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(2,957 products)
- Antibiotic(920 products)
- Antifection(23 products)
- DHFR(33 products)
- DNA/RNA Synthesis(708 products)
- HBV(176 products)
- HIV Protease(449 products)
- HSV(91 products)
- Integrase(2 products)
- Ribosome(13 products)
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Found 5842 products of "Microbiology/Virology"
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BO3482
CAS:<p>BO3482 is an antimicrobial compound and can inhibit the growth of methicillin-resistant Staphylococci (MIC90: 6.25 mg/mL).</p>Formula:C14H20N2NaO5S2Purity:98%Color and Shape:SolidMolecular weight:383.43Purfalcamine
CAS:<p>Purfalcamine, a selective PfCDPK1 inhibitor effective against malaria, has IC50 of 17 nM and EC50 of 230 nM; halts parasites at schizont stage.</p>Formula:C29H33FN8OColor and Shape:SolidMolecular weight:528.62Antiviral 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:371.39Tolindate
CAS:<p>Tolindate, a potent PXR agonist, demonstrates antifungal activity and possesses an EC50 value of 8.3 µM.</p>Formula:C18H19NOSColor and Shape:SolidMolecular weight:297.41PF-46396
CAS:<p>PF-46396 is a HIV maturation inhibitor and can be used against HIV-1 clade B and C.</p>Formula:C27H29F3N2OColor and Shape:SolidMolecular weight:454.53Antistaphylococcal agent 2
CAS:<p>Antistaphylococcal agent 2 is an anti-staphylococcal therapeutic agent.</p>Formula:C23H21N5O5Color and Shape:SolidMolecular weight:447.44Sch 25393
CAS:Sch 25393 is an antibacterial agent in vitro.Formula:C12H14F3NO4SPurity:98%Color and Shape:SolidMolecular weight:325.3CP-320626
CAS:<p>CP-320626 is an effective human liver glycogen phosphorylase (GP) inhibitor with cholesterol-lowering activity, used in type 2 diabetes research.</p>Formula:C23H23ClFN3O3Purity:98.06%Color and Shape:SolidMolecular weight:443.9B 669
CAS:<p>B 669 has antibacterial activity.</p>Formula:C30H28N4Color and Shape:SolidMolecular weight:444.57IACS-4759
CAS:<p>IACS-4759 is a novel potent and selective MTH1 inhibitor with excellent cell permeability and good metabolic stability in microsomes.</p>Formula:C10H17N3O2Color and Shape:SolidMolecular weight:211.26Antimicrobial agent-1
CAS:<p>Antimicrobial Agent-1 (compound 6C) shows strong activity (MIC = 2 μg/mL) against TolC mutant E.</p>Formula:C22H21N3O2SColor and Shape:SolidMolecular weight:391.49As-358 hydrochloride
CAS:<p>As-358 (hydrochloride) shows well in vivo safety as well as inhibits Ebola virus and Marburg virus with IC 50 values of 9.1 μM and 18.1 μM [1].</p>Formula:C18H32ClNO2Color and Shape:SolidMolecular weight:329.91Antiviral agent 9
<p>Antiviral agent 9: EC50 0.006 nM vs HIV-1, 300x more selective than TAF.</p>Formula:C38H50N7O8PColor and Shape:SolidMolecular weight:763.82ERCC1-XPF-IN-1
CAS:<p>ERCC1-XPF-IN-1: potent ERCC1-XPF inhibitor (IC50: 0.49 μM), hampers CPD removal, boosts UV toxicity, hinders DNA repair.</p>Formula:C28H32ClN5O2Color and Shape:SolidMolecular weight:506.04HIV-1 inhibitor-48
CAS:<p>HIV-1 inhibitor-48 is a novel non-nucleoside reverse transcriptase inhibitor (NNRTI) and exhibits anti-HIV-1 activity .</p>Formula:C19H16BrN5Color and Shape:SolidMolecular weight:394.27HIV-1 inhibitor-35
CAS:<p>HIV-1 inhibitor-35, potent against HIV (EC50: 80 nM LTR, 70 nM CMV), also suppresses HepG2 cells (CC50: 40 nM), may reverse HIV-1 latency.</p>Formula:C13H12Cl3N5OSColor and Shape:SolidMolecular weight:392.69ZG-10
