Pyridines and derivatives
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- (1)
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- (1)
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- (54)
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- (1)
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- (10)
- (2)
- (1)
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- (6)
- (7)
- (12)
- (1)
- (1)
- (39)
- (1)
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- (11)
- (4)
- (2)
- (2)
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- (15)
- (1)
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- (1)
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- (30)
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Filtered Search Results
Cayman Chemical 4methoxyaPyrrolidinopropiophe
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A cathinone whose physiological and toxicological properties are not known
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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Medchemexpress LLC 15-PGDH-IN-1 | 2241676-74-2 | C24H22N4O2 | 5 MG
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15-PGDH-IN-1 is a potent and orally active 15-PGDH inhibitor. It demonstrates inhibition activity against recombinant human 15-PGDH with an IC50 value of 3 nM and is utilized for research into tissue repair and regeneration.
- Potent and orally active 15-PGDH inhibitor
- Inhibits recombinant human 15-PGDH with an IC50 value of 3 nM
- Used for research of tissue repair and regeneration
- Molecular weight: 398.46
- Purity: 98.35%
- Appearance: Solid, light yellow to yellow
- Storage conditions: Powder at -20°C for 3 years, 4°C for 2 years; in solvent at -80°C for 6 months, -20°C for 1 month
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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Medchemexpress LLC Cp-113818 | 135025-12-6 | 99.7% | 470.8 g/mol | C24H42N2OS3 | 1 ML
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CP-113818 is a potent cholesterol acyltransferase (ACAT) inhibitor used in cell-based and animal studies to reduce Aβ production and amyloid pathology in Alzheimer's disease research. It is provided as a solid and as a ready-to-use 10 mM solution in DMSO for in vitro applications, with documented solubility and storage conditions for research use only.
- Potent ACAT inhibitory activity suitable for Alzheimer's disease research.
- High purity (99.7%).
- Molecular weight 470.8 g/mol.
- Soluble in DMSO at 100 mg/mL for in vitro use.
- Available as solution and multiple solid pack sizes.
- Storage conditions documented for powder and solutions.
- For research use only; not for human or clinical use.
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Cambridge Isotope Laboratories Galaxolidone (unlabeled) (mix of diastereomers) 100 ug/mL in acetonitrile 1 2 mL
Galaxolidone (unlabeled) (mix of diastereomers) 100 ug/mL in acetonitrile 1 2 mL
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Medchemexpress LLC 4-Methylbenzylidene camphor | 36861-47-9 | 99.9% | 254.37 | 25 MG
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4-Methylbenzylidene camphor (4-MBC) is an endocrine disrupter that produces estrogen-like effects. Functioning as a ultraviolet (UV) filter, it may also impact normal placental formation during early pregnancy. This compound has been observed to influence cellular processes by activating PI3K/AKT and ERK1/2 signaling pathways, elevating intracellular ROS production, and inhibiting cell proliferation. It is intended for research use only.
- Inhibits proliferation and reduces invasion of HTR8/SVneo cells
- Induces apoptotic cell death of human trophoblast cells
- Increases the proportion of cells in the SubG1 phase
- Activates PI3K/AKT and ERK1/2 signaling pathways
- Elevates intracellular ROS production
- Impacts uterine gene expression in neonates
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Cayman Chemical 5 deoxy5Fluorocytidine
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An intermediate metabolite of capecitabine
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eMolecules 182482-25-3 | 2,4,6-Trifluorobenzeneboronic acid | Apollo Scientific | MFCD01863169 | 175.900 | C6H4BF3O2 | 95.000 | OB(O)c1c(F)cc(F)cc1F | 1g | 562445090
2,4,6-Trifluorobenzeneboronic acid | Apollo Scientific | 182482-25-3 | MFCD01863169 | 175.900 | C6H4BF3O2 | 95.000 | OB(O)c1c(F)cc(F)cc1F | 1g | 562445090
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Medchemexpress LLC Enflicoxib | 251442-94-1 | 99.9% | 405.34 | 25 MG
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Enflicoxib (E 6087) is a nonsteroidal anti-inflammatory compound that selectively inhibits cyclooxygenase-2 (COX-2) but not cyclooxygenase-1 (COX-1). It demonstrates anti-inflammatory, analgesic, and antipyretic activities in animal models. Enflicoxib is the primary active compound, with a long elimination half-life and a relatively large volume of distribution. It is suitable for laboratory research.
