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| Product | Description | |
|---|---|---|
| Allyl 1,1,2,3,3,3-hexafluoropropyl ether | Allyl 1,1,2,3,3,3-hexafluoropropyl ether. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Allyl 2H-perfluoropropyl ether, 371939_ALDRICH, 2H-Perfluoropropyl 2-propenyl ether, EINECS 261-635-9, CID100972, ZINC04269689, Allyl 1,1,2,3,3,3-hexafluoropropyl ether, LT03496881, 3-(1,1,2,3,3,3-Hexafluoropropoxy)propene, 59158-81-5. Product Category: Heterocyclic Organic Compound. CAS No. 59158-81-5. Molecular formula: C6H6F6O. Mole weight: 208.1. Purity: 0.96. IUPACName: 3-(1,1,2,3,3,3-hexafluoropropoxy)prop-1-ene. Canonical SMILES: C=CCOC(C(C(F)(F)F)F)(F)F. Density: 1.305 g/mL at 25ºC(lit.). ECNumber: 261-635-9. Product ID: ACM59158815. Alfa Chemistry ISO 9001:2015 Certified. |  |
| Allyl-(1,1-dioxo-tetrahydro-1lambda6-thiophen-3-yl)-amine | Allyl-(1,1-dioxo-tetrahydro-1lambda6-thiophen-3-yl)-amine. Uses: Designed for use in research and industrial production. Additional or Alternative Names: ALLYL-(1,1-DIOXO-TETRAHYDRO-1LAMBDA6-THIOPHEN-3-YL)-AMINE;ALLYL-(1,1-DIOXO-TETRAHYDRO-1-THIOPHEN-3-YL)-AMINE;ALLYL-(1,1-DIOXO-TETRAHYDROTHIOPHEN-3-YL)-AMINE;IFLAB-BB F1294-0153;TIMTEC-BB SBB010585;Zinc03865800. Product Category: Heterocyclic Organic Compound. CAS No. 5553-32-2. Molecular formula: C7H13NO2S. Mole weight: 175.25. Product ID: ACM5553322. Alfa Chemistry ISO 9001:2015 Certified. Categories: 3-[(prop-2-en-1-yl)amino]-1lambda6-thiolane-1,1-dione hydrochloride. | |
| Allyl[1,3-bis(2,6-diisopropylphenyl)imidazol-2-ylidene]chloropalladium(II) | Allyl[1,3-bis(2,6-diisopropylphenyl)imidazol-2-ylidene]chloropalladium(II). Uses: Catalyst for the cross-coupling of aryl chlorides with boronic acids. catalyst for the diamination of conjugated dienes and trienes. catalyst for the dehalogenation of aryl chlorides. catalyst for anaerobic alcohol oxidation. catalyst for anaerobic ketone oxidation and domino oxidation/α-arylation. Additional or Alternative Names: Palladium, [1,?3-bis[2,?6-bis(1-methylethyl)?phenyl]?-1,?3-dihydro-2H-imidazol-2-ylidene]?chloro(η3-2-propen-1-yl)?-. Product Category: Organic Phosphine Compounds. Appearance: white solid. CAS No. 478980-03-9. Molecular formula: C30H42ClN2Pd. Mole weight: 572.54. Purity: 98%, Pd>18.5%. Product ID: ACM478980039. Alfa Chemistry ISO 9001:2015 Certified. | |
| ALLYL 1-BENZOTRIAZOLYL CARBONATE, 95% | ALLYL 1-BENZOTRIAZOLYL CARBONATE, 95%. Uses: Designed for use in research and industrial production. Additional or Alternative Names: ST50976201, 102423-16-5, Carbonic acid,1H-benzotriazol-1-yl 2-propen-1-yl ester, AC1MVKWE, Benzotriazol-1-yl Prop-2-enyl Carbonate, ACMC-20m5er, Allyl 1-benzotriazolyl carbonate, CTK4A1037, benzotriazolyl prop-2-enyloxyformate, AG-D-11445, MCULE-6568511672, 1-(Allyloxycarbonyloxy)-1H-benzotriazole, 1H-Benzotriazole,1-[[(2-propenyloxy)carbonyl]oxy]- (9CI); Allyl 1-benzotriazolyl carbonate. Product Category: Heterocyclic Organic Compound. CAS No. 102423-16-5. Molecular formula: C10H9N3O3. Mole weight: 219.196760 [g/mol]. Purity: 0.96. IUPACName: benzotriazol-1-yl prop-2-enyl carbonate. Canonical SMILES: C=CCOC(=O)ON1C2=CC=CC=C2N=N1. Product ID: ACM102423165. Alfa Chemistry ISO 9001:2015 Certified. | |
