
Microbiology/Virology
Microbiology and virology inhibitors are compounds that target microorganisms, including bacteria, viruses, and fungi, disrupting their growth, replication, or survival. These inhibitors are essential for studying microbial pathogenesis, understanding resistance mechanisms, and developing new antimicrobial and antiviral therapies. Inhibitors in this category are used to combat infectious diseases, explore microbial ecology, and investigate host-pathogen interactions. At CymitQuimica, we provide a broad selection of high-quality microbiology and virology inhibitors to support your research in infectious diseases, microbiology, and virology.
Subcategories of "Microbiology/Virology"
- Antibacterial(2,966 products)
- Antibiotic(922 products)
- Antifection(23 products)
- DHFR(33 products)
- DNA/RNA Synthesis(710 products)
- HBV(177 products)
- HIV Protease(450 products)
- HSV(91 products)
- Integrase(2 products)
- Ribosome(13 products)
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Found 5858 products of "Microbiology/Virology"
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Neuraminidase-IN-10
CAS:<p>Neuraminidase-IN-10 inhibits flu virus strains H1N1, H5N1, and H5N8 with IC50 values of 2.6, 5.1, and 1.65 nM respectively.</p>Formula:C26H34N2O5SColor and Shape:SolidMolecular weight:486.62Chlorfenson
CAS:<p>Chlorfenson is used to treat onychomycosis as the primary indication.</p>Formula:C12H8Cl2O3SColor and Shape:SolidMolecular weight:303.16Tromantadine
CAS:Tromantadine is an amantadine derivative with antiherpetic activity (inhibits HSV-1 and HSV-2 replication).Formula:C16H28N2O2Purity:98%Color and Shape:SolidMolecular weight:280.41S 2720
CAS:<p>S 2720 is a human immunodeficiency virus type 1 (HIV-1)-specific reverse transcriptase (RT) inhibitor quinoxaline.</p>Formula:C14H15ClN2O2SColor and Shape:SolidMolecular weight:310.8UNC10201652
CAS:<p>UNC10201652 inhibits intestinal L1-specific β-glucuronidases; effective against E. coli (IC50: 0.117 μM).</p>Formula:C20H25N7OSColor and Shape:SolidMolecular weight:411.52Epsiprantel
CAS:<p>Epsiprantel is an orally active antiparasitic drug that inhibits various tapeworms, including Echinococcus granulosus (granular echinococcus), in dogs.</p>Formula:C20H26N2O2Purity:98.09%Color and Shape:SolidMolecular weight:326.43ThrRS-IN-1
CAS:<p>ThrRS-IN-1 inhibits Salmonella ThrRS with IC50 1.4μM, Kd 1.36μM, targets tRNA/L-threonine sites, has strong antibacterial effects.</p>Formula:C16H18Cl2N4O3Color and Shape:SolidMolecular weight:385.25Methenamine mandelate
CAS:<p>Methenamine mandelate-loaded nanoparticles can induce DNA damage and apoptosis of cancer cells.</p>Formula:C14H20N4O3Color and Shape:SolidMolecular weight:292.33TKB245
CAS:<p>TKB245为SARS-CoV-2 Mpro的高效抑制剂,能有效抑制VeroE6细胞内SARS-CoV-2的复制。</p>Formula:C30H35F4N5O5SPurity:98%Color and Shape:SolidMolecular weight:653.69HBV-IN-19
CAS:<p>HBV-IN19 suppresses HBV, cutting HBsAg output, useful for chronic HBV study.</p>Formula:C24H30N2O6Color and Shape:SolidMolecular weight:442.5Antimalarial agent 24
