What is the Uridine-5'-diphosphate?

Uridine-5'-diphosphate is , while it's Molecular Formula is C9H14N2O12P2. Used in Biochemical Reactions: Uridine-5'-diphosphate is used as a precursor in the synthesis of glycogen for the production of UDP-glucose, which is essential for glycogen formation. Used in the Pharmaceutical Industry: Uridine-5'-diphosphate is utilized as a key molecule in the biosynthesis of glycoproteins, glycolipids, and polysaccharides, which are vital for the development of various pharmaceutical compounds and therapies. Used in Cell Communication and Signaling: In the field of cellular biology, UDP is employed as a component of signaling pathways and cell communication, contributing to the regulation of cellular processes and functions.

What is the CAS number for Uridine-5'-diphosphate?

The CAS number of Uridine-5'-diphosphate is 58-98-0.

What is Uridine-5'-diphosphate (58-98-0) used for?

Uridine-5'-diphosphate (UDP) is a nucleotide that serves as a fundamental building block of RNA, composed of a uracil base, a ribose sugar, and two phosphate groups. It is integral to the synthesis of glycogen, acting as a precursor for the production of UDP-glucose, a pivotal molecule in glycogen formation. Furthermore, UDP is engaged in a multitude of biochemical reactions, encompassing the biosynthesis of glycoproteins, glycolipids, and polysaccharides. Its involvement extends to signaling pathways and cell communication, underscoring its critical role in cellular function.

What is the Uridine-5'-diphosphate?

Uridine-5'-diphosphate is , while it's Molecular Formula is C9H14N2O12P2. Used in Biochemical Reactions: Uridine-5'-diphosphate is used as a precursor in the synthesis of glycogen for the production of UDP-glucose, which is essential for glycogen formation. Used in the Pharmaceutical Industry: Uridine-5'-diphosphate is utilized as a key molecule in the biosynthesis of glycoproteins, glycolipids, and polysaccharides, which are vital for the development of various pharmaceutical compounds and therapies. Used in Cell Communication and Signaling: In the field of cellular biology, UDP is employed as a component of signaling pathways and cell communication, contributing to the regulation of cellular processes and functions.

What is the CAS number for Uridine-5'-diphosphate?

The CAS number of Uridine-5'-diphosphate is 58-98-0.

What is Uridine-5'-diphosphate (58-98-0) used for?

Uridine-5'-diphosphate (UDP) is a nucleotide that serves as a fundamental building block of RNA, composed of a uracil base, a ribose sugar, and two phosphate groups. It is integral to the synthesis of glycogen, acting as a precursor for the production of UDP-glucose, a pivotal molecule in glycogen formation. Furthermore, UDP is engaged in a multitude of biochemical reactions, encompassing the biosynthesis of glycoproteins, glycolipids, and polysaccharides. Its involvement extends to signaling pathways and cell communication, underscoring its critical role in cellular function.

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Uridine-5'-diphosphate

CAS 58-98-0
Purity 99%

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Cost-effective and customizable Uridine-5'-diphosphate 58-98-0 factory

Molecular Formula: C9H14N2O12P2
Molecular Weight: 404.164
PKA: 1.04±0.50(Predicted)
PSA： 252.35000
Density: 2.003 g/cm³
LogP: -1.80580

58-98-0 Relevant articles

Analysis of the Mildiomycin Biosynthesis Gene Cluster in Streptoverticillum remofaciens ZJU5119 and Characterization of MilC, a Hydroxymethyl cytosyl-glucuronic Acid Synthase

Wu, Jun,Li, Li,Deng, Zixin,Zabriskie, T. Mark,He, Xinyi

, p. 1613 - 1621 (2012)

Mildiomycin (MIL) is a peptidyl-nucleosi...

DUAL-ACTIVITY NICOTINAMIDE PHOSPHORIBOSYLTRANSFERASE INHIBITORS

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Paragraph 00128; 00133; 00134; 00136; 00138; 00140-00142, (2018/05/24)

The present disclosure describes NAMPT m...

Enzymatic Synthesis of the Ribosylated Glycyl-Uridine Disaccharide Core of Peptidyl Nucleoside Antibiotics

Cui, Zheng,Liu, Xiaodong,Overbay, Jonathan,Cai, Wenlong,Wang, Xiachang,Lemke, Anke,Wiegmann, Daniel,Niro, Giuliana,Thorson, Jon S.,Ducho, Christian,Van Lanen, Steven G.

, p. 7239 - 7249 (2018/05/29)

Muraymycins belong to a family of nucleo...

Identification and characterization of UDP-mannose in human cell lines and mouse organs: Differential distribution across brain regions and organs

Nakajima, Kazuki,Kizuka, Yasuhiko,Yamaguchi, Yoshiki,Hirabayashi, Yoshio,Takahashi, Kazuo,Yuzawa, Yukio,Taniguchi, Naoyuki

, p. 401 - 407 (2017/11/17)

Mannosylation in the endoplasmic reticul...

Biosynthesis of CMP-legionaminic acid from fructose-6-P

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Paragraph 0082, (2015/09/22)

The sialic acid-like sugar legionaminic ...

58-98-0 Process route

: 5'-cap-ApppU

: 58-97-9,27416-86-0
5'-Uridylic Acid

: 61-19-8,24937-83-5,67583-85-1
5'-adenosine monophosphate

: 58-98-0
UDP

: 58-64-0,905904-58-7
adenosine 5'-diphosphate

Conditions

Conditions	Yield
With 1,4-bis(2,2':6',2''-terpyridin-4'-yloxy)butane; water; copper(II) nitrate; at 60 ℃; pH=7; Reagent/catalyst; Temperature; Kinetics; aq. buffer;