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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PXYC13
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:329.38Dabequin
CAS:<p>Dabequin is a derivative of aminoquinoline. It is said to have pharmacological activity against Plasmodium fukiparum.</p>Formula:C19H29N3O8P2Color and Shape:SolidMolecular weight:489.4MMV024101
CAS:<p>MMV024101: PI4K inhibitor, P. falciparum NF54 IC50 543 nM, poor solubility (<5 μM), fast mouse liver clearance.</p>Formula:C16H12N6O2SColor and Shape:SolidMolecular weight:352.37A3N19
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:593.7SARS-CoV-2 Mpro-IN-4
<p>SARS-CoV-2 Mpro-IN-4 inhibits Mpro (IC50: 900 nM) & CatL (IC50: 60 nM), blocks virus replication (IC50: 8.2 nM).</p>Formula:C30H38N4O5Color and Shape:SolidMolecular weight:534.65ATD-3169
CAS:<p>ATD-3169 is a ROS generator with antibacterial activity.</p>Formula:C15H14O3Purity:98%Color and Shape:SolidMolecular weight:242.27Berteroin
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:175.31INSCoV-601I(1)
CAS:<p>INSCoV-601I(1) is a strong 3CLpro inhibitor, key in SARS-CoV-2 replication; potential for research use - WO2021219089A1.</p>Formula:C23H22ClF2N5O2SColor and Shape:SolidMolecular weight:505.97Cefepime 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:517.02CAY10704
CAS:<p>CAY10704: Potent HCV inhibitor, EC50=17 nM, low cytotoxicity, good in mice, liver-targeted, not hepatotoxic, weak against dengue.</p>Formula:C18H20Cl2N2Color and Shape:SolidMolecular weight:335.27Anti-infective agent 4
CAS:<p>Oral Trypanosoma cruzi inhibitor (IC50: 0.016 μM), Anti-infective agent 4 reduces in vivo parasite load.</p>Formula:C19H12F3N5O4Color and Shape:SolidMolecular weight:431.32HIV-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:383.66Antitubercular 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:346.18Antimalarial 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:509.572-Hydroxydocosanoic acid
CAS:<p>2-Hydroxydocosanoic acid exhibits antioxidant, cholinesterase inhibitory, and antimicrobial properties [1].</p>Formula:C22H44O3Color and Shape:SolidMolecular weight:356.58Antibacterial agent 73
CAS:<p>Compound 7a: antitubercular (MIC 0.65 μg/mL Mtb), antibacterial, antifungal; cytotoxic (IC50 8.20 μM MCF-7).</p>Formula:C15H17FN2OColor and Shape:SolidMolecular weight:260.31Antileishmanial agent-11
CAS:<p>Antileishmanial agent-11: Potent against L. brazilensis (28.3 μM), L. infantum (24.8 μM), T. cruzi (13.0 μM) with strong antiprotozoal efficacy.</p>Formula:C27H24ClN3O4Color and Shape:SolidMolecular weight:489.95Antifungal agent 73
CAS:<p>Antifungal agent 73 (compound A32) effectively combats azole-resistant candidiasis by disrupting the fungal cell wall and membrane.</p>Formula:C21H16Cl2N2O3Color and Shape:SolidMolecular weight:415.27Mycobactin-IN-1
CAS:<p>Mycobactin-IN-1, a pyrazoline analogue, inhibits MbtA, key in mycobactin synthesis, targeting mycobacteria.</p>Formula:C15H13ClN2OColor and Shape:SolidMolecular weight:272.73Chitin synthase inhibitor 3
CAS:<p>Compound 2d is a potent chitin synthase inhibitor (IC50: 0.16 mM, MIC: 1 μg/mL vs. Candida albicans) with antifungal properties.</p>Formula:C20H19N3O4Color and Shape:SolidMolecular weight:365.38Fosclevudine alafenamide
CAS:<p>Fosclevudine alafenamide (Compound EIDD-02173) is an antiviral agent that acts against HBV (EC50: 1.71 μM).</p>Formula:C22H29FN3O9PColor and Shape:SolidMolecular weight:529.45Diamthazole hydrochloride
CAS:<p>Diamthazole (Dimazole) hydrochloride, an antifungal agent, is utilized in infection research.</p>Formula:C15H24ClN3OSColor and Shape:SolidMolecular weight:329.89MurA-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:229.75SARS-CoV-2 Mpro-IN-1
