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제품정보 (DICE 배송 시 비용 별도)
Linear Formula:
C9H12N3O8PNa2
CAS 번호:
Molecular Weight:
367.16
NACRES:
NA.51
PubChem Substance ID:
UNSPSC Code:
41106305
EC Number:
229-819-3
MDL number:
Assay:
≥99%
Biological source:
synthetic
Form:
crystalline
Solubility:
water: 100 mg/mL, clear to very slightly hazy, colorless to very faintly yellow
Storage temp.:
2-8°C
제품 이름
Cytidine 5′-monophosphate disodium salt, Sigma Grade, ≥99%, crystalline
InChI key
RCIPNLSOCXMZDD-UHFFFAOYSA-N
InChI
1S/C9H14N3O8P.Na.H/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);;
SMILES string
[Na].NC1=NC(=O)N(C=C1)C2OC(COP(O)(O)=O)C(O)C2O
biological source
synthetic
grade
Sigma Grade
assay
≥99%
form
crystalline
solubility
water: 100 mg/mL, clear to very slightly hazy, colorless to very faintly yellow
storage temp.
2-8°C
Quality Level
Application
Cytidine 5′-monophosphate disodium salt has been used:
- in nucleotide stock solution
- as an ectonucleotidase (ENTase) inhibitor to probe 5′-ENTase activity in cortical neurons
- in in vitro studies to estimate its effect on growth response of selected bacteria strains that dominate the piglets′ small intestine
Biochem/physiol Actions
Cytidine 5′-monophosphate (CMP) is 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.
Cytidine monophosphate (CMP) serve as a nucleotide carrier for sugars.
저장 등급
11 - Combustible Solids
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
Carbohydrate Metabolism III: Glycoproteins, Glycolipids, GPI Anchors, Proteoglycans, and Peptidoglycans
Medical Biochemistry, 307-330 (2002)
Nucleotides modify growth of selected intestinal bacteria in vitro
Sauer N, et al.
Livestock Science, 133(1), 161-163 (2010)
Nicotinamide riboside, a form of vitamin B3, protects against excitotoxicity-induced axonal degeneration
Vaur P, et al.
Faseb Journal (2017)
Charuni A Amarasekara et al.
Journal of chromatography. A, 1638, 461892-461892 (2021-01-22)
With advances in the design and fabrication of nanofluidic devices during the last decade, there have been a few reports on nucleic acid analysis using nanoscale electrophoresis. The attractive nature of nanofluidics is the unique phenomena associated with this length
P Briozzo et al.
Structure (London, England : 1993), 6(12), 1517-1527 (1998-12-24)
. Nucleoside monophosphate kinases (NMP kinases) catalyze the reversible transfer of a phosphoryl group from a nucleoside triphosphate to a nucleoside monophosphate. Among them, cytidine monophosphate kinase from Escherichia coli has a striking particularity: it is specific for CMP, whereas
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