Antibiotic

Cephalosporinase, bacillus, are enzymes produced by Bacillus; these enzymes inactivate and degrade the effectiveness of cephalosporin antibiotics. Cephalosporins are a class of β-lactam antibiotics widely used to treat bacterial infections [1].

Pyrazine-2-carbaldehyde inhibits nicotinamidase in Mycobacterium tuberculosis and can be used for tuberculosis research

Saframycin S, an antibiotic featuring a Racemomycin group, demonstrates inhibitory effects against Ehrlich ascites tumor. The LD50 value of Saframycin S in ddY mice is 3.2 mg/kg (i.p.).

Siccanin is an antifungal antibiotic with antidermatophytic properties.

Garenoxacin (BMS284756) is a novel oral des-fluoro(6) quinolone for the treatment of Gram-positive and Gram-negative bacterial infections.

Ristocetin, an antibiotic from Amycolatopsis lurida, treated staph infections but was discontinued due to causing thrombocytopenia.

Cefotiam hydrochloride is a third-gen cephalosporin that disrupts bacterial cell wall synthesis by inhibiting PBPs.

X 14547-A is a biochemical product.

Malonomicin is a useful organic compound for research related to life sciences and the catalog number is T124924.

RK 1441B is a bacteriophage antibiotic related to neothramycin.

CC 1014 is a polypeptide antibiotic isolated from Penicillium lilacinum that inhibits phosphorylation of ADP, Mg ATPase.

Nikkomycin is used as an insecticide.

Kuguacin R is a natural product that can be used as a reference standard.

Ambruticin is a biochemical.

Epithienamycin E is a member of the class of carbapenems. Epithienamycin E has a role as a bacterial metabolite.

Cefoxitin sodium (Betacef) is a semisynthetic cephamycin antibiotic resistant to beta-lactamase.

Streptonigrin, from Streptomyces flocculus, has anti-tumor and anti-bacterial properties, inhibiting PAD1-4.

Nystatin A3 (Fungicidin) , which belongs to the polyene group of antimycotics, is frequently used as a topical agent in the treatment of oro-pharyngeal

Gliotoxin, a mycotoxin, inhibits Wnt pathway, causing apoptosis in mutated colorectal cancer cells and blocks NF-κB by preserving IκB.

Amorolfine HCL is an antifungal reagent.

T.cruzi-IN-1 (MDK1088) is a Trypanosoma cruzi inhibitor.

Oxacillin sodium monohydrate (Stapenor monohydrate) is an antibacterial agent and is a narrow spectrum beta-lactam antibiotic of the penicillin class.

3′-Deoxyuridine is a potential anticancer and antiviral agent. 3'-deoxyuridine inhibits the production of bovine diarrhoea virus (BVDV) [1].

2-Nitrobenzaldehyde Semicarbazone (Standard) is the standard substance of 2-Nitrobenzaldehyde Semicarbazone, and it is applicable for quantitative analysis, quality control, and related research in biochemical experiments. 2-Nitrobenzaldehyde Semicarbazone is a metabolite marker for the detection of Nitrofurazone, a highly restricted antibiotic. This compound, derived from Semicarbazide, exhibits significant potential in identifying the presence of Nitrofurazone.

Ceftriaxone Sodium is a sporotaxin antibiotic that inhibits GSK3β and Aurora B. It is used in the study of sepsis and infective endocarditis.

Desmethyl Levofloxacin, a levofloxacin metabolite, is a synthetic fluoroquinolone antibiotic that inhibits bacterial DNA gyrase.

Cefaclor (Panoral) is a cephalosporin antibiotic.

Halofantrine hydrochloride (SKF-102886) is an orally administered antimalarial drug effective against drug-resistant P. falciparum and P. vivax. SKF-102886 has cardiac toxicity, inhibiting hERG and delayed rectifier potassium channel I Kr, leading to prolonged QTc and PR intervals.

EDTA copper(II) disodium salt is a metal chelator with antimicrobial, anti-inflammatory, and antioxidant activities for the study of neurological disorders.

