Pyridines and derivatives
- (4)
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- (60)
- (867)
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- (19)
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- (1)
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- (1)
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- (54)
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- (1)
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- (1)
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- (1)
- (1)
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- (1)
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- (49)
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- (1)
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- (1)
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- (1)
- (1)
- (1)
- (1)
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- (1)
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- (1)
- (1)
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- (1)
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- (7)
- (5)
- (1)
- (1)
- (3)
- (5)
- (10)
- (2)
- (1)
- (6)
- (6)
- (7)
- (12)
- (1)
- (1)
- (39)
- (1)
- (12)
- (11)
- (4)
- (2)
- (2)
- (15)
- (15)
- (1)
- (1)
- (1)
- (2)
- (9)
- (3)
- (2)
- (1)
- (1)
- (3)
- (6)
- (3)
- (3)
- (1)
- (3)
- (1)
- (1)
- (1)
- (3)
- (3)
- (1)
- (6)
- (5)
- (2)
- (1)
- (19)
- (9)
- (1)
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- (1)
- (1)
- (1)
- (22)
- (22)
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Filtered Search Results
Medchemexpress LLC Cyproconazole | 94361-06-5 | 98.7% | C15H18ClN3O | 50 MG
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Cyproconazole is a triazole fungicide that effectively protects crops, fruits, and vegetables from a wide range of fungal pathogens. It has been observed to induce hepatocellular adenomas and carcinomas in CD-1 mice. Furthermore, this compound demonstrates low toxicity to zebrafish embryos and impacts their locomotor activity.
- Triazole fungicide
- Protects against fungal pathogens
- Low toxicity to zebrafish embryos
- Affects zebrafish locomotor activity
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Medchemexpress LLC Tellimagrandin II (Eugeniin) | 81571-72-4 | 98.8% | 938.66 | 5 MG
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Tellimagrandin II (Eugeniin) is the first intermediate of the ellagitannin series, derived from 4C1-glucose, and possesses oral activity. It has shown potential for research in antibacterial, anti-inflammatory, and neurodegenerative diseases due to its diverse biological effects.
- Inhibits resistance of Staphylococcus aureus by disrupting cell wall integrity.
- Exhibits anti-inflammatory effects by inhibiting NO production and COX-2 levels in macrophages.
- Improves memory impairment by inhibiting acetylcholinesterase (AChE) activity.
- Demonstrates improved learning and memory functions in scopolamine-induced amnesiac mice.
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Medchemexpress LLC Ythdf2-in-1 | 99.4% | 358.35 | 100 MG
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YTHDF2-IN-1 (Compound CK-75) is an inhibitor for YT521-B homology domain family 2 YTHDF2 (Kd=26.2 μM), which blocks the interaction between YTHDF2 and m6A RNA.
- It inhibits the colony formation of JAR cells.
- It exhibits antiproliferative activity in various cancer cells (IC50 in micromolar levels).
- It arrests the cell cycle at G0/G1 phase.
- It induces apoptosis in K562.
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Medchemexpress LLC 2-FLUOROFLUOREN-9-ON 5G | 5G
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2-FLUOROFLUOREN-9-ON 5G | 5G
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Medchemexpress LLC Trisbenzyltriazolylm 500mg | 510758-28-8 | 530.6 g/mol | C30H30N10 | 500 MG
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Tris(benzyltriazolylmethyl)amine (TBTA) is a tertiary amine ligand containing three 1,2,3-triazole groups. It complexes with and stabilizes copper(I) to accelerate azide-alkyne cycloadditions (click chemistry), and is supplied as a high-purity crystalline solid for use as a biochemical tool in protein and enzyme tagging.
- Complexes with and stabilizes copper(I) to support Cu(I)-catalyzed reactions.
- Accelerates azide-alkyne cycloadditions (click chemistry).
- Supplied as a crystalline solid.
- High purity (≥98%).
- Molecular formula C30H30N10; molecular weight 530.6 g/mol.
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Medchemexpress LLC 2-Aminotetralin | 2048491-06-9 | 98.06% | 269.36 | 50 MG
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FPT is a 2-Aminotetralin that acts as an efficacious partial agonist at 5-HT1A receptors and a full agonist at 5-HT1B and 5-HT1D receptors. It has demonstrated antiepileptic effects in Fmr1 knockout mice and exhibits anxiolytic-like and prosocial effects in various mouse models. This compound is used in research related to neurological conditions.
- Efficacious partial agonist at 5-HT1A receptors
- Full agonist at 5-HT1B and 5-HT1D receptors
- Weak agonist at 5-HT7R
- Antiepileptic effects in Fmr1 knockout mice
- Anxiolytic-like and prosocial effects in mouse models
- Purity of 98.06%
- Available in various sizes and forms
- Storage at 4°C, protected from light
- Shipping at room temperature
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Medchemexpress LLC JNK-IN-13 | 345986-38-1 | 97.6% | C13H7ClN4S | 25 MG
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JNK-IN-13 is a potent and selective JNK inhibitor that exhibits IC50s of 290 nM for JNK3 and 500 nM for JNK2. This product is intended for research use only and appears as a solid, typically white to yellow in color.
- Potent and selective JNK inhibitor
- IC50s of 290 nM for JNK3 and 500 nM for JNK2
- For research use only
- Appears as a solid
- White to yellow color
- Store at 4°C under nitrogen
- If in solvent, store at -80°C for 6 months or -20°C for 1 month under nitrogen
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Medchemexpress LLC Phospho-TAK1 (Ser439) Antibody (YA144) | 10 UL
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This Phospho-TAK1 (Ser439) Antibody (YA144) is a rabbit-derived, non-conjugated IgG monoclonal antibody specifically targeting Phospho-TAK1 (Ser439). It is affinity purified with a molecular weight of 67-78 kDa. Intended for research use only, it is stored at -20°C for up to one year, with precautions against repeated freeze/thaw cycles.
