3-[(4,4-dimethyl-8-methylidene-3-azabicyclo[3.3.1]nonan-2-yl)methyl]-1H-indole

Details

Top
Internal ID 6ae23147-7283-4a90-8d0c-08e05c627d23
Taxonomy Organoheterocyclic compounds > Indoles and derivatives > Indoles > 3-alkylindoles
IUPAC Name 3-[(4,4-dimethyl-8-methylidene-3-azabicyclo[3.3.1]nonan-2-yl)methyl]-1H-indole
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C20H26N2/c1-13-8-9-15-11-17(13)19(22-20(15,2)3)10-14-12-21-18-7-5-4-6-16(14)18/h4-7,12,15,17,19,21-22H,1,8-11H2,2-3H3
InChI Key GELMCGOPWNCDHN-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

Top
Molecular Formula C20H26N2
Molecular Weight 294.40 g/mol
Exact Mass 294.209598838 g/mol
Topological Polar Surface Area (TPSA) 27.80 Ų
XlogP 3.90
Atomic LogP (AlogP) 4.43
H-Bond Acceptor 1
H-Bond Donor 2
Rotatable Bonds 2

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of 3-[(4,4-dimethyl-8-methylidene-3-azabicyclo[3.3.1]nonan-2-yl)methyl]-1H-indole

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9922 99.22%
Caco-2 + 0.6257 62.57%
Blood Brain Barrier + 0.8500 85.00%
Human oral bioavailability + 0.5429 54.29%
Subcellular localzation Nucleus 0.3338 33.38%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8890 88.90%
OATP1B3 inhibitior + 0.9383 93.83%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior + 0.5250 52.50%
BSEP inhibitior + 0.5979 59.79%
P-glycoprotein inhibitior - 0.7334 73.34%
P-glycoprotein substrate - 0.6086 60.86%
CYP3A4 substrate + 0.6568 65.68%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate + 0.5157 51.57%
CYP3A4 inhibition - 0.5508 55.08%
CYP2C9 inhibition - 0.6192 61.92%
CYP2C19 inhibition - 0.6257 62.57%
CYP2D6 inhibition - 0.6333 63.33%
CYP1A2 inhibition + 0.5254 52.54%
CYP2C8 inhibition + 0.6465 64.65%
CYP inhibitory promiscuity + 0.6468 64.68%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8800 88.00%
Carcinogenicity (trinary) Non-required 0.6795 67.95%
Eye corrosion - 0.9860 98.60%
Eye irritation - 0.9900 99.00%
Skin irritation - 0.7317 73.17%
Skin corrosion - 0.8735 87.35%
Ames mutagenesis - 0.6600 66.00%
Human Ether-a-go-go-Related Gene inhibition + 0.9522 95.22%
Micronuclear - 0.6100 61.00%
Hepatotoxicity - 0.5733 57.33%
skin sensitisation - 0.7158 71.58%
Respiratory toxicity + 0.7000 70.00%
Reproductive toxicity + 0.7889 78.89%
Mitochondrial toxicity + 0.9000 90.00%
Nephrotoxicity - 0.8019 80.19%
Acute Oral Toxicity (c) III 0.6165 61.65%
Estrogen receptor binding + 0.6726 67.26%
Androgen receptor binding - 0.5559 55.59%
Thyroid receptor binding + 0.6128 61.28%
Glucocorticoid receptor binding + 0.6223 62.23%
Aromatase binding + 0.8009 80.09%
PPAR gamma - 0.4868 48.68%
Honey bee toxicity - 0.8442 84.42%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity + 0.5700 57.00%
Fish aquatic toxicity + 0.9886 98.86%

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 99.43% 91.11%
CHEMBL3137262 O60341 LSD1/CoREST complex 96.57% 97.09%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 96.06% 94.62%
CHEMBL3192 Q9BY41 Histone deacetylase 8 95.96% 93.99%
CHEMBL3155 P34969 Serotonin 7 (5-HT7) receptor 95.74% 90.71%
CHEMBL240 Q12809 HERG 95.50% 89.76%
CHEMBL2996 Q05655 Protein kinase C delta 95.27% 97.79%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 93.32% 92.62%
CHEMBL3310 Q96DB2 Histone deacetylase 11 92.92% 88.56%
CHEMBL253 P34972 Cannabinoid CB2 receptor 92.04% 97.25%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.95% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.57% 96.09%
CHEMBL216 P11229 Muscarinic acetylcholine receptor M1 91.11% 94.23%
CHEMBL3920 Q04759 Protein kinase C theta 90.07% 97.69%
CHEMBL2581 P07339 Cathepsin D 89.26% 98.95%
CHEMBL1951 P21397 Monoamine oxidase A 88.26% 91.49%
CHEMBL255 P29275 Adenosine A2b receptor 85.50% 98.59%
CHEMBL2693 Q9UIQ6 Cystinyl aminopeptidase 85.44% 97.64%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 84.90% 89.62%
CHEMBL1937 Q92769 Histone deacetylase 2 84.04% 94.75%
CHEMBL1994 P08235 Mineralocorticoid receptor 83.78% 100.00%
CHEMBL1821 P08173 Muscarinic acetylcholine receptor M4 82.08% 94.08%
CHEMBL3045 P05771 Protein kinase C beta 81.97% 97.63%
CHEMBL5103 Q969S8 Histone deacetylase 10 81.88% 90.08%
CHEMBL213 P08588 Beta-1 adrenergic receptor 81.76% 95.56%
CHEMBL5608 Q16288 NT-3 growth factor receptor 81.75% 95.89%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 80.12% 94.45%

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.
Aristotelia serrata

Cross-Links

Top
PubChem 73880786
LOTUS LTS0155806
wikiData Q105007220