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Home >> Signaling Pathways >> DNA Damage/DNA Repair

DNA Damage/DNA Repair

Products for  DNA Damage/DNA Repair

  1. Cat.No. Product Name Information
  2. 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
  3. 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
  4. GC45332 3'-Dephosphocoenzyme A

    depCoA, Dephospho-CoA

     An intermediate in the biosynthesis of CoA 3'-Dephosphocoenzyme A Chemical Structure
  5. GC34384 3,6-DMAD hydrochloride 3,6-DMAD hydrochloride, an acridine derivative, is a potent IRE1α-XBP1s pathway inhibitor. 3,6-DMAD hydrochloride promotes IL-6 secretion via the IRE1α-XBP1s pathway. 3,6-DMAD hydrochloride inhibits IRE1α oligomerization and endoribonuclease (RNase) activity. 3,6-DMAD hydrochloride can be used for research of cancer. 3,6-DMAD hydrochloride Chemical Structure
  6. GC34452 3,7,4'-Trihydroxyflavone 3,7,4'-Trihydroxyflavone, isolated from Rhus javanica var. 3,7,4'-Trihydroxyflavone Chemical Structure
  7. GC52129 3-Amino-5-hydroxybenzoic Acid

    AHBA

     3-Amino-5-hydroxybenzoic Acid Chemical Structure
  8. GC13510 3-AP

    3-Aminopyridine-2-Carboxyaldehyde Thiosemicarbazone,NSC 663249,Triapine™

     ribonucleotide reductase inhibitor and iron chelator with antitumor activity 3-AP Chemical Structure
  9. GC48457 3-keto Fusidic Acid

    3-keto FA, 3-Oxofusidic Acid

     An active metabolite of fusidic acid 3-keto Fusidic Acid Chemical Structure
  10. 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
  11. GC52391 306-O12B-3 An ionizable cationic lipidoid 306-O12B-3 Chemical Structure
  12. GC15389 360A 360A Chemical Structure
  13. GC10115 360A iodide 360A iodide Chemical Structure
  14. GC14493 4μ8C

    4u8C

    IRE1 Rnase inhibitor, potent and non-toxic

     4μ8C Chemical Structure
  15. GC17271 4'-Demethylepipodophyllotoxin

    (-)-4′-Demethylepipodophyllotoxin

     An inhibitor of tubulin polymerization 4'-Demethylepipodophyllotoxin Chemical Structure
  16. GC46607 4-(Methylnitrosamino)-1-(3-pyridyl)-1-butanone

    NNK

     A tobacco-specific nitrosamine carcinogen 4-(Methylnitrosamino)-1-(3-pyridyl)-1-butanone Chemical Structure
  17. GC11761 4-amino-1,8-Naphthalimide

    4-Aminonaphthalimide,4-ANI

     4-amino-1,8-Naphthalimide is a potent PARP inhibitor and potentiates the cytotoxicity of γ-radiation in cancer cells. 4-amino-1,8-Naphthalimide Chemical Structure
  18. GC42401 4-hydroperoxy Cyclophosphamide

    4-OOH-CY

     4-hydroperoxy Cyclophosphamide, the active metabolite of cyclophosphamide, can cross-link DNA and induce T cell apoptosis independently of caspase receptor activation. It also activates the mitochondrial death pathway through the production of reactive oxygen species (ROS). 4-hydroperoxy Cyclophosphamide Chemical Structure
  19. GC68332 4-Hydroperoxy Cyclophosphamide-d4 4-Hydroperoxy Cyclophosphamide-d4 Chemical Structure
  20. GC18853 4-isocyanato TEMPO 4-isocyanato TEMPO is a spin labeling reagent used to label the 2'-position in RNA. 4-isocyanato TEMPO Chemical Structure
  21. GC61683 4-Methoxyphenethyl alcohol 4-Methoxyphenethyl alcohol, an aromatic alcohol, is the major component in the anise-like odour produced by A. 4-Methoxyphenethyl alcohol Chemical Structure
  22. GC49127 4-oxo Cyclophosphamide

    4-keto CP, 4-keto Cyclophosphamide, NSC 139488, 4-oxo CP

     An inactive metabolite of cyclophosphamide 4-oxo Cyclophosphamide Chemical Structure
  23. GC42464 4-oxo-2-Nonenal

    4-ONE

    4-hydroxy Nonenal is a lipid peroxidation product derived from oxidized ω-6 polyunsaturated fatty acids such as arachidonic acid and linoleic acid.

