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Cat. No. | Product Name | Target | Signaling Pathways |
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T22297 |
Clindamycin hydrochloride monohydrate
Clindamycin alcoholate |
Antibiotic | Microbiology/Virology |
Clindamycin hydrochloride monohydrate(Clindamycin alcoholate)是一种口服蛋白质合成抑制剂,具有在金黄色葡萄球菌中以亚抑制浓度(sub-MICs)抑制毒力因子表达的能力。其抗性来源于50S核糖体亚基(23S rRNA)的抗生素结合位点通过酶促甲基化。此外,Clindamycin hydrochloride monohydrate能显著减少杀白细胞毒素(PVL)、毒性休克-葡萄球菌毒素(TSST-1)或α-溶血素(Hla)的产生。 | |||
T1142 |
Clindamycin phosphate
Clindamycin 2-phosphate,Clindamycin 2-dihydrogen phosphate,NSC 618653,U-28508,克林霉素磷酸酯 |
ribosome; Antibacterial; Antibiotic; Parasite | Microbiology/Virology |
Clindamycin phosphate (Clindamycin 2-dihydrogen phosphate) 是一种抗生素,抑制微生物的核糖体作用。可研究厌氧菌感染和原虫疾病。 | |||
T6448 |
Clindamycin hydrochloride
盐酸克林霉素,Sobelin HCl,Cleocin,Clindamycin HCl,Clinimycin HCl |
Antibacterial; Antibiotic | Microbiology/Virology |
Clindamycin hydrochloride (Clinimycin HCl) 是一种半合成的林可胺类抗生素,作用于50S ribosomal 抑制蛋白质合成。 | |||
T35730 |
Clindamycin Sulfoxide
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Clindamycin sulfoxide is an active metabolite of the antibiotic clindamycin . It is formed via S-oxidation of clindamycin primarily by the cytochrome P450 (CYP) isoform CYP3A4. Clindamycin sulfoxide inhibits the growth of P. prevotti, B. fragilis, and C. sordelli in vitro with MIC values of 2, 2, and 1 mg/L, respectively. | |||
T6449 |
Clindamycin palmitate hydrochloride
Cleocin Pediatric,盐酸克林霉素棕榈酸酯,Clindamycin palmitate HCl |
Antibacterial; Antibiotic | Microbiology/Virology |
Clindamycin palmitate hydrochloride (Clindamycin palmitate HCl) 是克林霉素和棕榈酸酯的盐酸盐,是一种林可酰胺抗生素。 | |||
T18322 |
MC-Val-Cit-PAB-clindamycin
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Others | Others |
MC-Val-Cit-PAB-clindamycin is an antibody-drug conjugate (ADC) linker that combines the potent antitumor properties of clindamycin, a protein synthesis inhibitor, with the ADC linker MC-Val-Cit-PAB, to enhance its ability to target and kill cancer cells effectively. | |||
T75306 | Clindamycin phosphate hydrochloride | ||
Clindamycin phosphate (Clindamycin 2-phosphate) hydrochloride 是一种广谱抑菌林可酰胺类抗生素 (antibiotic)。Clindamycin phosphate hydrochloride 是Clindamycin 的前体活性分子,在体外不具有抗菌活性 ,但在体内可通过磷酸酶酯水解迅速转化为具有活性的母体活性分子 Clindamycin。Clindamycin phosphate hydrochloride 可用于痤疮和细菌性阴道病的研究。 | |||
T25965 |
Pirlimycin HCl
U 57930E,Pirsue,U-57930E,U57930E,Pirlimycin hydrochloride |
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Pirlimycin Hydrochloride, a Clindamycin analog, is a semi-synthetic lincosaminide antibiotic. | |||
T25815 |
Mirincamycin HCl
U24,729A,U-24,729A,U-24729 A,U 24729 A,U 24,729A,Mirincamycin hydrochloride |
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Mirincamycin HCl is a close analog of the drug clindamycin used for the treatment of Plasmodium falciparum blood stages. |
Cat. No. | Product Name | Target | Signaling Pathways |
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T6447 |
Clindamycin
Clinimycin,Sobelin,Chlolincocin,克林霉素 |
Antibacterial; Antibiotic | Microbiology/Virology |
Clindamycin (Sobelin) 从细菌核糖体中解离肽基-tRNA,破坏细菌蛋白质合成。 它是一种半合成广谱抗生素,由母体化合物林可霉素化学修饰而成。 |