benzyl 3-(1H-indol-3-yl)propanoate

Details

Top
Internal ID bbf01eb3-92d2-428f-b9f6-2429971d3f08
Taxonomy Organoheterocyclic compounds > Indoles and derivatives > Indolyl carboxylic acids and derivatives
IUPAC Name benzyl 3-(1H-indol-3-yl)propanoate
SMILES (Canonical) C1=CC=C(C=C1)COC(=O)CCC2=CNC3=CC=CC=C32
SMILES (Isomeric) C1=CC=C(C=C1)COC(=O)CCC2=CNC3=CC=CC=C32
InChI InChI=1S/C18H17NO2/c20-18(21-13-14-6-2-1-3-7-14)11-10-15-12-19-17-9-5-4-8-16(15)17/h1-9,12,19H,10-11,13H2
InChI Key FLEDMTNAZUAUSS-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C18H17NO2
Molecular Weight 279.30 g/mol
Exact Mass 279.125928785 g/mol
Topological Polar Surface Area (TPSA) 42.10 Ų
XlogP 3.60
Atomic LogP (AlogP) 3.84
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 5

Synonyms

Top
AKOS000814910
NCGC00329868-01
AB01199969-03
Z13758694

2D Structure

Top
2D Structure of benzyl 3-(1H-indol-3-yl)propanoate

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 1.0000 100.00%
Caco-2 + 0.6504 65.04%
Blood Brain Barrier + 0.8000 80.00%
Human oral bioavailability - 0.6000 60.00%
Subcellular localzation Mitochondria 0.6443 64.43%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9294 92.94%
OATP1B3 inhibitior + 0.9473 94.73%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.6250 62.50%
BSEP inhibitior + 0.8034 80.34%
P-glycoprotein inhibitior - 0.8365 83.65%
P-glycoprotein substrate - 0.9168 91.68%
CYP3A4 substrate + 0.5315 53.15%
CYP2C9 substrate - 0.8074 80.74%
CYP2D6 substrate - 0.7572 75.72%
CYP3A4 inhibition - 0.7179 71.79%
CYP2C9 inhibition + 0.9163 91.63%
CYP2C19 inhibition + 0.9168 91.68%
CYP2D6 inhibition - 0.7897 78.97%
CYP1A2 inhibition + 0.8962 89.62%
CYP2C8 inhibition + 0.5283 52.83%
CYP inhibitory promiscuity + 0.8515 85.15%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Non-required 0.6433 64.33%
Eye corrosion - 0.9798 97.98%
Eye irritation - 0.5752 57.52%
Skin irritation - 0.8336 83.36%
Skin corrosion - 0.9596 95.96%
Ames mutagenesis - 0.8600 86.00%
Human Ether-a-go-go-Related Gene inhibition + 0.9009 90.09%
Micronuclear - 0.5800 58.00%
Hepatotoxicity - 0.7323 73.23%
skin sensitisation - 0.8920 89.20%
Respiratory toxicity - 0.6667 66.67%
Reproductive toxicity + 0.7778 77.78%
Mitochondrial toxicity - 0.5000 50.00%
Nephrotoxicity - 0.8849 88.49%
Acute Oral Toxicity (c) III 0.7000 70.00%
Estrogen receptor binding + 0.9406 94.06%
Androgen receptor binding - 0.7715 77.15%
Thyroid receptor binding - 0.6526 65.26%
Glucocorticoid receptor binding - 0.5358 53.58%
Aromatase binding + 0.7502 75.02%
PPAR gamma - 0.5894 58.94%
Honey bee toxicity - 0.8602 86.02%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.7055 70.55%
Fish aquatic toxicity + 0.9036 90.36%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.09% 91.11%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 96.60% 94.62%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.55% 96.09%
CHEMBL2581 P07339 Cathepsin D 92.65% 98.95%
CHEMBL2095172 P14867 GABA-A receptor; alpha-1/beta-2/gamma-2 91.84% 92.67%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.07% 95.56%
CHEMBL2693 Q9UIQ6 Cystinyl aminopeptidase 90.28% 97.64%
CHEMBL3060 Q9Y345 Glycine transporter 2 90.11% 99.17%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 88.29% 91.71%
CHEMBL221 P23219 Cyclooxygenase-1 84.75% 90.17%
CHEMBL5939 Q9NZ08 Endoplasmic reticulum aminopeptidase 1 84.01% 100.00%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 82.88% 92.62%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 81.36% 95.50%
CHEMBL2535 P11166 Glucose transporter 80.48% 98.75%

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.
Rauvolfia serpentina

Cross-Links

Top
PubChem 13855378
LOTUS LTS0202660
wikiData Q104996999