Bruceolline D

Details

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Internal ID 214a87ee-58b9-4b0b-ad2d-4fc89a36649e
Taxonomy Organoheterocyclic compounds > Indoles and derivatives > Indoles > 3-alkylindoles
IUPAC Name 3,3-dimethyl-1,4-dihydrocyclopenta[b]indol-2-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C13H13NO/c1-13(2)11(15)7-9-8-5-3-4-6-10(8)14-12(9)13/h3-6,14H,7H2,1-2H3
InChI Key TVRRJWCBPHZRIR-UHFFFAOYSA-N
Popularity 6 references in papers

Physical and Chemical Properties

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Molecular Formula C13H13NO
Molecular Weight 199.25 g/mol
Exact Mass 199.099714038 g/mol
Topological Polar Surface Area (TPSA) 32.90 Ų
XlogP 2.40
Atomic LogP (AlogP) 2.57
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 0

Synonyms

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3,3-Dimethyl-1,4-dihydrocyclopenta[b]indol-2-one

2D Structure

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2D Structure of Bruceolline D

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 - 0.6284 62.84%
Blood Brain Barrier + 0.8379 83.79%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Mitochondria 0.5269 52.69%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9227 92.27%
OATP1B3 inhibitior + 0.9558 95.58%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.7798 77.98%
P-glycoprotein inhibitior - 0.9737 97.37%
P-glycoprotein substrate - 0.9591 95.91%
CYP3A4 substrate - 0.5159 51.59%
CYP2C9 substrate - 0.5735 57.35%
CYP2D6 substrate - 0.7268 72.68%
CYP3A4 inhibition + 0.5000 50.00%
CYP2C9 inhibition - 0.8292 82.92%
CYP2C19 inhibition + 0.5380 53.80%
CYP2D6 inhibition - 0.8385 83.85%
CYP1A2 inhibition + 0.5825 58.25%
CYP2C8 inhibition - 0.9104 91.04%
CYP inhibitory promiscuity - 0.5987 59.87%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8800 88.00%
Carcinogenicity (trinary) Non-required 0.5763 57.63%
Eye corrosion - 0.9904 99.04%
Eye irritation - 0.7345 73.45%
Skin irritation - 0.6926 69.26%
Skin corrosion - 0.8908 89.08%
Ames mutagenesis + 0.6600 66.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4890 48.90%
Micronuclear - 0.6041 60.41%
Hepatotoxicity + 0.6948 69.48%
skin sensitisation - 0.6951 69.51%
Respiratory toxicity + 0.6889 68.89%
Reproductive toxicity + 0.7444 74.44%
Mitochondrial toxicity + 0.5375 53.75%
Nephrotoxicity + 0.6345 63.45%
Acute Oral Toxicity (c) III 0.6040 60.40%
Estrogen receptor binding - 0.5168 51.68%
Androgen receptor binding - 0.5800 58.00%
Thyroid receptor binding - 0.7175 71.75%
Glucocorticoid receptor binding - 0.5201 52.01%
Aromatase binding + 0.6080 60.80%
PPAR gamma + 0.6097 60.97%
Honey bee toxicity - 0.9390 93.90%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity + 0.6100 61.00%
Fish aquatic toxicity + 0.7323 73.23%

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 96.84% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.83% 91.11%
CHEMBL2581 P07339 Cathepsin D 93.75% 98.95%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 90.54% 99.23%
CHEMBL3310 Q96DB2 Histone deacetylase 11 90.49% 88.56%
CHEMBL4145 Q9UKV0 Histone deacetylase 9 89.10% 85.49%
CHEMBL1937 Q92769 Histone deacetylase 2 87.86% 94.75%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 87.54% 94.45%
CHEMBL3192 Q9BY41 Histone deacetylase 8 86.84% 93.99%
CHEMBL3524 P56524 Histone deacetylase 4 85.38% 92.97%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 84.44% 96.09%
CHEMBL2535 P11166 Glucose transporter 84.33% 98.75%
CHEMBL2717 Q9HCR9 Phosphodiesterase 11A 84.17% 85.00%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 84.10% 82.69%
CHEMBL2708 Q16584 Mitogen-activated protein kinase kinase kinase 11 83.56% 81.14%
CHEMBL255 P29275 Adenosine A2b receptor 82.66% 98.59%
CHEMBL3137262 O60341 LSD1/CoREST complex 82.19% 97.09%
CHEMBL4040 P28482 MAP kinase ERK2 81.23% 83.82%
CHEMBL2094127 P06493 Cyclin-dependent kinase 1/cyclin B 80.57% 96.00%
CHEMBL1951 P21397 Monoamine oxidase A 80.33% 91.49%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 80.26% 94.62%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 80.15% 85.30%
CHEMBL5103 Q969S8 Histone deacetylase 10 80.01% 90.08%

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 12387437
LOTUS LTS0220230
wikiData Q105265521