BOC Sciences provides a wide range of research chemicals and biochemicals including inhibitors, building blocks, GMP Products, impurities and metabolites, APIs for Veterinary, Natural Compounds, ADCs, Stem Cell Molecule and chiral compounds.
| Product | Description | |
|---|---|---|
| 6-Chloro-3-indolyl 2-acetamido-2-deoxy-b-D-galactopyranoside | 6-Chloro-3-indolyl 2-acetamido-2-deoxy-b-D-galactopyranoside, a potent biomedicine compound, serves as a crucial tool in scientific research. Its utility lies in precisely detecting and localizing targeted enzymes, making it indispensable in biomedicine exploration. Researchers harness its potential to unravel the intricacies of drug resistance, microbial infections, and various diseases, which expedites the progress of drug discovery and development. Synonyms: 6-Chloro-3-indolyl-N-acetyl-b-D-galactosaminide; Salmon-b-D-GalNAc; 6-Chloro-3-(2-acetamido-2-deoxy-b-D-galactopyranosyloxy)indole; 6-Chloro-1H-indol-3-yl 2-(acetylamino)-2-deoxy-β-D-galactopyranoside; N-((2S,3R,4R,5R,6R)-2-((6-Chloro-1H-indol-3-yl)oxy)-4,5-dihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-3-yl)acetamide. CAS No. 501432-61-7. Molecular formula: C16H19ClN2O6. Mole weight: 370.78. |  |
| 6-Chloro-3-indolyl 2-acetamido-2-deoxy-b-D-glucopyranoside | 6-Chloro-3-indolyl 2-acetamido-2-deoxy-b-D-glucopyranoside is a highly potent and invaluable instrument within the realm of biomedicine, exhibiting its prominence in the context of cellular analysis. With its proficient utility in cell staining, it showcasing a profound ability to monitor and gauge the functionality of β-glucosidases. Additionally, this remarkable compound's inherent capabilities render it conducive to the comprehensive investigation of various afflictions, encompassing lysosomal storage disorders, cancer is and neurological maladies. Synonyms: 6-Chloro-3-indolyl N-acetyl-b-D-glucosaminide; Salmon-b-D-GlcNAc; 6-Chloro-3-(2-acetamido-2-deoxy-b-D-glucopyranosyloxy)indole; 6-Chloro-1H-indol-3-yl 2-(acetylamino)-2-deoxy-β-D-glucopyranoside. CAS No. 156117-44-1. Molecular formula: C16H19ClN2O6. Mole weight: 370.78. | |
| 6-Chloro-3-indolyl a-D-galactopyranoside | 6-Chloro-3-indolyl α-D-galactopyranoside is a biochemical compound used in the compound industry. It acts as a substrate for the detection of β-galactosidase enzyme activity. This enzymatic reaction is widely utilized in diagnostics and research, providing valuable information about lac gene expression and cellular processes. Synonyms: 6-Chloro-1H-indol-3-yl α-D-galactopyranoside; Salmon alpha-Gal; (2R,3R,4S,5R,6R)-2-((6-Chloro-1H-indol-3-yl)oxy)-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-triol; 6-Chloro-3-indoxyl alpha-D-galactopyranoside. CAS No. 198402-61-8. Molecular formula: C14H16ClNO6. Mole weight: 329.73. | |
| 6-Chloro-3-indolyl a-D-glucopyranoside | 6-Chloro-3-indolyl α-D-glucopyranoside is a biochemical reagent used in biomedicine. It is commonly employed as a substrate for the detection of glucosidase enzymes, aiding the study of carbohydrate metabolism. This compound plays a crucial role in the development of therapeutic strategies for diseases related to carbohydrate metabolism disorders such as diabetes mellitus. Synonyms: Salmon a-glucoside; 6-Chloro-3-(a-D-glucopyranosyloxy)indole; 6-Chloro-1H-indol-3-yl α-D-glucopyranoside; 6-Chloro-3-indoxyl-alpha-D-glucopyranoside; (2R,3R,4S,5S,6R)-2-(6-chloro-1H-indol-3-yloxy)-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-triol. CAS No. 467214-46-6. Molecular formula: C14H16ClNO6. Mole weight: 329.73. | |
| 6-Chloro-3-indolyl a-D-mannopyranoside | 6-Chloro-3-indolyl a-D-mannopyranoside is a compound widely used in biomedicine for the detection and quantification of β-D-galactosidase activity. It acts as a chromogenic substrate, producing a blue product when cleaved by this enzyme. This product can be utilized in various research fields, including the study of diseases and drug development. Synonyms: Rose a-mannoside; 6-Chloro-3-(a-D-mannopyranosyloxy)indole; 6-Chloro-3-indoxyl-alpha-D-mannopyranoside; 6-Chloro-1H-indol-3-yl α-D-mannopyranoside; (2R,3S,4S,5S,6R)-2-(6-chloro-1H-indol-3-yloxy)-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-triol. CAS No. 425427-88-9. Molecular formula: C14H16ClNO6. Mole weight: 329.73. | |
| 6-Chloro-3-indolyl b-D-cellobioside | 6-Chloro-3-indolyl β-D-cellobioside, a remarkable substrate extensively utilized in the field of biomedicine, serves as a potent tool for detecting and scrutinizing the activity of β-glucosidase enzymes. Manifesting as a chromogenic substrate of utmost significance, it has found widespread usage in the investigation of inhibitory and inductive effects on β-glucosidases within diverse maladies and pharmaceutical advancements. Synonyms: Salmon-cellobioside; 6-Chloro-1H-indol-3-yl 4-O-β-D-glucopyranosyl-β-D-glucopyranoside; β-D-Glucopyranoside, 6-chloro-1H-indol-3-yl 4-O-β-D-glucopyranosyl-; 6-Chloro-1H-indol-3-yl β-D-cellobioside. CAS No. 425427-87-8. Molecular formula: C20H26ClNO11. Mole weight: 491.87. | |
| 6-Chloro-3-indolyl b-D-galactopyranoside | 6-Chloro-3-indolyl b-D-galactopyranoside is a colorless substrate used to detect β-galactosidase activity, which is an extensively studied enzyme in molecular biology. This compound can be hydrolyzed by β-galactosidase to form an insoluble blue precipitate, commonly used in reporter assays to monitor gene expression or analyze protein interactions. Synonyms: Salmon Gal; 6-Chloro-3-(b-D-galactopyranosyloxy)indole; Rose Gal; Red-Gal; 6-Chloro-1H-indol-3-yl β-D-galactopyranoside; (2S,3R,4S,5R,6R)-2-((6-Chloro-1H-indol-3-yl)oxy)-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-triol; 6-Chloro-3-indoxyl-beta-D-galactopyranoside. CAS No. 138182-21-5. Molecular formula: C14H16ClNO6. Mole weight: 329.73. | |