CAS:<p>SARS-CoV-2 Mpro-IN-1 (compound 16b-3) is a potent, selective and irreversible SARS-CoV-2 main protease (Mpro) inhibitor (IC 50 = 116 nM) [1].</p>Formula:C15H11FN2O2SColor and Shape:SolidMolecular weight:302.32Anthrarobin
CAS:<p>Anthrarobin is an antipsoriatic.</p>Formula:C14H10O3Purity:98%Color and Shape:SolidMolecular weight:226.23Antitubercular agent-39
CAS:<p>Antitubercular agent-39 (Compound P1) is a potent agent effective against both drug-resistant strains and drug-susceptible clinical isolates of tuberculosis,</p>Formula:C26H30N4O2Color and Shape:SolidMolecular weight:430.54Antifungal 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:446.18PNU-176798
CAS:<p>PNU-176798 is an agent with antimicrobial.</p>Formula:C16H13FN4O3SPurity:98%Color and Shape:SolidMolecular weight:360.36Antiviral 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:506.04(-)-Pinocembrin
CAS:<p>(-)-Pinocembrin: Anti-tuberculosis (IC50: 1.11 mg/mL dormant, 1.21 mg/mL active), antiproliferative (IC50: 1.88-11 mg/mL on various cell lines).</p>Formula:C15H12O4Color and Shape:SolidMolecular weight:256.25RO5464466
CAS:<p>RO5464466 is an inhibitor of influenza A virus (H1N1) fusion.</p>Formula:C16H26N2O3SColor and Shape:SolidMolecular weight:326.45SARS-CoV-2 Mpro-IN-6
CAS:<p>SARS-CoV-2 Mpro-IN-6: irreversible Mpro inhibitor, IC50 0.18 μM, selective; doesn't block cathepsins B/F/K/L or caspase 3.</p>Formula:C18H18Cl3N3O2SColor and Shape:SolidMolecular weight:446.78Antistaphylococcal 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:354.19Antiviral 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:477.59pUL89 Endonuclease-IN-1
CAS:<p>Compound 13d: potent pUL89 endonuclease inhibitor, IC50 0.88 μM, anti-HCMV activity.</p>Formula:C10H8N2O4SColor and Shape:SolidMolecular weight:252.25Antibacterial 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:606.07Diamthazole
CAS:<p>Diamthazole (Dimazole) is an antifungal agent that can be used in the infection research[1].</p>Formula:C15H23N3OSColor and Shape:SolidMolecular weight:293.43SARS-CoV-2 3CLpro-IN-6
CAS:<p>SARS-CoV-2 3CLpro-IN-6: reversible inhibitor for COVID-19 3CL protease, IC50 4.9 μM, useful in research.</p>Formula:C22H15NO7Color and Shape:SolidMolecular weight:405.36Vebufloxacin
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:418.5Antimycobacterial agent-1
CAS:<p>Compound 33: antimycobacterial, MIC 1 μg/ml vs M. tuberculosis H37Ra, low toxicity (IC50 143.2 μg/ml in Vero cells).</p>Formula:C18H12N4O5SColor and Shape:SolidMolecular weight:396.38P163-0892
CAS:<p>P163-0892: potent, specific antifungal for Cryptococcus; moderate blood-brain barrier penetration.</p>Formula:C19H20N2O3SColor and Shape:SolidMolecular weight:356.44Mycobacterial Zmp1-IN-1
<p>Zmp1-IN-1: An inhibitor of mycobacterial Zmp1 with dose-dependent anti-tuberculosis effects.</p>Formula:C26H27N3O7SColor and Shape:SolidMolecular weight:525.57Edelfosine
CAS:<p>inhibits phosphatidylinositol phospholipase C</p>Formula:C27H58NO6PPurity:98%Color and Shape:SolidMolecular weight:523.73Mt KARI-IN-5
CAS:<p>Mt KARI-IN-5 inhibits MtbKARI with Ki 4.72 μM, has MIC 1.56 μM against MtbH37Rv, and is low in cytotoxicity with IC50 >64 μg/mL in HEK.</p>Formula:C14H10N4O5S3Color and Shape:SolidMolecular weight:410.45RMI 10874
CAS:<p>RMI 10874 is a tilorone analogue. Tilorone is an orally bioavailable antiviral agent.</p>Formula:C21H26N2O4Purity:98%Color and Shape:SolidMolecular weight:370.44Soporidine
CAS:<p>Soporidine, a strigolactone antagonist, blocks AtHTL, hindering SL signaling and seed germination.</p>Formula:C27H30F3NO3Purity:98%Color and Shape:SolidMolecular weight:473.53DLC27-14
CAS:<p>DLC27-14 is an HIV-1 Nef specific protein disorder catalyzer.</p>Formula:C25H25NO4Color and Shape:SolidMolecular weight:403.47HIV-1 inhibitor-50
