Products for microbiology and virology
- Antibiotic(139)
- NA(7)
- HSV(7)
- Bacterial lipoprotein targeting chaperone(1)
- HIV(20)
- SARS-CoV(1)
- HCV(9)
- CMV(7)
- HBV(6)
- Reverse Transcriptase(11)
- Influenza A virus(1)
- gp120/CD4(5)
- RXR(1)
- Antifungal(2)
- Antimalaria(3)
- SRPK(1)
- Interleukin Related(5)
- CCR5(1)
- RSV(1)
- Orthopoxvirus(1)
- Cat.No. Product Name Information
-
BCC1108
Tenofovir Disoproxil Fumarate
Tenofovir Disoproxil Fumarate is a nucleotide reverse transcriptase inhibitor used to treat HIV and chronic Hepatitis B.
-
BCC3780
Flucytosine
Flucytosine (5-Fluorocytosine, 5-FC, Ancobon), a fluorinated pyrimidine analogue, is an antifungal drug.
-
BCC5414
Helioxanthin derivative 5-4-2
Helioxanthin derivative 5-4-2 is an analogue of helioxanthin, exhibites significant in vitro anti-HBV activity with EC50 of 0.08 uM in HepG2.2.15 cells.
-
BCC4690
Oseltamivir phosphate
Oseltamivir phosphate (GS 4104) is a neuraminidase inhibitor recommended for the treatment and prophylaxis of influenza A and B.
-
BCC4261
Tenofovir hydrate
Tenofovir hydrate is a nucleotide reverse transcriptase inhibitor to treat HIV and chronic Hepatitis B.
-
BCC1109
Entecavir Hydrate
Entecavir monohydrate (BMS200475 monohydrate; SQ34676 monohydrate) is a potent and selective inhibitor of HBV, with an EC50 of 3.75 nM in HepG2 cell.
-
BCC5467
Flumorph
Flumorph(SYP-L190) is a carboxylic acid amide (CAA) fungicide.
-
BCC2019
Tulathromycin A
Tulathromycin A is a macrolide antibiotic.
-
BCC4849
SRPIN340
SRPIN340 is an ATP-competitive serine-arginine-rich protein kinase (SRPK) inhibitor, with a Ki of 0.89 μM for SRPK1.
-
BCC4837
Retapamulin
Retapamulin(SB-275833) is a topical antibiotic, which binds to both E.
-
BCC4137
TAK-779
TAK-779 is a potent and selective nonpeptide antagonist of CCR5 and CXCR3, with a Ki of 1.1 nM for CCR5, and effectively and selectively inhibits R5 HIV-1, with EC50 and EC90 of 1.2 nM and 5.7 nM, respectively, in MAGI-CCR5 cells.
-
BCC4096
Cephalexin monohydrate
Cefalexin monohydrate is a cephalosporin antibiotic.
-
BCC5083
Daunorubicin HCl
Daunorubicin Hydrochloride (Daunomycin Hydrochloride; RP 13057 Hydrochloride; Rubidomycin Hydrochloride) is a topoisomerase II inhibitor with potent antineoplastic activities. Daunorubicin Hydrochloride (Daunomycin Hydrochloride; RP 13057 Hydrochloride; Rubidomycin Hydrochloride) inhibites DNA and RNA synthesis in sensitive and resistant Ehrlich ascites tumor cells.
-
BCC3755
Clotrimazole
Clotrimazole is an imidazole derivative, an antifungal compound and is a CYP (cytochrome P450) inhibitor. Clotrimazole has antibacterial activity.
-
BCC5515
Isavuconazole
Isavuconazole (BAL-4815) is a triazole prodrug with antifungal activity against yeasts, molds, and dimorphic fungi. Isavuconazole inhibits ergosterol biosynthesis and results in the disruption of fungal membrane structure and function. Isavuconazole is a moderate inhibitor of CYP3A4.
-
BCC3882
Dapivirine (TMC120)
Dapivirine(TMC 120, TMC 120 R147681) is a NNRTI for HIV reverse transcriptase with IC50 of 24 nM, inhibits a broad panel of HIV-1 isolates from different classes, inclucing a wide range of NNRTI-resistant isolates.
