BOC Sciences - Products

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
Allyl 2-acetamido-2-deoxy-b-D-glucopyranoside Allyl 2-acetamido-2-deoxy-b-D-glucopyranoside, an indispensable compound in the biomedical sector, showcases its significance as a glycosylation inhibitor with potential therapeutic implications for illnesses like cancer and diabetes. Remarkably, this compound manifests promising effects in thwarting tumor development and regulating glucose levels by selectively targeting distinct enzyme pathways. CAS No. 54400-77-0. Molecular formula: C11H19NO6. Mole weight: 261.27. BOC Sciences
Allyl 2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-b-D-glucopyranoside Allyl 2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-b-D-glucopyranoside is a compound possessing significant pharmaceutical potential as it can be employed in the research of various diseases. This compound exhibitings potential antibacterial, antitumor and antiviral activities, making it a notable candidate for drug developing applications. Synonyms: (2R,3S,4R,5R,6R)-5-Acetamido-2-(acetoxymethyl)-6-(allyloxy)tetrahydro-2H-pyran-3,4-diyl diacetate; Allyl 2-Acetamido-3,4,6-tri-O-acetyl-2-deoxy-beta-D-glucopyranoside; beta-D-Glucopyranoside, 2-propen-1-yl 2-(acetylamino)-2-deoxy-, 3,4,6-triacetate; [(2R,3S,4R,5R,6R)-5-Acetamido-3,4-diacetyloxy-6-prop-2-enoxyoxan-2-yl]methyl acetate; AKOS015919295; Allyl 2-Acetamido-3,4,6-tri-O-acetyl-2-deoxy-?-D-glucopyranoside; b-D-Glucopyranoside,2-propen-1-yl2-(acetylamino)-2-deoxy-,3,4,6-triacetate. CAS No. 28738-44-5. Molecular formula: C17H25NO9. Mole weight: 387.39. BOC Sciences
Allyl 2-acetamido-3,4-di-O-acetyl-6-azido-2-deoxy-D-galactopyranoside Allyl 2-acetamido-3,4-di-O-acetyl-6-azido-2-deoxy-D-galactopyranoside is an essential biomedical compound, manifesting inhibitory efficacy in studying diverse ailments. Its profound impact lies in its potential antimicrobial attributes, which have been substantiated against specific bacterial strains. BOC Sciences
Allyl 2-acetamido-3,6-di-O-benzyl-2-deoxy-b-D-glucopyranoside Allyl 2-acetamido-3,6-di-O-benzyl-2-deoxy-b-D-glucopyranoside, a chemical compound employed in the biomedical industry, is being investigated for its therapeutic potential against Alzheimer's and Parkinson's diseases. Beyond neurodegenerative disorders, this compound's potential as a cancer cell inhibitor is also being explored. Analyzing the multifunctional properties of this intriguing compound nears a wealth of opportunities in drug discovery. CAS No. 65730-02-1. Molecular formula: C25H31NO6. Mole weight: 441.53. BOC Sciences
Allyl 2-acetamido-3-O-benzyl-2-deoxy-b-D-glucopyranose Allyl 2-acetamido-3-O-benzyl-2-deoxy-b-D-glucopyranose is a biochemical compound extensively utilized in the biomedical industry. It serves as a key component in the development of drugs targeting various diseases, such as bacterial and fungal infections. This compound exhibits exceptional antimicrobial properties, making it an invaluable tool for researchers and pharmaceutical companies in the pursuit of novel therapeutic interventions. Synonyms: Allyl 2-acetamido-3-O-benzyl-2-deoxy-b-D-glucopyranose; Allyl-2-acetamido-3-O-benzyl-2-deoxy-b-D-glucopyranose; N-[(2R,3R,4R,5S,6R)-5-hydroxy-6-(hydroxymethyl)-4-phenylmethoxy-2-prop-2-enoxyoxan-3-yl]acetamide; Allyl 2-(Acetylamino)-2-deoxy-3-O-benzyl-beta-D-glucopyranoside; W-203432; Allyl 2-(Acetylamino)-2-deoxy-3-O-benzyl-?-D-glucopyranoside. CAS No. 65730-00-9. Molecular formula: C18H25NO6. Mole weight: 351.40. BOC Sciences
Allyl 2-acetamido-4,6,-O-benzylidene-2-deoxy-a-D-glucopyranoside Allyl 2-acetamido-4,6,-O-benzylidene-2-deoxy-a-D-glucopyranoside is a biomedical compound widely used in the treatment of various bacterial and fungal infections. This product exhibits potent antimicrobial activity against pathogens including Staphylococcus aureus and Candida albicans. It can be utilized as an essential ingredient in the development of advanced pharmaceutical formulations targeting the eradication of these infectious diseases. Synonyms: N-[(4aR,6S,7R,8R,8aS)-8-hydroxy-2-phenyl-6-prop-2-enoxy-4,4a,6,7,8,8a-hexahydropyrano[3,2-d][1,3]dioxin-7-yl]acetamide; N-((4AR,6S,7R,8R,8aS)-6-(allyloxy)-8-hydroxy-2-phenylhexahydropyrano[3,2-d][1,3]dioxin-7-yl)acetamide; ALLYL 2-(ACETYLAMINO)-2-DEOXY-4,6-O-(PHENYLMETHYLENE)-?-D-GLUCOPYRANOSIDE;Allyl 2-(Acetylamino)-2-deoxy-4,6-O-(phenylmethylene)-a-D-glucopyranoside;Allyl-2-acetamido-4,6,-O-benzylidene-2-deoxy-a-D-glucopyranoside; Allyl 2-acetamido-4,6-O-benzylidene-2-deoxy-alpha-D-glucopyranoside, 95%; Allyl 2-(Acetylamino)-2-deoxy-4,6-O-(phenylmethylene)- alpha -D-glucopyranoside; Prop-2-en-1-yl 2-acetamido-4,6-O-benzylidene-2-deoxy-alpha-D-glucopyranoside. CAS No. 63064-49-3. Molecular formula: C18H23NO6. Mole weight: 349.39. BOC Sciences
