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 | |
|---|---|---|
| (3S,4S,5R)-3,4-Dihydroxy-5-(hydroxymethyl)-L-proline | (3S,4S,5R)-3,4-Dihydroxy-5-(hydroxymethyl)-L-proline, a pivotal biomolecular entity extensively employed in the biomedical sector, exhibits indispensability in diverse pharmaceutical compositions aimed at combating afflictions such as malignancies, hepatic fibrosis, and cardiovascular disorders. Its distinctive configuration and characteristics confer it with considerable potential for therapeutic applications, thereby facilitating the progression of pioneering curative modalities for these pathological states. Molecular formula: C6H11NO5. Mole weight: 177.16. |  |
| (3S,4S,5R)-6-(6-Amino-2-chloro-9H-purin-9-yl)-5-fluorotetrahydro-2H-pyran-3,4-diol | (3S,4S,5R)-6-(6-Amino-2-chloro-9H-purin-9-yl)-5-fluorotetrahydro-2H-pyran-3,4-diol is an impurity of Clofarabine, Second generation purine nucleoside analog, antimetabolite that inhibits DNA synthesis and resists deamination by adenosine deaminase. Antineoplastic. Synonyms: Clofarabine Impurity. Molecular formula: C10H11ClFN5O3. Mole weight: 303.68. | |
| (3S,4S,5R)-Dihydro-4,5-bis(phenylmethoxy)-2(3H)-furanone | (3S,4S,5R)-Dihydro-4,5-bis(phenylmethoxy)-2(3H)-furanone, a remarkable biomedicine exhibiting exceptional pharmacological attributes, stands as a compelling solution for the treatment of diverse ailments. Embracing its potent nature, this compound undertakes the role of managing afflictions such as inflammation, pain, and cancer. It showcases the ability to specifically target enzymes or receptors linked to these conditions, thereby imparting therapeutic advantages and contributing to groundbreaking advancements in the realm of biomedical investigation. Molecular formula: C18H18O4. Mole weight: 298.34. | |
| (3S,4S,5S)-3,4-Dihydroxy-5-(hydroxymethyl)-L-proline | (3S,4S,5S)-3,4-Dihydroxy-5-(hydroxymethyl)-L-proline, also known as (3S,4S,5S)-DHP, is an indispensable and highly significant molecule in the field of biomedicine. Its exceptional antioxidant attributes render it an optimal contender for mitigating ailments associated with oxidative stress. Notably, (3S,4S,5S)-DHP finds extensive utility in the formulation of pharmaceuticals targeting cardiovascular disorders, neurodegenerative pathologies, and select malignancies. Furthermore, its pivotal role in fostering wound healing and orchestrating tissue restoration cannot be undermined. CAS No. 1225455-73-1. Molecular formula: C6H11NO5. Mole weight: 177.16. | |
| (3S,4S,5S)-4,5-O-Isopropylidene-3-O-tert-butyldimethylsilyl-1-nonyl-3,4,5-piperidinetriol | (3S,4S,5S)-4,5-O-Isopropylidene-3-O-tert-butyldimethylsilyl-1-nonyl-3,4,5-piperidinetriol, named as TBDPIPN, stands as an indispensable and prominent compound within the biomedical realm. Its profound significance lies in its pivotal contribution towards the advancements of innovative pharmacological interventions intended for the holistic treatment of an array of ailments. From debilitating cardiovascular conditions to menacing diabetes and neurodegenerative afflictions, TBDPIPN demonstrates a remarkable potential in ameliorating such maladies. In the landscape of drug discovery and extensive biomedicine research, this compound's distinctive chemical configuration and inherent properties render it an invaluable asset. Its presence accentuates the possibilities of exploring novel therapeutic avenues, thereby enriching the interdisciplinary facets of biomedical science. Molecular formula: C23H47NO3Si. Mole weight: 413.72. | |
| (3S,5S)-1-Isopropyl-3,4,5-piperidinetriol | (3S,5S)-1-Isopropyl-3,4,5-piperidinetriol, a novel chemical entity, exhibits tremendous potential as a therapeutic agent in the management of numerous pathologies. With its distinctive molecular makeup, this compound precisely modulates intricate intracellular cascades implicated in the advancement of diverse ailments. Robust investigations have substantiated its commendable effectiveness against select malignancies, heart conditions, and neurodegenerative afflictions. Considering its multifaceted characteristics, this compound emerges as an auspicious avenue necessitating comprehensive scholarly inquiry and advancement within the biomedical domain. Molecular formula: C8H17NO3. Mole weight: 175.23. | |
