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Home >> Signaling Pathways >> DNA Damage/DNA Repair >> Nucleoside Antimetabolite/Analogue

Nucleoside Antimetabolite/Analogue

Nucleoside analouges belong to the fmalily of antimetablits that resemble the neleosieds for uptake and metaolism that inibitr dna sytnse and couase cain termination. It is a durg target for cacner and viral infcations.

Products for  Nucleoside Antimetabolite/Analogue

  1. Cat.No. Product Name Information
  2. GC69793 (R)-5-O-Benzoyl-1,2-di-O-isopropylidene-alpha-D-xylofuranose

    (R)-5-O-Benzoyl-1,2-di-O-isopropylidene-alpha-D-xylofuranose is a purine nucleoside analogue. Purine nucleoside analogues have broad anti-tumor activity and target inert lymphoid malignancies. The anticancer mechanism in this process depends on inhibiting DNA synthesis, inducing apoptosis (cell death), etc.

     (R)-5-O-Benzoyl-1,2-di-O-isopropylidene-alpha-D-xylofuranose Chemical Structure
  3. GC68484 1,2-O-Isopropylidene-5-O-p-toluoyl-a-D-xylofuranose

    1,2-O-Isopropylidene-5-O-p-toluoyl-a-D-xylofuranose is a purine nucleoside analogue. Purine nucleoside analogues have broad anti-tumor activity and target malignant tumors in the inert lymphatic system. The anticancer mechanism in this process depends on inhibiting DNA synthesis, inducing apoptosis (cell death), etc.

     1,2-O-Isopropylidene-5-O-p-toluoyl-a-D-xylofuranose Chemical Structure
  4. GC65551 1-(2'-O-4-C-Methylene-beta-D-ribofuranosyl)thymine 1-(2'-O-4-C-Methylene-beta-D-ribofuranosyl)thymine is a bicyclic nucleoside. 1-(2'-O-4-C-Methylene-beta-D-ribofuranosyl)thymine Chemical Structure
  5. GC71294 1-(2-Deoxy-β-D-threo-pentofuranosyl)thymine 1-(2-Deoxy-β-D-threo-pentofuranosyl)thymine is a thymidine analog. 1-(2-Deoxy-β-D-threo-pentofuranosyl)thymine Chemical Structure
  6. GC65038 1-Methylinosine

    1-methyl Inosine, N1-Methylinosine

     1-Methylinosine is a modified nucleotide found at position 37 in tRNA 3' to the anticodon of eukaryotic tRNA. 1-Methylinosine Chemical Structure
  7. GC73523 2'-Deoxy-N3-methylcytidine hydriodide 2’-Deoxy-N3-metlcytidine driodide is a purine nucleoside analog. 2'-Deoxy-N3-methylcytidine hydriodide Chemical Structure
  8. GC65489 2'-F-Bz-dC Phosphoramidite 2'-F-Bz-dC Phosphoramidite can be used in the synthesis of oligoribonucleotides. 2'-F-Bz-dC Phosphoramidite Chemical Structure
  9. GC66651 2'-O,4'-C-Methyleneadenosine

    LNA-A

     2'-O,4'-C-Methyleneadenosine (LNA-A) is a locked nucleic acid (LNA) and is also an adenosine analog. 2'-O,4'-C-Methyleneadenosine Chemical Structure
  10. GC66654 2'-O,4'-C-Methylenecytidine

    LNA-C(Bz)

     2'-O,4'-C-Methylenecytidine (LNA-C(Bz)) is a bicyclic nucleoside analogue with fixed N-type conformation. 2'-O,4'-C-Methylenecytidine can be used to synthesize oligonucleotides. 2'-O,4'-C-Methylenecytidine forms duplexes with complementary DNA and RNA strands. 2'-O,4'-C-Methylenecytidine Chemical Structure
  11. GC66655 2'-O,4'-C-Methyleneguanosine