- Selectively inhibits cyclooxygenase-2 (COX-2)
- Does not inhibit cyclooxygenase-1 (COX-1)
- Exhibits anti-inflammatory properties
- Provides analgesic and antipyretic activities in animal models
- Has a long elimination half-life
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Medchemexpress LLC Lin28-let-7a antagonist 1 | 2024548-03-4 | 99.5% | 583.59 g/mol | C31H29N5O7 | 25 MG
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Lin28-let-7a antagonist 1 is a small-molecule inhibitor that disrupts Lin28 binding to pre-let-7 RNAs, promoting maturation of let-7 microRNAs. It shows an IC50 of 4.03 μM for the Lin28A-let-7a-1 interaction and is supplied in solid and DMSO solution formats for research use.
- Antagonizes Lin28-let-7 interaction, increasing mature let-7 levels.
- IC50 4.03 μM for Lin28A-let-7a-1 in biochemical assay.
- Available as solid packs and 10 mM solution in DMSO for convenience.
- High chemical purity, supporting reproducible experimental results.
- Soluble in DMSO at high concentration for in vitro use.
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![Medchemexpress LLC Acetamide, 2-[(8-ethyl-5H-1,2,4-triazino[5,6-b]indol-3-yl)thio]-N-(2-methylphenyl)- | 3070282-38-8 | 99.05% | 377.46 | 50 MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000386973-logo.png-250.jpg){kind=logo}
Medchemexpress LLC Acetamide, 2-[(8-ethyl-5H-1,2,4-triazino[5,6-b]indol-3-yl)thio]-N-(2-methylphenyl)- | 3070282-38-8 | 99.05% | 377.46 | 50 MG
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IGF2BP3-IN-1 (Compound I3IN-122) is an inhibitor of IGF2BP3, an RNA binding protein, with an IC50 of > 50 μM. It can be used for cancer research. This product is for research use only and is not sold to patients.
- Inhibitor of IGF2BP3 (a RNA binding protein)
- Can be used for cancer research
- Purity: 99.05%
- Available in various quantities
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Medchemexpress LLC UCB-35440 | 299460-62-1 | 99.4% | 576.09 | 1 MG
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UCB-35440 is an orally active histamine H1 receptor antagonist and 5-lipoxygenase inhibitor. It inhibits LTB4 formation in human whole blood and reduces polymorphonuclear cell infiltration in mouse models. It inhibits histamine-stimulated bronchoconstriction and reduces skin inflammation in guinea pigs, and can be used for research on asthma and skin inflammation.
- Orally active histamine H1 receptor antagonist and 5-lipoxygenase inhibitor.
- Inhibits LTB4 formation in human whole blood.
- Reduces polymorphonuclear cell infiltration in mouse models.
- Inhibits histamine-stimulated bronchoconstriction.
- Reduces skin inflammation in guinea pigs.
- Can be used for research on asthma and skin inflammation.
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Apexbio Technology LLC Vildagliptin (LAF-237) 274901-16-5 50mg
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Vildagliptin (LAF-237 CAS 274901-16-5) is an inhibitor of dipeptidyl peptidase-4 (DPP-4) a widely expressed antigenic enzyme with roles in signal transduction apoptosis and immunoregulation Vildagliptin inhibits DPP-4 enzymatic activity at an IC50 of approximately 2 3 nM preventing the degradation of glucagon-like peptide-1 (GLP-1) Through enhanced GLP-1 activity it promotes insulin secretion and reduces glucagon release Animal model studies including experiments in obese Zucker rats demonstrated improved glucose tolerance increased beta-cell proliferation decreased apoptosis and neuroprotective effects Vildagliptin is thus relevant for diabetes mellitus type 2 and related biomedical research
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Medchemexpress LLC LANA-DNA-IN-1 | 10 MG
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LANA-DNA-IN-1 | 10mg
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Ambeed 11bR 4 4Morpholinyl dinaphtho
(11bR)-4-(4-Morpholinyl)dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin, 636559-56-3, 97% 99%ee
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Medchemexpress LLC 20α-dihydroprogesterone | 145-14-2 | MFCD00009823 | 97.1% | 316.5 g/mol | C21H32O2 | 5 MG
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20α-dihydroprogesterone is an endogenous metabolite of progesterone supplied as a research-grade powder for laboratory use. It is used as an analytical reference and in biochemical or pharmacological studies. Chemical identity: C21H32O2, molecular weight 316.5 g/mol, CAS 145-14-2. Typical purity is about 97.1%, and the product is commonly supplied in 5 mg amounts. Store and handle per supplier documentation.
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