CAS:<p>Compound 24 (Compound 7), an in vitro antimalarial agent, demonstrates inhibitory activity against the Plasmodium falciparum W2 strain with an IC50 of 0.81 μM</p>Formula:C20H16N4O2Purity:98%Color and Shape:SolidMolecular weight:344.37SARS-CoV-2 nsp14-IN-3
CAS:<p>SARS-CoV-2 nsp14-IN-3 (4975) is a potent inhibitor targeting the N7-Methyltransferase activity of SARS-CoV-2 nonstructural protein 14 (Nsp14), with an IC50</p>Formula:C17H17N3O3SPurity:98%Color and Shape:SolidMolecular weight:343.4Nifuroxime
CAS:<p>Nifuroxime, an anti-infective agent, is utilized in researching fungal infections.</p>Formula:C5H4N2O4Color and Shape:SolidMolecular weight:156.1Ofurace
CAS:<p>Ofurace is a fungicide.</p>Formula:C14H16ClNO3Purity:98%Color and Shape:SolidMolecular weight:281.73Antitrypanosomal agent 4
CAS:<p>Compound 19: potent, blood-brain penetrant antitrypanosomal; IC50: T. cruzi 1.2 μM, T.b. brucei 70 nM.</p>Formula:C18H14ClN3O5SColor and Shape:SolidMolecular weight:419.84VP-4556
CAS:<p>VP-4556 is a potent anti-MRSA compound with >95% inhibition at 8 μg/mL MIC.</p>Formula:C12H12N2O4SColor and Shape:SolidMolecular weight:280.3BPH-1358 free base
CAS:<p>BPH-1358 inhibits UPPS (IC50: 110 nM) and FPPS (IC50: 1.8 µM), effective against S. aureus (MIC ~250 ng/mL).</p>Formula:C32H28N6O2Purity:98%Color and Shape:SolidMolecular weight:528.6Flomoxef sodium
CAS:<p>Flomoxef sodium, an antibiotic belonging to the oxacephem group, exhibits excellent activity against a broad spectrum of Gram-positive bacteria.</p>Formula:C15H17F2N6NaO7S2Purity:97.88%Color and Shape:SolidMolecular weight:518.44Syncytial Virus Inhibitor-1
CAS:<p>Syncytial Virus Inhibitor-1: Potent, oral RSV fusion blocker (EC50: 0.002-0.004 μM for Long, A2, B strains).</p>Formula:C23H26N4O3SPurity:98%Color and Shape:SolidMolecular weight:438.54OX11
CAS:<p>OX11 is a selective inhibitor of S. pneumoniae, P. aeruginosa and E. coli bacteria.</p>Formula:C17H10Cl2N4O3S2Color and Shape:SolidMolecular weight:453.32RSV/IAV-IN-3
CAS:<p>RSV/IAV-IN-3 is a dual inhibitor of RSV (EC50: 2.92μM) and IAV (EC50:1.90μM), blocking virus replication post-entry.</p>Formula:C19H19BrN2O3SColor and Shape:SolidMolecular weight:435.3341F5
CAS:<p>41F5: Anti-fungal with MIC50 0.4-0.8 μM and IC50 0.87 μM against Histoplasma; 62x more selective for yeast vs host cells.</p>Formula:C21H22N2OSColor and Shape:SolidMolecular weight:350.48MMV008138
CAS:<p>MMV008138 inhibits the growth of P. falciparum Dd2 strain (IC50 of 250 nM).</p>Formula:C18H14Cl2N2O2Color and Shape:SolidMolecular weight:361.22BDM91514
CAS:<p>BDM91514 enhances antibiotic efficacy by inhibiting AcrB, effectively curbing the proliferation of E.</p>Formula:C13H19Cl3N6OColor and Shape:SolidMolecular weight:381.69PC190723
CAS:<p>PC190723 is an inhibitor of the bacterial cytosolic protein FtsZ with antimicrobial activity against Staphylococcus spp.</p>Formula:C14H8ClF2N3O2SPurity:97.64%Color and Shape:SolidMolecular weight:355.75SARS-CoV-2 nsp13-IN-5
