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Products for microbiology and virology

  1. Cat.No. Product Name Information
  2. BCC3836 Pentamidine Pentamidine (MP-601205) is an antimicrobial agent and interferes with DNA biosynthetics. Pentamidine inhibits parasite Leishmania infantum with an IC50 of 2.5 μM. Pentamidine is a potent and selective protein tyrosine phosphatases (PTPases) and phosphatase of regenerating liver (PRL) inhibitor. Pentamidine has the potential for Gambian trypanosomiasis, antimony-resistant leishmaniasis, and Pneumocystis carinii pneumonia treatment. Antitumor and antibacterial activities. Pentamidine
  3. BCC4791 Levofloxacin Levofloxacin, a synthetic fluoroquinolone, is an antibacterial agent that inhibits the supercoiling activity of bacterial DNA gyrase, halting DNA replication. Levofloxacin
  4. BCC4768 Butenafine HCl Butenafine Hydrochloride (KP363 Hydrochloride) is a synthetic benzylamine antifungal, works by inhibiting the synthesis of sterols by inhibiting squalene epoxidase. Butenafine HCl
  5. BCC4956 Peramivir Trihydrate Peramivir trihydrate (RWJ-270201 trihydrate;BCX-1812 trihydrate) is a highly potent, selective and orally active influenza virus neuraminidase (NA) inhibitor, with IC50 values ranging from 0.9 to 4.3 nM for nine NA subtypes. Peramivir Trihydrate
  6. BCC4780 Famciclovir Famciclovir(BRL 42810) is a guanine analogue antiviral drug used for the treatment of various herpesvirus infections. Famciclovir
  7. BCC4952 Tacrolimus (FK506) Tacrolimus (FK506), a macrocyclic lactone, binds to FK506 binding protein (FKBP) to form a complex. Tacrolimus inhibits calcineurin phosphatase, which inhibits T-lymphocyte signal transduction and IL-2 transcription. Immunosuppressive properties. Tacrolimus (FK506)
  8. BCC1370 Ascomycin(FK 520) Ascomycin(Immunomycin, FR-900520, FK520) is an ethyl analog of tacrolimus (FK506) with strong immunosuppressant properties. Ascomycin(FK 520)
  9. BCC1727 MAC13243 MAC13243, an antibacterial agent, is a likely inhibitor of the bacterial lipoprotein targeting chaperone, LolA. MAC13243
  10. BCC2116 Deuterated Atazanivir-D3-2 Deuterated Atazanivir-D3-2
  11. BCC2117 Deuterated Atazanivir-D3-3 Deuterated Atazanivir-D3-3
  12. BCC2115 Deuterated Atazanivir-D3-1 Deuterated Atazanivir-D3-1
  13. BCC5302 PLpro inhibitor PLpro inhibitor is a potent inhibitor of papain-like protease (PLpro) with IC50 of 2.6 uM. PLpro inhibitor
  14. BCC4129 ABT-333 Dasabuvir (ABT-333) is a nonnucleoside inhibitor of the RNA-dependent RNA polymerase encoded by the HCV NS5B gene, inhibits recombinant NS5B polymerases derived from HCV genotype 1a and 1b clinical isolates, with IC50 between 2.2 and 10.7 nM. ABT-333
  15. BCC5309 Moxidectin Moxidectin(ProHeart 6; CL301423; Cydectin) is an anthelmintic drug which kills parasitic worms (helminths), and is used for the prevention and control of heartworm and intestinal worms. Moxidectin
  16. BCC4229 Tigecycline mesylate Tigecycline mesylate (GAR-936 mesylate) is a broad-spectrum glycylcycline antibiotic. The mean inhibitory concentration (MIC) of Tigecycline for E. coli (MG1655 strain) is approximately 125 ng/mL. MIC50 and MIC90 are 1 and 2 mg/L for Acinetobacter baumannii (A. baumannii), respectively. Tigecycline mesylate
  17. BCC2546 Cidofovir Cidofovir suppresses virus replication by selective inhibition of viral DNA synthesis. Cidofovir
  18. BCC4778 Erythromycin Erythromycin is a macrolide antibiotic produced by actinomycete Streptomyces erythreus with a broad spectrum of antimicrobial activity. Erythromycin acts by binding to bacterial 50S ribosomal subunits and inhibits RNA-dependent protein synthesis by blockage of transpeptidation and/or translocation reactions, without affecting synthesis of nucleic acid. Erythromycin
  19. BCC2510 Marbofloxacin Marbofloxacin is a potent antibiotic of which depends upon its inhibition of DNA-gyrase. Marbofloxacin
