Quinolines and derivatives
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Filtered Search Results
Medchemexpress LLC Methyl 3,3-dimethoxypropionate | 7424-91-1 | MFCD00010650 | ≥98.0% | 148.16 g/mol | C6H12O4 | 50 G
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Methyl 3,3-dimethoxypropionate is the methyl ester of 3,3-dimethoxypropionic acid, provided as a high-purity biochemical reagent for organic synthesis and life-science research. It functions as a synthetic building block and intermediate for derivatization and coupling reactions.
- High purity ≥98.0%.
- Molecular formula C6H12O4.
- Molecular weight 148.16 g/mol.
- Available in multiple pack sizes including 50 g.
- Suitable as a building block for organic synthesis and derivatization.
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Medchemexpress LLC Azido-PEG9-amine | 1207714-69-9 | 98.5% | 482.57 g/mol | C20H42N4O9 | 250 MG
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Azido-PEG9-amine is an azide-terminated polyethylene glycol linker containing nine ethylene glycol units and a terminal primary amine, used as a click-chemistry reagent and as a non-cleavable PEG9 linker in bioconjugation applications.
- Azide-terminated PEG linker with nine ethylene glycol units.
- Terminal primary amine for further conjugation.
- Enables copper-catalyzed azide-alkyne cycloaddition (CuAAC) and strain-promoted azide-alkyne cycloaddition (SPAAC).
- Suitable for antibody-drug conjugate (ADC) and proteolysis targeting chimera (PROTAC) synthesis and general bioconjugation.
- CAS number 1207714-69-9; molecular weight 482.57 g/mol; formula C20H42N4O9; purity 98.5%.
- Supplied as 250 mg quantity for laboratory-scale synthesis.
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Medchemexpress LLC Tacalcitol monohydrate | 93129-94-3 | 99.9% | 434.65 | 5 MG
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Tacalcitol monohydrate promotes normal bone growth by regulating calcium ions. It also inhibits cancer cell proliferation and migration. This compound is suitable for research related to inflammation, cancer, and skin diseases.
- Promotes normal bone growth through calcium ion regulation.
- Inhibits cancer cell proliferation and migration.
- Inhibits the synthesis of IL-6 and IL-8 in nasal polyp fibroblast cultures in a dose-dependent manner.
- Induces cell differentiation in normal human keratinocytes.
- Inhibits the growth of normal and psoriatic human keratinocytes.
- Inhibits DNA synthesis in normal human keratinocytes.
- Strongly reduces the proliferation of human glioblastoma.
- Inhibits human glioblastoma migration.
- Significantly inhibits TPA-induced cutaneous inflammation and improves epidermal differentiation in hairless mice.
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TARGETMOL CHEMICALS INC PF-04979064 25MG
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Also available in 2 mg 5 mg 10 mg 50 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. PF-04979064 is a potent and selective PI3K and mTOR dual kinase inhibitor(Ki of 0.13 nM and 1.42 nMrespectively). purity: 98%
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TARGETMOL CHEMICALS INC ASTX660 5MG
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Also available in 1 mg 10 mg 25 mg 50 mg 100 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. ASTX660 is an orally bioavailable dual antagonist of cIAP and XIAP. purity: 99%
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TARGETMOL CHEMICALS INC CIS-5-DODECENOIC ACID 100MG
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Also available in 10 mg 25 mg 50 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. Cis-5-Dodecenoic Acid is a monounsaturated fatty acid that has a C12 chain as a backbone and a cis double bond at the C5 position. purity: 99%
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TARGETMOL CHEMICALS INC MOXIDECTIN 50MG
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Also available in 5 mg 10 mg 25 mg 100 mg 500 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. Moxidectin (CL301423) is an anthelmintic drug which kills parasitic worms and is used for the prevention and control of heartworm and intestinal worms. It can be found in treatments prescribed for animals such as dogs cats horses cattle and sheep. Application methods for moxidectin vary by treatment and include oral topical and injectable solutions. Cydectin Pour On is a trade name for a formulation for use on cattle and red deer. purity: 99%
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Medchemexpress LLC Gemifloxacin mesylate | 210353-53-0 | 99.59% | 5 MG
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Gemifloxacin mesylate (SB-265805S; LB-20304a) is an orally active broad-spectrum quinolone antibacterial antibiotic. It inhibits DNA synthesis by inhibiting DNA gyrase and Topoisomerase IV activities. Gemifloxacin mesylate has potent antibacterial activities against gram-positive bacteria in in vitro efficacy study, particularly Streptococci and Staphylococci. It has been used in the research of respiratory tract infections.
