2. Infection

Infection

Infection

Related Products

PDF 70.44 MB

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-W016969
    2-Undecanone 112-12-9 99.90%
    2-Undecanone is an orally active organic ketone. 2-Undecanone exerts antibacterial effects by inhibiting bacterial chaperone systems and interfering with the refolding of heat-inactivated proteins. 2-Undecanone also ameliorates asthmatic inflammation and airway remodeling by blocking the NF-κB pathway, and activates the Nrf2 pathway to reduce oxidative damage and prevent lung cancer induced by Benzo[a]pyrene (HY-107377). 2-Undecanone can be used in research related to cancer, asthma and infections.
    2-Undecanone
  • HY-W018758
    1-Phenylpropane-1,2-dione 579-07-7 99.76%
    1-Phenylpropane-1,2-dione is a SARS-CoV-2 helicase binder. 1-Phenylpropane-1,2-dione can be isolated from the young stems of Ephedra sinica. 1-Phenylpropane-1,2-dione is commonly used as an edible flavoring and a basic raw material in synthetic chemistry. 1-Phenylpropane-1,2-dione can be applied to research related to COVID-19.
    1-Phenylpropane-1,2-dione
  • HY-W042191
    Oxychlororaphine 550-89-0 ≥98.0%
    Oxychloroaphine could be isolated from the bacterium Pantoea agglomerans naturally present in soil. Oxychloroaphine has broad-spectrum antifungal activity. Oxychloroaphine has cytotoxicity in a dose-dependent manner and induces apoptosis. Oxychloroaphine can be used in research of cancer.
    Oxychlororaphine
  • HY-W047709
    N,N,N',N'-Tetrakis(2-hydroxyethyl)ethylenediamine 140-07-8 99.89%
    N,N,N',N'-Tetrakis(2-hydroxyethyl)ethylenediamine (THEED; THEEN) is a tetrapodal pentadentate chelating ligand that functions as a chelator to form stable complexes with metal ions. N,N,N',N'-Tetrakis(2-hydroxyethyl)ethylenediamine serves as a versatile building block for organic synthesis, a reagent for metal extraction, and an auxiliary for catalytic reactions. N,N,N',N'-Tetrakis(2-hydroxyethyl)ethylenediamine-derived metal complexes exhibit antibacterial, antifungal, and anticancer activities. N,N,N',N'-Tetrakis(2-hydroxyethyl)ethylenediamine and its metal complexes can be used for research related to breast cancer, leukemia, various bacterial and fungal infections.
    N,N,N',N'-Tetrakis(2-hydroxyethyl)ethylenediamine
  • HY-77995
    2-Methoxybenzaldehyde 135-02-4 99.83%
    2-Methoxybenzaldehyde (o-Anisaldehyde) is a bacterial/fungal inhibitor with a BA50 value of 0.19 for Salmonella. 2-Methoxybenzaldehyde can be used for the study of bacterial and fungal infectious diseases.
    2-Methoxybenzaldehyde
  • HY-B1300
    Cefonicid sodium 61270-78-8
    Cefonicid sodium is a long-acting cephalosporin antibiotic. Cefonicid sodium also acts as a noncompetitive class I β-lactamase inhibitor with a Ki value of 0.8 μM. Cefonicid sodium exhibits broad-spectrum antimicrobial activity and is effective against a variety of Gram-positive and Gram-negative bacteria. Cefonicid sodium can be used for research on infections.
    Cefonicid sodium
  • HY-N1434
    Methyl p-coumarate 3943-97-3
    Methyl p-coumarate (Methyl 4-hydroxycinnamate), an orally active esterified derivative of p-Coumaric acid (pCA), can be isolated from the flower of Trixis michuacana var longifolia. Methyl p-coumarate could inhibit the melanin formation in B16 mouse melanoma cells. Methyl p-coumarate also has strong in vitro inhibitory effect on A. alternata and other pathogens.
    Methyl p-coumarate
  • HY-15602B
    Ledipasvir D-tartrate 1502654-87-6 99.20%
    Ledipasvir D-tartrate is an inhibitor of the hepatitis C virus NS5A, with EC50 values of 34 pM against GT1a and 4 pM against GT1b replicon.
    Ledipasvir D-tartrate
  • HY-158761
    Polyaminopropyl biguanide 133029-32-0
    Polyaminopropyl biguanide (PAPB) is a positively charged antimicrobial polymer and cosmetic preservative. Polyaminopropyl biguanide inhibits the growth and division of negatively charged microorganisms via charge-based adsorption. Polyaminopropyl biguanide exhibits broad-spectrum in vitro activity against foodborne microorganisms and postharvest fruit pathogens. Polyaminopropyl biguanide can be used in studies related to citrus postharvest diseases and foodborne bacterial infections.
    Polyaminopropyl biguanide
  • HY-B1369R
    Imipenem monohydrate (Standard) 74431-23-5 99.52%
