antibiotics

Aminothiazole (2-Aminothiazole), a thyroid inhibitor, displays antibacterial activity.

Rifamycin S is a potent DNA-dependent RNA polymerase inhibitor,is a quinone and an antibiotic agnet against Gram-positive bacteria

Metallo β-lactamase ligand 1 is an inhibitor of class B β-lactamase exhibiting antibacterial activities.

Cinoxacin (Compound 64716), an older synthetic antimicrobial, was related to the quinolone class of antibiotics. Its activity was similar to oxolinic acid and nalidixic acid.

Nanaomycin A, a quinone antibiotics, reactivates silenced tumor suppressor genes in human cancer cells. Nanaomycin A is a selective inhibitor of DNMT3B (IC50 = 500 nM).

Midecamycin (Medecamycin A1), an acetoxy-substituted macrolide antibiotic, has effective on gram-positive and gram-negative bacteria acts by inhibiting bacterial protein synthesis.

Dactimicin is a new aminoglycoside. It also has in vitro activity, post-antibiotic effect, and interaction with other antibiotics.

Antibiotic SB 202742 is a useful organic compound for research related to life sciences. The catalog number is T124135 and the CAS number is 83173-24-4.

Antibiotic Sch 378167 is a useful organic compound for research related to life sciences. The catalog number is T125021 and the CAS number is 336108-99-7.

Antibiotic Sch 60057 is a useful organic compound for research related to life sciences. The catalog number is T125403 and the CAS number is 203061-35-2.

Antibiotic Sch 60061 is a useful organic compound for research related to life sciences. The catalog number is T125404 and the CAS number is 203061-33-0.

Antibiotic Sch 60065 is a useful organic compound for research related to life sciences. The catalog number is T125405 and the CAS number is 203061-31-8.

Antibiotic Sch 60059 is a useful organic compound for research related to life sciences. The catalog number is T125406 and the CAS number is 203061-30-7.

K-252a is a protein kinase inhibitor targeting serine-threonine, tyrosine, and CAM kinases. In vitro, it blocks NGF-induced TrkA signalling and neural differentiation, exhibiting antitumour, antibacterial, anti-inflammatory, and neuroprotective activities.

Cyclosporin B is an immunosuppressant that has revolutionized organ transplantation through its use in the prevention of graft rejection. Cyclosporin B displays antiviral properties, inhibiting the entry of hepatitis B into hepatocytes. Cyclosporin B also

Bilanafos is an agent of Anti-Bacterial.

Antibiotic SF 2132 is a bioactive chemical.

GSK-598809 L-tartrate sesquihydrate is an acute D3 antagonist.

1-Deamino-1-hydroxygentamicin C1a (AntibioticSU-2) is an aminoglycoside antibiotic effective against both gram-positive and gram-negative bacteria.

1-Deamino-1-hydroxygentamicin C2 (AntibioticSU-1) is an aminoglycoside antibiotic effective against both Gram-positive and Gram-negative bacteria.

1-Deamino-1-hydroxysagamicin (AntibioticSUM-3) is an aminoglycoside antibiotic that is effective against both Gram-positive and Gram-negative bacteria.

Ampicillin (Aminobenzylpenicillin) is a semi-synthetic penicillin belonging to the β-lactam group of antibiotics. Ampicillin has bactericidal activity against a wide range of Gram-positive and Gram-negative bacteria.

Penicillamine (Artamine), possessing antineoplastic properties, induces apoptosis by a p53-mediated mechanism and inhibits angiogenesis by chelating with copper, a cofactor for angiogenesis. Artamine is a beta dimethyl analog of the amino acid cysteine. As a degradation product of penicillin antibiotics, Artamine chelates with heavy metals and increases their urinary excretion.

Doxorubicin hydrochloride is an anthracycline antibiotic with cytotoxic and antitumor activity. It is an effective inhibitor of human DNA topoisomerase I and II, with IC50 values of 0.8 μM and 2.67 μM, respectively. In addition to inhibiting DNA topoisomerases, it can reduce the phosphorylation of AMPK and its downstream target, acetyl-CoA carboxylase. Doxorubicin hydrochloride also induces apoptosis and autophagy. In animal studies, it is commonly used to induce models of acute renal failure, chronic kidney injury, and heart failure.