| 6-Chloro-3-indolyl b-D-glucopyranoside | 6-Chloro-3-indolyl β-D-glucopyranoside is a compound used for studying the activity of β-glucosidase enzymes in various biological samples. It is a chromogenic substrate that produces a blue color upon enzymatic cleavage by β-glucosidase. This compound is also utilized as a chemical tool in drug discovery and pharmaceutical research related to glycobiology and carbohydrates. Synonyms: Rose glucoside; Salmon-glc; 6-Chloro-1H-indol-3-yl β-D-glucopyranoside; (2S,3R,4S,5S,6R)-2-((6-Chloro-1H-indol-3-yl)oxy)-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-triol. CAS No. 159954-28-6. Molecular formula: C14H16ClNO6. Mole weight: 329.73. | |
| 6-Chloro-3-indolyl b-D-glucuronide sodium salt | 6-Chloro-3-indolyl b-D-glucuronide sodium salt, known for its significant contribution in the field of biomedical research, serves as an invaluable asset. Primarily utilized as a substrate for the purpose of β-glucuronidase detection and localization, this compound serves as a catalyst in the identification and analysis of drugs metabolized via glucuronidation. It assumes a pivotal role in the comprehensive examination of drug metabolism, intricate drug-drug interactions, and the pathogenesis of multifarious diseases. Synonyms: Rose glucuronide Na; β-D-Glucopyranosiduronic acid, 6-chloro-1H-indol-3-yl, sodium salt (1:1); β-D-Glucopyranosiduronic acid, 6-chloro-1H-indol-3-yl, monosodium salt; 6-Chloro-1H-indol-3-yl β-D-glucopyranosiduronic acid sodium salt; 6-Chloro-3-indolyl-β-D-glucuronide sodium salt. CAS No. 216971-56-1. Molecular formula: C14H13ClNNaO7. Mole weight: 365.70. | |
| 6-Chloro-3-indolyl-β-D-Glucuronide cyclohexylammonium salt | 6-Chloro-3-indolyl-β-D-Glucuronide cyclohexylammonium salt is the chromogenic substrate of β-glucuronidase used for histochemical analysis of β-glucuronidase activity. Synonyms: β-D-Glucopyranosiduronic acid, 6-chloro-1H-indol-3-yl, compd. with cyclohexanamine (1:1); Rose-β-D-GlcU CHA; Salmon-β-D-GlcU cyclohexylammonium salt; Salmon glca cyclohexylammonium salt; 6-Chloro-3-indolyl-β-D-glucuronic acid cyclohexylammonium salt; Rose glucuronide CHA. Grade: ≥95%. CAS No. 138182-20-4. Molecular formula: C14H14ClNO7.C6H13N. Mole weight: 442.89. | |
| 6-Chloro 3-Methyl Uracil | 6-Chloro 3-Methyl Uracil is an impurity of Sacubitril. Sacubitril is a prodrug neprilysin inhibitor used in combination with valsartan to reduce the risk of cardiovascular events in patients with chronic heart failure (NYHA Class II-IV) and reduced ejection fraction. Synonyms: 6-Chloro-3-methyluracil; 6-Chloro-3-methyl-2,4(1H,3H)-pyrimidinedione; 3-Methyl-6-chlorouracil; 6-Chloro-3-methylpyrimidine-2,4(1H,3H)-dione; 6-Chloro-3-methylpyrimidine-2,4-dione; 6-Chloro-2-hydroxy-3-methylpyrimidin-4(3H)-one. CAS No. 4318-56-3. Molecular formula: C5H5ClN2O2. Mole weight: 160.56. | |
| 6-Chloro-4-methylumbelliferyl 2-Acetamido-2-deoxy-β-D-glucopyranoside | 6-Chloro-4-methylumbelliferyl-2-acetamido-2-deoxy-β-D-glucopyranoside is a fluorogenic glycoside suitable for the ß-glucosidase assay. This assay monitors the hydrolysis of glycosidic bond by ß-glucosidase and its enzymatic activity has clinic applications for investigating Gaucher's disease. In addition, novel fluorogenic substrates may find utility in high-throughput and sensitive detection applications such as metagenomic screening. CAS No. 1867162-08-0. Molecular formula: C18H20ClNO8. Mole weight: 413.81. | |
| 6-Chloro-4-methylumbelliferyl α-L-Fucopyranoside | 6-Chloro-4-methylumbelliferyl-α-L-fucopyranoside is a fluorogenic glycoside suitable for the ß-glucosidase assay. This assay monitors the hydrolysis of glycosidic bond by ß-glucosidase and its enzymatic activity has clinic applications for investigating Gaucher's disease. In addition, novel fluorogenic substrates may find utility in high-throughput and sensitive detection applications such as metagenomic screening. Synonyms: 6-Chloro-7-[(6-deoxy-α-L-galactopyranosyl)oxy]-4-methyl-2H-1-benzopyran-2-one. CAS No. 1867162-11-5. Molecular formula: C16H17ClO7. Mole weight: 356.75. | |
| 6-Chloro-4-methylumbelliferyl b-D glucuronide | 6-Chloro-4-methylumbelliferyl b-D glucuronide is a fluorogenic substrate for the β-glucosidase assay. Synonyms: CMUG; 6-Chloro-4-methylumbelliferyl β-D-glucopyranosiduronic Acid; 6-Chloro-4-methyl-2-oxo-2H-1-benzopyran-7-yl beta-D-glucopyranosiduronic acid; 2H-1-Benzopyran-2-one, 6-chloro-7-(β-D-glucopyranuronosyloxy)-4-methyl-. CAS No. 947175-17-9. Molecular formula: C16H15ClO9. Mole weight: 386.74. | |
| 6-Chloro-4-methylumbelliferyl β-D-Galactopyranoside | 6-Chloro-4-methylumbelliferyl-β-D-galactopyranoside is a fluorogenic substrate for the ß-glucosidase assay. This assay monitors the hydrolysis of glycosidic bond by ß-glucosidase and its enzymatic activity has clinic applications for investigating Gaucher's disease. In addition, novel fluorogenic substrates may find utility in high-throughput and sensitive detection applications such as metagenomic screening. Synonyms: 6-Chloro-4-methylumbelliferyl beta-D-Galactopyranoside; 1867162-06-8. CAS No. 1867162-06-8. Molecular formula: C16H17ClO8. Mole weight: 372.75. | |
