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Results for "

heterocycle

" in TargetMol Product Catalog
  • Inhibitors & Agonists
    11
    TargetMol | Inhibitors_Agonists
  • Natural Products
    3
    TargetMol | Natural_Products
CL097
CL097
T384231026249-18-2
CL097 is an effective agonist of TLR7 and TLR8. CL097 induces pro-inflammatory cytokines in macrophages and NADPH oxidase priming, thereby increasing the fMLF-stimulated ROS production.
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Clomazone
Magister, Gamit, FMC 57020, Dimethazone, Command
T1978181777-89-1
Clomazone (Magister) is an agricultural herbicide. The molecule consists of a 2-chlorobenzyl group bound to an N-O heterocycle called Isoxazole. Clomazone suppresses the biosynthesis of chlorophyll and other plant pigments.
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Thianthrene
NSC-439, NSC439, NSC 439, Dibenzodithiodioxane, dibenzo-1,4-dithiin, AI3-00638, AI300638, AI3 00638, 9,10-Dithiaanthracene
T2029092-85-3
Thianthrene (Dibenzodithiodioxane) is a sulfur-containing heterocyclic chemical compound that is a derivative of the parent heterocycle called dithiin and is easy to oxidize.
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TargetMol | Inhibitor Sale
2,2':5',2''-Terthiophene
α-Terthienyl, Trithiophene
T56501081-34-1
2,2':5',2''-Terthiophene (Trithiophene) (α-Terthiophene) is an oligomer of the heterocyclic compound thiophene, used as a building block for the organic semiconductor polythiophene.
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DDCPPB-Glu
T25296149325-95-1
DDCPPB-Glu is a 6-5 fused ring heterocycle antifolate that shows antitumor activity.
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10-14 weeks
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Celecoxib Carboxylic Acid Acyl-β-D-Glucuronide
T37251264236-79-5
Celecoxib carboxylic acid acyl-β-D-glucuronide is a phase II metabolite of celecoxib . Celecoxib is an anti-inflammatory compound from the diaryl heterocycle class that selectively inhibits cyclooxygenase-2 (COX-2; IC50s = 22.9 and 0.05 μM for COX-1 and COX-2, respectively). Celecoxib carboxylic acid acyl-β-D-glucuronide is a minor metabolite, accounting for 2% of the administered dose in human urine and rat bile.
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Spinacine
T3729859981-63-4
Spinacine has been isolated from spinach and the roots of Panax ginseng. This conformationally constrained amino acid is a structural element in certain biologically active compounds as glucagon antagonists and angiotensin II receptor antagonists. Spinacine can be inserted as a His replacement with a locked imidazole moiety for elucidating the role of the lateral heterocycle in the activity of a peptide.
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SC-560
SC560
T4101188817-13-2
SC-560 is a member of the diaryl heterocycle class of cyclooxygenase (COX) inhibitors.
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TargetMol | Inhibitor Sale
C-2′-Decoumaroylaloeresin G
T827991059182-21-6
Compound 1059182-21-6 features a cyclic structure characterized by a nitrogen atom occupying an apex (corner) within the heterocycle. Its molecular scaffold integrates aromatic properties due to the presence of a conjugated system, while the inclusion of hydroxyl (-OH) groups confers reactive potential for subsequent modification. Additionally, a halogenated component, specifically a bromine atom, is attached to the aromatic ring, enhancing its propensity for undergoing further synthetic transformations.
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1,3-Dicyclohexiylimidazolium chloride
TNU0684181422-72-0
Other heterocycle, fine chemical, catalyst
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7-10 days
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6-Oxo-1,6-dihydropyridazine-3-carboxylic acid methyl ester
TNU079663001-30-9
Heterocyclic Compound - Other heterocycle; Intermediate - Electrophile; Fine Chemicals
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7-10 days
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