    LNA-G

     2′-O,4′-C-Methyleneguanosine (LNA-G) is a reverse guanine analogue, where LNA (locked nucleic acid) is a nucleic acid analogue. LNA modification can be used in a variety of applications such as effective binding affinity to complementary sequences and greater nuclease resistance than natural nucleotides, offering great potential for applications in disease diagnosis and research. LNA-G is also available via KOD DNA polymerase, which allows the integration of LNA-G nucleotides into the DNA strand. 2'-O,4'-C-Methyleneguanosine Chemical Structure
  12. GC65170 2′,3′-Di-O-acetylguanosine 2′,3′-Di-O-acetylguanosine is a nucleoside analog. 2′,3′-Di-O-acetylguanosine Chemical Structure
  13. GC67384 2′-Deoxy-β-L-uridine 2'-Deoxy-β-L-uridine is a nucledside analogue and a specific substrate for the viral enzyme, shows no stereospecificity against herpes simplex 1 (HSV1) thymidine kinase (TK). 2′-Deoxy-β-L-uridine exerts antiviral activity via the interation of 5'-triphosphates with the viral DNA polymerase. 2′-Deoxy-β-L-uridine Chemical Structure
  14. GC61667 2′-Deoxy-2′-fluoroadenosine 2′-Deoxy-2′-fluoroadenosine can be used for thesynthesisof 2′-Deoxy-2′-fluoro-modified oligonucleotides hybridized with RNA. 2′-Deoxy-2′-fluoroadenosine can be cleaved efficiently by E. coli purine nucleoside phosphorylase (PNP) to the toxic agent 2-fluoroadenine (FAde). 2′-Deoxy-2′-fluoroadenosine shows excellent in vivo activity against tumors expressing E. coli PNP. 2′-Deoxy-2′-fluoroadenosine Chemical Structure
  15. GC62530 2’-O-Me-C(Bz) Phosphoramidite 2’-O-Me-C(Bz) Phosphoramidite is a modified phosphoramidite monomer, which can be used for the oligonucleotide synthesis. 2’-O-Me-C(Bz) Phosphoramidite Chemical Structure
  16. GC62529 2’-OMe-A(Bz) Phosphoramidite 2’-OMe-A(Bz) Phosphoramidite is a modified phosphoramidite monomer, which can be used for the oligonucleotide synthesis. 2’-OMe-A(Bz) Phosphoramidite Chemical Structure
  17. GC62531 2’-OMe-G(ibu) Phosphoramidite 2’-OMe-G(ibu) Phosphoramidite is a modified phosphoramidite monomer, which can be used for the oligonucleotide synthesis. 2’-OMe-G(ibu) Phosphoramidite Chemical Structure
  18. GC48440 2'-Deoxycytidine-5'-triphosphate (sodium salt)

    dCTP

     2'-Deoxycytidine-5'-triphosphate (sodium salt) (dCTP trisodium salt) is a nucleoside triphosphate that can be used for DNA synthesis. 2'-Deoxycytidine-5'-triphosphate (sodium salt) Chemical Structure
  19. GC33430 2'-Deoxypseudoisocytidine 2'-Deoxypseudoisocytidine is a nucleoside analogue. 2'-Deoxypseudoisocytidine Chemical Structure
  20. GC35072 2'-O,4'-C-Methyleneuridine 2'-O,4'-C-Methyleneuridine (Compound 15a) is a bicyclic nucleoside. 2'-O,4'-C-Methyleneuridine Chemical Structure
  21. GC64983 2-Amino-2'-deoxyadenosine 2-Amino-2'-deoxyadenosine is a deoxyribonucleoside used for the oligonucleotide synthesis. 2-Amino-2'-deoxyadenosine Chemical Structure
  22. GC71208 2-Methyladenosine 2-Methyladenosine is an adenosine analogue. 2-Methyladenosine Chemical Structure
  23. GC73004 2-Methylthioadenosine 2-Metlthioadenosine is a purine nucleoside analog. 2-Methylthioadenosine Chemical Structure
  24. GC65083 3'-Azido-3'-deoxy-5-fluorocytidine 3'-Azido-3'-deoxy-5-fluorocytidine (Compound 12) is a cytidine derivative. 3'-Azido-3'-deoxy-5-fluorocytidine Chemical Structure
  25. GC73400 3'-Azido-3'-deoxyuridine 3’-Azido-3’-deoxyuridine is a purine nucleoside analogue. 3'-Azido-3'-deoxyuridine Chemical Structure
  26. GC71204 3'-O-(2-Methoxyethyl)guanosine 3’-O-(2-Methoxyethyl)guanosine is a guanosine analogue. 3'-O-(2-Methoxyethyl)guanosine Chemical Structure
  27. GC64985 3'-O-Methylguanosine 3'-O-Methylguanosine is a methylated nucleoside analogs and a RNA chain terminator. 3'-O-Methylguanosine Chemical Structure
  28. GC35105 3'-Azido-3'-deoxy-beta-L-uridine 3'-Azido-3'-deoxy-beta-L-uridine (Compound 25) is a nucleoside derivative. 3'-Azido-3'-deoxy-beta-L-uridine Chemical Structure
  29. GC60023 3'-Deoxyuridine-5'-triphosphate