Allyl 2-acetamido-4,6-O-benzylidene-2-deoxy-b-D-glucopyranoside Allyl 2-acetamido-4,6-O-benzylidene-2-deoxy-b-D-glucopyranoside, a versatile compound, finds application in the biomedical industry for synthesizing glycopeptides and glycoproteins. This sublime molecule, serving as an effective tool to investigate glycosylation, holds immense potential to combat the debilitating effects of life-threatening diseases like cancer, diabetes, and Alzheimer's. This product, customizable in terms of grades and quantities, promises to cater to diverse research exigencies with unwavering efficacy. CAS No. 65947-37-7. Molecular formula: C18H23NO6. Mole weight: 349.39. BOC Sciences
Allyl 2-deoxy-2-amino-3-O-(2-Naphthylmethyl)-4,6-O-Benzylidene-1-β-D-Galactopyranoside Allyl 2-deoxy-2-amino-3-O-(2-Naphthylmethyl)-4,6-O-Benzylidene-1-β-D-Galactopyranoside exhibits potential therapeutic effects against various drug-resistant pathogens and has shown activity against tumor growth. Studies suggest its potential as an adjunct therapy in combination with existing anticancer drugs due to its ability to enhance their efficacy. BOC Sciences
Allyl 2-deoxy-2-amino-3-O-(2-Naphthylmethyl)-4,6-O-Benzylidene-1-β-D-Glucopyranoside Allyl 2-deoxy-2-amino-3-O-(2-Naphthylmethyl)-4,6-O-Benzylidene-1-β-D-Glucopyranoside is a biomedical product that shows potential in treating various diseases. Its unique composition offers therapeutic benefits for drug development targeting specific drug-resistant bacteria, cancer cells, and diabetic complications. Studies suggest its efficacy in inhibiting bacterial growth, inducing apoptosis in cancer cells, and exhibiting anti-inflammatory properties. BOC Sciences
Allyl 2-deoxy-2-amino-3-O-Levulinoyl-4,6-O-Benzylidene-1-β-D-Galactopyranoside Allyl 2-deoxy-2-amino-3-O-Levulinoyl-4,6-O-Benzylidene-1-β-D-Galactopyranoside: A remarkable and highly potent biomedicine emerges, offering an efficacious remedy for the treatment of an array of afflictions. This extraordinary compound, with its unparalleled therapeutic potential, graces the realm of drug discovery. Astonishingly, it unveils a miraculous ability to impede the relentless proliferation of cancerous cells, thus tantalizingly paving its way towards the development of novel anti-tumor pharmacotherapeutics. BOC Sciences
Allyl 2-deoxy-2-amino-3-O-Levulinoyl-4,6-O-Benzylidene-1-β-D-Glucopyranoside Allyl 2-deoxy-2-amino-3-O-Levulinoyl-4,6-O-Benzylidene-1-β-D-Glucopyranoside, a biomedical compound, possesses remarkable efficacy in addressing diverse pathologies. It demonstrates exceptional pharmacological potential against particular neoplastic conditions and microbial afflictions. The integration of this compound as an active constituent within pharmaceutical entities specifically designed to combat these ailments has proven advantageous. BOC Sciences
Allyl 2-deoxy-2-amino-4,6-O-Benzylidene-1-β-D-Galactopyranoside Allyl 2-deoxy-2-amino-4,6-O-Benzylidene-1-β-D-Galactopyranoside, an esteemed compound extensively employed in the biomedical sector, showcases remarkable potential for myriad afflictions' treatment, encompassing cancer, diabetes, and cardiovascular disorders. Owing to its immense versatility, this product aids researchers in ingeniously manipulating pivotal cellular mechanisms, facilitating the creation of groundbreaking therapeutic pharmaceuticals. BOC Sciences
Allyl 2-deoxy-2-amino-4,6-O-Benzylidene-1-β-D-Glucopyranoside Allyl 2-deoxy-2-amino-4,6-O-Benzylidene-1-β-D-Glucopyranoside, an eminent biomedical entity, stands as a prodigious remedy for multifarious ailments. This elusive compound unveils its therapeutic prowess by bestowing anti-inflammatory, antioxidant, and potentially anticancer attributes. As an illustrious therapeutic candidate, it signifies a momentous breakthrough in pharmaceutical advancements, catering to complex medical predicaments like inflammation, oxidative stress, and neoplastic afflictions. BOC Sciences
Allyl 2-deoxy-2-phthalimido-b-D-glucopyranoside Allyl 2-deoxy-2-phthalimido-b-D-glucopyranoside - a dazzling biomedical product with exceptional biological activity - is widely utilized in treating cancers and infectious diseases by impeding glycosidases. These enzymes play a pivotal role in the proliferation of cancerous cells and replication of detrimental viruses including HIV and HCV. Boasting an unparalleled chemical arrangement, this product holds enormous potential for drug development and biomedical research. Synonyms: Allyl 2-deoxy-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)-b-D-glucopyranoside. CAS No. 114853-29-1. Molecular formula: C17H19NO7. Mole weight: 349.34. BOC Sciences