  20. BCC4898 Cefditoren Pivoxil Cefditoren pivoxil is a new-third generation cephalosporin antibiotic that has a broad spectrum of activity against Gram-positive and Gram-negative bacteria, including common respiratory and skin pathogens. Cefditoren Pivoxil
  21. BCC1536 Doramectin Doramectin is an antiparasitic agent. Doramectin
  22. BCN6057 Limonin Limonin is a triterpenoid enriched in citrus fruits, which has antivirus and antitumor ability. Limonin
  23. BCC4226 Meropenem trihydrate Meropenem trihydrate (SM 7338 trihydrate) is a carbapenem antibiotic with broad-spectrum antibacterial activity. Meropenem trihydrate
  24. BCC2031 VCH-916 VCH-916 is a novel nonnucleoside HCV NS5B polymerase inhibitor. VCH-916
  25. BCC1071 Biapenem Biapenem (CLI 86815; L 627; LJC 10627) a parenteral carbapenem antibacterial agent with a broad spectrum. Biapenem
  26. BCC6376 TMC647055 TMC647055
  27. BCC4224 Gatifloxacin hydrochloride Gatifloxacin hydrochloride (AM-1155; BMS-206584; PD135432) is a potent fluoroquinolone antibiotic with broad-spectrum antibacterial activity. Gatifloxacin hydrochloride inhibits bacterial type II topoisomerases (IC50=13.8 μg/ml for S. aureus topoisomerase IV) and E. coli DNA gyrase (IC50 = 0.109 μg/ml). Gatifloxacin hydrochloride can be used to treat bacterial conjunctivitis in vivo. Gatifloxacin hydrochloride
  28. BCC4092 Cefoselis Cefoselis is a widely used beta-lactam antibiotic. Cefoselis
  29. BCC4769 Cefoselis Sulfate Cefoselis sulfate is a widely used beta-lactam antibiotic. Cefoselis Sulfate
  30. BCC1602 GS-9620 Vesatolimod (GS-9620) is a potent, selective and orally active agonist of Toll-Like Receptor (TLR7) with an EC50 of 291 nM. GS-9620
  31. BCC5261 Cefepime Dihydrochloride Monohydrate Cefepime Dihydrochloride Monohydrate is a broad-spectrum cephalosporin with enhanced coverage against Gram-positive and Gram-negative bacteria. Cefepime Dihydrochloride Monohydrate
  32. BCC4262 Tenofovir maleate Tenofovir Disoproxil Fumarate is a nucleotide reverse transcriptase inhibitor to treat HIV and chronic Hepatitis B. Tenofovir maleate
  33. BCC2025 Valaciclovir Valacyclovir is an antiviral drug used in the management of herpes simplex, herpes zoster, and herpes B. Valaciclovir
  34. BCC4051 Valacyclovir hydrochloride Valacyclovir hydrochloride is an antiviral drug used in the management of herpes simplex, herpes zoster, and herpes B. Valacyclovir hydrochloride
  35. BCC1696 Ledipasvir Ledipasvir is an inhibitor of the hepatitis C virus NS5A, with EC50s of 34 pM and 4 pM against genotype 1a and 1b replicon, respectively. Ledipasvir
  36. BCC6459 TBA354 TBA-354 is a potent anti-tuberculosis compound; maintains activity against Mycobacterium tuberculosis H37Rv isogenic monoresistant strains. TBA354
  37. BCC5175 GNF179 GNF179 is an optimized 8,8-dimethyl IP analog that exhibited the potency(4.8 nM against the multidrug resistant strain W2) in vitro metabolic stability and in vivo oral bioavailability. GNF179
  38. BCC5205 Sulfamerazine sodium salt Sulfamerazine Sodium is a sulfonamide antibacterial. Sulfamerazine sodium salt
  39. BCC4892 Balofloxacin Balofloxacin is a quinolone antibiotic, inhibiting the synthesis of bacterial DNA by interference with the enqyme DNA gyrase. Balofloxacin
  40. BCC3820 Nevirapine Nevirapine is a non-nucleoside inhibitor of HIV-1 reverse transcriptase used to treat and prevent HIV/AIDS; with a Ki of 270 μM. Nevirapine
  41. BCC5236 Mafenide Acetate Mafenide Acetate is a sulfonamide-type medication. Mafenide Acetate
  42. BCC5176 GNF179 Metabolite GNF179 metabolite is the metabolite of GNF179, which is an optimized 8,8-dimethyl IP analog that exhibited the potency(4.8 nM against the multidrug resistant strain W2) in vitro metabolic stability and in vivo oral bioavailability. GNF179 Metabolite
  43. BCC6148 PF 5081090 PF 5081090
