11 Results for "

3-phenyllactic acid

" in MedChemExpress (MCE) Product Catalog:
Products (11)

11 Results for "3-phenyllactic acid" in MCE Product Catalog:

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1 Cited Publications
Cat. No.: HY-30219
CAS No.: 7326-19-4
Synonyms: D-3-phenyllactic acid
D-​(+)​-​Phenyllactic acid is an anti-bacterial agent, excreted by Geotrichum candidum, inhibits a range of Gram-positive from humans and foodstuffs and Gram-negative bacteria found in humans .
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1 Cited Publications
Cat. No.: HY-30220
CAS No.: 20312-36-1
Synonyms: L-(-)-3-phenyllactic acid
(S)-2-Hydroxy-3-phenylpropanoic acid is the L-configuration of 2-Hydroxy-3-phenylpropanoic acid, and its level is closely related to some diseases, such as phenylketonuria .
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Cat. No.: HY-W016203
CAS No.: 114-76-1
Synonyms: Sodium phenylpyruvate
Research Areas:  

Infection Metabolic Disease

Phenylpyruvic acid sodium is a endogenous metabolite that participates in the synthesis of 3-phenyllactic acid (PLA) by lactate dehydrogenase. Phenylpyruvic acid is a precursor of the antifungal compound phenyllactic acid. Phenylpyruvic acid can improve the antifungal activity of eight lactic acid bacterial strains through the addition into a dedined growth medium. Phenylpyruvic acid demonstrates improved inhibitory activity against fungal bread contaminants Aspergillus niger and Penicillium roqueforti. Phenylpyruvic acid affects enzyme activity of the pentose phosphate pathway involved in the oxidative phase in rat brain homogenates. Phenylpyruvic acid can reduce glucose-6-phosphate dehydrogenase activity .
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Cat. No.: HY-W017162S
CAS No.: 490034-49-6
DL-3-Phenyllactic acid-d3 is a deuterated labeled DL-3-Phenyllactic acid . DL-3-Phenyllactic acid is a broad-spectrum antimicrobial compound.
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Cat. No.: HY-W017162R
CAS No.: 828-01-3
DL-3-Phenyllactic acid (Standard) is the analytical standard of DL-3-Phenyllactic acid. This product is intended for research and analytical applications. DL-3-Phenyllactic acid is a broad-spectrum antimicrobial compound.
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Cat. No.: HY-P10563
CAS No.: 2580150-96-3
Synonyms: BHV-1100
Target:  

CD38 IFNAR

Research Areas:  

Cancer

Noraramtide (BHV-1100) is an antibody-recruiting molecule. Noraramtide binds to CD38 and recruits natural killer (NK) cells to mediate antibody-dependent cellular cytotoxicity. Noraramtide enhances the capacity of autologous cytokine-induced memory-like (CIML) NK cells to produce IFNγ and CD107a, thereby improving their cytotoxicity against multiple myeloma cells. Noraramtide can be used in the research of multiple myeloma .
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Cat. No.: HY-W753181
Synonyms: L-(-)-3-phenyllactic acid-13C9
(S)-2-Hydroxy-3-phenylpropanoic acid- 13C9 (L-(-)-3-Phenyllactic Acid- 13C9) is the 13C-labeled (S)-2-Hydroxy-3-phenylpropanoic acid (HY-30220). (S)-2-Hydroxy-3-phenylpropanoic acid is the L-configuration of 2-Hydroxy-3-phenylpropanoic acid, and its level is closely related to some diseases, such as phenylketonuria .
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Cat. No.: HY-30219R
CAS No.: 7326-19-4
Synonyms: D-3-phenyllactic acid (Standard)
D-​(+)​-​Phenyllactic acid (Standard) is the analytical standard of D-​(+)​-​Phenyllactic acid. This product is intended for research and analytical applications. D-​(+)​-​Phenyllactic acid is an anti-bacterial agent, excreted by Geotrichum candidum, inhibits a range of Gram-positive from humans and foodstuffs and Gram-negative bacteria found in humans[1].
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Cat. No.: HY-30220R
CAS No.: 20312-36-1
Synonyms: L-(-)-3-phenyllactic acid (Standard)
(S)-2-Hydroxy-3-phenylpropanoic acid (Standard) is the analytical standard of (S)-2-Hydroxy-3-phenylpropanoic acid. This product is intended for research and analytical applications. (S)-2-Hydroxy-3-phenylpropanoic acid is the L-configuration of 2-Hydroxy-3-phenylpropanoic acid, and its level is closely related to some diseases, such as phenylketonuria .
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Cat. No.: HY-126840
CAS No.: 139026-54-3
Target:  

Others

Research Areas:  

Others

Antho-riamide I is a neuropeptide and an inhibitor of spontaneous contraction of endodermal muscle groups. Antho-riamide I can be isolated from the sea anemone Anthopleura elegantissima. Antho-riamide I resists degradation by non-specific aminopeptidases via the L-3-phenyllactic acid blocking group at its amino terminus .
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