Quinolines and derivatives

Ambeed Tetraphenylphosphonium chlorid

Tetraphenylphosphonium chloride, 2001-45-8, 97%

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TARGETMOL CHEMICALS INC 8-Deoxygartanin 5MG

Also available in 1 mL, 1 mg, 10 mg, 25 mg, 50 mg and bulk. Please contact Fisher for quotes. 8-Deoxygartanin is a butyrylcholinesterase (BChE) selective inhibitor, it exhibits significant inhibition of self-induced alpha2-amyloid (Aalpha2) aggregation, it has multifunctional activities against Alzheimer's disease (AD) and could be promising compounds for the therapy of AD. Purity 99.76%

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Medchemexpress LLC Tolmetin sodium dihydrate | 64490-92-2 | 99.94% | 1 ML

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Tolmetin sodium dihydrate is an orally active and potent COX inhibitor, with IC50s of 0.35 μM and 0.82 μM for human COX-1 and COX-2, respectively. It is a non-steroidal anti-inflammatory drug (NSAID).

• Orally active and potent COX inhibitor.
• Non-steroidal anti-inflammatory drug (NSAID).
• Shows anticancer activity against HT-29 colon cancer cell line in a dose-dependent manner.
• Can attenuate quinolinic acid (QA)-induced neurotoxicity.

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eMolecules​ 121689-23-4 | 8-AMINOQUINOLINE-4-CARBOXYLIC ACID | AstaTech | MFCD08690743 | 188.186 | C10H8N2O2 | 95.000 | Nc1cccc2c(ccnc12)C(O)=O | 1g | 449740747

8-AMINOQUINOLINE-4-CARBOXYLIC ACID | AstaTech | 121689-23-4 | MFCD08690743 | 188.186 | C10H8N2O2 | 95.000 | Nc1cccc2c(ccnc12)C(O)=O | 1g | 449740747

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Medchemexpress LLC Quin-C7 | 871100-12-8 | MFCD34182190 | 99.8% | 431.48 g/mol | C25H25N3O4 | 5 MG

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Quin-C7 is an orally active antagonist of the formyl peptide receptor 2 (FPR2/ALX) with reported anti-inflammatory activity; it has been shown to ameliorate dextran sulfate sodium (DSS)-induced colitis in mice and is used in preclinical studies of inflammatory responses and inflammatory bowel disease.

• Orally active FPR2/ALX antagonist used in inflammation research.
• Validated in DSS-induced colitis models in mice.
• High purity suitable for in vivo and in vitro studies (≈99.8%).
• Molecular weight 431.48 g/mol; formula C25H25N3O4.
• Supplied as a powder with COA and SDS available.
• Recommended storage at -20°C to maintain stability.

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Medchemexpress LLC 5-Hydroxyquinoline | 578-67-6 | 99.51% | 145.16 | 50 G

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5-Hydroxyquinoline is an organic compound commonly used in certain chemical reactions and biological research. It can be used in the manufacture of dyes, cellulase, oxidants and passivators, etc., and is widely used in the pigment, paint and rubber industries. Additionally, the compound is utilized as a precursor, intermediate, and metal ion complexing agent for specific drugs. It is a biochemical reagent that can be used as a biological material or organic compound for life science related research.

• Used in chemical reactions and biological research.
• Utilized in the manufacture of dyes, cellulase, oxidants and passivators.
• Widely applied in pigment, paint, and rubber industries.
• Functions as a precursor, intermediate, and metal ion complexing agent for specific drugs.
• Biochemical reagent for life science-related research.

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eMolecules​ 103476-89-7 | Ambeed | (S)-2-Acetamido-N-((S)-1-(((S)-5-guanidino-1-oxopentan-2-yl)amino)-4-methyl-1-oxopentan-2-yl)-4-methylpentanamide hemisulfate | 1mg | 761012742 | A663950 | MFCD00037012 | 951.2 | C40H78N12O12S

2-(Pyridyldithio)ethylamine HCl | Ambeed | 106139-15-5 | MFCD01863453 | 222.750 | C7H11ClN2S2 | 97.000 | Cl.NCCSSc1ccccn1 | 1g | 490550027

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Medchemexpress LLC Lobeglitazone (sulfate) | 763108-62-9 | 99.6% | 578.61 | 25 MG

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Lobeglitazone sulfate is a new type of thiazolidinedione, acting as an orally active agonist for PPARγ and PPARα. It inhibits the ERK/JNK/Smad/NF-κB signaling pathway and possesses various therapeutic properties.