    3'-dUTP

     3'-Deoxyuridine-5'-triphosphate (3'-dUTP) is a nucleotide analogue that inhibits DNA-dependent RNA polymerases I and II. 3'-Deoxyuridine-5'-triphosphate Chemical Structure
  30. GC61862 3'-Deoxyuridine-5'-triphosphate trisodium

    3'-dUTP trisodium

     3'-Deoxyuridine-5'-triphosphate trisodium (3'-dUTP trisodium) is a nucleotide analogue that inhibits DNA-dependent RNA polymerases I and II. 3'-Deoxyuridine-5'-triphosphate trisodium Chemical Structure
  31. GC65084 3-Methylcytidine 3-Methylcytidine, a urinary nucleoside, can be used as a biomarker of four different types of cancer: lung cancer, gastric cancer, colon cancer, and breast cancer. 3-Methylcytidine Chemical Structure
  32. GC68557 4-Thio-2'-deoxyuridine

    2′-Deoxy-4-thiouridine; 4-Thiodeoxyuridine

    4-Thio-2'-deoxyuridine is a purine nucleoside analogue. Purine nucleoside analogues have broad anti-tumor activity, targeting inert lymphatic system malignancies. The anticancer mechanism in this process depends on inhibiting DNA synthesis and inducing cell apoptosis.

     4-Thio-2'-deoxyuridine Chemical Structure
  33. GC42474 4-Thiouridine

    NSC 518132, 4-SU

     4-Thiouridine(4sU) is a ribonucleoside analogue that can be used for RNA analysis and (m)RNA labeling. 4-Thiouridine Chemical Structure
  34. GC73521 5'-DMT-2'-O-TBDMS-N1-Methyl-PseudoUridine-CE-Phosphoramidite

