| Cat. No. | Product Name | Field of Application | Chemical Structure |
|---|---|---|---|
| DC22546 | Antibiotic-5d | A synthetic antimicrobial compound that antibacterial activity in vitro against various Gram-positive and Gram-negative bacteria, fungi and yeast.. |
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| DC23906 | Butenafine hydrochloride Featured | A synthetic benzylamine antifungal that inhibits the synthesis of ergosterol by inhibiting squalene epoxidase. |
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| DC20656 | AM-2201 | A synthetic cannabinoid that acts as a potent, nonselective full agonist for the cannabinoid receptor with EC50 of 38 and 58 nM for CB1 and CB2, respectively. |
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| DC23209 | HO-3867 Featured | A synthetic curcuminoid that selectively inhibits STAT3 phosphorylation, transcription, and DNA binding without affecting the expression of other active STATs. |
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| DC11517 | Benzodrocortisone | A synthetic glucocorticoid corticosteroid.. |
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| DC11525 | Mocravimod | A synthetic immunosuppressant that functions as a S1P1 receptor agonist. |
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| DC23705 | Lenabasum | A synthetic nonpsychoactive cannabinoid acid with potent analgesic and anti-inflammatory activity in vivo, binds directly and selectively to PPARγ. |
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| DC22494 | ST-2825 | A synthetic peptido-mimetic compound that inhibits MyD88 dimerization in a TIR-dependent manner. |
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| DC22357 | Benfotiamine | A synthetic S-acyl derivative of thiamine (vitamin B1) that possesses anti-inflammatory effects. |
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| DC22458 | RX-055 | A tailored WOBE437-derived diazirine-containing photoaffinity probe that irreversibly blocks membrane transport of both endocannabinoids. |
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| DC22474 | Demeclocycline hydrochloride | A tetracycline antibiotic that acts by binding to the 30S ribosomal subunit to inhibit binding of aminoacyl tRNA which impairs protein synthesis by bacteria. |
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| DC23965 | Clopidogrel thiolactone Featured | A thienopyridine-class antiplatelet agent that works by irreversibly inhibiting P2Y12 receptor on platelets. |
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| DC7517 | THIACETAZONE Featured | A thiosemicarbazone that is used in association with other antimycobacterial agents in the initial and continuation phases of antituberculosis regimens. Thiacetazone containing regimens are less effective than the short-course regimen recommended by the I |
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| DC25059 | BMS-986001 | A thymidine analogue nucleoside reverse transcriptase inhibitor (NRTI) that inhibits HIV-2 isolates from treatment-naive individuals with EC50 of 30-81 nM. |
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| DC9633 | Toll-like receptor modulator | A Toll-like receptor modulator. |
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| DC24097 | Ufenamate | A topical analgesic that possesses anti-inflammatory effect for treatment of skin diseases, such as acute and chronic eczema, contact dermatitis, diaper dermatitis, miliaria and atopic dermatitis.. |
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| DC22457 | NAPQI Featured | A toxic byproduct, iminoquinone metabolite of acetaminophen that covalently binds to the active site of MIF. |
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| DC24092 | Posaconazole hydrate Featured | A triazole antifungal agent that blocks the synthesis of ergosterol by inhibiting of the enzyme lanosterol 14α-demethylase and accumulation of methylated sterol precursors, more potent at inhibiting 14α-demethylase than itraconazole.. |
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| DC21517 | Mithramycin A | A tricyclic pentaglycosidic, antineoplastic antibiotic from Streptomyces strains that inhibits RNA and protein synthesis by adhering to DNA. |
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| DC21638 | SLV peptide | A tripeptide representing the Fas-C terminus that specifically blocks the interaction of Fap1 with Fas. |
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| DC24136 | Amitifadine hydrochloride | A triple monoamine reuptake inhibitor that inhibits the reuptake of [3H]serotonin, [3H]norepinephrine, and [3H]dopamine in HEK 293 cells expressing the corresponding human recombinant transporters (IC50 values of 12, 23, and 96 nM, respectively). |
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| DC22736 | Amitifadine | A triple monoamine reuptake inhibitor, inhibits the reuptake of 5-HT, norepinephrine and dopamine in HEK 293 cells with IC50 of 12, 23 and 96 nM, respectively. |
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| DC21185 | Cucurbitacin I | A triterpenoid compound that potently and selectively inhibits JAK/STAT3 pathway, suppresses the levels of phosphotyrosine STAT3 in A549 cell with IC50 of 500 nM. |
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| DC23062 | RAMX3 | A tritium-labeled allosteric modulator of the human chemokine receptor CXCR3 with Kd of 1.08 nM. |
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| DC22473 | Loxapine | A typical antipsychotic agent that displays an extremely strong binding affinity for dopamine D4 and serotonin 5-HT2 receptors.. |
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| DC22477 | Loxapine succinate | A typical antipsychotic agent that displays an extremely strong binding affinity for dopamine D4 and serotonin 5-HT2 receptors.. |
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| DC8197 | Tyrosine kinase inhibitor Featured | A Tyrosine kinase inhibitor. |
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| DC22811 | TX-1123 | A tyrphostin AG17 analog that exihibits potent Src-K inhibitory activity with IC50 of 2.2 uM. |
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| DC24189 | Closantel sodium | A veterinary anthelmintic with known proton ionophore activities. |
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| DC24190 | Closantel | A veterinary anthelmintic with known proton ionophore activities. |
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