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Results for "

microbiota

" in TargetMol Product Catalog.
  • Inhibitors & Agonists
    60
    TargetMol | All_Pathways
  • Compound Libraries
    1
    TargetMol | Compound_Libraries
  • Natural Products
    32
    TargetMol | Natural_Products
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    TargetMol | Recombinant_Protein
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    TargetMol | Isotope_Products
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    TargetMol | Disease_Modeling_Products
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    TargetMol | Standard_Products
  • Stachyose hydrate
    T580954261-98-2
    Stachyose hydrate is a natual product,it highly promotes proliferation of lactic acid bacteria (LAB) by inducing LAB to produce more α-galactosidase to hydrolyze stachyose.
    • $33
    In Stock
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    QTY
  • methyl 2-hydroxy-4-methylvalerate
    T950940348-72-9
    Methyl 2-hydroxy-4-methylvalerate [Methyl 2-hydroxyisovalerate] is a predominant volatile compound found in Zhenjiang aromatic vinegar.
    • $36
    In Stock
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  • Carbendazim
    Mercarzole, Carbendazole, Bavistin
    T312410605-21-7
    Carbendazim (Mercarzole) is a broad-spectrum benzimidazole antifungal with potential antimitotic and antineoplastic activities. Although the exact mechanism of action is unclear, carbendazim appears to binds to an unspecified site on tubulin and suppresses microtubule assembly dynamic. This results in cell cycle arrest at the G2/M phase and an induction of apoptosis.
    • $35
    In Stock
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    TargetMol | Citations Cited
  • Theaflavin digallate
    Theaflavine bisgallate, theaflavin digallate, TFBG
    T4S055433377-72-9
    Theaflavin digallate and lactic acid together could reduce herpes simplex virus transmission.
    • $98
    In Stock
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  • Dextran sulfate sodium salt (MW 36,000 - 50,000)
    DSS
    T13647L
    Dextran sulfate sodium salt (MW 36,000–50,000) is a medium molecular weight polyanionic dextran derivative with strong intestinal epithelial permeability. It is the most commonly used agent for inducing inflammatory bowel disease (IBD) models, effectively inducing both acute and chronic colitis. Its mechanism may involve macrophage dysfunction and gut microbiota dysbiosis. Due to its colonic epithelial toxicity, long-term use can also induce colorectal cancer models.
    • $30
    In Stock
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    TargetMol | Inhibitor Hot
  • Trimethylamine N-oxide
    T412451184-78-7
    Trimethylamine N-oxide (TMAO) is a gut microbiota-dependent metabolite derived from dietary choline, betaine, and carnitine. It induces inflammation by activating the ROS/NLRP3 inflammasome and promotes fibroblast differentiation through the activation of the TGF-β/Smad2 signaling pathway. TMAO is commonly used to induce cardiac fibrosis models.
    • $29
    In Stock
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    TargetMol | Inhibitor Hot
  • 2-Hydroxy-4-methoxybenzoic acid
    4-Methoxysalicylic acid, 2-Hydroxy-p-anisic Acid
    T2A24282237-36-7
    2-Hydroxy-4-methoxybenzoic acid (2-Hydroxy-p-anisic Acid) is a predicted metabolite generated by BioTransformer1 that is produced by the metabolism of 3-(2-hydroxy-4-methoxyphenyl)propanoic acid. It is generated by unspecified-gutmicro enzyme via a beta-oxidation-of-carbxoylic-acid reaction. This beta-oxidation-of-carbxoylic-acid occurs in human gut microbiota.
    • $30
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  • 4-hydroxyphenylacetic acid
    p-Hydroxyphenylacetic acid, parahydroxy phenylacetate
    T3743156-38-7
    4-hydroxyphenylacetic acid (parahydroxy phenylacetate) is a major microbiota-derived metabolite of polyphenols. 4-hydroxyphenylacetic acid(p-Hydroxyphenylacetic acid) is involved in the antioxidative action. 4-hydroxyphenylacetic acid(p-Hydroxyphenylacetic acid) induces expression of Nrf2.
