12 Results for "

aromatic nucleophilic substitution

" in MedChemExpress (MCE) Product Catalog:
Products (12)

12 Results for "aromatic nucleophilic substitution" in MCE Product Catalog:

Cat. No.: HY-W093017
CAS No.: 626-61-9
Research Areas:  

Others

4-Chloropyridine is a NNMT (Nicotinamide N-methyltransferase) substrate and suicide inhibition-based protein labeling scaffold precursor.4-Chloropyridine undergoes NNMT-catalyzed pyridine nitrogen methylation to increase C4 electrophilicity, enabling aromatic nucleophilic substitution by NNMT cysteine C159 for covalent NNMT modification and inactivation.4-Chloropyridine can be used for the research of various cancers .
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Cat. No.: HY-Y0779
CAS No.: 403-42-9
Synonyms: 1-(4-Fluorophenyl)ethan-1-one
4'-Fluoroacetophenone (1-(4-Fluorophenyl)ethan-1-one) is p-fluoroacetophenone, and serves as a substrate for both SNAr dimerization reactions and cross SNAr reactions. 4'-Fluoroacetophenone is also an important intermediate that can be used in the synthesis of other active compounds, such as aromatic diketones .
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Cat. No.: HY-W007690
CAS No.: 626-64-2
Pyridin-4-ol is a pyridinol and can be used as synthetic intermediate .
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Cat. No.: HY-148629
CAS No.: 1637394-01-4
Purity:  99.18%
Target:  

JNK

Research Areas:  

Neurological Disease

GDC-0134 (RG6000) is a modulator targeting dual leucine zipper kinase (DLK) that can cross the blood-brain barrier. By inhibiting the kinase activity of DLK, GDC-0134 blocks the activation of the downstream JNK signaling pathway, suppresses DLK-dependent retrograde signal transduction of axon-to-soma degeneration, and exerts neuroprotective activity. GDC-0134 reduces TDP-43 protein aggregation and decreases the degree of neuromuscular junction denervation in motor neurons. GDC-0134 can be used in the research of amyotrophic lateral sclerosis (ALS), Alzheimer's disease and other DLK-related neurodegenerative diseases .
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Cat. No.: HY-34054
CAS No.: 4487-56-3
2,4-Dichloro-5-nitropyridine is a pyridine derivative, which can be used as a precursor to synthesize polyfluorinated pyrrolidine derivatives [3][4].
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Cat. No.: HY-W005118
CAS No.: 944401-77-8
Synonyms: 4-Fluoropyridin-2-amine
Target:  

Drug Intermediate

Research Areas:  

Others

2-Amino-4-fluoropyridine (4-Fluoropyridin-2-amine) is an intermediate. 2-Amino-4-fluoropyridine can be used in research on the synthesis of PKCζ inhibitors .
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Cat. No.: HY-W025838
CAS No.: 3171-45-7
Target:  

Drug Intermediate

Research Areas:  

Others

4,5-Dimethylbenzene-1,2-diamine is a substitute for aromatic diamine compound. 4,5-Dimethylbenzene-1,2-diamine act as a bidentate nucleophilic reagent and participates in the palladium (II)-mediated isocyanate addition reaction to construct a diaminocarbene palladium complex with potential catalytic activity .
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Cat. No.: HY-120188
CAS No.: 1680204-90-3
Purity:  99.94%
Target:  

PPAR

Research Areas:  

Others

CC618 is a selective PPARβ/δ antagonist. CC618 covalently modifies conserved Cys249 in the PPARβ/δ ligand-binding pocket via nucleophilic aromatic substitution, converting its thiol moiety to a 5-trifluoromethyl-2-pyridylthioether .
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Cat. No.: HY-206852
CAS No.: 2055777-51-8
PF-06445974 precursor (Compound 28) is a nitro precursor and synthetic intermediate. PF-06445974 precursor can be used for the synthesis of PF-06445974 (HY-119190). PF-06445974 is a positron emission tomography (PET) compound that acts potently on PDE4B .
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Cat. No.: HY-187359
Target:  

SARS-CoV Virus Protease

Research Areas:  

Infection

SR-B-182 is a SARS-CoV-2 main protease (MPro) inhibitor with an IC50 of 0.015 μM. SR-B-182 can be used for the research of COVID-19 .
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Cat. No.: HY-158616
CAS No.: 1286479-53-5
4-Methyl-7-(2-nitrophenoxy)-2H-chromen-2-one (compound 2f) is a selenol fluorescent probe designed based on a nucleophilic aromatic substitution mechanism. It can selectively recognize selenols in neutral aqueous solution without significant interference from biological thiols, amines or alcohols. It can be used to quantify the selenium content in selenoenzymes and to image the activity of endogenous selenols in living cells.
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Cat. No.: HY-187684
CAS No.: 3054389-11-3
Target:  

CRM1 Apoptosis

Research Areas:  

Neurological Disease Cancer

FR-027 is an orally active, blood-brain barrier permeable XPO1 inhibitor with an EC50 value of 54-69 nM in human cells. FR-027 covalently modifies Cys528 of XPO1 via nucleophilic aromatic substitution, maintaining the nuclear export signal binding groove of XPO1 in a closed conformation to block the nuclear export process, and inhibits XPO1 function without inducing its protein degradation. FR-027 promotes cancer cell apoptosis and inhibits the growth of hematological and solid tumor cells. FR-027 can be used in research related to acute lymphoblastic leukemia, ovarian cancer, glioblastoma, and primary central nervous system lymphoma .
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