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 | |
|---|---|---|
| 2'-Deoxy-2'-fluorouridine-5'-triphosphate sodium salt | 2'-Deoxy-2'-fluorouridine-5'-triphosphate sodium salt is a vital component in the biomedicine field. It is commonly used in molecular biology research and drug development. This compound serves as a substrate for reverse transcriptases and DNA polymerases, playing a crucial role in the synthesis of various modified nucleic acids. It is particularly utilized in the study of RNA function and structure and the development of antiviral drugs targeting RNA viruses. Synonyms: 2'F-dUTP.Na. Grades: 95%. Molecular formula: C9H14FN2O14P3·Na. Mole weight: 509.12 (free acid). |  |
| 2'-Deoxy-2'-fluorouridine-5'-triphosphate tetralithium salt | 2'-Deoxy-2'-fluorouridine-5'-triphosphate tetralithium salt is a vital compound in biomedicine used for various research purposes. It serves as a nucleotide analog that incorporates into DNA during synthesis, aiding in the study of DNA replication, repair, and mutagenesis. This compound can also be utilized in the development of antiviral drugs targeting RNA viruses such as hepatitis C and HIV. Synonyms: 2'-Fluoro-2'-deoxyuridine-5'-triphosphate. Grades: 95%. Molecular formula: C9H11FN2O14P3Li4. Mole weight: 510.87 (free acid). | |
| 2'-Deoxy-2'-methylcytidine | 2'-Deoxy-2'-methylcytidine, a remarkable compound employed within the biomedical sector, boasts remarkable potency as an antiviral agent. Its efficacy extends to combating a multitude of RNA viruses, encompassing both flaviviruses and coronaviruses, rendering it indispensable in the creation of therapeutic antiviral medications to tackle afflictions like hepatitis C, Zika virus infection, and COVID-19. Synonyms: 2'-Methyl-2'-deoxycytidine; 2/'-Methyl-2/'-deoxycytidine; 4-amino-1-[(2R,3R,4S,5R)-4-hydroxy-5-(hydroxymethyl)-3-methyloxolan-2-yl]pyrimidin-2-one; 2',2'-Dmc; 2'-Deoxy-2'-methylcytidine; 2-C-Ethynyl-cytidine; 2'C-Me-dC;4-amino-1-[(2R,3R,4S,5R)-4-hydroxy-5-(hydroxymethyl)-3-methyl-tetrahydrofuran-2-yl]pyrimidin-2-one; 4-Amino-1-[(2R,3R,4S,5R)-4-Hydroxy-5-(Hydroxymethyl)-3-Methyl-Tetrahydrofuran-2-Yl]Pyrimidin-2-One; 4-Amino-1-[(2R,3R,4S,5R)-4-Hydroxy-5-(Hydroxymethyl)-3-Methyl-2-Tetrahydrofuranyl]-2-Pyrimidinone; 4-Amino-1-[(2R,3R,4S,5R)-4-Hydroxy-3-Methyl-5-Methylol-Tetrahydrofuran-2-Yl]Pyrimidin-2-One. CAS No. 115494-53-6. Molecular formula: C10H15N3O4. Mole weight: 241.24. | |
| 2'-Deoxy-2'-methyleneadenosine | 2'-Deoxy-2'-methyleneadenosine is a potent compound utilized in the biomedical industry for its unique pharmacological properties. Primarily, it acts as an adenosine analog, contributing to the treatment of various diseases, including certain forms of cancer. This product serves as a critical component in research involving nucleotide modification and drug development, ultimately enhancing our understanding and treatment options for complex biomedical conditions. CAS No. 104409-41-8. Molecular formula: C11H13N5O3. Mole weight: 263.25. | |
| 2'-Deoxy-2-O-ethyluridine | 2'-Deoxy-2-O-ethyluridine is an intermediate for synthesizing 2-Thio 2'-Deoxyuridine, a metabolite of 2-Thiouracil. Synonyms: O2-Ethyldeoxyuridine; 1-(2-Deoxy-β-D-erythro-pentofuranosyl)-2-ethoxy-4(1H)-pyrimidinone. CAS No. 66656-47-1. Molecular formula: C11H16N2O5. Mole weight: 256.26. | |
| 2'-Deoxy-2-thiouridine | A metabolite of 2-Thiouracil. Synonyms: 2-Thio-2'-Deoxyuridine; 1-(2-Deoxy-β-D-erythro-pentofuranosyl)-2-thiouracil; 2-Thiodeoxyuridine; 1-[(2R,4S,5R)-4-hydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl]-2-thioxo-pyrimidin-4-one; 4(1H)-Pyrimidinone, 1-(2-deoxy-b-D-erythro-pentofuranosyl)-2,3-dihydro-2-thioxo-. Grades: ≥95%. CAS No. 35059-12-2. Molecular formula: C9H12N2O4S. Mole weight: 244.27. | |
| 2'-Deoxy-3',5'-bis-O-[(1,1-dimethylethyl)dimethylsilyl]-8-[(1-methyl-6-phenyl-1H-imidazo[4,5-b]pyridin-2-yl)amino]-6-O-(phenylmethyl)guanosine | 2'-Deoxy-3',5'-bis-O-[(1,1-dimethylethyl)dimethylsilyl]-8-[(1-methyl-6-phenyl-1H-imidazo[4,5-b]pyridin-2-yl)amino]-6-O-(phenylmethyl)guanosine is an intermediate in the synthesis of 2'-Deoxyguanosine-C8 adducts with mutagenic/carcinogenic heterocyclic amines. CAS No. 896719-58-7. Molecular formula: C42H57N9O4Si2. Mole weight: 808.13. | |
| 2'-Deoxy-3',5'-bis-O-[(1,1-dimethylethyl)dimethylsilyl]-8-[(1-methyl-6-phenyl-1H-imidazo[4,5-b]pyridin-2-yl)amino]-guanosine | 2'-Deoxy-3',5'-bis-O-[(1,1-dimethylethyl)dimethylsilyl]-8-[(1-methyl-6-phenyl-1H-imidazo[4,5-b]pyridin-2-yl)amino]-guanosine is an intermediate in the synthesis of 2'-Deoxyguanosine-C8 adducts with mutagenic/carcinogenic heterocyclic amines. Synonyms: 2'-Deoxy-3',5'-bis-O-[(1,1-dimethylethyl)dimethylsilyl]-8-[(1-methyl-6-phenyl-1H-imidazo[4,5-b]pyridin-2-yl)amino]-guanosine; 915092-62-5. CAS No. 915092-62-5. Molecular formula: C35H51N9O4Si2. Mole weight: 718.01. | |
| 2'-Deoxy-3,5-dimethylcytidine | 2'-Deoxy-3,5-dimethylcytidine is a profoundly potent antiviral compound widely embraced in the biomedical domain, exhibiting remarkable capacity to impede viral replication. Grades: 98%. CAS No. 198198-29-7. Molecular formula: C11H17N3O4. Mole weight: 255.27. | |
| 2'-Deoxy-3',5'-di-O-benzoyl-2',2'-difluorocytidine | A (β-anomer) intermediate of Gemcitabine; antitumor compound. Synonyms: 2'-Deoxy-2',2'-difluoro-3',5'-bis-O-benzoylcytidine. Grades: 98 %. CAS No. 134790-39-9. Molecular formula: C23H19F2N3O6. Mole weight: 471.41. | |
