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Targeted therapy! The Capetin Prize winning "Click Chemistry" can be used like this!Targeted therapy! The Nobel Prize winning "Click Chemistry" can be used like this!2025-02-06
41 Results for "
mutase
" in MedChemExpress (MCE) Product Catalog:
Products (41)
41 Results for "mutase" in MCE Product Catalog:
Cat. No.: HY-138877A
Target:
Research Areas:
Phosphoglycolic acid (lithium) is a competitive inhibitor of phosphoglycerate mutase (PGAM)-B, an enzyme of the glycolytic pathway. Phosphoglycolic acid increases basal and fMLF-induced levels of G6P in intact neutrophils. Phosphoglycolic acid thereby increases upstream intermediates in neutrophils, thereby amplifying the respiratory oxidative burst .
Cat. No.: HY-E71591
Target:
Research Areas:
2-Methyleneglutarate mutase (EC 5.4.99.4) requires a cobamide coenzyme.
Cat. No.: HY-E71629
Target:
Research Areas:
3-(hydroxyamino)Phenol mutase (EC 5.4.4.3) belongs to the family of isomerases, specifically those intramolecular transferases transferring hydroxy groups.
Cat. No.: HY-E71807
Target:
Research Areas:
4-Carboxymethyl-4-methylbutenolide mutase (EC 5.4.99.14) is an isomerase that can convert 4-methylmuconolactone into 3-methylmuconolactone.
Cat. No.: HY-E71462
Target:
Research Areas:
2-Acetolactate mutase (EC 5.4.99.3) requires ascorbic acid; also converts 2-aceto-2-hydroxybutanoate to 3-hydroxy-3-methyl-2-oxopentanoate.
Cat. No.: HY-E71563
Target:
Research Areas:
2-Hydroxyisobutanoyl-CoA mutase (EC 5.3.3.20), characterized from the bacterium Aquincola tertiaricarbonis, uses radical chemistry to rearrange the positions of both a methyl group and a hydroxyl group, and consists of two subunits, the smaller one containing a cobalamin cofactor.
Cat. No.: HY-E71890
Target:
Research Areas:
5-(Carboxyamino)Imidazole ribonucleotide mutase (EC 5.4.99.18) is an isomerase that can convert 5-carboxyamino-1-(5-phospho-D-ribosyl)imidazole and H + into 5-amino-1- (5-phospho-D-ribosyl)imidazole-4-carboxylate.
Cat. No.: HY-128753A
CAS No.: 65-42-9
Target:
Cat. No.: HY-P701963
Purity: ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: PGAM1; Phosphoglycerate mutase Isozyme B; Prev. PGAMA; HEL-S-35; PGAM-B; Epididymis Secretory Protein Li 35; Phosphoglycerate mutase A, Nonmuscle Form; Phosphoglycerate mutase; Phosphoglycerate mutase 1 (Brain); Phosphoglycerate mutase 1; BPG-Dependent PG
Species:
Human
Source:
E. coli
Cat. No.: HY-P7665
Purity: ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: BPGM; DPGM; Bisphosphoglycerate mutase; Testis Secretory Sperm-Binding Protein Li 202a; 2,3-Bisphosphoglycerate mutase, Erythrocyte; Erythrocyte 2,3-Bisphosphoglycerate mutase; 2,3-Bisphosphoglycerate Synthase; 2,3-Bisphosphoglycerate mutase; 2,3-Diphosph
Species:
Human
Source:
E. coli
Cat. No.: HY-P703173
Purity: ≥ 80%, as determined by reducing SDS-PAGE.
Synonyms: PGM3; N-Acetylglucosamine-Phosphate mutase; Phosphoglucomutase 3; DKFZP434B187; PAGM; PGM 3; Phosphoacetylglucosamine mutase; N-Acetylglucosamine-Phosphate mutase 1; Acetylglucosamine Phosphomutase; Phosphoglucomutase-3; AGM1; IMD23
Species:
Human
Source:
E. coli
Category:
Target:
Cat. No.: HY-115804
CAS No.: 957762-36-6
Target:
Research Areas:
MJE3 is a cell-permeable small-molecule phosphoglycerate mutase 1 (PGAM1) inhibitor. MJE3 is applicable to research related to breast cancer and melanoma .
Cat. No.: HY-113652
CAS No.: 1027102-49-3
UGM-IN-2 is a UGM inhibitor with a Kd of 20 μM. It binds to the UGM isoforms of K. pneumoniae (Klebsiella pneumoniae) and M. tuberculosis (Mycobacterium tuberculosis) and inhibits mycobacterial growth. UGM-IN-2 can be used in studies related to mycobacterial infections and tuberculosis .
Cat. No.: HY-180407
CAS No.: 1027102-50-6
UGM-IN-1 (compound 107) is a selective competitive inhibitor of Mycobacterium tuberculosis UDP-Galp mutase (UGM), encoded by Rv3809c. UGM-IN-1 inhibits the conversion of UDP-galactopyranose (UDP-Galp) to UDP-galactofuranose (UDP-Galf), thereby blocking the synthesis of key components of the mycobacterial cell wall, including mycolic acid-arabinogalactan (mAG) and liparabinomannan (LAM), leading to anti-mycobacterial activity against Mycobacterium tuberculosis. UGM-IN-1 is useful for research on tuberculosis, including drug-resistant tuberculosis .
Cat. No.: HY-P702869
Purity: ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: PGAM5; BXLBv68; PGAM Family Member 5, Mitochondrial Serine/Threonine Protein Phosphatase; PGAM Family Member 5, Serine/Threonine Protein Phosphatase, Mitochondrial; Phosphoglycerate mutase Family Member 5; MGC5352; Serine/Threonine-Protein Phosphatase PGA
Species:
Human
Source:
E. coli
Cat. No.: HY-P75162
Purity: ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: GLO1; Aldoketomutase; Glyoxalase I; Glx I; Lactoylglutathione Lyase; Epididymis Secretory Protein Li 74; GLOD1; Glyoxalase Domain Containing 1; S-D-Lactoylglutathione Methylglyoxal Lyase; Lactoyl Glutathione Lyase; Ketone-Aldehyde mutase; HEL-S-74; Methyl
Species:
Mouse
Source:
E. coli
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Protocols
Targeted therapy! The Capetin Prize winning "Click Chemistry" can be used like this!Targeted therapy! The Nobel Prize winning "Click Chemistry" can be used like this!A suitable model is crucial in drug screening experiments. Organs can mimic the three-dimensional functional structure of internal organs, have similar spatial organization to corresponding organs, maintain some key characteristics, and reproduce some physiological functions. They are widely used for modeling and personalized drug screening physiological functions.2025-02-06
