DNA/RNA Synthesis
Inhibitors of DNA and RNA synthesis are compounds that interfere with the replication and transcription processes in cells, thereby preventing the production of essential genetic material. These inhibitors can target various enzymes and proteins involved in nucleic acid synthesis, making them valuable tools for studying the mechanisms of replication, transcription, and translation. They are also used in developing treatments for infections and cancer. At CymitQuimica, we offer a broad spectrum of DNA/RNA synthesis inhibitors to support your research in molecular biology, virology, and therapeutic development.
Found 706 products of "DNA/RNA Synthesis"
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DMTr-TNA-U-amidite
CAS:<p>DMTr-TNA-U-amidite is a Nucleoside Phosphoramidite.</p>Formula:C38H45N4O8PColor and Shape:SolidMolecular weight:716.76Antipain dihydrochloride
CAS:<p>Antipain dihydrochloride (Antipain 2HCl) is a protease inhibitor derived from Actinomycetes with analgesic activity.</p>Formula:C27H46Cl2N10O6Purity:95%Color and Shape:White To Off-White PowderMolecular weight:677.625'-O-DMT-N6-Me-2'-dA
CAS:<p>5'-O-DMT-N6-Me-2'-dA is a nucleoside with protective and modification effects.</p>Formula:C32H33N5O5Color and Shape:SolidMolecular weight:567.635'-O-DMT-2'-TBDMS-Uridine
CAS:<p>5’-O-DMT-2’-TBDMS-Uridine is a deoxyribonucleoside used for the oligonucleotide synthesis.</p>Formula:C36H44N2O8SiColor and Shape:SolidMolecular weight:660.83DMTr-MOE-Inosine-3-CED-phosphoramidite
<p>DMTr-MOE-Inosine-3-CED-phosphoramidite is a useful organic compound for research related to life sciences and the catalog number is TNU1574.</p>Color and Shape:SolidBPN-15477
CAS:<p>BPN-15477 is a splicing modulator compound (SMC) that which restores correct splicing of exon 20 in ELP1 (Elongator complex protein 1).</p>Formula:C12H10ClN5Purity:99.84%Color and Shape:SolidMolecular weight:259.692'-O-MOE-U
CAS:<p>2'-O-MOE-U is a Nucleoside Phosphoramidite; Nucleoside Derivative - 2'-Modified nucleoside.</p>Formula:C42H53N4O10PColor and Shape:SolidMolecular weight:804.86DMT-dG(dmf) Phosphoramidite
CAS:<p>DMT-dG(dmf) Phosphoramidite is a phosphinamide monomer employed for oligonucleotide synthesis.</p>Formula:C43H53N8O7PColor and Shape:SolidMolecular weight:824.92'-MOE-G(iBu)-3'-phosphoramidite
CAS:<p>2'-MOE-G(iBu)-3'-phosphoramidite is a Nucleoside Phosphoramidite;Nucleoside Derivative - 2'-Modified nucleoside;.</p>Formula:C47H60N7O10PColor and Shape:SolidMolecular weight:913.99DMTr-LNA-U-3-CED-phosphoramidite
CAS:<p>Nucleoside Phosphoramidites; Nucleoside Derivatives - LNA-related nucleosides</p>Formula:C40H47N4O9PColor and Shape:SolidMolecular weight:758.8Branaplam hydrochloride
CAS:<p>Branaplam hydrochloride (LMI070; NVS-SM1) is an orally active SMN2 splicing modulator (EC50 20 nM) that also inhibits hERG channels (IC50 6.3 μM).</p>Formula:C22H28ClN5O2Purity:98.45%Color and Shape:SolidMolecular weight:429.95HDGFRP2/PSIP1-IN-1
CAS:<p>Compound BPP (HDGFRP2/PSIP1-IN-1) is a dual inhibitor targeting the PWWP domains of Hepatoma-derived Growth Factor Related Protein 2 (HDGFRP2) and its homologue PSIP1. This compound effectively hinders the occurrence and progression of Diffuse Intrinsic Pontine Glioma (DIPG). It demonstrates binding affinity with a Kd value of 7 μM for HDGFRP2, indicative of its efficient ligand efficacy at 0.47. Additionally, Compound BPP exhibits a Kd value of 27 μM when binding to the PSIP1 PWWP domain, and a Kd value of 14 μM against HDGFRP3, confirming its potency as an inhibitor within the HDGFRP2 PWWP subfamily.</p>Formula:C8H6BrN3Color and Shape:SolidMolecular weight:224.063'-Deoxy-5'-O-(4,4'-dimethoxytrityl)-3'-fluorouridine-2'-CED-phosphoramidite
CAS:<p>3'-Deoxy-5'-O-(4,4'-dimethoxytrityl)-3'-fluorouridine-2'-CED-phosphoramidite is a Nucleoside Phosphoramidite.</p>Formula:C12H5Cl3F3N5O4Color and Shape:SolidMolecular weight:446.55Uridine 5'-diphosphate sodium salt
CAS:<p>Uridine 5'-diphosphate sodium, P2Y6 agonist (EC50: 300 nM), P2Y14 antagonist (pEC50: 7.28).</p>Formula:C9H11N2Na3O12P2Purity:98%Color and Shape:SolidMolecular weight:470.106RNase L-IN-1
<p>RNase L-IN-1 is an RNase L inhibitor with potential anticancer activity and inhibits viral replication.</p>Formula:C27H35FN6O3SPurity:98.55%Color and Shape:SolidMolecular weight:542.67DMT-locMeC(bz) phosphoramidite
CAS:<p>Nucleoside Derivatives - LNA-related nucleosides; Nucleoside Phorphoramidites</p>Formula:C48H54N5O9PColor and Shape:SolidMolecular weight:875.94ML216
CAS:<p>ML216 (CID-49852229) inhibits BLM helicase (IC50: 1.8 μM), 28-fold selective over RECQ1, RECQ5, and UvrD (IC50s > 50 μM).</p>Formula:C15H9F4N5OSPurity:98.12%Color and Shape:SolidMolecular weight:383.32Lurbinectedin
CAS:<p>Lurbinectedin (PM01183) is a DNA minor groove covalent binder. Lurbinectedin also shows effective anti-tumor activity.</p>Formula:C41H44N4O10SPurity:98.11%Color and Shape:SolidMolecular weight:784.87Dasabuvir sodium
CAS:<p>Dasabuvir sodium (ABT-333) inhibits HCV NS5B polymerase, targeting genotypes 1a (EC50: 7.7 nM) and 1b (EC50: 1.8 nM).</p>Formula:C26H26N3NaO5SColor and Shape:SolidMolecular weight:515.56TH5427 hydrochloride
CAS:<p>TH5427 HCl inhibits NUDT5 with 29 nM IC50; 690x more selective over MTH1; blocks ATP in breast cancer cells, hindering growth.</p>Formula:C20H21Cl3N8O3Color and Shape:SolidMolecular weight:527.79