  44. BCC3722 Arbidol HCl Umifenovir hydrochloride is an broad-spectrum antiviral chemical agent which can inhibit cell entry of enveloped viruses by blocking viral fusion with host cell membrane. Arbidol HCl
  45. BCC4839 Rifampin Rifampicin is a potent and broad spectrum antibiotic against bacterial pathogens. Rifampicin has anti-influenza virus activities. Rifampin
  46. BCC4263 Stavudine sodium Stavudine sodium is a nucleoside analog that inhibits reverse transcriptase and has in vitro activity against HIV. Stavudine sodium
  47. BCC3801 Lamivudine Lamivudine (BCH-189) is a nucleoside reverse transcriptase inhibitors (NRTIs). Lamivudine (BCH-189) can inhibit HIV reverse transcriptase 1/2 and also the reverse transcriptase of hepatitis B virus. Lamivudine
  48. BCC5436 Pneumocandin B0 Pneumocandin B0(L-688786), a key intermediate in the synthesis of the antifungal agent, Cancidas, has led to the identification of several materials with potential for improved performance. Pneumocandin B0
  49. BCC4679 Minocycline HCl Minocycline hydrochloride is a broad-spectrum tetracycline antibiotic, acting by binding to the bacterial 30S ribosomal subunit and inhibiting protein synthesis. Minocycline HCl
  50. BCC4300 Delavirdine Delavirdine(U 90152) is a potent non-nucleoside reverse transcriptase inhibitor (NNRTI). Delavirdine
  51. BCC5237 Mafenide Mafenide is a sulfonamide-type medication. Mafenide
  52. BCC4946 Zanamivir Zanamivir is an influenza viral neuraminidase inhibitor with IC50 values of 0.95 nM and 2.7 nM for influenza A and B, respectively. Zanamivir
  53. BCN2564 Amphotericin B Amphotericin B is a polyene antifungal agent against a wide variety of fungal pathogens. It binds irreversibly to ergosterol, resulting in disruption of membrane integrity and ultimately cell death. Amphotericin B
  54. BCC5644 Pentamidine isethionate Pentamidine isethionate (MP-601205 isethionate) is an antimicrobial agent and interferes with DNA biosynthetics. Pentamidine isethionate inhibits parasite Leishmania infantum with an IC50 of 2.5 μM. Pentamidine isethionate is a potent and selective protein tyrosine phosphatases (PTPases) and phosphatase of regenerating liver (PRL) inhibitor. Pentamidine isethionate has the potential for Gambian trypanosomiasis, antimony-resistant leishmaniasis, and Pneumocystis carinii pneumonia treatment. Antitumor and antibacterial activities. Pentamidine isethionate
  55. BCC4813 Nystatin (Fungicidin) Nystatin is an orally active polyene antifungal antibiotic effective against yeast and mycoplasma. Nystatin increases the permeability of plasma membranes to small monovalent ions, including chloridion. Nystatin is a cholesterol-sequestering agent, partially prevents Oxaliplatin-induced lipid raft aggregation, DR4 and DR5 clustering, and thereby reduces apoptosis. Nystatin (Fungicidin)
  56. BCC4232 Vancomycin hydrochloride Vancomycin hydrochloride is an antibiotic for the treatment of bacterial infections. It acts by inhibiting the second stage of cell wall synthesis of susceptible bacteria. Vancomycin also alters the permeability of the cell membrane and selectively inhibits ribonucleic acid synthesis. Vancomycin hydrochloride
  57. BCC5551 Tylosin phosphate Tylosin phosphate(Fradizine; Tylocine; Tylosin A) is a broad spectrum antibiotic against Gram-positive organisms and a limited range of Gram-negative organisms. Tylosin phosphate
  58. BCC4633 Bacitracin Zinc Bacitracin Zinc is a dephosphorylation of the C55-isoprenyl pyrophosphate interference for inhibition of cleavage of Tyr from Met-enkephalin with IC50 of 10 μM. Bacitracin Zinc
  59. BCC1571 Faropenem daloxate Faropenem daloxate is the first oral penem in a new class of beta-lactam antibiotics. Faropenem daloxate
  60. BCC5025 Adefovir Dipivoxil Adefovir Dipivoxil works by blocking reverse transcriptase, an enzyme that is crucial for the hepatitis B virus (HBV) to reproduce in the body. Adefovir Dipivoxil