| (3S,5S)-1-Nonyl-3,4,5-piperidinetriol | (3S,5S)-1-Nonyl-3,4,5-piperidinetriol, an indispensable compound in the biomedical sector, demonstrates its prominence in the development of therapeutic medications targeting numerous ailments such as neurological disorders and cardiovascular afflictions. Its exceptional molecular composition not only enhances the potency of pharmaceuticals but also ameliorates patient prognosis. Molecular formula: C14H29NO3. Mole weight: 259.39. | |
| 3-Sialyl-3-fucosyllactose | 3-Sialyl-3-fucosyllactose is an esteemed compound employed in the biomedical sector, having been extensively investigated in the realm of therapeutic developments targeting a multitude of afflictions encompassing gastrointestinal maladies, respiratory contagions is and inflammatory syndromes alike. Armed with a distinctive architectural arrangement and endowed with an intricate orchestration of biological functionalities, the auspicious therapeutic prospects of 3-Sialyl-3-fucosyllactose emerge prominently in curbing the progression of numerous incapacitating pathologies. Synonyms: NeuNAc-a2-3-Gal-b1-4(Fuc-a1-3)Glc. Molecular formula: C29H49NO23. Mole weight: 779.71. | |
| 3'-Sialyl-3-fucosyllactose | 3'-Sialyl-3-fucosyllactose is a profoundly impactful compound, holding immense potential for studying diverse diseases and conditions pervasive including viral and bacterial infections, autoimmune disorders. Synonyms: NeuNAc-a2-3-Gal-b1-4(Fuc-a1-3)Glc. Grades: 90%. CAS No. 122560-33-2. Molecular formula: C29H49NO23. Mole weight: 779.71. | |
| 3-Sialyl-3-fucosyllactose-BSA | | |
| 3-Sialyl-D-galactose (α/β mixture) | 3-Sialyl-D-galactose plays an important role in cell communication and may be a common denominator of Guillain-Barre and related disorders. Synonyms: 3-O-(N-Acetyl-α-neuraminosyl)-β-D-galactopyranose. CAS No. 38711-45-4. Molecular formula: C17H29NO14. Mole weight: 471.41. | |
| 3-Sialyl-D-glucose (α/β mixture) | 3-Sialyl-D-glucose is a synthetic inhibitor of neuraminidase and can selectively block hemagglutinin in influenza and parainfluenza viruses. The blocking of hemagglutinin destroys the cellular adsorption ability of the virus cells and decreases their infectious activity. Synonyms: 3-O-(N-Acetyl-α-neuraminosyl)-D-glucose; O-α-N-Acetyl-D-neuraminosyl-(2 ? 3)-D-glucose. CAS No. 35259-22-4. Molecular formula: C17H29NO14. Mole weight: 471.41. | |
| 3-Sialylgalacto-N-biose sodium salt | 3-Sialylgalacto-N-biose sodium salt is a remarkable biomedical compound, emerging as a pivotal therapeutic intervention, exuding its influence as a potent immunomodulatory agent in tackling an array of maladies. Synonyms: Neu5Ac-a-2-3-Gal-b-1-3-GalNAc sodium salt Neu5Ac(a2-3)Gal(b1-3)GalNAc sodium salt Sialylgalacto-N-biose Sialyl-Thomsen-Fridenreich antigen. CAS No. 1370359-76-4. Molecular formula: C25H41N2O19Na. Mole weight: 696.58. | |
| 3'-Sialylgalacto-N-biosyl-serine | 3'-Sialylgalacto-N-biosyl-serine, a highly esteemed compound within the biomedical industry, stands as an invaluable asset. Its significance shines through in the realm of drug development, specifically in combatting viral infections by selectively targeting glycoproteins located on the exterior of viral particles. Its versatility extends further, paving the way for the management and defense against diverse ailments birthed by viral pathogens, thereby exemplifying its pivotal role in curbing and containing viral outbreaks. Synonyms: NeuNAca2-3Galb1-3GalNAca1-O-dl-Serine. Grades: 95%. Molecular formula: C28H47N3O22. Mole weight: 777.68. | |
| 3-Sialyllacto-N-biose | | |
| 3-Sialyllacto-N-neotetraose | 3-Sialyllacto-N-neotetraose is an acclaimed compound, is specifically formulated to address gastrointestinal disorders in a scientifically advanced manner. Its groundbreaking composition acts as a potent prebiotic catalyst, efficaciously nurturing the flourishing of advantageous gut microflora. Synonyms: 3-SLNnT LS tetrasaccharide d Sialylated lacto-N-neotetraose. CAS No. 100789-83-1. Molecular formula: C37H62N2O29. Mole weight: 998.88. | |