| Allyl 1-Pyrrolidinecarbodithio ate | Allyl 1-Pyrrolidinecarbodithio ate. Group: Biochemicals. Alternative Names: Allyl Pyrrolidinodithiocarba mate; 1-Pyrrolidinecarbodithio ic Acid Allyl Ester; Pyrrolidinodithiocarba mic Acid Allyl Ester. Grades: Highly Purified. CAS No. 701-13-3. Pack Sizes: 5g, 10g, 25g, 50g, 100g. US Biological Life Sciences. |  Worldwide |
| Allyl 2,2,2-trichloroacet | Allyl 2,2,2-trichloroacet. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Allyl 2,2,2-Trichloroacetimidate, 51479-73-3, 2,2,2-Trichloroacetimidic acid allyl ester, O-Allyl 2,2,2-trichloroacetimidate, NSC245512, ACMC-209ktx, AC1L7UWB, 678414_ALDRICH, CTK8B1798, ANW-31267, NSC-245512, prop-2-enyl 2,2,2-trichloroethanimidate, I14-58876. Product Category: Heterocyclic Organic Compound. CAS No. 51479-73-3. Molecular formula: C5H6Cl3NO. Mole weight: 202.47. Purity: 0.96. IUPACName: prop-2-enyl 2,2,2-trichloroethanimidate. Canonical SMILES: C=CCOC(=N)C(Cl)(Cl)Cl. Density: 1.36g/cm³. Product ID: ACM51479733. Alfa Chemistry ISO 9001:2015 Certified. | |
| Allyl 2,2,2-trifluoroethyl ether | Allyl 2,2,2-trifluoroethyl ether. Group: Biochemicals. Grades: Highly Purified. CAS No. 1524-54-5. Pack Sizes: 1g, 2g, 5g, 10g, 25g. Molecular Formula: C5H7F3O. US Biological Life Sciences. | Worldwide |
| Allyl 2,3,4,6-tetra-O-acetyl-a-D-mannopyranoside | Allyl 2,3,4,6-tetra-O-acetyl-α-D-mannopyranoside is an extraordinary biomedical compound with profound impact stemming from its distinctive structure and acetylation intricacies, used in the research of cancer and inflammation. Synonyms: Allyl 2,3,4,6-tetra-O-acetyl-a-D-mannopyranoside; (2R,3R,4S,5S,6S)-2-(Acetoxymethyl)-6-(allyloxy)tetrahydro-2H-pyran-3,4,5-triyl triacetate; [(2R,3R,4S,5S,6S)-3,4,5-Triacetyloxy-6-prop-2-enoxyoxan-2-yl]methyl acetate; Allyl 2,3,4,6-tetra-O-acetyl-alpha-D-mannopyranoside; SCHEMBL121340; |A-D-Mannopyranoside, 2-propen-1-yl, 2,3,4,6-tetraacetate; CS-0093469; A892652; ?-D-Mannopyranoside, 2-propen-1-yl, 2,3,4,6-tetraacetate; alpha-D-Mannopyranoside, 2-propen-1-yl, 2,3,4,6-tetraacetate. CAS No. 119111-31-8. Molecular formula: C17H24O10. Mole weight: 388.37. |  |
| Allyl 2,3,4,6-tetra-O-acetyl-b-D-glucopyranoside | Allyl 2,3,4,6-tetra-O-acetyl-b-D-glucopyranoside is an astounding biomedical compound, standing resolute in the relentless pursuit of studying myriad diseases such as inflammation, cancer and microbial infestations. Synonyms: Allyl-tetra-O-acetyl-b-D-glucopyranoside. CAS No. 10343-15-4. Molecular formula: C17H24O10. Mole weight: 388.37. | |
| Allyl 2,3,4,6-tetra-O-benzyl-a-D-glucopyranoside | Allyl 2,3,4,6-tetra-O-benzyl-α-D-glucopyranoside, a remarkable biomedicine compound, stands as an intriguing therapeutic solution against diverse ailments. Its intricate molecular configuration bestows it with immense potential in combating tumors, eradicating bacteria, and countering viruses. CAS No. 6207-45-0. Molecular formula: C37H40O6. Mole weight: 580.71. | |
| Allyl 2,3,4,6-tetra-O-benzyl-α-D-glucopyranoside | Allyl 2,3,4,6-tetra-O-benzyl-α-D-glucopyranoside. CAS No. 6207-45-0. Product ID: 3-02712. |  |
