Pyrimidines And Derivatives
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Filtered Search Results
Aobchem AOBCHEM
5000945050 2-METHYL-1- 9-PHENANTHRENYL -1
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Ambeed AMBEED
5000891175 4-2-2-METHOXYETHOXYETHOX 250MG
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[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O | 25g | 794198065](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000489909.jpg-250.jpg)
eMolecules 1341-23-7 | 3-Carbamoyl-1-((2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)pyridin-1-ium | Combi-Blocks, Inc. | MFCD16621007 | 255.249 | C11H15N2O5 | 95.000 | NC(=O)c1ccc[n+](c1)[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O | 25g | 794198065
3-Carbamoyl-1-((2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)pyridin-1-ium | Combi-Blocks, Inc. | 1341-23-7 | MFCD16621007 | 255.249 | C11H15N2O5 | 95.000 | NC(=O)c1ccc[n+](c1)[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O | 25g | 794198065
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Apexbio Technology LLC DMBA-250mg
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DMBA (CAS No 57-97-6) is a chemical compound commonly studied in the field of biomedical research notably for its role as a polycyclic aromatic hydrocarbon Originating from both natural sources and anthropogenic activities it is crucial in exploring carcinogenic processes DMBA functions by inducing DNA adduct formation leading to mutagenesis which makes it a valuable tool in understanding cancer initiation and progression In vitro DMBA exhibits activity typically in the nanomolar to low micromolar range demonstrating its potency It is frequently used in various experimental models including cell lines and animal studies to investigate carcinogenesis and the efficacy of potential chemopreventive agents Additionally its role in drug screening for anti-cancer properties is significant Experimental concentrations typically depend on the specific research design ensuring precise and relevant findings
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eMolecules EMOLECULES INC
5000567311 2-METHYLPYRIMIDINE-5-BORONI 5G
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Apexbio Technology LLC 3-AZIDOPROPYLAMINE-250MG
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3-Azidopropylamine (CAS No 88192-19-2) is a compound of interest in biomedical research due to its potential applications in drug discovery and development Originating from synthetic organic chemistry this molecule is studied for its ability to interact with biological targets through azide-functional group-mediated reactions which can facilitate bioconjugation and labeling Its mechanism involves pathways where azide groups participate in click chemistry making it valuable in modifying biomolecules Common in vitro activities of 3-azidopropylamine occur in nanomolar to low micromolar ranges demonstrating its efficacy in cell assays It is often utilized in cell models and animal studies for drug screening purposes Experimental concentrations typically depend on the specific research design allowing flexibility in application for various biomedical investigations
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eMolecules 54198-89-9 | 5-Chloro-2-methylpyrimidine | Ambeed | MFCD10574686 | 128.560 | C5H5ClN2 | 95.000 | Cc1ncc(Cl)cn1 | 1g | 588342371
5-Chloro-2-methylpyrimidine | Ambeed | 54198-89-9 | MFCD10574686 | 128.560 | C5H5ClN2 | 95.000 | Cc1ncc(Cl)cn1 | 1g | 588342371
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Apexbio Technology LLC HALAZONE-250MG
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Halazone (CAS No 80-13-7) is a chemical compound studied in the context of antimicrobial research Originating from efforts to develop water purification methods Halazone functions by releasing active chlorinated species targeting pathogenic microorganisms by disrupting cellular metabolism and integrity Its mechanism of action involves oxidation and chlorination pathways proving effective in reducing microbial viability in various conditions In vitro activities are often observed in the nanomolar to low micromolar range indicating potent efficacy in controlled environments Typical applications for Halazone include studies using bacterial cultures and animal models to explore its potential as a disinfectant and therapeutic agent It is also utilized in drug screening to identify compounds with similar antimicrobial properties Experimental concentrations typically depend on the specific research design allowing for tailored investigation into its efficacy and safety profile
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Medchemexpress LLC Pyrimidine | 289-95-2 | MFCD00006059 | 100.0% | 80.09 g/mol | C4H4N2 | 1g
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Pyrimidine is a nitrogen-containing heterocyclic compound and endogenous metabolite Pyrimidine derivatives can be used in pancreatic cancer triple-negative breast cancer colon carcinoma and neuron research[1][2][3]
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000712121 GUVACINE ETHYL ESTER 50MG
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Medchemexpress LLC Ethyl 6-(4-aminophenyl)-1-(4-methoxyphenyl)-7-oxo-4,5-dihydropyrazolo[3,4-c]pyridine-3-carbox | 503615-07-4 | MFCD18251628 | 98.6% | C22H22N4O4 | 10 G
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This product is Ethyl 6-(4-aminophenyl)-1-(4-methoxyphenyl)-7-oxo-4,5-dihydropyrazolo[3,4-c]pyridine-3-carboxylate, a chemical compound that appears as a light green to green solid. It has been tested and complies with given specifications, showing a purity of 98.6% by LCMS. This product is for research use only and has not been fully validated for medical applications.
- Appears as a light green to green solid
- Purity of 98.6% confirmed by LCMS
- Tested and complies with specifications
- Store at 4°C, protected from light
- Store in solvent at -80°C for up to 6 months or -20°C for up to 1 month, protected from light
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Medchemexpress LLC 4-(4,5-diphenyl-1H-imidazol-2-yl)benzoic acid | 5496-35-5 | MFCD00999654 | 99.7% | 340.37 | C22H16N2O2 | 250 MG
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I-XW-053 is a small-molecule inhibitor of the HIV-1 capsid protein used in antiviral research; it disrupts the capsid N-terminal domain (NTD-NTD) interface and exhibits micromolar-range activity.
- Inhibits HIV-1 capsid protein by blocking the NTD-NTD interface.
- Shows micromolar antiviral activity (reported IC50 ≈ 164.2 μM).
- High purity suitable for research applications.
- Available in multiple pack sizes for flexible experimental needs.
- Solid form; soluble in DMSO for solution preparation.
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Medchemexpress LLC ANTILEISHMANIAL AGEN 250MG
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5000204649 ANTILEISHMANIAL AGEN 250MG
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Matrix Scientific 4-PYRIMIDINECARBOXYLIC ACID-1G
4-Pyrimidinecarboxylic acid, >95%; 1g,C5H4N2O2, MFCD00129737, mw 124.10, [31462-59-6]
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eMolecules 64987-85-5 | SMCC | Medchem Express | MFCD00009634 | 334.328 | C16H18N2O6 | 98.000 | O=C(ON1C(=O)CCC1=O)C1CCC(CN2C(=O)C=CC2=O)CC1 | 500mg | 746319431
SMCC | Medchem Express | 64987-85-5 | MFCD00009634 | 334.328 | C16H18N2O6 | 98.000 | O=C(ON1C(=O)CCC1=O)C1CCC(CN2C(=O)C=CC2=O)CC1 | 500mg | 746319431
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