| 6-Chloro-4-methylumbelliferyl β-D-Glucopyranoside | 6-Chloro-4-methylumbelliferyl-β-D-glucopyranoside is a fluorogenic substrate for the ß-glucosidase assay. This assay monitors the hydrolysis of glycosidic bond by ß-glucosidase and its enzymatic activity has clinic applications for investigating Gaucher's disease. In addition, novel fluorogenic substrates may find utility in high-throughput and sensitive detection applications such as metagenomic screening. Synonyms: 6-Chloro-7-(β-D-glucopyranosyloxy)-4-methyl-2H-1-benzopyran-2-one. CAS No. 1421228-15-0. Molecular formula: C16H17ClO8. Mole weight: 372.75. | |
| 6-Chloro-4-methylumbelliferyl β-D-Xyloside | 6-Chloro-4-methylumbelliferyl-β-xyloside is a fluorogenic substrate for the ß-glucosidase assay. This assay monitors the hydrolysis of glycosidic bond by ß-glucosidase and its enzymatic activity has clinic applications for investigating Gaucher's disease. In addition, novel fluorogenic substrates may find utility in high-throughput and sensitive detection applications such as metagenomic screening. Synonyms: 6-Chloro-4-methyl-7-(β-D-xylopyranosyloxy)-2H-1-benzopyran-2-one. CAS No. 1867162-20-6. Molecular formula: C15H15ClO7. Mole weight: 342.73. | |
| 6-Chloro-4-methylumbelliferyl β-Lactoside | 6-Chloro-4-methylumbelliferyl-β-lactoside is a fluorogenic substrate for the ß-glucosidase assay. This assay monitors the hydrolysis of carbohydrates by ß-glucosidase and its enzymatic activity has clinic applications for investigating Gaucher's disease. In addition, novel fluorogenic substrates may find utility in high-throughput and sensitive detection applications such as metagenomic screening. Synonyms: 6-Chloro-7-[(4-O-β-D-galactopyranosyl-β-D-glucopyranosyl)oxy]-4-methyl-2H-1-benzopyran-2-one. CAS No. 1867162-15-9. Molecular formula: C22H27ClO13. Mole weight: 534.89. | |
| 6-Chloro-4-methylumbelliferyl b-xylobioside | 6-Chloro-4-methylumbelliferyl b-xylobioside is a vital tool in the biomedical industry for studying xylanase enzymes and their role in various diseases. This compound serves as a substrate to measure xylanase activity aiding in the detection and characterization of xylanolytic enzymes. Synonyms: 6-Chloro-4-methyl-7-[(4-O-β-D-xylopyranosyl-β-D-xylopyranosyl)oxy]-2H-1-benzopyran-2-one; 6-Chloro-2-oxo-4-methylchromen-7-yl 4-O-beta-D-xylopyranosyl-beta-D-xylopyranoside; 6-Chloro-4-methylumbelliferyl β-Xylobioside. CAS No. 1867162-18-2. Molecular formula: C20H23ClO11. Mole weight: 474.84. | |
| 6-Chloro-4-(trifluoromethyl)umbelliferyl b-D-cellotetraoside | 6-Chloro-4-(trifluoromethyl)umbelliferyl b-D-cellotetraoside is a biomedical compound used in the study of enzyme activity and diagnosis of diseases. It acts as a substrate for cellulases and endoglucanases aiding in the detection and characterization of these enzymes. this compound finds utility in biomedical research related to drug development for studying cellulase-related disorders and understanding cellulose degradation pathways. Molecular formula: C34H44ClF3O23. Mole weight: 913.15. | |
| 6-Chloro-4-(trifluoromethyl)umbelliferyl b-D-galactopyranoside | 6-Chloro-4-(trifluoromethyl)umbelliferyl b-D-galactopyranoside is a specialized biochemical compound serving as a substrate for the detection and measurement of β-D-galactosidase activity in various biological samples. This compound enables researchers to study diseases related to β-D-galactosidase deficiency, such as galactosialidosand Morquio B syndrome. Its unique structure and properties make it an important tool for enzymatic assays and molecular biology research. Synonyms: CTU-Gal; 6-chloro-4-(trifluoromethyl)-7-(((2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)oxy)-2H-chromen-2-one. Molecular formula: C16H14ClF3O8. Mole weight: 426.73. | |
| 6-Chloro-4-trifluoromethylumbelliferyl b-D-galactopyranoside | 6-Chloro-4-trifluoromethylumbelliferyl b-D-galactopyranoside is a highly significant recompound in the biomedical realm, serving as a pivotal component in enzymatic assays. Its utility lies primarily in the detection of b-galactosidase activity. By virtue of its involvement in biochemical investigations, this compound assumes a critical function in the exploration of altered b-galactosidase expression linked to ailments like lysosomal storage disorders and select cancer variants. Synonyms: 6-Chloro-4-trifluoromethylumbelliferyl β-D-galactopyranoside; 6-chloro-4-(trifluoromethyl)-7-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-2-one. Grade: 95%. Molecular formula: C16H14ClF3O8. Mole weight: 426.03. | |
| 6-Chloro-5-[2-(1-piperazinyl)ethyl]-1,3-dihydro-2H-indol-2-one | 6-Chloro-5-[2-(1-piperazinyl)ethyl]-1,3-dihydro-2H-indol-2-one is a pharmaceutical agent possessing remarkable capability as a formidable antagonist of serotonin receptors. This distinctive attribute empowers its efficacy in studying multifarious afflictions, including anxiety, depression and psychosis. Synonyms: 2H-Indol-2-one, 6-chloro-1,3-dihydro-5-[2-(1-piperazinyl)ethyl]-; 6-Chloro-1,3-dihydro-5-[2-(1-piperazinyl)ethyl]-2H-Indol-2-one. Grade: 96%. CAS No. 188797-79-7. Molecular formula: C14H18ClN3O. Mole weight: 279.76. | |
| 6-Chloro-5-(2-chloroethyl)oxindole | An impurity of Ziprasidone, a combined serotonin (5HT2) and dopamine (D2) receptor antagonist. Synonyms: 5-(2-Chloroethyl)-6-chlorooxindole. CAS No. 118289-55-7. Molecular formula: C10H9Cl2NO. Mole weight: 230.09. | |
| 6-Chloro-6-deoxy-a-cyclodextrin | 6-Chloro-6-deoxy-α-cyclodextrin is a compound renowned for its remarkable versatility owing to its unrivaled aptitude for drug delivery. Engineered with utmost precision, this cyclodextrin derivative impeccably augments solubility, stability and bioavailability of a myriad of therapeutic compounds. Molecular formula: C36H54Cl6O24. Mole weight: 1083.52. | |
