2-Bromo-3-(3,4,5-trimethoxyphenyl)pyridine

Details

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Internal ID ab70aab8-9428-4eed-9347-4e18e64ba712
Taxonomy Organoheterocyclic compounds > Pyridines and derivatives > Phenylpyridines
IUPAC Name 2-bromo-3-(3,4,5-trimethoxyphenyl)pyridine
SMILES (Canonical) COC1=CC(=CC(=C1OC)OC)C2=C(N=CC=C2)Br
SMILES (Isomeric) COC1=CC(=CC(=C1OC)OC)C2=C(N=CC=C2)Br
InChI InChI=1S/C14H14BrNO3/c1-17-11-7-9(8-12(18-2)13(11)19-3)10-5-4-6-16-14(10)15/h4-8H,1-3H3
InChI Key FLBYXYAXXCTQAW-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C14H14BrNO3
Molecular Weight 324.17 g/mol
Exact Mass 323.01571 g/mol
Topological Polar Surface Area (TPSA) 40.60 Ų
XlogP 3.40
Atomic LogP (AlogP) 3.54
H-Bond Acceptor 4
H-Bond Donor 0
Rotatable Bonds 4

Synonyms

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AKOS015962566
847063-30-3

2D Structure

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2D Structure of 2-Bromo-3-(3,4,5-trimethoxyphenyl)pyridine

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9955 99.55%
Caco-2 + 0.8511 85.11%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability + 0.7286 72.86%
Subcellular localzation Mitochondria 0.5981 59.81%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9644 96.44%
OATP1B3 inhibitior + 0.9662 96.62%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior + 0.5928 59.28%
P-glycoprotein inhibitior - 0.9192 91.92%
P-glycoprotein substrate - 0.8399 83.99%
CYP3A4 substrate - 0.5176 51.76%
CYP2C9 substrate - 0.6198 61.98%
CYP2D6 substrate - 0.7309 73.09%
CYP3A4 inhibition - 0.5973 59.73%
CYP2C9 inhibition - 0.6356 63.56%
CYP2C19 inhibition + 0.8712 87.12%
CYP2D6 inhibition - 0.7894 78.94%
CYP1A2 inhibition + 0.7096 70.96%
CYP2C8 inhibition + 0.7801 78.01%
CYP inhibitory promiscuity + 0.9053 90.53%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8551 85.51%
Carcinogenicity (trinary) Non-required 0.4460 44.60%
Eye corrosion - 0.9814 98.14%
Eye irritation + 0.7852 78.52%
Skin irritation - 0.8542 85.42%
Skin corrosion - 0.9700 97.00%
Ames mutagenesis - 0.6600 66.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7513 75.13%
Micronuclear + 0.6533 65.33%
Hepatotoxicity + 0.6125 61.25%
skin sensitisation - 0.9249 92.49%
Respiratory toxicity - 0.6333 63.33%
Reproductive toxicity + 0.7333 73.33%
Mitochondrial toxicity - 0.6125 61.25%
Nephrotoxicity - 0.6235 62.35%
Acute Oral Toxicity (c) III 0.5106 51.06%
Estrogen receptor binding + 0.8931 89.31%
Androgen receptor binding - 0.6131 61.31%
Thyroid receptor binding + 0.7736 77.36%
Glucocorticoid receptor binding + 0.7330 73.30%
Aromatase binding + 0.8536 85.36%
PPAR gamma + 0.6910 69.10%
Honey bee toxicity - 0.8928 89.28%
Biodegradation - 0.9250 92.50%
Crustacea aquatic toxicity + 0.6100 61.00%
Fish aquatic toxicity + 0.7614 76.14%

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 95.76% 96.09%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 94.11% 94.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 94.02% 86.33%
CHEMBL5747 Q92793 CREB-binding protein 93.97% 95.12%
CHEMBL4302 P08183 P-glycoprotein 1 93.54% 92.98%
CHEMBL4306 P22460 Voltage-gated potassium channel subunit Kv1.5 93.31% 94.03%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 90.40% 96.00%
CHEMBL5903 Q04771 Activin receptor type-1 89.24% 89.93%
CHEMBL1907 P15144 Aminopeptidase N 89.10% 93.31%
CHEMBL2535 P11166 Glucose transporter 88.60% 98.75%
CHEMBL2581 P07339 Cathepsin D 88.26% 98.95%
CHEMBL2094127 P06493 Cyclin-dependent kinase 1/cyclin B 87.31% 96.00%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 86.94% 85.14%
CHEMBL4208 P20618 Proteasome component C5 85.44% 90.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.60% 95.56%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.49% 99.17%
CHEMBL1966 Q02127 Dihydroorotate dehydrogenase 84.42% 96.09%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 83.82% 100.00%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 83.29% 96.67%
CHEMBL4145 Q9UKV0 Histone deacetylase 9 81.97% 85.49%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 81.94% 95.50%
CHEMBL3401 O75469 Pregnane X receptor 81.26% 94.73%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 80.69% 99.15%

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.
Codonopsis pilosula
Cynomorium coccineum subsp. songaricum

Cross-Links

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PubChem 11738823
NPASS NPC260995