-
BCC5311
Bruceine A
-
BCC4130
T 705
Favipiravir (T-705) is a novel viral RNA polymerase inhibitor, it is phosphoribosylated by cellular enzymes to its active form, Favipiravir-ribofuranosyl-5′-triphosphate (RTP). Favipiravir-RTP inhibits the influenza viral RNA-dependent RNA polymerase (RdRP) activity with IC50 of 341 nM.
-
BCC5027
Etravirine (TMC125)
Etravirine is a non-nucleoside reverse transcriptase inhibitor (NNRTI) used for the treatment of HIV.
-
BCC5404
Tyrphostin A1
Tyrphostin A1(AG9) inhibits CD40L-stimulated IL-12 production in macrophage cultures and antigen-induced generation of Th1 cells.
-
BCC5202
Y-320
Y-320 is a new phenylpyrazoleanilide immunomodulator; inhibits IL-17 production by CD4 T cells stimulated with IL-15 with IC50 values of 20 to 60 nM.
-
BCC5028
Stavudine (d4T)
Stavudine is a nucleoside analog that inhibits reverse transcriptase and has in vitro activity against HIV.
-
BCC4225
Gatifloxacin mesylate
Gatifloxacin mesylate (AM-1155; BMS-206584; PD135432) is a potent fluoroquinolone antibiotic with broad-spectrum antibacterial activity. Gatifloxacin mesylate 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 mesylate can be used to treat bacterial conjunctivitis in vivo.
-
BCC5478
Tildipirosin
Tildipirosin, a long-acting macrolide, has antibiotic activity.
-
BCC1846
Peramivir
Peramivir (RWJ-270201;BCX-1812) is a highly potent, selective and orally active influenza virus neuraminidase (NA) inhibitor, with IC50 values ranging form 0.9 to 4.3 nM for nine NA subtypes.
-
BCC1637
I2906
I2906 showed antimycobacterial and cytotoxic activity against mycobacterium tuberculosis.
-
BCC1791
NBD-557
NBD-557 is a potentially HIV-1 inhibitor.
-
BCC1790
NBD-556
NBD-556 is small molecule mimetic of CD4, NBD-556 recognizes the HIV-1 envelope protein gp120 and induces restructuring of gp120 analogous to CD4 binding.
-
BCC1811
Nucleozin
Nucleozin targets influenza A nucleoprotein (NP), a multifunctional, RNA-binding protein necessary for virus replication.
-
BCC3862
Telbivudine
Telbivudine, a specific inhibitor of hepatitis B virus (HBV) replication, is an antiviral drug used in the treatment of hepatitis B infection.
-
BCC1311
5-hydroxypyrazine-2-carboxylic acid
5-Hydroxypyrazine-2-Carboxylic Acid, a metabolite of anti-tuberculosis drug pyrazinamide (PZA).
-
BCC4050
BAY 57-1293
Pritelivir (BAY 57-1293; AIC316), an inhibitor of the viral helicase-primase complex, exhibits antiviral activity in vitro and in animal models of herpes simplex virus (HSV) infection. Pritelivir is active against herpes simplex virus types 1 and 2 (HSV-1 and HSV-2) with the IC50 of 0.02 μM against HSV1-2.
-
BCC1669
JC-1
JC-1, a fluorescent lipophilic carbocyanine dye, that can be used to measure mitochondrial membrane potential.
-
BCC1523
Delafloxacin meglumine
-
BCC4505
BMS-378806
BMS-378806 selectively inhibits the binding of HIV-1 gp120 to the CD4 receptor with EC50 of 0.85-26.5 nM in virus.
-
BCC1160
Doripenem Hydrate
Doripenem monohydrate is a new member of the carbapenem class of beta-lactam antibiotics with broad-spectrum coverage of Gram-positive, Gram-negative and anaerobic pathogens.
-
BCC5206
Amikacin
-
BCC3675
Maraviroc
Maraviroc (UK-427857) is a selective CCR5 antagonist with activity against human HIV.
