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Results for "

skin infection

" in TargetMol Product Catalog
  • Inhibitors & Agonists
    10
    TargetMol | Inhibitors_Agonists
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Luliconazole
NND 502
T2411187164-19-8
Luliconazole (NND 502) is an Azole Antifungal. The mechanism of action of luliconazole is as a Cytochrome P450 2C19 Inhibitor.
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Dehydroemetine
T150954914-30-1In house
Dehydroemetine is an effective antigenic insecticide, which is a synthetic analogue of Emetine dihydrochloride. It can be used to prevent and treat amoeba infections and diseases. It has the effect of treating leishmania infection with skin damage and resistance to metronidazole amoebiosis.
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8-10weeks
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Hexylresorcinol
4-Hexylresorcinol
T0314136-77-6
Hexylresorcinol (4-Hexylresorcinol) is a substituted dihydroxybenzene utilized topically as an antiseptic for minor skin infection treatment.
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Benzyl benzoate
Scabitox, Novoscabin, Benzoic acid benzyl ester, Ascabiol
T0729120-51-4
Benzyl benzoate (Benzoic acid benzyl ester) is one of the older preparations used for the therapy of scabies. Scabies is a skin infection caused by the Sarcoptes scabiei. Its symptoms are red spots, severe itching (particularly at night), and may lead to a secondary infection. Benzyl benzoate is useful in the therapy of scabies because it is lethal to this mite. It is also used for the therapy of lice affection of the body and head. Benzyl benzoate is not the therapy of choice for scabies because of its irritant properties.
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Imiquimod 2HCl
Imiquimod 2HCl(99011-02-6 Free base)
T0134L2995277-02-4
Imiquimod 2HCl is a toll-like receptor 7 (TLR7) agonist and an immunomodulator with antiviral and antitumor activity.Imiquimod 2HCl can be used to construct a psoriasis-like mouse model, which can be used to study periocular skin cancers, pemphigus foliaceus, and COVID-19 infection.
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Lenampicillin hydrochloride
KBT 1585 hydrochloride
T1573480734-02-7
Lenampicillin hydrochloride is an orally active prodrug of Ampicillin. Lenampicillin hydrochloride is an effective beta-lactam antibacterial agent that inhibits bacterial penicillin-binding proteins. It is applied in the investigation of suppurative skin
    7-10 days
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    3-Acetyl-28-N-(3-guanidinobutoxy)-oleanolic acid
    T201012
    3-Acetyl-28-N–(3–guanidinobutoxy)-oleanolic acid (compound J1) serves as an effective antimicrobial agent, displaying activity against both Gram-positive bacteria and fungi. In addition to its primary use, it can also function as an adjuvant in antibiotic treatments. The mechanism of action for compound J1 involves disrupting bacterial cell membranes, integrating into DNA, and binding with DNA gyrase. Furthermore, it has been shown to reduce microbial counts and accelerate wound healing in a mouse MRSA skin infection model.
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    K6PC-5
    K6PC5, K6PC 5
    T27710756875-51-1
    K6PC-5 is a ceramide derivative that acts as an activator of sphingosine kinase 1 (SPHK1), inducing a swift and temporary rise in intracellular calcium levels. With its potential applications in skin diseases associated with abnormal keratinocyte function, as well as in studies on neurodegeneration and virus infection, K6PC-5 presents a promising compound for research purposes.
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    6-8 weeks
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    Sauchinone
    T6S1572177931-17-8
    1. Sauchinone is a useful adjunctive treatment for bacterial infection. 2. Sauchinone, an active lignan found in Saururus chinensis, to regulate the activation of HSCs, to prevent liver fibrosis, and to inhibit oxidative stress in vivo and in vitro. 3. Sa
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    Ambuic acid
    T71860340774-69-8
    Ambuic acid is a cyclohexanone that has phytopathogenic antifungal, quorum sensing inhibitory, and antibacterial activities. Ambuic acid inhibits the biosynthesis of cyclic peptides involved in quorum sensing, including gelatinase biosynthesis-activating pheromone (GBAP) in E. faecalis, autoinducing peptide I (AIP-I) in S. aureus, and LsrD698 and LsrD826 in L. innocua. It suppresses abcess formation in a mouse model of skin infection induced by methicillin-resistant S. aureus (MRSA) when administered at a dose of 5 µg and decreases the activity of the agr quorum sensing system in an in vivo reporter assay.
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    10-14 weeks
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