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

DNA/RNA Synthesis

RNA synthesis, which is also called DNA transcription, is a highly selective process. Transcription by RNA polymerase II extends beyond RNA synthesis, towards a more active role in mRNA maturation, surveillance and export to the cytoplasm.

Single-strand breaks are repaired by DNA ligase using the complementary strand of the double helix as a template, with DNA ligase creating the final phosphodiester bond to fully repair the DNA.DNA ligases discriminate against substrates containing RNA strands or mismatched base pairs at positions near the ends of the nickedDNA. Bleomycin (BLM) exerts its genotoxicity by generating free radicals, whichattack C-4′ in the deoxyribose backbone of DNA, leading to opening of the ribose ring and strand breakage; it is an S-independentradiomimetic agent that causes double-strand breaks in DNA.

First strand cDNA is synthesized using random hexamer primers and M-MuLV Reverse Transcriptase (RNase H). Second strand cDNA synthesis is subsequently performed using DNA Polymerase I and RNase H. The remaining overhangs are converted into blunt ends using exonuclease/polymerase activity. After adenylation of the 3′ ends of DNA fragments, NEBNext Adaptor with hairpin loop structure is ligated to prepare the samples for hybridization. Cell cycle and DNA replication are the top two pathways regulated by BET bromodomain inhibition. Cycloheximide blocks the translation of mRNA to protein.

Targets for  DNA/RNA Synthesis

Products for  DNA/RNA Synthesis

  1. Cat.No. Product Name Information
  2. GC38000 β-Boswellic acid A pentacyclic triterpene with diverse bioactivities β-Boswellic acid  Chemical Structure
  3. GC10867 (+)-Aphidicolin

    Aphidicolin ((+)-Aphidicolin), a reversible inhibitor of eukaryotic nuclear DNA replication, can block the cell cycle at the pre-S phase[1].