CAS:<p>ZG-10 (JNK-IN-2) is an inhibitor of JNK, blocking JNK1, JNK2, and JNK3, and is used in studies of SARS-CoV-2 virus infection.</p>Formula:C28H27N7O2Purity:99.41% - 99.91%Color and Shape:SolidMolecular weight:493.56Vebufloxacin
CAS:<p>Vebufloxacin (OPC-7251) shows potent antibacterial activity against gram-positive and -negative bacteria, including Staphylococcus aureus and Pseudomonas</p>Formula:C19H22FN3O3Purity:98%Color and Shape:SolidMolecular weight:359.39Influenza virus-IN-4
CAS:<p>Influenza virus-IN-4 (compound 11e) is a potent inhibitor of influenza virus neuraminidase, acting on H5N1 (IC50: 3.4 μM), H5N2 (IC50: 0.094 μM), H5N6 (IC50: 0.</p>Formula:C23H31FN2O4Color and Shape:SolidMolecular weight:418.5Nucleoside-Analog-2
CAS:<p>Nucleoside-Analog-2 is a 4'-Azidocytidine analogue, used to against Hepatitis C virus (HCV) replication.</p>Formula:C9H11N5O6Purity:98%Color and Shape:SolidMolecular weight:285.21Pam 1392
CAS:<p>Pam 1392 is a chemotherapeutic agent.</p>Formula:C15H13Cl2N5Color and Shape:SolidMolecular weight:334.2NSC666715
CAS:<p>NSC666715 is the strand-displacement activity of DNA polymerase inhibitor.</p>Formula:C15H13Cl2N5O2S2Purity:98%Color and Shape:SolidMolecular weight:430.33Mtb-cyt-bd oxidase-IN-4
<p>Mtb-cyt-bd oxidase inhibitor; IC50=0.25μM; MIC=8μM against Mycobacterium tuberculosis; for TB research.</p>Formula:C25H32FNOColor and Shape:SolidMolecular weight:381.53BA38017
CAS:<p>BA38017 is a potent assembly modulator of HBV core protein that inhibits the replication of HBV (EC50 = 0.20 μM) [1].</p>Formula:C15H11ClFNO3Color and Shape:SolidMolecular weight:307.7Efavirenz, (R)-
CAS:<p>Efavirenz, (R)- is an antiviral agent and a nonnucleoside HIV-1 reverse transcriptase inhibitor.</p>Formula:C14H9ClF3NO2Color and Shape:SolidMolecular weight:315.67Antimycobacterial agent-3
CAS:<p>Antimycobacterial agent-3: low toxicity, fights MTB H37Rv and drug-resistant strains (MIC 0.029-0.110 μM).</p>Formula:C21H15F6N5O4SColor and Shape:SolidMolecular weight:547.43Antistaphylococcal agent 1
CAS:<p>Antistaphylococcal agent 1 is an antistaphylococcal therapeutic agent.</p>Formula:C22H16N6O2Color and Shape:SolidMolecular weight:396.4Enisamium iodide
CAS:<p>Enisamium iodide is used as an antiviral agent.</p>Formula:C14H15IN2OColor and Shape:SolidMolecular weight:354.19Biclotymol
CAS:<p>Biclotymol is used in the study about infectious oropharyngeal diseases.</p>Formula:C21H26Cl2O2Purity:98.56%Color and Shape:SolidMolecular weight:381.34M2 ion channel blocker
CAS:<p>M2 ion channel blocker ,Antiviral agent, is capable of inhibiting and blocking the activity of M2 ion channel.</p>Formula:C18H27N3O2Purity:98%Color and Shape:SolidMolecular weight:317.43Antiviral agent 19
CAS:<p>Antiviral agent 19 (Compound 3) is a selective inhibitor of Zika virus (EC50: 1.3 μM) with low cytotoxicity.</p>Formula:C29H35NO5Color and Shape:SolidMolecular weight:477.59Antibacterial agent 64
CAS:<p>Potent antibacterial, YycG inhibitor with 6.1 µM IC50. Synergistic with ampicillin against biofilm bacteria.</p>Formula:C29H20ClN3O6S2Color and Shape:SolidMolecular weight:606.07Antibacterial agent 115
CAS:<p>Antibacterial agent 115 is an antibacterial and anti-inflammatory agent that is active when taken orally.</p>Formula:C35H48N2O3Color and Shape:SolidMolecular weight:544.77Covidcil-19