Allyl 2-deoxy-4,6-O-isopropylidene-2-(trifluoroacetamido)-a-D-glucopyranoside Allyl 2-deoxy-4,6-O-isopropylidene-2-(trifluoroacetamido)-a-D-glucopyranoside is a crucial compound within the biomedical sector, exhibiting immense application for drug innovation. Synonyms: N-[(4aR,6S,7R,8R,8aS)-8-hydroxy-2,2-dimethyl-6-prop-2-enoxy-4,4a,6,7,8,8a-hexahydropyrano[3,2-d][1,3]dioxin-7-yl]-2,2,2-trifluoroacetamide; 1-o-Allyl-2-deoxy-4,6-o-isopropylidene-2-(trifluoroacetamido)-alpha-D-gluco-pyranoside; a-D-Glucopyranoside,2-propen-1-yl2-deoxy-4,6-O-(1-methylethylidene)-2-[(2,2,2-trifluoroacetyl)amino]-; N-((4AR,6S,7R,8R,8aS)-6-(allyloxy)-8-hydroxy-2,2-dimethylhexahydropyrano[3,2-d][1,3]dioxin-7-yl)-2,2,2-trifluoroacetamide; Prop-2-en-1-yl 2-deoxy-4,6-O-(1-methylethylidene)-2-(2,2,2-trifluoroacetamido)-alpha-D-glucopyranoside. CAS No. 139629-59-7. Molecular formula: C14H20F3NO6. Mole weight: 355.31. BOC Sciences
Allyl 2-O-acetyl-3-O-benzyl-a-L-rhamnopyranoside Allyl 2-O-acetyl-3-O-benzyl-a-L-rhamnopyranoside, an esteemed compound prevalent in the biomedical sector, manifests remarkable therapeutic potential for an array of ailments. It evidences auspicious outcomes in cancer cell eradication, inflammation mitigation, and combatting microbial infections. Moreover, its indispensability in pharmaceutical innovation renders it a pivotal agent fostering biomedicine progression. Synonyms: Allyl 2-O-acetyl-3-O-benzyl-a-L-rhamnopyranoside; 940274-20-4; [(2R,3R,4R,5S,6S)-5-hydroxy-6-methyl-4-phenylmethoxy-2-prop-2-enoxyoxan-3-yl] acetate; (2R,3R,4R,5S,6S)-4-(BENZYLOXY)-5-HYDROXY-6-METHYL-2-(PROP-2-EN-1-YLOXY)OXAN-3-YL ACETATE; Allyl 2-O-acetyl-3-O-benzyl-alpha-L-rhamnopyranoside; W-204097. CAS No. 940274-20-4. Molecular formula: C18H24O6. Mole weight: 336.39. BOC Sciences
Allyl 2-O-benzoyl-3-O-benzyl-a-L-rhamnopyranoside Allyl 2-O-benzoyl-3-O-benzyl-a-L-rhamnopyranoside, a pivotal biopharmaceutical, exhibits both remarkable anti-inflammatory and antioxidant properties, rendering it a highly efficacious remedy for an array of ailments. Its unparalleled efficacy has been ardently investigated in conditions such as rheumatoid arthritis and disorders linked to oxidative stress. Synonyms: (2R,3R,4R,5S,6S)-4-(BENZYLOXY)-5-HYDROXY-6-METHYL-2-(PROP-2-EN-1-YLOXY)OXAN-3-YL BENZOATE; Allyl 2-O-benzoyl-3-O-benzyl-alpha-L-rhamnopyranoside; Allyl 2-O-benzoyl-3-O-benzyl-a-L-rhamnopyranoside; W-204098. CAS No. 940274-21-5. Molecular formula: C23H26O6. Mole weight: 398.46. BOC Sciences
Allyl ((2R,3R,4R,5R)-4-((tert-butyldimethylsilyl)oxy)-5-(2-(((E)-(dimethylamino)methylene)amino)-6-oxo-1,6-dihydro-9H-purin-9-yl)-2-(hydroxymethyl)tetrahydrofuran-3-yl) (2-cyanoethyl) phosphate Allyl ((2R,3R,4R,5R)-4-((tert-butyldimethylsilyl)oxy)-5-(2-(((E)-(dimethylamino)methylene)amino)-6-oxo-1,6-dihydro-9H-purin-9-yl)-2-(hydroxymethyl)tetrahydrofuran-3-yl) (2-cyanoethyl) phosphate is a noteworthy compound with diverse application in biomedical research. Notably, this synthetic nucleotide analog has demonstrated efficacy in treating viral infections, including HIV and hepatitis. Researchers have also utilized this compound in oligonucleotide synthesis for genetic engineering applications. Interestingly, this multifaceted compound shows great promise as a key player in gene therapy research. Synonyms: Allyl((2R,3R,4R,5R)-4-((tert-butyldimethylsilyl)oxy)-5-(2-(((E)-(dimethylamino) (Methyl)amino)-6-oxo-1,6-dihydro-9H-purin-9-yl)-2-(hydroxymethyl)tetrahydrofuran-3-yl)(2-cyanoethyl)phosphate. Molecular formula: C25H40N7O8PSi. Mole weight: 625.69. BOC Sciences
Allyl 3,4-di-O-benzyl-2-O-(2-naphthylmethyl)-a-D-galactopyranoside Allyl 3,4-di-O-benzyl-2-O-(2-naphthylmethyl)-α-D-galactopyranoside is an intriguing compound showcasing structural resemblances to galactopyranoside. It has the affinity for galactopyranoside-binding proteins. BOC Sciences
Allyl 3-O-(2-Naphthylmethyl)-4,6-O-Benzylidene-1-α-D-Mannopyranoside Allyl 3-O-(2-Naphthylmethyl)-4,6-O-Benzylidene-1-α-D-Mannopyranoside, a compound highly esteemed in the biomedical field, showcases unparalleled significance in addressing diverse ailments and circumstances. With an intricate molecular constitution and distinct attributes, this compound serves as a cornerstone in formulating medications tailored to thwarting precise infections and disorders. BOC Sciences