| 2'-Deoxy-3-methyladenosine | 2'-Deoxy-3-methyladenosine is a vital compound in the biomedical field used for research and drug development. It plays a crucial role in the study of nucleic acids and nucleotide metabolism. This product is widely employed in investigating the effects of modified nucleosides on gene expression and can be used to treat various diseases associated with nucleotide imbalances and abnormalities. CAS No. 76227-25-3. Molecular formula: C11H15N. Mole weight: 161.24. | |
| 2'-?Deoxy-?3'-?O-?[ (1, ?1-?dimethylethyl) ?dimethylsilyl]?-?N, ?5-?dimethyl-cytidine | 2'-Deoxy-3'-O-[(1,?1-dimethylethyl)?dimethylsilyl]?-N,?5-dimethyl-cytidine is an intermediate in synthesizing N4,5-Dimethyldeoxycytidine, which has been shown to participate in cytidine deaminase inhibition. CAS No. 1569273-35-3. Molecular formula: C17H31N3O4Si. Mole weight: 369.53. | |
| 2'-Deoxy-3'-O-DMT-N2-Isobutyrylguanosine | 2'-Deoxy-3'-O-DMT-N2-Isobutyrylguanosine, a compound highly esteemed in the biomedical industry, serves as a nucleotide analogue and harbors immense potential for antiviral drugs and cancer therapies. With its auspicious pharmacological attributes, this compound assumes a pivotal role in pioneering revolutionary remedies for a plethora of ailments. Synonyms: N2-isobutyryl-3'-O-(4,4'-dimethoxytrityl)-2'-deoxyguanosine. CAS No. 140712-81-8. Molecular formula: C35H37N5O7. Mole weight: 639.71. | |
| 2'-Deoxy-4-hydazone uridine | 2'-Deoxy-4-hydazone uridine is an intriguing compound under investigation, renowned for its antiviral prowess against a repertoire of RNA viruses namely influenza, enterovirus, and hepatitis C. This nucleoside analogue holds promise in thwarting the replication of these noxious pathogens. Synonyms: N4-amino-2'-deoxycytidine. CAS No. 52725-05-0. Molecular formula: C9H14N4O4. Mole weight: 242.23. | |
| 2'-Deoxy-4'-thioadenosine | 2-Deoxy-4-thioadenosine is a paramount biochemical compound extensively characterized by its profound inhibitory prowess upon enzymes engaged in pivotal metabolic pathways. With its idiosyncratic attributes, it assuming indispensability as a primary instrument in the realm of biomedical examination and pharmacological advancement. Synonyms: 2'-deoxy-4'-thioadenosine; 135656-35-8. CAS No. 135656-35-8. Molecular formula: C10H13N5O2S. Mole weight: 267.31. | |
| 2'-Deoxy-4'-thiouridine | 2'-Deoxy-4'-thiouridine, a vital compound utilized in the field of biomedicine, holds immense promise for therapeutic interventions. Its profound antiviral capabilities against HIV-1 derive from its distinctive nucleoside analog properties. In-depth investigations have been conducted to explore its remarkable efficiency in impeding viral replication. Synonyms: 1-(2-deoxy-4-thio-beta-d-ribofuranosyl)uracil. CAS No. 134111-32-3. Molecular formula: C9H12N2O4S. Mole weight: 244.27. | |
| 2'-Deoxy-5-(2-hydroxyethyl)-2',3'-di-O-toluoyluridine | 2'-Deoxy-5-(2-hydroxyethyl)-2',3'-di-O-toluoyluridine, a prominent pharmaceutical compound extensively utilized in the biomedical sector, showcases remarkable efficacy in selectively modulating intricate cellular processes, rendering it a valuable therapeutic agent against a diverse range of afflictions. Intriguingly, investigations allude to its potential in combatting viral infections, specific malignancies, and autoimmune maladies. Molecular formula: C27H28N2O8. Mole weight: 508.53. | |
| 2'-Deoxy-5-(2-iodoethyl)uridine | 2'-Deoxy-5-(2-iodoethyl)uridine, an indispensable component utilized extensively in the realm of biomedical research, assumes a pivotal position in the progress of antiviral pharmaceuticals aimed at addressing viral afflictions. Remarkably intricate in its composition, this compound exhibits unparalleled proficiency in selectively honing in on viral enzymes, effectively impeding the replication of virulent agents. Synonyms: 5-(2-Iodoethyl)-2'-deoxyuridine; 1-(4-Hydroxy-5-hydroxymethyl-tetrahydro-furan-2-yl)-5-(2-iodo-ethyl)-1H-pyrimidine-2,4-dione. CAS No. 90301-67-0. Molecular formula: C11H15IN2O5. Mole weight: 382.15. | |
| 2'-Deoxy-5-[3-[[[(3',6'-dihydroxy-3-oxospiro[isobenzofuran-1(3H),9'-[9H]xanthen]-5-yl)amino]thioxomethyl]amino]-1-propynyl]uridine 5'-(Tetrahydrogen Triphosphate) Triethylamine Salt | 2'-Deoxy-5-[3-[[[(3',6'-dihydroxy-3-oxospiro[isobenzofuran-1(3H),9'-[9H]xanthen]-5-yl)amino]thioxomethyl]amino]-1-propynyl]uridine 5'-(Tetrahydrogen Triphosphate) is a fluorescence-labelled DNA that is readily detectable without using radioactive substances. Synonyms: Spiro[isobenzofuran-1(3H),9'-[9H]xanthene] Uridine 5'-(Tetrahydrogen Triphosphate) Deriv. Triethylamine Salt; FITC-dUTP Triethylamine Salt. Molecular formula: C33H29N4O19P3S XC6H15N. Mole weight: 910.59. | |
| 2'-Deoxy-5,6-dihydrouridine | It is used to screen or bind to nucleic acid targets, such as RNA or related fragments associated with a disease, disorder, or condition. Synonyms: 5,6-Dihydro-2'-deoxyuridine; 1-(2-deoxy-β-D-ribofuranoshydrouracil; 5,6-Dihydrodeoxyuridine; Dihydrodeoxyuridine. Grades: ≥95%. CAS No. 5626-99-3. Molecular formula: C9H14N2O5. Mole weight: 230.22. | |
| 2'-Deoxy-5-azacytidylyl-(3'?5')-2'-deoxy-guanosine Sodium Salt | 2'-Deoxy-5-azacytidylyl-(3'?5')-2'-deoxy-guanosine is an DNA methylation inhibitor in vivo and was shown to effectively tolerated in tumor-free mouse and was found to be similarly effective in reducing tumor growth. Uses: Antineoplastic agents. Synonyms: Guadecitabine sodium;SGI-110; Guadecitabine sodium [USAN]; S110 sodium salt; SGI-110 sodium salt; sodium; [(2R,3S,5R)-5-(2-amino-6-oxo-1H-purin-9-yl)-3-hydroxyoxolan-2-yl]methyl [(2R,3S,5R)-5-(4-amino-2-oxo-1,3,5-triazin-1-yl)-2-(hydroxymethyl)oxolan-3-yl] phosphate; 0RB89YH367; 2'-Deoxy-5-azacytidylyl-(3'-->5')-2'-deoxy-guanosine Sodium Salt; Guanosine, 2'-deoxy-5-azacytidylyl-(3'-5')-2'-deoxy-, sodium salt (1:1); SGI 110; SGI-110 sodium; S-110 sodium;Guadecitabine sodium (JAN/USAN);2'-Deoxy-5-azacytidylyl-(3'?5')-2'-deoxy-guanosine SodiuM Salt; Guadecitabine sodium; SGI-110 sodium. CAS No. 929904-85-8. Molecular formula: C18H23N9NaO10P. Mole weight: 579.39. | |
