6 Results for "

Saccharomyces sp.

" in MedChemExpress (MCE) Product Catalog:
Products (6)

6 Results for "Saccharomyces sp." in MCE Product Catalog:

Cat. No.: HY-W009417
CAS No.: 77-54-3
Cedryl acetate is an orally active α-glucosidase inhibitor with an IC50 of 94 μM against yeast α-glucosidase. Cedryl acetate reduces high-fat diet-induced body weight gain, visceral fat pad weight, adipocyte hypertrophy, hepatic lipid accumulation, glucose intolerance, insulin resistance and gluconeogenesis. Cedryl acetate can be used in the research of obesity and obesity-related metabolic syndrome .
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Cat. No.: HY-N13962
CAS No.: 377775-45-6
Target:  

Bacterial Fungal

Bagremycin A is found in the strain of Streptomyce sp. Tu 4128. Bagremycin A has weak activity against Gram-positive bacteria, Saccharomyces cerevisiae and Candida albicans .
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Cat. No.: HY-N13963
CAS No.: 93316-63-3
Target:  

Bacterial Fungal

Bagremycin B is found in the strain of Streptomyce sp. Tu 4128. Bagremycin B has weak activity against Gram-positive bacteria, Saccharomyces cerevisiae and Candida albicans .
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Cat. No.: HY-N20641
CAS No.: 3059457-35-8
Turonicin A is an anti-fungal and anti-bacterial agent found in Australian Streptomyces sp. MST-123921. Turonicin A inhibits growth of Candida albicans and Saccharomyces cerevisiae fungi. Turonicin A inhibits growth of Bacillus subtilis and Staphylococcus aureus bacteria. Turonicin A can be used for the research of fungal infections, bacterial infections .
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Cat. No.: HY-184340
Target:  

Glycosidase

Research Areas:  

Metabolic Disease

α-Glucosidase-IN-118 is a non-competitive inhibitor of α-glucosidase with a IC50 of 2.77 μM, and it shows no inhibitory activity against β-glucosidase. α-Glucosidase-IN-118 binds to the entrance of the α-glucosidase active site to block substrate release. α-Glucosidase-IN-118 can be used in the research of diabetes, obesity and lysosomal storage diseases .
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Cat. No.: HY-N21836
CAS No.: 76551-64-9
Category:  

Microorganisms Antibiotics

Target:  

Parasite Fungal

Partricin A is an antimicrobial agent with affinity for ergosterol and cholesterol. Partricin A inhibits growth of fungal species and Trichomonas vaginalis. Partricin A induces hemolysis of rat erythrocytes. Partricin A causes acute toxicity in mice via intraperitoneal or intravenous administration. Partricin A serves as a starting material for synthesis of semisynthetic amide derivatives. Partricin A can be used for the research of fungal infections, trichomonas vaginalis infection .
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