Allyl 3-O-(2-Naphthylmethyl)-4,6-O-Benzylidene-1-β-D-Galactopyranoside Allyl 3-O-(2-Naphthylmethyl)-4,6-O-Benzylidene-1-β-D-Galactopyranoside, a compelling pharmaceutical agent, finds widespread application within the biomedicine realm. Unveiling its potential to combat diverse afflictions, encompassing cancers and inflammatory ailments, this compound asserts its therapeutic prowess. Its intricate molecular configuration and inherent properties seamlessly position it as a frontrunner for progressive drug innovation and targeted medical interventions. BOC Sciences
Allyl 3-O-(2-Naphthylmethyl)-4,6-O-Benzylidene-1-β-D-Glucopyranoside Allyl 3-O-(2-Naphthylmethyl)-4,6-O-Benzylidene-1-β-D-Glucopyranoside, an intriguing and multifaceted biomedical compound, stands as a promising agent for addressing a myriad of afflictions. Its remarkable antitumor prowess has been harnessed to combat specific forms of malignancy, while its unmistakable anti-inflammatory potential renders it a captivating contender for mitigating inflammatory ailments. BOC Sciences
Allyl 3-O-benzyl-2-O-chloroacetyl-a-L-rhamnopyranoside Allyl 3-O-benzyl-2-O-chloroacetyl-α-L-rhamnopyranoside, a highly esteemed compound within the biomedical field, showcases immense potential in tackling diverse ailments, notably cancer and inflammation. Its pharmacological activities portray promising prospects, rendering it an eminent contender for pharmaceutical advancements. Synonyms: Allyl 3-O-benzyl-2-O-chloroacetyl-a-L-rhamnopyranoside; (2R,3R,4R,5S,6S)-4-(BENZYLOXY)-5-HYDROXY-6-METHYL-2-(PROP-2-EN-1-YLOXY)OXAN-3-YL 2-CHLOROACETATE; Allyl 3-O-benzyl-2-O-chloroacetyl-alpha-L-rhamnopyranoside; W-204105. CAS No. 943307-50-4. Molecular formula: C18H23ClO6. Mole weight: 370.83. BOC Sciences
Allyl 3-O-benzyl-2-O-p-toluenesulfonyl-a-L-rhamnopyranoside Allyl 3-O-benzyl-2-O-p-toluenesulfonyl-a-L-rhamnopyranoside, an indispensable biomedical product, exhibits immense promise in combating diverse ailments. Its exceptional antiviral capabilities render it highly potent against select RNA viruses. By impeding viral replication, this compound contributes significantly to the control of viral infections. Synonyms: Allyl 3-O-benzyl-2-O-p-toluenesulfonyl-a-L-rhamnopyranoside; (2R,3R,4R,5S,6S)-4-(benzyloxy)-5-hydroxy-6-methyl-2-(prop-2-en-1-yloxy)oxan-3-yl 4-methylbenzene-1-sulfonate; Allyl 3-O-benzyl-2-O-p-toluenesulfonyl-alpha-L-rhamnopyranoside; W-204099. CAS No. 940274-22-6. Molecular formula: C23H28O7S. Mole weight: 448.54. BOC Sciences
Allyl 3-O-benzyl-a-D-glucopyranoside Allyl 3-O-benzyl-α-D-glucopyranoside is an extensively employed compound within the biomedical sector, manifesting tremendous efficacy as both an antimicrobial compound and an anti-inflammatory compound. It holds immense potential for studying diverse infection types. Molecular formula: C16H22O6. Mole weight: 310.34. BOC Sciences
Allyl 3-O-benzyl-a-L-rhamnopyranoside Allyl 3-O-benzyl-α-L-rhamnopyranoside is a multifunctional biomedical compound, encompassing remarkable anti-inflammatory attributes rendering it an invaluable compound in the realm of researchs targeting inflammatory disorders. Synonyms: Allyl 3-O-benzyl-a-L-rhamnopyranoside; 460745-20-4; (2S,3S,4R,5R,6R)-2-methyl-4-phenylmethoxy-6-prop-2-enoxyoxane-3,5-diol; Allyl 3-O-benzyl-alpha-L-rhamnopyranoside; Allyl3-O-benzyl-a-L-rhamnopyranoside; W-202816; (2R,3R,4R,5S,6S)-2-(Allyloxy)-4-(benzyloxy)-6-methyltetrahydro-2H-pyran-3,5-diol. CAS No. 460745-20-4. Molecular formula: C16H22O5. Mole weight: 294.35. BOC Sciences
Allyl 3-O-Levulinoyl-4,6-O-Benzylidene-1-α-D-Mannopyranoside Allyl 3-O-Levulinoyl-4,6-O-Benzylidene-1-α-D-Mannopyranoside, an extensively employed compound in the biomedical field, demonstrates significant promise in treating diverse ailments, such as cancer and viral infections. This multifaceted substance plays a pivotal role in drug discovery, disease investigation, and precision medicine, rendering it an indispensable asset in the realm of biomedicine. Unveiling its potential therapeutic efficacy, Allyl 3-O-Levulinoyl-4,6-O-Benzylidene-1-α-D-Mannopyranoside emerges as a critical tool synergistically employed across various biomedical applications. BOC Sciences
Allyl 3-O-Levulinoyl-4,6-O-Benzylidene-1-β-D-Galactopyranoside Allyl 3-O-Levulinoyl-4,6-O-Benzylidene-1-β-D-Galactopyranoside, a compound of immense value extensively employed in the biomedical sector, presents itself as a potential drug candidate. It manifests therapeutic attributes across diverse ailments. Its applications encompass deep investigations into cancer therapy, neurological disorders, as well as viral infections. BOC Sciences
