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| Cat. No. | Product Name | Field of Application | Chemical Structure |
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| DC28443 | DHQZ 36 |
DHQZ 36 is a potent inhibitor of retrograde trafficking. DHQZ 36 inhibits Leishmania amazonensis infection in macrophages with an EC50 of 13.63 μM. DHQZ 36 has potent anti-parasite activity.
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| DC28438 | Nigranoic acid |
Nigranoic acid is a triterpenoid separated from Schisandra chinensis. Nigranoic acid inhibits HIV-1 reverse transcriptase. Nigranoic acid exhibits protective effects on brain through PARP/AIF signaling pathway in cerebral ischemia-reperfusion animal model.
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| DC28431 | (S)-BI-1001 |
(S)-BI-1001 (Compound 11) is an active S-enantiomer of BI-1001. (S)-BI-1001 exhibits antiviral potency against HIV-1 integrase with an IC50 of 28 nM, an EC50 of 450 nM and a Kd of 4.7 μM.
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| DC28424 | Dehydroemetine |
Dehydroemetine, a synthetic analogue of emetine dihydrochloride, is used for visceral leishmaniasis. Dehydroemetine used for anti-parasites.
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| DC28403 | Psicofuranine |
Psicofuramine a nucleoside antibiotic and has the inhibition of xanthosine 5'-phosphate aminase. Psicofuranine also specifically inhibits GMP synthase, and interrupts parasite growth. Psicofuranine exhibits a dose-dependent inhibition of P. falciparum growth.
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| DC28282 | (3R,4R)-A2-32-01 |
(3R,4R)-A2-32-01 (compound 2), an anti-virulence drug, is a specific caseinolytic protein proteases (ClpP) inhibitor with an EC50 of 4.5 μM, and shows a tolerable cytotoxicity.
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| DC28259 | BM635 mesylate |
BM635 mesylate is a MmpL3 inhibitor with outstanding anti-mycobacterial activity. BM635 mesylate has a MIC50 of 0.6 μM against M. tuberculosis H37Rv. BM635 mesylate significantly improves the bioavailability compared to free-base BM635.
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| DC28258 | BM635 hydrochloride |
BM635 hydrochloride is a MmpL3 inhibitor with outstanding anti-mycobacterial activity. BM635 hydrochloride has an MIC50 of 0.08 μM against M.tuberculosis H37Rv. BM635 hydrochloride doubles the in vivo exposure with respect to the free base BM635.
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| DC28221 | Rezafungin acetate |
Rezafungin acetate (Biafungin acetate) is a next-generation, broad-spectrum, and long-lasting echinocandin. Rezafungin acetate shows potent antifungal activity against Candida spp., Aspergillus spp., and Pneumocystis spp..
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| DC28191 | Cefathiamidine |
Cefathiamidine is a first-generation cephalosporin antibacterial agent and is used to treat infections caused by susceptible bacteria. Cefathiamidine exhibits a wide spectrum of antimicrobial activity against bacteria. Cefathiamidine is used for the treatment of respiratory, liver, five senses, urinary tract infections, endocarditis and sepsis.
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| DC28181 | Vapendavir diphosphate |
Vapendavir diphosphate (BTA798 diphosphate) is a potent enteroviral capsid binder (CB). Vapendavir diphosphate (BTA798 diphosphate) possesses potent antiviral activity for enterovirus 71 (EV71) replication, with EC50 values of 0.5-1.4 μM in different EV71 strains.
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| DC28135 | Formycin A |
Formycin A (NSC 102811), a ribonucleoside analog, is a potent Human immunodeficiency virus type 1 (HIV-1) inhibitor with an EC50 of 10 μM .
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| DC28108 | Flurofamide |
Flurofamide is a potent bacterial urease inhibitor with potential clinical utility in the treatment of infection induced urinary stones.
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| DC11102 | Taniborbactam |
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| DC10497 | VXc-486 Featured |
VXc-486 is active against drug-resistant isolates, has bactericidal activity, and kills intracellular and dormant M. tuberculosis bacteria in a low-oxygen environment.
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| DCAPI1041 | Valaciclovir HCl |
Valaciclovir HCl
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| DC10286 | Vaborbactam Featured |
Vaborbactam is a cyclic boronic acid pharmacophore β-lactamase inhibitor.
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| DC9618 | TMC353121 |
TMC353121 is a potent RSV fusion inhibitor with pEC50 of 9.9(t1/2 in lung = 25 h).
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| DCAPI1383 | Terbinafine (Lamisil, Terbinex) |
Terbinafine (Lamisil, Terbinex)
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| DC7940 | TBA-354 |
TBA-354 is a potent anti-tuberculosis compound; maintains activity against Mycobacterium tuberculosis H37Rv isogenic monoresistant strains and clinical drug-sensitive and drug-resistant isolates.
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| DC10180 | ST-193 hydrochlorid |
ST-193 hydrochloride is a potent broad-spectrum arenavirus inhibitor; inhibits Guanarito, Junin, Lassa and Machupo virus with IC50 values of 0.44, 0.62, 1.4 and 3.1 nM, respectively.
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| DC8612 | Simeprevir(TMC-435) |
Simeprevir (TMC 435350) is a potent inhibitor of HCV NS3/4A protease (Ki = 0.36 nM) and viral replication (replicon EC50 = 7.8 nM).
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| DC9864 | Azidothymidine (AZT) |
Selective reverse transcriptase inhibitor. Exhibits 100-fold selectivity for HIV reverse transcriptase over DNA polymerase α.
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| DC8628 | Saquinavir Mesylate Featured |
Saquinavir(Ro 31-8959) is an HIV Protease inhibitor used in antiretroviral therapy.
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| DC8627 | Saquinavir Featured |
Saquinavir(Ro 31-8959) is an HIV Protease inhibitor used in antiretroviral therapy.
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| DC10435 | RSV604 racemate |
RSV604 racemate is a racemic mixture, shows less potency against strains of respiratory syncytial virus (RSV) than the S-isomer.
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| DCAPI1325 | Rifabutin (Mycobutin) |
Rifabutin (Mycobutin)
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| DC4148 | Retapamulin |
Retapamulin is a topical antibiotic, which binds to both E. coli and S. aureus ribosomes with similar potencies with Kd of 3 nM.
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| DC9479 | Raltegravir (potassium salt) |
Raltegravir potassium salt(MK0518 potassium salt) is a potent integrase (IN) inhibitor, used to treat HIV infection.
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| DC8930 | Rafoxanide |
Rafoxanide is a salicylanilide used as an antiparasitic agent.
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