| 2'-Deoxy-5-chloro-2',2'-difluorocytidine | 2'-Deoxy-5-chloro-2',2'-difluorocytidine, a vital compound in the field of biomedicine, holds immense significance. Falling under the category of nucleoside analogs, it finds extensive application in the treatment of a diverse array of ailments such as viral infections and cancer. Exhibiting its prowess as an antiviral and antitumor agent, this compound effectively thwarts viral DNA replication and disrupts DNA synthesis within cancer cells. CAS No. 132786-39-1. Molecular formula: C9H10ClF2N3O4. Mole weight: 297.64. | |
| 2'-Deoxy-5'-DMT-5-[3-(trifluoroacetylamino)-1-E-propenyl]-uridine 3-CE phosphoramidite | 2'-Deoxy-5'-DMT-5-[3-(trifluoroacetylamino)-1-E-propenyl]-uridine 3-CE phosphoramidite, derived from nucleobase uracil, is a highly significant chemical entity within the realm of biomedicine. Widely recognized as a fundamental phosphoramidite building block, it plays a pivotal role in the synthesis of oligonucleotides for diverse biomedical applications. Its indispensable role extends to the development of nucleotide-based therapeutics, targeting formidable ailments such as viral infections, genetic disorders, and select cancer variants. CAS No. 851520-76-8. | |
| 2'-Deoxy-5'-DMT-5-[3-(trifluoroacetylamino)-1-propynyl]-uridine 3'-CE phosphoramidite | 2'-Deoxy-5'-DMT-5-[3-(trifluoroacetylamino)-1-propynyl]-uridine 3'-CE phosphoramidite is a highly intricate and cutting-edge phosphoramidite derivative, manifesting immense potential in the realm of biomedical applications. Synonyms: 5-TFA-ap-dU phosphoramidite; alpha-[2- (Trifluoroacetylamino)ethylidyne]-3'-O-[2-cyanoethoxy (diisopropylamino)phosphino]-5'-O- (4, 4'-dimethoxytrityl)thymidine; Uridine, 5'-O-[bis(4-methoxyphenyl)phenylmethyl]-2'-deoxy-5-[3-[(2,2,2-trifluoroacetyl)amino]-1-propyn-1-yl]-, 3'-[2-cyanoethyl N,N-bis(1-methylethyl)phosphoramidite]; 5'-O-[Bis (4-methoxyphenyl) (phenyl)methyl]-3'-O-[ (2-cyanoethoxy) (diisopropylamino)phosphino]-2'-deoxy-5-{3-[ (trifluoroacetyl)amino]-1-propyn-1-yl}uridine. Grades: ≥98% by HPLC. CAS No. 120016-98-0. Molecular formula: C44H49F3N5O9P. Mole weight: 879.86. | |
| 2'-Deoxy-5-fluorocytidine 5'-monophosphate | 2'-Deoxy-5-fluorocytidine 5'-monophosphate, a pivotal compound within the biomedical sector, assumes a critical role in the management of diverse ailments. By impeding RNA virus replication, particularly those associated with influenza, hepatitis C, and HIV, this product exerts its therapeutic effect. Moreover, it serves as a precursor for antiviral nucleoside analog synthesis, rendering it an invaluable asset in the realm of pharmaceutical research against viral infections. Uses: Enzyme inhibitors. Synonyms: 5-FLUORO-2'-DEOXY-CYTIDINE-5'-MONOPHOSPHATE. CAS No. 847-22-3. Molecular formula: C9H13FN3O7P. Mole weight: 325.19. | |
| 2'-Deoxy-5-fluoro-N-methylcytidine | 2'-Deoxy-5-fluoro-N-methylcytidine is a vital compound in biomedicine used to treat various viral infections. Known for its potent antiviral properties, this nucleoside analog is particularly effective against influenza viruses and respiratory syncytial virus (RSV). Extensively studied for its ability to inhibit viral replication, it has great potential for the development of antiviral therapies and vaccines. Synonyms: N-Methyl-5-fluorodeoxycytidine; 5-Fluoro-N4-methyl-2'-deoxycytidine; 5-Fluoro-N(sup 4)-methyl-2'-deoxycytidine. CAS No. 2248-73-9. Molecular formula: C10H14FN3O4. Mole weight: 259.23. | |
| 2'-Deoxy-5-fluorouridine 5'-diphosphate sodium salt | 2'-Deoxy-5-fluorouridine 5'-diphosphate sodium salt, a remarkable biomedical innovation, emerges as a promising solution in combating select malignancies. Exhibiting its prowess as an antineoplastic agent, this compound effectively impedes the replication of DNA, harnessing the power to thwart malignant cell proliferation. Uniquely tailored to combat cancer, it diligently targets aberrant cells, actively hindering their expansion and rendering it indispensable within the realm of chemotherapeutic interventions. Unraveling its transformative potential, the sodium salt form ensures unparalleled stability and bioavailability, thereby maximizing therapeutic efficacy and affording unprecedented clinical outcomes. Synonyms: 5F-dUDP. CAS No. 82122-52-9. Molecular formula: C9H13FN2O11P2·xNa. Mole weight: 406.15. | |
| 2'-Deoxy-5-fluorouridine 5'-monophosphate sodium salt | 2'-Deoxy-5-fluorouridine 5'-monophosphate sodium salt, a remarkable compound extensively employed in the biomedical domain due to its exceptional antiviral attributes, brings forth intricacy and diversity. It showcases remarkable effectiveness in combatting various viral infections, chiefly instigated by RNA viruses. This compound profoundly suppresses the replication of distinct viruses, exhibiting immense promise in alleviating ailments like hepatitis C, Zika virus, and respiratory syncytial virus. Synonyms: 5F-dUMP; 5-Fluoro-2'-deoxyuridine 5'-monophosphate sodium salt. Grades: ≥ 85% (HPLC). CAS No. 103226-10-4. Molecular formula: C9H10FN2Na2O8P. Mole weight: 370.14. | |