CAS:<p>SARS-CoV-2 nsp13-IN-5 inhibits nsp13, affects ssDNA+/-ATPase (IC50: 50/55 μM), useful for COVID-19 research.</p>Formula:C28H30N4O4SColor and Shape:SolidMolecular weight:518.63LY 186826
CAS:<p>LY 186826 is an antibacterial agent with bicyclic pyrazolidinone properties.</p>Formula:C15H16N6O6SPurity:98%Color and Shape:SolidMolecular weight:408.39Tromantadine hydrochloride
CAS:Tromantadine hydrochloride is an amantadine derivative with antiherpetic activity (inhibits HSV-1 and HSV-2 replication).Formula:C16H29ClN2O2Purity:98%Color and Shape:SolidMolecular weight:316.87RO-9187
CAS:<p>RO-9187 is an effective HCV virus replication inhibitor(IC50: 171 nM).</p>Formula:C9H12N6O5Purity:98%Color and Shape:SolidMolecular weight:284.23Selgantolimod
CAS:Selgantolimod is an effective and selective toll-like receptor 8 agonists for the treatment of the hepatitis B virus and human immunodeficiency virus infection.Formula:C14H20FN5OPurity:98%Color and Shape:SolidMolecular weight:293.34SARS-CoV-IN-3
CAS:SARS-CoV-IN-3 is an effective SARS-CoV replication inhibitor.Formula:C25H28ClFeN3OPurity:98%Color and Shape:SolidMolecular weight:477.8116,17-Dihydroheronamide C
CAS:<p>16,17-Dihydroheronamide C is a probe used for the analysis of the mode of action of heronamide C, which has antifungal properties.</p>Formula:C29H41NO3Color and Shape:SolidMolecular weight:451.64(3R,4R)-A2-32-01
CAS:(3R,4R)-A2-32-01 is the (R,R)-enantiomer of A2-32-01 and has potential antibacterial activity.Formula:C19H27NO2Purity:98.19%Color and Shape:SolidMolecular weight:301.42Antitubercular agent-31
CAS:<p>Antitubercular agent-31 is an antitubercular agent that inhibits M. tuberculosisH37Rv (MIC: 0.03 μM) and also inhibits DprE1 (IC50: 1.1 μM).</p>Formula:C20H24F2N4O5S2Color and Shape:SolidMolecular weight:502.56SABA1
CAS:<p>SABA1 has antibacterial activity, inhibiting Pseudomonas aeruginosa and Escherichia coli, and also inhibits biotin carboxylase.</p>Formula:C22H19ClN2O5SPurity:98.36%Color and Shape:SolidMolecular weight:458.92Antibacterial agent 100
CAS:<p>Compound 7c: Antibacterial/fungal, effective on S. aureus, C. albicans (MIC 4 μg/mL), C. neoformans (MIC 8 μg/mL).</p>Formula:C28H29BrN2Color and Shape:SolidMolecular weight:473.458BM635
CAS:<p>BM635 is an MmpL3 inhibitor with outstanding anti-mycobacterial activity (MIC50: 0.12 μM against M. tuberculosis H37Rv).</p>Formula:C25H29FN2OColor and Shape:SolidMolecular weight:392.51Anti-Influenza agent 4
CAS:<p>Anti-Influenza agent 4 selectively inhibits A/Parma (EC50: 62 nM) and A/Roma (EC50: 150 nM) influenza strains.</p>Formula:C19H18N2O5SPurity:98.94% - 98.95%Color and Shape:SolidMolecular weight:386.42HIV-1 inhibitor-34
CAS:<p>HIV-1 inhibitor-34 (5q): potent, selective; EC50: 6.4 nM; MT-4 CC50: 16 μM; useful in AIDS research.</p>Formula:C26H27N7OColor and Shape:SolidMolecular weight:453.54Antifungal agent 36
CAS:<p>Antifungal agent 36 is a potent anti-fungal agent that shows anti-fungal activity for Basidiomycetes [1].</p>Formula:C14H21NO2Color and Shape:SolidMolecular weight:235.32PXYC2