CAS:<p>Covidcil-19 targets SARS-CoV-2 FSE with 11 nM affinity, cuts frameshifting, and lowers infectivity sharply.</p>Formula:C16H14N4O2Color and Shape:SolidMolecular weight:294.31HCV-IN-37
CAS:<p>HCV-IN-37: potent HCV inhibitor, stable in rat plasma post-oral dose (15 mg/kg), blocks virus entry phase.</p>Formula:C31H35F2N5Color and Shape:SolidMolecular weight:515.64ML344
CAS:<p>ML344 is a CqsS/LuxQ agonist probe that acts as an inducer of light production without autoinducers.</p>Formula:C13H19N5Purity:98%Color and Shape:SolidMolecular weight:245.32Linogliride fumarate
CAS:<p>Linogliride fumarate, a guanidine derivative, stimulates insulin release by blocking ATP-sensitive K+ channels, enhancing glucose tolerance.</p>Formula:C20H26N4O5Purity:98%Color and Shape:SolidMolecular weight:402.451Antifungal agent 22
CAS:<p>Orally active antifungal D16 (IC50: 0.5 μg/mL) passes blood-brain barrier, stable, low toxicity, targets C. neoformansH99 cells.</p>Formula:C21H26Cl3NOSColor and Shape:SolidMolecular weight:446.86Ditalimfos
CAS:<p>Ditalimfos is a fungicide.</p>Formula:C12H14NO4PSColor and Shape:SolidMolecular weight:299.28DDD01035881
CAS:<p>DDD01035881 is a anti-malarial drug that blocks parasite-to-mosquito transmission by targeting the Plasmodium vesicle membrane protein Pfs16.</p>Formula:C14H14BrNO4S2Purity:99.78%Color and Shape:SolidMolecular weight:404.3Succinate dehydrogenase-IN-1
CAS:<p>Succinate dehydrogenase-IN-1 (Compound 34) acts as an inhibitor of succinate dehydrogenase (SDH), exhibiting an IC50 value of 0.94 μM and a KD of 22.4 μM. This compound also demonstrates antifungal activity, with EC50 values against Rhizoctonia solani, Sclerotinia sclerotiorum, Monilinia fructicola, and Botrytis cinerea measured at 0.04 μM, 1.13 μM, 1.61 μM, and 1.21 μM, respectively.</p>Formula:C20H13F6N3OColor and Shape:SolidMolecular weight:425.33Antitubercular agent-28
CAS:<p>Antitubercular agent-28 targets resistant Mycobacterium tuberculosis; MIC: 4.5 μM, IC50: 1.5 μM, IC90: 2.5 μM; low cytotoxicity.</p>Formula:C17H14N4O2Color and Shape:SolidMolecular weight:306.32DprE1-IN-4
CAS:<p>DprE1-IN-4: Potent DprE1 inhibitor (IC50: 0.90 μg/mL), good pharmacokinetics, kills TB bacteria in mice.</p>Formula:C20H21N3O5SColor and Shape:SolidMolecular weight:415.46SARS-CoV-2-IN-32
CAS:<p>SARS-CoV-2-IN-32 inhibits COVID-19 (Mpro; PDB: 6LU7) and has anti-cancer effects; useful for related research.</p>Formula:C27H23N5O4Color and Shape:SolidMolecular weight:481.5Sulfametrole
CAS:<p>Sulfametrole: oral, potent antibacterial for HIV, severe pneumonia, UTIs research.</p>Formula:C9H10N4O3S2Color and Shape:SolidMolecular weight:286.33Soporidine
CAS:<p>Soporidine, a strigolactone antagonist, blocks AtHTL, hindering SL signaling and seed germination.</p>Formula:C27H30F3NO3Purity:98%Color and Shape:SolidMolecular weight:473.53Dapabutan
CAS:<p>Dapabutan is an antimicrobial agent active against Gram-positive bacteria.</p>Formula:C19H40N2O2Color and Shape:SolidMolecular weight:328.53Tuberculosis inhibitor 3
CAS:<p>Tuberculosis inhibitor 3 is a highly potent and oral anti-tuberculosis drug against both drug-sensitive and drug-resistant Mycobacterium , H37RV & MDR-TB.</p>Formula:C21H22F6N4O3SPurity:98.8%Color and Shape:SolidMolecular weight:524.48Antiviral agent 10