| 2'-Deoxy-5-fluorouridine-5'-triphosphate sodium salt | 2'-Deoxy-5-fluorouridine-5'-triphosphate sodium salt, a compound of utmost importance in the realm of biomedicine, proves indispensable for the therapeutic intervention against diverse viral infections. Leveraging its potent inhibitory properties, this substance effectively hampers the replication processes of viral DNA or RNA, establishing it as a pivotal tool in biomedicine research and the ongoing battle against viral afflictions. Synonyms: 5F-dUTP. Grades: ≥ 95% (HPLC). CAS No. 1630828-71-5. Molecular formula: C9H14FN2O14P3·xNa. Mole weight: 486.13 (free acid). | |
| 2'-Deoxy-5-formyluridine | 2'-Deoxy-5-formyluridine is an indispensable nucleoside analog extensively employed in biomedicine due to its remarkable antiviral attributes, manifesting an exceptional ability to impede the duplication of viral DNA. Particularly significant in the reserch of herpes simplex virus (HSV) infections, this compound exerts its action by inducing disruptions in the intricate viral replication machinery. Synonyms: 1-((2R,4S,5R)-4-hydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)-2,4-dioxo-1,2,3,4-tetrahydropyrimidine-5-carbaldehyde; 5-Formyl-2'-deoxyuridine; NSC 148297; 1,2,3,4-Tetrahydro-1-(2-deoxy-beta-D-ribofuranosyl)-2,4-dioxo-5-pyrimidinecarboxaldehyde; 5-formyldeoxyuridine; 5-Formyl-dU. Grades: ≥95% by HPLC. CAS No. 4494-26-2. Molecular formula: C10H12N2O6. Mole weight: 256.21. | |
| 2'-Deoxy-5-hydroxymethylcytidine 5'-monophosphate sodium salt | 2'-Deoxy-5-hydroxymethylcytidine 5'-monophosphate sodium salt, a remarkable biomedicine, manifests immense potential in combating select viral infections. Mechanistically, it thwarts viral replication and diminishes viral load, largely attributed to its profound antiviral properties. Furthermore, owing to its unique pharmacological attributes, this compound aptly targets specific viral enzymes, thereby promulgating its efficacy against afflictions induced by such insidious viral strains. Molecular formula: C10H14N3Na2O8P. Mole weight: 381.19. | |
| 2'-Deoxy-5-hydroxymethylcytidine-5'-triphosphate sodium salt | 2'-Deoxy-5-hydroxymethylcytidine-5'-triphosphate sodium salt, an indispensable compound in the realm of biomedical research, takes center stage. This vital component unfailingly immerses itself in the ever-evolving studies concerning DNA sequencing and gene expression analysis. Precisely due to its unparalleled chemical structure, this compound spearheads the march towards unraveling biomedical complexities and blazing a revolutionary trail in therapeutic advancements. Synonyms: 5-Hydroxymethyl-dCTP Na. Grades: ≥ 90% (HPLC). Molecular formula: C10H18N3O14P3·xNa. Mole weight: 497.18 (free acid). | |
| 2'-Deoxy-5-hydroxymethyluridine-5'-triphosphate triethylammonium salt | 2'-Deoxy-5-hydroxymethyluridine-5'-triphosphate triethylammonium salt is an indispensable recompound employed in biomedical research across diverse applications, functioning as a fundamental constituent for the enzymatic synthesis of altered DNA molecules. It simultaneously serving as a DNA polymerase substrate enabling PCR amplification. This product assuming a pivotal role in comprehending and manipulating DNA's intricate structure and functionality, thereby expediting investigations concerning genetic disorders, mutagenesis, and the advancement of therapeutic pharmaceuticals. Synonyms: Hydroxymethyldeoxyuridine triphosphate. Grades: ≥ 90%. Molecular formula: C10H13N2O15P3·4C6H16N. Mole weight: 902.93. | |
| 2'-Deoxy-5-hydroxyuridine 5'-triphosphate | 2'-Deoxy-5-hydroxyuridine 5'-triphosphate is an essential nucleotide substrate utilized in molecular biology research for DNA sequencing. This modified form of uridine triphosphate is incorporated into DNA during PCR amplification and enables identification of single nucleotide polymorphisms (SNPs) linked to diseases such as cancer and genetic disorders. Synonyms: 5-Hydroxydeoxyuridine triphosphate; 27972-89-0; 2'-Deoxy-5-hydroxyuridine 5'-triphosphate; [(2R,3S,5R)-3-hydroxy-5-(5-hydroxy-2,4-dioxopyrimidin-1-yl)oxolan-2-yl]methyl [hydroxy(phosphonooxy)phosphoryl] hydrogen phosphate; 5-Ohdutp; SCHEMBL149769; 5-Hydroxy-2'-deoxyuridine 5'-triphosphate; Uridine 5'-(tetrahydrogen triphosphate), 2'-deoxy-5-hydroxy-. CAS No. 27972-89-0. Molecular formula: C9H15N2O15P3. Mole weight: 484.14. | |
| 2'-Deoxy-5-iodo-2-pytimidinone-D-ribose | 2'-Deoxy-5-iodo-2-pytimidinone-D-ribose, a highly sought-after compound within the biomedical sector, showcases immense value. Its profound utility lies in combating an array of viral infections, making it an indispensable weapon in viral disease treatment. Operating through its strategic focus on designated enzymes or receptors, this remarkable product effectively impedes viral replication and minimizes viral load. | |
| 2'-?Deoxy-?5-?iodouridine 3',5'-bis(4-Methylbenzoate) | 2'-Deoxy-5-iodouridine 3',5'-Dibenzoate is a protected intermediate of Idoxuridine, antitumor nucleoside enantiomer thymidine kinase used as potential antiviral agents. Synonyms: 2'-Deoxy-5-iodouridine 3',5'-di-p-toluate. CAS No. 31356-86-2. Molecular formula: C23H19IN2O7. Mole weight: 562.31. | |
| 2'-Deoxy-5-methylcytidine | A Cytidine analog and also an isostere of Thymidine. Synonyms: 5-Methyl-2'-deoxy Cytidine; 5-Methyldeoxycytidine; 1-(2-Deoxy-β-D-ribofuranosyl)-5-methylcytosine; 4-Amino-1-((2R,4S,5R)-4-hydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)-5-methylpyrimidin-2(1H)-one. Grades: ≥ 95 %. CAS No. 838-07-3. Molecular formula: C10H15N3O4. Mole weight: 241.24. | |
