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Uridine - for cell culture, ≥99% , CAS No.58-96-8

CAS: 58-96-8 Cat. No.: U108811 分子式: C9H12N2O6 分子量: 244.20 Beilstein Registry Number: 754902 EC番号: 200-407-5
84 Citations COA
Uridine - for cell culture, ≥99% CAS No(58-96-8) by Aladdin Scientific
注文可能
グレード＆純度 for Cell culture ? Cell-culture grade — low endotoxin and contaminants to support viable cell growth. Use in mammalian/other cell culture media and supplements. ≥99%
Synonyms
1af2 | 1-beta-D-Ribofuranosyluracil | NCGC00017312-02 | Urd | ADENOSINE IMPURITY F (EP IMPURITY) | 1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-1,2,3,4-tetrahydropyrimidine-2,4-dione | URIDINE (MART.) | EINECS 200-407-5 | URIDINE [USP IMPU
Storage
Store at 2-8°C
Shipped In
Wet ice
★
サイズ
USA
ドイツ (EU)*
価格
個数
5g
U108811-5g
4 在庫あり
—

$10.90

$12.90
保存 $2.00 (15.50%)
25g
U108811-25g
6 在庫あり
—

$33.90

$41.90
保存 $8.00 (19.09%)
100g
U108811-100g
2 在庫あり
—
$114.90
500g
U108811-500g
1 在庫あり
—
$399.90
Enter a quantity for the sizes you want to add.
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COA
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DS
データシート
SP
仕様書
概要 仕様 名前と識別子 ドキュメント 詳細データ Taxonomic Classification 3 D構造 関連ターゲット（人間） 関連ターゲット（非人間） 作用メカニズム 証明書（CoA、COO、BSE/TSEと分析図） 化学的性質と物理的性質 よくある質問と記事 Citations of This Product ソリューション計算機 レビュー
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このグレードを選ぶ理由

for cell culture, ≥99% 細胞培養用 ベースライン干渉を最小限に抑える必要がある、感度の高いクロマトグラフィーおよび分析ワークフロー向け。

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保管・配送

Store at 2-8°C Wet ice に出荷。正確な仕様については、ロット固有の COA をご確認ください。

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品質書類

SDS、COA、データシート、仕様書をダウンロードできます。ロット固有の COA はロット番号検索で入手可能です。

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文献的裏付け

クロマトグラフィー、有機合成、クロスカップリング反応に関する 84 件の査読済み論文で引用されています。

概要

Product Introduction

Uridine is a uracil nucleoside, specific for RNA sequence. Uridine is present in blood, seminal fluid and cerebrospinal fluid. Uridine is a substrate for nucleotide synthesis in living organisms by de- novo and salvage pathways.


Application

Uridine has been used:

as an inhibitor of schwann cell proliferation in rat dorsal root ganglia (DRG) neurons culture

as a medium supplement for epiblasts culture

as a component of 5-fluoro-2′-deoxyuridine stock solution used for neuronal culture

仕様

同義語
1af2 | 1-beta-D-Ribofuranosyluracil | NCGC00017312-02 | Urd | ADENOSINE IMPURITY F (EP IMPURITY) | 1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-1,2,3,4-tetrahydropyrimidine-2,4-dione | URIDINE (MART.) | EINECS 200-407-5 | URIDINE [USP IMPU
仕様と純度
for cell culture, ≥99%
保管条件
Store at 2-8°C
入荷
Wet ice
この製品は冷冷この冷このこの製品の運送が必要です。地上およびその他の経済サービスは利用できません。
等級
細胞培養用
純度
≥99%
名前と識別子
パブケム・シド
488179988
パブケム・シド・ウル
https://pubchem.ncbi.nlm.nih.gov/substance/488179988
カノニカル・スマイル
C1=CN(C(=O)NC1=O)C2C(C(C(O2)CO)O)O
IUPAC Name
1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]pyrimidine-2,4-dione
InChIKey
DRTQHJPVMGBUCF-XVFCMESISA-N
INCHI
1S/C9H12N2O6/c12-3-4-6(14)7(15)8(17-4)11-2-1-5(13)10-9(11)16/h1-2,4,6-8,12,14-15H,3H2,(H,10,13,16)/t4-,6-,7-,8-/m1/s1
異性体SMILES
C1=CN(C(=O)NC1=O)[C@H]2[C@@H]([C@@H]([C@H](O2)CO)O)O
WGKドイツ
3
分子量
244.20
Beilstein
754902
Reaxy-Rn
4699706
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=4699706&ln=

