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Products for microbiology and virology

  1. Cat.No. Product Name Information
  2. BCC4908 Ganciclovir Ganciclovir is a potent herpes simplex virus (HSV)inhibitor, including cytomegalovirus (CMV), with an IC50 of 5.2 μM for feline herpesvirus type-1 (FHV-1). Ganciclovir
  3. BCC6174 LF 11 LF 11
  4. BCC6175 Lauryl-LF 11 Lauryl-LF 11
  5. BCC4385 Azithromycin Azithromycin is a macrolide antibiotic useful for the treatment of a number of bacterial infections. Azithromycin
  6. BCC5415 Helioxanthin 8-1 Helioxanthin 8-1 is an analogue of helioxanthin, exhibites significant in vitro anti-HBV/HCV/HSV-1/HIV activity with EC50 of >5/10/1.4/15 uM. Helioxanthin 8-1
  7. BCC5246 Bedaquiline Bedaquiline (TMC207) is a diarylquinoline drug and inhibits Mycobacterium tuberculosis (Mtb) F1FO-ATP synthase through targeting of both the c- and the ε-subunit. Bedaquiline has uncoupler activity. Bedaquiline is used for the multi-drug resistant tuberculosis. Bedaquiline
  8. BCC5245 Bedaquiline fumarate Bedaquiline fumarate, a diarylquinoline antibiotic that targets ATP synthase, is effective for the treatment of Mycobacterium tuberculosis infections. Bedaquiline fumarate
  9. BCC4914 Itraconazole Itraconazole (R51211) is a triazole antifungal agent and a potent and orally active Hedgehog (Hh) signaling pathway antagonist with an IC50 of ~800 nM. Itraconazole potently inhibits lanosterol 14α-demethylase (cytochrome P450 enzyme), thereby inhibits the oxidative conversion of lanosterol to ergosterol. Itraconazole has anticancer and antiangiogenic effects. Itraconazole
  10. BCC1990 Tedizolid Tedizolid (TR 700; Torezolid; DA-7157) is a novel oxazolidinone, acting through inhibition of bacterial protein synthesis by binding to 23S ribosomal RNA (rRNA) of the 50S subunit of the ribosome. Tedizolid
  11. BCC2004 TMC353121 TMC353121 is a potent respiratory syncytial virus (RSV) fusion inhibitor with pEC50 of 9.9. TMC353121
  12. BCC4905 Fluconazole Fluconazole is a triazole antifungal drug used in the treatment and prevention of superficial and systemic fungal infections. Fluconazole
  13. BCC5201 Mc-MMAE Mc-MMAE is a protective group (maleimidocaproyl)-conjugated monomethyl auristatin E (MMAE), which is a potent tubulin inhibitor. Mc-MMAE is a drug-linker conjugate for ADC. Mc-MMAE
  14. BCC1428 BMS-663068 Fostemsavir (BMS-663068) is the phosphonooxymethyl prodrug of BMS-626529. Fostemsavir (BMS-663068) is a novel attachment inhibitor that targets HIV-1 gp120 and prevents its binding to CD4+ T cells. BMS-663068
  15. BCC1429 BMS-663068 Tris Fostemsavir Tris (BMS-663068 (Tris)) is the phosphonooxymethyl prodrug of BMS-626529. Fostemsavir Tris (BMS-663068 (Tris)) is a novel attachment inhibitor that targets HIV-1 gp120 and prevents its binding to CD4+ T cells. BMS-663068 Tris
  16. BCC5518 Tecovirimat Tecovirimat
  17. BCC1882 Radezolid Radezolid is a novel oxazolidinone antibiotic agent. Radezolid
  18. BCC5287 Apilimod mesylate Apilimod mesylate
  19. BCC5156 Walrycin B Walrycin B is a novel antibacterial compound specifically targeting the essential WalR response regulator. Walrycin B
  20. BCC2026 Valganciclovir Valganciclovir
  21. BCC5437 Buparvaquone Buparvaquone is a hydroxynaphthoquinone antiprotozoal drug related to parvaquone and atovaquone. Buparvaquone
  22. BCC6172 PF 945863 PF 945863
  23. BCC5407 AVX 13616 AVX 13616 shows the potent in vivo antibacterial activity of Avexa’s lead antibacterial candidate; particularly against drug-resistant Staphylococcus pathogens. AVX 13616
  24. BCC4093 Cefoselis hydrochloride Cefoselis is a widely used beta-lactam antibiotic. Cefoselis hydrochloride
  25. BCC3865 Terbinafine Terbinafine (TDT 067) is an antifungal medication used to treat fungal infections. It is a potent non-competitive inhibitor of squalene epoxidase from Candida with a Ki of 30 nM. Terbinafine also antibacterial activity against certain Gram-positive and Gram-negative bacteria. Terbinafine
  26. BCC1700 Letermovir AIC246 is a novel anti-CMV compound which targets the viral terminase complex and remains active against virus resistant to DNA polymerase inhibitors. Letermovir
  27. BCC3747 Cefdinir Cefdinir (FK-482) is a semi-synthetic, broad-spectrum antibiotic, which is proved to be effective for common bacterial infections of the ear, sinus, throat, and skin. Cefdinir
  28. BCC1880 R-7128 Mericitabine (RG 7128; R-7128) is a nucleoside inhibitor of the HCV NS5B polymerase that acts as an RNA chain terminator and prevents elongation of RNA transcripts during replication. R-7128
  29. BCC2489 Meropenem Meropenem (SM 7338) is a carbapenem antibiotic, which displaying a broad spectrum of antibacterial activity. Meropenem
  30. BCC5216 Ceftibuten Ceftibuten(Sch39720) is a third-generation cephalosporin antibiotic. Ceftibuten
  31. BCC4932 Pyrazinamide Pyrazinamide is a pyrazine that is used therapeutically as an antitubercular agent. Pyrazinamide

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