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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
25 Results for "
Nocardia
" in MedChemExpress (MCE) Product Catalog:
Products (25)
25 Results for "Nocardia" in MCE Product Catalog:
30
30 Publications Verification
Referencia número: HY-B0509B
No. CAS: 39831-55-5
Synonyms: BAY 41-6551 disulfate
Target:
Amikacin disulfate (BAY 41-6551 dissulfate) is an aminoglycoside antibiotic and a semisynthetic analog of kanamycin. Amikacin disulfate is bactericidal, acting directly on the 30S and 50S bacerial ribosomal subunits to inhibit protein synthesis. Amikacin disulfate is very active against most Gram-negative bacteria including gentamicin- and tobramycin-resistant strains. Amikacin disulfate also inhibits the infections caused by susceptible Nocardia and nontuberculous mycobacteria .
30
30 Publications Verification
Synonyms: BAY 41-6551 sulfate
Target:
Amikacin sulfate (BAY 41-6551 sulfate) is an aminoglycoside antibiotic and a semisynthetic analog of kanamycin. Amikacin sulfate is bactericidal, acting directly on the 30S and 50S bacerial ribosomal subunits to inhibit protein synthesis. Amikacin sulfate is very active against most Gram-negative bacteria including gentamicin- and tobramycin-resistant strains. Amikacin sulfate also inhibits the infections caused by susceptible Nocardia and nontuberculous mycobacteria .
30
30 Publications Verification
Referencia número: HY-B0509
No. CAS: 1257517-67-1
Synonyms: BAY 41-6551 hydrate
Target:
Amikacin hydrate (BAY 41-6551 hydrate) is an aminoglycoside antibiotic and a semisynthetic analog of kanamycin. Amikacin hydrate is bactericidal, acting directly on the 30S and 50S bacerial ribosomal subunits to inhibit protein synthesis. Amikacin hydrate is very active against most Gram-negative bacteria including gentamicin- and tobramycin-resistant strains. Amikacin hydrate also inhibits the infections caused by susceptible Nocardia and nontuberculous mycobacteria .
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2 Cited Publications
Cotrimoxazole (Trimethoprim/sulfamethoxazole 1:19), an antibacterial agent, is a Trimethoprim (HY-B0510) and Sulfamethoxazole (HY-B0322) mixture. The ratio of Trimethoprim to Sulfamethoxazole in the combination mixture is 1 : 19 .
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Cotrimoxazole (Trimethoprim/sulfamethoxazole 1:5), an antibacterial agent, is a Trimethoprim (HY-B0510) and Sulfamethoxazole (HY-B0322) mixture. The ratio of Trimethoprim to Sulfamethoxazole in the combination mixture is 1 : 5 .
Referencia número: HY-W001963
No. CAS: 634-97-9
Category:
Microorganisms Ketones, Aldehydes, Acids Marine natural products Other Diseases Endogenous metabolite Disease Research Fields Marine microorganism
Target:
Target:
Referencia número: HY-N13150A
No. CAS: 198774-23-1
Synonyms: N-Demethylvancomycin hydrochloride; NVCM hydrochloride
Target:
Áreas de investigación:
Norvancomycin hydrochloride is a glycopeptide antibiotic which can be found in Nocardia orientalis and active against several strains of S. aureus and S. epidermidis. Norvancomycin hydrochloride can be used for infection research .
Referencia número: HY-E70406
No. CAS: 67775-34-2
Synonyms: CHDH-5
Target:
Áreas de investigación:
Cholesterol Dehydrogenase, Nocardia sp. is an enzyme that uses nicotinamide adenine dinucleotide/nicotinamide adenine dinucleotide phosphate (NAD(P)) as its cofactor in oxidizing cholesterol to form cholest-4-en-3-one. This enzyme oxidizes the hydroxyl group at the 3 position of the sterol ring to form a ketone.
Referencia número: HY-162836
No. CAS: 13929-35-6
Synonyms: 4-O-(Carboxymethyl)-Rifamycin
Target:
Áreas de investigación:
Rifamycin B (4-O-(Carboxymethyl)-Rifamycin) is a member of ansamycin antibiotics family with an anti-mycobacterial activity against tuberculosis, leprosy and AIDS-related mycobacterial infections. Rifamycin B is a metabolic product of Nocardia inediterranei, which can yield Rifamycin O and Rifamycin S (HY-125365) by microbial transformation .
Referencia número: HY-N13150
No. CAS: 91700-98-0
Synonyms: N-Demethylvancomycin; NVCM
Category:
Target:
Referencia número: HY-N14497
No. CAS: 199173-81-4
Category:
Target:
Referencia número: HY-N14313
No. CAS: 199173-82-5
Category:
Target:
Referencia número: HY-P2848D
Synonyms: ChOx, Nocardia sp.
Target:
Áreas de investigación:
Cholesterol oxidase, Nocardia sp. (ChOx, Nocardia sp.) (EC 1.1.3.6) is a cholesterol oxidase identified from bacterial sources. Cholesterol oxidase, Nocardia sp. catalyzes the oxidation of cholesterol to 4-cholesten-3-one, while simultaneously reducing oxygen to hydrogen peroxide. Cholesterol oxidase, Nocardia sp. retains its enzymatic activity and exhibits improved catalytic efficiency upon immobilization. Cholesterol oxidase, Nocardia sp. is applicable for cholesterol detection, steroid biotransformation, and research on tuberculosis-related diseases .
Referencia número: HY-N14475
No. CAS: 86470-27-1
Category:
Target:
Referencia número: HY-W777997
No. CAS: 60134-71-6
Target:
Referencia número: HY-136828
No. CAS: 52932-62-4
Target:
Áreas de investigación:
LL-BM123α is a basic antibiotic isolated from Nocardia sp. LL-BM123α exhibits moderate activity against Gram-negative bacteria.
Referencia número: HY-N11485
No. CAS: 50888-50-1
Category:
Target:
Referencia número: HY-W550259
No. CAS: 321-54-0
Synonyms: Coumaphos oxon
Target:
Áreas de investigación:
Coroxon (Coumaphos oxon) is an oxidative metabolite of the organophosphate insecticide Coumaphos (HY-W653717) and an active AChE inhibitor with insecticidal and acaricidal properties. Coroxon can be hydrolyzed by phosphotriesterases of microorganisms such as Nocardia asteroides to produce the fluorescent product Chlorferon .
Referencia número: HY-125042
No. CAS: 130756-15-9
Sarothralin G is an antibacterial compound isolated from Hypericum japonicum Thunb. (Japanese spurfle). The structure of Sarothralin G contains phenolic and aromatic acid moieties and shows excellent antibacterial activity against Gram-positive bacteria such as Staphylococcus aureus, Bacillus subtilis and Nocardia spp., which is stronger than Sarothralen A, B and Saroaspidin A, B, C. Sarothralin G exhibits significant antibacterial potential.
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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
