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Home >> Signaling Pathways >> Microbiology & Virology >> Parasite

Parasite

Antiparasitics are a class of medications which are indicated for the treatment of parasitic diseases such as nematodes, cestodes, trematodes, and infectious protozoa.

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Products for  Parasite

  1. Cat.No. Product Name Information
  2. GC50054 Quinine hydrochloride Antimalarial Quinine hydrochloride Chemical Structure
  3. GC61231 Quinine hydrochloride dihydrate Quinine hydrochloride dihydrate (Qualaquin) is an orally active and can be used in anti-malarial studies. Quinine hydrochloride dihydrate Chemical Structure
  4. GC32683 Rafoxanide An anthelmintic Rafoxanide Chemical Structure
  5. GC63860 Rapanone Rapanone is a natural benzoquinone. Rapanone Chemical Structure
  6. GC64981 Resorantel Resorantel is an anthelmintic. Resorantel Chemical Structure
  7. GC32106 Robenidine hydrochloride Robenidine hydrochloride is an anticoccidial agent which is also active against MRSA and VRE with MIC50s of 8.1 and 4.7 μM, respectively. Robenidine hydrochloride Chemical Structure
  8. GC15728 Ronidazole antiprotozoal agent Ronidazole Chemical Structure
  9. GC65451 RR-11a analog RR-11a analog is a potent and irreversible inhibitor of Schistosoma mansoni legumain, with an IC50 of 31 nM. RR-11a analog Chemical Structure
  10. GC32066 RRx-001 RRx-001 is an aerospace-derived anticancer agent with reactive nitrogen species (RNS)-generating chemistry that leads to epigenetic alterations, such as DNA methylation and histone acetylation in cancer cells. RRx-001 Chemical Structure
  11. GC13442 Sanguinarine chloride Inhibitor of PP2C and MKP-1 Sanguinarine chloride Chemical Structure
  12. GC38666 Santonin A sesquiterpenoid lactone Santonin Chemical Structure
  13. GC34774 Sarolaner Sarolaner (PF-6450567) is an orally active and broad-spectrum ectoparasiticide. Sarolaner Chemical Structure
  14. GC39562 SARS-CoV-IN-1 SARS-CoV-IN-1 is an effective inhibitor of SARS-CoV replication. SARS-CoV-IN-1 Chemical Structure
  15. GC39642 SARS-CoV-IN-2 SARS-CoV-IN-2 is an effective inhibitor of SARS-CoV replication. SARS-CoV-IN-2 Chemical Structure
  16. GC39563 SARS-CoV-IN-3 SARS-CoV-IN-3 is an effective inhibitor of SARS-CoV replication. SARS-CoV-IN-3 Chemical Structure
  17. GC61465 SDZ285428 SDZ285428 is a CYP51 inhibitor. SDZ285428 Chemical Structure
  18. GC16933 Secnidazole nitroimidazole anti-infective Secnidazole Chemical Structure
  19. GC32174 Selamectin An anthelmintic antibiotic Selamectin Chemical Structure
  20. GC50700 SGC 6870N SGC 6870N Chemical Structure
  21. GC10377 SID 26681509 SID 26681509 Chemical Structure
  22. GC61791 SID 26681509 quarterhydrate SID 26681509 quarterhydrate is a potent, reversible, competitive, and selective inhibitor of human cathepsin L with an IC50 of 56 nM. SID 26681509 quarterhydrate Chemical Structure
  23. GC48455 Sitamaquine (tosylate) An antileishmanial agent Sitamaquine (tosylate) Chemical Structure
  24. GC18047 Spiramycin 16-membered ring macrolide (antibiotic) Spiramycin Chemical Structure
  25. GC65563 Spiramycin I Spiramycin I is a macrolide antibiotic and antiparasitic. Spiramycin I Chemical Structure
  26. GC33967 Spirodiclofen (BAJ-2740) Spirodiclofen (BAJ-2740) is a broad spectrum acaricide acting via lipid biosynthesis inhibition (LBI) with no cross resistance to currently available acaricides and with additional insecticidal properties. Spirodiclofen (BAJ-2740) Chemical Structure
  27. GC12722 SQ109 SQ109 Chemical Structure
  28. GC64572 Strictosamide Strictosamide has important effects on inflammation and inflammatory pain. Strictosamide Chemical Structure
  29. GC32146 Sulfaclozine (Sulfachloropyrazine) Sulfaclozine (Sulfachloropyrazine) (Sulfachloropyrazine) is an efficacious sulphonamide derivative with antibacterial and anticoccidial effects. Sulfaclozine (Sulfachloropyrazine) Chemical Structure
  30. GC38852 Sulfaclozine sodium A sulfonamide antibiotic with antiprotozoal activity Sulfaclozine sodium Chemical Structure
  31. GC60347 Sulfadiazine sodium Sulfadiazine sodium is a sulfonamide?antibiotic with antimalarial activity. Sulfadiazine sodium Chemical Structure
  32. GC16950 Sulfadoxine synthetic analog of para-aminobenzoic acid (PABA) Sulfadoxine Chemical Structure
  33. GC67935 Sulfadoxine D3 Sulfadoxine D3 Chemical Structure
  34. GC32351 Sulfalene (Sulfametopyrazine) Sulfalene (Sulfametopyrazine) (Sulfametopyrazine) is an antimalarial agent. Sulfalene (Sulfametopyrazine) Chemical Structure
  35. GC32261 Symetine (L 16726) Symetine (L 16726) is an antiparasitic and antispirochete agent. Symetine (L 16726) Chemical Structure
  36. GC61950 T.cruzi-IN-1 T.cruzi-IN-1 is a potent?Trypanosoma cruzi?inhibitor with an?IC50?of 8 nM. T.cruzi-IN-1, a 4-trifluoromethyl substituted analog, has the potential for both the acute and chronic stages of Chagas disease. T.cruzi-IN-1 Chemical Structure
  37. GC32314 Tafenoquine (WR 238605) Tafenoquine (WR 238605) (WR 238605) is an 8-aminoquinoline. Tafenoquine (WR 238605) Chemical Structure
  38. GC32206 Tafenoquine Succinate (WR 238605 (Succinate)) Tafenoquine Succinate (WR 238605 (Succinate)) (WR 238605 Succinate) is an 8-aminoquinoline. Tafenoquine Succinate (WR 238605 (Succinate)) Chemical Structure
  39. GC39162 TCMDC-135051 TCMDC-135051 is a highly selective and potent protein kinase PfCLK3 inhibitor with low off-target toxicity. TCMDC-135051 Chemical Structure
  40. GC39755 TCMDC-135051 hydrochloride TCMDC-135051 hydrochloride is a highly selective and potent protein kinase PfCLK3 inhibitor with low off-target toxicity. TCMDC-135051 hydrochloride Chemical Structure
  41. GC63904 Teclozan Teclozan (WIN 13146) is an antiprotozoal agent, class in benzylamine derivatives. Teclozan Chemical Structure
  42. GC61318 Tectol Tectol, isolated from Lippia sidoides, exhibits significant activity against human leukemia cell lines HL60 and CEM. Tectol Chemical Structure
  43. GC32245 Temephos (Temefos) Temefos is an organophosphate larvicide, used to treat water infested with disease-carrying insects including mosquitoes, midges, and black fly larvae. Temephos (Temefos) Chemical Structure
  44. GC11352 Tetramisole HCl Tetramisole HCl is an inhibitor of alkaline phosphatases, is a high purity antiparasitic. Tetramisole HCl Chemical Structure
  45. GC17228 Thiabendazole Fungicide Thiabendazole Chemical Structure
  46. GC66398 Thiabendazole-d4 Thiabendazole-d4 is the deuterium labeled EIDD-1931. EIDD-1931 (Beta-d-N4-hydroxycytidine; NHC) is a novel nucleoside analog and behaves as a potent anti-virus agent. EIDD-1931 effectively inhibits the replication activity of venezuelan equine encephaliti Thiabendazole-d4 Chemical Structure
  47. GC48164 Thiacloprid A neonicotinoid insecticide Thiacloprid Chemical Structure
  48. GC37792 Tilbroquinol Tilbroquinol is an orally active antiparasite agent, can be used in study of amoebiasis. Tilbroquinol Chemical Structure
  49. GC70031 Tioxazafen

