Click Here for 5% Off Your First Aladdin Purchase!

2-Deoxy-D-glucose - 98%, high purity , CAS No.154-17-6

  • ≥98%
Item Number
D109194
Grouped product items
SKUSizeAvailabilityPrice Qty
D109194-1g
1g
In stock
$58.90
D109194-5g
5g
In stock
$189.90
D109194-25g
25g
In stock
$855.90
D109194-100g
100g
In stock
$3,078.90

Non-metabolizable glucose analog and glycolytic inhibitor. Antitumor agent.

Basic Description

Synonyms2-deoxy-D-glucose|Deoxyglucose|154-17-6|2-Desoxy-D-glucose|2-DG|(3R,4S,5R)-3,4,5,6-tetrahydroxyhexanal|2-Deoxy-D-mannose|2-Deoxy-D-arabinohexose|D-2-Deoxyglucose|D-arabino-2-desoxyhexose|D-Arabino-hexose, 2-deoxy-|HSDB 5484|D-Glucose, 2-deoxy-|9G2MP84A8W|
Specifications & Purity≥98%
Biochemical and Physiological Mechanisms2-Deoxy-D-Glucose (2-Deoxyglucose) is a glucose analog that inhibits glycolysis via its actions on hexokinase, the rate limiting step of glycolysis. It is phosphorylated by hexokinase to 2-DG-P which can not be further metabolized by phosphoglucose isomer
Storage TempStore at 2-8°C
Shipped InWet ice
NoteWherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20°C. Generally, these will be useable for up to one month. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour. Need more advice on solubility, usage and handling? Please visit our frequently asked questions (FAQ) page for more details.
Product Description

2-Deoxy-D-glucose is used in the development of anti-cancer strategies that involve radio- and chemosensitization and oxidative stress.

Associated Targets

SLC16A7 Tchem Monocarboxylate transporter 2 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

SLC16A1 Tchem Monocarboxylate transporter 1 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

Names and Identifiers

Pubchem Sid488187422
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/488187422
IUPAC Name (3R,4S,5R)-3,4,5,6-tetrahydroxyhexanal
INCHI InChI=1S/C6H12O5/c7-2-1-4(9)6(11)5(10)3-8/h2,4-6,8-11H,1,3H2/t4-,5-,6+/m1/s1
InChi Key VRYALKFFQXWPIH-PBXRRBTRSA-N
Canonical SMILES C(C=O)C(C(C(CO)O)O)O
Isomeric SMILES C(C=O)[C@H]([C@@H]([C@@H](CO)O)O)O
WGK Germany 3
RTECS MQ3325000
PubChem CID 108223
Molecular Weight 164.16
Beilstein 1723331
Reaxy-Rn 1723331

Certificates

Certificate of Analysis(COA)

Enter Lot Number to search for COA:

To view the certificate results,please click on a Lot number.For Lot numbers from past orders,please use our order status section

20 results found

Lot NumberCertificate TypeDateItem
H2430351Certificate of AnalysisAug 19, 2024 D109194
H2430350Certificate of AnalysisAug 19, 2024 D109194
H2430349Certificate of AnalysisAug 19, 2024 D109194
H2430348Certificate of AnalysisAug 19, 2024 D109194
G2312775Certificate of AnalysisJun 07, 2023 D109194
G2312792Certificate of AnalysisJun 07, 2023 D109194
G2312790Certificate of AnalysisJun 07, 2023 D109194
G2312784Certificate of AnalysisJun 07, 2023 D109194
G2312783Certificate of AnalysisJun 07, 2023 D109194
G2312782Certificate of AnalysisJun 07, 2023 D109194
D2408085Certificate of AnalysisJun 07, 2023 D109194
G2312774Certificate of AnalysisJun 07, 2023 D109194
F2312717Certificate of AnalysisMay 15, 2023 D109194
G2205112Certificate of AnalysisJun 01, 2022 D109194
G2205098Certificate of AnalysisJun 01, 2022 D109194
G2205097Certificate of AnalysisJun 01, 2022 D109194
G2205096Certificate of AnalysisJun 01, 2022 D109194
E2124231Certificate of AnalysisMar 17, 2021 D109194
E2124230Certificate of AnalysisMar 17, 2021 D109194
E2124150Certificate of AnalysisMar 17, 2021 D109194

more

Chemical and Physical Properties

SolubilitySoluble in water.
Specific Rotation[α]46.5 ° (C=1, H2O)
Melt Point(°C)146-147°C

Safety and Hazards(GHS)

WGK Germany 3
RTECS MQ3325000
Reaxy-Rn 1723331
Merck Index 2904

Related Documents

Alternative Products

References

1. Cabezas-Cruz A et al..  (2017)  Anaplasma phagocytophilum Infection Subverts Carbohydrate Metabolic Pathways in the Tick Vector, Ixodes scapularis..  Front Cell Infect Microbiol,  (23).  [PMID:28229048]
2. Morein D et al..  (2021)  Continuous Inflammatory Stimulation Leads via Metabolic Plasticity to a Prometastatic Phenotype in Triple-Negative Breast Cancer Cells..  Cells,  10  (6):   [PMID:34072893]
3. Blancke Soares A et al..  (2021)  High-resolution spatiotemporal pHe and pO2 imaging in head and neck and oesophageal carcinoma cells..  Cancer Metab,  (21).  [PMID:33947450]
4. Wang Z et al..  (2022)  The Fibrillin-1/VEGFR2/STAT2 signaling axis promotes chemoresistance via modulating glycolysis and angiogenesis in ovarian cancer organoids and cells..  Cancer Commun (Lond),  42  (3): (245-265).  [PMID:35234370]

Solution Calculators