CAS:<p>PXYC2 is an RpsA-CTD antagonist; Kd: 6.35 μM for RpsA-CTD, 5.11 μM for RpsA-CTD Δ438A; vital in trans-translation.</p>Formula:C7H6N4O3SColor and Shape:SolidMolecular weight:226.21WAY 150138
CAS:<p>WAY 150138 inhibits the herpes simplex virus.</p>Formula:C22H18Cl2FN3O3SColor and Shape:SolidMolecular weight:494.37Benzylurea
CAS:<p>Benzylurea (AI3-61350) competitively inhibits dehydrogenase/cytokinin oxidase.</p>Formula:C8H10N2OPurity:98%Color and Shape:SolidMolecular weight:150.18S-(N-PhenethylthiocarbaMoyl)-L-cysteine
CAS:<p>PEITC-Cys: anticarcinogenic, antileukemic, inhibits DNA synthesis in HL60, P450 inhibitor.</p>Formula:C12H16N2O2S2Color and Shape:SolidMolecular weight:284.4D77
CAS:D77 is anti-HIV-1 inhibitor. D77 inhibits HIV-1(IIIB) replication by EC50 value of 23.8 μg/ml in MT-4 cell (5.03 μg/ml for C8166 cells).Formula:C28H22BrNO7SPurity:98%Color and Shape:SolidMolecular weight:596.45Direct Black 38 free acid
CAS:<p>Ferristatin II (Direct Black 38 free acid) is a polysulphonated dye and promotes the degradation of transferrin receptor-1 in vitro and in vivo.</p>Formula:C34H27N9O7S2Purity:98%Color and Shape:SolidMolecular weight:737.77Adafosbuvir PM
CAS:<p>Adafosbuvir PM (AL-335 PM) is a small molecule NS5B inhibitor that can be used to study chronic hepatitis C.</p>Formula:C10H13FN2O6Purity:97.08%Color and Shape:SolidMolecular weight:276.22MurA-IN-3
CAS:<p>MurA-IN-3, a reversible pyrrolidinedione-based MurA inhibitor, exhibits an IC50 of 4.5 μM against MurA and demonstrates antibacterial activity [1].</p>Formula:C27H23ClN2O5SColor and Shape:SolidMolecular weight:523Antitubercular agent-26
CAS:<p>Compound 32: oral antitubercular, acts on M. tuberculosis, IC50 ~0.50μM, stable, low cardiotoxicity, non-genotoxic.</p>Formula:C22H23N5O3S2Color and Shape:SolidMolecular weight:469.58Berteroin
CAS:<p>Berteroin, found in cruciferous veggies like rucola and mustard, may act as an antioxidant, reducing inflammation and androgen receptors in cancer.</p>Formula:C7H13NS2Color and Shape:SolidMolecular weight:175.31ATD-3169
CAS:<p>ATD-3169 is a ROS generator with antibacterial activity.</p>Formula:C15H14O3Purity:98%Color and Shape:SolidMolecular weight:242.27A3N19
CAS:<p>A3N19 is a potent inhibitor of HIV-1 non-nucleoside reverse transcriptase and is able to act on HIV-1 IIIB (EC50: 3.28 nM).</p>Formula:C31H31N9O2SColor and Shape:SolidMolecular weight:593.7PXYC13
CAS:<p>PXYC13 inhibits Mtb RpsA essential for trans-translation with Kd of 7.61 μM; less effective on RpsA-CTD Δ438A (Kd 8.50 μM).</p>Formula:C15H15N5O2SColor and Shape:SolidMolecular weight:329.38Cefepime chloride
CAS:<p>Cefepime chloride, a broad-spectrum cephalosporin, combats Gram-positive/negative bacteria and can induce neurotoxicity.</p>Formula:C19H25ClN6O5S2Color and Shape:SolidMolecular weight:517.02Urease-IN-5
<p>Urease-IN-5: urease inhibitor, IC50 1.473 µM, low cytotoxicity, IC50 17.78 µg/mL on P. vulgaris.</p>Formula:C16H20N2O3SColor and Shape:SolidMolecular weight:320.41HBV-IN-16
CAS:<p>HBV-IN-16, a quinoline derivative, inhibits HBV cccDNA, key for viral replication (from patent WO2019121357A1).</p>Formula:C22H20ClNO4Color and Shape:SolidMolecular weight:397.85Isobellidifolin
