1-Ethyl-4-methoxy-9H-pyrido[3,4-b]indole

Details

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Internal ID 66e0e04e-b82b-4d80-8420-80d0bee3d749
Taxonomy Alkaloids and derivatives > Harmala alkaloids
IUPAC Name 1-ethyl-4-methoxy-9H-pyrido[3,4-b]indole
SMILES (Canonical) CCC1=NC=C(C2=C1NC3=CC=CC=C32)OC
SMILES (Isomeric) CCC1=NC=C(C2=C1NC3=CC=CC=C32)OC
InChI InChI=1S/C14H14N2O/c1-3-10-14-13(12(17-2)8-15-10)9-6-4-5-7-11(9)16-14/h4-8,16H,3H2,1-2H3
InChI Key LWWRUTVIAQDHRE-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C14H14N2O
Molecular Weight 226.27 g/mol
Exact Mass 226.110613074 g/mol
Topological Polar Surface Area (TPSA) 37.90 Ų
XlogP 3.10
Atomic LogP (AlogP) 3.29
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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26585-14-8
1-Ethyl-4-methoxy-9H-pyrido[3,4-b]indole
Crenatin
9H-Pyrido(3,4-b)indole, 1-ethyl-4-methoxy-
1-Ethyl-4-methoxy-9H-pyrido[3,4-b]indole; 1-Ethyl-4-methoxy-beta-carboline; Crenatin
CHEMBL3400668
DTXSID90181150
1-Ethyl-4-methoxy-beta-carboline
LWWRUTVIAQDHRE-UHFFFAOYSA-N
BBA58514
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 1-Ethyl-4-methoxy-9H-pyrido[3,4-b]indole

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 - 0.5220 52.20%
Blood Brain Barrier + 0.8605 86.05%
Human oral bioavailability + 0.5857 58.57%
Subcellular localzation Mitochondria 0.7860 78.60%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8973 89.73%
OATP1B3 inhibitior + 0.9431 94.31%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior - 0.4946 49.46%
P-glycoprotein inhibitior - 0.9505 95.05%
P-glycoprotein substrate - 0.5000 50.00%
CYP3A4 substrate + 0.5594 55.94%
CYP2C9 substrate - 0.8116 81.16%
CYP2D6 substrate + 0.4144 41.44%
CYP3A4 inhibition + 0.6061 60.61%
CYP2C9 inhibition - 0.8938 89.38%
CYP2C19 inhibition - 0.6181 61.81%
CYP2D6 inhibition + 0.7420 74.20%
CYP1A2 inhibition + 0.9202 92.02%
CYP2C8 inhibition + 0.8678 86.78%
CYP inhibitory promiscuity + 0.8268 82.68%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9323 93.23%
Carcinogenicity (trinary) Non-required 0.6169 61.69%
Eye corrosion - 0.9903 99.03%
Eye irritation - 0.6561 65.61%
Skin irritation - 0.8230 82.30%
Skin corrosion - 0.9412 94.12%
Ames mutagenesis + 0.7300 73.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3843 38.43%
Micronuclear + 0.7000 70.00%
Hepatotoxicity + 0.6625 66.25%
skin sensitisation - 0.8885 88.85%
Respiratory toxicity + 0.6444 64.44%
Reproductive toxicity + 0.7889 78.89%
Mitochondrial toxicity + 0.5250 52.50%
Nephrotoxicity - 0.6193 61.93%
Acute Oral Toxicity (c) III 0.6931 69.31%
Estrogen receptor binding + 0.7666 76.66%
Androgen receptor binding + 0.7924 79.24%
Thyroid receptor binding + 0.6354 63.54%
Glucocorticoid receptor binding - 0.4784 47.84%
Aromatase binding + 0.6786 67.86%
PPAR gamma - 0.5769 57.69%
Honey bee toxicity - 0.8042 80.42%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity + 0.6200 62.00%
Fish aquatic toxicity - 0.7701 77.01%

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 96.79% 96.09%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 93.43% 94.00%
CHEMBL3192 Q9BY41 Histone deacetylase 8 92.30% 93.99%
CHEMBL2535 P11166 Glucose transporter 90.53% 98.75%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.04% 95.56%
CHEMBL255 P29275 Adenosine A2b receptor 89.03% 98.59%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 87.69% 94.45%
CHEMBL1937 Q92769 Histone deacetylase 2 87.32% 94.75%
CHEMBL202 P00374 Dihydrofolate reductase 86.79% 89.92%
CHEMBL213 P08588 Beta-1 adrenergic receptor 86.69% 95.56%
CHEMBL4145 Q9UKV0 Histone deacetylase 9 86.29% 85.49%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 86.22% 96.00%
CHEMBL1781 P11387 DNA topoisomerase I 85.45% 97.00%
CHEMBL2885 P07451 Carbonic anhydrase III 85.34% 87.45%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.55% 86.33%
CHEMBL2717 Q9HCR9 Phosphodiesterase 11A 84.20% 85.00%
CHEMBL2716 Q8WUI4 Histone deacetylase 7 83.71% 89.44%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 83.50% 91.11%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.26% 99.17%
CHEMBL1907 P15144 Aminopeptidase N 82.24% 93.31%
CHEMBL2581 P07339 Cathepsin D 82.24% 98.95%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 81.18% 95.50%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 80.50% 93.65%

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.
Ailanthus triphysa
Picrasma crenata
Picrasma javanica
Picrasma quassioides
Quassia undulata

Cross-Links

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PubChem 5317256
NPASS NPC19872
LOTUS LTS0014313
wikiData Q72461691