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Cytidine 5'-monophosphate - 10mM in Water, high purity , CAS No.63-37-6

    Grade & Purity:
  • 10mM in Water
  • Cas Number:  63-37-6
  • Molecular Weight:  323.2
  • Beilstein Registry Number:   46982
  • EC Number:   200-556-6
  • PubChem CID: 6131
In stock
Item Number
C427232
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Price Qty
C427232-1ml
1ml
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$241.90

Nucleoside monophosphate.

Basic Description

Synonyms 5'-CYTIDYLIC ACID | Cytidine 5'-monophosphate | 63-37-6 | cytidylic acid | Cytidine monophosphate | Cytidine-5'-monophosphate | 5'-CMP | cytidylate | Cytidine 5'-phosphate | CMP (nucleotide) | Cytidine 5'-phosphoric acid | Cytidine 5'-monophosphoric acid | ((2R,3S,4R,5R)-5-(4-am
Specifications & Purity 10mM in Water
Biochemical and Physiological Mechanisms Nucleoside monophosphate used as a substrate of uridine monophosphate (UMP)/cytidine monophosphate (CMP) kinase (EC 2.7.4.4) to form CDP which upon phosphorylation to CTP supports DNA and RNA biosynthesis.
Storage Temp Store at -80°C
Shipped In
Ice chest + Ice pads
This product requires cold chain shipping. Ground and other economy services are not available.

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
Superclass Nucleosides, nucleotides, and analogues
Class Pyrimidine nucleotides
Subclass Pyrimidine ribonucleotides
Intermediate Tree Nodes Not available
Direct Parent Pyrimidine ribonucleoside monophosphates
Alternative Parents Pentose phosphates  Glycosylamines  Monosaccharide phosphates  Monoalkyl phosphates  Aminopyrimidines and derivatives  Pyrimidones  Imidolactams  Hydropyrimidines  Heteroaromatic compounds  Tetrahydrofurans  Secondary alcohols  1,2-diols  Oxacyclic compounds  Azacyclic compounds  Primary amines  Organopnictogen compounds  Organic oxides  Hydrocarbon derivatives  
Molecular Framework Aromatic heteromonocyclic compounds
Substituents Pyrimidine ribonucleoside monophosphate - Pentose phosphate - Pentose-5-phosphate - Glycosyl compound - N-glycosyl compound - Monosaccharide phosphate - Pentose monosaccharide - Aminopyrimidine - Pyrimidone - Monoalkyl phosphate - Hydropyrimidine - Monosaccharide - Organic phosphoric acid derivative - Phosphoric acid ester - Pyrimidine - Alkyl phosphate - Imidolactam - Tetrahydrofuran - Heteroaromatic compound - Secondary alcohol - 1,2-diol - Oxacycle - Organoheterocyclic compound - Azacycle - Organopnictogen compound - Amine - Alcohol - Organic oxide - Organonitrogen compound - Organooxygen compound - Hydrocarbon derivative - Organic nitrogen compound - Primary amine - Organic oxygen compound - Aromatic heteromonocyclic compound
Description This compound belongs to the class of organic compounds known as pyrimidine ribonucleoside monophosphates. These are pyrimidine ribobucleotides with monophosphate group linked to the ribose moiety.
External Descriptors Ribonucleotides

Associated Targets(Human)

UCK2 Tbio Uridine-cytidine kinase 2 (58 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
CCRF-CEM (65223 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
RNASE1 Tchem Ribonuclease pancreatic (45 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
UMPS Tclin Uridine 5'-monophosphate synthase (20 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
CMPK1 Tchem UMP-CMP kinase (152 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID

Associated Targets(non-human)

St6gal1 CMP-N-acetylneuraminate-beta-galactosamide-alpha-2,6-sialyltransferase (61 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
St3gal3 CMP-N-acetylneuraminate-beta-1,4-galactoside alpha-2,3-sialyltransferase (29 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Mus musculus (284745 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
B16 (5829 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
L1210 (27553 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
L1210/ara C (6 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
ompdc Orotidine phosphate decarboxylase (9 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
pyrF Orotidine 5'-phosphate decarboxylase (39 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID

Mechanisms of Action

Mechanism of Action Action Type target ID Target Name Target Type Target Organism Binding Site Name References