| Allyl 2,3,4-tri-O-acetyl-b-D-galacturonide methyl ester | Allyl 2,3,4-tri-O-acetyl-b-D-galacturonide methyl ester, an esteemed biomedical product, emerges as a veritable panacea in the realm of medical treatment. Its multi-tasking prowess is evidenced by its remarkable anti-inflammatory, anti-cancer, and anti-bacterial attributes. Notably, this compound harbors immense potential in combating drug-resistant bacterial strains, warranting its integration into cancer therapeutics and inflammatory interventions. CAS No. 130506-36-4. Molecular formula: C16H22O10. Mole weight: 374.34. | |
| Allyl 2,3,4-tri-O-benzyl a-D-galactopyranoside | Allyl 2,3,4-tri-O-benzyl α-D-galactopyranoside has potential biomedical applications as a glycosylation recompound used in research studies focused on investigating galactosylation processes and carbohydrate chemistry. | |
| Allyl-2,3,4-tri-O-benzyl-a-D-galactopyranoside | Allyl-2,3,4-tri-O-benzyl-a-D-galactopyranoside is a crucial compound utilized in the biomedical industry employed for the research of various diseases, including cancer. | |
| Allyl 2,3,4-tri-O-benzyl-a-D-glucopyranoside | Allyl 2,3,4-tri-O-benzyl-a-D-glucopyranoside, a biomedical product renowned for its potential therapeutic effects on various ailments, stands as a promising avenue in the realm of disease management. Its distinct chemical composition unlocks doors to novel treatment modalities. CAS No. 78184-40-4. Molecular formula: C30H34O6. Mole weight: 490.59. | |
| Allyl 2,3,4-tri-O-benzyl-alpha-D-glucopyranoside | Allyl 2,3,4-tri-O-benzyl-alpha-D-glucopyranoside, a chemical compound with antitumor properties, is a subject of interdisciplinary research. Its ability to curb cancer cell growth not only shows promise in slowing tumor progression but also in addressing other ailments, including diabetes and inflammation. Investigating this compound's pharmacological mechanisms underscores the potential for new therapeutic treatments. Synonyms: ((2R,3R,4S,5R,6S)-6-(Allyloxy)-3,4,5-tris(benzyloxy)tetrahydro-2H-pyran-2-yl)methanol. Molecular formula: C30H34O6. Mole weight: 490.59. | |
| Allyl 2,3,4-tri-O-benzyl b-D-galactopyranoside | Allyl 2,3,4-tri-O-benzyl b-D-galactopyranoside is an esteemed compound commodity,functioning as a pivotal precursor. This compound facilitates the compoundion of a diverse range of pharmaceutical drugs curated to specifically address prevailing diseases. | |
| Allyl 2,3,4,-tri-O-benzyl-b-L-fucopyranoside | Allyl 2,3,4,-tri-O-benzyl-b-L-fucopyranoside is a profound biomedical compound, extensively applied in studying a myriad of ailments associated with aberrant cellular proliferation. Its mechanism of action entails the precise modulation of cellular signaling cascades, ensuring the targeted restraint of particular neoplastic cells. Molecular formula: C30H34O5. Mole weight: 474.59. | |
| Allyl 2,3-anhydro-4,6-O-benzylidene-a-L-mannopyranoside | Allyl 2,3-anhydro-4,6-O-benzylidene-α-L-mannopyranoside is an intricate biomedical substance, manifesting widely biomedical researching applications by actively hindering enzymes associated with cancer, diabetes and inflammation. Molecular formula: C16H18O5. Mole weight: 290.31. | |