- Rabbit-derived IgG monoclonal antibody
- Non-conjugated
- Specifically targets Phospho-TAK1 (Ser439)
- Affinity purified
- Molecular weight of 67-78 kDa
- For research use only
- Stable for 1 year when stored at -20°C
- Avoid repeated freeze/thaw cycles
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Medchemexpress LLC Antide | 112568-12-4 | 99.53% | 1591.29 | 25 MG
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Antide (D-21074) is a potent LHRH antagonist. It can also be used for the research of prostatic cancer.
- Potent LHRH antagonist
- Used for prostatic cancer research
- Induces long-term chemical castration in adult male rats and cynomolgus monkeys
- Sealed storage, away from moisture and light
- For powder: -80°C for 2 years; -20°C for 1 year
- In solvent: -80°C for 6 months; -20°C for 1 month
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Medchemexpress LLC Belapectin 1mg | 1980787-47-0 | 1 MG
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Belapectin is a carbohydrate-based galectin-3 inhibitor for preclinical research. It binds Gal-3 with a reported Ki of 2.8 μM, and is supplied as a solid with high purity.
- Carbohydrate-based galectin-3 inhibitor
- Reported binding affinity Ki = 2.8 μM
- High purity (98.9%) suitable for research applications
- Solid formulation with recommended cold storage
- Available in small quantities for laboratory studies
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BIOHIPPO SREBP1-TAR-BSD LV
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SREBP1-TAR-BSD is a transcription factor reporter lentiviral vector designed to monitor SREBP1 lipid metabolism and cholesterol regulatory pathway in living cells The construct carries a fluorescent reporter gene under the control of pathway responsive elements and includes a blasticidin selection marker to generate stable cell pools The lentivirus is provided as a ready to use VSV G pseudotyped preparation for efficient gene delivery and stable genomic integration Each vial provides a nominal titer of 5x10E6 transducing units TU Typical applications include pathway activation studies assay development compound screening and mechanism of action research The system is suitable for human and mouse cells and can be read using standard fluorescence microscopy flow cytometry or luciferase assays depending on the reporter gene This product is intended for research use only and is not for diagnostic or therapeutic procedures
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Medchemexpress LLC Lecirelin | 61012-19-9 | 99.6% | 1209.40 | 50 MG
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Lecirelin is a synthetic gonadotropin-releasing hormone (GnRH) analogue that acts as a GnRH agonist. It is widely used for the research of bovine ovarian follicular cysts. In studies, Lecirelin (2.07 μM) significantly increases the tension and frequency of contractions in preovulatory follicles (PF), small follicular cysts (FC-S), and large follicular cysts (FC-L). It also causes strips from preovulatory follicles to contract significantly more than strips from cysts.
- Synthetic gonadotropin-releasing hormone (GnRH) analogue
- Acts as a GnRH agonist
- Used in research of bovine ovarian follicular cysts
- Increases tension and frequency of contractions in preovulatory follicles
- Increases tension and frequency of contractions in small follicular cysts
- Increases tension and frequency of contractions in large follicular cysts
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![Medchemexpress LLC 2,4-Pyrimidinediamine, N4-(cyclopropylmethyl)-6-[(3R)-3-(methylamino)-1-pyrrolidinyl]-, hydrochloride | 2096455-90-0 | 98.0% | 371.74 | 50 MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000402746-logo.png-250.jpg){kind=logo}
Medchemexpress LLC 2,4-Pyrimidinediamine, N4-(cyclopropylmethyl)-6-[(3R)-3-(methylamino)-1-pyrrolidinyl]-, hydrochloride | 2096455-90-0 | 98.0% | 371.74 | 50 MG
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Adriforant hydrochloride (PF-3893787 hydrochloride) is a novel histamine H4 receptor antagonist. It exhibits a binding affinity (Ki) of 2.4 nM and a functional (Ki) antagonist at 1.56 nM, making it suitable for research use.
- Novel histamine H4 receptor antagonist.
- Binding affinity (Ki) of 2.4 nM for H4R.
- Functional (Ki) of 1.56 nM for H4R.
- Fast on/fast off characteristic on rhH4R.
- In vitro IC50 on human native isolated eosinophils assessing actin polymerisation is 1.16 nM.
- Completely blocks imetit-induced shape change in whole blood GAFS assay at 30 nM total blood concentration.
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Medchemexpress LLC 3-Aminophenylacetic acid | 14338-36-4 | 151.16 | 5 G
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3-Aminophenylacetic acid is an organic compound with a molecular weight of 151.16 and the chemical formula C8H9NO2. It appears as a solid, ranging from light yellow to yellow in color, and has a confirmed purity of 98.58%. This compound is intended for research use only.
- Organic compound.
- High purity of 98.58%.
- Molecular weight of 151.16.
- Available in solid form.
- Detailed documentation, including Data Sheet, SDS, COA, HNMR, RP-HPLC, and Handling Instructions, is provided.
- Specific storage recommendations are given for both powder and in-solvent forms to maintain stability.
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Medchemexpress LLC Protein Kinase C (19-31) | 121545-65-1 | 99.7% | 1543.82 | 5 MG
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Protein Kinase C (19-31) is a peptide inhibitor of protein kinase C (PKC). It is derived from the pseudo-substrate regulatory domain of PKCa (residues 19-31) and is utilized as a protein kinase C substrate peptide for testing PKC activity.
- Peptide inhibitor of protein kinase C
- Derived from PKCa (residues 19-31)
- Used as a substrate peptide for testing protein kinase C activity
- Purity of 99.7%
- For research use only
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