| 2'-Deoxy-5-methyl-isocytidine triphosphate | 2'-Deoxy-5-methyl-isocytidine triphosphate, a paramount substance in the realm of biomedical research, serves as an indispensable component for synthesizing intricate DNA and RNA molecules. Its significance lies in its role as a substrate for DNA polymerases, thereby assuming a pivotal position in an array of molecular biology methodologies encompassing PCR, DNA sequencing, and mutagenesis investigations. Synonyms: 4(1H)-Pyrimidinone, 2-amino-1-[2-deoxy-5-O-[hydroxy[[hydroxy (phosphonooxy) phosphinyl]oxy]phosphinyl]-β -D-erythro-pentofuranosyl]-5-methyl-; 2-Amino-1-[2-deoxy-5-O-[hydroxy[[hydroxy (phosphonooxy) phosphinyl]oxy]phosphinyl]-β -D-erythro-pentofuranosyl]-5-methyl-4 (1H) -pyrimidinone; ((2R,3S,5R)-5-(2-amino-5-methyl-4-oxopyrimidin-1(4H)-yl)-3-hydroxytetrahydrofuran-2-yl)methyl tetrahydrogen triphosphate; 2'-Deoxy-5-methylisocytidine 5'-triphosphoric acid. CAS No. 139157-80-5. Molecular formula: C10H18N3O13P3. Mole weight: 481.18. | |
| 2'-Deoxy-5-(methylthio)-uridine | 2'-Deoxy-5-(methylthio)-uridine, a pivotal compound within the biomedical industry, plays a crucial role in deciphering the intricate consequences of methylthio alterations on uridine nucleotides. By harnessing its potential, researchers can delve into the realm of novel nucleoside analogs which hold promise in antiviral and anticancer therapeutics. These advancements aim to tackle the complexities of afflictions like viral infections and malignant neoplasms. Synonyms: 5-(Methylthio)-2'-deoxyuridine. CAS No. 14985-32-1. Molecular formula: C10H14N2O5S. Mole weight: 274.29. | |
| 2'-?Deoxy-?5'-?O-?[ (1, ?1-?dimethylethyl) ?dimethylsilyl]?-?2', ?2'-?difluorocytidine | 2'-Deoxy-5'-O-[(1, 1-dimethylethyl)dimethylsilyl]-2', 2'-difluorocytidine is an intermediate in the synthesis of Gemcitabine metabolites. Synonyms: 4-amino-1-((2R,4R,5R)-5-((tert-butyldimethylsilyloxy)methyl)-3,3-difluoro-4-hydroxytetrahydrofuran-2-yl)pyrimidin-2(1H)-one; 4-amino-1-[(2R,4R,5R)-5-[[tert-butyl(dimethyl)silyl]oxymethyl]-3,3-difluoro-4-hydroxyoxolan-2-yl]pyrimidin-2-one; 2'-Deoxy-5'-O-[(1, 1-dimethylethyl)dimethylsilyl]-2', 2'-difluorocytidine; 5'-O-(t-butyldimethylsilyl)-2'-deoxy-2',2'-difluorocytidine; 4-Amino-1-((2R,4R,5R)-5-(((tert-butyldimethylsilyl)oxy)methyl)-3,3-difluoro-4-hydroxytetrahydrofuran-2-yl)pyrimidin-2(1H)-one. CAS No. 1151528-36-7. Molecular formula: C15H25F2N3O4Si. Mole weight: 377.46. | |
| 2'-Deoxy-5'-O-DMT-2'-fluoro-5-methyluridine | 2'-Deoxy-5'-O-DMT-2'-fluoro-5-methyluridine, a paramount compound in the realm of biomedicine, assumes a significant role in the advancement of antiviral drugs and therapies targeting an array of ailments, ranging from viral infections to malignant neoplasms and hereditary disorders. Embodied within its distinctive structural attributes lies robust antiviral efficacy, endowing this compound with immense potential as a hopeful contender for combating viral afflictions like HIV and hepatitis. Synonyms: 5'-O-[Bis(4-methoxyphenyl)phenylmethyl]-2'-deoxy-2'-fluoro-5-methyluridine; 5'-ODMT-2'-fluoro-5-methyl-2'-deoxyuridine. Grades: ≥ 98% (HPLC). CAS No. 133324-02-4. Molecular formula: C31H31FN2O7. Mole weight: 562.59. | |
| 2'-Deoxy-5'-O-DMT-2'-fluoroinosine 3'-CE phosphoramidite | 2'-Deoxy-5'-O-DMT-2'-fluoroinosine 3'-CE phosphoramidite harmonizes with current medical advancements as an indispensable entity, employed extensively in constructing nucleoside analogs. This invaluable compound transpires as an utmost necessity during the creation of DNA and RNA fragments, empowering precise administration of therapeutic drugs while propelling relentless exploration in oncology, virology, and genetic engineering domains. Synonyms: DMT-2'-F-dI-CE phosphoramidite. Molecular formula: C40H46FN6O7P. Mole weight: 772.80. | |
| 2'-Deoxy-5'-O-DMT-2'-fluoro-N2-isobutyrylguanosine | 2'-Deoxy-5'-O-DMT-2'-fluoro-N2-isobutyrylguanosine is a remarkable nucleoside analog emerging as a potent weapon against the replication of virus. Through deftly thwarting viral proliferation, this miraculous antiviral compound disrupts the sacred domain of viral DNA synthesis. Synonyms: N2-iBu-DMT-2'-F-dG; 2'-Deoxy-5'-O-DMT-2'-fluoro-N2-isobutyryl-D-guanosine; 5'-O-DMT-2'-fluoro-N2-isobutyryl-2'-deoxyguanosine. Molecular formula: C35H36FN5O7. Mole weight: 657.70. | |
| 2'-Deoxy-5'-O-DMT-2'-fluoro-N2-isobutyrylguanosine 3'-O-succinate triethylammonium salt | 2'-Deoxy-5'-O-DMT-2'-fluoro-N2-isobutyrylguanosine 3'-O-succinate triethylammonium salt, an esteemed compound extensively utilized within the biomedical sector, assumes a pivotal function in combating a myriad of ailments encompassing viral infections and specific malignancies. Boasting profound anti-viral and anti-tumor capabilities, this product manifests as an indispensable asset for both scientific researchers and pharmaceutical enterprises seeking to forge pioneering therapeutic interventions that exemplify innovation and efficacy. Synonyms: 2'-Deoxy-5'-O-DMT-2'-fluoro-N2-isobutyryl-D-guanosine 3'-O-succinate triethylammonium salt; 5'-O-DMT-2'-fluoro-N2-isobutyryl-2'-deoxyguanosine 3'-O-succinate triethylammonium salt. Molecular formula: C39H40FN5O10·C6H16N. Mole weight: 859.98. | |