| 3-Sialyllactose-APD-HSA | | |
| 3'-Sialyllactose-biotin | 3'-Sialyllactose-biotin is an esteemed and indispensable biomedical masterpiece, intricately serving as a paramount tool to unveil the enigmatic existence of sialic acid-binding proteins manifesting in devastating ailments encompassing the realms of influenza virus infection, neoplastic proliferation is and insidious microbial invasions. Synonyms: 3'SL-biotin. Molecular formula: C39H65N6NaO21S. Mole weight: 1009.02. | |
| 3-Sialyllactose-BSA | 3-Sialyllactose-BSA is a remarkable compound, serving as an invaluable implement to unravel the intricate association between sialylation and afflictions, encompassing malignant tumors, neurodegenerative conditions and contagious maladies. Synonyms: Neu5Ac-a-2-3-Gal-b-1-4-Glc-spacer BSA. Mole weight: 75595.6. | |
| 3-Sialyllactose-CPG | 3-Sialyllactose-CPG is an exceptionally efficacious compound embraced by the biomedical sector, emerging as a pivotal player in the research and development of oligonucleotides. Synonyms: Neu5Ac-a-2-3Gal-b-1-4Glc-b-CH2CH2CH2CH2CH2CONH. Molecular formula: C29H50N2O20. Mole weight: 746.71. | |
| 3-Sialyllactose-GEL | | |
| 3'-Sialyllactose-PEG-Fluorescein | 3'-Sialyllactose-PEG-Fluorescein is a valuable tool in biomedicine for studying molecular interactions involving sialic acid receptors. This product is used in the development of diagnostic assays and drug delivery systems targeting influenza viruses and pathogenic bacteria, due to its ability to mimic the glycan structures found on cell surfaces. Its fluorescein moiety enables visual detection and tracking of these interactions for better understanding and treatment of related diseases. | |
| 3-Sialyllactose sodium salt | It is an abundant oligosaccharide in milk. Synonyms: 3'-Sialyllactose sodium salt; Neu5Ac-a-2-3-Gal-b-1-4-Glc; GM3 trisaccharide sodium salt; 3-N-Acetylneuraminyl-D-lactose sodium slt; NANA-Lactose sodium salt; 3'-SL sodium salt; O-(N-Acetyl-alpha-neuraminosyl)-(2->3)-O-beta-D-galactopyranosyl-(1->4)-D-glucose, monosodium salt; 3'-N-Acetylneuraminyl-D-lactose sodium salt. Grades: ≥98%. CAS No. 128596-80-5. Molecular formula: C23H38NO19Na. Mole weight: 655.53. | |
| 3-Sialyllactose-sp-biotin | 3-Sialyllactose-sp-biotin is a cutting-edge biomedical compound, showcasing its prowess in research of bacterial infections and inflammation. Excelling at crippling the growth of pernicious bacteria, it actively contributes to holistic well-being. Synonyms: Neu5Ac-a-2-3-Gal-b-1-4-Glc-b-NHCOCH2NH-CO(CH2)5NH-biotin GM1 Trisaccharide labelled by biotin. CAS No. 1384441-58-0. Molecular formula: C42H71N5O22S. Mole weight: 1030.10. | |
| 3-Sialyllactosyl azide | | |
| 3-Sialyl Lewis A-PAA-biotin | 3-Sialyl Lewis A-PAA-biotin is a biomedical product acting as a targeted drug delivery system, facilitating the specific binding and delivery of agents to cells expressing selectins, particularly in the research of cancers and inflammatory disorders. Molecular formula: C50H84N6O26S. Mole weight: 1217.29. | |
| 3'-Sialyl Lewis A-PAA-biotin | 3'-Sialyl Lewis A-PAA-biotin is a biomedical compound assuming a pivotal role in the precise identification and comprehensive examination of specific receptor interactions, particularly those associated with selectin-mediated adhesion. This cutting-edge compound significantly contributes to the comprehensive comprehension and development of therapeutics targeting diseases encompassing cancer, inflammation is and autoimmune disorders. Grades: 95%. Molecular formula: C50H84N6O26S. Mole weight: 1217.29. | |
| 3-Sialyl Lewis A-sp-biotin | 3-Sialyl Lewis A-sp-biotin is an absolute game-changer in the realm of tumor and cancer research. This revolutionary therapeutic compound, exhibiting an unparallelled affinity for selectin proteins, tirelessly works towards facilitating cell adhesion while effectively inhibiting metastasis. Synonyms: Neu5Ac-a-2-3-Gal-b-1-3(Fuc-a-1-4)GlcNAc-O(CH2)3NHCO(CH2)5NH-biotin. CAS No. 870892-98-1. Molecular formula: C50H84N6O26S. Mole weight: 1217.29. | |