| 6-Chloro-6-deoxy-α-D-glucopyranose | 6-Chloro-6-deoxy-α-D-glucopyranose is a reactant used in the synthesis of 6-chloro-6-deoxy-1,2,3,4-tetra-O-galloyl-α-D-glucopyranose which may be used as an antidiabetic. Synonyms: (2S,3R,4S,5S,6S)-6-(Chloromethyl)tetrahydro-2H-pyran-2,3,4,5-tetraol. Grade: 95%. CAS No. 28528-86-1. Molecular formula: C6H11ClO5. Mole weight: 198.60. | |
| 6-Chloro-6-deoxy-b-cyclodextrin | 6-Chloro-6-deoxy-β-cyclodextrin is a meticulously engineered cyclodextrin derivative standing as a quintessential exemplar for drug delivery and encapsulation purposes. Its exceptional properties allow it to profoundly enhance the solubility and stability of hydrophobic drugs. Synonyms: Heptakis-(6-chloro-6-deoxy)-b-cyclodextrin. Molecular formula: C42H63Cl7O28. Mole weight: 1264.10. | |
| 6-Chloro-6-deoxy-D-allitol | 6-Chloro-6-deoxy-D-allitol is a potent pharmaceutical compound renowned for its remarkable antimicrobial attributes. Molecular formula: C6H13ClO5. Mole weight: 200.62. | |
| 6-Chloro-6-deoxy-D-allose | 6-Chloro-6-deoxy-D-allose is an intriguing pharmaceutical compound existing in the biomedical industry, showcasing remarkable antimicrobial attributes in inhibiting an array of pernicious bacterial invasions. Molecular formula: C6H11ClO5. Mole weight: 198.60. | |
| 6-Chloro-6-deoxy-D-altrose | 6-Chloro-6-deoxy-D-altrose is an exceptional biomedical compound unveiling its formidable prowess by effectively impeding the replication of specific viral strains. Extensive and rigorous scientific exploration has unequivocally revealed its remarkable efficacy in tackling a wide array of menacing viral afflictions. Molecular formula: C6H11ClO5. Mole weight: 198.60. | |
| 6-Chloro-6-deoxy-D-galactitol | 6-Chloro-6-deoxy-D-galactitol is an indispensable biomedical compound with an assertive antimicrobial prowess against select bacterial and fungal strains. This compound intrigues the scientific community by manifesting its competence in research of diabetes. Molecular formula: C6H13ClO5. Mole weight: 200.62. | |
| 6-Chloro-6-deoxy-D-galactose | 6-Chloro-6-deoxy-D-galactose is a significant constituent employed in the pharmaceutical realm, bearing paramount significance in synthesizing diverse medications. Its pivotal role unfolds in research and development of antiviral and antitumor therapies. CAS No. 18465-32-2. Molecular formula: C6H11ClO5. Mole weight: 198.60. | |
| 6-Chloro-6-deoxy-D-glucitol | 6-Chloro-6-deoxy-D-glucitol is a pharmacological compound, dominating the realm of biomedical breakthroughs in diabetes research by invigorating glucose utilization. Synonyms: 6-Chloro-6-deoxyglucitol; Glucitol, 6-chloro-6-deoxy-; 1-Chloro-1-deoxyhexitol. CAS No. 76986-26-0. Molecular formula: C6H13ClO5. Mole weight: 200.62. | |
| 6-Chloro-6-deoxy-D-glucose | 6-Chloro-6-deoxy-D-glucose, known for its remarkable pharmacological attributes, finds surprising utility within positron emission tomography (PET) analyses, warranting its potential potency as a radiopharmaceutical agent. This glucose mimic, boasting an unparalleled affinity towards malignant cells, substantially facilitates the research of neoplastic metabolic patterns. Synonyms: (2R,3S,4S,5S)-6-Chloro-2,3,4,5-tetrahydroxyhexanal. CAS No. 40656-44-8. Molecular formula: C6H11ClO5. Mole weight: 198.60. | |
| 6-Chloro-6-deoxy-D-mannono-1,4-lactone | 6-Chloro-6-deoxy-D-mannono-1,4-lactone is a remarkable compound, emerging as a prodigious weapon in the research of intransigent bacterial and fungal infections. This compounds holds the capacity to perturb and deter the proliferation of malevolent microorganisms. Molecular formula: C6H9ClO5. Mole weight: 196.59. | |
| 6-Chloro-6-deoxy-D-mannose | 6-Chloro-6-deoxy-D-mannose acts as an antimicrobial agent, inhibiting the growth of certain bacteria and fungi. It displays potent activity against specific drug-resistant strains, making it an essential tool in combating these infections. Its mechanism of action involves targeting key enzymes required for microbial growth, offering a promising solution for drug resistance challenges. CAS No. 4990-81-2. Molecular formula: C6H11ClO5. Mole weight: 198.60. | |
| 6-Chloro-7-deaza-9-(2',3',5'-tri-O-acetyl-β-D-ribofuranoysyl)purine | 6-Chloro-7-deaza-9-(2',3',5'-tri-O-acetyl-β-D-ribofuranoysyl)purine is a compound useful in organic synthesis. Synonyms: (2R,3R,4R,5R)-2-(Acetoxymethyl)-5-(4-chloro-7H-pyrrolo[2,3-d]pyrimidin-7-yl)tetrahydrofuran-3,4-diyl diacetate; 4-Chloro-7-(2,3,5-tri-O-acetyl-β-D-ribofuranosyl)-7H-pyrrolo[2,3-d]pyrimidine; 4-Chloro-7-β-D-ribofuranosyl-7H-pyrrolo[2,3-d]pyrimidine 2',3',5'-Triacetate. Grade: ≥95%. CAS No. 16754-79-3. Molecular formula: C17H18ClN3O7. Mole weight: 411.79. | |
| 6-Chloro-7-deaza-9-(5'-O-tert-butyldimethylsilyl-2',3'-O-isopropylidine-β-D-ribofuranosyl)purine | 6-Chloro-7-deaza-9-(5'-O-tert-butyldimethylsilyl-2',3'-O-isopropylidine-β-D-ribofuranosyl)purine is a compound useful in organic synthesis. Synonyms: 4-Chloro-7-[(5-O-t-butyldimethylsilyl)-2,3-O-isopropyli-dene-β-D-ribofuranosyl]-7H-pyrrolo[2,3-d]pyrimidine; 4-Chloro-7-[5-O-[(1,1-dimethylethyl)dimethylsilyl]-2,3-O-(1-methylethylidene)-β-D-ribofuranosyl]-7H-pyrrolo[2,3-d]pyrimidine; 7-((3aR,4R,6R,6aR)-6-(((tert-butyldimethylsilyl)oxy)methyl)-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol-4-yl)-4-chloro-7H-pyrrolo[2,3-d]pyrimidine; 4-Chloro-7-{5-O-[dimethyl(2-methyl-2-propanyl)silyl]-2,3-O-isopropylidene-β-D-ribofuranosyl}-7H-pyrrolo[2,3-d]pyrimidine. Grade: ≥95%. CAS No. 115479-39-5. Molecular formula: C20H30ClN3O4Si. Mole weight: 440.01. | |
