2,2,7-Trimethylspiro[3-azatricyclo[5.2.2.04,8]undecane-6,3'-indole]

Details

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Internal ID a2644911-d127-475f-9c16-366b508fa7d9
Taxonomy Organoheterocyclic compounds > Indoles and derivatives > Indoles > 3-alkylindoles
IUPAC Name 2,2,7-trimethylspiro[3-azatricyclo[5.2.2.04,8]undecane-6,3'-indole]
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C20H26N2/c1-18(2)13-8-9-19(3)15(10-13)17(22-18)11-20(19)12-21-16-7-5-4-6-14(16)20/h4-7,12-13,15,17,22H,8-11H2,1-3H3
InChI Key OHXDSOCCYBBGAP-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C20H26N2
Molecular Weight 294.40 g/mol
Exact Mass 294.209598838 g/mol
Topological Polar Surface Area (TPSA) 24.40 Ų
XlogP 3.20
Atomic LogP (AlogP) 4.22
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2,2,7-Trimethylspiro[3-azatricyclo[5.2.2.04,8]undecane-6,3'-indole]

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9951 99.51%
Caco-2 + 0.7293 72.93%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability + 0.6000 60.00%
Subcellular localzation Lysosomes 0.5125 51.25%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9081 90.81%
OATP1B3 inhibitior + 0.9390 93.90%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior + 0.6250 62.50%
BSEP inhibitior - 0.5925 59.25%
P-glycoprotein inhibitior - 0.8867 88.67%
P-glycoprotein substrate - 0.6380 63.80%
CYP3A4 substrate + 0.6418 64.18%
CYP2C9 substrate - 0.8042 80.42%
CYP2D6 substrate + 0.3596 35.96%
CYP3A4 inhibition - 0.7299 72.99%
CYP2C9 inhibition - 0.7869 78.69%
CYP2C19 inhibition - 0.7128 71.28%
CYP2D6 inhibition - 0.6099 60.99%
CYP1A2 inhibition - 0.7421 74.21%
CYP2C8 inhibition + 0.6231 62.31%
CYP inhibitory promiscuity - 0.7203 72.03%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8300 83.00%
Carcinogenicity (trinary) Non-required 0.6759 67.59%
Eye corrosion - 0.9765 97.65%
Eye irritation - 0.9963 99.63%
Skin irritation - 0.6919 69.19%
Skin corrosion - 0.7768 77.68%
Ames mutagenesis - 0.7000 70.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8208 82.08%
Micronuclear - 0.6300 63.00%
Hepatotoxicity - 0.5894 58.94%
skin sensitisation - 0.7159 71.59%
Respiratory toxicity + 0.7000 70.00%
Reproductive toxicity + 0.7667 76.67%
Mitochondrial toxicity + 0.7500 75.00%
Nephrotoxicity + 0.5166 51.66%
Acute Oral Toxicity (c) III 0.5656 56.56%
Estrogen receptor binding + 0.6311 63.11%
Androgen receptor binding + 0.5741 57.41%
Thyroid receptor binding + 0.5750 57.50%
Glucocorticoid receptor binding - 0.5662 56.62%
Aromatase binding + 0.6930 69.30%
PPAR gamma - 0.7064 70.64%
Honey bee toxicity - 0.8777 87.77%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity + 0.8000 80.00%
Fish aquatic toxicity + 0.9765 97.65%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.44% 96.09%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 95.60% 82.69%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 95.44% 94.62%
CHEMBL3137262 O60341 LSD1/CoREST complex 94.68% 97.09%
CHEMBL216 P11229 Muscarinic acetylcholine receptor M1 90.93% 94.23%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 90.00% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.71% 95.56%
CHEMBL1994 P08235 Mineralocorticoid receptor 85.51% 100.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 85.07% 94.45%
CHEMBL3902 P09211 Glutathione S-transferase Pi 83.85% 93.81%
CHEMBL2095226 P05556 Integrin alpha-5/beta-1 82.68% 96.39%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 81.91% 100.00%
CHEMBL1937 Q92769 Histone deacetylase 2 81.54% 94.75%
CHEMBL226 P30542 Adenosine A1 receptor 81.32% 95.93%
CHEMBL1293249 Q13887 Kruppel-like factor 5 81.32% 86.33%
CHEMBL1821 P08173 Muscarinic acetylcholine receptor M4 81.02% 94.08%
CHEMBL221 P23219 Cyclooxygenase-1 80.03% 90.17%

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.
Aristotelia serrata

Cross-Links

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PubChem 15601039
LOTUS LTS0020720
wikiData Q105192359