52 Results for "

quinoline-based hydrazones

" in MedChemExpress (MCE) Product Catalog:
Products (52)

52 Results for "quinoline-based hydrazones" in MCE Product Catalog:

5
5 Cited Publications
Cat. No.: HY-16261B
CAS No.: 480998-12-7
Synonyms: (E/Z)-Aldoxorubicin hydrochloride; Doxorubicin(6-maleimidocaproyl)hydrazone hydrochloride
Research Areas:  

Cancer

MC-DOXHZN ((E/Z)-Aldoxorubicin; Doxorubicin(6-maleimidocaproyl)hydrazone) hydrochloride is an albumin-binding proagent of Doxorubicin (HY-15142A) (DNA topoisomerase II inhibitor), with acid-sensitive properties. MC-DOXHZN hydrochloride can be used to synthesize ADC .
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4
4 Cited Publications
Cat. No.: HY-114758
CAS No.: 737-86-0
Purity:  99.96%
Pyridoxal isonicotinoyl hydrazone is an orally active and lipophilic iron-specific chelator that acts as a non-competitive inhibitor of ferrochelatase (FECH) by binding iron ions. Pyridoxal isonicotinoyl hydrazone disrupts heme biosynthesis, leading to reduced FECH stability and increased protoporphyrin IX (PPIX) accumulation. Pyridoxal isonicotinoyl hydrazone is promising for research of iron-overload diseases (e.g., β-thalassemia) .
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4
4 Cited Publications
Cat. No.: HY-10522
CAS No.: 957890-42-5
Purity:  99.62%
Synonyms: CX05168; CX04328
Target:  

HIV HIV Integrase

Research Areas:  

Infection

LEDGIN6 (CX05168) is a quinoline-based protein-protein interaction inhibitor of LEDGF/p75 and HIV integrase .
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3
3 Cited Publications
Cat. No.: HY-137331
CAS No.: 2374782-04-2
Purity:  98.57%
Synonyms: FAPI-46
Target:  

FAP

Research Areas:  

Cancer

FAPI-46 is a quinoline-based fibroblast activation protein (FAP)-targeted tracer. Use radioactivity FAPI-46 labeled with 68Ga or 177Lu can be used for tumor imaging in a variety of cancers and has higher tumor uptake rates and longer tumor accumulation .
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1
1 Cited Publications
Cat. No.: HY-W077680
CAS No.: 1126-58-5
Research Areas:  

Others

Girard's P reagent is a reagent used in organic chemistry. Girard's P reagent is used to react with vanillin to form a hydrazone derivative, which is then combined with an ion selective electrode (ISE) to develop a potentiometric method for the determination of vanillin. Girard's P reagent can be used in the development of ion selective electrodes and in the study of organic analysis .
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Cat. No.: HY-15932
CAS No.: 82692-93-1
Synonyms: TOOS sodium salt
TOOS (TOOS sodium salt) is a highly water-soluble aniline derivative widely used in diagnostics and biological experiments. TOOS can be combined with 3-methyl-2-benzothiazolinone hydrazone hydrochloride (MBTH) to form a chromogenic system to measure oxidase activity. In the MBTH-TOOS chromogenic system, MBTH is catalytically oxidized to produce (-NH) free radicals, which react with TOOS to form colorless compounds. Furthermore, the colorless compound undergoes a disproportionation reaction to produce a blue-violet quinoid compound .
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Cat. No.: HY-Y0760
CAS No.: 586-38-9
Synonyms: 3-Anisic acid; NSC 27014; m-Methoxybenzoic acid
3-Methoxybenzoic acid (3-Anisic acid; NSC 27014; m-Methoxybenzoic acid) is a substituted benzoic acid and precursor for synthesis of hydrazide-hydrazone derivatives active against Gram-positive bacteria, including Bacillus spp .
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Cat. No.: HY-W074541
CAS No.: 123-46-6
Synonyms: Trimethylacetohydrazideammonium chloride
Girard's reagent T is often used in analytical chemistry as a derivatizing agent for carbonyl compounds. Girard's reagent T reacts with ketones and aldehydes to form stable hydrazones that can be readily analyzed by various techniques including chromatography and spectrophotometry. In addition, Girard's Reagent T has been used in the synthesis of a variety of organic compounds, including pharmaceuticals and agrochemicals.
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Cat. No.: HY-16261A
CAS No.: 151038-96-9
Synonyms: (E/Z)-Aldoxorubicin; Doxorubicin(6-maleimidocaproyl)hydrazone
Research Areas:  

Cancer

MC-DOXHZN ((E/Z)-Aldoxorubicin; Doxorubicin(6-maleimidocaproyl)hydrazone) is an albumin-binding proagent of Doxorubicin (HY-15142A) (DNA topoisomerase II inhibitor), with acid-sensitive properties. MC-DOXHZN can be used to synthesize ADC .
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Cat. No.: HY-161752
CAS No.: 16371-55-4
Target:  