-
BCC8066
Tenofovir alafenamide
Tenofovir alafenamide (GS-7340) is an investigational oral prodrug of Tenofovir. Tenofovir is a HIV-1 nucleotide reverse transcriptase inhibitor.
-
BCC8067
Tenofovir Alafenamide Fumarate
Tenofovir alafenamide fumarate (GS-7340 fumarate) is an investigational oral prodrug of Tenofovir. Tenofovir is a HIV-1 nucleotide reverse transcriptase inhibitor.
-
BCC6447
tenofovir diphosphate
-
BCC5266
Ceftaroline fosamil
Ceftaroline fosamil (TAK-599) is a cephalosporin with activity against Gram-positive pathogens, including methicillin-resistant Staphylococcus aureus (MRSA).
-
BCC4764
Besifloxacin HCl
Besifloxacin hydrochloride is a fourth-generation fluoroquinolone antibiotic.
-
BCC4106
CMX001
CMX001 (Brincidofovir; HDP-CDV) was developed as an orally active, lipophilic form of cidofovir (CDV); has enhanced activity in vitro and in vivo compared to CDV against certain herpesviruses, adenoviruses and orthopoxviruses.
-
BCC5192
Carbenicillin
Carbenicillin is broad-spectrum semisynthetic penicillin derivative used parenterally.
-
BCC1698
Lersivirine
Lersivirine(UK-453061) is a next-generation non-nucleoside reverse transcriptase inhibitor (NNRTI, IC50=119 nM) with a unique resistance profile that exhibits potent antiretroviral activity against wild-type human immunodeficiency virus and clinically relevant NNRTI-resistant strains.
-
BCC1878
R-1479
R-1479 is a specific inhibitor of HCV replication in the HCV subgenomic replicon system (IC50=1.28 μM).
-
BCC1800
Nifuratel
Nifuratel(NF 113, SAP 113) is a broad antibacterial spectrum agent, which is used as an antibacterial, antifungal, and antiprotozoal (Trichomonas).
-
BCC1897
Rilpivirine
Rilpivirine (R278474; TMC278) is a type of anti-HIV medicine called a non-nucleoside reverse transcriptase inhibitor (NNRTI).
-
BCC1962
SQ109
SQ109 is a potent inhibitor of the trypomastigote form of the parasite, with IC50 for cell killing of 50±8 nM. SQ109, targets MmpL3, is an antitubercular agent.
-
BCC5194
Pentamidine dihydrochloride
Pentamidine dihydrochloride (MP-601205 dihydrochloride) is an antimicrobial agent and interferes with DNA biosynthetics. Pentamidine dihydrochloride inhibits parasite Leishmania infantum with an IC50 of 2.5 μM. Pentamidine dihydrochloride is a potent and selective protein tyrosine phosphatases (PTPases) and phosphatase of regenerating liver (PRL) inhibitor. Pentamidine dihydrochloride has the potential for Gambian trypanosomiasis, antimony-resistant leishmaniasis, and Pneumocystis carinii pneumonia treatment. Antitumor and antibacterial activities.
-
BCC6379
Carminomycin
-
BCC1737
Mefloquine hydrochloride
Mefloquine hydrochloride is a quinoline antimalarial drug that is structurally related to the antiarrhythmic agent quinidine.
-
BCC3778
Ethionamide
Ethionamide(2-ethylthioisonicotinamide) is an antibiotic used in the treatment of tuberculosis.
-
BCC2527
Cefaclor
Cefaclor is an effective antibiotic agent, and specifically binds to penicillin-binding protein 3 (PBP 3).
-
BCC5286
Apilimod
Apilimod is a potent IL-12/IL-23 inhibitor, and strongly inhibits IL-12 with IC50s of 1 nM and 2 nM, in IFN-γ/SAC-stimulated human PBMCs and SAC-treated monkey PBMCs, respectively.
-
BCC4136
BMS-538203
BMS-538203 is a highly efficient HIV integrase inhibitor and antiviral agent.
-
BCC3718
Albendazole
Albendazole is a member of the benzimidazole compounds used as a drug indicated for the treatment of a variety of worm infestations.
-
BCC4829
Praziquantel
Praziquantel is an anthelmintic effective against flatworms.
