Pyridines and derivatives
- (4)
- (1)
- (5)
- (5)
- (597)
- (22)
- (2,186)
- (22)
- (2)
- (5)
- (5)
- (309)
- (181)
- (1)
- (14)
- (51)
- (2)
- (303)
- (87)
- (245)
- (6)
- (4)
- (2)
- (2)
- (3)
- (1)
- (1)
- (1)
- (1)
- (5)
- (1)
- (12)
- (4)
- (8)
- (7)
- (12)
- (60)
- (875)
- (6)
- (56)
- (66)
- (58)
- (19)
- (357)
- (2)
- (4)
- (2)
- (1)
- (1)
- (5)
- (303)
- (1)
- (1,713)
- (2)
- (29)
- (7)
- (1)
- (92)
- (4)
- (15)
- (86)
- (128)
- (55)
- (60)
- (2)
- (1)
- (1)
- (2)
- (1)
- (1)
- (1)
- (1)
- (1)
- (2)
- (5)
- (2)
- (2)
- (1)
- (2)
- (1)
- (2)
- (3)
- (3)
- (1)
- (1)
- (1)
- (2)
- (1)
- (2)
- (9)
- (4)
- (1)
- (2)
- (4)
- (2)
- (1)
- (6)
- (17)
- (23)
- (1)
- (1)
- (63)
- (21)
- (1)
- (1)
- (29)
- (50)
- (7)
- (2)
- (1)
- (5)
- (6)
- (12)
- (1)
- (1)
- (1)
- (1)
- (18)
- (1)
- (14)
- (4)
- (1)
- (11)
- (5)
- (1)
- (10)
- (17)
- (2)
- (1)
- (2)
- (1)
- (1)
- (1)
- (1)
- (1)
- (9)
- (7)
- (1)
- (2)
- (1)
- (4)
- (6)
- (2)
- (1)
- (1)
- (1)
- (4)
- (4)
- (1)
- (1)
- (5)
- (15)
- (1)
- (1)
- (1)
- (1)
- (1)
- (1)
- (1)
- (1)
- (12)
- (1)
- (2)
- (1)
- (2)
- (4)
- (1)
- (1)
- (1)
- (2)
- (2)
- (1)
- (15)
- (18)
- (4)
- (2)
- (2)
- (5)
- (2)
- (3)
- (1)
- (1)
- (1)
- (1)
- (1)
- (1)
- (7)
- (5)
- (9)
- (1)
- (2)
- (1)
- (1)
- (1)
- (1)
- (2)
- (2)
- (16)
- (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)
- (1)
- (4)
- (6)
- (3)
- (3)
- (1)
- (4)
- (1)
- (1)
- (1)
- (3)
- (3)
- (1)
- (6)
- (5)
- (2)
- (1)
- (19)
- (9)
- (1)
- (2)
- (1)
- (1)
- (1)
- (22)
- (24)
- (2)
- (2)
- (1)
- (1)
- (2)
- (2)
- (22)
- (16)
- (6)
- (2)
- (1)
- (1)
- (3)
- (7)
- (1)
- (2)
- (3)
- (1)
- (1)
- (2)
- (1)
- (8)
- (17)
- (3)
- (1)
- (8)
- (1)
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- (1)
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- (1)
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- (3)
- (4)
- (2)
- (1)
- (1)
- (1)
- (6)
- (3)
- (3)
- (3)
- (3)
- (5)
- (1)
- (1)
- (1)
- (1)
- (1)
- (1)
- (6)
- (1)
- (1)
- (2)
- (5)
- (3)
- (1)
- (4)
- (12)
- (49)
- (1)
- (4)
- (2)
- (3)
- (1)
- (2)
- (1)
- (1)
- (7)
- (10)
- (22)
- (30)
- (1)
- (1)
- (1)
- (3)
- (2)
- (2)
- (4)
- (11)
- (5)
- (1)
- (1)
- (55)
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- (1)
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- (1)
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- (1)
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- (23)
- (1)
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- (1)
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- (1)
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- (1)
- (1)
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- (35)
- (3)
- (4)
- (4)
- (3)
- (1)
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- (1)
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- (1)
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- (1)
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- (1)
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- (8)
- (6)
- (2)
- (3)
- (2)
- (2)
- (1)
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- (1)
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- (2)
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- (2)
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- (1)
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- (1)
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- (1)
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- (33)
- (2)
- (75)
- (1)
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- (53)
- (1)
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- (1)
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- (1)
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- (1)
- (1)
- (106)
- (1)
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- (544)
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- (462)
- (42)
- (22)
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- (1)
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- (1)
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- (1)
- (11)
- (373)
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- (138)
- (1)
- (1,048)
- (4)
- (2)
- (1)
- (2)
- (3)
- (12)
- (924)
- (7)
- (35)
- (7)
- (2)
- (1)
- (501)
- (26)
- (1)
- (1)
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- (18)
- (1)
- (1)
- (1)
- (4)
- (4)
- (1)
- (2)
- (6)
- (4)
- (4)
- (1)
- (1)
- (4)
- (1)
- (3)
- (19)
- (2)
- (8)
- (72)
- (4)
- (1,561)
- (2)
- (4)
- (12)
- (9)
- (1)
- (14)
- (3)
- (9)
- (3)
- (2)
- (5)
- (4)
- (2)
- (1)
- (16)
- (3)
- (13)
- (11)
- (13)
- (10)
- (2)
- (2)
- (1)
- (2)
- (2)
- (408)
- (5)
- (6)
- (2)
- (7)
- (2)
- (3)
- (2)
- (237)
- (3)
- (2)
- (3)
- (18)
- (5)
- (2)
- (264)
- (3)
- (4)
- (4)
- (1)
- (2)
- (1)
- (4)
- (1)
- (2)
- (2)
- (2)
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- (2)
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- (3)
- (2)
- (2)
- (2)
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- (1)
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- (1)
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- (2)
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- (2)
- (2)
- (2)
- (2)
- (1)
- (1)
- (1)
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- (1)
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- (1)
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- (2)
- (2)
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- (1)
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- (2)
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- (3)
- (3)
- (2)
- (6)
- (1)
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Filtered Search Results
Medchemexpress LLC Asengeprast | 1001288-58-9 | MFCD28502026 | 99.3% | 351.35 | C20H17NO5 | 50 MG
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Small and/or specialty supplier based on Federal laws and SBA requirements.