| 6-Chloro-7-deaza-9-(a-D-ribofuranosyl)purine | 6-Chloro-7-deaza-9-(a-D-ribofuranosyl)purine, an influential antiviral compound, stands as a stronghold in the biomedical industry, combating diverse viral infections, especially those instigated by RNA viruses. Showcasing its supremacy, this nucleoside analog unveils formidable antiviral prowess against RNA viruses such as influenza, hepatitis C, and dengue. Its ability to impede viral replication not only restrains the onslaught of viral ailments but also augments overall patient prognosis in unprecedented measures. Synonyms: 4-Chloro-7-α-D-ribofuranosyl-7H-pyrrolo[2,3-d]pyrimidine; 7H-Pyrrolo[2,3-d]pyrimidine, 4-chloro-7-α-D-ribofuranosyl-. CAS No. 120401-32-3. Molecular formula: C11H12ClN3O4. Mole weight: 285.68. | |
| 6-Chloro-7-deazapurine | One of the impurities of Tofacitinib, which is a Janus kinase inhibitor and could be used against rheumatoid arthritis. Synonyms: 4-Chloro-1H-pyrrolo[2,3-d]pyrimidine; 4-Chloropyrrolo[2,3-d]pyrimidine; NSC 64952. Grade: ≥98% by HPLC. CAS No. 3680-69-1. Molecular formula: C6H4ClN3. Mole weight: 153.57. | |
| 6-Chloro-7-deazapurine-2F-β-D-arabinofuranose | 4-Chloro-7-(2-deoxy-2-fluoro-beta-D-arabinofuranosyl)-7H-pyrrolo[2.3-d]pyrimidine, known for its potent antiviral properties, is mainly used to study a wide array of viral infections such as HIV and hepatitis B. By impeding viral DNA replication, it effectively curtails the viral burden within the host organism. Synonyms: 169516-60-3; 4-Chloro-7-(2-deoxy-2-fluoro-beta-D-arabinofuranosyl)-7H-pyrrolo[2.3-d]pyriMidine; (2R,3R,4S,5R)-5-(4-chloro-7H-pyrrolo[2,3-d]pyrimidin-7-yl)-4-fluoro-2-(hydroxymethyl)tetrahydrofuran-3-ol; (2R,3R,4S,5R)-5-(4-chloropyrrolo[2,3-d]pyrimidin-7-yl)-4-fluoro-2-(hydroxymethyl)oxolan-3-ol; XFKDBYKOIYHLSC-FBSDJGSXSA-N; SCHEMBL1689451; DTXSID601137565; (2R,3R,4S,5R)-5-{4-chloro-7H-pyrrolo[2,3-d]pyrimidin-7-yl}-4-fluoro-2-(hydroxymethyl)oxolan-3-ol; DA-60342; F12818; A900689; 4-chloro-7-(2-deoxy-2-fluoro-beta-D-arabinofuranosyl)-7H-pyrrolo[2,3-d]pyrimidine; 4-Chloro-7-(2-deoxy-2-fluoro-I(2)-D-arabinofuranosyl)-7H-pyrrolo[2,3-d]pyrimidine. Grade: ≥95%. CAS No. 169516-60-3. Molecular formula: C11H11ClFN3O3. Mole weight: 287.67. | |
| 6-Chloro-7-deazapurine-β-D-riboside | 6-Chloro-7-deazapurine-β-D-riboside is an adenosine kinase inhibitor. 6-Chloro-7-deazapurine-β-D-riboside is a valuable nucleoside analog used in biochemical and pharmacological research. Its modified structure allows scientists to study the effects of chlorination and deaza modifications on nucleotide function, enzyme interactions, and potential therapeutic applications in antiviral and anticancer treatments. This compound provides insights into the role of modified nucleosides in various biological processes and the development of novel therapeutic agents. Synonyms: 6-Chloro-7-deazapurine-9-b-D-ribofuranose; 4-Chloro-7-(b-D-ribofuranosyl)-7H-pyrrolo[2.3-d]pyrimidine; 4-Chloro-7-(β-D-ribofuranosyl)pyrrolo[2,3-d]pyrimidine; 6-Chloro-9-(β-D-ribofuranosyl)-7-deazapurine; 6-Deamino-6-chlorotubercidin; NSC 101161. Grade: ≥95%. CAS No. 16754-80-6. Molecular formula: C11H12ClN3O4. Mole weight: 285.68. | |
| 6-Chloro-7-iodo-7-deazapurine | 4-Chloro-5-iodopyrrolo[2,3-d]pyrimidine can be used to synthesize compounds that can act as analogs of Axl kinase inhibitors. Furthermore, it can be used to prepare nucleoside prodrugs for treating viral infections. Synonyms: 4-Chloro-5-iodopyrrolo[2,3-d]pyrimidine; 4-Chloro-5-iodo-1H-pyrrolo[2,3-d]pyrimidine; 7H-Pyrrolo[2,3-d]pyriMidine, 4-chloro-5-iodo-. Grade: 97.0 %. CAS No. 123148-78-7. Molecular formula: C6H3ClIN3. Mole weight: 279.47. | |
| 6-?Chloro-?9-?[(1R,?4S)?-?4-?[(1,?1-?dimethylethoxy)?methyl]?-?2-?cyclopenten-?1-?yl]?-?9H-?purin-?2-?amine | 6-Chloro-9-[(1R,?4S)?-4-[(1,?1-dimethylethoxy)?methyl]?-2-cyclopenten-1-yl]?-9H-purin-2-amine is an intermediate in synthesizing N6-Cyclopropyl-9-[(1R,4S)-4-[(1,1-dimethylethoxy)methyl]-2-cyclopenten-1-yl]-9H-purine-2,6-diamine (Abacavir EP Impurity F) , an impurity of Abacavir, a guanosine analog that inhibits reverse transcriptase (NRTI). Synonyms: 9-((1R,4S)-4-(tert-Butoxymethyl)cyclopent-2-en-1-yl)-6-chloro-9H-purin-2-amine. Molecular formula: C15H20ClN5O. Mole weight: 321.81. | |
| 6-Chloro-9-(2',3',5'-tri-O-acetyl-b-D-ribofuranosyl)purine | 6-Chloro-9-(2',3',5'-tri-O-acetyl-b-D-ribofuranosyl)purine, a highly potent nucleoside analog, finds extensive applications in the field of biomedical research. By impeding the replication process of specific viruses, this compound showcases remarkable antiviral properties. Its utilization prospects extend to the treatment of various viral ailments including hepatitis B and C, herpes, and HIV. Molecular formula: C16H17ClN4O7. Mole weight: 412.79. | |
| 6-Chloro-9-(2,3,5-tri-O-benzoyl-2-C-methyl-β-D-ribofuranosyl)-9H-purine | 6-Chloro-9-(2,3,5-tri-O-benzoyl-2-C-methyl-β-D-ribofuranosyl)-9H-purine, commonly known as a remarkable antiviral agent, holds immense significance in the biomedical realm. It emerges as a key player in combating RNA viruses, through its intricate interactions with viral enzymes. By impeding their replication, this compound effectively curtails viral proliferation and transmission. Synonyms: (2R,3R,4R,5R)-5-((Benzoyloxy)methyl)-2-(6-chloro-9H-purin-9-yl)-3-methyltetrahydrofuran-3,4-diyl dibenzoate; 9H-Purine, 6-chloro-9-(2,3,5-tri-O-benzoyl-2-C-methyl-β-D-ribofuranosyl)-. Grade: ≥95%. CAS No. 205171-04-6. Molecular formula: C32H25ClN4O7. Mole weight: 613.02. | |