  61. BCC1294 (S)-Tedizolid (S)-Tedizolid is the S-enantiomer of Tedizolid. Tedizolid is a novel oxazolidinone with activity against Gram-positive pathogens. (S)-Tedizolid is the less active isomer. (S)-Tedizolid
  62. BCC3774 Emtricitabine Emtricitabine is a nucleoside reverse transcriptase inhibitor (NRTI) with an EC50 of 0.01 µM in PBMC cell. It is an antiviral drug for the treatment of HIV infection. Emtricitabine
  63. BCC5207 Sulfathiazole sodium Sulfathiazole sodium is an organosulfur compound that has been used as a short-acting sulfa drug. Sulfathiazole sodium
  64. BCC4729 Sulfapyridine Sulfapyridine(Dagenan) is a sulfonamide antibacterial. Sulfapyridine
  65. BCC4046 Ledipasvir acetone Ledipasvir acetone (GS-5885 acetone) is the active ingredient of Ledipasvir. Ledipasvir is an inhibitor of the hepatitis C virus NS5A, with EC50 values of 34 pM against GT1a and 4 pM against GT1b replicon. Ledipasvir acetone
  66. BCC5346 YYA-021 YYA-021 is a small-molecule CD4 mimic that inhibits HIV entry, with high anti-HIV activity and low cytotoxicity. YYA-021
  67. BCC6372 GSK2838232 GSK2838232
  68. BCC2500 Tenofovir Tenofovir (GS 1278) is a nucleotide reverse transcriptase inhibitor to treat HIV and chronic Hepatitis B (HBV). Tenofovir
  69. BCC4069 Delavirdine mesylate Delavirdine mesylate (U 90152 mesylate) is a potent non-nucleoside HIV-1 reverse transcriptase inhibitor (NNRTI) of HIV-1. Delavirdine mesylate
  70. BCC4094 Doripenem Doripenem is a new member of the carbapenem class of beta-lactam antibiotics with broad-spectrum coverage of Gram-positive, Gram-negative and anaerobic pathogens. Doripenem
  71. BCC5089 Pefloxacin Mesylate Dihydrate Pefloxacin mesylate dehydrate is a an antibacterial agent and prevents bacterial DNA replication by inhibiting DNA gyrase (topoisomerse) Target: DNA gyrase Pefloxacin is a synthetic chemotherapeutic agent used to treat severe and life-threatening bacterial infections. Pefloxacin Mesylate Dihydrate
  72. BCC4047 Ledipasvir D-tartrate Ledipasvir D-tartrate is an inhibitor of the hepatitis C virus NS5A, with EC50 values of 34 pM against GT1a and 4 pM against GT1b replicon. Ledipasvir D-tartrate
  73. BCC4227 Moxifloxacin Moxifloxacin is an orally active 8-methoxyquinolone antimicrobial for use in the treatment of acute bacterial sinusitis, acute bacterial exacerbations of chronic bronchitis, and community-acquired pneumonia. Moxifloxacin
  74. BCC3737 Bexarotene Bexarotene (LGD1069) is a selective retinoid X receptors (RXR) agonist for the treatment of cutaneous T-cell lymphoma. Bexarotene
  75. BCC4135 Efavirenz Efavirenz is a potent inhibitor of the wild-type HIV-1 reverse transcriptase with a Ki of 2.93 nM and exhibits an IC95 of 1.5 nM for the inhibition of HIV-1 replicative spread in cell culture. Efavirenz
  76. BCC4235 Fluconazole hydrate Fluconazole (hydrate) is a triazole antifungal drug used in the treatment and prevention of superficial and systemic fungal infections. Fluconazole hydrate
  77. BCC4646 Cephalexin Cefalexin is a cephalosporin antibiotic. Cephalexin
  78. BCC4236 Fluconazole mesylate Fluconazole (mesylate) is a triazole antifungal drug used in the treatment and prevention of superficial and systemic fungal infections. Fluconazole mesylate
  79. BCC5550 Tebipenem Tebipenem is an orally available carbapenem antibiotic, shows broad-spectrum activity against Gram-positive and -negative bacteria, except for Pseudomonas aeruginosa. Tebipenem
  80. BCC5523 Efinaconazole Efinaconazole (KP-103) is a triazole antifungal agent and againsts T. mentagrophytes SM-110 and C. albicans ATCC 10231 with MICs of 0.0039 μg/mL and 0.00098 μg/mL, respectively. Efinaconazole has a potent in vitro activity against fungal pathogens including dermatophytes, Candida and Malassezia species. Efinaconazole
