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-N15127
    3-O-Demethyl-2'-N-glylfortimicin B 71640-65-8
    3-O-Demethyl-2'-N-glylfortimicin B is an aminoglycoside antibiotic.
    3-O-Demethyl-2'-N-glylfortimicin B
  • HY-N15128
    7β,8β-Epoxyroridin H 64687-85-0
    7β,8β-2′,3′-Diepoxyroridin H is an antibiotic with anti-Gram-positive and negative bacteria activity.
    7β,8β-Epoxyroridin H
  • HY-N15129
    7β,8β-2′,3′-Diepoxyroridin H 64687-84-9
    7β,8β-2′,3′-Diepoxyroridin H is an antibiotic with anti-Gram-positive and negative bacteria activity.
    7β,8β-2′,3′-Diepoxyroridin H
  • HY-N15138
    Sativanone 70561-31-8
    Sativanone is a compound that can be isolated from Dalbergia tonkinensis. Sativanone is a potent α-glucosidase inhibitor, with an EC50 of 0.357 mg/mL for rat α-glucosidase. Sativanone has antibacterial activity against Ralstonia solanacearum. Sativanone also has anti-senescent and antioxidant effects.
    Sativanone
  • HY-N15146
    Aralia-saponin I 289649-54-3
    Aralia-saponin I is a saponin that can be isolated from Aralia elata, possessing high binding affinity for aerolysin and capable of binding to amino acids critical for aerolysin function. Aralia-saponin I can be utilized in research on infections caused by Aeromonas hydrophila.
    Aralia-saponin I
  • HY-N15179
    Minosaminomycin 51746-09-9
    Minosaminomycin is an antibiotic containing myo-inosamine that can be extracted from Streptomyces No. MA514A1. Minosaminomycin exerts antimicrobial activity against Mycobacterium smegrnatis ATCC 607 and Mycobacterium phlei (MIC= 1.56/6.25 mcg/mL).
    Minosaminomycin
  • HY-N15181
    Fluostatin B 158906-40-2
    Fluostatin B is a dipeptidyl peptidase 3 (DPP-3) inhibitor with an IC50 value of 24 µg/mL. Fluostatin B is a fluorenone, which is found in Streptomyces.
    Fluostatin B
  • HY-N15182
    4-Trehalosamine 51855-99-3
    4-Trehalosamine is a derivative of trehalose with weak antibacterial activity. 4-Trehalosamine shows no toxic effects when injected intravenously into mice at a dose of 625 mg/kg.
    4-Trehalosamine
  • HY-N15183
    Aselacin C 156223-08-4
    Aselacin C is a cyclic peptide that can be isolated from the fungus Acremonium spp..
    Aselacin C
  • HY-N15184
    Benanomicin B 116249-66-2
    Benanomicin B (Pradimicin C) is an antifungal antibiotic that also has antibacterial activity against two Gram-positive bacteria: Micrococcus luteus and Corynebacterium bovis.
    Benanomicin B
  • HY-N15187
    Acronycidine 521-43-7
    Acronycidine is a quinoline alkaloid with antimalarial activity and can be extracted from Acronychia baueri Schott. Acronycidine can be utilized in malari research.
    Acronycidine
  • HY-N15262
    Schinlignan B 77881-08-4
    Schinlignan B (Angeloylgomisin P) is a lignan with antioxidant, anti-HIV, anti-HBV activities, which is found in plants of the Schisandra genus. Schinlignan B is promising for research of antioxidant-associated diseases.
    Schinlignan B
  • HY-N15266
    Mukonidine 24949-00-6
    Mukonidine is a carbazole alkaloid with antibacterial activity.
    Mukonidine
  • HY-N15268
    Koenine 28200-63-7
    Koenine is a carbazole alkaloid. It is predicted that Koenine has strong binding affinity and inhibitory ability to SARS-CoV-2 main protease (Mpro), which can be used in the research of anti-novel coronavirus drugs.
    Koenine
  • HY-N15272
    Artocarpesin 3162-09-2
    Artocarpesin is a flavonoid compound. Artocarpesin has inhibitory effects on methicillin-resistant Staphylococcus aureus (MRSA). Artocarpesin inhibits the production of NO, PGE2 and ROS by inhibiting COX-2 and iNOS expression, and plays an anti-inflammatory role. In addition, Artocarpesin inhibits platelet aggregation by inhibiting cyclic nucleotides and MAPKs, which can be used in the study of cardiovascular diseases.
    Artocarpesin
  • HY-N15283
    Baculiferin A 1141448-57-8
    Baculiferins A is a DOPA-derived pyrrole alkaloid. Baculiferins A can be isolated from the Chinese marine sponge Iotrochota baculifera. Baculiferins A have anti-HIV activity.
    Baculiferin A
  • HY-N15288
    Cavipetin C 128552-90-9
    Cavipetin C is a diterpene that can be isolated from B. cavipes. Cavipetin C exhibits antifungal activity that blocks the Cladosporium cucumericum spore formation.
    Cavipetin C
  • HY-N15294
    3β-Hydroxy-27-p-Z-coumaroyloxyurs-12-en-28-oic acid
    3β-Hydroxy-27-p-Z-coumaroyloxyurs-12-en-28-oic acid (compound 8) is a triterpenoid ester HIV-1 protease inhibitor with the potential for use in the antiretroviral combination therapy of AIDS.
    3β-Hydroxy-27-p-Z-coumaroyloxyurs-12-en-28-oic acid
  • HY-N15302
    Ostamycin A
    Ostamycin A is a cyclic diterpene with antiviral activity. Ostamycin A inhibits the replication of influenza A virus by targeting the nucleoprotein, with an IC50 of 4.72 μM.
    Ostamycin A
  • HY-N15309
    Torvoside C 185012-38-8
    Torvoside C (Torvoside K) is a compound found in Solanum torvum with antifungal activity. The ZOIs and MIC values of Torvoside C against the tested fungi (Alternaria brassicicola, Alternaria geophila, Aspergillus flavus, etc.) range from 33.4% to 87.4% and 31.25 to 250 μg/mL, respectively. Additionally, it exhibits a dose-dependent inhibitory effect on the production of mycotoxins aflatoxin B1 and fumonisin B1, which are produced by A. flavus and F. verticillioides, respectively. Torvoside C can be used for research in the field of antifungal infection.
    Torvoside C
Cat. No. Product Name / Synonyms Application Reactivity