CAS:<p>Antiviral agent 10 effectively inhibits the respiratory syncytial virus (RSV) [1], serving as a potent anti-viral compound.</p>Formula:C22H24N2O5Color and Shape:SolidMolecular weight:396.44Pafuramidine maleate
CAS:<p>Pafuramidine is an orally bioavailable prodrug of formamidine which was developed for the treatment of human African trypanosomiasis.</p>Formula:C24H24N4O7Purity:98%Color and Shape:SolidMolecular weight:480.163-Chlorogentisyl alcohol
CAS:<p>3-Chlorogentisyl alcohol: E. coli β-glucuronidase inhibitor (IC50=0.74µM, Ki=0.58µM), antiproliferative, for anti-cancer/inflammatory research.</p>Formula:C7H7ClO3Color and Shape:SolidMolecular weight:174.58Influenza A virus-IN-4
CAS:<p>Influenza A virus-IN-4 (23b), a potent neuraminidase inhibitor derived from Oseltamivir, effectively targets influenza viruses.</p>Formula:C19H28N4O4Color and Shape:SolidMolecular weight:376.45Silthiofam
CAS:<p>Silthiofam effectively combats Ggt, a wheat take-all fungus, now widely used for control in China.</p>Formula:C13H21NOSSiPurity:98%Color and Shape:SolidMolecular weight:267.46FtsZ-IN-2
CAS:<p>FtsZ-IN-2, a bacterial FtsZ inhibitor, hampers GTPase; has anti-MRSA/MSSA effects with 2 μg/ml MIC.</p>Formula:C30H35N5SColor and Shape:SolidMolecular weight:497.7GNF6702
CAS:<p>GNF6702 inhibits kinetoplastid proteasome, treating leishmaniasis, Chagas, and trypanosomiasis in mice.</p>Formula:C22H16FN7O2Color and Shape:SolidMolecular weight:429.41SARS-CoV-2-IN-33
CAS:<p>SARS-CoV-2-IN-33 inhibits COVID-19 with strong affinity for Mpro and combats cancer cell growth.</p>Formula:C30H30N4O5Color and Shape:SolidMolecular weight:526.58Robenidine
CAS:<p>Robenidine, an anticoccidial guanidine, is used as an additive in rabbit fodder.</p>Formula:C15H13Cl2N5Purity:98%Color and Shape:SolidMolecular weight:334.2Enviroxime
CAS:<p>Enviroxime(LY 122772, NSC 346230) is an anti-infective and anti-disease agent. Enviroxime targets the 3A coding region of rhinovirus and poliovirus.</p>Formula:C17H18N4O3SColor and Shape:SolidMolecular weight:358.41Pterophyllin 2
CAS:<p>Pterophyllin 2 is an agent of natural antifungal. It also against postharvest fruit pathogenic fungi.</p>Formula:C15H12O3Purity:98%Color and Shape:SolidMolecular weight:240.25Phenosulfazole
CAS:<p>Phenosulfazole is a potent antiviral agent which has the potential for the research of poliomyelitis virus [1].</p>Formula:C9H8N2O3S2Color and Shape:SolidMolecular weight:256.3NEU617
CAS:<p>NEU617 is an inhibitor of the growth of protozoan parasites, against T. brucei bloodstream proliferation.</p>Formula:C31H26ClFN4O2Color and Shape:SolidMolecular weight:541.02Fumaramidmycin
CAS:<p>Fumaramidmycin is an antibiotic that is produced by Streptomyces kurssanovii NR-7GG1.</p>Formula:C12H12N2O3Purity:98%Color and Shape:SolidMolecular weight:232.24Cylindrospermopsin
CAS:<p>Cylindrospermopsin: a toxic cyanobacterial uracil derivative, disrupts protein/glutathione synthesis in hepatocytes, and is genotoxic.</p>Formula:C15H21N5O7SColor and Shape:SolidMolecular weight:415.42SARS-CoV-2-IN-36
<p>SARS-CoV-2-IN-36: strong Mpro inhibitor, IC50=2.37μM, Kd=1.19μM, fights UC-1074/RG2674/NVDBB-2220 variants.</p>Formula:C17H21N5O3Color and Shape:SolidMolecular weight:343.38MMT5-14
CAS:<p>MMT5-14: potent SARS-CoV-2 inhibitor, improves antiviral activity (2-7x), boosts prodrug in plasma/lungs (200-300x), raises NTP in lungs (5x).</p>Formula:C39H55N6O8PColor and Shape:SolidMolecular weight:766.86SSF-109