Bacterial

Research Areas:  

Infection

Antibacterial agent 224 is a potent and selective synthetic hydrazone inhibitor against the Salmonella PhoP/PhoQ system .
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Cat. No.: HY-136131
Target:  

ADC Linkers

Research Areas:  

Cancer

NH2-PEG4-hydrazone-DBCO is a cleavable 4 unit PEG ADC linker used in the synthesis of antibody-drug conjugates (ADCs) . NH2-PEG4-hydrazone-DBCO is a click chemistry reagent, it contains a DBCO group that can undergo strain-promoted alkyne-azide cycloaddition (SPAAC) with molecules containing Azide groups.
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Cat. No.: HY-14801
CAS No.: 2675-35-6
Purity:  99.41%
Synonyms: A-007
Target:  

Drug Derivative

Research Areas:  

Inflammation/Immunology Cancer

Sivifene (A-007) is a triaryl hydrazone. Sivifene has anticancer activity and immunomodulatory effects. Sivifene regulates immune regulation by upregulating CD45 T lymphocyte surface receptors .
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Cat. No.: HY-W009411
CAS No.: 33008-06-9
Dansyl hydrazine is a carbohydrate-specific fluorescent dye (Ex/Em = 340 nm/525 nm). Dansyl hydrazine undergoes a condensation reaction with aldehyde groups generated by periodate oxidation on carbohydrate-containing structures to form fluorescent hydrazone compounds. Dansyl hydrazine selectively stains polysaccharides in formalin-fixed, paraffin-embedded human post-mortem brain tissues, revealing detailed structural features. Dansyl hydrazine is applicable to research related to Alzheimer's disease, Lafora disease, and polyglucosan body disease .
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Cat. No.: HY-W012617
CAS No.: 553-53-7
Synonyms: Nicotinic acid hydrazide
Target:  

Drug Intermediate

Research Areas:  

Infection

Nicotinohydrazide (Nicotinic acid hydrazide) is a precursor used for synthesizing hydrazone derivatives with antibacterial and antifungal activities. Nicotinohydrazide can be used in studies of bacterial and fungal infections .
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Cat. No.: HY-W013677
CAS No.: 456-22-4
4-Fluorobenzoic acid is a drug intermediate that can be used to synthesize a series of hydrazone derivatives with antituberculosis activity and Schiff bases with DPPH radical scavenging activity .
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Cat. No.: HY-155908
CAS No.: 474922-26-4
Synonyms: DSPE-PEG10000-NH2 ammonium
Target:  

Liposome

Research Areas:  

Others

DSPE-PEG10000-Amine ammonium (DSPE-PEG10000-NH2 ammonium) is a PEGylated distearoylphosphatidylethanolamine lipid with a terminal primary amino group. DSPE-PEG10000-Amine ammonium serves as a liposome component, and its surface bears reactive primary amino groups that enable covalent conjugation via the formation of bis-aryl hydrazone bonds .
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Cat. No.: HY-128642
CAS No.: 2370952-98-8
Purity:  98.94%
Target:  

FAP

Research Areas:  

Cancer

FAPI-2 is a quinoline-based fibroblast activation protein (FAP)-targeting ligand that can be labeled as 68Ga-FAPI-2 and used as a PET tracer for cancer diagnosis. FAPI-2 has advantages such as fast tracer kinetics, no need for fasting preparation, and being unaffected by blood glucose .
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Cat. No.: HY-136079
Target:  

ADC Linkers

Research Areas:  

Cancer

Methyltetrazine-PEG4-hydrazone-DBCO is a cleavable 4 unit PEG ADC linker used in the synthesis of antibody-drug conjugates (ADCs) . Methyltetrazine-PEG4-hydrazone-DBCO is a click chemistry reagent, it contains a DBCO group that can undergo strain-promoted alkyne-azide cycloaddition (SPAAC) with molecules containing Azide groups. Methyltetrazine-PEG4-hydrazone-DBCO also contains a Tetrazine group that can undergo an inverse electron demand Diels-Alder reaction (iEDDA) with molecules containing TCO groups.
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Cat. No.: HY-B0994
CAS No.: 140-87-4
Synonyms: Cyanoacetic hydrazide; 2-Cyanoacetohydrazide
Target:  

Drug Intermediate

Research Areas:  

Infection

Cyanoacetohydrazide is a pharmaceutical intermediate. Cyanoacetohydrazide can be used to synthesize acylhydrazide hydrazone derivatives with antibacterial or anti-tumor activity .
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Cat. No.: HY-19221
CAS No.: 133012-05-2
Target:  

Lipoxygenase

Research Areas:  

Inflammation/Immunology

Bay-y-1015 is an orally active quinoline-based 5-lipoxygenase inhibitor. Bay-y-1015 inhibits LTB4 and LTC4 synthesis. Bay-y-1015 can be used in the research of inflammatory diseases .
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