UDP-G - 10mM in DMSO , CAS No.28053-08-9

CAS: 28053-08-9 Cat. No.: U422983 Summenformel: C15H22N2Na2O17P2 Molekulargewicht: 610.27 EG-Nummer: 248-801-6 PubChem CID: 119803
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GRADE & PURITY 10mM in DMSO
Synonyms
28053-08-9|UDPG sodium salt|Uridine(5')disodiodiphospho(1)-alpha-D-glucose|Uridine 5'-diphosphoglucose disodium|UYD77NZ2JQ|Uridine 5'-diphosphoglucose disodium salt|disodium;[[(2R,3S,4R,5R)-5-(2,4-dioxopyrimidin-1-yl)-3,4-dihydroxyoxolan-2-yl]methoxy-oxid
Storage
Store at -80°C
Shipped In
Dry ice packs + Cold packs
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Size
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Price
Qty
1ml
U422983-1ml
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Why this grade

10mM in DMSO for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

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Storage & shipping

Store at -80°C Ships Dry ice packs + Cold packs 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 9 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Specifications

Synonyme
28053-08-9 | UDPG sodium salt | Uridine(5')disodiodiphospho(1)-alpha-D-glucose | Uridine 5'-diphosphoglucose disodium | UYD77NZ2JQ | Uridine 5'-diphosphoglucose disodium salt | disodium;[[(2R,3S,4R,5R)-5-(2,4-dioxopyrimidin-1-yl)-3,4-dihydroxyoxolan-2-yl]methoxy-oxid
Spezifikationen & Reinheit
10mM in DMSO
Biochemische und physiologische Mechanismen
Highly potent, endogenous P2Y 14 agonist (EC 50 = 82 nM). Involved in modulation of gastric function. UDP also available .
Storage
Store at -80°C
Verschickt in
Dry ice packs + Cold packs
Dieses Produkt erfordert Kühlkettenversand. Grundversand und andere Economy-Optionen sind nicht verfügbar.
Namen und Kennungen
Pubchem Sid528769741
Kanonisches LächelnC1=CN(C(=O)NC1=O)C2C(C(C(O2)COP(=O)([O-])OP(=O)([O-])OC3C(C(C(C(O3)CO)O)O)O)O)O.[Na+].[Na+]
IUPAC Namedisodium;[[(2R,3S,4R,5R)-5-(2,4-dioxopyrimidin-1-yl)-3,4-dihydroxyoxolan-2-yl]methoxy-oxidophosphoryl] [(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] phosphate
InChIKeyPKJQEQVCYGYYMM-QBNUFUENSA-L
INCHI1S/C15H24N2O17P2.2Na/c18-3-5-8(20)10(22)12(24)14(32-5)33-36(28,29)34-35(26,27)30-4-6-9(21)11(23)13(31-6)17-2-1-7(19)16-15(17)25;;/h1-2,5-6,8-14,18,20-24H,3-4H2,(H,26,27)(H,28,29)(H,16,19,25);;/q;2*+1/p-2/t5-,6-,8-,9-,10+,11-,12-,13-,14-;;/m1../s1
Isomere SMILES C1=CN(C(=O)NC1=O)[C@H]2[C@@H]([C@@H]([C@H](O2)COP(=O)([O-])OP(=O)([O-])O[C@@H]3[C@@H]([C@H]([C@@H]([C@H](O3)CO)O)O)O)O)O.[Na+].[Na+]
Alternative CAS-Nummer 117756-22-6
PubChem CID 119803
Molekulargewicht 610.27

