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134 Pancharatna Char Rasta G I D C,Vapi,Gujarat,India India
5,6-Dichloro-1- -D-ribofuranosylbenzimidazole (DRB) is a chemical compound that inhibits transcription elongation by RNA Polymerase II.
5-Ethynyl-2-deoxyuridine (EdU) is a novel thymidine analogue, that is incorporated into dividing cells. At high doses it can be cytotoxic.
5-Methylcytidine is a modified nucleoside derived from 5-methylcytosine. It is found in ribonucleic acids of animal, plant, and bacterial origin
The chemical compound 5-methyluridine, also called ribothymidine, is a pyrimidine nucleoside. It is the ribonucleoside counterpart to the deoxyribonuc
7-Methylguanosine is a modified purine nucleobase. It is a methylated version of guanosine and when found in human urine, it may be a biomarker of som
8-Hydroxyguanosine is a nucleoside which is an oxidative derivative of guanosine. Measurement of the levels of 8-hydroxyguanosine is used as a biomark
8-Oxo-2'-deoxyguanosine (8-oxo-dG) is an oxidized derivative of deoxyguanosine. 8-oxo-dG is one of the major products of DNA oxidation.[1] Concent
Azacitidine is mainly used in the treatment of myelodysplastic syndrome (MDS), for which it received approval by the U.S. Food and Drug Administration
Bromodeoxyuridine (5-bromo-2'-deoxyuridine, BrdU) is a synthetic nucleoside that is an analogue of thymidine. BrdU is commonly used in the detecti
Therefore, it can participate in certain biochemical reactions (for example, be incorporated into an RNA molecule, thus causing the premature terminat
Cytarabine was first synthesized in 1959 by Richard Walwick, Walden Roberts, and Charles Dekker at the University of California, Berkeley.[4]
Cytidine is a nucleoside molecule that is formed when cytosine is attached to a ribose ring (also known as a ribofuranose) via a -N1-glycosidic bond.
It is a hypomethylating agent.[1][2] It hypomethylates DNA by inhibiting DNA methyltransferase.
Deoxyadenosine is a deoxyribonucleoside. It is a derivative of the nucleoside adenosine, differing from the latter by the replacement of a hydroxyl gr
Deoxycytidine is a deoxyribonucleoside. It is like cytidine, but with one oxygen atom removed.
It is similar to guanosine, but with one hydroxyl group removed from the 2' position of the ribose sugar (making it deoxyribose). If a phosphate g
Deoxyuridine is a compound and a nucleoside. It is similar in chemical structure to uridine, but without the 2'-hydroxyl group.
Dexelvucitabine is a failed experimental agent for the treatment of HIV. Dexelvucitabine is a cytidine nucleoside analog and nucleoside reverse transc
Dihydrouridine (abbreviated as D, DHU, or UH2) is a pyrimidine which is the result of adding two hydrogen atoms to a uridine, making it a fully satura
Floxuridine works because it is broken down by the body into its active form, which is the same as a metabolite of 5-Fluorouracil.
The antiviral drug aciclovir, often used in herpes treatment, is structurally similar to guanosine.
Inosine is also an intermediate in a chain of purine nucleotides reactions required for muscle movements.
A Phase II study with maribavir demonstrated that prophylaxis with maribavir displayed strong antiviral activity, as measured by statistically signifi
N4-Chloroacetylcytosine arabinoside is a GABA agonist.[1][dubious discuss]
It has mainly cardiovascular effects with only subtle alterations of behavior.[2] CPA is widely used in scientific research into the adenosine recepto
It is also found in tRNA, rRNA, and small nuclear RNA (snRNA) as well as several long non-coding RNA, such as Xist.[13][14]
Nelarabine is a chemotherapy drug used in T-cell acute lymphoblastic leukemia. It was previously known as 506U78.
Orotidine is a nucleoside formed by attaching orotic acid to a ribose ring via a -N1-glycosidic bond
Pentostatin is used to treat hairy cell leukemia.[3] It is given by intravenous infusion once every two weeks for three to six months.
Pseudouridine (abbreviated by the Greek letter psi- ) is the C-glycoside isomer of the nucleoside uridine, and it is the most prevalent of the over o
Queuosine is a modified nucleoside that is present in certain tRNAs in bacteria and eukaryotes.
Regadenoson (INN, code named CVT-3146) is an A2A adenosine receptor agonist that is a coronary vasodilator. It produces maximal hyperemia quickly and
S-Adenosyl-L-homocysteine (SAH) is an amino acid derivative used in several metabolic pathways in most organisms. It is an intermediate in the synthes
Sapacitabine is an oral nucleoside analog prodrug that acts through a dual mechanism. The compound interferes with DNA synthesis by causing single-str
Telbivudine is a synthetic thymidine nucleoside analogue; it is the L-isomer of thymidine. It is taken once daily.
Tezacitabine is a ribonucleotide reductase inhibitor. It is a synthetic purine nucleoside analogue with potential antineoplastic activity. It is used
Thymidine (more precisely called deoxythymidine; can also be labelled deoxyribosylthymine, and thymine deoxyriboside) is a chemical compound, more pre
Uridine is a molecule (known as a nucleoside) that is formed when uracil is attached to a ribose ring (also known as a ribofuranose) via a -N1-glycos
Xanthosine is a nucleoside derived from xanthine and ribose.
Persona de contacto Mr. Kamlesh Singh
Dirección 134 Pancharatna Char Rasta G I D C, Vapi, Gujarat
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