| Allyl 2,3-di-O-benzyl-4,6-O-benzylidene-a-D-glucopyranoside | Allyl 2,3-di-O-benzyl-4,6-O-benzylidene-α-D-glucopyranoside is a biomedical compound with targeted action on viral enzymes, unveiling remarkable antiviral activity. Synonyms: Allyl 2,3-di-O-benzyl-4,6-O-benzylidene-a-D-glucopyranoside; 20746-71-8; (4aR,6S,7R,8S,8aR)-2-phenyl-7,8-bis(phenylmethoxy)-6-prop-2-enoxy-4,4a,6,7,8,8a-hexahydropyrano[3,2-d][1,3]dioxine; SCHEMBL2175284; DTXSID201131634; 87326-31-6; W-201814; 2-Propen-1-yl 2,3-bis-O-(phenylmethyl)-4,6-O-(phenylmethylene)-alpha-D-glucopyranoside; A-D-GALACTOPYRANOSIDE,2-PROPEN-1-YL 2,3-BIS-O-(PHENYLMETHYL)-4,6-O-(PHENYLMETHYLENE)-. CAS No. 20746-71-8. Molecular formula: C30H32O6. Mole weight: 488.57. | |
| Allyl 2,3-di-O-benzyl-a-D-glucopyranoside | Allyl 2,3-di-O-benzyl-a-D-glucopyranoside. CAS No. 87326-32-7. Product ID: 3-02745. Molecular formula: C23H28O6. Mole weight: 400.46. | |
| Allyl 2,3-di-O-benzyl-a-D-glucopyranoside | Allyl 2,3-di-O-benzyl-a-D-glucopyranoside is a valuable compound utilized in the development of drugs targeting various diseases like cancer, cardiovascular disorders and neurodegenerative conditions. CAS No. 87326-32-7. Molecular formula: C23H28O6. Mole weight: 400.46. | |
| Allyl-2,3-di-O-benzyl-alpha-D-glucopyranoside | Allyl-2,3-di-O-benzyl-alpha-D-glucopyranoside. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Allyl-2,3-di-O-benzyl-alpha-D-glucopyranoside, SCHEMBL2534111, W0507, 87326-32-7. Product Category: Heterocyclic Organic Compound. CAS No. 87326-32-7. Molecular formula: C23H28O6. Mole weight: 400.46482. Purity: 0.96. IUPACName: (2R,3R,4S,5R,6S)-2-(hydroxymethyl)-4,5-bis(phenylmethoxy)-6-prop-2-enoxyoxan-3-ol. Canonical SMILES: C=CCOC1C(C(C(C(O1)CO)O)OCC2=CC=CC=C2)OCC3=CC=CC=C3. Product ID: ACM87326327. Alfa Chemistry ISO 9001:2015 Certified. | |
| Allyl 2,3-di-O-benzyl-b-D-glucopyranoside | Allyl 2,3-di-O-benzyl-b-D-glucopyranoside, a highly esteemed compound within the biomedical sector, showcases significant potential as an antitumor agent through its commendable inhibitory effect on cancer cell proliferation. Remarkable outcomes have been observed in the treatment of diverse tumor categories, rendering it an invaluable inclusion within anti-cancer therapeutic regimens. Synonyms: Allyl 2,3-di-O-benzyl-b-D-glucopyranoside; Allyl-2,3-di-O-benzyl-beta-D-glucopyranoside; (2R,3R,4S,5R,6R)-2-(hydroxymethyl)-4,5-bis(phenylmethoxy)-6-prop-2-enoxyoxan-3-ol; SCHEMBL2536430; DTXSID101192611; 2-Propen-1-yl 2,3-bis-O-(phenylmethyl)-beta-D-glucopyranoside; W-203906; (2R,3R,4S,5R,6R)-4,5-BIS(BENZYLOXY)-2-(HYDROXYMETHYL)-6-(PROP-2-EN-1-YLOXY)OXAN-3-OL; (2R,3R,4S,5R,6R)-6-(Allyloxy)-4,5-bis(benzyloxy)-2-(hydroxymethyl)tetrahydro-2H-pyran-3-ol. CAS No. 84218-68-8. Molecular formula: C23H28O6. Mole weight: 400.46. | |
| Allyl 2,3-O-isopropylidene-a-L-rhamnopyranoside | Allyl 2,3-O-isopropylidene-a-L-rhamnopyranoside. CAS No. 71695-57-3. Product ID: 3-02690. | |
| Allyl 2,3-O-isopropylidene-a-L-rhamnopyranoside | Allyl 2,3-O-isopropylidene-a-L-rhamnopyranoside is a prominent compound serving as a crucial building block for glycoside research. This development technique finds particular relevance in drug discovery endeavors aimed at studying afflictions such as cancer, inflammation and microbial infections. CAS No. 71695-57-3. Molecular formula: C12H20O5. Mole weight: 244.29. | |