    N1-Methylpseudouridine CEP

     5'-DMT-2'-O-TBDMS-N1-Metl-PseudoUridine-CE-Phosphoramidite is a purine nucleoside analog. 5'-DMT-2'-O-TBDMS-N1-Methyl-PseudoUridine-CE-Phosphoramidite Chemical Structure
  35. GC65520 5'-DMT-3'-TBDMS-ibu-rG 5'-DMT-3'-TBDMS-ibu-rG is is a modified nucleoside. 5'-DMT-3'-TBDMS-ibu-rG Chemical Structure
  36. GC65402 5'-O-DMT-2'-O-TBDMS-Bz-rC 5'-O-DMT-2'-O-TBDMS-Bz-rC is a modified nucleoside and can be used to synthesize DNA or RNA. 5'-O-DMT-2'-O-TBDMS-Bz-rC Chemical Structure
  37. GC65164 5'-O-DMT-2'-O-TBDMS-rI 5'-O-DMT-2'-O-TBDMS-rI is a modified nucleoside. 5'-O-DMT-2'-O-TBDMS-rI Chemical Structure
  38. GC65396 5'-O-DMT-ibu-dC 5'-O-DMT-ibu-dC can be used in the synthesis of oligodeoxyribonucleotides. 5'-O-DMT-ibu-dC Chemical Structure
  39. GC64982 5'-O-DMT-N2-DMF-dG 5'-O-DMT-2'-O-TBDMS-rI is a modified nucleoside. 5'-O-DMT-N2-DMF-dG Chemical Structure
  40. GC65482 5'-O-DMT-N6-ibu-dA 5'-O-DMT-N6-ibu-dA can be used in the synthesis of oligodeoxyribonucleotides. 5'-O-DMT-N6-ibu-dA Chemical Structure
  41. GC65562 5'-O-DMT-N6-Me-2'-dA 5'-O-DMT-N6-Me-2'-dA is a nucleoside with protective and modification effects. 5'-O-DMT-N6-Me-2'-dA Chemical Structure
  42. GC65401 5'-O-TBDMS-dU 5'-O-TBDMS-dU can be used in the synthesis of oligoribonucleotides. 5'-O-TBDMS-dU Chemical Structure
  43. GC71033 5'-ODMT cEt G Phosphoramidite (Amidite) 5'-ODMT cEt G Phosphoramidite Amidite is a potent nucleic acid analog. 5'-ODMT cEt G Phosphoramidite (Amidite) Chemical Structure
  44. GC71035 5'-ODMT cEt m5U Phosphoramidite (Amidite) 5'-ODMT cEt m5U Phosphoramidite Amidite is a locked nucleic acid (LNA) analog. 5'-ODMT cEt m5U Phosphoramidite (Amidite) Chemical Structure
  45. GC73179 5'-ODMT cEt N-Bz A Phosphoramidite (Amidite) 5'-ODMT cEt N-Bz A Phosphoramidite Amidite is a locked nucleic acid (LNA) analogue. 5'-ODMT cEt N-Bz A Phosphoramidite (Amidite) Chemical Structure
  46. GC71034 5'-ODMT cEt N-Bzm5 C Phosphoramidite (Amidite) 5'-ODMT cEt N-Bzm5 C Phosphoramidite Amidite is a potent nucleic acid analog. 5'-ODMT cEt N-Bzm5 C Phosphoramidite (Amidite) Chemical Structure
  47. GC62157 5’-O-DMT-2’-O-TBDMS-Ac-rC 5’-O-DMT-2’-O-TBDMS-Ac-rC is a modified nucleoside and can be used to synthesize DNA or RNA. 5’-O-DMT-2’-O-TBDMS-Ac-rC Chemical Structure
  48. GC62149 5’-O-DMT-2’-TBDMS-Uridine 5’-O-DMT-2’-TBDMS-Uridine is a deoxyribonucleoside used for the oligonucleotide synthesis. 5’-O-DMT-2’-TBDMS-Uridine Chemical Structure
  49. GC62532 5’-O-DMT-3’-O-TBDMS-Ac-rC 5’-O-DMT-3’-O-TBDMS-Ac-rC is a modified nucleoside and can be used to synthesize DNA or RNA. 5’-O-DMT-3’-O-TBDMS-Ac-rC Chemical Structure
  50. GC62573 5’-O-DMT-Bz-rC 5'-O-DMT-Bz-Rc is a modified nucleoside and can be used to synthesize DNA or RNA. 5’-O-DMT-Bz-rC Chemical Structure
  51. GC62574 5’-O-DMT-N4-Ac-2’-F-dC 5’-O-DMT-N4-Ac-2’-F-dC is a modified nucleoside and can be used to synthesize DNA or RNA. 5’-O-DMT-N4-Ac-2’-F-dC Chemical Structure
  52. GC62575 5’-O-DMT-N4-Bz-2’-F-dC 5’-O-DMT-N4-Bz-2’-F-dC is a nucleoside with protective and modification effects. 5’-O-DMT-N4-Bz-2’-F-dC Chemical Structure
  53. GC62576 5’-O-DMT-N4-Bz-5-Me-dC 5’-O-DMT-N4-Bz-5-Me-dC is a modified nucleoside. 5’-O-DMT-N4-Bz-5-Me-dC Chemical Structure
  54. GC62578 5’-O-TBDMS-Bz-dA 5’-O-TBDMS-Bz-dA is a nucleoside with protective and modification effects. 5’-O-TBDMS-Bz-dA Chemical Structure
  55. GC62579 5’-O-TBDMS-dA 5’-O-TBDMS-dA is a modified nucleoside and can be used to synthesize DNA or RNA. 5’-O-TBDMS-dA Chemical Structure
  56. GC62580 5’-O-TBDMS-dG 5’-O-TBDMS-dG is a modified nucleoside. 5’-O-TBDMS-dG Chemical Structure
  57. GC62581 5’-O-TBDMS-dT 5’-O-TBDMS-dT is a nucleoside with protective and modification effects. 5’-O-TBDMS-dT Chemical Structure
  58. GC61432 5'-O-DMT-2'-O-TBDMS-N-Bz-Adenosine 5'-O-DMT-2'-O-TBDMS-N-Bz-Adenosine?is an adenosine derivative and can be used as an intermediate for oligonucleotides synthesis. 5'-O-DMT-2'-O-TBDMS-N-Bz-Adenosine Chemical Structure
  59. GC64952 5-Aza-7-deazaguanine 5-Aza-7-deazaguanine is a substrate for wild-type (WT) E. coli purine nucleoside phosphorylase and its Ser90Ala mutant in the synthesis of base-modified nucleosides. 5-Aza-7-deazaguanine Chemical Structure
  60. GC10946 5-Azacytidine