Metronidazole acetic acid, a mutagenic metabolite of an antibiotic, targets protozoa and anaerobic bacteria.

"Ribavirin-13C5, an antiviral guanosine analog, aids in ribavirin quantification via GC/LC-MS, effective against various viruses with diverse EC50 values."

Praziquantel (Standard) is the standard substance of Praziquantel, and it is applicable for quantitative analysis, quality control, and related research in biochemical experiments. Praziquantel (Droncit) increases the permeability of the tegument of susceptible worms, resulting in an influx and increase in intra-tegumental calcium leading to rapid contractions and paralysis of the worm's musculature through a subsequent increase in levels of calcium in the sarcoplasmic reticulum. Praziquantel is a pyrazinoisoquinoline derivative with anthelminthic property. In addition, vacuolization of the tegumental syncytium and blebbing results in tegument disintegration, leads to antigen exposure and elicit host defense responses to the worm.

Surfen dihydrochloride (Aminoquinuride dihydrochloride) is a heparin sulfate antagonist with antimicrobial properties and inhibits blockade of signaling.

3-Desacetyl Cefotaxime lactone, the active metabolite of Cefotaxime, is derived from its sodium salt form, which is recognized as a third-generation

2-Nitrosopyridine: used in antibiotic synthesis, Click/Diels-Alder reactions, excellent dienophile.

AMOZ has a wide range of applications in life science related research.

D-4-Hydroxyphenylglycine is key in making β-lactam antibiotics like Amoxicillin and Cefadroxil.

2-Nitrobenzaldehyde Semicarbazone, a Semicarbazide derivative, detects antibiotic Nitrofurazone use.

Cerulenin is a natural inhibitor of fatty acid synthase (FAS). It is produced by the fungus Cephalosporium caeruleus.

Bleomycin A2, a DNA-degrading antitumor antibiotic, functions as an inhibitor of aspartate/asparagine-β-hydroxylase (AspH), exhibiting an inhibitory

17β-Estradiol sulfate sodium (17β-Estradiol 3-sulfate sodium) is a neuroactive estrogen with vasoprotective properties that inhibits the growth of Neisseria brasiliensis and disrupts aquatic ecosystems.

Amikacin hydrate (BAY 41-6551 hydrate) is an aminoglycoside antibiotic with bacteriostatic properties.

Validamycin A is an antibiotic and fungicide that inhibits the alginate enzyme trehalase Rhizoctonia solani, reversible inhibitor of tyrosinase.

Tirilazad: a 21-aminosteroid preventing lipid peroxidation; aids in neuroprotection and treats ischemic conditions.

Dextramycine is an optic isomer of chloramphenicol.

Fenbendazole-d3 is a deuterated compound of Fenbendazole. Fenbendazole has a CAS number of 43210-67-9. Fenbendazole is an antinematodal benzimidazole used in veterinary medicine.

Ganciclovir mono-O-acetate: an oral antiviral derivative targeting CMV, part of nucleoside analogues.

Sulfathiazole-d4 is a deuterated isotope of Sulfathiazole for isotope tracing. Sulfathiazole is a short-acting sulfonamide antibiotic.

PD 404182 is a DDAH1 inhibitor with antiangiogenic and antiviral activities that can be used to study cardiovascular disease and viral infections.

Amikacin disulfate (BAY-416651 sulfate) is a semi-synthetic aminoglycoside antibiotic derived from kanamycin A.

Piromidic acid, an antibacterial, targets gram-negative bacteria and staphylococci; used for urinary and intestinal infections.

Calcimycin (A-23187) is a polyether antibiotic that transports Ca²⁺, uncouples phosphorylation, and inhibits ATPase in mitochondria.

Besifloxacin Hydrochloride (BOL-303224-A) is a fourth-generation fluoroquinolone antibiotic.

Leucomycin (Turimycin) is a macrolide antibiotic.

Brefeldin A (Cyanein) belongs to the class of macrolide antibiotics and is an ATPase inhibitor (IC50=0.2 μM).