| Allyl 2,4,6-tri-O-(3,4,6-tri-O-acetyl-2-deoxy-2-phthalimido-b-D-glucopyranosyl)-3-O-benzyl-a-D-mannopyranoside | Allyl-2,4,6-tri-O-(3,4,6-tri-O-acetyl-2-deoxy-2-phthalimido-b-D-glucopyranosyl)-3-O-benzyl-a-D-mannopyranoside is a preeminent glycosylation recompound, profoundly aiding in the research of glycoconjugate modification. Synonyms: Allyl 2,4,6-tri-o-(3,4,6-tri-o-acetyl-2-deoxy-2-phthalimido-b-d-glucopyranosyl)-3-o-benzyl-a-d-mannopyranoside. Molecular formula: C76H79N3O33. Mole weight: 1562.44. | |
| Allyl 2-acetamido-2-deoxy-a-D-glucopyranoside | Allyl 2-acetamido-2-deoxy-a-D-glucopyranoside is a glycosylation recompound, facilitating the research and development of intricate carbohydrates and glycoconjugates. Such an extraordinary compound assumes a pivotal role in the development of therapeutic drugs targeting a myriad of ailments including cancer, bacterial infections and inflammatory disorders. Synonyms: ALLYL 2-ACETAMIDO-2-DEOXY-ALPHA-D-GLUCOPYRANOSIDE; Allyl 2-acetamido-2-deoxy-a-D-glucopyranoside; N-((2S,3R,4R,5S,6R)-2-(Allyloxy)-4,5-dihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-3-yl)acetamide; N-[(2S,3R,4R,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-2-prop-2-enoxyoxan-3-yl]acetamide; SCHEMBL687195; MFCD08274526; AKOS015919294; s11561; A830156; W-203051. CAS No. 54400-75-8. Molecular formula: C11H19NO6. Mole weight: 261.27. | |
| 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. | |
| 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. | |
| 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. | |
| 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. | |
| 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. | |
| 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. | |
| 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. | |
| Allyl 2-(acetylamino)-2-deoxy-3-O-benzyl-β-D-glucopyranoside | Allyl 2-(acetylamino)-2-deoxy-3-O-benzyl-β-D-glucopyranoside. Uses: Designed for use in research and industrial production. Additional or Alternative Names: CTK8F7653, 65730-00-9, AG-G-47430, Allyl 2-(Acetylamino)-2-deoxy-3-O-benzyl-beta-D-glucopyranoside. Product Category: Heterocyclic Organic Compound. CAS No. 65730-00-9. Molecular formula: C18H25NO6. Mole weight: 351.39. Purity: 0.96. IUPACName: N-[(2R,4R,5S)-5-hydroxy-6-(hydroxymethyl)-4-phenylmethoxy-2-prop-2-enoxyoxan-3-yl]acetamide. Product ID: ACM65730009. Alfa Chemistry ISO 9001:2015 Certified. | |
| Allyl 2-(acetylamino)-2-deoxy-4,6-O-(phenylmethylene)-α-D-glucopyranoside | Allyl 2-(acetylamino)-2-deoxy-4,6-O-(phenylmethylene)-α-D-glucopyranoside. Uses: Designed for use in research and industrial production. Additional or Alternative Names: 63064-49-3, CTK8F7654, 2-Propenyl 2-(Acetylamino)-2-deoxy-4,6-O-(phenylmethylene)-|A-D-glucopyranoside, Allyl 2-(Acetylamino)-2-deoxy-4,6-O-(phenylmethylene)-|A-D-glucopyranoside, AG-G-33050, Allyl 2-(Acetylamino)-2-deoxy-4,6-O-(phenylmethylene)-alpha-D-glucopyranoside. Product Category: Heterocyclic Organic Compound. CAS No. 63064-49-3. Molecular formula: C18H23NO6. Mole weight: 349.38. Purity: 0.96. IUPACName: 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. Product ID: ACM63064493. Alfa Chemistry ISO 9001:2015 Certified. | |