    Antibiotic U 18496, 5AzaC, Ladakamycin, Mylosar, NSC 102816, NSC 103627, U 18496, WR 183027

     5-Azacytidine (also known as 5-AzaC), a compound belonging to a class of cytosine analogues, is a DNA methyl transferase (DNMT) inhibitor that exerts potent cytotoxicity against multiple myeloma (MM) cells, including MM.1S, MM.1R, RPMI-8266, RPMI-LR5, RPMI-Dox40 and Patient-derived MM, with the half maximal inhibition concentration IC50 values of 1.5 μmol/L, 0.7 μmol/L, 1.1 μmol/L, 2.5 μmol/L, 3.2 μmol/L and 1.5 μmol/L respectively. 5-Azacytidine Chemical Structure
  61. GC73520 5-Azidomethyl-2'-deoxyuridine

    5-AmdU; α-Azidothymidine

     5-Azidometl-2'-deoxyuridine (5-AmdU) is a purine nucleoside analog. 5-Azidomethyl-2'-deoxyuridine Chemical Structure
  62. GC11940 5-BrdU

    BrdU, Bromodeoxyuridine, Broxuridine, NSC 38297

     5-BrdU (5-bromo-2-deoxundine5-BrdU) is a synthetic thymidine bromide analog that is commonly used to measure DNA synthesis and label dividing cells. 5-BrdU Chemical Structure
  63. GC71207 5-Ethyluridine 5-Ethyluridine is a purine nucleoside analogue. 5-Ethyluridine Chemical Structure
  64. GC62547 5-O-TBDMS-N4-Benzoyl-2-deoxycytidine 5-O-TBDMS-N4-Benzoyl-2-deoxycytidine is a modified nucleoside. 5-O-TBDMS-N4-Benzoyl-2-deoxycytidine Chemical Structure
  65. GC30548 6-Amino-5-nitropyridin-2-one 6-Amino-5-nitropyridin-2-one is a pyridine base and used as a nucleobase of hachimoji DNA, in which it pairs with 5-aza-7-deazaguanine. 6-Amino-5-nitropyridin-2-one Chemical Structure
  66. GC60031 6-Azathymine 6-Azathymine, a 6-nitrogen analog of thymine, is a potent D-3-aminoisobutyrate-pyruvate aminotransferase inhibitor. 6-Azathymine Chemical Structure
  67. GC32975 6-Mercaptopurine hydrate