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
KlassePyrimidine nucleotides
SubclassPyrimidine nucleotide sugars
Intermediate Tree Nodes Not available
Direct ParentPyrimidine nucleotide sugars
Alternative Parents Pyrimidine ribonucleoside diphosphates  Pentose phosphates  Glycosylamines  Monosaccharide phosphates  Organic pyrophosphates  Pyrimidones  Alkyl phosphates  Hydropyrimidines  Oxanes  Vinylogous amides  Tetrahydrofurans  Heteroaromatic compounds  Ureas  Secondary alcohols  Lactams  Oxacyclic compounds  Azacyclic compounds  Polyols  Organic oxides  Hydrocarbon derivatives  Primary alcohols  Organopnictogen compounds  Organic sodium salts  Organonitrogen compounds  
Molecular FrameworkAromatic heteromonocyclic compounds
Substituents Pyrimidine nucleotide sugar - Pyrimidine ribonucleoside diphosphate - Pentose phosphate - Pentose-5-phosphate - Glycosyl compound - N-glycosyl compound - Monosaccharide phosphate - Organic pyrophosphate - Pyrimidone - Hydropyrimidine - Monosaccharide - Organic phosphoric acid derivative - Oxane - Phosphoric acid ester - Pyrimidine - Alkyl phosphate - Vinylogous amide - Heteroaromatic compound - Tetrahydrofuran - Secondary alcohol - Lactam - Urea - Organoheterocyclic compound - Organic alkali metal salt - Azacycle - Oxacycle - Polyol - Organooxygen compound - Organonitrogen compound - Organic nitrogen compound - Organic sodium salt - Primary alcohol - Hydrocarbon derivative - Organic oxygen compound - Organopnictogen compound - Organic oxide - Organic salt - Alcohol - Aromatic heteromonocyclic compound
BeschreibungThis compound belongs to the class of organic compounds known as pyrimidine nucleotide sugars. These are pyrimidine nucleotides bound to a saccharide derivative through the terminal phosphate group.
External Descriptors Not available
3D-Struktur
Interaktives chemisches Strukturmodell