| 2'-Deoxy-5'-O-DMT-2'-fluoro-N4-phenoxyacetylcytidine | Demonstrating remarkable potential in the therapeutic realm, 2'-Deoxy-5'-O-DMT-2'-fluoro-N4-phenoxyacetylcytidine emerges as a cutting-edge biomedicine compound. Embracing antiviral prowess, it selectively hampers RNA synthesis, effectively combating the replication of targeted viruses. Its multifaceted properties position it as a promising weapon against a spectrum of viral infections, including respiratory illnesses and consequential outbreaks propelled by these insidious intruders. Molecular formula: C38H36FN3O8. Mole weight: 681.71. | |
| 2'-Deoxy-5'-O-DMT-2'-fluoro-N4-phenoxyacetylcytidine 3'-CE-phosphoramidite | 2'-Deoxy-5'-O-DMT-2'-fluoro-N4-phenoxyacetylcytidine 3'-CE-phosphoramidite, an indispensable element in the ever-evolving biomedical sector, finds its use in synthesizing altered nucleosides tailored for investigative ventures. Within the realm of antiviral drug advancement and nucleic acid-oriented therapeutics, this specimen assumes a pivotal role in comprehending the intricate interplay between pharmaceutical compounds and maladies. Distinguished by its unparalleled attributes, this offering facilitates precision-based enhancements, thereby augmenting the effectiveness and distinctiveness of potential drug candidates. Grades: 98%. Molecular formula: C47H55N5O9FP. Mole weight: 883.94. | |
| 2'-Deoxy-5'-O-DMT-2'-fluorouridine 3'-O-succinate triethylammonium salt | 2'-Deoxy-5'-O-DMT-2'-fluorouridine 3'-O-succinate triethylammonium salt is an invaluable triethylammonium salt of 2'-Deoxy-5'-O-DMT-2'-fluorouridine 3'-O-succinate is revered as a crucial precursor in the synthesis of nucleoside analogs, apexing with paramount significance in antiviral and anticancer drug research. Synonyms: 2'-Deoxy-5'-O-DMT-2'-fluoro-D-uridine 3'-CE succinate triethylammonium salt; 5'-O-DMT-2'-fluoro-2'-deoxyuridine 3'-CE succinate triethylammonium salt. Molecular formula: C34H32FN2O10·C6H16N. Mole weight: 749.84. | |
| 2'-Deoxy-5'-O-DMT-2'-trifluoroacetamidouridine | 2'-Deoxy-5'-O-DMT-2'-trifluoroacetamidouridine is a biomedical product used in the research of viral infections and cancer. It acts as an antiviral and antitumor agent, targeting viral RNA and inhibiting tumor cell proliferation. Derived from uridine, this compound shows potential in nucleoside analog therapy due to its ability to selectively target infected or cancerous cells while minimizing toxicity to healthy cells. Molecular formula: C32H30F3N3O8. Mole weight: 641.61. | |
| 2'-Deoxy-5'-O-DMT-3'-C-methyluridine | 2'-Deoxy-5'-O-DMT-3'-C-methyluridine, being an essential compound in the field of biomedicine, finds widespread application due to its unique characteristics. It serves as a fundamental constituent in the synthesis of medicinal drugs, particularly those designed to combat viral infections and specific malignancies. | |
| 2'-Deoxy-5'-O-DMT-5-acetoxymethyluridine 3'-CE phosphoramidite | The compound known as 2'-Deoxy-5'-O-DMT-5-acetoxymethyluridine 3'-CE phosphoramidite serves a significant purpose within the biomedical domain by facilitating the synthesis of altered RNA molecules. Combining this specialized substance with oligonucleotides during the solid-phase synthesis process results in the successful integration of the 5'-acetoxymethyluridine modification. Such a modified RNA species has proven invaluable in the pursuit of advancing drug discovery and investigating RNA-targeted treatments for multiple afflictions encompassing cancer, viral infections, and genetic abnormalities. Synonyms: 2'-Deoxy-5'-O-DMT-5-acetoxymethyl-D-uridine 3'-CE phosphoramidite. Molecular formula: C42H51N4O10P. Mole weight: 802.85. | |
| 2'-Deoxy-5'-O-DMT-5-D-uridine 3'-CE phosphoramidite | 2'-Deoxy-5'-O-DMT-5-D-uridine 3'-CE phosphoramidite is an indispensable compound extensively employed in the synthesis of oligonucleotides for the realms of biomedical research and diagnostic undertakings, showcasing an imperative significance in advancing nucleic acid-based therapeutic approaches and interventions. Remarkably, its unparalleled configuration facilitates the optimal integration of modified nucleotides into oligonucleotide strands, thus enhancing the efficacy and precision of reserch modalities. Molecular formula: C39H46N4O8PD. Mole weight: 731.81. | |
| 2'-Deoxy-5'-O-DMT-5-fluorouridine | 2'-Deoxy-5'-O-DMT-5-fluorouridine, a cutting-edge biomedicine marvel, emerges as a paramount solution for an extensive array of cancerous afflictions. Its unwavering potency arises from its compelling efficacy in thwarting the formidable RNA and DNA synthesis within malignant cells. An unparalleled therapeutic breakthrough, this compound holds immense promise to revolutionize chemotherapy protocols in combating pernicious diseases like breast, colon, and lung cancer. Synonyms: 2'-Deoxy-5'-O-DMT-5-fluoro-D-uridine; 5'-O-DMT-5-fluoro-2'-deoxyuridine. Molecular formula: C30H29FN2O7. Mole weight: 548.57. | |
| 2'-Deoxy-5'-O-DMT-5-fluorouridine 3'-CE phosphoramidite | 2'-Deoxy-5'-O-DMT-5-fluorouridine 3'-CE phosphoramidite, an indispensable component within the biomedical sector, serves as a pivotal pharmaceutical intermediate. Its application lies in the synthesis of altered nucleosides, consequently facilitating the creation of medications tackling diverse ailments such as viral infections and cancers. Furthermore, this compound showcases its potential in generating nucleotide analogs that precisely target enzymes or pathways, presenting a promising avenue for groundbreaking therapeutic interventions. This multifaceted product epitomizes the intersection of scientific advancements and pharmaceutical innovation. Synonyms: 5-F-dU-CE Phosphoramidite; 2'-Deoxy-5-fluoro-D-uridine 3'-CE phosphoramidite; 2'-Fluoro-2'-deoxyuridine 3'-CE phosphoramidite. Molecular formula: C39H46FN4O8P. Mole weight: 748.80. | |
