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  • Inhibitors & Agonists
    30
    TargetMol | All_Pathways
  • Compound Libraries
    6
    TargetMol | Compound_Libraries
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    1
    TargetMol | Peptide_Products
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    TargetMol | All_Dye_Reagents
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    TargetMol | Natural_Products
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    8
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    TargetMol | Standard_Products
  • Spectinomycin dihydrochloride
    Spectinomycin 2HCl, Actinospectacin
    T078821736-83-4
    Spectinomycin dihydrochloride (Actinospectacin) is an antibiotic produced by Streptomyces spectabilis. It is active against gram-negative bacteria and used for the treatment of gonorrhea.
    • $30
    In Stock
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    TargetMol | Citations Cited
  • Spectinomycin dihydrochloride pentahydrate
    Trobicin, Spectogard, Spectinomycin hydrochloride hydrate
    T0788L22189-32-8
    Spectinomycin dihydrochloride pentahydrate (Spectogard) is an antibiotic produced by Streptomyces spectabilis. It is active against gram-negative bacteria and used for the treatment of gonorrhea.
    • $37
    In Stock
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  • 1-Undecanol
    Undecyl alcohol, 1-Hendecanol
    T7480112-42-5
    1-Undecanol (1-Hendecanol) is a natural product in many foods such as fruits, butter, eggs and cooked pork, is used as a flavoring ingredient.
    • $29
    In Stock
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  • Trehalase, Microorganism
    T2044939025-52-9
    Trehalase, Microorganism (EC 3.2.1.28), is an enzyme that effectively degrades trehalose in certain bacteria. It serves as a biomarker for acute kidney injury resulting from proximal tubule damage.
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  • Xanthine dehydrogenase, Microorganism
    TRP-00755
    Xanthine dehydrogenase, Microorganism (EC 1.17.1.4), is part of the molybdenum hydroxylase family and plays a role in the oxidative metabolism of purines. This homodimeric enzyme can be converted to xanthine oxidase through reversible thiol oxidation or irreversible proteolytic modification.
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  • L-α-glycerophosphate oxidase, Microorganism
    TRP-00977
    L-α-glycerophosphate oxidase, Microorganism (EC 1.1.3.21) refers to an oxidoreductase enzyme that acts on the CH-OH group of the donor molecule with oxygen as the acceptor. It is involved in glycerophospholipid metabolism and utilizes the cofactor FAD.
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  • Phenylethyl isothiocyanate
    JC-5411, JC5411, JC 5411
    T196872257-09-2
    Phenylethyl isothiocyanate (JC5411) is an HDAC inhibitor. It potentially for the treatment of benign prostatic hypertrophy.
    • $30
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  • Collagenase Type I
    Collagenase Type I (From microorganisms), Collagenase I, 9001-12-1
    T64812
    Collagenase Type I is a proteolytic enzyme that primarily targets collagen and is able to break down peptide bonds in collagen. Collagenase is used as a potential therapeutic option to break up the herniated disc material, thereby reducing compression of nearby nerves. Collagenase may aid in the breakdown and reorganization of excessive scar tissue, potentially improving tissue function and appearance. Collagenase has the potential to treat intervertebral disc herniation, keloid, fat mass, lipoma, as well as Peyronie's disease and palmar fibromatosis.
    • $39
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  • Diazolidinyl urea
    Germall II
    T812378491-02-8
    Diazolidinyl urea (Germall II) is a formaldehyde-releasing preservative used in cosmetics and personal-care products,
    • $29
    In Stock
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  • Glyco-Obeticholic acid
    T11428863239-60-5
    Glyco-Obeticholic acid is an active metabolite of Obeticholic acid. Obeticholic acid is an agonist of the farnesoid X receptor (FXR).
    • $44
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  • Tauro-Obeticholic acid
    T13092863239-61-6
    Tauro-Obeticholic acid is an active Obeticholic acid metabolite. Obeticholic acid is an orally bioavailable agonist of farnesoid-X receptor (FXR).
    • $119
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  • Oritavancin diphosphate
    LY333328 diphosphate
    T2691192564-14-0
    Oritavancin diphosphate (LY333328 diphosphate) is a novel semisynthetic glycopeptide antibiotic developed for treating serious Gram-positive bacterial infections.
    • $30
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  • Bisdionin C
    T4086374857-22-0
    Bisdionin C is a potent inhibitor of GH18 chitinase with an IC50 of 0.2 μM for A. fumigatus ChiB1. Bisdionin C inhibits human macrophage chitotriosidase(HCHT, IC50 = 8.3 μM) and acidic mammalian chitinase (AMCase, IC50 = 3.4 μM).
    • $34
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  • Cefoselis Sulfate
    FK-037, FK 037 Sulfate
    T6438122841-12-7
    Cefoselis Sulfate is a widely used beta-lactam antibiotic.