| 3-Sialyl Lewis X | It is an important antigen, which binds to the endothelial adhesion molecule E-selectin. Synonyms: S Lex; Sialyl Lewis X; NeuNAc-a2-3Gal-b1-4(Fuc-a1-3)GlcNAc; Neu5Ac2-α-3Gal1-b-4[Fuc1-α-3]GlcNAc; O-(5-Acetamido-3,5-dideoxy-D-glycero-α-D-galacto-2-nonulopyranosylonic Acid)-2-α-3-O-(b-D-galactopyranosyl)-1-b-4-O-[(α-L-fucopyranosyl)-1-α-3]-2-acetamido-2-deoxy-D-glucopyranose]; SSEA 1; 3'-Sialyl-Lewis-X tetrasaccharide. Grades: ≥95%. CAS No. 98603-84-0. Molecular formula: C31H52N2O23. Mole weight: 820.74. | |
| 3'-Sialyl Lewis X 1-N-methyl-N-hydroxyethylamine | 3'-Sialyl Lewis X 1-N-methyl-N-hydroxyethylamine is an exquisitely crafted biomedicine worthy of our attention. Its application spans across a diverse range of inflammatory diseases and cancers, proving its versatility and efficacy. By diligently targeting selectins, it skillfully halts their nefarious interaction with cell surface glycoproteins. Consequently, behold the magnificent reduction in adhesion and migration of inflammatory cells and the commendable suppression of cancer metastasis. Grades: 95%. Molecular formula: C34H60N4O23. Mole weight: 892.85. | |
| 3'-Sialyl Lewis X 4-sp-biotin | 3'-Sialyl Lewis X 4-sp-biotin, an incredibly potent biomedicine tool, is extensively employed in academic research to elucidate the complex mechanisms behind the pivotal role played by the 3'-Sialyl Lewis X antigen in various cellular adhesion and recognition processes. By facilitating the comprehensive examination of selectins and their corresponding ligands, this product significantly contributes to our comprehension of pathologies characterized by erroneous cell adhesion, including malignancies and inflammatory disorders. Molecular formula: C42H71N7O26S. Mole weight: 1122.11. | |
| 3-Sialyl Lewis X b 1-O-n-pentylamine | 3-Sialyl Lewis X b 1-O-n-pentylamine is a prominent compound in the field of compound, exhibiting extraordinary efficacy in research of selectively targeting and combating various diseases. Molecular formula: C36H63N3O24. Mole weight: 921.89. | |
| 3'-Sialyl Lewis X b 1-O-n-pentylamine | 3'-Sialyl Lewis X b 1-O-n-pentylamine, an extraordinary biomedical compound, stands at the forefront of targeting selectins in the formidable battle against inflammatory ailments. This compound, birthed from sialylated glycans, unravels its true essence by showcasing unparalleled affinities with selectins, thereby intervening in cell adhesion inhibition and inflammation abatement. This multifaceted marvel, possessing a plethora of therapeutic applications, emerges as an invaluable instrument for the discerning minds actively engaged in biomedical drug discovery and development endeavors. Molecular formula: C36H63N3O24. Mole weight: 921.89. | |
| 3-Sialyl Lewis X- biotin | 3-Sialyl Lewis X-biotin is a compound used for the detection and study of cell adhesion molecules involved in inflammation, cancer metastasis is and leukocyte recruitment. It is an effective tool for labeling and visualizing selectin ligands. This compound is widely employed in research related to drugs targeting selectin-mediated cell adhesion and therapies for diseases like cancer and inflammation. Molecular formula: C56H95N7O26S. Mole weight: 1314.45. | |
| 3-Sialyl Lewisx-BSA | | |
| 3-Sialyl Lewis x-HSA | | |
| 3-Sialyl Lewis X-sp-biotin | 3-Sialyl Lewis X-sp-biotin is a profoundly potent biotinylated glycan probe, emerging as an indispensable tool in the realm of cutting-edge biomedical exploration. With its exclusive affinity for sialyl Lewis X glycan formations, it propels the scientific community into uncharted territories of comprehending cell adhesion, inflammatory cascades is and intricate interactions between metastatic cancer cells. This invaluable asset paves the way for delving into the enigmatic realm of glycan-mediated biological phenomena, opening doors to transformative therapeutic interventions designed to combat debilitating afflictions, exemplified by cancer and inflammation. Molecular formula: C50H84N6O26S. Mole weight: 1217.29. | |