| 2'-Deoxy-5'-O-DMT-5-iodocytidine | 2'-Deoxy-5'-O-DMT-5-iodocytidine, an exceptional antiviral nucleoside analog utilized in biomedicine, exhibits remarkable potential in combating viral infections, specifically those engendered by DNA viruses. Its profound efficacy lies in its ability to impede viral replication through precise targeting of viral DNA synthesis and subsequent integration into replicating viral genomes. The extensive research conducted on this compound underscores its formidable antiviral activity against an array of DNA viruses encompassing herpes simplex virus (HSV), cytomegalovirus (CMV), and Epstein-Barr virus (EBV). | |
| 2'-Deoxy-5'-O-DMT-5-methylcytidine | 2'-Deoxy-5'-O-DMT-5-methylcytidine is a remarkable biomedicine distinguished by its potent antiviral properties, widely employed for the research of viral infections and malignant conditions. Functioning as a nucleoside analogue, it exerts its action by impeding viral replication and restraining the growth of tumor cells. Leveraging its exceptional chemical composition, this product manifesting unparalleled specificity and efficacy against pathogens and malignant cells of interest. Synonyms: 5-Methyl-5'-O-DMT-deoxycytidine; 2'-Deoxy-5'-O-DMT-5-methyl-D-cytidine; 5'-O-DMT-5-methyl-2'-deoxycytidine. Molecular formula: C31H33N3O6. Mole weight: 543.63. | |
| 2'-Deoxy-5'-O-DMT-5-(methylthio)-uridine 3'-CE phosphoramidite | 2'-Deoxy-5'-O-DMT-5-(methylthio)-uridine 3'-CE phosphoramidite is a crucial compound in the biomedical industry used for DNA synthesis and modification. It is commonly employed in the development of oligonucleotides and nucleic acid probes for various applications, including gene expression analysis, genetic engineering, and targeted drug delivery. This phosphoramidite facilitates the introduction of phosphate and other desired modifications in the synthesized DNA strands, enabling precise control over their structure and function. CAS No. 212075-46-2. Molecular formula: C40H49N4O8PS. Mole weight: 776.88. | |
| 2'-Deoxy-5'-O-DMT-5-propargyloxyuridine | 2'-Deoxy-5'-O-DMT-5-propargyloxyuridine, also known as PDU, is an indispensable entity in the realm of biomedicine. Its multifaceted properties make it indispensable in the production of groundbreaking antiviral pharmaceuticals and as an invaluable instrument for genetic investigation. With its remarkable ability to impede the proliferation of diverse viral strains, it stands poised as a prospective remedy for combating viral afflictions. Capitalizing on its idiosyncratic architecture, this compound exhibits precision in selectively targeting viral DNA or RNA sequences, thus presenting an exquisitely tailored therapeutic modality. Synonyms: 2'-Deoxy-5'-O-DMT-5-propargyloxy-D-uridine; 5'-O-DMT-5-propargyloxy-2'-deoxyuridine. Molecular formula: C33H32N2O8. Mole weight: 584.63. | |
| 2'-Deoxy-5'-O-DMT-cytidine | 2'-Deoxy-5'-O-DMT-cytidine, a significant and indispensable compound utilized extensively in the realm of biomedicine, finds its purpose deeply rooted in research and development. This pivotal product showcases its utmost importance when exploring the intricacies of nucleosides and nucleotides. Its exceptional structure and properties provide an invaluable pathway towards comprehending the synthesis and interactions of nucleic acids. Synonyms: 5'-O-(4,4'-Dimethoxytrityl)-2'-deoxycytidine; DMT-dC; 4-Amino-1- ( (2R, 4S, 5R)-5- ( (bis (4-methoxyphenyl) (phenyl)methoxy)methyl)-4-hydroxytetrahydrofuran-2-yl)pyrimidin-2 (1H)-one; 5'-O-[Bis(4-methoxyphenyl)(phenyl)methyl]-2'-deoxycytidine. Grades: ≥95%. CAS No. 76512-82-8. Molecular formula: C30H31N3O6. Mole weight: 529.58. | |
| 2'-Deoxy-5'-O-DMT-guanosine-3'-O-P(OMe)N(iPr)2 | 2'-Deoxy-5'-O-DMT-guanosine-3'-O-P(OMe)N(iPr)2, a fascinating biochemical entity of great scientific interest, finds extensive application within the esteemed biomedical realm. Its multifaceted nature has rendered it a subject of thorough investigation, owing to the potential it holds in combatting sundry ailments. Notable focus has been directed towards its utilization for drug development targeting intricate molecular pathways, establishing it as an instrumental resource. Synonyms: DMT-5'-O-dG-3'-O-P(OMe)N(iPr)2. | |
| 2'-Deoxy-5'-O-DMT-guanosine-(DMF)-3'-Q Linker CPG | 2'-Deoxy-5'-O-DMT-guanosine-(DMF)-3'-Q Linker CPG is a specialized biomedical product utilized for the synthesis of nucleotides and oligonucleotides. It acts as a linker providing stability and compatibility during the solid-phase synthesis process. This product facilitates the efficient coupling of guanosine residues, enabling the targeted treatment of various diseases related to genetic disorders, cancer, and viral infections. | |
| 2'-Deoxy-5-O-DMT-guanosine-(DMF)-succinyl-CPG | 2'-Deoxy-5-O-DMT-guanosine-(DMF)-succinyl-CPG, an indispensable asset in the biomedical realm for oligonucleotide synthesis, manifests itself as a paramount instrument. It bestows upon us the capability to fabricate altered DNA sequences with utmost efficacy and prodigious output. These sequences hold great significance in combatting genetic disorders, viral afflictions, and neoplastic conditions. | |
