4 Results for "

Fru-6-P

" in MedChemExpress (MCE) Product Catalog:
Products (4)

4 Results for "Fru-6-P" in MCE Product Catalog:

1
1 Cited Publications
Cat. No.: HY-110156
CAS No.: 6093-71-6
Purity:  98.56%
Target:  

Phosphatase

Research Areas:  

Cancer

Y29 is a potent PFKFB3 inhibitor with an IC50 of 0.183 µM, and acts as a competitive inhibitor against Fru-6-P with a Ki value of 0.094 µM. Y29 exhibits antitumor effects against cervical cancer .
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Cat. No.: HY-124890
CAS No.: 727664-79-1
Purity:  99.36%
Thr101 is an inhibitor (IC50=2.9 μM) of phosphomannose isomerase (PMI).PMI can compete with phosphomannose mutase 2 (PMM2) for the binding site of Man-6-P and convert mannose-6-phosphate (Man-6-P) into fructose-6-phosphate (Fru-6-P) .Thr101 only specifically inhibits PMI and not PMM2. Thr101 can be used for research of congenital disorder of glycosylation type Ia (CDG-Ia) .
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Cat. No.: HY-E70120
CAS No.: 9023-88-5
Target:  

Fungal

Research Areas:  

Infection

Phosphomannose isomerase is the first enzyme involved in the biosynthesis pathway of GDP-Man. Phosphomannose isomerase catalyzes the conversion between fructose-6-phosphate (Fru6P) and mannose-6-phosphate (Man6P). Phosphomannose isomerase is important for cell wall synthesis and protein glycosylation. Phosphomannose isomerase is a potent antifungal target to curb the threats posed by A. flavus .
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Cat. No.: HY-110156R
CAS No.: 6093-71-6
Research Areas:  

Cancer

YZ9 (Standard) is the analytical standard of YZ9 (HY-110156). This product is intended for research and analytical applications. Y29 is a potent PFKFB3 inhibitor with an IC50 of 0.183 µM, and acts as a competitive inhibitor against Fru-6-P with a Ki value of 0.094 µM. Y29 exhibits antitumor effects against cervical cancer .
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