     4-oxo-2-Nonenal Chemical Structure
  24. GC45353 4-oxo-27-TBDMS Withaferin A 4-oxo-27-TBDMS Withaferin A, a withaferin A derivative, exhibits potent antiproliferative effects on the tumor cells.4-oxo-27-TBDMS Withaferin A induces tumor cells apoptosis. 4-oxo-27-TBDMS Withaferin A is a anticancer agent. 4-oxo-27-TBDMS Withaferin A Chemical Structure
  25. 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
  26. GC40477 4-Thiouracil

    2-hydroxy-4-Mercaptopyrimidine, NSC 43288, 4-Thiopyrimidin-2-one, 4-TU

     4-Thiouracil is a site-specific, photoactivatable probe used to detect RNA structures and nucleic acid-nucleic acid contacts. 4-Thiouracil Chemical Structure
  27. 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
  28. GC13104 4E1RCat

    eIF4E/eIF4G Interaction Inhibitor II

     Dual inhibitor of eIF4E:eIF4G and eIF4E:4E-BP1 interaction 4E1RCat Chemical Structure
  29. GC30785 4E2RCat 4E2RCat is an inhibitor of eIF4E-eIF4G interaction with an IC50 of 13.5 μM. 4E2RCat Chemical Structure
  30. GC10468 4EGI-1

    eIF4E/eIF4G Interaction Inhibitor

     Competitive eIF4E/eIF4G interaction inhibitor 4EGI-1 Chemical Structure
  31. GC12667 4SC-202 4SC-202 (4SC-202) is a selective class I HDAC inhibitor with IC50 of 1.20 μM, 1.12 μM, and 0.57 μM for HDAC1, HDAC2, and HDAC3, respectively. It also displays inhibitory activity against Lysine specific demethylase 1 (LSD1). 4SC-202 Chemical Structure
  32. 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
  33. 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
  34. 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
  35. 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
  36. 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
  37. 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
  38. 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
  39. 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
  40. GC65401 5'-O-TBDMS-dU 5'-O-TBDMS-dU can be used in the synthesis of oligoribonucleotides. 5'-O-TBDMS-dU Chemical Structure
  41. 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
  42. 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
  43. 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
  44. 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
  45. 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
  46. 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
  47. 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
  48. 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
  49. 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
  50. 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
  51. 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
  52. GC62812 5’-O-DMT-PAC-dA 5’-O-DMT-PAC-dA can be used in the synthesis of oligoribonucleotides. 5’-O-DMT-PAC-dA Chemical Structure
  53. GC62813 5’-O-DMT-rI 5'-O-DMT-Ri can be used in the synthesis of oligoribonucleotides. 5’-O-DMT-rI 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. GC40641 5'-Ethynyl-2'-deoxycytidine

    EdC, 2'-deoxy-5-Ethynylcytidine

     5'-Ethynyl-2'-deoxycytidine (EdC) is a nucleoside analog that inhibits replication of the herpes simplex virus-1 (HSV-1) KOS strain (ID50 = 0.2 μg/mL). 5'-Ethynyl-2'-deoxycytidine Chemical Structure
  59. 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
  60. GC61726 5'-O-DMT-N4-Ac-dC 5'-O-DMT-N4-Ac-dC (N4-Acetyl-2'-deoxy-5'-O-DMT-cytidine, compound 7), a deoxynucleoside, can be used to synthesize of dodecyl phosphoramidite which is the raw material for dod‐DNA (amphiphilic DNA containing an internal hydrophobic region consisting of dodecyl phosphotriester linkages) synthesis. 5'-O-DMT-N4-Ac-dC Chemical Structure
  61. GC48662 5'-Thymidylic Acid (sodium salt)

    Deoxythymidine-5’-monophosphate, Thymidine monophosphate, Thymidine-5’-monophosphate, dTMP

