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Microbiology/Virology

Chemical Structure Cat. No. Product Name CAS No.
Valnivudine hydrochloride Chemical Structure
 BCP38558 Valnivudine hydrochloride 956483-03-7
Valnivudine hydrochloride is a potential fast-acting, once-daily therapy for herpes zoster (shingles) and for the reduction of shingles-associated pain and post-herpetic neuralgia (PHN).
Florfenicol Chemical Structure
 BCP38556 Florfenicol 73231-34-2
Florfenicol is a fluorinated synthetic analog of thiamphenicol with broad-spectrum, primarily bacteriostatic activity.
Porfiromycin Chemical Structure
 BCP38467 Porfiromycin 801-52-5
Porfiromycin is a quinone antibiotic produced by Str. ardus NRRL 2817. It has anti-Gram-positive and negative bacteria activity. It can inhibit sarcoma-180, Ehrlich ascites carcinoma, L-1210, H leukemia (solid type). The dose of inhibiting KB cell protein synthesis was 0.5 μg/mL.
Atpenin A5 Chemical Structure
 BCP38457 Atpenin A5 119509-24-9
Atpenin A5, an antifungal antibiotic, is an ubiquinone-binding site inhibitor of succinate dehydrogenase. Atpenin A5 has cardioprotective effects against simulated ischemia-reperfusion injury in cardiomyocytes.
Gramicidin Chemical Structure
 BCP38466 Gramicidin 1405-97-6
Gramicidin is produced by the strain of Bacillus brevis. It is a family of linear pentadecapeptides isolated from bacillus brevis, and it is a complex of six closely related analogues A1, A2, B1, B2, C1 and C2 where A1 and A2 are the dominant components. It acts by forming channels in cell membranes causing ion leakage, and is an essential bioprobe for understanding the nature of the cell membranes.
Amoscanate Chemical Structure
 BCP38451 Amoscanate 100990-46-3
Amoscanate is an experimental anthelmintic agent of the arylisothiocyanate class which was found to be highly effective in animals against the four major species of schistosomes which infect humans,and is also highly active against hookworm
Cyclosporin U Chemical Structure
 BCP38347 Cyclosporin U 108027-45-8
NITD008 Chemical Structure
 BCP38313 NITD008 1044589-82-3
NITD008 is a flavivirus inhibitor. It was developed as a potential treatment for flavivirus infections, and shows broad spectrum antiviral activity.
Troleandomycin Chemical Structure
 BCP38232 Troleandomycin 2751-09-9
Troleandomycin is a macrolide antibiotic that is similar to Erythromycin.
Ronidazole Chemical Structure
 BCP38196 Ronidazole 7681-76-7
Ronidazole is an antiprotozoal agent.
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