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FT011 (asengeprast) is an anti-fibrotic small molecule and alkyne-containing click-chemistry reagent for research use. It reduces mRNA expression of collagen I and III, inhibits collagen synthesis, and can be conjugated via copper-catalyzed azide-alkyne cycloaddition for probe development and bioconjugation.
- Reduces collagen I and III mRNA expression and inhibits collagen synthesis.
- Contains an alkyne moiety enabling copper-catalyzed azide-alkyne cycloaddition for bioconjugation.
- High purity suitable for research applications.
- Available as a solid in multiple quantities and as a DMSO solution for convenience.
- Intended for research use only.
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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Selleck Chemical LLC MINA53 inhibitor-E1064-5MG
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MINA53 inhibitor (Compound 10 2-((3-Phenylpropyl)thio)-3 4-dihydro-4-oxopyrimidine-5-carboxylic Acid) is a first-in-class inhibitor of the ribosomal oxygenase MINA53 with an IC50 of 1 5 M in vitro
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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Medchemexpress LLC IL-2-IN-1 | 245747-10-8 | 99.9% | 418.29 | 5 MG
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Small and/or specialty supplier based on Federal laws and SBA requirements.
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IL-2-IN-1 is a potent IL-2 inhibitor with an IC50 value of 1978 nM. It exhibits antiproliferative activities. This product is for research use only.
- Targets IL-2
- Has an IC50 of 1978 nM
- Inhibits antiproliferative activities in human PBMC with an IC50 of 340 nM
- Inhibits antiproliferative activities in rat PBMC with an IC50 of 1266 nM
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Selleck Chemical LLC BIIB059-A2598-1MG
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BIIB059 is a humanized IgG1- antibody targeting to C-type lectin domain family 4 member C (CLEC4C) It can be used for cutaneous lupus erythematosus (CLE) study MW 146 34 KD
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![Medchemexpress LLC (2E)-2-[4-(1-benzimidazolyl)-3-methoxyphenyl]-3-nitro-2-propenoic acid. | 108883-90-5 | 98.7% | 285.25 g·mol⁻¹ | C14H11N3O4 | 1 G](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000283012.png-250.jpg)
Medchemexpress LLC (2E)-2-[4-(1-benzimidazolyl)-3-methoxyphenyl]-3-nitro-2-propenoic acid. | 108883-90-5 | 98.7% | 285.25 g·mol⁻¹ | C14H11N3O4 | 1 G
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CB096 is a small-molecule research compound that inhibits repeat-associated non-AUG (RAN) translation by binding the 5′CGG/3′GGC internal loop of pathogenic r(G4C2)exp RNA, reducing production of toxic dipeptide repeats and mitigating RNA-mediated cellular dysfunctions. Intended for laboratory research use.
- Inhibits RAN translation with reported IC50 of 20 μM in HEK293T cells.
- Binds the 5′CGG/3′GGC internal loop of r(G4C2)exp RNA.
- Reduces generation of toxic dipeptide repeats produced by RAN translation.
- High purity (98.7%) suitable for research applications.
- Available in multiple pack sizes including 1 G.
- Molecular formula C14H11N3O4 and molecular weight 285.25 g·mol⁻¹.
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Medchemexpress LLC Pivalyloxymethyl butyrate | 122110-53-6 | >=95.0% | 100 MG
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Pivalyloxymethyl butyrate (AN-9) is a liquid histone deacetylase (HDAC) inhibitor used in research applications such as epigenetic modulation and preclinical oncology studies. It is typically supplied for laboratory use and may be prepared as solutions in DMSO for in vitro assays.