CAS:<p>SSF-109 is a broad-spectrum fungicide, has protective activity against plant disease.</p>Formula:C15H18ClN3OPurity:98%Color and Shape:SolidMolecular weight:291.78Helioxanthin 8-1
CAS:<p>Helioxanthin 8-1, an analogue of helioxanthin, exhibits significant in vitro anti-HBV/HCV/HSV-1/HIV activity with EC50 of >5/10/1.4/15 μM.</p>Formula:C20H12N2O6Purity:98%Color and Shape:SolidMolecular weight:376.32HCV-IN-34
CAS:<p>HCV-IN-35, an oral HCV blocker, has an EC50 of 0.010 μM and a CC50 of 7.5 μM, indicating strong antiviral effects.</p>Formula:C31H36ClN5Color and Shape:SolidMolecular weight:514.1MAC173979
CAS:<p>MAC173979 inhibits E. coli de novo PABA biosynthesis and growth.</p>Formula:C9H5Cl2NO3Purity:98%Color and Shape:SolidMolecular weight:246.05SARS-CoV-2-IN-17
CAS:<p>SARS-CoV-2-IN-17 inhibits NPro effectively, with EC50 of 2.18 μM and Kd of 7.82 μM, showing strong anti-viral properties.</p>Formula:C19H19F3N2O3Color and Shape:SolidMolecular weight:380.36Mab Aspartate Decarboxylase-IN-1
CAS:<p>Mab Aspartate Decarboxylase-IN-1 is a potent inhibitor of aspartate decarboxylase (PanD) (IC50 = 56.3 μM) with antibacterial activity [1].</p>Formula:C16H11N3O3Color and Shape:SolidMolecular weight:293.28Antiparasitic agent-4
CAS:<p>Compound 4q: Antiparasitic; IC50: 8.51 μM (L. infantum), 2.20 μM (T. cruzi); HepG2 cytotoxicity: CC50 18.97 μM.</p>Formula:C16H13N3O2Color and Shape:SolidMolecular weight:279.29DprE1-IN-1
CAS:<p>DprE1-IN-1: Potent, oral DprE1 inhibitor; stable in hepatocytes, low toxicity, anti-bacilli in macrophages, -1.29 log10 CFU.</p>Formula:C19H21N3O6S2Color and Shape:SolidMolecular weight:451.52AIC-292
CAS:<p>AIC-292 is a potent, tolerable reverse transcriptase inhibitor active against various HIV-1 strains, including NNRTI-resistant K103N, G190A, Y181C.</p>Formula:C19H12Cl2F2N4O2Color and Shape:SolidMolecular weight:437.23HIV-1 protease-IN-2
CAS:<p>HIV-1 protease-IN-2: strong HIV-1 protease blocker, IC50 2.53 nM, fights DRV-sensitive/resistant HIV-1.</p>Formula:C27H34N4O7SColor and Shape:SolidMolecular weight:558.65Antifungal agent 59
CAS:<p>Antifungal agent 59 exhibits potent activity, reflected by MIC values ranging from 0.01 to 1 μg/mL, and inhibits the formation of fungal biofilms, while</p>Formula:C18H15BrF2N2SeColor and Shape:SolidMolecular weight:456.19TH-Z93
CAS:<p>TH-Z93 is a potent FPPS inhibitor (IC50:90 nM) and a lipophilic bisphosphonate.</p>Formula:C12H22N2O7P2Purity:98.37%Color and Shape:SolidMolecular weight:368.26CK-2-68
CAS:<p>CK-2-68 is a potent inhibitor of PfNDH2.</p>Formula:C24H17ClF3NO2Purity:98%Color and Shape:SolidMolecular weight:443.85BMS-585248
CAS:<p>BMS-585248 is a highly effective HIV-1 adhesion inhibitor that targets the viral envelope protein gp120.</p>Formula:C22H18FN7O3Color and Shape:SolidMolecular weight:447.42GNF179 (Metabolite)
CAS:<p>GNF179 metabolite is a potent (4.8 nM vs. W2 strain) derivative of 8,8-dimethyl IP with strong in vitro stability and oral bioavailability.</p>Formula:C14H16FN3Purity:98%Color and Shape:SolidMolecular weight:245.3Cap-dependent endonuclease-IN-8
CAS:<p>Cap-dependent endonuclease-IN-8, from CN111410661A (I-196), inhibits CENs, halting orthomyxovirus replication, like influenza A/B/C.</p>Formula:C29H23F2N3O6SColor and Shape:SolidMolecular weight:579.57SARS-CoV-IN-1
CAS:<p>SARS-CoV-IN-1 is an effective SARS-CoV replication inhibitor(EC50 of 4.9 μM in Vero cells).</p>Formula:C23H24ClFeN3OPurity:98%Color and Shape:SolidMolecular weight:449.76MmpL3-IN-3
