5-(1H-indol-3-yl)-5-methoxyimidazolidine-2,4-dione

Details

Top
Internal ID 016429b2-a0d5-4b21-8b1d-5582611a4215
Taxonomy Organoheterocyclic compounds > Azolidines > Imidazolidines > Hydantoins
IUPAC Name 5-(1H-indol-3-yl)-5-methoxyimidazolidine-2,4-dione
SMILES (Canonical) COC1(C(=O)NC(=O)N1)C2=CNC3=CC=CC=C32
SMILES (Isomeric) COC1(C(=O)NC(=O)N1)C2=CNC3=CC=CC=C32
InChI InChI=1S/C12H11N3O3/c1-18-12(10(16)14-11(17)15-12)8-6-13-9-5-3-2-4-7(8)9/h2-6,13H,1H3,(H2,14,15,16,17)
InChI Key HFMPWSSOWNDCKQ-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C12H11N3O3
Molecular Weight 245.23 g/mol
Exact Mass 245.08004122 g/mol
Topological Polar Surface Area (TPSA) 83.20 Ų
XlogP 0.50
Atomic LogP (AlogP) 0.81
H-Bond Acceptor 3
H-Bond Donor 3
Rotatable Bonds 2

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of 5-(1H-indol-3-yl)-5-methoxyimidazolidine-2,4-dione

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9693 96.93%
Caco-2 + 0.6478 64.78%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability + 0.6571 65.71%
Subcellular localzation Mitochondria 0.5983 59.83%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9248 92.48%
OATP1B3 inhibitior + 0.9499 94.99%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.9071 90.71%
BSEP inhibitior - 0.7163 71.63%
P-glycoprotein inhibitior - 0.9533 95.33%
P-glycoprotein substrate - 0.7930 79.30%
CYP3A4 substrate + 0.5785 57.85%
CYP2C9 substrate - 0.5992 59.92%
CYP2D6 substrate - 0.8174 81.74%
CYP3A4 inhibition - 0.8092 80.92%
CYP2C9 inhibition - 0.8156 81.56%
CYP2C19 inhibition - 0.7952 79.52%
CYP2D6 inhibition - 0.9259 92.59%
CYP1A2 inhibition - 0.5712 57.12%
CYP2C8 inhibition - 0.7277 72.77%
CYP inhibitory promiscuity - 0.8479 84.79%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8743 87.43%
Carcinogenicity (trinary) Non-required 0.6798 67.98%
Eye corrosion - 0.9884 98.84%
Eye irritation - 0.9796 97.96%
Skin irritation - 0.8478 84.78%
Skin corrosion - 0.9548 95.48%
Ames mutagenesis - 0.5354 53.54%
Human Ether-a-go-go-Related Gene inhibition - 0.6151 61.51%
Micronuclear + 0.9600 96.00%
Hepatotoxicity - 0.5000 50.00%
skin sensitisation - 0.9291 92.91%
Respiratory toxicity + 0.7333 73.33%
Reproductive toxicity + 0.5778 57.78%
Mitochondrial toxicity + 0.5875 58.75%
Nephrotoxicity + 0.5246 52.46%
Acute Oral Toxicity (c) III 0.6617 66.17%
Estrogen receptor binding - 0.5808 58.08%
Androgen receptor binding + 0.6197 61.97%
Thyroid receptor binding - 0.6887 68.87%
Glucocorticoid receptor binding - 0.6798 67.98%
Aromatase binding + 0.7008 70.08%
PPAR gamma - 0.5983 59.83%
Honey bee toxicity - 0.8214 82.14%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity + 0.6600 66.00%
Fish aquatic toxicity - 0.7281 72.81%

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 98.60% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.64% 95.56%
CHEMBL3192 Q9BY41 Histone deacetylase 8 95.54% 93.99%
CHEMBL1937 Q92769 Histone deacetylase 2 93.69% 94.75%
CHEMBL2581 P07339 Cathepsin D 93.68% 98.95%
CHEMBL2095172 P14867 GABA-A receptor; alpha-1/beta-2/gamma-2 93.01% 92.67%
CHEMBL1951 P21397 Monoamine oxidase A 88.84% 91.49%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.99% 96.09%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 86.61% 99.23%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 86.36% 94.00%
CHEMBL2535 P11166 Glucose transporter 85.27% 98.75%
CHEMBL3524 P56524 Histone deacetylase 4 84.94% 92.97%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 84.83% 94.62%
CHEMBL1821 P08173 Muscarinic acetylcholine receptor M4 82.95% 94.08%
CHEMBL4208 P20618 Proteasome component C5 82.81% 90.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 82.59% 94.45%
CHEMBL4051 P13569 Cystic fibrosis transmembrane conductance regulator 81.45% 95.71%
CHEMBL255 P29275 Adenosine A2b receptor 81.09% 98.59%
CHEMBL4145 Q9UKV0 Histone deacetylase 9 80.13% 85.49%

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.
There are no matching plants.

Cross-Links

Top
PubChem 14729464
LOTUS LTS0240879
wikiData Q105027403