N,N-Dimethyl-1H-indole-3-(methanaminium)

Details

Top
Internal ID b21d474b-142e-4ad6-8939-f31d89304bfa
Taxonomy Organoheterocyclic compounds > Indoles and derivatives > Indoles > 3-alkylindoles
IUPAC Name 1-(1H-indol-1-ium-3-yl)-N,N-dimethylmethanamine
SMILES (Canonical) CN(C)CC1=C[NH2+]C2=CC=CC=C21
SMILES (Isomeric) CN(C)CC1=C[NH2+]C2=CC=CC=C21
InChI InChI=1S/C11H14N2/c1-13(2)8-9-7-12-11-6-4-3-5-10(9)11/h3-7,12H,8H2,1-2H3/p+1
InChI Key OCDGBSUVYYVKQZ-UHFFFAOYSA-O
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C11H15N2+
Molecular Weight 175.25 g/mol
Exact Mass 175.123523487 g/mol
Topological Polar Surface Area (TPSA) 19.80 Ų
XlogP 1.40
Atomic LogP (AlogP) 0.80
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of N,N-Dimethyl-1H-indole-3-(methanaminium)

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9325 93.25%
Caco-2 + 0.9427 94.27%
Blood Brain Barrier + 0.8500 85.00%
Human oral bioavailability + 0.6571 65.71%
Subcellular localzation Mitochondria 0.4468 44.68%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8674 86.74%
OATP1B3 inhibitior + 0.9439 94.39%
MATE1 inhibitior - 0.7800 78.00%
OCT2 inhibitior - 0.5000 50.00%
BSEP inhibitior - 0.8290 82.90%
P-glycoprotein inhibitior - 0.9902 99.02%
P-glycoprotein substrate - 0.8727 87.27%
CYP3A4 substrate - 0.5213 52.13%
CYP2C9 substrate - 0.5948 59.48%
CYP2D6 substrate + 0.4552 45.52%
CYP3A4 inhibition - 0.6825 68.25%
CYP2C9 inhibition - 0.7929 79.29%
CYP2C19 inhibition - 0.8581 85.81%
CYP2D6 inhibition + 0.6334 63.34%
CYP1A2 inhibition - 0.5341 53.41%
CYP2C8 inhibition - 0.9488 94.88%
CYP inhibitory promiscuity + 0.5427 54.27%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8700 87.00%
Carcinogenicity (trinary) Non-required 0.6036 60.36%
Eye corrosion - 0.9715 97.15%
Eye irritation + 0.6079 60.79%
Skin irritation - 0.7060 70.60%
Skin corrosion - 0.8211 82.11%
Ames mutagenesis - 0.5600 56.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6606 66.06%
Micronuclear + 0.7100 71.00%
Hepatotoxicity + 0.6177 61.77%
skin sensitisation - 0.7848 78.48%
Respiratory toxicity + 0.8000 80.00%
Reproductive toxicity + 0.6889 68.89%
Mitochondrial toxicity + 0.8875 88.75%
Nephrotoxicity + 0.6232 62.32%
Acute Oral Toxicity (c) III 0.4750 47.50%
Estrogen receptor binding - 0.6636 66.36%
Androgen receptor binding - 0.6358 63.58%
Thyroid receptor binding - 0.7866 78.66%
Glucocorticoid receptor binding - 0.7509 75.09%
Aromatase binding - 0.5482 54.82%
PPAR gamma - 0.8653 86.53%
Honey bee toxicity - 0.8507 85.07%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity + 0.7500 75.00%
Fish aquatic toxicity + 0.9191 91.91%

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
CHEMBL2581 P07339 Cathepsin D 95.76% 98.95%
CHEMBL1293255 P15428 15-hydroxyprostaglandin dehydrogenase [NAD+] 94.00% 83.57%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.06% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.44% 95.56%
CHEMBL221 P23219 Cyclooxygenase-1 86.16% 90.17%
CHEMBL226 P30542 Adenosine A1 receptor 86.09% 95.93%
CHEMBL3492 P49721 Proteasome Macropain subunit 86.01% 90.24%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 83.25% 96.67%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 83.09% 96.00%
CHEMBL3401 O75469 Pregnane X receptor 82.45% 94.73%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 82.04% 91.11%

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.
Acer rubrum
Arundo donax
Dioscorea althaeoides
Dioscorea futschauensis
Dioscorea gracillima
Dioscorea septemloba
Hordeum vulgare
Loropetalum chinense
Smilax china
Tribulus terrestris

Cross-Links

Top
PubChem 101928958
NPASS NPC52197