CAS:<p>Isobellidifolin, a xanthone compound, serves as a free radical scavenger and antioxidant. It exhibits a potent antifungal effect.</p>Formula:C14H10O6Color and Shape:SolidMolecular weight:274.23DMJ-I-228
CAS:<p>DMJ-I-228 is a specific inhibitor of HIV-1 entry through interaction with the Env spike by virtue of the incorporation of a guandinium group.</p>Formula:C19H19ClFN5O4Color and Shape:SolidMolecular weight:435.84HIV-1 inhibitor-38
CAS:<p>HIV-1 inhibitor-38, or Compound 91, shows promise as a strong latency reversing agent against HIV-1.</p>Formula:C15H13Cl3N6Color and Shape:SolidMolecular weight:383.66SARS-CoV-2-IN-16
CAS:<p>SARS-CoV-2-IN-16 strongly inhibits NPro, with EC50 of 3.69 μM and Kd of 7.82 μM, suggesting effective binding and antiviral properties.</p>Formula:C17H20N2O2Color and Shape:SolidMolecular weight:284.35MurA-IN-2
CAS:<p>MurA-IN-2: potent MurA inhibitor, IC50 of 39μM, chloroacetamide with aliphatic amine; has antibacterial properties.</p>Formula:C12H20ClNOColor and Shape:SolidMolecular weight:229.75Anthrarobin
CAS:<p>Anthrarobin is an antipsoriatic.</p>Formula:C14H10O3Purity:98%Color and Shape:SolidMolecular weight:226.23Antitubercular agent-18
CAS:<p>Antitubercular agent-18 (9a) MIC: 2 μg/ml for H37Rv, Spec 192, 210; 128 μg/ml for Spec 800. Selective antimycobacterial.</p>Formula:C14H12BrN5OColor and Shape:SolidMolecular weight:346.18F8-S43-S3
CAS:<p>F8-S43-S3 is a SARS-CoV-2 main protease inhibitor (IC 50 = 9.69 μM) [1].</p>Formula:C12H10N4O3SColor and Shape:SolidMolecular weight:290.3Antimalarial agent 16
CAS:<p>Antimalarial agent 16 is a parasite inhibitor that exhibits antimalarial effects and inhibits the growth of Plasmodium falciparum with an IC50 value of 2.0 nM.</p>Formula:C30H32N2O6Color and Shape:SolidMolecular weight:516.58Antifungal agent 30
CAS:<p>Potent antifungal, works against Candida albicans (MIC: 0.03 μg/mL) & Aspergillus fumigatus (MIC: 0.5 μg/mL) via CYP51 interactions.</p>Formula:C18H14Cl2F2N2SeColor and Shape:SolidMolecular weight:446.18Vps34-IN-2
CAS:<p>Vps34-IN-2 is a potent and selective Vps34 inhibitor (IC50s: 2 and 82 nM on the Vps34 enzymatic assay and the GFP-FYVE cellular assay, respectively).</p>Formula:C18H25F3N4O3Purity:98%Color and Shape:SolidMolecular weight:402.41Bunamidine hydrochloride
CAS:<p>Bunamidine hydrochloride is a veterinary anthelmintic that acts against Echinococcus granulosus and Tapeworm.</p>Formula:C25H39ClN2OColor and Shape:SolidMolecular weight:419.05SARS-CoV-2 3CLpro-IN-3
CAS:SARS-CoV-2 3CLpro-IN-3 is a SARS CoV-2 3CLpro inhibitor that exhibits antiviral, antibacterial, and antifungal effects.Formula:C23H21BrN6O2SColor and Shape:SolidMolecular weight:525.42Sotirimod
CAS:<p>Sotirimod(R850) is a novel immunomodulator with antitumor and antiviral activity for the study of actinic keratoses.</p>Formula:C14H17N5Purity:95.87%Color and Shape:SolidMolecular weight:255.32FR900098 (sodium salt)