    (+)-Aphidicolin  Chemical Structure
  4. GC48635 (-)-Cryptopleurine An alkaloid with diverse biological activities (-)-Cryptopleurine  Chemical Structure
  5. GC41695 (6R,S)-5,6,7,8-Tetrahydrofolic Acid (hydrochloride) (6R,S)-5,6,7,8-Tetrahydrofolic acid (THFA), the reduced form of folic acid, serves as a cofactor in methyltransferase reactions and is the major one-carbon carrier in one carbon metabolism. (6R,S)-5,6,7,8-Tetrahydrofolic Acid (hydrochloride)  Chemical Structure
  6. GC41088 (6S)-Tetrahydrofolic Acid (6S)-Tetrahydrofolic acid is a diastereomer of tetrahydrofolic acid, a reduced form of folic acid that serves as a cofactor in methyltransferase reactions and is the major one-carbon carrier in one carbon metabolism. (6S)-Tetrahydrofolic Acid  Chemical Structure
  7. GC41633 (R)-Prunasin (R)-Prunasin is a inhibitor of DNA Polymerase β. (R)-Prunasin  Chemical Structure
  8. GC41859 1,5,7-Triazabicyclo[4.4.0]dec-5-ene 1,5,7-Triazabicyclo[4.4.0]dec-5-ene is a bicyclic guanidine base that can be used as a catalyst for a variety of base-mediated organic transformations, including Michael additions, Wittig reactions, Henry reactions, and transesterification reactions. 1,5,7-Triazabicyclo[4.4.0]dec-5-ene  Chemical Structure
  9. GC48909 1-Hydroxyanthraquinone An anthraquinone with genotoxic and carcinogenic activities 1-Hydroxyanthraquinone  Chemical Structure
  10. GC49872 10-Formyltetrahydrofolate (sodium salt) (technical grade) 10-Formyltetrahydrofolate (sodium salt) (technical grade) is a form of tetrahydrofolic acid that acts as a donor of formyl groups in anabolism. 10-Formyltetrahydrofolate (sodium salt) (technical grade)  Chemical Structure
  11. GC63796 116-9e 116-9e (MAL2-11B) is a Hsp70 co-chaperone DNAJA1 inhibitor. 116-9e  Chemical Structure
  12. GC49759 13C17-Mycophenolic Acid An internal standard for the quantification of mycophenolic acid 13C17-Mycophenolic Acid  Chemical Structure
  13. GC46474 18-Deoxyherboxidiene A bacterial metabolite with antiangiogenic activity 18-Deoxyherboxidiene  Chemical Structure
  14. 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
  15. GC52183 2'-O-Methyl-5-methyluridine 2'-O-Methyl-5-methyluridine  Chemical Structure
  16. GC66713 2'-O-MOE-5-Me-C(Bz) 2'-O-MOE-5-Me-C (Bz) is a nucleotide for the stereoselective synthesis of nucleoside alkyl phosphonates. 2'-O-MOE-5-Me-C(Bz)  Chemical Structure
  17. GC66657 2'-O-MOE-5-Me-rC 2'-O-MOE-5-Me-rC is an active compound. 2'-O-MOE-5-Me-rC can be used for oligonucleotide synthesis. 2'-O-MOE-5-Me-rC  Chemical Structure
  18. GC66091 2'-O-MOE-5-Me-rU 2'-O-MOE-5-Me-rU is an active compound. 2'-O-MOE-5-Me-rU can be used for oligonucleotide synthesis. 2'-O-MOE-5-Me-rU  Chemical Structure
  19. GC66656 2'-O-MOE-rC 2'-O-MOE-rC is a 2'-O-MOE modified nucleoside. 2'-O-MOE-rC can be used for synthesis of DNA. 2'-O-MOE-rC  Chemical Structure
  20. GC66652 2'-O-MOE-U 2'-O-MOE-U is a phosphoramidite, can be used for oligonucleotide synthesis. 2'-O-MOE-U  Chemical Structure
  21. 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
  22. 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
  23. 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
  24. GC42061 2',3'-Dideoxyadenosine 5'-triphosphate 2',3'-Dideoxyadenosine 5'-triphosphate (2',3'-Dideoxyadenosine 5'-triphosphate), an active metabolite of 2',3'-dideoxyinosine, is a chain-elongating inhibitor of DNA polymerase. 2',3'-Dideoxyadenosine 5'-triphosphate  Chemical Structure
  25. GC46519 2',3'-O-Isopropylideneguanosine A building block 2',3'-O-Isopropylideneguanosine  Chemical Structure
  26. GC46540 2'-Deoxyadenosine-5'-triphosphate (sodium salt hydrate) A purine nucleotide 2'-Deoxyadenosine-5'-triphosphate (sodium salt hydrate)  Chemical Structure
  27. GC48440 2'-Deoxycytidine-5'-triphosphate (sodium salt) 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
  28. GC42151 2'-Deoxyguanosine 5'-monophosphate (sodium salt hydrate) 2'-Deoxyguanosine 5'-monophosphate (dGMP) is used as a substrate of guanylate kinases to generate dGDP, which in turn is phosphorylated to dGTP, a nucleotide precursor used in DNA synthesis. 2'-Deoxyguanosine 5'-monophosphate (sodium salt hydrate)  Chemical Structure
  29. GC42080 2'2'-cGAMP (sodium salt) 2'2'-cGAMP is a synthetic dinucleotide (CDN) that contains non-canonical 2'5'-phosphodiester bonds. 2'2'-cGAMP (sodium salt)  Chemical Structure
  30. GC60459 2,4-D (2,4-Dichlorophenoxyacetic acid) 2,4-D (2,4-Dichlorophenoxyacetic acid) (2,4-D (2,4-Dichlorophenoxyacetic acid) ichlorophenoxyacetic acid) is a selective systemic herbicide for the control of broad-leaved weeds. 2,4-D (2,4-Dichlorophenoxyacetic acid)   Chemical Structure
  31. GC46524 2,6-Dichloropurine-9-β-D-riboside