- Small-molecule HDAC inhibitor that modulates histone acetylation and gene expression.
- Liquid form suitable for solution preparation and in vitro assays.
- Typical purity approximately 95% by assay.
- Molecular weight 202.25 g/mol and formula C10H18O4.
- Commonly used in epigenetic research and preclinical cancer studies.
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![Alkali Scientific 5 Azacytosine [4 Amino 1,3.5 triazine 2 one], 1 G](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000660756.jpg-250.jpg)
Alkali Scientific 5 Azacytosine [4 Amino 1,3.5 triazine 2 one], 1 G
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5 Azacytosine (1g) is a cytidine analog and research compound used in DNA methylation studies. It is an essential tool for researchers studying gene expression, epigenetic modifications, and DNA methylation patterns. This compound is particularly useful for exploring mechanisms in cancer research, developmental biology, and genetics. As a nucleoside analog, Azacytosine is incorporated into DNA during replication, inhibiting DNA methyltransferase and preventing methylation at specific sites. It plays a significant role in understanding genetic regulation and the role of epigenetics in diseases. This 1g formulation is ideal for laboratory experiments focused on nucleic acid research.
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Selleck Chemical LLC Deutenzalutamide-E1502-5MG
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Deutenzalutamide (HC-1119 MDV3100) is an androgen receptor (AR) antagonist with an IC50 of 36 nM in LNCaP prostate cells It can be used in a treatment of advanced prostate cancer
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Medchemexpress LLC Rhodamine 6G | 989-38-8 | MFCD00012665 | 98.02% | 50 MG
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Rhodamine 6G is a membrane-permeable cationic fluorescent probe used to specifically recognize mitochondrial membrane potentials. It attaches to mitochondria, producing bright fluorescence, and exhibits low toxicity to cells at certain concentrations. This makes it a common choice for detecting mitochondria in animal cells, plant cells, and microorganisms.
- Recognizes mitochondrial membrane potentials
- Produces bright fluorescence
- Low toxicity to cells
- Used for detecting mitochondria
- Suitable for cell staining in suspension and adherent cells
- May inhibit tumor growth and reduce metastases
- Labels leukocytes in the circulatory system
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Medchemexpress LLC Napropamide | 15299-99-7 | 1 ML
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Napropamide is an amide herbicide that controls weeds in fruits, vegetables, tobacco, and ornamental plants by inhibiting DNA synthesis and cell division. It exhibits moderate to high persistence with a half-life of 24 to 131 days and is susceptible to photodegradation. Studies indicate low acute toxicity, no genotoxicity, carcinogenicity, neurotoxicity, or adverse effects on fertility, reproduction, embryotoxicity, or teratogenicity.
- Amide herbicide
- Controls weeds in fruits, vegetables, tobacco, and ornamental plants
- Inhibits DNA synthesis and cell division
- Moderate to high persistence in field
- Low acute toxicity
- No genotoxicity, carcinogenicity, or neurotoxicity
- No adverse effects on fertility, reproduction, embryotoxicity, or teratogenicity
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![Medchemexpress LLC 3,5-bis[(4-methylphenyl)methylene]-4-piperidone hydrochloride | 157654-67-6 | MFCD09753281 | 98.9% | 339.86 g/mol | C21H22ClNO | 50 MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000214536.png-250.jpg)
Medchemexpress LLC 3,5-bis[(4-methylphenyl)methylene]-4-piperidone hydrochloride | 157654-67-6 | MFCD09753281 | 98.9% | 339.86 g/mol | C21H22ClNO | 50 MG
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NSC632839 is a small-molecule, nonselective isopeptidase inhibitor used in biochemical and cell-based research to probe deubiquitinating enzymes and SUMO proteases. It shows mid-micromolar activity against USP2 and USP7 and greater potency against SENP2, and is supplied as a high-purity solid suitable for mechanistic studies.
- Nonselective isopeptidase inhibitor active against USP2, USP7, and SENP2 (EC50s: 45±4 μM, 37±1 μM, 9.8±1.8 μM).
- High purity suitable for research (≈98.9%).
- Solid form, light yellow to yellow appearance for easy handling.
- Soluble in DMSO (~4 mg/mL) with warming or sonication if required.
- Stable when stored sealed away from moisture; in solvent: -80°C up to 6 months, -20°C up to 1 month.
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Selleck Chemical LLC Enasidenib
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Enasidenib (AG-221) is a first-in-class oral potent reversible selective inhibitor of the IDH2 mutant enzyme
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Medchemexpress LLC Trifluralin (standard) | 1582-09-8 | Analytical Standard | 500 MG
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Trifluralin (standard) | 1582-09-8 | Analytical Standard | 500 MG
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Cayman Chemical 4hydroperoxy 2Nonenal
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The hydroperoxide precursor of 4-HNE
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Selleck Chemical LLC FIN56
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FIN56 is a specific inducer of ferroptosis
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