     5'-Thymidylic Acid (sodium salt) is an endogenous metabolite. 5'-Thymidylic Acid (sodium salt) Chemical Structure
  62. GC35150 5,7,4'-Trimethoxyflavone 5,7,4'-Trimethoxyflavone is isolated from Kaempferia parviflora (KP) that is a famous medicinal plant from Thailand. 5,7,4'-Trimethoxyflavone induces apoptosis, as evidenced by increments of sub-G1 phase, DNA fragmentation, annexin-V/PI staining, the Bax/Bcl-xL ratio, proteolytic activation of caspase-3, and degradation of poly (ADP-ribose) polymerase (PARP) protein.5,7,4'-Trimethoxyflavone is significantly effective at inhibiting proliferation of SNU-16 human gastric cancer cells in a concentration dependent manner. 5,7,4'-Trimethoxyflavone Chemical Structure
  63. GC90796 5-(3-Aminoallyl)-2'-deoxyuridine-5'-O-triphosphate (sodium salt)

    An amine-modified nucleotide

     5-(3-Aminoallyl)-2'-deoxyuridine-5'-O-triphosphate (sodium salt) Chemical Structure
  64. GC90823 5-(3-Aminoallyl)uridine-5'-O-triphosphate (sodium salt)

    An amine-modified nucleotide

     5-(3-Aminoallyl)uridine-5'-O-triphosphate (sodium salt) Chemical Structure
  65. GC68161 5-AIQ

    5-Aminoisoquinolin-1-one

     5-AIQ Chemical Structure
  66. GC90549 5-Aminoimidazole-4-carboxamide (hydrate)

    A synthetic precursor

     5-Aminoimidazole-4-carboxamide (hydrate) Chemical Structure
  67. GC73073 5-Aza-4'-thio-2'-deoxycytidine

    5-Aza-T-dCyd; NTX-301

     5-Aza-4'-thio-2'-deoxycytidine (5-Aza-T-dCyd) is an orally active DNA metltransferase I (DNMT1) inhibitor. 5-Aza-4'-thio-2'-deoxycytidine Chemical Structure
  68. 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
  69. 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
  70. 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
  71. 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
  72. GC46681 5-Bromouridine

    (-)-5-Bromouridine, BrU, BrUrd, NSC 38296

     A brominated uridine analog 5-Bromouridine Chemical Structure
  73. GC71207 5-Ethyluridine 5-Ethyluridine is a purine nucleoside analogue. 5-Ethyluridine Chemical Structure
  74. GC49245 5-Ethynyluridine 5-Ethynyluridine (5-EU) is a potent cell-permeable nucleoside can be used to label newly synthesized RNA. 5-Ethynyluridine Chemical Structure
  75. GC71361 5-Fluoro-2′-deoxy-UTP 5-Fluoro-2′-deoxy-UTP can be used as a substrate for DNA synthesis. 5-Fluoro-2′-deoxy-UTP Chemical Structure
  76. GC42545 5-Fluorouracil-13C,15N2

    5-FU-13C,15N2

     5-Fluorouracil-13C,15N2 is intended for use as an internal standard for the quantification of 5-flurouracil by GC- or LC-MS. 5-Fluorouracil-13C,15N2 Chemical Structure
  77. GC46033 5-Heneicosylresorcinol An alkylresorcinol 5-Heneicosylresorcinol Chemical Structure
  78. GC62389 5-Iminodaunorubicin 5-Iminodaunorubicin is a quinone-modified anthracycline that retains antitumor activity. 5-Iminodaunorubicin produces protein-concealed DNA strand breaks in cancer cells. 5-Iminodaunorubicin Chemical Structure
  79. GC35162 5-Iodo-indirubin-3'-monoxime 5-Iodo-indirubin-3'-monoxime is a potent GSK-3β, CDK5/P25 and CDK1/cyclin B inhibitor, competing with ATP for binding to the catalytic site of the kinase, with IC50s of 9, 20 and 25 nM, respectively. 5-Iodo-indirubin-3'-monoxime Chemical Structure
  80. GC66658 5-Me-dC(Ac) amidite 5-Me-dC(Ac) amidite is used for synthesizing DNA or RNA. 5-Me-dC(Ac) amidite Chemical Structure
  81. GC31187 5-Methoxyflavone 5-Methoxyflavone, belonged to Flavonoid family, is a DNA polymerase-beta inhibitor and neuroprotective agent against beta-amyloid toxicity. 5-Methoxyflavone Chemical Structure
  82. GC42562 5-Methyl-2'-deoxycytidine

    5Methyldeoxycytidine

     5-Methyl-2'-deoxycytidine is a pyrimidine nucleoside that when incorporated into single-stranded DNA can act in cis to signal de novo DNA methylation. 5-Methyl-2'-deoxycytidine Chemical Structure
  83. GC67671 5-Methylcytidine 5′-triphosphate trisodium