| Allyl 2-amino-5-iodobenzoate | Allyl 2-amino-5-iodobenzoate. Uses: Designed for use in research and industrial production. Additional or Alternative Names: allyl 2-amino-5-iodobenzoate, 1131605-37-2, CTK8E2096, SBB068195, ZINC39951613, AKOS015854673, AK133627, prop-2-enyl 2-azanyl-5-iodanyl-benzoate, KB-145432, FT-0658179, 2-amino-5-iodobenzoic acid prop-2-enyl ester, A802846, I14-5650. Product Category: Heterocyclic Organic Compound. CAS No. 1131605-37-2. Molecular formula: C10H10INO2. Mole weight: 303.096370 [g/mol]. Purity: 0.96. IUPACName: prop-2-enyl 2-amino-5-iodobenzoate. Product ID: ACM1131605372. Alfa Chemistry ISO 9001:2015 Certified. | |
| Allyl 2-bromo-2-methylpropionate | Allyl 2-bromo-2-methylpropionate. Uses: This product is suitable for scientific research. Additional or Alternative Names: prop-2-enyl 2-bromo-2-methylpropanoate; Allyl2-bromo-2-methylpropionate. Product Category: Polymer/MacromoleculeAllyl Monomers. CAS No. 40630-82-8. Molecular formula: C7H11BrO2. Mole weight: 207.07 g/mol. Purity: 0.98. Canonical SMILES: CC(C)(Br)C(=O)OCC=C. Density: 1.302 g/mL at 25 °C (lit.). Product ID: ACM-MO-40630828. Alfa Chemistry ISO 9001:2015 Certified. | |
| Allyl 2-bromopropionate | Allyl 2-bromopropionate. Uses: Designed for use in research and industrial production. Additional or Alternative Names: ALLYL ALPHA-BROMOPROPIONATE;ALLYL 2-BROMOPROPIONATE. Product Category: Heterocyclic Organic Compound. CAS No. 87129-38-2. Molecular formula: C6H9BrO2. Mole weight: 193.04. Purity: 0.96. IUPACName: prop-2-enyl 2-bromopropanoate. Density: 1.382g/cm³. Product ID: ACM87129382. Alfa Chemistry ISO 9001:2015 Certified. | |
| 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. | |
| 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. | |
| 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. | |
| 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. | |
| 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. | |
| 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. | |
| 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. | |
| 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. | |
| Allyl-(2-methoxy-phenyl)-amine | Allyl-(2-methoxy-phenyl)-amine. Uses: Designed for use in research and industrial production. Additional or Alternative Names: SureCN8631283, CTK4C7496, ZINC22003831, AKOS011421883, AG-D-99954, Benzenamine,2-methoxy-N-2-propen-1-yl-, 15258-47-6, Benzenamine,2-methoxy-N-2-propenyl- (9CI); o-Anisidine, N-allyl- (8CI);N-Allyl-2-methoxyaniline; N-Allyl-o-anisidine. Product Category: Heterocyclic Organic Compound. CAS No. 15258-47-6. Molecular formula: C10H13NO. Mole weight: 163.216320 [g/mol]. Purity: 0.96. IUPACName: 2-methoxy-N-prop-2-enylaniline. Density: 1.013g/cm³. Product ID: ACM15258476. Alfa Chemistry ISO 9001:2015 Certified. | |
| Allyl 2-O-acetyl-3-O-benzyl-α-L-rhamnopyranoside | Allyl 2-O-acetyl-3-O-benzyl-α-L-rhamnopyranoside. CAS No. 940274-20-4. Product ID: 3-02693. | |
| 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. | |
