 95.22%
CYP2C8 inhibition + 0.5233 52.33%
CYP inhibitory promiscuity + 0.6989 69.89%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9300 93.00%
Carcinogenicity (trinary) Non-required 0.7454 74.54%
Eye corrosion - 0.9793 97.93%
Eye irritation + 0.9773 97.73%
Skin irritation + 0.7975 79.75%
Skin corrosion - 0.9428 94.28%
Ames mutagenesis + 0.7600 76.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6985 69.85%
Micronuclear + 0.6859 68.59%
Hepatotoxicity + 0.8356 83.56%
skin sensitisation - 0.7138 71.38%
Respiratory toxicity - 0.5889 58.89%
Reproductive toxicity + 0.7000 70.00%
Mitochondrial toxicity - 0.7250 72.50%
Nephrotoxicity + 0.6762 67.62%
Acute Oral Toxicity (c) III 0.7218 72.18%
Estrogen receptor binding + 0.9272 92.72%
Androgen receptor binding + 0.8531 85.31%
Thyroid receptor binding + 0.8336 83.36%
Glucocorticoid receptor binding + 0.8567 85.67%
Aromatase binding + 0.8925 89.25%
PPAR gamma + 0.7736 77.36%
Honey bee toxicity - 0.9093 90.93%
Biodegradation - 0.9750 97.50%
Crustacea aquatic toxicity + 0.7800 78.00%
Fish aquatic toxicity - 0.4625 46.25%

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 98.27% 91.49%
CHEMBL2637 P53779 c-Jun N-terminal kinase 3 91.20% 92.75%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 90.96% 96.67%
CHEMBL308 P06493 Cyclin-dependent kinase 1 89.80% 91.73%
CHEMBL2828 P48730 Casein kinase I delta 89.70% 93.08%
CHEMBL4179 P45984 c-Jun N-terminal kinase 2 87.29% 90.75%
CHEMBL3116 P50750 Cyclin-dependent kinase 9 84.29% 96.31%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 83.28% 94.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 82.67% 86.33%
CHEMBL2581 P07339 Cathepsin D 82.23% 98.95%
CHEMBL1868 P17948 Vascular endothelial growth factor receptor 1 81.97% 96.47%
CHEMBL301 P24941 Cyclin-dependent kinase 2 80.34% 91.23%

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.
Ambavia gerrardii
Cleistopholis patens
Eupomatia laurina

Cross-Links

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PubChem 72486
LOTUS LTS0194660
wikiData Q5851990