Bruceolline E

Details

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Internal ID 2435cb86-1267-4323-aa92-1102a4262709
Taxonomy Organoheterocyclic compounds > Indoles and derivatives > Indoles
IUPAC Name 3,3-dimethyl-4H-cyclopenta[b]indole-1,2-dione
SMILES (Canonical) CC1(C2=C(C3=CC=CC=C3N2)C(=O)C1=O)C
SMILES (Isomeric) CC1(C2=C(C3=CC=CC=C3N2)C(=O)C1=O)C
InChI InChI=1S/C13H11NO2/c1-13(2)11-9(10(15)12(13)16)7-5-3-4-6-8(7)14-11/h3-6,14H,1-2H3
InChI Key ARBFRFGYYIWHSN-UHFFFAOYSA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C13H11NO2
Molecular Weight 213.23 g/mol
Exact Mass 213.078978594 g/mol
Topological Polar Surface Area (TPSA) 49.90 Ų
XlogP 2.00
Atomic LogP (AlogP) 2.21
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 0

Synonyms

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CHEBI:68926
CHEMBL1922996
Q27137281
3,3-dimethyl-3,4-dihydrocyclopenta[b]indole-1,2-dione

2D Structure

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2D Structure of Bruceolline E

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 1.0000 100.00%
Caco-2 - 0.6045 60.45%
Blood Brain Barrier + 0.7879 78.79%
Human oral bioavailability + 0.6571 65.71%
Subcellular localzation Mitochondria 0.7289 72.89%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8945 89.45%
OATP1B3 inhibitior + 0.9565 95.65%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.8768 87.68%
P-glycoprotein inhibitior - 0.9530 95.30%
P-glycoprotein substrate - 0.9703 97.03%
CYP3A4 substrate - 0.5097 50.97%
CYP2C9 substrate - 0.6095 60.95%
CYP2D6 substrate - 0.8468 84.68%
CYP3A4 inhibition - 0.6887 68.87%
CYP2C9 inhibition - 0.7908 79.08%
CYP2C19 inhibition - 0.5782 57.82%
CYP2D6 inhibition - 0.7662 76.62%
CYP1A2 inhibition + 0.8098 80.98%
CYP2C8 inhibition - 0.7821 78.21%
CYP inhibitory promiscuity - 0.5297 52.97%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8543 85.43%
Carcinogenicity (trinary) Non-required 0.5350 53.50%
Eye corrosion - 0.9876 98.76%
Eye irritation - 0.6445 64.45%
Skin irritation - 0.7316 73.16%
Skin corrosion - 0.9212 92.12%
Ames mutagenesis + 0.6400 64.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6472 64.72%
Micronuclear + 0.6459 64.59%
Hepatotoxicity + 0.6198 61.98%
skin sensitisation - 0.7208 72.08%
Respiratory toxicity + 0.5778 57.78%
Reproductive toxicity - 0.5000 50.00%
Mitochondrial toxicity - 0.5375 53.75%
Nephrotoxicity + 0.7218 72.18%
Acute Oral Toxicity (c) III 0.6361 63.61%
Estrogen receptor binding - 0.5276 52.76%
Androgen receptor binding + 0.6735 67.35%
Thyroid receptor binding - 0.6171 61.71%
Glucocorticoid receptor binding - 0.6082 60.82%
Aromatase binding + 0.6392 63.92%
PPAR gamma - 0.6168 61.68%
Honey bee toxicity - 0.9220 92.20%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity + 0.5500 55.00%
Fish aquatic toxicity - 0.3746 37.46%

Targets

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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
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 96.93% 95.56%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 96.14% 94.45%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.92% 91.11%
CHEMBL2581 P07339 Cathepsin D 92.65% 98.95%
CHEMBL1937 Q92769 Histone deacetylase 2 89.85% 94.75%
CHEMBL255 P29275 Adenosine A2b receptor 88.90% 98.59%
CHEMBL3310 Q96DB2 Histone deacetylase 11 88.90% 88.56%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 87.85% 99.23%
CHEMBL2708 Q16584 Mitogen-activated protein kinase kinase kinase 11 86.73% 81.14%
CHEMBL3192 Q9BY41 Histone deacetylase 8 85.52% 93.99%
CHEMBL3524 P56524 Histone deacetylase 4 85.01% 92.97%
CHEMBL1806 P11388 DNA topoisomerase II alpha 84.14% 89.00%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 83.32% 96.67%
CHEMBL4145 Q9UKV0 Histone deacetylase 9 82.09% 85.49%
CHEMBL2717 Q9HCR9 Phosphodiesterase 11A 81.68% 85.00%
CHEMBL5103 Q969S8 Histone deacetylase 10 80.78% 90.08%
CHEMBL1951 P21397 Monoamine oxidase A 80.60% 91.49%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 80.32% 96.09%
CHEMBL3401 O75469 Pregnane X receptor 80.30% 94.73%

Plants that contains it

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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.
Brucea mollis

Cross-Links

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PubChem 56945466
LOTUS LTS0143120
wikiData Q27137281