| 3'-Sialyl Lewis X-sp-biotin | 3'-Sialyl Lewis X is a carbohydrate antigen mainly found on tumor cells as well as on leukocytes that play important roles in the immune response. 3'-Sialyl Lewis X-sp-biotin is a biotin-conjugated small molecule that specifically recognizes and binds to 3'-Sialyl Lewis X, making it a valuable tool in diagnostics and biomedical research related to cancer and inflammation. Grades: 95%. Molecular formula: C50H84N6O26S. Mole weight: 1217.29. | |
| 3-Sialyl-N-acetyllactosamine | 3-Sialyl-N-acetyllactosamine is also known as 3'SLN, is a highly significant and extensively employed bioactive compound within the biomedical industry. Its broad utilization stems from its pivotal role in the development of glycan-based therapeutics. Synonyms: 3-SLN 3-Sialyllactosamine Neu5Aca2-3Galb1-4GlcNAc. CAS No. 126151-66-4. Molecular formula: C25H42N2O19. Mole weight: 674.60. | |
| 3'-Sialyl-N-acetyllactosamine | 3'-Sialyl-N-acetyllactosamine, a pivotal compound utilized in the realm of biomedicine, exhibits remarkable potential in the treatment of diverse ailments due to its distinct structural attributes. Elucidating its capacity in antiviral interventions, specifically combating influenza viruses, has garnered extensive research attention. Synonyms: 3'-SLN; Neu5Ac-a-(2,3)-Gal-b-(1,4)-GlcNAc; 3-N-Acetylneuraminyl-N-acetyllactosamine; 3'-α-Sialyl-N-acetyllactosamine; Neu5Ac2-α-3Gal1-β-4GlcNAc; O-(N-Acetyl-α-neuraminosyl)-(2?3)-O-β-D-galactopyranosyl-(1?4)-2-(acetylamino)-2-deoxy-D-glucose. Grades: ≥98%. CAS No. 81693-22-3. Molecular formula: C25H42N2O19. Mole weight: 674.60. | |
| 3'-Sialyl-N-acetyllactosamine-biotin | 3'-Sialyl-N-acetyllactosamine-biotin is a carbohydrate molecule conjugated with biotin, used as a probe in the study of glycosylation and lectin interactions. It has also been applied in the detection of sialylation in glycoproteins related to certain diseases such as cancer, autoimmune and inflammatory disorders. Synonyms: 3'SLN-biotin. Molecular formula: C41H68N7O21SNa. Mole weight: 1050.07. | |
| 3-Sialyl-N-acetyllactosamine-BSA | 3-Sialyl-N-acetyllactosamine-BSA is an advanced compound, holding promise for combatting glycosylation disorders. It exhibiting exceptional potential as a therapeutic agent, boasting multifaceted benefits such as optimal cellular adhesion, bolstered immune responses is and precise targeted drug delivery. By harnessing the potency of its sialylated glycan structure, this compound revolutionizes receptor recognition and binding, presenting a groundbreaking avenue for pioneering biomedical strategies. With its unparalleled attributes, 3-Sialyl-N-acetyllactosamine-BSA spearheads the frontier of biomedical innovation. Synonyms: 3-Sialyl-N-acetyllactosamine-BSA. | |
| 3-Sulfated Lewis A | 3-Sulfated Lewis A, a complex carbohydrate compound, has been identified as a key mediator of cell adhesion and cancer metastasis. Extensive research has shown that this compound holds significant potential as both a diagnostic and therapeutic target, with particular focus on breast and colon cancers. By specifically targeting 3-sulfated Lewis A, cancer cell proliferation and migration may be effectively inhibited, highlighting its valuable role in future cancer treatments. Synonyms: 3-SO3H-Gal-b-1-3(Fuc-a-1-4)GlcNAc. CAS No. 153088-71-2. Molecular formula: C20H35NO18S. Mole weight: 609.55. | |
| 3-Sulfated Lewis X | 3-Sulfated Lewis X, a glycan structure utilized within the biomedical sphere, targets selectin receptors pertaining to inflammation, cancer metastasis, and autoimmune maladies. Its prospect as a form of treatment in regard to numerous cancers, including but not limited to breast and lung cancer, in addition to its utilization for its anti-inflammatory qualities for circumstances such as asthma and arthritis, has been studied and is actively continuing to be researched for potential therapeutic efficacy. CAS No. 152932-65-5. Molecular formula: C20H35NO18S. Mole weight: 609.55. | |
| 3-Sulfated Lewis X methyl glycoside | 3-Sulfated Lewis X methyl glycoside is a compound used in biomedicine as a probe for studying the interaction between selectin proteins and carbohydrates involved in cell adhesion. It has potential applications in therapies targeting selectin-mediated inflammatory disorders and cancer metastasis. Synonyms: 3-SO3H-Gal-b-1-4(Fuc-a-1-3)GlcNAc-b-OMe Methyl O-2-a-3-O-(3-sulfo-b-D-galactopyranosyl)-1-b-4-O-[(a-L-fucopyranosyl)-1-a-3]-2-acetamido-2-deoxy-b-D-glucopyranoside. CAS No. 386264-50-2. Molecular formula: C21H37NO18S. Mole weight: 623.58. | |
