deoxycytidine monophosphate


"deoxycytidine monophosphate." Unter physiologischen Bedingungen desaminiert ein geringer Teil des in der DNA enthaltenen Desoxycytidins zu Desoxyuridin, wofür spezielle Reparatursysteme in den Zellen existieren. The others are adenine (A), cytosine (C), and guanine (G). From Infogalactic: the planetary knowledge core, InChI=1S/C9H14N3O7P/c10-7-1-2-12(9(14)11-7)8-3-5(13)6(19-8)4-18-20(15,16)17/h1-2,5-6,8,13H,3-4H2,(H2,10,11,14)(H2,15,16,17)/t5-,6+,8+/m0/s1, InChI=1/C9H14N3O7P/c10-7-1-2-12(9(14)11-7)8-3-5(13)6(19-8)4-18-20(15,16)17/h1-2,5-6,8,13H,3-4H2,(H2,10,11,14)(H2,15,16,17)/t5-,6+,8+/m0/s1, c1cn(c(=O)nc1N)[C@H]2C[C@@H]([C@H](O2)COP(=O)(O)O)O, Except where otherwise noted, data are given for materials in their, https://infogalactic.com/w/index.php?title=Deoxycytidine_monophosphate&oldid=378027, Chemical articles using a fixed chemical formula, Creative Commons Attribution-ShareAlike License, About Infogalactic: the planetary knowledge core. It is an ester of phosphoric acid with the nucleoside uridine. They are the basic building blocks of DNA and RNA. Deoxycytidine monophosphate, also known as deoxycytidylate, or dCMP, is a deoxynucleotide, and one of the four monomers that make up DNA. It is an ester of phosphoric acid with the nucleoside guanosine. Lot and Batch Numbers can be found on a product's label

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dTMP consists of a phosphate group, the pentose sugar deoxyribose, and the nucleobase thymine. Destruction of nucleic acid is a catabolic reaction. We're doing our best to make sure our content is useful, accurate and safe.If by any chance you spot an inappropriate image within your search results please use this form to let us know, and we'll take care of it shortly.
a cytosine attached to the deoxyribose sugar. We're doing our best to make sure our content is useful, accurate and safe.If by any chance you spot an inappropriate comment while navigating through our website please use this form to let us know, and we'll take care of it shortly. Deoxycytidine (dihydrogen phosphate). 2′-Deoxycytidine 5′-monophosphate … There has been recent biomedical research interest in investigating dCK's … The monomer itself from ribonucleotides forms the basic building blocks for RNA. Deoxyadenosine monophosphate is abbreviated dAMP. Uracil is a demethylated form of thymine. Type in Product Names, Product Numbers, or CAS Numbers to see suggestions. Guanosine monophosphate (GMP), also known as 5'-guanidylic acid or guanylic acid, is a nucleotide that is used as a monomer in RNA.
2′-Deoxycytidine 5′-monophosphate sodium salt has been used:• in nucleoside stability studies in human renal cell carcinoma (RCC) cell line SN12C• in the cell proliferation studies of human intestinal Caco-2 cell line and peripheral blood mononuclear cells (PBMCs)• as a ligand in dsDNA activation-induced cytidine deaminase crystallization. It is an ester of phosphoric acid with the nucleoside thymidine.

Information and translations of deoxycytidine monophosphate in the most comprehensive dictionary definitions resource on the web. Cytidine monophosphate, also known as 5'-cytidylic acid or simply cytidylate, and abbreviated CMP, is a nucleotide that is used as a monomer in RNA. We truly appreciate your support.

presented with a COA Request form. Deoxycytidylic acid, Bei der Desaminierung von 5-Methyldesoxycytidin entsteht jedoch das auch normalerweise in der DNA enthaltene Desoxythymidin, das nicht als fehlerhaft erkannt werden kann, wodurch es sich in der nächsten Replikationsrunde mit Desoxyadenosin paaren kann, woraus sich dann eine Transition von Desoxycytidin nach Desoxythymidin und auf dem gegenüberliegenden DNA-Strang von Desoxyguanosin nach Desoxyadenosin ergeben wird. GMP consists of the phosphate group, the pentose sugar ribose, and the nucleobase guanine; hence it is a ribonucleoside monophosphate. It is an ester of phosphoric acid with the nucleoside cytidine. Known as: Acid, Deoxycytidylic, DCMP, Monophosphate, Deoxycytidine Expand Deoxycytidine (dihydrogen phosphate). In DNA, the uracil nucleobase is replaced by thymine. Deoxycytidine kinase (dCK) is an enzyme which is encoded by the DCK gene in humans. Nucleotidyltransferases are transferase enzymes of phosphorus-containing groups, e.g., substituents of nucleotidylic acids or simply nucleoside monophosphates. Since tetrahydrofolate is needed to make both purines and pyrimidines, which are building blocks of DNA and RNA, dihydrofolate reductase is targeted by various drugs to prevent nucleic acid synthesis. -021. [4], https://de.wikipedia.org/w/index.php?title=Desoxycytidin&oldid=198318240, „Creative Commons Attribution/Share Alike“.