  81. BCC2496 Linezolid Linezolid (PNU-100766) is the first member of the class of oxazolidinone synthetic antibiotic. Linezolid acts by inhibiting the initiation of bacterial protein synthesis. Linezolid is used for the treatment of serious infections caused by Gram-positive bacteria that are resistant to several other antibiotics. Linezolid
  82. BCC5177 Eperezolid Eperezolid(PNU-100592) is a oxazolidinone antibacterial agent, Eperezolid demonstrated good in vitro inhibitory activity, regardless of methicillin susceptibility for staphylococci(MIC90= 1-4 mg/ml). Eperezolid
  83. BCC4233 Anidulafungin Anidulafungin is a new semisynthetic echinocandin with antifungal potency. Anidulafungin
  84. BCC1582 Furagin Furagin, nitrofurantoin analog, is an anti-bacterial agent. Furagin is 2-substituted 5-nitrofuran, chemically and structurally similar to well-known antibacterial compound nitrofurantoin. Furagin
  85. BCC1784 Naphthoquine phosphate Naphthoquine phosphate is antimalarial drug. Naphthoquine phosphate
  86. BCC5312 Bevirimat Bevirimat (PA-457; MPC-4326; YK FH312) is an anti-HIV drug derived from a betulinic acid-like compound; is believed to inhibit HIV by a novel mechanism, so-called maturation inhibition. Bevirimat
  87. BCC1360 AN-2690 Tavaborole (AN-2690) is an antifungal agent with activity against Trichophyton species, in a topical solution formulation for the potential treatment of onychomycosis. AN-2690
  88. BCC4745 Valganciclovir HCl Valganciclovir (hydrochloride), the L-valyl ester of ganciclovir, is actually a prodrug for ganciclovir. Valganciclovir HCl
  89. BCC5259 Maribavir Maribavir is a potent inhibitor of histone phosphorylation catalyzed by wild-type pUL97 in vitro, with an IC50 of 3 nM. Maribavir has potent antiviral activity against HCMV and Epstein-Barr virus (EBV). Maribavir
  90. BCC5264 Chlorhexidine digluconate Chlorhexidine digluconate is an antiseptic effective against a wide variety of gram-negative and gram-positive organisms. Chlorhexidine digluconate
  91. BCC1832 Pafuramidine Pafuramidine (DB289) is an orally bioavailable prodrug of furamidine, which has activity against Pneumocystis pneumonia. Pafuramidine
  92. BCC1711 Luliconazole Luliconazole(NND 502) is an azole antifungal indicated for the topical treatment of interdigital tinea pedis. Luliconazole
  93. BCC1826 Oseltamivir acid Oseltamivir acid (GS 4071), the active metabolite of Oseltamivir phosphate, is an orally bioavailable, potent and selective inhibitor of influenza virus neuraminidase (IC50=2 nM) with activity against both influenza A and B viruses. Oseltamivir acid
  94. BCC5413 Helioxanthin Helioxanthin
  95. BCC1522 Delafloxacin Delafloxacin (RX-3341; WQ-3034; ABT492) is a broad-spectrum fluoroquinolone antibiotic. Delafloxacin has a broad spectrum of activity that includes drug-resistant Staphylococcus aureus, Streptococcus pneumoniae, and Klebsiella pneumonia. Delafloxacin
  96. BCC1554 Epothilone D Epothilone D (KOS 862) is a potent microtubule stabilizer. Epothilone D
  97. BCC5273 Telithromycin Telithromycin(HMR3647) is a ketolide antibiotic to treat community acquired pneumonia of mild to moderate severity. Telithromycin
  98. BCC4866 Tinidazole Tinidazole is a synthesized imidazole derivative used in antiprotozoal treatment with antiamebic and antibacterial properties. Tinidazole
  99. BCC1825 Oseltamivir Oseltamivir
  100. BCC4228 Tigecycline hydrochloride Tigecycline hydrochloride (GAR-936 hydrochloride) is a broad-spectrum glycylcycline antibiotic. The mean inhibitory concentration (MIC) of Tigecycline for E. coli (MG1655 strain) is approximately 125 ng/mL. MIC50 and MIC90 are 1 and 2 mg/L for Acinetobacter baumannii (A. baumannii), respectively. Tigecycline hydrochloride
  101. BCC4128 Merimepodib Merimepodib is a novel noncompetitive inhibitor of IMPDH (Inosine monophosphate dehydrogenase). Merimepodib

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