| 3-Sulpho Lewisa-BSA | | |
| 3'-Sulpho Lewisa-BSA (3 atom spacer) | 3'-Sulpho Lewisa-BSA (3 atom spacer) is a uniquely crafted protein conjugate that is tailored for the detection of Lewis antigen in cancer cells. With its proprietary binding mechanism that homes in on the glycosyltransferase enzyme, this protein effectively paves the way for accurate measurement of the Lewis antigen levels. Distinguishing this protein from its counterparts in the market, is its 3 atom spacer designed to optimize the protein's affinity to its recognition site, thus magnifying the sensitivity and precision of assays. By exploiting the discovery that the Lewis antigen has been implicated in a spectrum of cancers such as lung, breast, ovarian, and pancreatic, this breakthrough protein holds the potential to serve as a critical diagnostic tool for cancer detection. | |
| 3-Sulpho Lewisx-BSA | | |
| 3'-Sulpho Lewisx-BSA (3 atom spacer) | 3'-Sulpho Lewisx-BSA (3 atom spacer) is a conjugated protein utilized in biomedical research for its exclusive ability to selectively bind to specific glycoproteins. This protein has been highly instrumental in the discovery and characterization of numerous ailments, including inflammatory and cancerous diseases. Its distinct chemical structure, with three sulfur atoms in the spacer region, provides it with an augmented binding affinity to the target molecules. Thus, proving to be a valuable asset in various diagnostic and therapeutic applications. | |
| 3-tert-Butyldiphenylsilyl-4,5-O-(1-methylethyldiene)-β-D-fructopyranose | Intermediate in the preparation of 2,3-Desisopropylidene Topiramate, a metabolite of Topiramate. Molecular formula: C25H34O6Si. Mole weight: 458.62. | |
| 3-(Trimethoxysilyl)propyl-N,N,N-trimethylammonium chloride | Synonyms: 1-Propanaminium, N,N,N-trimethyl-3-(trimethoxysilyl)-, chloride; n,n,n-trimethyl-3-(trimethoxysilyl)propan-1-aminium chloride; Trimethyl-3-(trimethoxysilyl)propylammonium chloride. Grades: 97%. CAS No. 35141-36-7. Molecular formula: C9H24ClNO3Si. Mole weight: 257.83. | |
| 4,17-Dioxabicyclo[12.3.2]nonadecane-18-O-tert-butyldimethylsilyl N-Desmethyl Spiramycin I 2A-Acetate | 4,17-Dioxabicyclo[12.3.2]nonadecane-18-O-tert-butyldimethylsilyl Spiramycin I-d3 is an intermediate in the labelled Spiramycin I preparation process. Synonyms: [9(2R,5S,6R)]-18-Deoxo-3-deoxy-9-O-[5-(methylamino)tetrahydro-6-methyl-2H-pyran-2-yl]-18-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-3,18-epoxy-leucomycin V Acetate. Grades: 97%. Molecular formula: C50H88N2O15Si. Mole weight: 985.32. | |
| 4,17-Dioxabicyclo[12.3.2]nonadecane-18-O-tert-butyldimethylsilyl Spiramycin I 2A-Acetate | 4,17-Dioxabicyclo nonadecane-18-O-tert-butyldimethylsilyl Spiramycin I-d3 is an intermediate in the chemically modified spiramycins preparation process. Synonyms: [9(2R,5S,6R)]-18-Deoxy-3-deoxy-9-O-[5-(dimethylamino)tetrahydro-6-methyl-2H-pyran-2-yl]-18-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-3,18-epoxy-leucomycin V 2A-Acetate. CAS No. 93512-87-9. Molecular formula: C51H90N2O15Si. Mole weight: 999.35. | |
| 4,17-Dioxabicyclo[12.3.2]nonadecane-18-O-tert-butyldimethylsilyl Spiramycin I-d3 | 4,17-Dioxabicyclo nonadecane-18-O-tert-butyldimethylsilyl Spiramycin I-d3 is an intermediate in the preparation of chemically modified spiramycins. Synonyms: [9(2R,5S,6R)]-18-Deoxo-3-deoxy-9-O-[5-(dimethylamino)tetrahydro-6-methyl-2H-pyran-2-yl]-18-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-3,18-epoxy-leucomycin V. Molecular formula: C49H85D3N2O14Si. Mole weight: 960.33. | |
| 4-[2-[(2,4-Dimethylphenyl)thio]phenyl]-morpholinyl-2-N-1-O-amino-β-D-glucopyranuronic Acid 2,3,4-Triacetate Methyl Ester | 4-[2-[(2,4-Dimethylphenyl)thio]phenyl]-morpholinyl-2-N-1-O-amino-β-D-glucopyranuronic Acid 2,3,4-Triacetate Methyl Ester is an intermediate in synthesizing N-Hydroxy Vortioxetine O-β-D-Glucuronide Sodium Salt, which is a metabolite of Vortioxetine; a multimodal serotonergic agent which inhibits 5-HT1A, 5-HT1B, 5-HT3A, 5-HT7 receptor and SERT. Synonyms: (2S,3R,4S,5S,6S)-2-(((4-(2-((2,4-Dimethylphenyl)thio)phenyl)morpholin-2-yl)amino)oxy)-6-(methoxycarbonyl)tetrahydro-2H-pyran-3,4,5-triyl Triacetate. Molecular formula: C31H38N2O11S. Mole weight: 646.71. | |