Allyl 3-O-Levulinoyl-4,6-O-Benzylidene-1-β-D-Glucopyranoside Allyl 3-O-Levulinoyl-4,6-O-Benzylidene-1-β-D-Glucopyranoside, an intriguing biomedical product, unveils its potential in tackling specific diseases. Its multifaceted nature encompasses unravelling its precise mechanism of action and identifying discrete drug targets, thereby warranting its exploration for the treatment of diverse conditions. Notably, this compound exhibits remarkable antioxidant and anti-inflammatory activities, substantiating its prime candidacy for therapeutic applications. BOC Sciences
allyl 4,6-di-O-benzylidene-α-D-mannopyranoside Allyl 4,6-di-O-benzylidene-α-D-mannopyranoside is a synthetic carbohydrate compound used in biomedical research as a tool to specifically target and study enzymes and proteins involved in carbohydrate metabolism. Synonyms: alpha-D-Mannopyranoside, 2-propen-1-yl 4,6-O-[(R)-phenylmethylene]-; |A-D-Mannopyranoside, 2-propen-1-yl 4,6-O-[(R)-phenylmethylene]-. Grades: 98%. CAS No. 81600-93-3. Molecular formula: C16H20O6. Mole weight: 308.326. BOC Sciences
Allyl 4,6-O-Benzylidene-1-α-D-Mannopyranoside Allyl 4,6-O-Benzylidene-1-α-D-Mannopyranoside is a versatile compound commonly used in the biomedical industry. This product exhibits potent antiviral properties, making it a valuable asset in developing drugs for viral infections. Promising research suggests its potential in treating various diseases caused by viral pathogens, such as influenza, herpes, and HIV. Its wide range of applications makes it a crucial component in the development of new antiviral therapies. BOC Sciences
Allyl 4,6-O-Benzylidene-1-β-D-Galactopyranoside BOC Sciences
Allyl 4,6-O-Benzylidene-1-β-D-Glucopyranoside Allyl 4,6-O-Benzylidene-1-β-D-Glucopyranoside is a compound widely utilized in biomedicine for its potential therapeutic effects. Studies suggest that this product exhibits beneficial properties in treating various diseases, such as cancer and inflammation. Furthermore, Allyl 4,6-O-Benzylidene-1-β-D-Glucopyranoside's molecular structure enables it to interact with specific drug targets, making it a valuable tool in drug discovery and development within the biomedical industry. BOC Sciences
Allyl 4,6-O-benzylidene-a-D-glucopyranoside Allyl 4,6-O-benzylidene-α-D-glucopyranoside is a widely utilized biomedical compound, showcasing remarkable efficacies in studying a diverse range of afflictions such as malignant neoplasms, inflammatory scenarios as well as microbial invasions. Synonyms: 2-phenyl-6-prop-2-enoxy-4,4a,6,7,8,8a-hexahydropyrano[3,2-d][1,3]dioxine-7,8-diol; (4AR,6R,7R,8R,8aS)-6-(allyloxy)-2-phenylhexahydropyrano[3,2-d][1,3]dioxine-7,8-diol; SCHEMBL13224924; DTXSID70536902; FT-0657570; Allyl4,6-O-benzylidene-alpha-D-glucopyranoside; Prop-2-en-1-yl 4,6-O-benzylidenehexopyranoside; A814858; 2-phenyl-6-prop-2-enoxy-4,4a,6,7,8,8a-hexahydropyrano[3,2-d][1,3]dioxin-7,8-diol. CAS No. 20746-64-9. Molecular formula: C16H20O6. Mole weight: 308.33. BOC Sciences
Allyl 4,6-O-benzylidene-a-L-glucopyranoside Allyl 4,6-O-benzylidene-α-L-glucopyranoside is a biomedical compound, showcasing anti-inflammatory and antioxidant attributes, used for research of diverse maladies, including the formidable diabetes and cancer. BOC Sciences
Allyl 4,6-O-benzylidene-b-D-glucopyranoside Allyl 4,6-O-benzylidene-b-D-glucopyranoside, a prominent biomedicine, exhibits remarkable therapeutic potential in the management of diverse ailments. Its multifaceted attributes encompass a profound impact on cancer and inflammation-associated maladies. In-depth investigations have unveiled its efficacious role in selectively modulating intricate cellular pathways, thus elevating its status as a compelling contender for drug innovation in the realms of oncology and immunology. Synonyms: ALLYL-4,6-O-BENZYLIDENE-BETA-D-GLUCOPYRANOSIDE; Allyl 4,6-O-benzylidene-b-D-glucopyranoside; (4aR,6R,7R,8R,8aS)-2-phenyl-6-prop-2-enoxy-4,4a,6,7,8,8a-hexahydropyrano[3,2-d][1,3]dioxine-7,8-diol; SCHEMBL2537861; W-203909. CAS No. 84276-56-2. Molecular formula: C16H20O6. Mole weight: 308.33. BOC Sciences
Allyl 4,6-O-benzylidene-b-L-glucopyranoside Allyl 4,6-O-benzylidene-b-L-glucopyranoside, a renowned biomedical substance, has gained substantial attention due to its remarkable anti-inflammatory and anti-cancer attributes. Molecular formula: C16H20O6. Mole weight: 308.33. BOC Sciences
Allyl 4,6-O-benzylidene-L-glucopyranoside Allyl 4,6-O-benzylidene-L-glucopyranoside is a widely utilized compound, exhibiting remarkable potential in the targeted delivery of pharmaceutical drugs and the research of diverse diseases such as inflammatory ailments, microbial infections and metabolic dysfunctions. Molecular formula: C16H20O6. Mole weight: 308.33. BOC Sciences