    Tioxazafen is a broad-spectrum seed treatment nematicide that belongs to the class of 2-substituted oxazolines. It provides consistent control against nematodes in corn, soybean, and cotton crops.

     Tioxazafen Chemical Structure
  50. GC11105 Toltrazuril antiprotozoal agent Toltrazuril Chemical Structure
  51. GC37813 Toltrazuril sulfone An active metabolite of toltrazuril Toltrazuril sulfone Chemical Structure
  52. GC62371 trans-4-Methylcyclohexanamine trans-4-Methylcyclohexanamine is an intermediate and can be used for the development of T. trans-4-Methylcyclohexanamine Chemical Structure
  53. GC10537 Triclabendazole Microtubule associated inhibitor Triclabendazole Chemical Structure
  54. GC61360 Tuberostemonine Tuberostemonine, an alkaloid, is an antimalarial agent that targets Plasmodium falciparum ferredoxin-NADP+ reductases (pfFNR). Tuberostemonine Chemical Structure
  55. GC65454 UCT943 UCT943 is a next-generation Plasmodium falciparum PI4K inhibitor. UCT943 Chemical Structure
  56. GC62163 VU041 VU041 is a first submicromolar-affinity inhibitor of Anopheles (An. VU041 Chemical Structure
  57. GC30857 Warangalone (Scandenolone) Warangalone (Scandenolone) is an anti-malarial compound which can inhibit the growth of both strains of parasite 3D7 (chloroquine sensitive) and K1 (chloroquine resistant) with IC50s of 4.8 μg/mL and 3.7 μg/mL, respectively. Warangalone (Scandenolone) Chemical Structure
  58. GC70146 WM382

    WM382 is an orally effective dual plasma proteinase inhibitor of factor IX/X (PMIX/X), with IC50 values of 1.4 nM and 0.03 nM, respectively. WM382 has good in vivo efficacy and resistance to multiple stages of the malaria parasite life cycle.

     WM382 Chemical Structure

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