Cytidine - Moligand™, suitable for cell culture,Endotoxin

CAS: 65-46-3 Cat. No.: GMP1508351 분자식: C9H13N3O5 분자량: 243.22 Beilstein Registry Number: 89173 EC 번호: 200-610-9
주문 가능
GRADE & PURITY Moligand™ ? Moligand™ — Aladdin's line of ligands and bioactive small molecules. Use for receptor, pathway, and binding studies needing defined small-molecule tools. suitable for cell culture,Endotoxin<500EU/g;Microbial Limit≤100cfu/g
Storage
Store at 2-8°C,Argon charged
Shipped In
Wet ice
★
Size
USA
독일 (EU)*
Price
Qty
5g
GMP1508351-5g
주문제작 · 8~12주
US$79.90
25g
GMP1508351-25g
주문제작 · 8~12주
US$259.90
100g
GMP1508351-100g
주문제작 · 8~12주
US$799.90
Enter a quantity for the sizes you want to add.
🧪
Why this grade

Moligand™, suitable for cell culture,Endotoxin<500EU/g;Microbial Limit≤100cfu/g Moligand™ for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Store at 2-8°C,Argon charged Ships Wet ice Check lot-specific COA for exact specifications.

📋

Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

📚

Literature proof

Cited in 72 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

개요

A constituent of nucleic acids originally isolated in yeast

Cytidine is a pyrimidine nucleoside and acts as a component of RNA. Cytidine is a precursor of uridine. Cytidine controls neuronal-glial glutamate cycling, affecting cerebral phospholipid metabolism, catecholamine synthesis, and mitochondrial function.

Application

Cytidine is used to synthesize enzyme inhibitors, antiviral agents, and anticancer agents. And also used as constituent of nucleic acids.

Specifications

사양 및 순도
Moligand™, suitable for cell culture,Endotoxin<500EU/g;Microbial Limit≤100cfu/g
보관 조건
Store at 2-8°C,Argon charged
배송
Wet ice
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등급
Moligand™
이름과 식별자
정식 스마일
C1=CN(C(=O)N=C1N)C2C(C(C(O2)CO)O)O
IUPAC Name
4-amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]pyrimidin-2-one
InChIKey
UHDGCWIWMRVCDJ-XVFCMESISA-N
INCHI
1S/C9H13N3O5/c10-5-1-2-12(9(16)11-5)8-7(15)6(14)4(3-13)17-8/h1-2,4,6-8,13-15H,3H2,(H2,10,11,16)/t4-,6-,7-,8-/m1/s1
이성체 SMILES
C1=CN(C(=O)N=C1N)[C@H]2[C@@H]([C@@H]([C@H](O2)CO)O)O
WGK 독일
3
RTECS
UW7370000
분자량
243.22
Beilstein
89173
Reaxy-Rn
753984
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=753984&ln=

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassNucleosides, nucleotides, and analogues
분류Pyrimidine nucleosides
SubclassNot available
Intermediate Tree Nodes Not available
Direct ParentPyrimidine nucleosides
Alternative Parents Glycosylamines  Pentoses  Pyrimidones  Aminopyrimidines and derivatives  Imidolactams  Hydropyrimidines  Tetrahydrofurans  Heteroaromatic compounds  Secondary alcohols  Azacyclic compounds  Oxacyclic compounds  Hydrocarbon derivatives  Organic oxides  Organopnictogen compounds  Primary alcohols  Primary amines  
Molecular FrameworkAromatic heteromonocyclic compounds
Substituents Pyrimidine nucleoside - Glycosyl compound - N-glycosyl compound - Pentose monosaccharide - Aminopyrimidine - Pyrimidone - Hydropyrimidine - Monosaccharide - Pyrimidine - Imidolactam - Tetrahydrofuran - Heteroaromatic compound - Secondary alcohol - Oxacycle - Azacycle - Organoheterocyclic compound - Organic nitrogen compound - Primary alcohol - Organic oxide - Organooxygen compound - Organonitrogen compound - Amine - Alcohol - Organopnictogen compound - Organic oxygen compound - Primary amine - Hydrocarbon derivative - Aromatic heteromonocyclic compound
설명This compound belongs to the class of organic compounds known as pyrimidine nucleosides. These are compounds comprising a pyrimidine base attached to a ribosyl or deoxyribosyl moiety.
External Descriptors Ribonucleosides
3D 구조
상호 작용 화학 구조 모델





인증서(CoA, COO, BSE/TSE 및 분석 차트)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

1 results found

Lot NumberCertificate Type날짜항목
GMG2608710Certificate of AnalysisJul 09, 2026 GMP1508351
화학 및 물리적 특성
용해성Soluble in water and dimethyl sulfoxide.
감도Air and moisture sensitive
특정 회전[α]34 ° (C=0.7, H2O)
녹는점(°C)224-225°C
분자량243.220 g/mol
XLogP3-2.100
Hydrogen Bond Donor Count4
Hydrogen Bond Acceptor Count5
Rotatable Bond Count2
Exact Mass243.086 Da
Monoisotopic Mass243.086 Da
Topological Polar Surface Area129.000 Ų
Heavy Atom Count17
Formal Charge0
Complexity383.000
Isotope Atom Count0
Defined Atom Stereocenter Count4
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
자주 묻는 질문과 기사
Pyrimidine Research Selection Guide: Structural Features, Typical Applications, and a Reagent/Building-Block Classification Navigator (Tables 1–5)
Functional Systems of Nucleoside Metabolism-Related Enzymes in Drug Response and Disease Biology
The Methodological Value of TPS-Cl: The Logic of Selective Activation and Representative Transformations in Nucleoside and Nucleotide Chemistry
Coupling Activators, Nucleoside Building Blocks, and Modification Design in Oligonucleotide Chemical Synthesis: Their Effects on Synthetic Efficiency, Purity, and Product Properties
Porous Graphitic Carbon (PGC) Chromatography Columns: Creating New Selectivity for Challenging Separations through Molecular Shape and the π-Electron Cloud on the Graphitic Surface
From Tumor Sequencing to “One Patient, One Drug”: Machine-Learning-Assisted Design of V940 Individualized Neoantigen mRNA and the Phase III Breakthrough in Melanoma
Glycosidic Bond Structure and Cleavage Mechanisms—Chemical and Enzymatic Cleavage of O-, N-, S-, and C-Glycosides
Citations of This Product
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