    A building block

    2,6-Dichloropurine-9-β-D-riboside  Chemical Structure
  32. GC33496 2-(Methylamino)-1H-purin-6(7H)-one (N2-methylguanine) 2-(Methylamino)-1H-purin-6(7H)-one (N2-methylguanine) (N2-Methylguanine) is a modified nucleoside. 2-(Methylamino)-1H-purin-6(7H)-one (N2-methylguanine)  Chemical Structure
  33. GC64983 2-Amino-2'-deoxyadenosine 2-Amino-2'-deoxyadenosine is a deoxyribonucleoside used for the oligonucleotide synthesis. 2-Amino-2'-deoxyadenosine  Chemical Structure
  34. GC39527 2-O-Methylcytosine 2-O-Methylcytosine, an O-alkylated analogue a DNA adduct, is the damaged nucleobase. 2-O-Methylcytosine  Chemical Structure
  35. GC49348 2-Thiocytidine A modified nucleobase 2-Thiocytidine  Chemical Structure
  36. GC42197 2-Thiouridine 2-Thiouridine (s2U) is a modified nucleobase found in tRNAs that is known to stabilize U:A pairs and modestly destabilize U:G wobble pairs. 2-Thiouridine  Chemical Structure
  37. GC40618 3',4',7-Trihydroxyisoflavone 3',4',7-Trihydroxyisoflavone, a major metabolite of Daidzein, is an ATP-competitive inhibitor of Cot (Tpl2/MAP3K8) and MKK4. 3',4',7-Trihydroxyisoflavone has anticancer, anti-angiogenic, chemoprotective, and free radical scavenging activities. 3',4',7-Trihydroxyisoflavone  Chemical Structure
  38. GC60023 3'-Deoxyuridine-5'-triphosphate 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
  39. GC61862 3'-Deoxyuridine-5'-triphosphate 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
  40. GC45332 3'-Dephosphocoenzyme A An intermediate in the biosynthesis of CoA 3'-Dephosphocoenzyme A  Chemical Structure
  41. GC34452 3,7,4'-Trihydroxyflavone 3,7,4'-Trihydroxyflavone, isolated from Rhus javanica var. 3,7,4'-Trihydroxyflavone  Chemical Structure
  42. GC13510 3-AP ribonucleotide reductase inhibitor and iron chelator with antitumor activity 3-AP  Chemical Structure
  43. GC48457 3-keto Fusidic Acid An active metabolite of fusidic acid 3-keto Fusidic Acid  Chemical Structure
  44. GC52391 306-O12B-3 An ionizable cationic lipidoid 306-O12B-3  Chemical Structure
  45. 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
  46. 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
  47. 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
  48. 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
  49. 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
  50. 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
  51. 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
  52. 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
  53. 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
  54. GC65401 5'-O-TBDMS-dU 5'-O-TBDMS-dU can be used in the synthesis of oligoribonucleotides. 5'-O-TBDMS-dU  Chemical Structure
  55. 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
  56. 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
  57. 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
  58. 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
  59. 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
  60. 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
  61. 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
  62. 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
  63. GC62813 5’-O-DMT-rI 5'-O-DMT-Ri can be used in the synthesis of oligoribonucleotides. 5’-O-DMT-rI  Chemical Structure
  64. GC62577 5’-O-DMT-rU 5’-O-DMT-rU is a modified nucleoside and can be used to synthesize RNA. 5’-O-DMT-rU  Chemical Structure
  65. 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
  66. 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
  67. GC62580 5’-O-TBDMS-dG 5’-O-TBDMS-dG is a modified nucleoside. 5’-O-TBDMS-dG  Chemical Structure
  68. GC62581 5’-O-TBDMS-dT 5’-O-TBDMS-dT is a nucleoside with protective and modification effects. 5’-O-TBDMS-dT  Chemical Structure
  69. GC40641 5'-Ethynyl-2'-deoxycytidine 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
  70. 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
  71. GC48662 5'-Thymidylic Acid (sodium salt) 5'-Thymidylic Acid (sodium salt) is an endogenous metabolite. 5'-Thymidylic Acid (sodium salt)  Chemical Structure
  72. GC46681 5-Bromouridine A brominated uridine analog 5-Bromouridine  Chemical Structure
  73. 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
  74. 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
  75. 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
  76. 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
  77. GC67671 5-Methylcytidine 5′-triphosphate trisodium 5-Methylcytidine 5′-triphosphate trisodium  Chemical Structure
  78. 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
  79. 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
  80. GC46713 5-Phospho-D-ribose 1-diphosphate (sodium salt hydrate) An intermediate in several biochemical pathways 5-Phospho-D-ribose 1-diphosphate (sodium salt hydrate)  Chemical Structure
  81. GC60031 6-Azathymine 6-Azathymine, a 6-nitrogen analog of thymine, is a potent D-3-aminoisobutyrate-pyruvate aminotransferase inhibitor. 6-Azathymine  Chemical Structure
  82. 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
  83. GC12193 6-Thio-dG 6-Thio-dG is a nucleoside analogue that can be incorporated into de novo-synthesized telomeres by telomerase. 6-Thio-dG  Chemical Structure
  84. GC33577 7-Aminoactinomycin D (7-AAD) 7-Aminoactinomycin D (7-AAD) (7-AAD) a fluorescent DNA stain, is a potent RNA polymerase inhibitor. 7-Aminoactinomycin D (7-AAD)  Chemical Structure
  85. GC65408 7-Deaza-2'-deoxy-7-iodoadenosine 7-Deaza-2'-deoxy-7-iodoadenosine is a modified oligonucleotide containing 7-Deazaadenine. 7-Deaza-2'-deoxy-7-iodoadenosine  Chemical Structure
  86. GC65675 7-Iodo-7-deaza-2'-deoxyguanosine 7-Iodo-7-deaza-2'-deoxyguanosine (7-Deaza-7-Iodo-2'-deoxyguanosine) is a deoxyguanosine derivative that can be used in DNA synthesis and sequencing reactions. 7-Iodo-7-deaza-2'-deoxyguanosine  Chemical Structure
  87. GC49561 7-Methylguanosine-d3 An internal standard for the quantification of 7-methylguanosine 7-Methylguanosine-d3  Chemical Structure
  88. GC66058 7-TFA-ap-7-Deaza-dA 7-TFA-ap-7-Deaza-dA is a modified nucleoside. 7-TFA-ap-7-Deaza-dA can be used in the synthesis of deoxyribonucleic acid or nucleic acid. 7-TFA-ap-7-Deaza-dA  Chemical Structure
  89. GC65525 7-TFA-ap-7-Deaza-dG 5'-O-TBDMS-dG is a modified nucleoside. 7-TFA-ap-7-Deaza-dG  Chemical Structure
  90. GC12777 8-Chloroadenosine Nucleoside analog, inhibits RNA synthesis 8-Chloroadenosine  Chemical Structure
  91. GC61763 Ac-rC Phosphoramidite Ac-rC Phosphoramidite is used for the oligoribonucleotide phosphorodithioate modification (PS2-RNA). Ac-rC Phosphoramidite  Chemical Structure
  92. GC34090 Acelarin (NUC-1031) Acelarin (NUC-1031) (NUC-1031) is a ProTide transformation and enhancement of the widely-used nucleoside analogue, gemcitabine. Acelarin (NUC-1031)  Chemical Structure
  93. GC16866 Actinomycin D

