Teladiazoline

Details

Top
Internal ID 039ef3f2-e136-42ee-883e-ecf6f9bd1b44
Taxonomy Alkaloids and derivatives > Aporphines
IUPAC Name 16-amino-14,15-dimethoxy-10-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/C18H14N2O3/c1-22-17-11-7-8-20-15-13(11)12(14(19)18(17)23-2)9-5-3-4-6-10(9)16(15)21/h3-8H,19H2,1-2H3
InChI Key KLUWUEZDQZTJES-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

Top
Molecular Formula C18H14N2O3
Molecular Weight 306.30 g/mol
Exact Mass 306.10044231 g/mol
Topological Polar Surface Area (TPSA) 74.40 Ų
XlogP 2.80
Atomic LogP (AlogP) 3.05
H-Bond Acceptor 5
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

Top
119763-88-1
DTXSID20923101
1-Amino-2,3-dimethoxy-7H-dibenzo[de,g]quinolin-7-one

2D Structure

Top
2D Structure of Teladiazoline

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9940 99.40%
Caco-2 + 0.7235 72.35%
Blood Brain Barrier + 0.8000 80.00%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Mitochondria 0.5524 55.24%
OATP2B1 inhibitior - 0.8573 85.73%
OATP1B1 inhibitior + 0.9636 96.36%
OATP1B3 inhibitior + 0.9678 96.78%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior + 0.6209 62.09%
P-glycoprotein inhibitior - 0.6681 66.81%
P-glycoprotein substrate - 0.7493 74.93%
CYP3A4 substrate + 0.5439 54.39%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate + 0.3553 35.53%
CYP3A4 inhibition + 0.7527 75.27%
CYP2C9 inhibition + 0.5629 56.29%
CYP2C19 inhibition + 0.7022 70.22%
CYP2D6 inhibition - 0.9062 90.62%
CYP1A2 inhibition + 0.8635 86.35%
CYP2C8 inhibition + 0.4752 47.52%
CYP inhibitory promiscuity + 0.8481 84.81%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9210 92.10%
Carcinogenicity (trinary) Warning 0.4142 41.42%
Eye corrosion - 0.9943 99.43%
Eye irritation - 0.6145 61.45%
Skin irritation - 0.8497 84.97%
Skin corrosion - 0.9477 94.77%
Ames mutagenesis + 0.8200 82.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5762 57.62%
Micronuclear + 0.7700 77.00%
Hepatotoxicity + 0.6125 61.25%
skin sensitisation - 0.9532 95.32%
Respiratory toxicity - 0.5333 53.33%
Reproductive toxicity + 0.6333 63.33%
Mitochondrial toxicity - 0.7625 76.25%
Nephrotoxicity - 0.6035 60.35%
Acute Oral Toxicity (c) III 0.6982 69.82%
Estrogen receptor binding + 0.8774 87.74%
Androgen receptor binding + 0.6464 64.64%
Thyroid receptor binding + 0.7327 73.27%
Glucocorticoid receptor binding + 0.9529 95.29%
Aromatase binding + 0.8344 83.44%
PPAR gamma + 0.6752 67.52%
Honey bee toxicity - 0.7847 78.47%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity + 0.5200 52.00%
Fish aquatic toxicity - 0.6244 62.44%

Targets

Top

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
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 94.94% 96.67%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.17% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.14% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.74% 95.56%
CHEMBL1806 P11388 DNA topoisomerase II alpha 92.68% 89.00%
CHEMBL2535 P11166 Glucose transporter 91.92% 98.75%
CHEMBL2581 P07339 Cathepsin D 91.02% 98.95%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 90.54% 94.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.59% 86.33%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 89.20% 99.23%
CHEMBL1868 P17948 Vascular endothelial growth factor receptor 1 87.79% 96.47%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 86.29% 96.00%
CHEMBL1907 P15144 Aminopeptidase N 85.12% 93.31%
CHEMBL4306 P22460 Voltage-gated potassium channel subunit Kv1.5 84.13% 94.03%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 83.31% 100.00%
CHEMBL2094127 P06493 Cyclin-dependent kinase 1/cyclin B 81.86% 96.00%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 80.89% 93.65%
CHEMBL1287628 Q9Y5S8 NADPH oxidase 1 80.48% 95.48%

Plants that contains it

Top
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.
Telitoxicum glaziovii
Telitoxicum peruvianum

Cross-Links

Top
PubChem 189692
LOTUS LTS0120767
wikiData Q82897008