-
BCC4877
Vidarabine
Vidarabine (Ara-A) an antiviral drug which is active against herpes simplex and varicella zoster viruses.
-
BCC1917
Salinomycin sodium salt
Salinomycin sodium salt (Salinomycin sodium), an antibiotic potassium ionophore, is a potent inhibitor of Wnt/β-catenin signaling. Salinomycin sodium salt (Salinomycin sodium) acts on the Wnt/Fzd/LRP complex, blocks Wnt-induced LRP6 phosphorylation, and causes degradation of the LRP6 protein. Salinomycin sodium salt (Salinomycin sodium) shows selective activity against human cancer stem cells.
-
BCC3825
Nitrofurazone
Nitrofurazone (NFZ;Nitrofural) is a bactericidal compound used as an antibiotic most commonly in the form of ointments.
-
BCC4095
Cephalexin hydrochloride
Cefalexin hydrochloride is a cephalosporin antibiotic.
-
BCC2038
Vicriviroc maleate
Vicriviroc maleate (SCH-417690 maleate; SCH-D maleate) is a potent, selective, oral bioavailable and CNS penetrated antagonist of CCR5, with a Ki of 2.5 nM, and also inhibits HIV-1 in PBMC cells, with IC90s of 3.3 nM (JrFL), 2.8 nM (ADA-M), 1.8 nM (301657), 4.9 nM (JV1083) and 10 nM (RU 570).
-
BCC3829
Olsalazine Sodium
Olsalazine Disodium is an anti-inflammatory drug used in the treatment of Inflammatory Bowel Disease and Ulcerative Colitis.
-
BCC8047
Toyocamycin
Toyocamycin (Vengicide) is an adenosine analog produced by Actinomycete, acts as an XBP1 inhibitor, inhibits IRE1α-induced ATP-dependent XBP1 mRNA cleavage, with an IC50 of 80 nM. Toyocamycin (Vengicide) induces apoptosis. Toyocamycin (Vengicide) shows no effect on IRE1α auto-phosphorylation.
-
BCC4937
Rifapentine
Rifapentine (DL 473) is an antibiotic compound used in the treatment of tuberculosis.
-
BCC3748
Cefoperazone
Cefoperazone is a cephalosporin antibiotic for inhibition of rMrp2-mediated [3H]E217βG uptake with IC50 of 199 μM.
-
BCC4706
Primaquine Diphosphate
Primaquine is the only generally available anti-malarial that prevents relapse in vivax and ovale malaria, and the only potent gametocytocide in falciparum malaria.
-
BCC4858
Sulfanilamide
Sulfanilamide is a competitive inhibitor for bacterial enzyme dihydropteroate synthetase with IC50 of 320 μM.
-
BCC5303
Demeclocycline hydrochloride
Demeclocycline hydrochloride is a tetracycline antibiotic; is an antibiotic in the treatment of Lyme disease, acne, and bronchitis.
-
BCC5253
Nimorazole
Nimorazole (K-1900) is a nitroimidazole anti-infective.
-
BCC4855
Sulfameter
Sulfameter(Bayrena) is a long-acting sulfonamide antibacterial.
-
BCC1382
Avermectin B1a
Avermectin B1a is an antiparasitic agent that paralyzes nematodes without causing hypercontraction or flaccid paralysis.
-
BCC1383
Avermectin B1b
-
BCC3859
Sulfadiazine
Sulfadiazine belongs to the class of sulfonamide antibiotics that are used for veterinary purposes worldwide, mainly in pig production. Sulfadiazine also used for toxoplasmosis.
-
BCC4230
Norfloxacin hydrochloride
Norfloxacin hydrochloride is a broad-spectrum antibiotic that is active against both Gram-positive and Gram-negative bacteria, which functions by inhibiting DNA gyrase.
-
BCC4870
Toltrazuril
Toltrazuril (BAY-i 9142) is an antiprotozoal agent that acts upon Coccidia parasites.
-
BCC2008
Toltrazuril sulfone
Toltrazuril sulfone is an antiprotozoal agent that acts upon Coccidia parasites.
