About 20 results found for searched term "Imidazole" (0.055 seconds)
| Cat.No. | Name | Target |
|---|---|---|
| M2216 | Dacarbazine | DNA Alkylator/Crosslinker |
| Imidazole Carboxamide | ||
| Dacarbazine (DTIC-Dome; DTIC) is an alkylating agent that acts as a purine nucleotide precursor analog to inhibit purine nucleotide synthesis, thereby inhibiting DNA/RNA Synthesis, and can be used in studies related to melanoma and Hodgkin's lymphoma. | ||
| M2640 | Dimetridazole | Parasite |
| 1,2-Dimethyl-5-nitroimidazole | ||
| Dimethyl azole is a nitroimidazole compound that is infected by antigenic animals. | ||
| M3315 | Thiabendazole | Mitochondrial Related |
| 2-(4-Thiazolyl)benzimidazole | ||
| Thiabendazole inhibites the mitochondrial helminth-specific enzyme, fumarate reductase, with anthelminthic property. | ||
| M5901 | Procodazole | Antibiotic |
| Propazol; 2-Benzimidazolepropionic acid | ||
| Procodazole is a non-specific active immunoprotective agent against viral and bacterial infections, used as a potentiator. | ||
| M6299 | Imidazole | Solvents & Excipients |
| 1,3-Diaza-2,4-cyclopentadiene; Glyoxaline | ||
| Imidazole is a planar 5-membered ring. Imidazole is a highly polar compound. | ||
| M8535 | Bis-Imidazole phenol IDH1 inhibitor | Isocitrate Dehydrogenase (IDH) |
| bis-Imidazole phenol is a potent and cell permeable inhibitor of isocitrate dehydrogenase 1 (IDH1) mutant R132H that inhibits D-2-hydroxyglutaric acid (2HG) production in cells. | ||
| M8823 | TBBz | Casein Kinase |
| 4,5,6,7-Tetrabromo-1H-benzimidazole | ||
| TBBz is a selective, cell-permeable, ATP-competitive inhibitor of casein kinase 2 (CK2). | ||
| M9777 | 4-Nitroimidazole | Others |
| 4-nitro-1H-imidazole | ||
| 4-Nitroimidazole is an intermediate during the synthesis of 1-methyl-2,4,5-trinitro imidazole. | ||
| M10080 | Saccharin 1-methylimidazole | DNA/RNA Synthesis |
| SMI | ||
| Saccharin 1-methylimidazole (also known as SMI) is an activator for DNA and RNA synthesis. | ||
| M14341 | Imidazoleacetic acid hydrochloride | Metabolite/Endogenous Metabolite |
| Imidazolyl-4-acetic acid hydrochloride | ||
| 2-(1H-Imidazol-5-yl)acetic acid hydrochloride is an endogenous metabolite. | ||
| M14352 | 5-Amino-3H-imidazole-4-Carboxamide | Metabolite/Endogenous Metabolite |
| 5-Aminoimidazole-4-carboxamide; AICA | ||
| 5-Amino-3H-imidazole-4-Carboxamide (AICA) is an important precursor for the synthesis of purines in general and of the nucleobases adenine and guanine in particular. | ||
| M19946 | Azomycin | Antibiotic |
| 2-Nitroimidazole | ||
| Azomycin is an antimicrobial antibiotic produced by a strain of Nocardia mesenterica. | ||
| M20493 | 2-Chloro-1-(4-fluorobenzyl)benzimidazole | Others |
| 2-Chloro-1-(4-fluorobenzyl)benzimidazole is an aldose reductase (ALR2) inhibitor which is used for preparation of disubstituted benzimidazole derivative. | ||
| M20781 | Bendazol | NO Synthase |
| 2-Benzylbenzimidazole, Dibazol, Dibazole, Bendazole, Tromasedan | ||
| Bendazol (2-Benzylbenzimidazole, Dibazol, Dibazole, Bendazole, Tromasedan) is a hypotensive drug that enhances NO synthase activity in renal glomeruli and collecting tubules. Bendazol inhibits the progression of form-deprivation myopia (FDM) and suppresses the upregulation of HIF-1α. | ||
| M28861 | Dacarbazine hydrochloride | Antibiotic |
| Imidazole Carboxamide hydrochloride | ||
| Dacarbazine hydrochloride is a cell cycle nonspecific antineoplastic alkylating agent. Dacarbazine hydrochloride inhibits T and B lymphoblastic response, with IC50 values of 50 and 10 μg/mL, respectively. Dacarbazine hydrochloride can be used for the research of metastatic malignant melanoma. | ||
| M30411 | Dacarbazine citrate | Apoptosis |
| Imidazole Carboxamide citrate | ||
| Dacarbazine citrate is a cell cycle nonspecific antineoplastic alkylating agent. Dacarbazine citrate inhibits T and B lymphoblastic response, with IC50 values of 50 and 10 μg/mL, respectively. Dacarbazine Citrate can be used for the research of apoptosis and various cancers such as metastatic malignant melanoma. | ||
| M31193 | 5,6-Dichlorobenzimidazole riboside | CDK |
| 5,6-Dichlorobenzimidazole riboside is a nucleoside analog that inhibits several carboxyl-terminal domain (CTD) kinases including casein kinase II and CDKs. 5,6-Dichlorobenzimidazole riboside trigger p53-dependent apoptosis of human colon adenocarcinoma cells without inducing genotoxic stress to healthy cells. | ||
| M38871 | 1H-Benzimidazole-6-carboxylic acid | Others |
| 1H-Benzimidazole-6-carboxylic acid is a biochemical reagent that can be used as a biological material or organic compound for life science related research. | ||
| M39602 | 1-Benzylimidazole | Others |
| 1-Benzyl-1H-imidazole is a biochemical reagent that can be used as a biological material or organic compound for life science related research. | ||
| M43867 | 1-Acetylimidazole | Others |
| 1-Acetylimidazole is an acetylation reagent that can be used to close the residual α-amino group remaining after coupling and to synthesize cyclic imidazole derivatives. | ||
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