CAS:<p>MmpL3-IN-3 (Compound 12), an MmpL3 inhibitor, exhibits potent anti-tuberculosis activity with a minimum inhibitory concentration (MIC) of 0.1 μM against H37Rv</p>Formula:C26H33ClN2SiColor and Shape:SolidMolecular weight:437.09Abimtrelvir
CAS:<p>Abimtrelvir exhibited antiviral activity.</p>Formula:C24H17ClF3N7O2Color and Shape:SolidMolecular weight:527.89Antimicrobial agent-5
<p>Antimicrobial agent-5: potent, selective for Gram-negative/positive bacteria, blocks LPS-CD14/TLR4, anti-inflammatory.</p>Formula:C32H48N16Color and Shape:SolidMolecular weight:656.83Vps34-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:402.41Synthalin sulfate
CAS:<p>Synthalin sulfate is a NMDA receptor antagonist.</p>Formula:C12H30N6O4SPurity:98%Color and Shape:SolidMolecular weight:354.47Antitubercular agent-19
CAS:<p>Antitubercular agent-19: effective against MTB H37Rv/MDR strains (MIC <0.016μg/ml), low cytotoxicity, high acute toxicity in BALB/c mice.</p>Formula:C24H20F6N4O3SColor and Shape:SolidMolecular weight:558.5GSK575594A
CAS:<p>GSK575594A is a selective agonist of GPR55.</p>Formula:C24H23F2N3O3SColor and Shape:SolidMolecular weight:471.52Acibenzolar-S-methyl
CAS:<p>Acibenzolar-S-methyl, a fungicide, boosts plant defenses by upregulating W-box genes like CAD1, NPR1, PR2.</p>Formula:C8H6N2OS2Purity:99.64% - 99.86%Color and Shape:Beige Fine PowderMolecular weight:210.28Chlordantoin
CAS:<p>Chlordantoin is an antifungal agent with the potential for vaginal candidiasis treatment.</p>Formula:C11H17Cl3N2O2SPurity:98%Color and Shape:SolidMolecular weight:347.69CWHM-1008
CAS:<p>CWHM-1008: Oral antimalarial, EC50 - 46 nM (3D7 strain), 21 nM (Dd2 resistant).</p>Formula:C22H26F3N3OColor and Shape:SolidMolecular weight:405.46VU0420373
CAS:<p>VU0420373 activates HssRS at EC50 10.7 μM, induces heme synthesis, toxic to S. aureus.</p>Formula:C15H11FN2OColor and Shape:SolidMolecular weight:254.26MtInhA-IN-1
<p>MtInhA-IN-1: an oral selective MtInhA inhibitor, IC50 0.23 μM, effective against M. tuberculosis with MIC 0.4 μM.</p>Formula:C21H22BrN3Color and Shape:SolidMolecular weight:396.32Furalazine
CAS:<p>Furalazine: antimicrobial, treats cholera, more effective than chloramphenicol in shortening stool culture positivity.</p>Formula:C9H7N5O3Purity:98%Color and Shape:SolidMolecular weight:233.18Nucleoside-Analog-1
CAS:<p>Nucleoside-Analog-1 is a 4′-Azidocytidine analogue, used to against Hepatitis C virus replication.</p>Formula:C9H9N5O5Purity:98%Color and Shape:SolidMolecular weight:267.2Acoziborole
CAS:<p>Acoziborole (SCYX-7158), a benzoxaborole derivative, is a novel, safe HAT agent with a MIC of 0.6 µg/mL against T. b. brucei S427.</p>Formula:C17H14BF4NO3Color and Shape:SolidMolecular weight:367.1Sisapronil
CAS:<p>Sisapronil is a member of the phenylpyrazole class of antiparasitics.</p>Formula:C15H6Cl2F8N4Color and Shape:SolidMolecular weight:465.13G0507
CAS:<p>G0507, a potent pyrrolopyrimidinedione, blocks E. coli growth by activating σE stress and targeting LolCDE ABC Transporter.</p>Formula:C18H15N3O3SColor and Shape:SolidMolecular weight:353.39Antimalarial agent 18
<p>Potent antimalarial, lipophilic, inhibits P. falciparum (IC50=50nM) & A. baumanii (IC50=390nM), blocks non-mevalonate pathway.</p>Formula:C23H44NO9PColor and Shape:SolidMolecular weight:509.57