- Inhibits DNA synthesis by inhibiting DNA gyrase and Topoisomerase IV activities.
- Potent antibacterial activities against gram-positive bacteria in in vitro efficacy study, particularly Streptococci and Staphylococci.
- Used in the research of respiratory tract infections.
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Medchemexpress LLC Quin-C7 | 871100-12-8 | MFCD34182190 | 99.8% | 431.48 g/mol | C25H25N3O4 | 10 MG
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Quin-C7 is an orally active antagonist of formyl peptide receptor 2 (FPR2/ALX) used as a research reagent to study inflammatory signaling pathways. It exhibits anti-inflammatory activity and has been reported to ameliorate dextran sulfate sodium (DSS)-induced colitis in mouse models.
- Orally active FPR2/ALX antagonist for in vivo and in vitro studies.
- Demonstrated anti-inflammatory effects and efficacy in DSS-induced colitis models.
- Chemical formula C25H25N3O4, molecular weight 431.48 g/mol.
- CAS number 871100-12-8.
- High purity (~99.8%) suitable for research applications.
- Available as a 10 MG solid; soluble in DMSO for stock solutions.
- For research use only; not for human or clinical use.
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Medchemexpress LLC Zm241385 | 139180-30-6 | 99.5% | 337.34 | 200 MG
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Zm241385 | 139180-30-6 | 99.5% | 337.34 | 200 MG
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TARGETMOL CHEMICALS INC BEPRIDIL HYDROCHLORIDE 50MG
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Also available in 5 mg 10 mg 25 mg 100 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. Bepridil hydrochloride (CERM 1978) is a calcium channel blocker and also inhibits Na+/Ca2+ exchange (NCX) sodium channels and cardiac sarcolemmal KATP channels. purity: 99%
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Ambeed 7Bromo1 2dihydroisoquinolin3 4
7-Bromo-1,2-dihydroisoquinolin-3(4H)-one, 943751-93-7, 95%
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Ambeed Dimethyl cyclohexane1 3dicarbo
Dimethyl cyclohexane-1,3-dicarboxylate, 62638-06-6, 95%
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Medchemexpress LLC Azido-PEG9-amine | 1207714-69-9 | 98.5% | 482.57 g/mol | C20H42N4O9 | 50 MG
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Azido-PEG9-amine is a non-cleavable nine-unit polyethylene glycol (PEG) linker bearing an azide and a terminal amine. It is used for antibody-drug conjugate and PROTAC synthesis and enables bioconjugation via click chemistry (CuAAC and SPAAC).
- Molecular formula: C20H42N4O9.
- Molecular weight: 482.57 g/mol.
- Cas number: 1207714-69-9.
- Purity: 98.52%.
- Available package sizes: 50 mg, 100 mg, 250 mg, 500 mg, 1 g.
- Storage: pure form -20°C (3 years) or 4°C (2 years); in solvent -80°C (6 months) or -20°C (1 month).
- Compatible with copper-catalyzed azide-alkyne cycloaddition and strain-promoted alkyne-azide cycloaddition for bioconjugation.
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Medchemexpress LLC ACT-1004-1239 | 2178049-58-4 | 98.8% | C27H28F2N6O3 | 1 MG
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ACT-1004-1239 is a potent, selective, orally active CXCR7 antagonist with an IC50 value of 3.2 nM. It is intended for research use only.
- Inhibits human, dog, rat, mouse, guinea pig, macaque CXCR7 with IC50s of 3.2, 2.3, 3.1, 2.3, 0.6, 1.5 nM respectively.
- Promotes oligodendrocyte precursor cell (OPC) differentiation by increasing CXCL12 levels.
- Increases plasma CXCL12 concentration in naive male DBA/1 mice.
- Reduces disease severity in MOG-induced experimental autoimmune encephalomyelitis (EAE) model.
- Increases myelination in the Cuprizone-induced demyelination model mice.
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