Zugehörige Ziele (menschlich)
ABL1 Tclin Tyrosine-protein kinase ABL (18331 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ADRB2 Tclin Beta-2 adrenergic receptor (11824 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ADRA2A Tclin Alpha-2a adrenergic receptor (9450 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
AGTR1 Tclin Type-1 angiotensin II receptor (5176 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
GSK3B Tclin Glycogen synthase kinase-3 beta (11785 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CSNK1D Tchem Casein kinase I delta (4546 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
S1PR1 Tclin Sphingosine 1-phosphate receptor Edg-1 (5806 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CDK2 Tchem Cyclin-dependent kinase 2 (9050 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
GLP1R Tclin Glucagon-like peptide 1 receptor (111429 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
C5AR1 Tclin C5a anaphylatoxin chemotactic receptor (2677 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
AURKA Tchem Serine/threonine-protein kinase Aurora-A (10240 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
U2OS (164939 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CX3CR1 Tchem C-X3-C chemokine receptor 1 (1686 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
FPR2 Tchem Lipoxin A4 receptor (3472 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
FFAR4 Tchem G-protein coupled receptor 120 (2999 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
BRD4 Tchem Bromodomain-containing protein 4 (13122 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
GPR35 Tchem G-protein coupled receptor 35 (2643 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
TRIM24 Tchem Transcription intermediary factor 1-alpha (2087 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
BRPF1 Tchem Peregrin (2217 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HEK-293T (167025 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Zugehörige Ziele (nicht menschlich)
Aplnr Apelin receptor (201 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mapk1 MAP kinase ERK2 (650 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Fgfr3 Fibroblast growth factor receptor 3 (21 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Gpr119 Glucose-dependent insulinotropic receptor (270 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Wirkungsmechanismen
Zertifikate (CoA, COO, BSE/TSE und Analyse-Diagramm)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:
Chemische und physikalische Eigenschaften
Molekulargewicht610.270 g/mol
XLogP3
Hydrogen Bond Donor Count7
Hydrogen Bond Acceptor Count17
Rotatable Bond Count9
Exact Mass610.019 Da
Monoisotopic Mass610.019 Da
Topological Polar Surface Area297.000 Ų
Heavy Atom Count38
Formal Charge0
Complexity948.000
Isotope Atom Count0
Defined Atom Stereocenter Count9
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count3
FAQs und Artikel
An Introduction to Research-Grade Carbohydrates: Decoding the “Glycan Language” and a Product-Selection Guide (with Tables 1–3)
Pyrimidine Research Selection Guide: Structural Features, Typical Applications, and a Reagent/Building-Block Classification Navigator (Tables 1–5)
Molecular Basis of Glycosylation Modification and Functional Release in Natural Products
From Sucrose to Monosaccharides: Key Enzymatic Nodes and Regulatory Logic in Sugar Conversion
Formation of Nucleotide-Sugar Precursors and Regulatory Mechanisms in Plant Growth and Development
Regulatory Mechanisms, Research Methods, and Modification-Omics Analysis of Protein Post-Translational Modifications
Citations of This Product
Referenzen
1. Xuqiu He, Ronghao Huang, Lipeng Liu, Yingying Li, Wenzhao Wang, Qingshan Xu, Youben Yu, Tianshan Zhou.  (2021)  CsUGT78A15 catalyzes the anthocyanidin 3-O-galactoside biosynthesis in tea plants.  PLANT PHYSIOLOGY AND BIOCHEMISTRY,      [PMID:34217130] [10.1016/j.plaphy.2021.06.029]
2. Cao Shiyang, Wang Tong, Ren Yifan, Wu Gengshan, Zhang Yuan, Tan Yafang, Zhou Yazhou, Chen Hongyan, Zhang Yu, Song Yajun, Yang Ruifu, Du Zongmin.  (2024)  A protein O-GlcNAc glycosyltransferase regulates the antioxidative response in Yersinia pestis.  Nature Communications,  15  (1): (1-16).  [PMID:39152136] [10.1038/s41467-024-50959-w]
3. Lin Ge, Yu Xia, Wenxin Xu, Ruobing Jia, Tingting Zhang.  (2025)  Efficient Biosynthesis of Gastrodin by UDP-Glycosyltransferase from Rauvolfia serpentina.  JOURNAL OF MICROBIOLOGY AND BIOTECHNOLOGY,      [PMID:40147927] [10.4014/jmb.2501.01002]
4. Yang Gu, Yaru Jiang, Changfan Li, Jiang Zhu, Xueyao Lu, Jianyue Ge, Mengchen Hu, Jieying Deng, Jingbo Ma, Zhiliang Yang, Xiaoman Sun, Feng Xue, Guocheng Du, Peng Xu, He Huang.  (2024)  High titer production of gastrodin enabled by systematic refactoring of yeast genome and an antisense-transcriptional regulation toolkit.  METABOLIC ENGINEERING,      [PMID:38428728] [10.1016/j.ymben.2024.02.016]
5. Xiaomeng Zhang, Xinquan Tian, Junyu Luo, Xiaoyang Wang, Shoupu He, Gaofei Sun, Ruidan Dong, Panhong Dai, Xiao Wang, Zhaoe Pan, Baojun Chen, Daowu Hu, Liru Wang, Baoyin Pang, Aishuang Xing, Guoyong Fu, Baoquan Wang, Jinjie Cui, Lei Ma, Xiongming Du.  (2025)  Identification of UDP-glucosyltransferase involved in the biosynthesis of phloridzin in Gossypium hirsutum.  PLANT JOURNAL,  121  (3): (e17248).  [PMID:39935137] [10.1111/tpj.17248]
6. Chen-Xin Guo, Jiyan Li, Yu Wang, Tang Li, Heng Yin.  (2025)  Functional characterization of a Stevia rebaudiana flavonoid glycosyltransferase.  ENZYME AND MICROBIAL TECHNOLOGY,      [PMID:40639146] [10.1016/j.enzmictec.2025.110708]
7. Yan Sun, Tayyab Shaheen, Jiali Guo, Bingjie Shi, Miaohan Li, Xiaoyan Li, Yongqiang Li, Gunghui Tang.  (2025)  Laboratory selection, resistance risk assessment, fitness costs and biochemical mechanism of Aphis gossypii to flonicamid.  PESTICIDE BIOCHEMISTRY AND PHYSIOLOGY,      [PMID:41326073] [10.1016/j.pestbp.2025.106757]
8. Shuocheng She, Jiachen Zuo, Yang Li, Liu Sun, Yaowei Dai, Zekun Yang, Jinwu Zhao, Lei Wang, Wenxia Wang, Pandeng Hou, Qiuhong Qu, Yizhu Zhang, Mingxia He.  (2026)  Terahertz Metasurface with Ultrastrong Hotspots Empowered by QBIC.  ANALYTICAL CHEMISTRY,      [PMID:41534007] [10.1021/acs.analchem.5c06405]
9. Song Jun, Qin Yutong, Jin Lu, Han Liang, Li Shihan, Wu Shijuan, Shen Pan, Chen Yanling, Liu Yaqi, Cao Yan, Li Juan, Li Ying, He Qi, Huang Wei.  (2026)  Discovery and Engineering of a Plant Glycosyltransferase for Efficient Benzylisoquinoline Alkaloid Glycosylation.  JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY,  74  (30): (23698-23711).  [PMID:42505063] [10.1021/acs.jafc.6c07405]
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