    • $34
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  • Pristane
    2,6,10,14-tetramethylpentadecane
    TN69251921-70-6
    Pristane (2,6,10,14-tetramethylpentadecane) is a natural product from shark liver oil and a non-antigenic adjuvant.
    • $40
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  • Ethionamide
    Ethinamide, Bayer 5312, 2-ethylthioisonicotinamide
    T1165536-33-4
    Ethionamide (2-ethylthioisonicotinamide) is a nicotinamide derivative, with antibacterial activity, used to treat tuberculosis. Although the exact mechanism of action of ethionamide is unknown, it may inhibit the synthesis of mycolic acid, a saturated fatty acid found in the bacterial cell wall, thereby inhibiting bacterial cell wall synthesis. This eventually leads to bacterial cell wall disruption and cell lysis. Ethionamide may be bacteriostatic or bactericidal in action, depending on the concentration of the drug at the site of infection and the susceptibility of the organism involved.
    • $31
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    TargetMol | Citations Cited
  • D-Xylose
    (2S,3R,4S,5R)-oxane-2,3,4,5-tetrol
    TN68266763-34-4
    D-Xylose ((2S,3R,4S,5R)-oxane-2,3,4,5-tetrol) is a monosaccharide widely found in yeast and involved in the metabolism of the organism.
    • $29
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    TargetMol | Citations Cited
  • Clavulanic Acid
    RX-10100, MM-14151, MM14151, MM 14151, BRL-14151, BRL14151, BRL 14151
    T1986058001-44-8
    Clavulanic Acid(RX-10100), a major beta-lactam antibiotic produced by the organism Streptomyces claveris, is a potent bacterial beta-lactamase inhibitor used in the study of infections caused by bacteria. Clavulanic Acid has a broad spectrum of biological activity and is active against a wide variety of Gram-positive and Gram-negative bacteria.
    • $40
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  • Anticandidal agent-2
    T218433
    Anticandidal agent-2 is an antifungal compound with a minimum inhibitory concentration (MIC) of 1.6 μg/mL. It disrupts Candida albicans biofilms and inhibits the growth of Candida albicans, making it useful for studying infections caused by this organism.
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  • Bisucaberin
    T38101112972-60-8
    Bisucaberin is a siderophore and bacterial metabolite that has been found inA. haloplanktisand has anticancer activity.1,2It inhibits the growth of L1210 and 1MC carcinoma cells (IC50s = 9.7 and 12.7 μM, respectively) and sensitizes fibrosarcoma 1023 cells to macrophage-mediated cytolysis. 1.Hou, Z., Raymond, K.N., O'Sullivan, B., et al.A preorganized siderophore: Thermodynamic and structural characterization of alcaligin and bisucaberin, microbial macrocyclic dihydroxamate chelating agentsInorg. Chem.37(26)6630-6637(1998) 2.Kameyama, T., Takahashi, A., Kurasawa, S., et al.Bisucaberin, a new siderophore, sensitizing tumor cells to macrophage-mediated cytolysis. I. Taxonomy of the producing organism, isolation and biological propertiesJ. Antibiot. (Tokyo)40(12)1664-1670(1987)
    • $1,410
    35 days
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  • Ethionamide HCl
    T693503684-73-9
    Ethionamide HCl is the salt form of Ethionamide, a second-line antitubercular agent that inhibits mycolic acid synthesis. Ethionamide is a nicotinamide derivative, with antibacterial activity, used to treat tuberculosis. Although the exact mechanism of action of ethionamide is unknown, it may inhibit the synthesis of mycolic acid, a saturated fatty acid found in the bacterial cell wall, thereby inhibiting bacterial cell wall synthesis. This eventually leads to bacterial cell wall disruption and cell lysis. Ethionamide may be bacteriostatic or bactericidal in action, depending on the concentration of the drug at the site of infection and the susceptibility of the organism involved. It binds with NAD+ to form an adduct.
    • $1,520
    1-2 weeks
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  • PD 0305970
    T69388351372-19-5
    PD 0305970 is new bacterial gyrase and topoisomerase inhibitor that possess outstanding in vitro and in vivo activities against a wide spectrum of bacterial species including quinolone- and multidrug-resistant gram-positive and fastidious organism groups.
    • $1,970
    8-10 weeks
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  • Sirtuin-1 inhibitor 1
    T79903945114-10-3
    Sirtuin-1 inhibitor 1 is an inhibitor against deacetylase-1 (Sirtuin-1) and can be used to study senescence and cell death in the organism.
    • $52
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  • Kaempferol-3-O-[2″,6″-di-O-E-p-coumaroyl]-β-D-glucopyranoside
    T81991121651-61-4
    Kaempferol-3-O-[2″,6″-di-O-E-p-coumaroyl]-β-D-glucopyranoside, an acylated kaempferol glucoside, can be extracted from the leaves of O. dentata and serves as a repellent for the fouling organism, the blue mussel M. edulis [1].
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