| 6-Chloro-9-(2-O-acetyl-5-O-benzoyl-3-azido-3-deoxy-beta-D-ribofuranosyl)-9H-purine | This compound is a potent nucleoside analogue widely used in the biomedical industry. Its antiviral properties make it an effective research for viral infections such as herpes and hepatitis. Additionally, it exhibits anticancer activity, particularly in the research of leukemia and solid tumors. This compound plays a crucial role in inhibiting viral replication and suppressing tumor growth. Synonyms: 9-(2-O-Acetyl-3-azido-5-O-benzoyl-3-deoxy-beta-D-ribofuranosyl)-6-chloro-9H-purine; ((2S,3R,4R,5R)-4-acetoxy-3-azido-5-(6-chloro-9H-purin-9-yl)tetrahydrofuran-2-yl)methyl benzoate. Grade: ≥95%. CAS No. 917239-29-3. Molecular formula: C19H16ClN7O5. Mole weight: 457.83. | |
| 6-Chloro-9-(2-O-acetyl-5-O-(p-toluoyl)-3-azido-3-deoxy-beta-D-ribofuranosyl)-9H-purine | 6-Chloro-9-(2-O-acetyl-5-O-(p-toluoyl)-3-azido-3-deoxy-beta-D-ribofuranosyl)-9H-purine, a formidable antiviral compound, boasts its efficacy in research of viral infections caused by both DNA and RNA viruses. With its broad-spectrum antiviral activity, it remarkably impedes viral replication and disrupts the enhancement of viral DNA. Operating by inhibiting viral reverse transcriptase and viral DNA polymerase, it fearlessly halts viral proliferation. Synonyms: 6-Chloro-9-(2-O-acetyl-5-O-(p-toluoyl)-3-azido-3-deoxy-β-D-ribofuranosyl)-9H-purine. Grade: ≥95%. Molecular formula: C20H18ClN7O5. Mole weight: 471.85. | |
| 6-Chloro-9-(3',5'-di-O-benzoyl-2'-Deoxy-2'-fluoro-b-D-arabinofuranosyl)purine | 6-Chloro-9-(3',5'-di-O-benzoyl-2'-Deoxy-2'-fluoro-b-D-arabinofuranosyl)purine is a potent antiviral compound used in the biomedical industry to treat various viral infections and diseases. It exhibits strong activity against RNA viruses, including influenza, HIV, and hepatitis C virus. This molecule functions by inhibiting viral replication and transcription, ultimately reducing the viral load and alleviating symptoms associated with these viral infections. Molecular formula: C24H18CIFN4O5. Mole weight: 496.89. | |
| 6-Chloro-9-(3,5-O-di-(p-toluoyl)-β-D-2-deoxyribofuranosyl)purine | It is a protected purine deoxynucleoside DNA adduct. Synonyms: 6-Chloro-9-[3,5-di-O-(p-toluoyl)-2-deoxy-β-D-ribofuranosyl]-9H-purine; 9-[2-Deoxy-3-O,5-O-bis(4-methylbenzoyl)-beta-D-erythro-pentofuranosyl]-6-chloro-9H-purine; 3,5-O-Ditoluoyl 6-Chloropurine-9-β-D-deoxyriboside; 6-Chloro-9-(2'-deoxy-3',5'-di-O-toluoyl-β-ribofuranosyl)purine; 6-Chloro-9-[2-deoxy-3,5-bis-O-(4-methylbenzoyl)-β-D-erythro-pentofuranosyl]-9H-purine. Grade: ≥95%. CAS No. 91713-46-1. Molecular formula: C26H23ClN4O5. Mole weight: 506.94. | |
| 6-chloro-9-((4-methoxy-3,5-dimethylpyridin-2-yl)methyl)-9H-purin-2-amine | BIIB021 is An orally active, purine-scaffold, small-molecule inhibitor of heat shock protein 90 (Hsp90) with potential antineoplastic activity. BIIB021 that is currently undergoing Phase II testing, may have broader application against tumors with acquired multidrug resistance or tumors located in organs protected by MDR proteins, such as the adrenal glands, brain and testis. Uses: Biib 021 an orally available, fully synthetic small-molecule inhibitor of the heat shock protein hsp90. studies show that biib 021 adminisitration led to degradation of hsp90 client proteins measured in tumor tissue and resulted in the inhibition of tumor. Synonyms: [6-Chloro-9-(4-methoxy-3,5-dimethylpyridin-2-ylmethyl)-9H-purin-2-yl]amine; CNF-2024; CNF 2024; CNF2024. Grade: >98%. CAS No. 848695-25-0. Molecular formula: C14H15ClN6O. Mole weight: 318.76. | |
| 6-Chloro-9-(5-O-dimethoxytrityl-β-D-2-deoxyribofuranosyl)purine | 6-Chloro-9-(5-O-dimethoxytrityl-β-D-2-deoxyribofuranosyl)purine is an immensely potent and exquisitely selective pharmaceutical compound, finding profound application within research of impeding the process of DNA enhancement. Manifesting exceptional attributes of pharmacological efficacy, this invaluable resource serves to propel developments in the research of anticancer therapeutics. Synonyms: 9-[5-O-[Bis(4-methoxyphenyl)phenylmethyl]-2-deoxy-beta-D-erythro-pentofuranosyl]-6-chloro-9H-purine. Grade: ≥ 97%. CAS No. 133931-96-1. Molecular formula: C31H29ClN4O5. Mole weight: 573.05. | |
| 6-Chloro-9-(β-D-2-deoxyribofuranosyl)purine | 6-Chloro-9-(β-D-2-deoxyribofuranosyl)purine, a remarkable compound utilized in the biomedical realm, showcases substantial prowess as an antiviral agent. Its key purpose lies within combatting diverse viral infections, emblematically those instigated by the herpes family. By thwarting viral DNA synthesis, this compound proficiently hampers the replication of these intrusive pathogens. The astute amalgamation of an exceptional chemical framework and an intricately orchestrated mechanism efficaciously endows this entity with an unparalleled potential to counteract a wide array of viral afflictions. Synonyms: 6-Chloropurine-2'-deoxyriboside; (2R,3S,5R)-5-(6-chloro-9H-purin-9-yl)-2-(hydroxymethyl)tetrahydrofuran-3-ol. Grade: ≥ 97%. CAS No. 4594-45-0. Molecular formula: C10H11ClN4O3. Mole weight: 270.68. | |