Names and Identifiers

IUPAC Name [(2R,3S,4R,5R)-5-(4-amino-2-oxopyrimidin-1-yl)-3,4-dihydroxyoxolan-2-yl]methyl dihydrogen phosphate
INCHI InChI=1S/C9H14N3O8P/c10-5-1-2-12(9(15)11-5)8-7(14)6(13)4(20-8)3-19-21(16,17)18/h1-2,4,6-8,13-14H,3H2,(H2,10,11,15)(H2,16,17,18)/t4-,6-,7-,8-/m1/s1
InChIKey IERHLVCPSMICTF-XVFCMESISA-N
Smiles C1=CN(C(=O)N=C1N)C2C(C(C(O2)COP(=O)(O)O)O)O
Isomeric SMILES C1=CN(C(=O)N=C1N)[C@H]2[C@@H]([C@@H]([C@H](O2)COP(=O)(O)O)O)O
WGK Germany 3
RTECS HA3980000
Molecular Weight 323.2
Beilstein 46982
Reaxy-Rn 14609599
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=14609599&ln=

Certificates(CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Chemical and Physical Properties

Specific Rotation[α] 9.8 ° (C=1, 0.5mol/L Na2HPO4)
Molecular Weight 323.200 g/mol
XLogP3 -3.400
Hydrogen Bond Donor Count 5
Hydrogen Bond Acceptor Count 8
Rotatable Bond Count 4
Exact Mass 323.052 Da
Monoisotopic Mass 323.052 Da
Topological Polar Surface Area 175.000 Ų
Heavy Atom Count 21
Formal Charge 0
Complexity 531.000
Isotope Atom Count 0
Defined Atom Stereocenter Count 4
Undefined Atom Stereocenter Count 0
Defined Bond Stereocenter Count 0
Undefined Bond Stereocenter Count 0
The total count of all stereochemical bonds 0
Covalently-Bonded Unit Count 1

