6-Bromo-1-(3,4-Dihydro-2H-Pyrrol-5-Yl)-9H-Pyrido(3,4-B)Indole

Details

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Internal ID 6598a9be-f62f-46bd-8ac1-58acf033bbad
Taxonomy Alkaloids and derivatives > Harmala alkaloids
IUPAC Name 6-bromo-1-(3,4-dihydro-2H-pyrrol-5-yl)-9H-pyrido[3,4-b]indole
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H12BrN3/c16-9-3-4-12-11(8-9)10-5-7-18-15(14(10)19-12)13-2-1-6-17-13/h3-5,7-8,19H,1-2,6H2
InChI Key BJVWSKGRRKQZGZ-UHFFFAOYSA-N
Popularity 8 references in papers

Physical and Chemical Properties

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Molecular Formula C15H12BrN3
Molecular Weight 314.18 g/mol
Exact Mass 313.02146 g/mol
Topological Polar Surface Area (TPSA) 41.00 Ų
XlogP 3.10
Atomic LogP (AlogP) 4.06
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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88704-44-3
CHEBI:80956
6-bromo-1-(3,4-dihydro-2H-pyrrol-5-yl)-9H-pyrido[3,4-b]indole
CHEMBL1994777
DTXSID10237269
NSC622807
NSC-622807
NCI60_006770
C17168
Q27154926
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 6-Bromo-1-(3,4-Dihydro-2H-Pyrrol-5-Yl)-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 + 0.9868 98.68%
Caco-2 + 0.5778 57.78%
Blood Brain Barrier + 0.9000 90.00%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Mitochondria 0.5857 58.57%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9426 94.26%
OATP1B3 inhibitior + 0.9456 94.56%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior + 0.7000 70.00%
BSEP inhibitior + 0.5762 57.62%
P-glycoprotein inhibitior - 0.8343 83.43%
P-glycoprotein substrate - 0.6705 67.05%
CYP3A4 substrate + 0.5204 52.04%
CYP2C9 substrate + 0.5764 57.64%
CYP2D6 substrate - 0.8080 80.80%
CYP3A4 inhibition - 0.6214 62.14%
CYP2C9 inhibition - 0.6126 61.26%
CYP2C19 inhibition - 0.7734 77.34%
CYP2D6 inhibition - 0.8763 87.63%
CYP1A2 inhibition + 0.8660 86.60%
CYP2C8 inhibition - 0.6667 66.67%
CYP inhibitory promiscuity + 0.6664 66.64%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8800 88.00%
Carcinogenicity (trinary) Non-required 0.7536 75.36%
Eye corrosion - 0.9828 98.28%
Eye irritation - 0.9021 90.21%
Skin irritation - 0.7263 72.63%
Skin corrosion - 0.8971 89.71%
Ames mutagenesis - 0.5200 52.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7546 75.46%
Micronuclear + 0.5200 52.00%
Hepatotoxicity + 0.6302 63.02%
skin sensitisation - 0.8257 82.57%
Respiratory toxicity + 0.8222 82.22%
Reproductive toxicity + 0.8667 86.67%
Mitochondrial toxicity + 0.8500 85.00%
Nephrotoxicity - 0.9336 93.36%
Acute Oral Toxicity (c) III 0.6032 60.32%
Estrogen receptor binding + 0.9326 93.26%
Androgen receptor binding + 0.7221 72.21%
Thyroid receptor binding + 0.7610 76.10%
Glucocorticoid receptor binding + 0.7860 78.60%
Aromatase binding + 0.8152 81.52%
PPAR gamma + 0.9334 93.34%
Honey bee toxicity - 0.8747 87.47%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity + 0.6200 62.00%
Fish aquatic toxicity + 0.8644 86.44%

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
CHEMBL240 Q12809 HERG 98.40% 89.76%
CHEMBL1951 P21397 Monoamine oxidase A 98.30% 91.49%
CHEMBL5443 O00311 Cell division cycle 7-related protein kinase 97.07% 96.11%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.55% 91.11%
CHEMBL1907594 P30926 Neuronal acetylcholine receptor; alpha3/beta4 94.00% 97.23%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.98% 96.09%
CHEMBL3192 Q9BY41 Histone deacetylase 8 93.93% 93.99%
CHEMBL241 Q14432 Phosphodiesterase 3A 90.08% 92.94%
CHEMBL1781 P11387 DNA topoisomerase I 89.85% 97.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 89.29% 89.00%
CHEMBL3310 Q96DB2 Histone deacetylase 11 89.21% 88.56%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 87.90% 94.00%
CHEMBL2292 Q13627 Dual-specificity tyrosine-phosphorylation regulated kinase 1A 87.82% 93.24%
CHEMBL2107 P61073 C-X-C chemokine receptor type 4 86.72% 93.10%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 86.39% 94.45%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 86.27% 96.67%
CHEMBL255 P29275 Adenosine A2b receptor 86.21% 98.59%
CHEMBL3155 P34969 Serotonin 7 (5-HT7) receptor 86.08% 90.71%
CHEMBL5747 Q92793 CREB-binding protein 85.05% 95.12%
CHEMBL202 P00374 Dihydrofolate reductase 84.87% 89.92%
CHEMBL1907598 P05106 Integrin alpha-V/beta-3 84.49% 95.71%
CHEMBL2581 P07339 Cathepsin D 84.20% 98.95%
CHEMBL213 P08588 Beta-1 adrenergic receptor 83.44% 95.56%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 83.32% 93.40%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 82.58% 91.71%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 81.48% 95.56%
CHEMBL2094127 P06493 Cyclin-dependent kinase 1/cyclin B 80.71% 96.00%
CHEMBL1952 P04818 Thymidylate synthase 80.50% 93.53%

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.
There are no matching plants.

Cross-Links

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PubChem 145929
LOTUS LTS0068375
wikiData Q27154926