2′-Deoxycytidine 5′-monophosphate (dCMP) is used as a substrate of uridine monophosphate (UMP)/cytidine monophosphate (CMP) kinase (EC 2.7.4.4) to form dCDP which upon phosphorylation to dCTP supports DNA biosynthesis. Its nucleoside contains a pyrimidinebase, i.e. The numerical value of deoxycytidine monophosphate in Chaldean Numerology is: 7, The numerical value of deoxycytidine monophosphate in Pythagorean Numerology is: 3. Linear Formula C 9 H 12 N 3 O 7 PNa 2. Deoxycytidine monophosphate (dCMP) is a nucleoside phosphate in being comprised of a deoxyribonucleosideand onephosphate group. IMPDH is a regulator of the intracelluar guanine nucleotide pool, and is therefore important for DNA and RNA synthesis, signal transduction, energy transfer, glycoprotein synthesis, as well as other process that are involved in cellular proliferation. In a DNA double helix, it will base pair with deoxyguanosine monophosphate. EC Number 235-995-2. Nucleotides are molecules consisting of a nucleoside and a phosphate group. Customer Service, Synonym: Deoxycytidine monophosphate (dCMP), also known as deoxycytidylic acid or deoxycytidylate in its conjugate acid and conjugate base forms, respectively, is a deoxynucleotide, and one of the four monomers that make up DNA. Deoxyadenosine monophosphate (dAMP), also known as deoxyadenylic acid or deoxyadenylate in its conjugate acid and conjugate base forms, respectively, is a derivative of the common nucleic acid AMP, or adenosine monophosphate, in which the -OH (hydroxyl) group on the 2' carbon on the nucleotide's pentose has been reduced to just a hydrogen atom. InChI=1S/C9H14N3O7P/c10-7-1-2-12(9(14)11-7)8-3-5(13)6(19-8)4-18-20(15,16)17/h1-2,5-6,8,13H,3-4H2,(H2,10,11,14)(H2,15,16,17)/t5-,6+,8+/m0/s1, InChI=1/C9H14N3O7P/c10-7-1-2-12(9(14)11-7)8-3-5(13)6(19-8)4-18-20(15,16)17/h1-2,5-6,8,13H,3-4H2,(H2,10,11,14)(H2,15,16,17)/t5-,6+,8+/m0/s1, c1cn(c(=O)nc1N)[C@H]2C[C@@H]([C@H](O2)COP(=O)(O)O)O, Except where otherwise noted, data are given for materials in their. Desoxycytidin (kurz dC oder in DNA-Sequenzen nur C) ist ein Nukleosid und besteht aus der Nukleinbase Cytosin und dem Zucker β-D-Desoxyribose. . Metabolites and Cofactors on the Metabolic Pathways Chart. 31 Oct. 2020. Unlike the other deoxyribonucleotides, thymidine monophosphate often does not contain the "deoxy" prefix in its name; nevertheless, its symbol often includes a "d" ("dTMP"). It is used as a monomer in DNA. dCMP. A deoxycytosine nucleotide containing one phosphate group esterified to the deoxyribose moiety in the 2'-,3… Deoxycytidine monophosphate, also known as deoxycytidylate, or dCMP, is a deoxynucleotide, and one of the four monomers that make up DNA. search was unable to find the COA you are looking for, you will be A nucleoside consists simply of a nucleobase and a five-carbon sugar, whereas a nucleotide is composed of a nucleobase, a five-carbon sugar, and one or more phosphate groups. to you upon submission of this form. If your

Meaning of deoxycytidine monophosphate. As a substituent or radical its name takes the form of the prefix uridylyl-. Definitions.net. STANDS4 LLC, 2020. Uridine is a glycosylated pyrimidine-analog containing uracil attached to a ribose ring (or more specifically, a ribofuranose) via a β-N1-glycosidic bond. It is a conjugate acid of a 2'-deoxycytosine 5'-monophosphate(2-) . How to say deoxycytidine monophosphate in sign language? This page was last modified on 7 July 2015, at 16:15. It is known as E number reference E626. Molecular Weight 351.16 . As a substituent it takes the form of the prefix cytidylyl-. Deoxyribose, or more precisely 2-deoxyribose, is a monosaccharide with idealized formula H−(C=O)−(CH2)−(CHOH)3−H. If you find a lot number with a filling-code such as Das Analogon mit Ribose ist das Cytidin. In a nucleoside, the anomeric carbon is linked through a glycosidic bond to the N9 of a purine or the N1 of a pyrimidine.

In RNA, uracil binds to adenine via two hydrogen bonds. This means that it has a deoxyribose as its sugar constituent with one phosphate group attached. 62K1064 – you will only find the COO if In a DNA double helix, it will base pair with deoxyguanosine monophosphate. The general reaction of transferring a nucleoside monophosphate moiety from A to B, can be written as: Inosine-5′-monophosphate dehydrogenase (IMPDH) is a purine biosynthetic enzyme that catalyzes the nicotinamide adenine dinucleotide (NAD+)-dependent oxidation of inosine monophosphate (IMP) to xanthosine monophosphate (XMP), the first committed and rate-limiting step towards the de novo biosynthesis of guanine nucleotides from IMP.

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