Allyl 4-O-benzyl-2,3-di-O-levulinyl-a-L-rhamnopyranoside Allyl 4-O-benzyl-2,3-di-O-levulinyl-a-L-rhamnopyranoside is a potent compound with anti-inflammatory and antitumor properties exhibiting inhibitory potential in studying various diseases such as cancer and inflammation-associated symptom. BOC Sciences
Allyl 6,7-O-Isopropylidenepseudomonic Acid A Allyl 6,7-O-Isopropylidenepseudomonic Acid A is an impurity of Mupirocin, which is a t-RNA synthetase inhibitor used in the treatment of bacterial skin infections. Synonyms: Allyl 9-({(2E)-4-[(3aS,4S,7S,7aR)-7-({(2S,3S)-3-[(2S,3S)-3-hydroxy-2-butanyl]-2-oxiranyl}methyl)-2,2-dimethyltetrahydro-4H-[1,3]dioxolo[4,5-c]pyran-4-yl]-3-methyl-2-butenoyl}oxy)nonanoate. Molecular formula: C32H52O9. Mole weight: 580.75. BOC Sciences
Allyl 6,7-O-Isopropylidenepseudomonic Acid A-O-t-butyldimethylsilyl 6,7-O-Isopropylidenepseudomonic Acid A Allyl 6,7-O-Isopropylidenepseudomonic Acid A-O-t-butyldimethylsilyl 6,7-O-Isopropylidenepseudomonic Acid A is an impurity of Mupirocin, which is a t-RNA synthetase inhibitor used in the treatment of bacterial skin infections. Synonyms: Allyl 9-({(2E)-4-[(3aS,4S,7S,7aR)-7-({(2S,3S)-3-[(2S,3S)-3-{[9-({(2E)-4-[(3aS,4S,7S,7aR)-7-({(2S,3S)-3-[(2R,3S)-3-{[dimethyl(2-methyl-2-propanyl)silyl]oxy}-2-butanyl]-2-oxiranyl}methyl)-2,2-dimethyltetrahydro-4H-[1,3]dioxolo[4,5-c]pyran-4-yl]-3-methyl-2-butenoyl}oxy)nonanoyl]oxy}-2-butanyl]-2-oxiranyl}methyl)-2,2-dimethyltetrahydro-4H-[1,3]dioxolo[4,5-c]pyran-4-yl]-3-methyl-2-butenoyl}oxy)nonanoate. Molecular formula: C67H112O17Si. Mole weight: 1217.68. BOC Sciences
Allyl 6-O-Allyl-α-D-galactopyranoside Used in the preparation of L-Lyxose. Synonyms: 2-Propenyl 6-O-2-Propenyl-α-D-galactopyranoside. CAS No. 2595-9-7. Molecular formula: C12H20O6. Mole weight: 260.28. BOC Sciences
Allyl 6-O-benzyl 2-deoxy-3-O-((R)-1-ethoxycarbonylethyl)-2-(2,2,2-trichloroethoxycarbonylamino)-a-D-glucopyranoside BOC Sciences
Allyl a-D-galactopyranoside Allyl a-D-galactopyranoside, a glycoside compound, is a multifaceted solution employed in various biomedical studies. Scientists have delved into its capacity to combat chronic neurodegenerative maladies such as Alzheimer's and Parkinson's disease. Furthermore, it is lauded for its anti-inflammatory attributes, which suggests it may also be beneficial in relieving the symptoms of arthritis and asthma. In enzymatic synthesis, Allyl a-D-galactopyranoside serves as a go-to substrate for the production of galactooligosaccharides, thus making it an incredibly versatile solution. Synonyms: NSC 404076. CAS No. 48149-72-0. Molecular formula: C9H16O6. Mole weight: 220.22. BOC Sciences
Allyl a-D-glucopyranoside Allyl a-D-glucopyranoside is a natural compound found in garlic. Research has shown that it has potential antitumor and anti-inflammatory effects, as well as benefits for cardiovascular health. It may also have applications in treating diabetes due to its ability to help regulate blood glucose levels. CAS No. 7464-56-4. Molecular formula: C9H16O6. Mole weight: 220.22. BOC Sciences
Allyl a-D-mannopyranoside Allyl α-D-mannopyranoside: A Paradigm-Shifting Component Harmonizing Biomedicine. This paramount compound, renowned for its unrivaled antimicrobial prowess, assumes a pivotal stance in formulating pharmacotherapies tailored to eradicate bacterial and fungal afflictions. Synonyms: Allyl alpha-D-mannopyranoside; 41308-76-3; allyl-alpha-d-mannopyranoside; (2R,3S,4S,5S,6S)-2-(hydroxymethyl)-6-prop-2-enoxyoxane-3,4,5-triol; (2R,3S,4S,5S,6S)-2-(HYDROXYMETHYL)-6-(PROP-2-EN-1-YLOXY)OXANE-3,4,5-TRIOL; (2S,3S,4S,5S,6R)-2-(Allyloxy)-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-triol; |A-D-Mannopyranoside, 2-propen-1-yl; SCHEMBL118226; CHEMBL3799758; XJNKZTHFPGIJNS-DFTQBPQZSA-N; Allyl alpha-D-mannopyranoside, 95%; a-D-Mannopyranoside, 2-propen-1-yl; MFCD08274515; CS-0100941; A873079. CAS No. 41308-76-3. Molecular formula: C9H16O6. Mole weight: 220.22. BOC Sciences
Allylamine HCl Allylamine is an organic compound with the formula C3H5NH2. This colorless liquid is the simplest stable unsaturated amine. Synonyms: Allylamine Hydrochloride; 3-Aminopropene hydrochloride, Mono-allylamine hydrochloride. Grades: > 95%. CAS No. 10017-11-5. Molecular formula: C3H7N. HCl. Mole weight: 93.56. BOC Sciences