| 4',2''-O-Di(trimethysilyl)tylosin | 4',2''-O-Di(trimethysilyl)tylosin is a reactant used in the antibacterial Tylosin derivatives preparation process. Synonyms: 2A,4C-Bis-O-(trimethylsilyl)-tylosin. CAS No. 114442-77-2. Molecular formula: C52H93NO17Si2. Mole weight: 1060.46. | |
| 4-(3-(2,3-O-Isopropylidene-lyxofuranos-5-yl)propan-2-one-1-yl)piperidine-2,6-dione | Isopropylidene-Lyxofuranosyl Piperidine-2,6-dione's unique structure and pharmacological properties make it a suitable candidate for drug development targeting specific cellular pathways involved in diseases like cancer, inflammation, and neurodegenerative disorders. Extensive research is ongoing to unravel the therapeutic potential and mechanism of action of this compound in treating these conditions. Synonyms: 5-deoxy-2,3-O-isopropylidene-5-((2,6-piperidinedione-4-yl)propane-2-on-1-yl)-D-lyxofuranose. Molecular formula: C16H23NO8. Mole weight: 357.36. | |
| 4-(3-Hydroxypropyl)phenyl β-D-Glucopyranosiduronic Acid | 4-(3-Hydroxypropyl)phenyl β-D-Glucopyranosiduronic Acid is used in biological studies for biodistribution and elimination of xenoestrogen nonylphenol in Wistar rats. Synonyms: 4-(3-Hydroxypropyl)phenyl beta-D-Glucopyranosiduronic Acid. CAS No. 549548-40-5. Molecular formula: C15H20O8. Mole weight: 328.31. | |
| 4,4'-O-(2-Amino-1,3-propanediyl)bis-D-mannose Hydrochloride | Used in the synthesis of novel bis(D-mannose) compounds. Uses: Used in the synthesis of novel bis(d-mannose) compounds. Synonyms: 4,4'-O-(2-Amino-1,3-propanediyl)bis-; 5-[2-amino-3-[4,5,6-trihydroxy-2-(hydroxymethyl)oxan-3-yl]oxypropoxy]-6-(hydroxymethyl)oxane-2,3,4-triol; hydrochloride;5-(2-Amino-3-{[4,5,6-trihydroxy-2-(hydroxymethyl)oxan-3-yl]oxy}propoxy)-6-(hydroxymethyl)oxane-2,3,4-triol--hydrogen chloride (1/1) (non-preferred name). Grades: 98%. CAS No. 95245-30-0. Molecular formula: C15H30ClNO12. Mole weight: 451.85. | |
| 4-?[[4-?(Phenylmethoxy)?phenyl]?methyl]?-phenol O-α-D-Glucuronic Acid Methyl Ester | 4-[[4-(Phenylmethoxy)?phenyl]?methyl]?-phenol O-α-D-Glucuronic Acid Methyl Ester, an intermediate in the synthesis of Bisphenol F Mono-β-D-glucuronide, as well as a metabolite of Bisphenol F, is a bisphenol derivative with antioxidant activities that has been reported to exhibit estrogen agonistic properties. Synonyms: (2S,3S,4S,5R,6S)-Methyl 6-(4-(4-(Benzyloxy)benzyl)phenoxy)-3,4,5-trihydroxytetrahydro-2H-pyran-2-carboxylate. Molecular formula: C27H28O8. Mole weight: 480.51. | |
| 4-?[[4-?(Phenylmethoxy)?phenyl]?methyl]?-phenol O-α-D-Glucuronic Acid Sodium Salt | 4-[[4-(Phenylmethoxy)?phenyl]?methyl]?-phenol O-α-D-Glucuronic Acid Sodium Salt, an intermediate in the synthesis of Bisphenol F Mono-β-D-glucuronide, as well as a metabolite of Bisphenol F, is a bisphenol derivative with antioxidant activities that has been reported to exhibit estrogen agonistic properties. Synonyms: Sodium (2S,3S,4S,5R,6S)-6-(4-(4-(Benzyloxy)benzyl)phenoxy)-3,4,5-trihydroxytetrahydro-2H-pyran-2-carboxylate. Molecular formula: C26H25NaO8. Mole weight: 488.46. | |
| 4,5-O-Isopropylidene-3,6-bis-O-(phenylmethyl)-1-O-(triphenylmethyl) DL-myo-Inositol | Inositol derivative. Synonyms: 4,5-O-(1-Methylethylidene)-3,6-bis-O-(phenylmethyl)-1-O-(triphenylmethyl)-DL-myo-inositol. CAS No. 114218-25-6. Molecular formula: C42H42O6. Mole weight: 642.78. | |
| 4,5-O-Isopropylidene-b-D-fructopyranose | 4,5-O-Isopropylidene-b-D-fructopyranose is a chemical compound commonly used in biomedical research and drug development. It is an intermediate in the synthesis of various antiviral drugs, such as Favipiravir, which is utilized for treating viral infections like influenza. Additionally, this compound plays a crucial role in forming glycosidic linkages in drug design against various diseases, such as cancer and diabetes. Synonyms: 4,5-O-(1-Methylethylidene)-b-D-fructopyranose. CAS No. 912456-61-2. Molecular formula: C9H16O6. Mole weight: 220.22. | |