ドキュメント

📋 安全データシート（SDS）

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<<<<<<< HEAD SDS をダウンロード → ======= SDS をダウンロード → >>>>>>> release248-p3

✅ 分析証明書（COA）

ロット固有の品質データ。ロット番号を入力して、正確な COA を取得してください。

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📊 データシート

製品仕様と用途のクイックリファレンス概要。

データシートを見る →

🔬 仕様書

このグレードの完全な品質特性と合格基準。

仕様書を見る →

詳細データ

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassNucleosides, nucleotides, and analogues
分類Pyrimidine nucleosides
SubclassNot available
Intermediate Tree Nodes Not available
Direct ParentPyrimidine nucleosides
Alternative Parents Glycosylamines  Pentoses  Pyrimidones  Hydropyrimidines  Tetrahydrofurans  Heteroaromatic compounds  Vinylogous amides  Ureas  Lactams  Secondary alcohols  Oxacyclic compounds  Azacyclic compounds  Primary alcohols  Organopnictogen compounds  Organonitrogen compounds  Organic oxides  Hydrocarbon derivatives  
Molecular FrameworkAromatic heteromonocyclic compounds
Substituents Pyrimidine nucleoside - Glycosyl compound - N-glycosyl compound - Pentose monosaccharide - Pyrimidone - Hydropyrimidine - Monosaccharide - Pyrimidine - Vinylogous amide - Tetrahydrofuran - Heteroaromatic compound - Urea - Secondary alcohol - Lactam - Organoheterocyclic compound - Oxacycle - Azacycle - Hydrocarbon derivative - Organopnictogen compound - Organooxygen compound - Organonitrogen compound - Primary alcohol - Alcohol - Organic oxygen compound - Organic oxide - Organic nitrogen compound - Aromatic heteromonocyclic compound
説明This 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
3 D構造
インタラクティブ化学構造モデル





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SLC28A1 Tbio Sodium/nucleoside cotransporter 1 (13 Activities)
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SLC28A2 Tchem Sodium/nucleoside cotransporter 2 (91 Activities)
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APEX1 Tchem DNA-(apurinic or apyrimidinic site) lyase (38016 Activities)
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CRBN Tclin Protein cereblon (139 Activities)
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関連ターゲット（非人間）
TK Thymidine kinase (276 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Cda Cytidine deaminase (37 Activities)
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deoA Thymidine phosphorylase (531 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Uck1 Uridine-cytidine kinase 1 (5 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Hdac6 Histone deacetylase 6 (222 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
B4GALT1 Beta-1,4-galactosyltransferase 1 (61 Activities)
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rep Replicase polyprotein 1ab (378 Activities)
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Trpa1 Transient receptor potential cation channel subfamily A member 1 (1003 Activities)
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Slc29a2 Equilibrative nucleoside transporter 2 (4 Activities)
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ffp 4'-phosphopantetheinyl transferase ffp (24982 Activities)
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lgtC Alpha 1,4 galactosyltransferase (29 Activities)
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作用メカニズム
証明書（CoA、COO、BSE/TSEと分析図）
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.