| 6-Chloro-9-(β-D-ribofuranosyl)purine | 6-Chloro-9-(β-D-ribofuranosyl)purine, a potent pharmaceutical compound, finds its application in combating chemotherapy-induced emesis and radiation sickness. Its remarkable antiviral activity thwarts diverse viral infections by effectively impeding viral replication. Additionally, this product serves as an invaluable nucleoside analog for cutting-edge research pertaining to nucleic acids and nucleotide metabolism. Synonyms: 6-Chloropurine riboside; Chloropurine riboside; 6-Chloro-9-ribofuranosyl-9H-purine; 6-Chloropurine ribonucleoside. Grade: 97%. CAS No. 2004-06-0. Molecular formula: C10H11ClN4O4. Mole weight: 286.67. | |
| 6-Chloro famciclovir | An impurity of Famciclovir. Famciclovir is used for the treatment of various herpesvirus infections, most commonly for herpes zoster. Synonyms: 9-[4-Acetoxy-3-(acetoxymethyl)butyl]-2-amino-6-chloropurine; Famciclovir Chloro Impurity. Grade: > 95%. CAS No. 97845-60-8. Molecular formula: C14H18ClN5O4. Mole weight: 355.78. | |
| 6-Chloro-GTP | 6-Chloro-GTP is a highly significant compound, playing a pivotal role due to its exceptional antiviral attributes which effectively impede viral replication. By selectively targeting viral RNA research and development-associated enzymes, this remarkable compound showcasing an outstanding inhibitory effect. Promisingly, it finds extensive application in studying various viral infections like hepatitis C and respiratory syncytial virus (RSV). Synonyms: (6Cl-GTP); 6-Chloro-guanosine-5'-triphosphate, Sodium salt; 2-Amino-6-chloro-9-(β-D-ribofuranosyl)-purine. Grade: ≥ 95% by HPLC. Molecular formula: C10H15N5O13P3Cl (free acid). Mole weight: 541.62 (free acid). | |
| 6-Chloroinosine monophosphate | 6-Chloroinosine monophosphate is a derivative of inosine monophosphate (IMP) where a chlorine atom is substituted at the 6th position of the purine ring. This modified nucleotide analog is utilized in biochemical and molecular biology research for probing nucleic acid structure, enzymatic reactions, and as a substrate for various enzymes. It can also serve as a precursor for the synthesis of modified nucleic acids for studying structure-function relationships or for therapeutic applications. Synonyms: 6-Cl-adenosine-5'-monophosphate; 6-Cl-AMP; 6-Cl-Purine Ribotide; 6-Chloropurine riboside 5'-monophosphate; 6-Chloropurine ribotide; 6-Chloropurine riboside 5'-phosphate; 6-Chloropurine 9-beta-D-ribofuranosyl 5'-monophosphate; 6-Chloro-9-(5-O-phosphono-beta-D-ribofuranosyl)-9H-purine; ((2R,3S,4R,5R)-5-(6-Chloro-9H-purin-9-yl)-3,4-dihydroxytetrahydrofuran-2-yl)methyl dihydrogen phosphate. CAS No. 5843-59-4. Molecular formula: C10H12ClN4O7P. Mole weight: 366.65. | |
| 6-Chloromelatonin | 6-Chloromelatonin is a potent agonist of the melatonin receptors, which is active at nanomolar concentrations. It shows higher affinity for binding to hamster brain membrane and chicken retina than melatonin. It has antiproliferative activity. Synonyms: N-[2-(6-Chloro-5-methoxyindol-3-yl)ethyl]acetamide; N-Acetyl-6-chloro-5-methoxytryptamine. Grade: ≥99% by HPLC. CAS No. 63762-74-3. Molecular formula: C13H15ClN2O2. Mole weight: 266.73. | |
| 6-chloro-N-((1R,2S)-2-(3,4-difluorophenyl)cyclopropyl)-5-nitro-2-(propylthio)pyrimidin-4-amine | An impurity of Ticagrelor which is a reversible P2Y12 receptor antagonist and is unique in its greater and more rapid and consistent, yet reversible, inhibition of the ADP receptor. Synonyms: Ticagrelor impurity 35. CAS No. 1427523-93-0. Molecular formula: C16H15ClF2N4O2S. Mole weight: 400.83. | |
| 6-?Chloro-?N4-?[(1R,?4S)?-?4-?[(1,?1-?dimethylethoxy)?methyl]?-?2-?cyclopenten-?1-?yl]?-?2,?4,?5-?pyrimidinetriamine | 6-Chloro-N4-[(1R,?4S)?-4-[(1,?1-dimethylethoxy)?methyl]?-2-cyclopenten-1-yl]?-2,?4,?5-pyrimidinetriamine is an intermediate in synthesizing N6-Cyclopropyl-9-[(1R,4S)-4-[(1,1-dimethylethoxy)methyl]-2-cyclopenten-1-yl]-9H-purine-2,6-diamine (Abacavir EP Impurity F), an impurity of Abacavir, a guanosine analog that inhibits reverse transcriptase (NRTI). Molecular formula: C14H22ClN5O. Mole weight: 311.81. | |
| 6-Chloro-N-phenyl-9-(2,3,5-tri-O-acetyl-b-D-ribofuranosyl)-9H-purin-2-amine | 6-Chloro-N-phenyl-9-(2,3,5-tri-O-acetyl-b-D-ribofuranosyl)-9H-purin-2-amine, commonly known as CPARTA, is a groundbreaking antiviral compound extensively applied in the biomedical sector. It exhibits remarkable efficacy in research of a range of viral afflictions, including hepatitis C and HIV. By impeding the propagation of viral RNA, CPARTA effectively curtails viral proliferation. Its intricate mode of action involves the selective targeting of pivotal viral enzymes indispensable for replication. Synonyms: 2-Phenylamino-6-chloro-9-(2,3,5-tri-O-acetyl-b-D-ribofuranosyl)purine. CAS No. 53296-14-3. Molecular formula: C22H22ClN5O7. Mole weight: 503.89. | |
| 6-Chloropurine | Astragaloside III has cardioprotective effects as well as causing improvement in cognitive function. Used in the prevention of cardio-cerebral vascular diseases. Antioxidant. Uses: Antiviral agents. Synonyms: 6-Chloro-9H-purine; NSC 744; 6-Chloro-1H-purine. Grade: 95 %. CAS No. 87-42-3. Molecular formula: C5H3ClN4. Mole weight: 154.56. | |
| 6-Chloropurine-2'-deoxyriboside-5'-Triphosphate | 6-Chloropurine-2'-deoxyriboside-5'-Triphosphate is a crucial recompound, serving as a substrate for DNA polymerases aiding in the research and development of modified nucleotides. This compound plays a vital role in studying DNA and RNA structure, replication and repair mechanisms. Its utility extends to investigating various diseases like cancer, genetic disorders and viral infections, providing insights into their molecular mechanisms. Synonyms: 6-Cl-purine-drTP. Grade: ≥95% by AX-HPLC. Molecular formula: C10H14N4O12P3Cl. Mole weight: 510.60. | |