    5-Methyl-CTP trisodium

     5-Methylcytidine 5′-triphosphate trisodium Chemical Structure
  84. GC35166 5-Methylcytosine 5-Methylcytosine is a well-characterized DNA modification, and is also predominantly in abundant non-coding RNAs in both prokaryotes and eukaryotes. 5-Methylcytosine Chemical Structure
  85. 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
  86. GC70654 5-PA-dUTP 5-PA-dUTP (5-Propargylamino-dUTP) is a C5-modified nucleotide and can be incorporated into DNA nanoparticles (DNPs) for photosensitizer delivery. 5-PA-dUTP Chemical Structure
  87. GC66055 5-Phenylpentan-2-one 5-Phenylpentan-2-one is a potent histone deacetylases (HDACs) inhibitor. 5-Phenylpentan-2-one can be used for urea cycle disorder research. 5-Phenylpentan-2-one Chemical Structure
  88. GC46713 5-Phospho-D-ribose 1-diphosphate (sodium salt hydrate)

    Phosphoribosyl Pyrophosphate, P-rib-PP, PRPP

     An intermediate in several biochemical pathways 5-Phospho-D-ribose 1-diphosphate (sodium salt hydrate) Chemical Structure
  89. GC73009 5-Propargylamino-3'-azidomethyl-dCTP TEA 5-Propargylamino-3'-azidometl-dCTP (TEA) is a nucleotide molecule that can be used in DNA synthesis and DNA sequencing. 5-Propargylamino-3'-azidomethyl-dCTP TEA Chemical Structure
  90. GC73008 5-Propargylamino-3'-azidomethyl-dUTP tristriethylamine 5-Propargylamino-3'-azidometl-dUTP tristrietlamine is a nucleotide molecule that can be used in DNA synthesis and DNA sequencing. 5-Propargylamino-3'-azidomethyl-dUTP tristriethylamine Chemical Structure
  91. GC70655 5-Propargylamino-ddCTP trisodium 5-Propargylamino-ddCTP (trisodium), a nucleoside molecule that can be used to synthesis of cyanine dye-nucleotide conjugate which is used in nucleic acid labeling or sequence analysis. 5-Propargylamino-ddCTP trisodium Chemical Structure
  92. GC46079 5-Tricosylresorcinol 5-Tricosylresorcinolthe is the first cyst lipid. 5-Tricosylresorcinol Chemical Structure
  93. GC45772 6(5H)-Phenanthridinone

    NSC 11021, NSC 40943, NSC 61083

     An inhibitor of PARP1 and 2 6(5H)-Phenanthridinone Chemical Structure
  94. GC60532 6-(Dimethylamino)purine 6-(Dimethylamino)purine is a dual inhibitor of protein kinase and CDK. 6-(Dimethylamino)purine Chemical Structure
  95. 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
  96. GC60031 6-Azathymine 6-Azathymine, a 6-nitrogen analog of thymine, is a potent D-3-aminoisobutyrate-pyruvate aminotransferase inhibitor. 6-Azathymine Chemical Structure
  97. GC50249 6-Hydroxy-DL-DOPA 6-Hydroxy-DL-DOPA is a selective and effective allosteric inhibitor of the RAD52 ssDNA binding domain. 6-Hydroxy-DL-DOPA can be used for the research of cancer. 6-Hydroxy-DL-DOPA Chemical Structure
  98. GC32975 6-Mercaptopurine hydrate

    6-MP

     An inhibitor of purine synthesis and interconversion 6-Mercaptopurine hydrate Chemical Structure
  99. GC35180 6-Methyl-5-azacytidine 6-Methyl-5-azacytidine is a potent DNMT inhibitor. 6-Methyl-5-azacytidine Chemical Structure
  100. GC49235 6-Methylmercaptopurine

    6-MMP, 6-(Methylthio)purine, NSC 20105, SQ 8,343

     A metabolite of 6-mercaptopurine 6-Methylmercaptopurine Chemical Structure
  101. GC49488 6-Methylmercaptopurine-d3

    6-MMP-d3, 6-(Methylthio)purine-d3

     An internal standard for the quantification of 6-MMP 6-Methylmercaptopurine-d3 Chemical Structure

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