1. Infection

Infection

Infection is a pathophysiological process that involves the invasion and colonization of a living organism (host) by disease-causing infectious agents, the reaction of host tissues to these agents and the toxins they produce, and the transmission of infectious agents to other hosts. Common infectious agents include viruses, viroids, prions, bacteria, nematodes, arthropods, and other macroparasites such as tapeworms. Hosts can fight infections using their immune system. Mammals often engage both innate and adaptive immune systems to eliminate infectious agents or inhibit their growth and transmission. When infection occurs, anti-infective drugs can suppress the infection. Several broad types of anti-infective drugs exist, depending on the type of organism targeted; they include antibacterial (antibiotic), antiviral, antifungal and antiparasitic agents.

Cat. No. Product Name CAS No. Purity Chemical Structure
  • HY-19892
    Brilacidin 1224095-98-0
    Brilacidin (PMX 30063) is an anti-infective antimicrobial with MIC90s of 1 and 8 μg/mL for Gram-positive bacteria Streptococcus pneumonia and Streptococcus viridans, and MIC90 of 8 and 4 μg/mL for Gram-negative bacteria Haemophilus influenza and Pseudomonas aeruginosa. Brilacidin is a defensin mimetic antibiotic compound.
    Brilacidin
  • HY-21210
    6-Quinoxalinecarboxylic acid, 2,3-bis(bromomethyl)- 32602-11-2 99.63%
    6-Quinoxalinecarboxylic acid, 2,3-bis(bromomethyl)-, derived from 2,3-Bis(bromomethyl)quinoxaline, shows antibacterial activity.
    6-Quinoxalinecarboxylic acid, 2,3-bis(bromomethyl)-
  • HY-21745
    MurA-IN-4 318280-69-2
    MurA-IN-4 has antibacterial activity and is a MurA inhibitor that inhibits bacterial cell wall synthesis.
    MurA-IN-4
  • HY-43060
    5'-DMT-3'-TBDMS-ibu-rG 81256-89-5 99.46%
    5'-DMT-3'-TBDMS-ibu-rG is is a modified nucleoside. 5'-DMT-3'-TBDMS-ibu-rG can be used in deoxyribonucleic acid synthesis.
    5'-DMT-3'-TBDMS-ibu-rG
  • HY-66035
    4-(Trifluoromethyl)nicotinic acid 158063-66-2
    4-(Trifluoromethyl)nicotinic acid (4-(Trifluoromethyl)pyridine-3-carboxylic acid) is a metabolite of the pyridinecarboxamide insecticide Flonicamid (HY-119649).
    4-(Trifluoromethyl)nicotinic acid
  • HY-75867
    M2 ion channel blocker-1 1190215-03-2
    M2 ion channel blocker-1 is capable of inhibiting and blocking the activity of M2 ion channel;Antiviral agent.
    M2 ion channel blocker-1
  • HY-76649
    NBD-557 333352-59-3 99.41%
    NBD-557 is a potentially HIV-1 inhibitor.
    NBD-557
  • HY-77651
    Nucleoside-Analog-1 876707-99-2
    Nucleoside-Analog-1 is a click chemistry reagent, it contains an Azide group and can undergo copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with molecules containing Alkyne groups. It can also undergo strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with molecules containing DBCO or BCN groups.
    Nucleoside-Analog-1
  • HY-78315
    2',3',4'-Trimethoxyacetophenone 13909-73-4
    2',3',4'-Trimethoxyacetophenone is an organic compound with a benzene ring and an acetyl group. 2',3',4'-Trimethoxyacetophenone can be used as a raw material for synthesizing dyes, fragrances, and certain pesticides.
    2',3',4'-Trimethoxyacetophenone
  • HY-79572
    4-Methyl-3-nitrophenol 2042-14-0 99.71%
    4-Methyl-3-nitrophenol is a phenolic compound classified as a soft electrophile. 4-Methyl-3-nitrophenol is toxic to ciliates, with a log IC50 value of -3.740 against T. pyriformis.
    4-Methyl-3-nitrophenol
  • HY-A0018
    Palonosetron 135729-61-2 98%
    Palonosetron is a 5-HT3 antagonist primarily used to prevent acute, delayed, and overall chemotherapy-induced nausea and vomiting. Palonosetron exhibits moderate anti-flavivirus activity and potent anti-Zika virus activity in mammalian cells. Palonosetron also possesses antidepressant activity.
    Palonosetron
  • HY-A0124
    Sapropterin 62989-33-7 98%
    Sapropterin ((6R)-BH4; (6R)-Tetrahydro-L-biopterin) is an orally active phenylalanine hydroxylase (PAH) cofactor, which is effective in reducing blood phenylalanine concentrations. Sapropterin can be used in study of phenylketonuria (PKU) phenylketonuria. Sapropterin can aggravate experimental autoimmune encephalomyelitis (EAE).
    Sapropterin
  • HY-B0186
    Cefoselis 122841-10-5 98%
    Cefoselis, the fourth gen-eration of cephalosporin, is a β-lactam antibiotic. Cefoselis exhibits good activity against a wide range of Gram-positive and Gram-negative organisms. Cefoselis penetrates the blood-brain barrier.
    Cefoselis
  • HY-B0525
    Carbenicillin 4697-36-3 98%
    Carbenicillin is a broad-spectrum semi-synthetic penicillin antibiotic for gram-negative bacteria. Carbenicillin can interfere the cell wall synthesis while displaying low toxicity to plant tissue.
    Carbenicillin
  • HY-B0698
    Ceftibuten 97519-39-6 98%
    Ceftibuten (Sch39720), an antibiotic, is an orally active cephalosporin, possesses potent activity in vitro against a wide range of gram-negative and certain gram-positive pathogens.
    Ceftibuten
  • HY-B0771
    Cefozopran 113359-04-9 98%
    Cefozopran (SCE-2787) is a potent antibiotic with broad-spectrum antibacterial activity. Cefozopran binds PBPs, induces cell wall destruction, cell elongation, filamentation, irregular septa formation, and bactericidal, bacteriolytic activity. Cefozopran reduces bacterial counts and eradicates bacteria in mouse respiratory, urinary, and thigh muscle infections. Cefozopran can be used for the research of bacterial infections.
    Cefozopran
  • HY-B0930
    Efloxate 119-41-5 99.73%
    Efloxate (Angorlisin) is a vasodilator used in the research of chronic coronary insufficiency and angina pectoris. Efloxate binds to Staphylococcus aureus sortase A.
    Efloxate
  • HY-B0945
    Nitromide 121-81-3 98.19%
    Nitromide is an anti-parasitic agent.
    Nitromide
  • HY-B0967
    Phthalylsulfacetamide 131-69-1 98.0%
    Phthalylsulfacetamide is an orally active sulfonamide antibiotic and New Delhi metallo-β-lactamase-1 (NDM-1) inhibitor with an IC50 of 15.4 μM. Phthalylsulfacetamide stably binds to the active hydrolysis center of NDM-1, interacts with Zn2+, and interacts with key amino acid residues Val73 and His122 to inhibit enzyme activity. Phthalylsulfacetamide can be used for the research of Escherichia coli infection.
    Phthalylsulfacetamide
  • HY-B0992
    Nithiamide 140-40-9 99.74%
    Nithiamide is a non-5-nitroimidazole drugs, is a antibiotic used in veterinary.
    Nithiamide
Cat. No. Product Name / Synonyms Application Reactivity