    A DNA-interacting transcription blocker with anti-cancer activity

    Actinomycin D  Chemical Structure
  94. GC35247 ACX-362E ACX-362E (ACX-362E) is a first-in-class, orally active DNA polymerase IIIC (pol IIIC) inhibitor, with a Ki of 0.325 μM for the DNA pol IIIC from C. ACX-362E  Chemical Structure
  95. GC17186 Acyclovir Antiviral agent Acyclovir  Chemical Structure
  96. GC13432 Adenine High affinity adenine receptor agonist Adenine  Chemical Structure
  97. GC11825 Adenine HCl Adenine HCl (6-Aminopurine hydrochloride), a purine, is one of the four nucleobases in the nucleic acid of DNA. Adenine HCl acts as a chemical component of DNA and RNA. Adenine HCl also plays an important role in biochemistry involved in cellular respiration, the form of both ATP and the cofactors (NAD and FAD), and protein synthesis. Adenine HCl  Chemical Structure
  98. GC17278 Adenine sulfate Adenine sulfate (6-Aminopurine hemisulfate), a purine, is one of the four nucleobases in the nucleic acid of DNA. Adenine sulfate acts as a chemical component of DNA and RNA. Adenine sulfate also plays an important role in biochemistry involved in cellular respiration, the form of both ATP and the cofactors (NAD and FAD), and protein synthesis. Adenine sulfate  Chemical Structure
  99. GC67946 Adenine-d1 Adenine-d1  Chemical Structure
  100. GC49004 Adenosine 3’-monophosphate (sodium salt hydrate) A nucleotide Adenosine 3’-monophosphate (sodium salt hydrate)  Chemical Structure
  101. GC42732 Adenosine 3',5'-diphosphate (sodium salt) Adenosine 3',5'-diphosphate (sodium salt) is an hydroxysteroid sulfotransferases inhibitor. Adenosine 3',5'-diphosphate (sodium salt)  Chemical Structure

Items 1 to 100 of 377 total

per page
  1. 1
  2. 2
  3. 3
  4. 4

Set Descending Direction