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Cat. No. | Product Name | Target | Signaling Pathways |
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T11427 |
Antibacterial compound 2
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Antifungal | Microbiology/Virology |
Antibacterial compound 2 是一种有效的抗菌剂,对许多人类兽医病原体有效,对多重耐药葡萄球菌、肠球菌和链球菌,以及厌氧菌有抑制作用。 | |||
T23639 |
Adicillin
NSC113137,NSC 113137,NSC-113137 |
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Adicillin is a penicillin antibiotic that works against vancomycin-resistant enterococci. | |||
T37881 |
Oritavancin(LY-333328)
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Oritavancin is a novel semisynthetic glycopeptide antibiotics. On August 6, 2014, the FDA approved oritavancin for treatment of skin infections. Oritavancin possesses potent and rapid bactericidal activity in vitro against a broad spectrum of both resistant and susceptible Gram-positive bacteria, including Staphylococcus aureus, MRSA, enterococci, and streptococci. | |||
T38125 |
Platencin
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Platencin is a natural, broad spectrum Gram-positive antibiotic isolated from S. platensis, which is also the source of platensimycin . Platencin inhibits two key enzymes in bacterial fatty acid synthesis, β-ketoacyl-ACP synthases II and III (FabF and FabH, respectively), unlike platensimycin which only targets FabF. The IC50 values for platencin against FabF and FabH are 1.95 and 3.91 μg/ml, respectively. It does not exhibit cross-resistance to antibiotic resistant bacterial strains, including ... | |||
T74821 |
Nemonoxacin
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Nemonoxacin (TG-873870) 是一种口服有效的广谱抗生素,对多种葡萄球菌、链球菌、肠球菌、淋病奈瑟菌和流感嗜血杆菌显示出强效的抑制活性。适用于研究细菌感染和社区获得性肺炎。 | |||
T73600 |
Cefaloglycin
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Cefaloglycin(Cephaloglycin)是一种β-内酰胺类(β-lactam)口服活性头孢菌素类抗生素,具有肾毒性和抗菌活性。该药物对革兰氏阳性球菌(除肠球菌外)有效,同时对线粒体底物摄取及呼吸具有毒性。 | |||
T38009 |
Kocurin
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Kocurin is a thiazolyl peptide originally isolated fromK. palustrisand has antibiotic activity.1It is active against methicillin-resistantS. aureus(MRSA; MIC = 0.25 μg/ml), as well asB. subtilisandE. faeciumin a solid agar test when used at a concentration of 8 μg/ml. Kocurin is also active againstE. faecium,E. faecalis,S. epidermidis, and clinical isolates of vancomycin-resistant enterococci (MICs = 0.004-1.025 μg/ml).2In vivo, kocurin (2.5, 5, and 10 mg/ml) increases survival in a mouse model ... | |||
T14359 |
AVX 13616
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Others | Others |
AVX 13616 shows the potent in vivo antibacterial activity of Avexa’s lead antibacterial candidate; particularly against drug-resistant Staphylococcus pathogens. IC50 value: 2-4 ug/ml (MICs) Target: antibacterial agent AVX13616 was as active as mupirocin i |
Cat. No. | Product Name | Target | Signaling Pathways |
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T3982 |
Vulpinic Acid
狐衣酸,Vulpic acid,Pulvinic acid methyl ester |
Others | Others |
Vulpinic Acid (Pulvinic acid methyl ester) 是地衣代谢物,可降低人脐静脉内皮细胞 (HUVEC) 中 H2O2诱导的ROS,氧化应激和氧化应激相关损伤,可作用于厌氧菌、葡萄球菌及肠球菌。它对脉粥样硬化的研究具有潜在的价值。 | |||
T0832 |
Vancomycin hydrochloride
盐酸万古霉素,Vancomycin HCl |
Cell wall; Antibacterial; Antibiotic; Autophagy | Autophagy; Immunology/Inflammation; Microbiology/Virology |
Vancomycin hydrochloride (Vancomycin HCl) 是Vancomycin 的盐酸盐,是一种支链三环糖基化肽,对大多数生物体具有杀菌活性,对肠球菌具有抑菌作用。 | |||
TN1342 |
8-Epidiosbulbin E acetate
8-表黄药子素E乙酸酯 |
Anti-infection; Antibacterial | Microbiology/Virology |
8-Epidiosbulbin E acetate 是从 Dioscorea bulbifera L.中发现的呋喃类化合物,对耐多药细菌具有广谱的质粒治疗活性。 | |||
TN4148 | Glyasperin C | Tyrosinase; Antifection | Microbiology/Virology; Proteases/Proteasome |
Glyasperin C acts as a partial estrogen antagonist, it shows tyrosinase inhibitory activity (IC (50) = 0.13 +/- 0.01 microg/mL), it could be a promising candidate in the design of skin-whitening agents. Glyasperin C shows potent anti-vancomycin-resistant |