| Allyl 2-O-benzoyl-3-O-benzyl-α-L-rhamnopyranoside | Allyl 2-O-benzoyl-3-O-benzyl-α-L-rhamnopyranoside. CAS No. 940274-21-5. Product ID: 3-02695. | |
| 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. | |
| 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. | |
| Allyl[3- (2-nitrobenzenesulfonamido) propyl]carbamate | Allyl[3- (2-nitrobenzenesulfonamido) propyl]carbamate. Group: Monomers. Alternative Names: ALLYL [3- (2-NITROBENZENESULFONAMIDO) PROPYL]CARBAMATE; [3- (2-NITROBENZENESULFONAMIDO) PROPYL]CARBAMIC ACID ALLYL ESTER. CAS No. 312283-45-7. Product ID: prop-2-enyl N-[3-[ (2-nitrophenyl) sulfonylamino]propyl]carbamate. Molecular formula: 343.36g/mol. Mole weight: C13H17N3O6S. C=CCOC (=O)NCCCNS (=O) (=O)C1=CC=CC=C1[N+] (=O)[O-]. InChI=1S/C13H17N3O6S/c1-2-10-22-13 (17)14-8-5-9-15-23 (20, 21)12-7-4-3-6-11 (12)16 (18)19/h2-4, 6-7, 15H, 1, 5, 8-10H2, (H, 14, 17). INKIDQWOEVNHHA-UHFFFAOYSA-N. |  |
| 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. | |
| Allyl(3-Chloropropyl)Dichlorosilane | Allyl(3-Chloropropyl)Dichlorosilane. Uses: Designed for use in research and industrial production. Additional or Alternative Names: allyl-3-chloropropyldichlorosilane; 4,4,7-trichloro-4-sila-1-heptene. Product Category: Halosilane. Appearance: Transparent liquid. CAS No. 166970-54-3. Molecular formula: C6H11Cl3Si. Mole weight: 217.6 g/mol. Purity: 95%+. IUPACName: dichloro-(3-chloropropyl)-prop-2-enylsilane. Canonical SMILES: C=CC[Si](CCCCl)(Cl)Cl. Density: 1.13g/cm³. Product ID: ACM166970543. Alfa Chemistry ISO 9001:2015 Certified. | |
| Allyl-(3-methyl-1,1-dioxo-tetrahydro-1lambda*6*-thiophen-3-yl)amine | Allyl-(3-methyl-1,1-dioxo-tetrahydro-1lambda*6*-thiophen-3-yl)amine. Uses: Designed for use in research and industrial production. Additional or Alternative Names: IFLAB-BB F1294-0166;CHEMBRDG-BB 4011821;ALLYL-(3-METHYL-1,1-DIOXO-TETRAHYDRO-1LAMBDA6-THIOPHEN-3-YL)-AMINE;ALLYL-(3-METHYL-1,1-DIOXO-TETRAHYDRO-1,6-THIOPHEN-3-YL)-AMINE;N-ALLYL-3-METHYLTETRAHYDROTHIOPHEN-3-AMINE 1,1-DIOXIDE. Product Category: Heterocyclic Organic Compound. CAS No. 151775-05-2. Molecular formula: C8H15NO2S. Mole weight: 189.28. Product ID: ACM151775052. Alfa Chemistry ISO 9001:2015 Certified. | |
| 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. | |
| 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. | |
| 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. | |
| Allyl 3-O-benzyl-2-O-chloroacetyl-α-L-rhamnopyranoside | Allyl 3-O-benzyl-2-O-chloroacetyl-α-L-rhamnopyranoside. CAS No. 943307-50-4. Product ID: 3-02694. | |
| 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. | |
| 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. | |
| Allyl 3-O-benzyl-2-O-p-tolylsulfonyl-α-L-rhamnopyranoside | Allyl 3-O-benzyl-2-O-p-tolylsulfonyl-α-L-rhamnopyranoside. CAS No. 940274-22-6. Product ID: 3-02692. | |
| 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. | |
| Allyl 3-O-benzyl-α-L-rhamnopyranoside | Allyl 3-O-benzyl-α-L-rhamnopyranoside. CAS No. 460745-20-4. Product ID: 3-02696. | |
| 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. | |
| 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. | |
| 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. | |
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