Citations of This Product

1. Yujuan Ren, Kaiwen Zhao, Guangyao Wu, Lianghai Hu.  (2023)  Highly Ordered Assembly of Templates on Molecular Imprinting toward Phosphorylated Compounds for Improved Performance.  ACS Applied Polymer Materials,     
2. Lai Liang, Zhang Mengyun, Liu Chusheng, Qu Jiahuan, Xu Dongsheng, Jiang Zhengjin.  (2023)  A comprehensive evaluation of a polymeric zwitterionic hydrophilic monolith for nucleotide separation.  ANALYTICAL SCIENCES,    (1-7). 
3. Tiantian Tang, Min Zhang, Yaping Liu.  (2023)  Valorization of meat and bone residue by ultrasound and high voltage electrostatic field assisted two-stage enzymatic hydrolysis: Nutritional characteristics and flavor analysis.  Food Bioscience,  56  (103203). 
4. Xu Shichao, Wu Haifeng, Liu Siyuan, Du Peidong, Wang Hui, Yang Haijun, Xu Wenjie, Chen Shuangming, Song Li, Li Jikun, Shi Xinghua, Wang Zhen-Gang.  (2023)  A supramolecular metalloenzyme possessing robust oxidase-mimetic catalytic function.  Nature Communications,  14  (1): (1-14). 
5. Peidong Du, Yanzhe Shen, Baoli Zhang, Shan Li, Minzheng Gao, Ting Wang, Xiaokang Ding, Bingran Yu, Zhen-Gang Wang, Fu-Jian Xu.  (2023)  A H2O2-Supplied Supramolecular Material for Post-irradiated Infected Wound Treatment.  Advanced Science,  10  (9): (2206851). 
6. Yuqin Wang, Pingping Fan, Shanyu Zhang, Liying Wang, Xinyue Li, Wendong Jia, Yao Liu, Kefan Wang, Xiaoyu Du, Panke Zhang, Shuo Huang.  (2022)  Discrimination of Ribonucleoside Mono-, Di-, and Triphosphates Using an Engineered Nanopore.  ACS Nano,  16  (12): (21356–21365). 
7. Yafei Hou, Xiaodan Pei, Yuancheng Wang, Luyuan Zhang, Xiaohui Wei, Hongyan Mao, Wuduo Zhao, Shusheng Zhang, Wenfen Zhang.  (2022)  Selective Detection of Nucleotides in Infant Formula Using an N-Rich Covalent Triazine Porous Polymer.  Nanomaterials,  12  (13): (2213). 
8. Jianghong Wu, Min Zhang, Lihui Zhang, Yaping Liu.  (2022)  Effect of ultrasound combined with sodium bicarbonate pretreatment on the taste and flavor of chicken broth.  JOURNAL OF FOOD PROCESS ENGINEERING,  46  (6): (e14072). 
9. Hui Hou, Chang Liu, Xiaoshuo Lu, Donglu Fang, Qiuhui Hu, Yuyu Zhang, Liyan Zhao.  (2021)  Characterization of flavor frame in shiitake mushrooms (Lentinula edodes) detected by HS-GC-IMS coupled with electronic tongue and sensory analysis: Influence of drying techniques.  LWT-FOOD SCIENCE AND TECHNOLOGY,  146  (111402). 
10. Chen Pengfei, Wu Jing, Zhou Lei, Pu Qiaosheng.  (2021)  In situ controllable synthesis of Schiff base networks porous polymer coatings for open-tubular capillary electrochromatography.  MICROCHIMICA ACTA,  188  (3): (1-9). 
11. Mei He, Ma Yange, Wu Huimin, Wang Xuedong.  (2021)  Fluorescent and visual assay of H2O2 and glucose based on a highly sensitive copper nanoclusters-Ce(III) fluoroprobe.  ANALYTICAL AND BIOANALYTICAL CHEMISTRY,  413  (8): (2135-2146). 
12. Hongying Li, Qiujin Zhu, Rui Chang, Ke Hu, Xuling Zhu, Aqi Xu, Shitao Xu, Pengyu Tang.  (2021)  Effects of Dietary 5′-CMP on Neu5Gc Contents in the Muscle and Viscera of Xiang Pigs.  JOURNAL OF FOOD PROTECTION,  84  (23). 
13. Fang Pu, Songrong Qu, Hao Qiu, Lu Zhang.  (2020)  Regulation of light-harvesting antenna based on silver ion-enhanced emission of dye-doped coordination polymer nanoparticles.  JOURNAL OF COLLOID AND INTERFACE SCIENCE,  578  (254). 
14. Fang Pu, Yanyan Huang, Zhiguang Yang, Hao Qiu, Jinsong Ren.  (2018)  Nucleotide-Based Assemblies for Green Synthesis of Silver Nanoparticles with Controlled Localized Surface Plasmon Resonances and Their Applications.  ACS Applied Materials & Interfaces,  10  (12): (9929–9937). 
15. Chusheng Liu, Haibin Li, Qiqin Wang, Jacques Crommen, Haibo Zhou, Zhengjin Jiang.  (2017)  Preparation and evaluation of 400 μm I.D. polymer-based hydrophilic interaction chromatography monolithic columns with high column efficiency.  JOURNAL OF CHROMATOGRAPHY A,  1509  (83). 
16. Ruiyong Wang, Xiaogai Wang, Zhigang Li, Yuanzhe Xie, Lingling Yang, Jie Shi, Junbiao Chang.  (2014)  Study on the interaction between bovine serum albumin and 4′-azido-2′-deoxyfluoroarabinocytidine or analogs by spectroscopy and molecular modeling.  SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY,  132  (786). 
17. Dianyuan Wang, Min Zhang, Yaping Liu.  (2024)  Effect of microwave combined with ultrasonic pretreatment on the flavor of composite stewed soup-stock.  JOURNAL OF FOOD PROCESS ENGINEERING,  47  (7): (e14697). 
18. Jiaxin Du, Jiapei Xi, Xiao Chen, Hailan Sun, Lei Zhong, Qiping Zhan, Liyan Zhao.  (2024)  Effects of different extraction methods on the release of non-volatile flavor components in shiitake mushroom (Lentinus edodes).  JOURNAL OF FOOD COMPOSITION AND ANALYSIS,  128  (106001). 
19. Zhongshuai Zhao, Ran Li, Ying Zhu, Zhongde Liu.  (2024)  Headspace separation combined fluorescence detection of hydrogen sulfide with silver-sensitized lanthanide coordination polymer via a simple self-made device.  MICROCHEMICAL JOURNAL,  206  (111617). 
20. Jihang Zhang, Xiao Zhang, Jinming Zhang, Jinglan Wu, Pengpeng Yang, Chenglun Tang, Fengxia Zou, Hanjie Ying, Wei Zhuang.  (2025)  Polyethylenimine-Assisted Interfacial Modulation Based on Electrostatic Balancing and Hierarchical Channel to the Cytidine 5′-Monophosphate Conversion Performance of Uridine-Cytosine Kinase.  JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY,  73  (14): (8426-8439). 

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