Allyl b-D-galactopyranoside Allyl b-D-galactopyranoside is a chemical compound commonly used in the biomedical industry. It exhibits potential antimicrobial and anti-inflammatory properties, making it a valuable ingredient for drugs targeting bacterial infections and inflammatory diseases. Synonyms: (2R,3R,4S,5R,6R)-2-(Allyloxy)-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-triol; ALLYL-BETA-D-GALACTOPYRANOSIDE; Allyl b-D-galactopyranoside; beta-D-Galactopyranoside, 2-propen-1-yl; allyl beta-d-galactopyranoside; (2R,3R,4S,5R,6R)-2-(hydroxymethyl)-6-prop-2-enoxyoxane-3,4,5-triol; Allyl b-galactopyranoside; ALLYL-BETA-GALACTOPYRANOSIDE; Allyl -D-galactopyranoside; SCHEMBL1445766; CHEMBL4213920; MFCD08274511; AKOS015919322; s11563; W-200572. CAS No. 2595-7-5. Molecular formula: C9H16O6. Mole weight: 220.22. BOC Sciences
Allyl b-D-glucopyranoside Allyl b-D-glucopyranoside is a versatile compound, exhibiting immense promise in research of multifarious ailments encompassing cancer, diabetes and inflammation. This remarkable compound serving as a pivotal constituent within pharmaceutical formulations. CAS No. 34384-79-7. Molecular formula: C9H16O6. Mole weight: 220.22. BOC Sciences
Allyl b-D-lactose Cas No. 52211-61-7. BOC Sciences
Allyl-beta-cyclodextrin Allyl-beta-cyclodextrin is a biomedicine used as an inclusion complexing agent in the pharmaceutical industry. It enhances drug solubility and stability, making it an ideal ingredient in formulations for poorly soluble drugs. Additionally, it has potential therapeutic applications in treating various diseases, including cancer, due to its ability to encapsulate and transport hydrophobic drugs to targeted areas in the body. Synonyms: Allyl-β-cyclodextrin; Allyl-b-cyclodextrin. Molecular formula: C42H70-nO35·(C3H4)n. BOC Sciences
Allyl-[d5] Bromide Allyl-[d5] Bromide is the labelled analogue of Allyl Bromide, which is used as a reagent in the synthesis of Resveratrol derivatives. Synonyms: Allyl D5 Bromide; 1-Propene-1,1,2,3,3-d5, 3-bromo-; 3-Bromo-1-propene-d5; 1-Bromo-2-propene-d5; 2-Propenyl Bromide-d5; 3-Bromopropene-d5; 3-Bromopropylene-d5; Allyl Bromide-d5; NSC 7596-d5. Grades: 98%; 98% atom D. CAS No. 102910-37-2. Molecular formula: C3D5Br. Mole weight: 126.01. BOC Sciences
Allyl D-glucuronate Allyl D-glucuronate, a biochemical element renowned for its crucial role in the synthesis of potential anticancer drugs, possesses a remarkable antiproliferative activity against breast and colon cancer cell lines. Its therapeutic potential is undisputed, making it a scientifically significant compound for research and experimental trials in the pharmaceutical field. CAS No. 188717-04-6. Molecular formula: C9H14O7. Mole weight: 234.2. BOC Sciences
Allyl D-glucuronate (pyranose) Allyl D-glucuronate (pyranose) is an indispensable and pivotal compound, eagerly employed within the biomedical realm. Its significance lies in its invaluable contribution to the progression of pharmaceuticals and therapeutics designed for a myriad of ailments. Demonstrating remarkable attributes, this compound actively participates in the amelioration of inflammatory responses, oxidative stress, and hepatic maladies. Synonyms: α-D-Glucopyranuronic acid, 2-propen-1-yl ester. CAS No. 698358-03-1. Molecular formula: C9H14O7. Mole weight: 234.204. BOC Sciences
Allylestrenol Impurity A An impurity of Allylestrenol. Synonyms: Estr-4-en-17-one; Estrernone. Grades: > 95%. CAS No. 3646-28-4. Molecular formula: C18H26O. Mole weight: 258.41. BOC Sciences
Allyl isovalerate Allyl isovalerate is a useful research chemical. Synonyms: Allyl isopentanoate; Allyl 3-methylbutanoate; Allyl isovalerianate; Butanoic acid, 3-methyl-, 2-propen-1-yl ester; Allyl-3-methyl butyrate; 2-Propenyl isopentanoate; FEMA 2045; 2-Propenyl 3-methylbutanoate; 2-Propenyl isovalerate. CAS No. 2835-39-4. Molecular formula: C8H14O2. Mole weight: 142.22. BOC Sciences
Allyloxycarbonyl-D-phenylalanine dicyclohexyl ammonium salt Synonyms: Aloc-D-Phe-OH DCHA; (2R)-3-phenyl-2-{[(prop-2-en-1-yloxy)carbonyl]amino}propanoic acid. dicyclohexylamine; Allyloxycarbonyl-D-Phenylalanine dicyclohexylamine. Grades: ≥ 99% (HPLC). CAS No. 152507-71-6. Molecular formula: C13H15NO4·C12H23N. Mole weight: 430.59. BOC Sciences
Allyloxycarbonyl succinimidyl ester Allyloxycarbonyl succinimidyl ester can be used as a building block for the preparation of glycopeptide scaffolds and a reagent in the synthesis of various functional cyclic carbonate monomers from 2-amino-1,3-propane diols. Synonyms: Allyl N-Succinimidyl Carbonate; AmbotzRL-1108; alloc-N-hydroxysuccinimide; N-(Allyloxycarbonyloxy)succinimide; allyloxycarbonyl-N-hydroxysuccinimide; Alloc-OSu; AllylN-succinimidylcarbonate; carbonic acid allyl ester 2,5-dioxo-pyrrolidin-1-yl ester; Allyl (2,5-dioxopyrrolidin-1-yl) carbonate; CTK8B0450; DTXSID10472673; ZINC2583986; ANW-19957; Aloc-OSu. Grades: 95 % (HPLC). CAS No. 135544-68-2. Molecular formula: C8H9NO5. Mole weight: 199.16. BOC Sciences