| 6-Chloropurine-9-(2,3-isopropylidene-β-D-ribofuranoside) | 6-Chloropurine-9-(2,3-isopropylidene-β-D-ribofuranoside) is a protected nucleoside analog used in chemical and biochemical research. The chlorination at the 6-position of the purine base and the isopropylidene protection of the ribose sugar allow for controlled synthesis and modification of nucleosides. This compound is valuable for studying nucleotide analog interactions, enzyme mechanisms, and potential therapeutic applications in antiviral and anticancer research. Synonyms: 6-Chloro-9-(2',3'-di-O-isopropylidene-beta-D-ribofuranosyl)purine; 6-Chloro-9-β-D-(2,3-isopropylidene)ribofuranosylpurine; 6-Chloro-9-[2,3-O-(1-methylethylidene)-beta-D-ribofuranosyl]-9H-Purine; [(3aR,4R,6R,6aR)-4-(6-chloropurin-9-yl)-2,2-dimethyl-3a,4,6,6a-tetrahydrofuro[3,4-d][1,3]dioxol-6-yl]methanol; 6-Chloro-9-(2,3-O-isopropylidene-β-D-ribofuranosyl)-9H-purine. Grade: 98%. CAS No. 39824-26-5. Molecular formula: C13H15ClN4O4. Mole weight: 326.74. | |
| 6-chloro-purine-9-b-D-(2-O-acetyl-3,5-di-O-benzoyl)xylo-furanoside | 6-Chloro-purine-9-b-D-(2-O-acetyl-3,5-di-O-benzoyl)xylo-furanoside is a biomedical compound used in the research of certain diseases. This compound possesses potential antiviral properties and is utilized in drug development against viral infections. It serves as a key component for the research and development of specific medications targeting viral diseases aiding in the development of biomedical research. Synonyms: 9-(2-O-Acetyl-3,5-di-O-benzoyl-b-D-xylofurano-syl)-9H-6-chloropurine; (2R,3S,4R,5R)-4-Acetoxy-2-((benzoyloxy)methyl)-5-(6-chloro-9H-purin-9-yl)tetrahydrofuran-3-yl benzoate. Grade: ≥95%. CAS No. 132370-61-7. Molecular formula: C26H21ClN4O7. Mole weight: 536.92. | |
| 6-Chloropurine-9-b-D-glucoside | 6-Chloropurine-9-b-D-glucoside, a quintessential compound widely utilized in the biomedical sector due to its immense potential in therapeutic applications, stands as a pivotal asset. Its efficacy surpasses boundaries as it battles an array of ailments, including select cancer variants and virulent infections. Scrutinized extensively, this compound emerges as a promising contender for the creation of specialized medications curated to subdue these afflictions. Synonyms: 9H-Purine, 6-chloro-9-β-D-glucopyranosyl-; 6-Chloro-9-β-D-glucopyranosyl-9H-purine; 9-β-D-Glucopyranosyl 6-chloropurine. CAS No. 66981-23-5. Molecular formula: C11H13CIN4O5. Mole weight: 316.70. | |
| 6-Chloropurine-9-beta-D-(3',5'-di-O-benzoyl-2'-deoxy-2'-fluoro)arabinoriboside | 6-Chloropurine-9-beta-D-(3',5'-di-O-benzoyl-2'-deoxy-2'-fluoro)arabinoriboside is an intriguing compound prevalent in the biomedical landscape, showcasing tremendous promise in research of ailments. Emanating from its unparalleled antiviral prowess against both DNA and RNA viruses, this compound emerges as an encouraging instrument in research of thwarting pervasive viral afflictions like herpes and hepatitis. Synonyms: 9-(3,5-Di-O-benzoyl-2-deoxy-2-fluoro-β-D-arabinofuranosyl)-9H-6-chloropurine; 6-Chloro-9-(3',5'-di-o-benzoyl-2'-deoxy-2'-fluoro-b-D-arabinofuranosyl)purine; ((2R,3R,4S,5R)-3-(Benzoyloxy)-5-(6-chloro-9H-purin-9-yl)-4-fluorotetrahydrofuran-2-yl)methyl benzoate. Grade: ≥95%. CAS No. 135473-15-3. Molecular formula: C24H18ClFN4O5. Mole weight: 496.88. | |
| 6-Chloropurine Riboside | 6-Chloropurine Riboside is an adenosine deaminase substrate. 6-Chloropurine Riboside is a modified nucleoside where a chlorine atom is attached to the 6-position of the purine base. It is used in biochemical research to study nucleic acid structure and function, and to investigate nucleic acid interactions. Additionally, it serves as a precursor in the synthesis of other modified nucleosides and nucleotides for therapeutic and diagnostic applications. Synonyms: 6-Chloro Inosine; 6-Chloro-9-(beta-D-ribofuranosyl)purine; 6-chloroinosine; 6-Chloropurine-9-β-D-ribofuranoside; 6-Chloro-6-deaminoadenosine; 6-Chloro-9-β-D-ribofuranosyl-9H-purine; 6-Chloro-9-β-D-ribofuranosylpurine; 6-Chloronebularine; 6-Chloropurine-D-riboside; 6-Chloropurinosine; 9-(β-D-Ribofuranosyl)-6-chloropurine; NSC 4910; Chloropurine riboside. Grade: ≥98% by HPLC. CAS No. 5399-87-1. Molecular formula: C10H11ClN4O4. Mole weight: 286.67. | |
| 6-Chloropurine-riboside-5'-monophosphate | 6-Chloropurine-riboside-5'-monophosphate, a synthetic nucleoside analog, has exhibited remarkable potential in imparting its anti-cancer prowess by implementing abrupt halt to DNA synthesis and disruption of the critical signaling pathways. Hence, promoting the death of cancer cells and facilitating the investigation of the underlying mechanisms that govern cancer cell apoptosis and assist in the development of novel cancer treatments. Consequently, it is widely utilized in research studies to uncover the various facets of cancer biology. Synonyms: 6-Chloropurine-riboside-5'-monophosphate, Sodium salt. Grade: ≥ 95% by HPLC. Molecular formula: C10H12N4O7PCl (free acid). Mole weight: 366.65 (free acid). | |
| 6-Chloropurine riboside-5'-O-triphosphate | 6-Chloropurine riboside-5'-O-triphosphate is a pivotal compound extensively employed in the biomedical sector for drug discovery and investigation, manifesting itself as a remarkably potent suppressor of specific enzymes, thus bestowing it with a noteworthy potential for research of diverse viral ailments. Synonyms: 6-Cl-PuTP; Cirtp. CAS No. 55673-61-5. Molecular formula: C10H14ClN4O13P3. Mole weight: 526.6. | |
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