CAS:<p>FR900098, a fosmidomycin derivative, has potent antimalarial effects, targeting DOXP reductoisomerase and eradicating P. vinckei in mice at >10 mg/kg.</p>Formula:C5H12NNaO5PColor and Shape:SolidMolecular weight:220.117Diamthazole hydrochloride
CAS:<p>Diamthazole (Dimazole) hydrochloride, an antifungal agent, is utilized in infection research.</p>Formula:C15H24ClN3OSColor and Shape:SolidMolecular weight:329.89SSJ-183
CAS:<p>SSJ-183 is a low-toxicity and orally available and anti-malarial drug with an IC50 = 7.6 nM against P. falciparum and no lethality at doses up to 2000 mg/kg po.</p>Formula:C25H22N4OPurity:99.71% - 99.83%Color and Shape:SolidMolecular weight:394.472-Hydroxydocosanoic acid
CAS:<p>2-Hydroxydocosanoic acid exhibits antioxidant, cholinesterase inhibitory, and antimicrobial properties [1].</p>Formula:C22H44O3Color and Shape:SolidMolecular weight:356.58Antitubercular agent-17
CAS:<p>Compound 8a: Antitubercular with MIC of 2 μg/ml for H37Rv, Spec 192, 210; 128 μg/ml for Spec 800. Selective effects.</p>Formula:C14H12BrN5OColor and Shape:SolidMolecular weight:346.18Antibacterial agent 121
CAS:<p>Antibacterial agent 121 exhibits anti-TB and anti-inflammatory properties.</p>Formula:C18H22N2O3SColor and Shape:SolidMolecular weight:346.44Lufotrelvir
CAS:Lufotrelvir (PF-07304814), a prodrug of PF-00835231, is a potent SARS-CoV-2 3CL protease inhibitor with antiviral properties, Ki 174nM.Formula:C24H33N4O9PPurity:99.43% - >99.99%Color and Shape:SolidMolecular weight:552.51(Rac)-SHIN2
CAS:(Rac)-SHIN2 is a serine hydroxymethyltransferase (SHMT) inhibitor for the study of T-cell acute lymphoblastic leukemia (T-ALL).Formula:C23H26N4O3Purity:98.165% - 99.48%Color and Shape:SolidMolecular weight:406.48Antimalarial agent 12
CAS:<p>Antimalarial 12 inhibits P. falciparum, EC50: 136-155 nM, not E. coli (MIC >250,000 nM), affects HEK-293/hPHep, CC50: 10,000-50,000 nM.</p>Formula:C26H18BrClN2O2Color and Shape:SolidMolecular weight:505.79Antitubercular agent-14
CAS:<p>Antitubercular agent-14 (Compound 1) shows antitubercular activity. The MIC value of Antitubercular agent-14 against M. tuberculosis is 0.3 μg/mL [1].</p>Formula:C20H27ClN2Color and Shape:SolidMolecular weight:330.89Anticandidal agent-1
CAS:<p>Compound C2 is a broad-spectrum anticandidal, blocking biofilm and filament growth with MIC50 of 13.51μg/mL (C. glabrata) and 8.65μg/mL (C. albicans).</p>Formula:C19H22O5Color and Shape:SolidMolecular weight:330.38LabMol-301
CAS:<p>LabMol-301 blocks NS5 RdRp/NS2B-NS3pro (IC50: 0.8/7.4µM), protects cells from ZIKV death.</p>Formula:C18H16N6Color and Shape:SolidMolecular weight:316.36SARS-CoV-2-IN-31
CAS:<p>SARS-CoV-2-IN-31: COVID-19 inhibitor, IC50: 28.84-38.36 μM, useful in cancer studies.</p>Formula:C29H28N4O2Color and Shape:SolidMolecular weight:464.56PXYD3
CAS:<p>PXYD3 inhibits RpsA-CTD (Kd: 5.66 μM) & RpsA-CTD Δ438A (Kd: 6.91 μM) crucial in Mtb translocation.</p>Formula:C25H21NO5Color and Shape:SolidMolecular weight:415.44Antitubercular agent 34
CAS:<p>Compound 42g: potent antitubercular, MIC 90 of 1.25 µg/mL, resists liver metabolism.</p>Formula:C19H14N4O2SColor and Shape:SolidMolecular weight:362.41Floxacrine
