Tricladin B

Details

Top
Internal ID 798b73aa-4ac2-4b5f-bbea-55b8f087ac14
Taxonomy Organoheterocyclic compounds > Indoles and derivatives > Indoles > 3-alkylindoles
IUPAC Name 2-ethyl-3-[2-(1H-indol-3-yl)ethyl]-2,5-dimethylimidazol-4-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C17H21N3O/c1-4-17(3)19-12(2)16(21)20(17)10-9-13-11-18-15-8-6-5-7-14(13)15/h5-8,11,18H,4,9-10H2,1-3H3
InChI Key YDMIZYMNWJPLBD-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

Top
Molecular Formula C17H21N3O
Molecular Weight 283.37 g/mol
Exact Mass 283.168462302 g/mol
Topological Polar Surface Area (TPSA) 48.50 Ų
XlogP 2.60
Atomic LogP (AlogP) 3.14
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 4

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of Tricladin B

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9856 98.56%
Caco-2 + 0.8883 88.83%
Blood Brain Barrier + 0.8000 80.00%
Human oral bioavailability + 0.5571 55.71%
Subcellular localzation Lysosomes 0.4829 48.29%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9416 94.16%
OATP1B3 inhibitior + 0.9214 92.14%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.6250 62.50%
BSEP inhibitior + 0.8254 82.54%
P-glycoprotein inhibitior - 0.7972 79.72%
P-glycoprotein substrate - 0.7415 74.15%
CYP3A4 substrate + 0.5798 57.98%
CYP2C9 substrate - 0.6147 61.47%
CYP2D6 substrate - 0.8390 83.90%
CYP3A4 inhibition - 0.6118 61.18%
CYP2C9 inhibition - 0.6342 63.42%
CYP2C19 inhibition - 0.5101 51.01%
CYP2D6 inhibition - 0.7668 76.68%
CYP1A2 inhibition + 0.5659 56.59%
CYP2C8 inhibition - 0.7283 72.83%
CYP inhibitory promiscuity + 0.5241 52.41%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9200 92.00%
Carcinogenicity (trinary) Non-required 0.7152 71.52%
Eye corrosion - 0.9881 98.81%
Eye irritation - 0.9792 97.92%
Skin irritation - 0.7833 78.33%
Skin corrosion - 0.8918 89.18%
Ames mutagenesis - 0.5500 55.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8101 81.01%
Micronuclear + 0.7000 70.00%
Hepatotoxicity + 0.6000 60.00%
skin sensitisation - 0.8623 86.23%
Respiratory toxicity + 0.8222 82.22%
Reproductive toxicity + 0.8778 87.78%
Mitochondrial toxicity + 0.8625 86.25%
Nephrotoxicity - 0.8593 85.93%
Acute Oral Toxicity (c) III 0.6056 60.56%
Estrogen receptor binding + 0.6600 66.00%
Androgen receptor binding - 0.5924 59.24%
Thyroid receptor binding + 0.5633 56.33%
Glucocorticoid receptor binding - 0.6583 65.83%
Aromatase binding + 0.5711 57.11%
PPAR gamma - 0.7706 77.06%
Honey bee toxicity - 0.8972 89.72%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity - 0.5600 56.00%
Fish aquatic toxicity + 0.9307 93.07%

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
CHEMBL1937 Q92769 Histone deacetylase 2 97.77% 94.75%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 97.09% 95.56%
CHEMBL3192 Q9BY41 Histone deacetylase 8 96.87% 93.99%
CHEMBL3310 Q96DB2 Histone deacetylase 11 96.60% 88.56%
CHEMBL2581 P07339 Cathepsin D 95.21% 98.95%
CHEMBL5103 Q969S8 Histone deacetylase 10 94.81% 90.08%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.21% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.02% 91.11%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 90.56% 94.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.52% 86.33%
CHEMBL255 P29275 Adenosine A2b receptor 87.88% 98.59%
CHEMBL230 P35354 Cyclooxygenase-2 87.41% 89.63%
CHEMBL3155 P34969 Serotonin 7 (5-HT7) receptor 87.35% 90.71%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 87.27% 99.23%
CHEMBL1829 O15379 Histone deacetylase 3 86.95% 95.00%
CHEMBL2095226 P05556 Integrin alpha-5/beta-1 85.32% 96.39%
CHEMBL325 Q13547 Histone deacetylase 1 85.31% 95.92%
CHEMBL5805 Q9NR97 Toll-like receptor 8 84.12% 96.25%
CHEMBL1806 P11388 DNA topoisomerase II alpha 82.69% 89.00%
CHEMBL332 P03956 Matrix metalloproteinase-1 81.02% 94.50%
CHEMBL2095172 P14867 GABA-A receptor; alpha-1/beta-2/gamma-2 80.29% 92.67%
CHEMBL253 P34972 Cannabinoid CB2 receptor 80.24% 97.25%

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 66555988
LOTUS LTS0100142
wikiData Q77278449