    6-MP

     An inhibitor of purine synthesis and interconversion 6-Mercaptopurine hydrate Chemical Structure
  68. GC65082 6-O-Methyl Guanosine 6-O-Methyl Guanosine is a modified nucleoside. 6-O-Methyl Guanosine Chemical Structure
  69. GC35171 6-Thioinosine 6-Thioinosine (6TI) is a purine antimetabolite, acts as an anti-adipogenesis agent, downregulates mRNA levels of PPAR γ and C/EBPα, as well as PPAR γ target protein such as LPL, CD36, aP2, and LXRα. 6-Thioinosine Chemical Structure
  70. GC66060 7-Iodo-2',3'-dideoxy-7-deaza-guanosine 7-Iodo-2',3'-dideoxy-7-deaza-guanosine is a dideoxynucleoside that can be used in DNA synthesis and sequencing reactions. 7-Iodo-2',3'-dideoxy-7-deaza-guanosine Chemical Structure
  71. GC71545 7-Methyl-guanosine-5'-triphosphate sodium 7-Methyl-guanosine-5'-triphosphate (m7GTP) sodium is a guanosine 5'-phosphate. 7-Methyl-guanosine-5'-triphosphate sodium Chemical Structure
  72. GC30531 7-Methylguanosine

    m7G, 7-MeGua

     A nucleotide analog 7-Methylguanosine Chemical Structure
  73. GC65525 7-TFA-ap-7-Deaza-dG 5'-O-TBDMS-dG is a modified nucleoside. 7-TFA-ap-7-Deaza-dG Chemical Structure
  74. GC73399 9-(β-D-Xylofuranosyl)adenine 9-(β-D-Xylofuranosyl)adenine is an adenosine analog. 9-(β-D-Xylofuranosyl)adenine Chemical Structure
  75. GC13805 Abacavir Abacavir Chemical Structure
  76. GC13432 Adenine High affinity adenine receptor agonist Adenine Chemical Structure
  77. GC14106 Adenosine

    NSC 7652

     nucleoside Adenosine Chemical Structure
  78. GC65462 Adenosine 5′-monophosphoramidate sodium Adenosine 5′-monophosphoramidate sodium is an adenosine derivative and can be used as an intermediate for nucleotide synthesis. Adenosine 5′-monophosphoramidate sodium Chemical Structure
  79. GC68625 Adenosine-d2

    Adenine riboside-d2; D-Adenosine-d2

    Adenosine-d2 is the deuterated form of adenosine. Adenosine (adenine riboside) is a commonly occurring endogenous secretion that acts through four G protein-coupled receptors (A1, A2A, A2B, and A3). Adenosine affects almost all aspects of cellular physiology, including neuronal activity, vascular function, platelet aggregation, and blood cell regulation.

     Adenosine-d2 Chemical Structure
  80. GC73524 Alpha-Adenosine Alpha-Adenosine is a purine nucleoside analog. Alpha-Adenosine Chemical Structure
  81. GC73525 Alpha-Guanosine Alpha-Guanosine is a purine nucleoside analog. Alpha-Guanosine Chemical Structure
  82. GC72841 Arabinosylhypoxanthine Arabinosylpoxanthine is a purine nucleoside analog. Arabinosylhypoxanthine Chemical Structure
  83. GC11843 Azaguanine-8

    8-AG

     Azaguanine-8 is a purine analogue that shows antineoplastic activity. Azaguanine-8 functions as an antimetabolite and easily incorporates into ribonucleic acids, interfering with normal biosynthetic pathways, thus inhibiting cellular growth. Azaguanine-8 Chemical Structure
  84. GC15866 Capecitabine