CAS:<p>Floxacrine is drug candidate for chemoprophylaxis of malaria.</p>Formula:C20H13ClF3NO3Purity:98%Color and Shape:SolidMolecular weight:407.77Mtb-cyt-bd oxidase-IN-6
CAS:<p>Mtb-cyt-bd oxidase-IN-6, a potent inhibitor of Mycobacterium tuberculosis (Mtb) cytochrome bd (cyt-bd) oxidase (MtbCyt-bd Oxidase), exhibits an inhibitory</p>Formula:C20H27NOColor and Shape:SolidMolecular weight:297.43Antitrypanosomal agent 10
<p>Antitrypanosomal agent 10, an antitrypanosomal compound, effectively inhibits Trypanosoma cruzi with an IC50 of 0.28 μM.</p>Formula:C17H9F6N5OColor and Shape:SolidMolecular weight:413.28Sitamaquine tosylate
CAS:<p>Sitamaquine: antileishmanial, targets L. donovani species, EC50 = 9.5-19.8 μM, inhibits mitochondrial complex II, induces apoptosis in promastigotes.</p>Formula:C28H41N3O4SColor and Shape:SolidMolecular weight:515.71Antimalarial agent 11
CAS:<p>Antimalarial compound 1: Spirocyclic chromane, EC50 - D6: 1.48 μM, ARC08-022: 1.81 μM.</p>Formula:C25H25F2NO3Color and Shape:SolidMolecular weight:425.47SARS-CoV-2 3CLpro-IN-7
CAS:<p>SARS-CoV-2 3CLpro-IN-7 is a reversible covalent inhibitor of the SARS-CoV-2 3CL protease, exhibiting an inhibitory concentration (IC50) value of 1.4 µM.</p>Formula:C24H17ClN2O6Color and Shape:SolidMolecular weight:464.85DHQZ 36
CAS:<p>DHQZ 36: retrograde trafficking inhibitor, anti-parasite, stops Leishmania amazonensis (EC50: 13.63 μM).</p>Formula:C21H18F2N2OSPurity:98%Color and Shape:SolidMolecular weight:384.44Halofantrine, (-)-
CAS:<p>Halofantrine, (-)- is an antimalarial agent.</p>Formula:C26H30Cl2F3NOColor and Shape:SolidMolecular weight:500.42Cap-dependent endonuclease-IN-21
CAS:<p>Cap-dependent endonuclease-IN-21 inhibits CEN and flu virus replication, potential against influenza A. (From patent WO2021233302A1, compound 8B/8A)</p>Formula:C26H23F2N3O7Color and Shape:SolidMolecular weight:527.47Afabicin
CAS:<p>Afabicin is an antibiotic targeting Staphylococcus aureus. treat acute bacterial skin and skin structure infections.the prodrug of Debio1452.</p>Formula:C23H24N3O7PPurity:98%Color and Shape:SolidMolecular weight:485.43GW-695634
CAS:<p>GW-695634, a non-nucleoside reverse transcriptase inhibitor, is used potentially for the treatment of HIV infection.</p>Formula:C26H21Cl2N3O6SColor and Shape:SolidMolecular weight:574.43HIV-1 inhibitor-31
CAS:<p>HIV-1 inhibitor-31 (compound 4) is a potent inhibitor of HIV-1. HIV-1 inhibitor-31 can be used in the study of AIDS.</p>Formula:C21H13Cl2N3O2Color and Shape:SolidMolecular weight:410.25S-1360
CAS:<p>S-1360 is an inhibitor of HIV-1 integrase.</p>Formula:C16H12FN3O3Purity:98%Color and Shape:SolidMolecular weight:313.28Antitumor agent-85
<p>Antitumor agent-85 stabilizes G4-DNA with potent anti-tumor effects.</p>Formula:C24H33N7Color and Shape:SolidMolecular weight:419.57Antiviral agent 23
CAS:<p>Antiviral agent 23 targets EV71 with 94 nM EC50 and suppresses METTL3/14, useful in infection research.</p>Formula:C18H21N5O4Color and Shape:SolidMolecular weight:371.39