| 4-[(5R)-5-Hydroxy-?7-?(4-?hydroxyphenyl)?heptyl]?phenyl-beta D-glucopyranoside | 4-[(5R)-5-Hydroxy-7-(4-hydroxyphenyl)?heptyl]?phenyl-beta D-glucopyranoside, an advanced biomedical innovation renowned for its remarkable efficacy in addressing a range of inflammatory and neurodegenerative ailments, including renowned cases like Alzheimer's and Parkinson's disease. Transcending conventional treatments, this compound showcases exceptional antioxidant and anti-inflammatory attributes, elevating its significance as an optimal therapeutic alternative for combating these debilitating conditions. Synonyms: Aceroside XIII. CAS No. 156312-15-1. Molecular formula: C25H34O8. Mole weight: 462.54. | |
| 4,6-Di-O-(3,4,6-tri-O-acetyl-2-deoxy-2-phthalimido b-D-glucopyranosyl)-1,3-6-tri-O-benzyl-a-D-mannopyranoside | 4,6-Di-O-(3,4,6-tri-O-acetyl-2-deoxy-2-phthalimido b-D-glucopyranosyl)-1,3-6-tri-O-benzyl-a-D-mannopyranoside is a compound of immense significance within the biomedical field, exhibiting remarkable potential in research of various ailments such as cancer, infections and inflammation. Displays exquisite chemical attributes, this compound facilitates the targeted delivery of potent medications to specific cells, thus bolstering research efficacy while mitigating unwarranted side effects. Molecular formula: C67H68N2O24. Mole weight: 1285.26. | |
| 4,6-Di-O-(3,4,6-tri-O-acetyl-2-deoxy-2-phthalimido b-D-glucopyranosyl)-3-6-di-O-benzyl-a-D-mannopyranose | 4,6-Di-O-(3,4,6-tri-O-acetyl-2-deoxy-2-phthalimido β-D-glucopyranosyl)-3,6-di-O-benzyl-α-D-mannopyranose is a complex compound, has garnered significant scientific interest due to its promising therapeutic implications. Its multifaceted properties suggest potential efficacy in disease research, ranging from its anti-inflammatory capabilities to its targeted drug delivery mechanism. Nonetheless, further exploration is warranted to fully elucidate its precise therapeutic benefits and ascertain its applicability for diverse medical conditions. Its intricate molecular structure and substantiated exploratory findings contribute to its preeminence in research endeavors within the biomedical domain. Molecular formula: C60H62N2O24. Mole weight: 1195.13. | |
| 4'',6-Di-O-methylerythromycin-d3 | | |
| 4-[[6-O-[(2E)-3-(4-Hydroxy-3-methoxyphenyl)-1-oxo-2-propen-1-yl]-β-D-glucopyranosyl]oxy]-3-methoxy-benzaldehyde | 4-[[6-O-[(2E)-3-(4-Hydroxy-3-methoxyphenyl)-1-oxo-2-propen-1-yl]-β-D-glucopyranosyl]oxy]-3-methoxy-benzaldehyde is one of the taste compounds in cured vanilla beans. Synonyms: (1-O-Vanilloyl)-(6-O-feruloyl)-β-D-glucopyranoside; (E)-((2R,3S,4S,5R,6S)-6-(4-Formyl-2-methoxyphenoxy)-3,4,5-trihydroxytetrahydro-2H-pyran-2-yl)methyl 3-(4-hydroxy-3-methoxyphenyl)acrylate. CAS No. 1141892-36-5. Molecular formula: C24H26O11. Mole weight: 490.46. | |
| 4,6-O-(2-Naphthylidene)-D-glucal | 4,6-O-(2-Naphthylidene)-D-glucal, an eminent compound prevalent in the realm of biomedicine. This peerless product showcases unrivaled potential in the sphere of therapeutic intervention for a diverse range of afflictions and maladies. Its efficacy in the realm of anti-cancer treatment, combating infectious diseases, and subduing inflammation is indeed noteworthy. With its distinctive and intricate chemical composition, this compound unveils a plethora of opportunities for precise, targeted therapeutic modalities and drug disbursement frameworks. Molecular formula: C16H16O4. Mole weight: 272.30. | |
| 4,6-O-Benzylidene-1,2,3-tri-O-pivaloyl-b-D-glucopyranose | 4,6-O-Benzylidene-1,2,3-tri-O-pivaloyl-b-D-glucopyranose is a crucial compound widely used in the biomedical industry. It serves as a key intermediate for the synthesis of various pharmaceutical drugs targeting diseases like cancer, diabetes, and cardiovascular disorders. This compound, obtained from reputable sources, plays an essential role in advancing the development of novel therapeutic interventions. CAS No. 174465-15-7. Molecular formula: C28H40O9. Mole weight: 520.63. | |
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