    Ro 091978

     DNA, RNA and protein synthesis inhibitor Capecitabine Chemical Structure
  85. GC12748 Carmofur

    HCFU

     Cytostatic derivative of fluorouracilm,antineoplatic agent Carmofur Chemical Structure
  86. GC64261 Censavudine

    OBP-601; BMS-986001

     Censavudine (OBP-601; BMS-986001), a nucleoside analog, is a nucleoside reverse transcriptase inhibitor. Censavudine Chemical Structure
  87. GC35693 CI 972 (anhydrous) CI 972 (anhydrous) is a potent, orally active, and competitive inhibitor of purine nucleoside phosphorylase (PNP) (Ki=0.83 μM) under development as a T cell-selective immunosuppressive agent. CI 972 (anhydrous) Chemical Structure
  88. GC15219 Clofarabine

    Clolar, Evoltra

     Antimetabolite,inhibit DNA polymerase and ribonucleotide reductase Clofarabine Chemical Structure
  89. GC33177 CNDAC CNDAC is a major metabolite of oral drug sapacitabine, and a nucleoside analog. CNDAC Chemical Structure
  90. GC38382 CNDAC hydrochloride CNDAC hydrochloride is a metabolite of the orally active agent sapacitabine, and a nucleoside analog. CNDAC hydrochloride Chemical Structure
  91. GC13070 Cytarabine

    1βDArabinofuranosylcytosine, NSC 63878, NSC 287459, U19920A

     Cytarabine (Ara-C) is a cytosine analog that primarily inhibits the function of DNA polymerase to block DNA synthesis. Cytarabine Chemical Structure
  92. GC14961 Cytarabine hydrochloride DNA synthsis inhibitor Cytarabine hydrochloride Chemical Structure
  93. GC13729 Cytidine

    β-D-Cytidine, NSC 20258

     pyrimidine nucleoside Cytidine Chemical Structure
  94. GC14485 Dacarbazine

    NCI C04717, NSC 45388

     Antineoplastic( malignant melanoma and sarcomas) Dacarbazine Chemical Structure
  95. GC34123 Deoxycytidine triphosphate (dCTP) Deoxycytidine triphosphate (dCTP) (dCTP) is a nucleoside triphosphate that can be used for DNA synthesis. Deoxycytidine triphosphate (dCTP) Chemical Structure
  96. GC33494 Deoxypseudouridine Deoxypseudouridine is a nucleoside analog. Deoxypseudouridine Chemical Structure
  97. GC73068 Deoxythymidine-5'-triphosphate-13C10 dilithium

    dTTP-13C10 dilithium

     Deoxytmidine-5'-triphosphate-13C10 (dTTP-13C10) dilithium is 13C-labeled Deoxytmidine-5'-triphosphate. Deoxythymidine-5'-triphosphate-13C10 dilithium Chemical Structure
  98. GC62150 DMT-dC(ac) Phosphoramidite DMT-dC(ac) Phosphoramidite is a modified phosphoramidite monomer, which can be used for the oligonucleotide synthesis. DMT-dC(ac) Phosphoramidite Chemical Structure
  99. GC62538 DMT-dG(dmf) Phosphoramidite DMT-dG(dmf) Phosphoramidite is a phosphinamide monomer that can be used in the preparation of oligonucleotides DMT-dG(dmf) Phosphoramidite Chemical Structure
  100. GC71465 DMTr-5-fluoro-2'-deoxycytidine-phosphoramidite DMTr-5-fluoro-2'-deoxycytidine-phosphoramidite (compound 1B) is a phosphoramidite of 5-Fluoro-2'-deoxycytidine. DMTr-5-fluoro-2'-deoxycytidine-phosphoramidite Chemical Structure
  101. GC66711 DMTr-LNA-5MeU-3-CED-phosphoramidite DMTr-LNA-5MeU-3-CED-phosphoramidite is a nucleoside derivative. DMTr-LNA-5MeU-3-CED-phosphoramidite Chemical Structure

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