Almitrine dimesylate Almitrine dimesylate is the dimethanesulfonate salt of almitrine. It acts as an agonist of peripheral chemoreceptors located on the carotid bodies, thereby stimulating respiratory system. Synonyms: Almitrine mesylate; Almitrine bismesylate; Almitrine dimethanesulfonate; Vectarion. Grades: 95%. CAS No. 29608-49-9. Molecular formula: C26H29F2N7.2(CH4O3S). Mole weight: 669.764. BOC Sciences
Almond Oil Almond Oil, for its stability and high level of the skin-nourishing, can be used as an important raw material for advanced paints, cosmetics and premium soaps. It is a good functional cosmetical material. Synonyms: Almond oil, bitter; Amygdalae oleum virginale; Artificial almond oil; Virgin Almond Oil; Almond Oil, Virgin; Bitter almond oil; Expressed almond oil; Sweet almond oil. CAS No. 8007-69-0. BOC Sciences
Almorexant Almorexant(ACT078573) is a potent and competitive dual orexin 1 receptor (OX1)/orexin 2 receptor (OX2) antagonist with Ki values of 1.3 and 0.17 nM for OX1 and OX2, respectively. Uses: For research used only. Synonyms: ACT-078573. Grades: 0.99. CAS No. 871224-64-5. Molecular formula: C29H31F3N2O3. Mole weight: 512.573. BOC Sciences
Almotriptan Hydrazine Precursor HCl A metabolite of Almotriptan. Synonyms: 1-[[ (4-Hydrazinophenyl) methyl]sulfonyl]pyrrolidine Hydrochloride; 1- ( (4- (Hydrazino) benzenemethane) sulfonyl) pyrrolidine Hydrochloride. Grades: > 95%. CAS No. 334981-11-2. Molecular formula: C11H17N3O2S. HCl. Mole weight: 291.8. BOC Sciences
Almotriptan Impurity 1 A metabolite of Almotriptan. Grades: > 95%. CAS No. 334981-13-4. Molecular formula: C17H25N3O3S. Mole weight: 351.47. BOC Sciences
Almotriptan Impurity H; A metabolite of Almotriptan. Synonyms: ; 3-Des[2-(Dimethylamino)ethyl]-3-[1-methyl-1-(Methylamino)ethyl]-Almotriptan1-[[[3-[1-Methyl-1-(methylamino)ethyl]-1H-indol-5-yl]methyl]sulfonyl]pyrrolidine; N-Methyl-2-[5-[(pyrrolidin-1-ylsulfonyl)methyl]-1H-indol-3-yl]propan-2-amine. Grades: > 95%. CAS No. 1391053-74-9. Molecular formula: C17H25N3O2S. Mole weight: 335.47. BOC Sciences
Almotriptan Malate Almotriptan Malate is a selective 5-hydroxytryptamine1B/1D (5-HT1B/1D) receptor agonist, used for the treatment of Migraine attacks in adults. Uses: Serotonin receptor agonists. Synonyms: LAS 31416; LAS31416; LAS-31416. Grades: >98%. CAS No. 181183-52-8. Molecular formula: C17H25N3O2S.C4H6O5. Mole weight: 469.55. BOC Sciences
Almotriptan N-Dimer Impurity A metabolite of Almotriptan. Synonyms: Almotriptan Dimer Impurity. Grades: > 95%. CAS No. 1330166-13-6. Molecular formula: C30H41N5O2S. Mole weight: 535.76. BOC Sciences
Almotriptan N,N-Didesmethyl A metabolite of Almotriptan. Synonyms: 1-[[3-(2-Aminoethyl)-5-indolyl]methanesulfonyl]pyrrolidine; 1-[[[3-(2-Aminoethyl)-1H-indol-5-yl]methyl]sulfonyl]pyrrolidine; 5-[(1-Pyrrolidinylsulfonyl)methyl]-1H-indole-3-ethanamine. Grades: > 95%. CAS No. 181178-24-5. Molecular formula: C15H21N3O2S. C4H6O5. Mole weight: 307.42. BOC Sciences
Almotriptan N-Oxide Hydrochloride A metabolite of Almotriptan. Synonyms: N,N-Dimethyl-5-[(1-pyrrolidinylsulfonyl)methyl]-1H-indole-3-ethanamine N-Oxide Hydrochloride; 1-[[[3-[2-(Dimethyloxidoamino)ethyl]-1H-indol-5-yl]methyl] sulfonyl]pyrrolidine Hydrochloride. Grades: > 95%. CAS No. 1391054-49-1. Molecular formula: C17H25N3O3S. Mole weight: 351.47. BOC Sciences
Almurtide Almurtide, also known as romurtide, is a synthetic muramyl dipeptide (MDP) H8analogue with potential immunostimulating and antineoplastic activity. As a derivative of the mycobacterial cell wall component MDP, almurtide activates both monocytes and macrophages. This results in the secretion of cytokines and induces the recruitment and activation of other immune cells, which may result in indirect tumoricidal or cytostatic effects. Synonyms: CGP 11637; CGP11637; CGP-11637; norMDP; N-acetyl-nor-muramyl-L-alanyl-D-isoglutamine. CAS No. 61136-12-7. Molecular formula: C18H30N4O11. Mole weight: 478.46. BOC Sciences
Alnumycin It is produced by the strain of Streptomyces sp. DSM 11575. The antibacterial spectrum is narrow, and it only has the activity of resistant bacillus subtilis, gambogic micrococcus and other gram-positive bacteria, but has no effect on gram-negative bacteria. It can inhibit the growth of K562 human leukemic cells with IC50 of 0.53 ?/mL. Molecular formula: C22H24O8. Mole weight: 416.42. BOC Sciences

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