    • $29
    In Stock
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    TargetMol | Citations Cited
  • Trimethylamine N-oxide dihydrate
    TMANO Dihydrate
    T524762637-93-8
    Trimethylamine N-oxide dihydrate (TMANO dihydrate) is a gut microbiota-dependent metabolite derived from dietary choline and other trimethylamine-containing nutrients. It induces inflammation by activating the ROS/NLRP3 inflammasome and promotes fibroblast differentiation and cardiac fibrosis via the TGF-β/Smad2 signaling pathway. TMANO dihydrate can be used to establish models of cardiac hypertrophy and cardiac fibrosis.
    • $35
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  • Terbuthylazine
    T131275915-41-3
    Terbuthylazine is a triazine herbicide and a selective acetolactate synthase (ALS) inhibitor, toxic to aquatic organisms, and capable of disrupting gut microbiota. Terbuthylazine induces significant damage to the jejunal barrier and mitochondrial quality control imbalance.
    • $33
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  • Fructo-oligosaccharide DP11/GF10
    T19328137405-36-8
    Fructo-oligosaccharide DP11/GF10 is a fructooligosaccharide (FOS) with a high degree of polymerization of approximately 11. It consists of multiple fructose units linearly linked via β(2→1) glycosidic bonds, with a glucose residue at the terminal end of the molecule. Fructo-oligosaccharide DP11/GF10 belongs to prebiotic substrates and can be selectively utilized by gut microbiota to modulate the structure and metabolic activity of the intestinal flora.
    • $123
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  • 5-(3',4'-Dihydroxyphenyl)-γ-valerolactone
    T20308121618-92-8
    5-(3',4'-Dihydroxyphenyl)-γ-valerolactone is a gut microbial metabolite of (-)-epicatechin and possesses antioxidant activity.
    • Inquiry Price
    10-14 weeks
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  • α-Glucosidase-IN-77
    T203496
    α-Glucosidase-IN-77 (Compound H7) is a non-competitive α-glucosidase inhibitor with an IC50 of 1.25 μM. It reduces blood glucose levels, improves glucose tolerance, regulates gut microbiota, and exhibits hepatoprotective effects in a mouse model of type 2 diabetes.
    • Inquiry Price
    Inquiry
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  • (3R,5R)-Octahydrocurcumin
    (3R,5R)-Hexahydrobisdemethoxycurcumin
    T203529408324-14-1
    (3R,5R)-Octahydrocurcumin (Compound 7) is a metabolite of Curcumin produced by gut microbiota. It exhibits neuroprotective effects against Aβ25-35-induced cell damage in SH-SY5Y cells and possesses anti-inflammatory properties in LPS-stimulated BV-2 mouse microglia.
    • Inquiry Price
    3-6 months
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  • β-Glucuronidase-IN-3
    T2069533081681-34-4
    β-Glucuronidase-IN-3 (Compound 49) is a covalent allosteric inhibitor targeting β-glucuronidase. It exhibits potent inhibitory activity against Escherichia coli β-glucuronidase (EcGUS) with an IC50 of 12.9 nM. The compound exerts its inhibitory effect through reversible covalent modification of cysteine residues (Cys28, Cys443, and Cys197) on EcGUS. It is applicable in research on gut microbiota-related diseases, particularly in reducing the toxic side effects of Irinotecan and non-steroidal anti-inflammatory drugs (NSAIDs).
    • Inquiry Price
    10-14 weeks
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  • Urobilinogens
    T20779911000-27-4
    Urobilinogens comprise a mixture of bilirubin metabolites, including D-urobilinogen, L-urobilinogen (stercobilinogen), and i-urobilinogen (mesobilirubinogen). These compounds are produced from bilirubin by gut microbiota. In mice on a high-fat diet, the cecal concentrations of D-urobilinogen, L-urobilinogen, and i-urobilinogen are increased. Furthermore, elevated fecal levels of L-urobilinogen are inversely associated with reduced blood hemoglobin levels in patients with heterozygous β-thalassemia.