-
BCC1574
Fiacitabine
Fiacitabine(NSC 382097; FIAC; FOAC) is a selective inhibitior of DNA replication of herpes simplex virus(HSV) with IC50 values of 2.5 nM and 12.6 nM for HSV1 and HSV2, respectively.
-
BCC3763
Didanosine
Didanosine(Videx) is a reverse transcriptase inhibitor with an IC50 of 0.49 μM.
-
BCC4231
Pefloxacin
Pefloxacin 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.
-
BCC4821
Pefloxacin Mesylate
Pefloxacin mesylate 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.
-
BCC4688
Norfloxacin
Norfloxacin (MK-0366) is a broad-spectrum antibiotic that is active against both Gram-positive and Gram-negative bacteria, which functions by inhibiting DNA gyrase.
-
BCC4033
Tilbroquinol
Tilbroquinol is an antiprotozoal agent effective against amoebiasis. It has also been used against Vibrio cholerae.
-
BCC1381
Avermectin B1
Avermectin B1 (Abamectin) is a widely used insecticide and anthelmintic.
-
BCC5274
Ceftazidime
Ceftazidime (GR20263) is a third generation cephalosporin administered intravenously or intramuscularly. Ceftazidime has a broad spectrum of in vitro activity against Gram-positive and Gram-negative aerobic bacteria. Ceftazidime is particularly active against Enterobacteriaceae (including beta-lactamase-positive strains) and is resistant to hydrolysis by most beta-lactamases.
-
BCC4936
Rifabutin
Rifabutin (Ansamycin) is a semisynthetic ansamycin antibiotic with potent antimycobacterial properties. Rifabutin inhibits DNA-dependent RNA polymerase.
-
BCC5212
Niclosamide monohydrate
Niclosamide monohydrate is an inhibitor of STAT with IC50 of 0.7 μM and inhibits DNA replication in a cell-free assay.
-
BCC5195
Ethambutol
Ethambutol is a bacteriostatic antimycobacterial agent, which obstructs the formation of cell wall by inhibiting arabinosyl transferases.
-
BCC3775
Enoxacin (Penetrex)
Enoxacin is a broad-spectrum 6-fluoronaphthyridinone antibacterial agent.
-
BCC5026
Zalcitabine
Zalcitabine is a potent nucleoside analogue reverse transcriptase inhibitor used in the treatment of HIV infection.
-
BCC6446
Solithromycin
Solithromycin (CEM-101) is an orally bioavailable, effective antimicrobial agent, with IC50s for inhibition of cell viability, protein synthesis, and growth rate are 7.5 ng/mL, 40 ng/mL, and 125 ng/mL for Streptococcus pneumonia, Staphylococcus aureus, and Haemophilus influenzae, respectively. Solithromycin binds to the large 50S subunit of the ribosome and inhibits protein biosynthesis.
-
BCC1392
Azathramycin
Azathramycin (Azaerythromycin A) is an antibiotic.
-
BCN2216
Pimaricin
Natamycin (pimaricin) is an antifungal macrolide polyene that binds to cell membrane sterols.
-
BCC2557
Aztreonam
Aztreonam (SQ-26,776) is a synthetic monocyclic beta-lactam antibiotic, which has a very high affinity for penicillin-binding protein 3 (PBP-3).
-
BCC4889
Amorolfine HCl
Amorolfine hydrochloride (Ro 14-4767/002) is a antifungal reagent.
-
BCC4819
Oxytetracycline (Terramycin)
Oxytetracycline is an antibiotic belonging to the tetracycline class. Oxytetracycline potent inhibits Gram-negative and Gram-positive bacteria. Oxytetracycline is a protein synthesis inhibitor and prevents the binding from aminoacil-tRNA to the complex m-ribosomal RNA. Oxytetracycline also possesses anti-HSV-1 activity.
-
BCC5220
Dapsone
Dapsone is a sulfone active against a wide range of bacteria but mainly employed for its actions against mycobacterium leprae.
-
BCC4916
Loteprednol etabonate
Loteprednol etabonate (LE) is an orally active "soft" steroid belonging to a unique class of glucocorticoids. Loteprednol etabonate (LE) exhibits anti-inflammatory activity and has been used in optometry and ophthalmology.