2. Infection

Infection

Infection

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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-118578
    Furalaxyl 57646-30-7 99.3%
    Furalaxyl (CGA 38140) is a potent fungicide. Furalaxyl is highly selective to fungi of the order of the Peronosporales.
    Furalaxyl
  • HY-118580
    RO-09-4609 279230-20-5 98%
    RO-09-4609 exhibits antimicrobial activity, that inhibits Candida albicans, Trypanosoma brucei and Plasmodium vivax through inhibition of N-myristoyl transferase.
    RO-09-4609
  • HY-118699
    Indole-3-thio carboxamide 59108-90-6 98%
    Indole-3-thio carboxamide is an antifungal agent. Indole-3-thio carboxamide is a biotransformation product of Camalexin (HY-119502) by plant pathogenic fungi Botrytis cinerea.
    Indole-3-thio carboxamide
  • HY-118703
    L-Ristosamine nucleoside 136035-11-5 98%
    L-Ristosamine nucleoside is a nucleoside compound with antiviral activity against HIV and HSV-1.
    L-Ristosamine nucleoside
  • HY-118730
    Flucycloxuron 113036-88-7 98%
    Flucycloxuron (Andalin) is an insect growth regulator (IGR), and a chitin synthesis inhibitor.
    Flucycloxuron
  • HY-118731
    TNK-6123 251481-69-3 98%
    TNK-6123 is a potent Emivirine (HY-15353) analogue with improved activity against drug-resistant HIV mutants. TNK-6123 improves activity against Lys103Asn mutant RT.
    TNK-6123
  • HY-118740
    L-708906 251963-74-3 98%
    L-708906 is a potent human immunodeficiency virus type 1 (HIV-1) inhibitor with an IC50 value of 12 μM. L-708906 inhibits HIV strains resistant to nonnucleoside or nucleoside reverse transcriptase inhibitors.
    L-708906
  • HY-118747
    Scirpusin A 69297-51-4 98%
    Scirpusin A is a naturally occurring compound extracted from the legume plant Caragana rosea Turcz, exhibiting anti-HIV activity. Scirpusin A demonstrates significant inhibitory effects against HIV-1 (EC50=7 μg/mL). Scirpusin A is utilized in research towards the development of anti-HIV therapeutics.
    Scirpusin A
  • HY-118839
    trans-Phenothrin 66036-31-5 98%
    Trans-Phenothrin is a synthetic pyrethroid with activity against adult fleas and ticks. Trans-Phenothrin has shown significant differences in biological activity between its different enantiomers in comparison with fenvalerate and d-trans-phenothrin. Trans-Phenothrin is used in agriculture for its potential insecticide activity against pests such as Plutella xylostella.
    trans-Phenothrin
  • HY-118843
    Lombazole 60628-98-0 98%
    Lombazole is an antimicrobial compound with activity that inhibits cell membrane synthesis. Lombazole had little effect on K+ permeability in S. aureus. Lombazole inhibited only de novo synthesis of cell enclosure in S. aureus, and this effect occurred before growth was affected. The main effect of lombazole was through inhibition of lipid synthesis. Lombazole may have an effect on key steps in lipid biosynthesis, as inferred from the lack of changes in lipid patterns after treatment. Lombazole also inhibited the sterol C-14 demethylation step in Candida albicans.
    Lombazole
  • HY-118896
    Acequinocyl 57960-19-7 98%
    Acequinocyl (CRM) is a certified reference material categorized as a naphthoquinone acaricide.1 Acequinocyl has been found in Cannabis. Formulations containing acequinocyl have been used to control mite populations in agriculture. This product is intended for research and forensic applications.
    Acequinocyl
  • HY-118906
    BO-1165 89426-64-2 98%
    BO-1165 is an antibiotic with good antibacterial activity against Gram-negative bacteria, but almost no activity against Gram-positive bacteria and anaerobic bacteria. BO-1165 has high antibacterial activity against Pseudomonas aeruginosa (MIC50=3.12 mg/L) and P. cepacia (MIC50=1.56 mg/L).
    BO-1165
  • HY-118932
    HCV-IN-45 301211-35-8 98%
    HCV-IN-45 (Compound EI-1) is an inhibitor for hepatitis C virus (HCV), that inhibits 1a and 1b HCV pseudoparticles with EC50 of 0.134 and 0.027 μM. HCV-IN-45 inhibits 1a/2a and 1b/2a cell culture-adapted HCV (HCVcc), with EC50 of 0.024 and 0.012μM. HCV-IN-45 inhibits the entry of the virus into hepatocyte, and blocks the cell-cell spread.
    HCV-IN-45
  • HY-118983
    Pivampicillin hydrochloride 26309-95-5 98%
    Pivampicillin hydrochloride is a penicillin antibiotic. Pivampicillin hydrochloride is a prodrug of Ampicillin (HY-B0522).
    Pivampicillin hydrochloride
  • HY-119057
    DSM74 898743-92-5 98%
    DSM74 (compound 21) is an orally active and potent antimalarial inhibitor of PfDHODH (IC50=0.28 μM) and PbDHODH (IC50=0.38 μM). DSM74 inhibits the growth of Plasmodium in animals.
    DSM74
  • HY-119067
    Aspirochlorine 59978-04-0 98%
    Aspirochlorine (A30641) is an antibiotc with activity against Gram-positive bacteria and fungi.
    Aspirochlorine
  • HY-119120
    JTK-101 503048-34-8 98%
    JTK-101 is a selective HIV inhibitor. JTK-101 selectively reduces HIV-1 mRNA synthesis by inhibiting Tat cofactors, including CDK9 and cyclin T1, thereby suppressing the transcriptional activity of HIV-1. JTK-101 may be used in the field of anti-HIV virus research.
    JTK-101
  • HY-119219
    Detoxin C1 74717-53-6 98%
    Detoxin C1 is an active principle of detoxin complex. Detoxin complex is an antagonist of Blasticidin S.
    Detoxin C1
  • HY-119246
    A-269A 38621-52-2 98%
    A-269A is a streptothricin-like compound derived from Streptomyces sp. with antimicrobial activity.
    A-269A
  • HY-119280
    Sch 29482 77646-83-4 98%
    Sch 29482 is an orally active penem antibiotic with broad-spectrum antibacterial activity.
    Sch 29482
Cat. No. Product Name / Synonyms Application Reactivity