| 2'-Deoxy-5'-O-DMT-guanosine-(DMF)-succinyl CPG | 2'-Deoxy-5'-O-DMT-guanosine-(DMF)-succinyl CPG, an indispensable asset in the realm of biomedical research. Leveraged for synthesizing oligonucleotides, this remarkable entity plays a pivotal role in nurturing nucleic acid-based therapeutics, anatomizing genetic disorders, and comprehending diseases. It spearheads the realm of drug discovery and personalized medicine by endowing scientists with efficacious and controlled DNA sequence synthesis. Prepare to embark on riveting scientific endeavors with this groundbreaking product. | |
| 2'-Deoxy-5'-O-DMT-guanosine-(iBu)-3'-succinyl CPG | 2'-Deoxy-5'-O-DMT-guanosine-(iBu)-3'-succinyl CPG, a pinnacle instrument harnessed within the ever-evolving biomedical realm for the profound synthesis of oligonucleotides. Its unparalleled prowess transcends boundaries, propelling therapeutic advancement towards combating afflictions like cancer, genetic anomalies, and viral onslaughts. | |
| 2'-Deoxy-5'-O-DMT-guanosine-(iBu)-succinyl CPG | 2'-Deoxy-5'-O-DMT-guanosine-(iBu)-succinyl CPG, an indispensable resource within the biomedical sector, holds significant prominence in the realm of oligonucleotide synthesis. Garnering immense importance, it is substantially utilized for the formulation of nucleic acid-centered therapeutics and diagnostics pertaining to an array of ailments encompassing cancer, infectious diseases, and genetic disorders. | |
| 2'-Deoxy-5'-O-DMT-inosine 3'-succinyl CPG | 2'-Deoxy-5'-O-DMT-inosine 3'-succinyl CPG is a crucial tool in biomedical research for the synthesis of modified oligonucleotides. It is extensively utilized as a solid support matrix for automated DNA/RNA synthesis, enabling the efficient incorporation of nucleotide modifications. This product plays a vital role in studying and developing various nucleic acid-based therapies, diagnostics, and drug delivery systems targeting specific diseases like cancer and viral infections. | |
| 2'-Deoxy-5'-O-DMT-N2-(4-isopropylphenoxyacetyl)guanosine | 2'-Deoxy-5'-O-DMT-N2-(4-isopropylphenoxyacetyl)guanosine is a modified nucleotide analog, showcasing the ability to inhibit viral replication. Its exceptional chemical configuration allows for site-specific inhibition of viral enzymes, inducing a substantial decline in viral replication dynamics. Synonyms: 5'-O-[Bis(4-methoxyphenyl)phenylmethyl]-2'-deoxy-N-[2-[4-(1-methylethyl)phenoxy]acetyl]guanosine. CAS No. 909415-65-2. Molecular formula: C42H43N5O8. Mole weight: 745.82. | |
| 2'-Deoxy 5'-O-DMT-N2-(4-isopropylphenoxyacetyl)guanosine 3'-CE phosphoramidite | 2'-Deoxy 5'-O-DMT-N2-(4-isopropylphenoxyacetyl)guanosine 3'-CE phosphoramidite, a compound of significant importance in the realm of biomedicine, finds applications in the synthesis of top-notch oligonucleotides, specifically within the domain of DNA and RNA research. Its distinctive structure facilitates seamless integration into oligonucleotide chains during solid-phase synthesis methods. This phosphoramidite assumes a pivotal role in the advancement of therapeutics, diagnostics, and a myriad of applications targeting genetic disorders, viral infections, and cancer, thus establishing its indispensability in these domains of study. Synonyms: 2'-Deoxy 5'-O-DMT-N2-(4-isopropylphenoxyacetyl)-D-guanosine 3'-CE phosphoramidite; 5'-O-DMT-N2-(4-isopropylphenoxyacetyl)-2'-deoxyguanosine 3'-CE phosphoramidite. Molecular formula: C51H60N7O9P. Mole weight: 946.06. | |
| 2'-Deoxy-5'-O-DMT-N2-(4-isopropylphenoxyacetyl)guanosine 3'-Me phosphoramidite | 2'-Deoxy-5'-O-DMT-N2-(4-isopropylphenoxyacetyl)guanosine 3'-Me phosphoramidite is a valuable tool in biomedicine, predominantly used in DNA synthesis and modification. This phosphoramidite is commonly employed for the introduction of the guanosine nucleotide within specific DNA sequences, aiding in the study and understanding of various diseases, genetics, and drug development. It offers precise site-specific modifications and plays a crucial role in targeted drug delivery systems and therapeutic approaches. Synonyms: 5'-(4,4'-Dimethoxytrityl)-N-(4-isopropylphenoxyacetyl)-2'-deoxyguanosine, 3'-[methyl-(N,N-diisopropyl)]-phosphoramidite; iPr-Pac-dG-Me Phosphoramidite; 2'-Deoxy-5'-O-DMT-N2-(4-isopropylphenoxyacetyl)-D-guanosine 3'-Me phosphonamidite; 5'-O-DMT-N2-(4-isopropylphenoxyacetyl)-2'-deoxyguanosine 3'-Me phosphonamidite. Molecular formula: C49H59N6O9P. Mole weight: 907.03. | |
| 2'-Deoxy-5'-O-DMT-N2-iBu-guanosine-3'-succinyl CPG | 2'-Deoxy-5'-O-DMT-N2-iBu-guanosine-3'-succinyl CPG, a paramount instrument in the realm of biomedicine, transcends boundaries as a solid support during the synthesis of altered oligonucleotides, specifically in the domain of drug discovery exploration, with a discerning focus on numerous ailments. An exemplar of efficacious pharmaceutical transportation, it empowers the amelioration of an array of afflictions, spanning genetic disorders to viral infestations. Its multifaceted applications herald its invaluable prowess within the biomedical sector. | |
| 2'-Deoxy-5'-O-DMT-N2-isobutyryl-3'-xanthylguanosine | 2'-Deoxy-5'-O-DMT-N2-isobutyryl-3'-xanthylguanosine, an exceptionally potent therapeutic agent, finds extensive application within the biomedical industry for combating a select set of viral infections. This unique compound showcases unparalleled antiviral properties that distinctly focus on impeding the proliferation and diffusion of specified viruses, providing substantial relief against associated ailments. Synonyms: 2'-Deoxy-5'-O-DMT-N2-isobutyryl-3'-xanthyl-D-guanosine; 5'-O-DMT-N2-isobutyryl-3'-xanthyl-2'-deoxyguanosine. Molecular formula: C46H49N5O8S. Mole weight: 832.00. | |
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