28 results found

Lot NumberCertificate Type日付商品
L2519486L2519486Certificate of AnalysisDec 03, 2025 U108811
L2519483L2519483Certificate of AnalysisDec 03, 2025 U108811
L2519480L2519480Certificate of AnalysisDec 03, 2025 U108811
L2519475L2519475Certificate of AnalysisDec 03, 2025 U108811
J2515110J2515110Certificate of AnalysisAug 24, 2024 U108811
J2515064J2515064Certificate of AnalysisAug 24, 2024 U108811
I2406535I2406535Certificate of AnalysisAug 24, 2024 U108811
I2406534I2406534Certificate of AnalysisAug 24, 2024 U108811
I2406529I2406529Certificate of AnalysisAug 24, 2024 U108811
I2406528I2406528Certificate of AnalysisAug 24, 2024 U108811
A2605012A2605012Certificate of AnalysisAug 24, 2024 U108811
D2417602D2417602Certificate of AnalysisApr 29, 2024 U108811
D2417603D2417603Certificate of AnalysisApr 29, 2024 U108811
G2308416G2308416Certificate of AnalysisJan 02, 2023 U108811
G2310635G2310635Certificate of AnalysisJan 02, 2023 U108811
G2310634G2310634Certificate of AnalysisJan 02, 2023 U108811
G2308419G2308419Certificate of AnalysisJan 02, 2023 U108811
G2308414G2308414Certificate of AnalysisJan 02, 2023 U108811
G2308410G2308410Certificate of AnalysisJan 02, 2023 U108811
G2308398G2308398Certificate of AnalysisJan 02, 2023 U108811
G2308394G2308394Certificate of AnalysisJan 02, 2023 U108811
G2223013G2223013Certificate of AnalysisJun 18, 2022 U108811
G2223012G2223012Certificate of AnalysisJun 18, 2022 U108811
G2222879G2222879Certificate of AnalysisJun 18, 2022 U108811
C2209330C2209330Certificate of AnalysisFeb 18, 2022 U108811
C2209321C2209321Certificate of AnalysisFeb 18, 2022 U108811
C2209317C2209317Certificate of AnalysisFeb 18, 2022 U108811
C2209310C2209310Certificate of AnalysisFeb 18, 2022 U108811
化学的性質と物理的性質
溶解度Soluble in water (50 mg/ml), DMSO, and methanol.
比旋光度［α］9 ° (C=2, H2O)
融点（°C）163-167°C
分子量244.200 g/mol
XLogP3-2.000
Hydrogen Bond Donor Count4
Hydrogen Bond Acceptor Count6
Rotatable Bond Count2
Exact Mass244.07 Da
Monoisotopic Mass244.07 Da
Topological Polar Surface Area119.000 Ų
Heavy Atom Count17
Formal Charge0
Complexity370.000
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
よくある質問と記事
For Cell Culture
Categories: Reagent Specifications, Grading and Purity
Tags:
For Cell Culture
Pyrimidine Research Selection Guide: Structural Features, Typical Applications, and a Reagent/Building-Block Classification Navigator (Tables 1–5)
Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides
Tags:
Pyrimidine Pyrimidine base
Functional Systems of Nucleoside Metabolism-Related Enzymes in Drug Response and Disease Biology
Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides
Tags:
Salvage synthesis Metabolic Reprogramming Nucleoside Metabolism Deoxycytidine Kinase Cytidine Deaminase Adenosine Kinase Purine Nucleoside Phosphorylase Thymidine Kinase Drug Response Disease Biology
The Methodological Value of TPS-Cl: The Logic of Selective Activation and Representative Transformations in Nucleoside and Nucleotide Chemistry
Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides
Tags:
TPS-Cl 2,4,6-triisopropylbenzenesulfonyl chloride
Coupling Activators, Nucleoside Building Blocks, and Modification Design in Oligonucleotide Chemical Synthesis: Their Effects on Synthetic Efficiency, Purity, and Product Properties
Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides
Tags:
Oligonucleotide chemical synthesis
Porous Graphitic Carbon (PGC) Chromatography Columns: Creating New Selectivity for Challenging Separations through Molecular Shape and the π-Electron Cloud on the Graphitic Surface
Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides
Tags:
High-performance liquid chromatography Porous Graphitic Carbon
From Tumor Sequencing to “One Patient, One Drug”: Machine-Learning-Assisted Design of V940 Individualized Neoantigen mRNA and the Phase III Breakthrough in Melanoma
Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides
Tags:
Tumors Tumor sequencing
Glycosidic Bond Structure and Cleavage Mechanisms—Chemical and Enzymatic Cleavage of O-, N-, S-, and C-Glycosides
Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides
Tags:
O-glycosides C-glycosides Glycosides
Citations of This Product
How to Cite Aladdin Scientific Products? Citations Search
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