Prulifloxacin (NM441) is a broad-spectrum fluoroquinolone that inhibits bacterial DNA synthesis by blocking topoisomerase II and IV.

Cefotaxime is an inhibitor of penicillin binding protein.

Cefapirin sodium is the sodium salt of Cephapirin, an antimicrobial agent.

Fenticonazole Nitrate (Lomexin) is an azole agent with antifungal activity.

Levofloxacin ((-)-Ofloxacin) is a synthetic fluoroquinolone antibiotic that prevents DNA replication. Cost-effective and quality-assured.

Tedizolid (DA-7157)is a novel oxazolidinone-class antibiotic that inhibits bacterial protein synthesis by binding to the 23S ribosomal RNA of the 50S subunit of

ML406 shows anti-tubercular activity via MtbbioA (DAPA synthase) enzyme inhibition(IC50 : 30 nM)

Dacarbazine ( imidazole carboxamide) is a chemotherapy drug used to treat melanoma and Hodgkin's lymphoma.

Oligomycin A (MCH 32) is an inhibitor of ATP synthase, inhibits oxidative phosphorylation and all the ATP-dependent processes occurring on the coupling membrane

2-Phenylethanol (Phenylethanol) is an antimicrobial, antiseptic, and disinfectant.

Pneumocandin B0 (L-688786) is a natural product and a key intermediate in the synthesis of the antifungal agent.

Pleuromutilin (Drosophilin B) is an inhibitor of bacterial protein synthesis by binding to the 50S ribosomal subunit of bacteria.

Gatifloxacin hydrochloride, a fourth-gen fluoroquinolone antibiotic, blocks bacterial DNA rotase and topoisomerase IV.

Buparvaquone (BW 720C) is a hydroxynaphthoquinone antiprotozoal drug related to atovaquone and parvaquone.

Avermectin B1a is a macrocyclic lactone disaccharide anthelmintic agent .

Ceftizoxime (Epocelin), a broad-spectrum cephalosporin antibiotic, resists beta-lactamases, effective IV/suppository.

Cefteram pivoxil (T-2588, CFTM-PI), an oral antibiotic in powder and tablet forms, treats bacterial infections in China.

Niclosamide (BAY2353) sodium: oral antihelminthic, STAT3 inhibitor (IC50 0.25 μM), anti-cancer, and DNA replication blocker.

Doripenem is a new parenteral carbapenem antibiotic with broad-spectrum activity against gram-negative and gram-positive pathogens.

Sibofimloc (Antibiotic-202), an antibiotic compound, is used in treating bacterial infections.

Sulfamethoxazole sodium (Ro 4-2130 sodium) is a sulfonamide bacteriostatic antibiotic

Oxiconazole is a broad-spectrum imidazole antifungal, inhibiting ergosterol biosynthesi by disrupting cytochrome P450 enzymes (lanosterol 14- α demethylase).

Bedaquiline, a diarylquinoline antibiotic, targets ATP synthase in Mycobacterium tuberculosis.

Ganciclovir hydrate: oral anti-cytomegalovirus; inhibits HSV 1/2, CMV, adenoviruses, FHV-1; brain-penetrating.

Puromycin dihydrochloride, from Streptomyces alboniger, blocks protein synthesis, acting as an antineoplastic and antitrypanosomal agent.

Chloroquine: antimalarial, anti-inflammatory, autophagy/TLRs inhibitor, treats arthritis, effective against COVID-19 in vitro. EC50: 1.13 μM.

Bekanamycin (Kanamycin B) is an aminoglycoside antibiotic, which inhibits a range of Gram-positive and Gram-negative bacteria. High-Quality, Low-Cost!

Luliconazole (NND 502) is an Azole Antifungal. The mechanism of action of luliconazole is as a Cytochrome P450 2C19 Inhibitor.

Rifamycin sodium (Rifamycin sodium salt) salt is an antibiotic that inhibits bacterial DNA-dependent RNA polymerase.

Nigericin sodium salt, an antibiotic and NLRP3 activator from S. hygroscopicus, inhibits Golgi and gram-positive bacteria, blocking viral activation.