    • Inquiry Price
    Inquiry
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  • LK-60
    T209048
    LK-60 is a potent inhibitor of DprE1. It effectively suppresses the proliferation of Mycobacterium tuberculosis. Additionally, LK-60 demonstrates good safety profiles for gut microbiota and human cells.
    • Inquiry Price
    Inquiry
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  • Prosulfuron
    T21881394125-34-5
    Prosulfuron is a fluorinated sulfonylurea herbicide with an acute oral LD50 of 546 mg/kg in female rats. It inhibits weed growth by blocking the biosynthesis of branched-chain amino acids (valine, leucine, and isoleucine) through the inhibition of acetolactate synthase (ALS). Additionally, Prosulfuron may disrupt the balance of soil microbiota in alkaline soils and has minimal chemical degradation. It is noted for its low toxicity to humans and mammals and is utilized in studies for controlling broadleaf weeds in corn and sweet corn fields.
    • Inquiry Price
    10-14 weeks
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  • Lunularin
    T3295937116-80-6
    Lunularin is a naturally occurring bibenzyl compound widely distributed in liverworts (such as Conocephalum conicum) and is also a major gut microbiota-derived metabolite of resveratrol. Research indicates that Lunularin possesses significant antioxidant and anti-inflammatory properties and can selectively inhibit 11beta-hydroxysteroid dehydrogenase 1 (11beta-HSD1). Due to its role in regulating glucocorticoid activation and metabolic homeostasis, this molecule is of great interest in studies involving metabolic diseases, skin health, and neuroprotection.
    • $30
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  • 3-(2,4-Dihydroxyphenyl)propanoic acid
    Hydroumbellic acid, 2,4-Dihydroxyhydrocinnamic acid
    T37375631-68-5
    3-(2,4-Dihydroxyphenyl)propanoic acid (Hydroumbellic acid) is a predicted metabolite generated by BioTransformer1 from the metabolism of 3-(2,4-dihydroxyphenyl)prop-2-enoic acid. It is produced by the abkar1 enzyme via a reduction-of-alpha-beta-unsaturated-compounds-pattern1 reaction in human gut microbiota.
    • $30
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  • Dihydroresveratrol
    3,4',5-Trihydroxybibenzyl
    T384058436-28-5
    Dihydroresveratrol (3,4',5-Trihydroxybibenzyl) is a major metabolite of resveratrol that is produced by animal-associated bacteria, including the gut microbiota. Dihydroresveratrol and dihydroresveratrol monosulfate are detectable in urine. The physiological effects of dihydroresveratrol have not been investigated.
    • $30
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  • Stachyose
    T65444470-55-3
    Stachyose is an oligosaccharide that inhibits the proliferation of vancomycin-resistant enterococci.Stachyose regulates the intestinal microbiota and attenuates dextran sulfate sodium-induced acute colitis in mice.
    • $31
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  • ADL 08-0011 HCl
    T70267170098-43-8
    ADL 08-0011 is an active metabolite of the μ-opioid receptor antagonist alvimopan. It is produced from alvimopan via amide hydrolysis by gut microbiota. ADL 08-0011 is a μ-opioid receptor antagonist (Ki = 0.25 nM). It is selective for μ-opioid receptors over κ- and δ-opioid receptors (Kis = 15.8 and 31.6 nM, respectively). ADL 08-0011 inhibits endomorphin 1-induced inhibition of electrically induced contraction of isolated guinea pig ileum (pA2 = 9.4). In vivo, ADL 08-0011 (0.03-1 mg/kg) reverses loperamide-induced delayed gastric emptying in a rat model of castor oil-induced diarrhea.
    • $2,700
    35 days
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  • FFA3 agonist 1
    T71663886358-51-6
    FFA3 Agonist 1, a potent agonist of the free fatty acid receptor 3 (FFA3), plays a crucial role in mediating the health-promoting effects of the intestinal microbiota through the activation of FFA3.
    • Inquiry Price
    6-8 weeks
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