• Agonist for PPARγ (EC50 of 137.4 nM) and PPARα (EC50 of 546.3 nM)
• Inhibits ERK/JNK/Smad/NF-κB signaling pathway
• Exhibits anti-inflammatory, anti-diabetic, anti-fibrotic, and anti-atherosclerotic properties
• Increases glucose uptake in 3T3-L1 adipocytes and L6 muscle cells
• Inhibits NO generation and pro-inflammatory cytokines in LPS-stimulated BMDMs
• Inhibits TGF-β1-induced expression of α-SMA and fibronectin
• Inhibits PDGF-induced proliferation and migration of vascular smooth muscle cells

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Medchemexpress LLC 8-Hydroxyquinoline hemisulfate | 134-31-6 | 100.0% | 194.20 | 100 MG

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8-Hydroxyquinoline hemisulfate is a monoprotic bidentate chelating agent. It exhibits antiseptic, disinfectant, and pesticide properties, functioning as a transcription inhibitor. This product is for research use only.

• Functions as a monoprotic bidentate chelating agent.
• Exhibits antiseptic properties.
• Acts as a disinfectant.
• Functions as a pesticide.
• Functions as a transcription inhibitor.
• For research use only.

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Aobchem 3-Hydroxyquinoline | 97% | CAS 580-18-7 | C9H7NO | 500g

3-Hydroxyquinoline | 97% | CAS 580-18-7 | C9H7NO | 500g

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eMolecules​ 103476-89-7 | Leupeptin hemisulfate | Ambeed | MFCD00037012 | 951.200 | C40H78N12O12S | 97.000 | OS(O)(=O)=O.CC(C)C[C@H](NC(C)=O)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCCNC(N)=N)C=O.CC(C)C[C@H](NC(C)=O)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCCNC(N)=N)C=O | 250mg | 528956477

Leupeptin hemisulfate | Ambeed | 103476-89-7 | MFCD00037012 | 951.200 | C40H78N12O12S | 97.000 | OS(O)(=O)=O.CC(C)C[C@H](NC(C)=O)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCCNC(N)=N)C=O.CC(C)C[C@H](NC(C)=O)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCCNC(N)=N)C=O | 250mg | 528956477

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eMolecules​ 103476-89-7 | Leupeptin hemisulfate | Ambeed | MFCD00037012 | 951.200 | C40H78N12O12S | 97.000 | OS(O)(=O)=O.CC(C)C[C@H](NC(C)=O)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCCNC(N)=N)C=O.CC(C)C[C@H](NC(C)=O)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCCNC(N)=N)C=O | 50mg | 552750159

Leupeptin hemisulfate | Ambeed | 103476-89-7 | MFCD00037012 | 951.200 | C40H78N12O12S | 97.000 | OS(O)(=O)=O.CC(C)C[C@H](NC(C)=O)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCCNC(N)=N)C=O.CC(C)C[C@H](NC(C)=O)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCCNC(N)=N)C=O | 50mg | 552750159

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eMolecules​ 103476-89-7 | Leupeptin hemisulfate | Ambeed | MFCD00037012 | 951.200 | C40H78N12O12S | 97.000 | OS(O)(=O)=O.CC(C)C[C@H](NC(C)=O)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCCNC(N)=N)C=O.CC(C)C[C@H](NC(C)=O)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCCNC(N)=N)C=O | 10mg | 552750157

Leupeptin hemisulfate | Ambeed | 103476-89-7 | MFCD00037012 | 951.200 | C40H78N12O12S | 97.000 | OS(O)(=O)=O.CC(C)C[C@H](NC(C)=O)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCCNC(N)=N)C=O.CC(C)C[C@H](NC(C)=O)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCCNC(N)=N)C=O | 10mg | 552750157

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Medchemexpress LLC 8-Hydroxyquinoline hemisulfate | 134-31-6 | 99.6% | 194.20 | 50 MG

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8-Hydroxyquinoline (hemisulfate) (Standard) serves as the analytical standard for 8-Hydroxyquinoline (hemisulfate), and is designated for research and analytical applications. It is recognized as a monoprotic bidentate chelating agent that possesses antiseptic, disinfectant, and pesticide properties, and also functions as a transcription inhibitor.

• Analytical standard for 8-Hydroxyquinoline (hemisulfate).
• Intended for research and analytical applications.
• Functions as a monoprotic bidentate chelating agent.
• Exhibits antiseptic, disinfectant, and pesticide properties.
• Acts as a transcription inhibitor.
• Commonly used in qualitative, quantitative, and methodological research experiments in HPLC, GC, and MS.

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Medchemexpress LLC Lobeglitazone (sulfate) | 763108-62-9 | 99.6% | 578.61 | 50 MG

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Lobeglitazone sulfate is a new type of thiazolidinedione and an orally active agonist for PPAR with EC50 of 137.4 nM and 546.3 nM for PPARγ and PPARα. It is an inhibitor for the ERK/JNK/Smad/NF-κB signaling pathway and exhibits anti-inflammatory, anti-diabetic, anti-fibrotic, and anti-atherosclerotic properties.

• Orally active agonist for PPAR.
• Inhibits the ERK/JNK/Smad/NF-κB signaling pathway.
• Exhibits anti-inflammatory properties.
• Possesses anti-diabetic properties.
• Demonstrates anti-fibrotic and anti-atherosclerotic properties.

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