7-methoxy-9H-pyrido(3,4-b)indole

Details

Top
Internal ID 853f05ee-a96f-43f8-8b5c-e31a1a89904d
Taxonomy Organoheterocyclic compounds > Indoles and derivatives > Pyridoindoles > Beta carbolines
IUPAC Name 7-methoxy-9H-pyrido[3,4-b]indole
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C12H10N2O/c1-15-8-2-3-9-10-4-5-13-7-12(10)14-11(9)6-8/h2-7,14H,1H3
InChI Key LMDPJJFWLNRVEH-UHFFFAOYSA-N
Popularity 8 references in papers

Physical and Chemical Properties

Top
Molecular Formula C12H10N2O
Molecular Weight 198.22 g/mol
Exact Mass 198.079312947 g/mol
Topological Polar Surface Area (TPSA) 37.90 Ų
XlogP 3.10
Atomic LogP (AlogP) 2.72
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

Top
NORHARMINE
6253-19-6
PVU54KD9C5
7-Methoxy-9H-pyrido(3,4-b)indole
9H-Pyrido(3,4-b)indole, 7-methoxy-
UNII-PVU54KD9C5
CHEMBL6470
SCHEMBL4823690
DTXSID30431161
PD183149
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

Top
2D Structure of 7-methoxy-9H-pyrido(3,4-b)indole

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 1.0000 100.00%
Caco-2 + 0.5449 54.49%
Blood Brain Barrier + 0.8129 81.29%
Human oral bioavailability + 0.6000 60.00%
Subcellular localzation Mitochondria 0.8227 82.27%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9344 93.44%
OATP1B3 inhibitior + 0.9660 96.60%
MATE1 inhibitior - 0.7800 78.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.5550 55.50%
P-glycoprotein inhibitior - 0.9606 96.06%
P-glycoprotein substrate - 0.7700 77.00%
CYP3A4 substrate - 0.6168 61.68%
CYP2C9 substrate - 0.8134 81.34%
CYP2D6 substrate + 0.3643 36.43%
CYP3A4 inhibition + 0.6126 61.26%
CYP2C9 inhibition - 0.9172 91.72%
CYP2C19 inhibition - 0.8101 81.01%
CYP2D6 inhibition + 0.8987 89.87%
CYP1A2 inhibition + 0.9704 97.04%
CYP2C8 inhibition + 0.7668 76.68%
CYP inhibitory promiscuity + 0.6625 66.25%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9823 98.23%
Carcinogenicity (trinary) Non-required 0.4801 48.01%
Eye corrosion - 0.9877 98.77%
Eye irritation + 0.9123 91.23%
Skin irritation - 0.8230 82.30%
Skin corrosion - 0.9624 96.24%
Ames mutagenesis + 0.5846 58.46%
Human Ether-a-go-go-Related Gene inhibition - 0.5184 51.84%
Micronuclear + 0.8200 82.00%
Hepatotoxicity + 0.6138 61.38%
skin sensitisation - 0.9260 92.60%
Respiratory toxicity + 0.6333 63.33%
Reproductive toxicity + 0.6889 68.89%
Mitochondrial toxicity - 0.6875 68.75%
Nephrotoxicity - 0.8126 81.26%
Acute Oral Toxicity (c) III 0.6511 65.11%
Estrogen receptor binding + 0.7143 71.43%
Androgen receptor binding + 0.7380 73.80%
Thyroid receptor binding + 0.7620 76.20%
Glucocorticoid receptor binding + 0.8047 80.47%
Aromatase binding + 0.8846 88.46%
PPAR gamma - 0.5000 50.00%
Honey bee toxicity - 0.9304 93.04%
Biodegradation - 0.9250 92.50%
Crustacea aquatic toxicity + 0.7600 76.00%
Fish aquatic toxicity - 0.7897 78.97%

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
CHEMBL2292 Q13627 Dual-specificity tyrosine-phosphorylation regulated kinase 1A 99.26% 93.24%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 98.94% 94.45%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 98.23% 85.30%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.25% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.95% 96.09%
CHEMBL255 P29275 Adenosine A2b receptor 93.82% 98.59%
CHEMBL1951 P21397 Monoamine oxidase A 92.71% 91.49%
CHEMBL1907 P15144 Aminopeptidase N 92.39% 93.31%
CHEMBL2424504 P29375 Lysine-specific demethylase 5A 91.60% 99.23%
CHEMBL3714130 P46095 G-protein coupled receptor 6 91.29% 97.36%
CHEMBL1868 P17948 Vascular endothelial growth factor receptor 1 90.45% 96.47%
CHEMBL308 P06493 Cyclin-dependent kinase 1 90.28% 91.73%
CHEMBL4225 P49760 Dual specificity protein kinase CLK2 90.19% 80.96%
CHEMBL2535 P11166 Glucose transporter 89.91% 98.75%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 89.09% 94.00%
CHEMBL4208 P20618 Proteasome component C5 89.06% 90.00%
CHEMBL3231 Q13464 Rho-associated protein kinase 1 88.38% 95.55%
CHEMBL3192 Q9BY41 Histone deacetylase 8 85.82% 93.99%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.13% 86.33%
CHEMBL1821 P08173 Muscarinic acetylcholine receptor M4 82.56% 94.08%
CHEMBL2094127 P06493 Cyclin-dependent kinase 1/cyclin B 82.41% 96.00%
CHEMBL5443 O00311 Cell division cycle 7-related protein kinase 81.79% 96.11%
CHEMBL1781 P11387 DNA topoisomerase I 81.32% 97.00%
CHEMBL5543 Q9Y463 Dual specificity tyrosine-phosphorylation-regulated kinase 1B 81.20% 94.70%
CHEMBL2095172 P14867 GABA-A receptor; alpha-1/beta-2/gamma-2 80.78% 92.67%
CHEMBL5747 Q92793 CREB-binding protein 80.49% 95.12%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 80.39% 94.62%
CHEMBL2000 P03952 Plasma kallikrein 80.16% 93.92%

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.
Peganum harmala

Cross-Links

Top
PubChem 9815570
LOTUS LTS0191686
wikiData Q15425761