Ethyl beta-carboline-1-propionate

Details

Top
Internal ID 223b1432-b6d5-4f05-a12d-1256b66ce890
Taxonomy Alkaloids and derivatives > Harmala alkaloids
IUPAC Name ethyl 3-(9H-pyrido[3,4-b]indol-1-yl)propanoate
SMILES (Canonical) CCOC(=O)CCC1=NC=CC2=C1NC3=CC=CC=C23
SMILES (Isomeric) CCOC(=O)CCC1=NC=CC2=C1NC3=CC=CC=C23
InChI InChI=1S/C16H16N2O2/c1-2-20-15(19)8-7-14-16-12(9-10-17-14)11-5-3-4-6-13(11)18-16/h3-6,9-10,18H,2,7-8H2,1H3
InChI Key MVOYJHIRYQUBIR-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C16H16N2O2
Molecular Weight 268.31 g/mol
Exact Mass 268.121177757 g/mol
Topological Polar Surface Area (TPSA) 55.00 Ų
XlogP 2.80
Atomic LogP (AlogP) 3.21
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 4

Synonyms

Top
90686-24-1
Ethyl 3-(9H-pyrido[3,4-b]indol-1-yl)propanoate
AKOS040734114
FS-7953

2D Structure

Top
2D Structure of Ethyl beta-carboline-1-propionate

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 1.0000 100.00%
Caco-2 + 0.5000 50.00%
Blood Brain Barrier + 0.8250 82.50%
Human oral bioavailability + 0.5286 52.86%
Subcellular localzation Mitochondria 0.7801 78.01%
OATP2B1 inhibitior - 0.8575 85.75%
OATP1B1 inhibitior + 0.9049 90.49%
OATP1B3 inhibitior + 0.9429 94.29%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.5500 55.00%
BSEP inhibitior + 0.6398 63.98%
P-glycoprotein inhibitior - 0.8966 89.66%
P-glycoprotein substrate - 0.7484 74.84%
CYP3A4 substrate + 0.6215 62.15%
CYP2C9 substrate - 0.6044 60.44%
CYP2D6 substrate - 0.8227 82.27%
CYP3A4 inhibition - 0.7172 71.72%
CYP2C9 inhibition + 0.8093 80.93%
CYP2C19 inhibition + 0.7610 76.10%
CYP2D6 inhibition - 0.6462 64.62%
CYP1A2 inhibition + 0.8016 80.16%
CYP2C8 inhibition + 0.7466 74.66%
CYP inhibitory promiscuity + 0.7636 76.36%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Non-required 0.6971 69.71%
Eye corrosion - 0.9878 98.78%
Eye irritation - 0.9245 92.45%
Skin irritation - 0.8210 82.10%
Skin corrosion - 0.9548 95.48%
Ames mutagenesis - 0.5200 52.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8068 80.68%
Micronuclear - 0.5800 58.00%
Hepatotoxicity + 0.6375 63.75%
skin sensitisation - 0.8924 89.24%
Respiratory toxicity - 0.5667 56.67%
Reproductive toxicity + 0.8333 83.33%
Mitochondrial toxicity + 0.8125 81.25%
Nephrotoxicity - 0.7863 78.63%
Acute Oral Toxicity (c) III 0.7205 72.05%
Estrogen receptor binding + 0.8172 81.72%
Androgen receptor binding + 0.5756 57.56%
Thyroid receptor binding + 0.6184 61.84%
Glucocorticoid receptor binding + 0.5950 59.50%
Aromatase binding + 0.5749 57.49%
PPAR gamma + 0.6998 69.98%
Honey bee toxicity - 0.9111 91.11%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity - 0.5100 51.00%
Fish aquatic toxicity + 0.8501 85.01%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.74% 96.09%
CHEMBL255 P29275 Adenosine A2b receptor 91.97% 98.59%
CHEMBL1806 P11388 DNA topoisomerase II alpha 89.76% 89.00%
CHEMBL1781 P11387 DNA topoisomerase I 88.56% 97.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 88.53% 99.17%
CHEMBL3401 O75469 Pregnane X receptor 88.18% 94.73%
CHEMBL2581 P07339 Cathepsin D 87.58% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.20% 86.33%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 87.07% 99.23%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.79% 95.56%
CHEMBL1868 P17948 Vascular endothelial growth factor receptor 1 85.26% 96.47%
CHEMBL2095172 P14867 GABA-A receptor; alpha-1/beta-2/gamma-2 84.67% 92.67%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 84.48% 85.14%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 84.22% 91.71%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 83.77% 95.50%
CHEMBL1951 P21397 Monoamine oxidase A 83.48% 91.49%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 82.96% 94.62%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 82.90% 91.11%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 82.39% 93.65%
CHEMBL202 P00374 Dihydrofolate reductase 82.07% 89.92%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 81.08% 94.00%
CHEMBL2535 P11166 Glucose transporter 80.98% 98.75%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 80.50% 96.00%

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.
Quassia undulata

Cross-Links

Top
PubChem 54093642
LOTUS LTS0027748
wikiData Q105173202