    Imipenem (monohydrate) (Standard) is the analytical standard of Imipenem (monohydrate). This product is intended for research and analytical applications. Imipenem monohydrate, a stable crystalline derivative of thienamycin, is an antibiotic and has the excellent activity against a broad range of gram-positive and gram-negative aerobic and anaerobic bacteria. Imipenem monohydrate can be used for the research of carbapenem-nonsusceptible and P. aeruginosa biofilm infections.
    Imipenem monohydrate (Standard)
  • HY-N10544
    δ-Cadinene 483-76-1
    δ-Cadinene ((+)-δ-Cadinene) is a sesquiterpene in essential oils. δ-Cadinene shows antiproliferative and pro-apoptotic effects on human ovary cancer (OVCAR-3) cells. δ-Cadinene has trichomonacidal, antimicrobial, antifungal and anticancer properties.
    δ-Cadinene
  • HY-W010538
    trans-4-Methylcyclohexanamine 2523-55-9 ≥98.0%
    trans-4-Methylcyclohexanamine is an intermediate and can be used for the development of T. cruzi enzyme inhibitor.
    trans-4-Methylcyclohexanamine
  • HY-W012892
    Methylphenylethyne 673-32-5 98%
    Methylphenylethyne (Phenylmethylacetylene) is an intermediate of bioactive compounds. Methylphenylethyne has antifeedant activities for larvae of Pieris rapae crucivora. Methylphenylethyne can be used for pest control research.
    Methylphenylethyne
  • HY-W018582
    N-Phenylacrylamide 2210-24-4 ≥98.0%
    N-Phenylacrylamide is a special polymer showing high affinity with Ochratoxin A, a colorless and crystalline mycotoxin compound. N-Phenylacrylamide can be applied in the field of mycotoxin extraction, and be used for the security research of agricultural commodities and foods made from cereals and grapes.
    N-Phenylacrylamide
  • HY-W040128
    Kanamycins sulfate 70560-51-9 99.22%
    Kanamycins sulfate is a blood-brain barrier-permeable JNK1 and Bcl-2 modulator as well as an antibiotic, with broad-spectrum antibacterial, and biofilm-inhibiting activities, and it induces autophagy. Kanamycins sulfate promotes Bcl-2 phosphorylation to upregulate autophagy levels, triggering changes such as mitochondrial swelling and endoplasmic reticulum expansion. Consequently, it causes reversible neuronal damage in the dorsal cochlear nucleus without inducing significant neuronal apoptosis. In the presence of exogenous alanine or glucose, Kanamycins sulfate effectively kills drug-resistant bacteria, restores drug sensitivity of multidrug-resistant bacteria, and alleviates urinary tract and kidney infections in mice. Kanamycins sulfate can be applied to scientific research related to Mycobacterium tuberculosis, salmonellosis, brucellosis, shigellosis, urinary tract infections, and reversible neurotoxicity.
    Kanamycins sulfate
  • HY-18351
    Indotecan 915303-09-2 98.0%
    Indotecan (LMP-400), an indenoisoquinoline derivative, is a potent Topoisomerase I inhibitor, with IC50s of 300, 1200, 560 nM for P388, HCT116, MCF-7 cell lines, respectively. Indotecan prevents the relaxation of supercoiled DNA and can be used for the research of visceral leishmaniasis.
    Indotecan
  • HY-76260
    Faropenem sodium 122547-49-3 99.74%
    Faropenem sodium is an orally bioavailable penem antibiotic. Faropenem sodium regulates inorganic phosphate transporter Npt1. Faropenem sodium inhibits M. tuberculosis (MIC of 1.3 μg/mL) and B. anthracis.
    Faropenem sodium
  • HY-B0977
    Dicloxacillin Sodium hydrate 13412-64-1
    Dicloxacillin Sodium hydrate (Dicloxacillin sodium salt monohydrate) is a narrow-spectrum β-Lactam antibiotic of the penicillin class, is used to treat infections caused by susceptible Gram-positive bacteria, active against beta-lactamase-producing organisms such as Staphylococcus aureus.
    Dicloxacillin Sodium hydrate
  • HY-G0021
    N-Desmethylclozapine 6104-71-8 99.10%
    N-Desmethylclozapine is a major active metabolite of the atypical antipsychotic agent Clozapine. N-Desmethylclozapine is a potent, allosteric and partial M1 receptors agonist (EC50=115 nM) and is able to potentiate hippocampal N-methyl-d-aspartate (NMDA) receptor currents through M1 receptor activation. N-Desmethylclozapine is also a δ-opioid agonist.
    N-Desmethylclozapine
  • HY-103017
    JH-X-119-01 hydrochloride 2591344-30-6 99.14%
    JH-X-119-01 hydrochloride is a potent and selective interleukin-1 receptor-associated kinases 1 (IRAK1) inhibitor. JH-X-119-01 hydrochloride ameliorates LPS-induced sepsis in mice.
    JH-X-119-01 hydrochloride
Cat. No. Product Name / Synonyms Application Reactivity