CAS:<p>HIV-1 inhibitor-50 is a non-nucleoside reverse transcriptase inhibitor (NNRTI) that targets HIV-1 reverse transcriptase (IC50 = 50 nM).</p>Formula:C24H18FN5O2Color and Shape:SolidMolecular weight:427.43Neuraminidase-IN-8
CAS:<p>Neuraminidase-IN-8 (Compound 6d) is a powerful inhibitor of neuraminidase, exhibiting a low half-maximal inhibitory concentration (IC50) of 0.027 μM and</p>Formula:C18H16FN3O3SColor and Shape:SolidMolecular weight:373.4Neuraminidase-IN-3
CAS:<p>Neuraminidase-IN-3 inhibits flu NA: H1N1 IC50=0.73nM, H5N1=0.26nM, H5N8=0.63nM.</p>Formula:C27H32N2O4SColor and Shape:SolidMolecular weight:480.62Afabicin disodium
CAS:<p>Afabicin (Debio 1450), a Debio1452 precursor, targets Staphylococcus by inhibiting lipid synthesis.</p>Formula:C23H22N3Na2O7PColor and Shape:SolidMolecular weight:529.396HBV-IN-32
CAS:<p>HBV-IN-32 is a strong cccDNA inhibitor with an IC50 of 0.14 µM against HBsAg, also halting cell growth.</p>Formula:C22H19ClO5SColor and Shape:SolidMolecular weight:430.9EP39
<p>EP39 is a potent HIV-1 inhibitor, stabilizing the SP1 domain's helix and blocking virus maturation.</p>Formula:C38H62N2O5Color and Shape:SolidMolecular weight:626.91Posaconazole hydrate
CAS:<p>Posaconazole: broad-spectrum antifungal, second-gen triazole, strong C14α demethylase inhibitor (IC50: 0.25 nM).</p>Formula:C37H44F2N8O5Purity:98%Color and Shape:SolidMolecular weight:718.79Antileishmanial agent-3
CAS:<p>Antileishmanial agent-3 (Compound 13) effectively inhibits the growth of Leishmania major [1].</p>Formula:C14H13ClN6O4Color and Shape:SolidMolecular weight:364.74Influenza 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:497.74,4'-Dicyanostilbene
CAS:<p>4,4'-Dicyanostilbene: potent anti-Dd2 malaria, EC50=27nM; effective vs. MRSA.</p>Formula:C16H10N2Color and Shape:SolidMolecular weight:230.26HSV-1/HSV-2-IN-1
CAS:<p>HSV-1/HSV-2-IN-1 inhibits HSV-1, HSV-2, and cowpox virus with EC50 values of 7.6, 7.6, 4, and 12 μM, respectively.</p>Formula:C18H14F4N4OSColor and Shape:SolidMolecular weight:410.39Phenosulfazole
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:541.02Antibacterial agent 104
CAS:<p>Antibacterial agent 104 is an effective antibacterial agent with significant antibacterial effects in vitro and good anti-MRSA effects in vivo.</p>Formula:C28H39NO4SColor and Shape:SolidMolecular weight:485.68Pralurbactam
CAS:<p>Pralurbactam is a β-Lactamase inhibitor utilized in the research of bacterial infections.</p>Formula:C10H18N6O8SColor and Shape:SolidMolecular weight:382.35LpxC-IN-9
CAS:<p>LpxC-IN-9 (compound 19) is a potent inhibitor of LpxC and exhibits antibacterial and hypotensive activity.</p>Formula:C23H25N5O3SColor and Shape:SolidMolecular weight:451.54SARS-CoV-2-IN-15
CAS:<p>SARS-CoV-2-IN-15, a stable niclosamide analogue, enhances bioavailability and half-life, with potent antiviral activity (IC50: 0.49 μM).</p>Formula:C14H9ClF3NO2Color and Shape:SolidMolecular weight:315.67HCV-IN-36
CAS:<p>HCV-IN-36: oral HCV inhibitor, EC50 0.016 μM, CC50 8.78 μM, potent antiviral.</p>Formula:C30H36ClN5Color and Shape:SolidMolecular weight:502.09CL-55
CAS:<p>CL-55 is a novel inhibitor of T3SS.</p>Formula:C19H17F2N3O4SColor and Shape:SolidMolecular weight:421.42BPH-1086
CAS:<p>BPH-1086 inhibits IspH, which with RPS1 binds mRNA or integrates into bacterial ribosomes.</p>Formula:C4H8O7P2Color and Shape:SolidMolecular weight:230.05Globosuxanthone A
CAS:<p>Globosuxanthone A: a dihydroxanthenone with anticancer and antifungal properties (MIC: F. graminearum 4, F. solani 8, B. cinerea 16 μg/mL).</p>Formula:C15H12O7Color and Shape:SolidMolecular weight:304.25HIV-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:456.19Metallo-β-lactamase-IN-2
CAS:<p>Metallo-β-lactamase-IN-4 (compound 40) is a potent metallo-β-lactamases (MBL) inhibitor with IC 50 values of 0.1 μM for VIM-1, 1.3 μM for NDM-1 and 5.0 μM for</p>Formula:C9H9Cl2NOSColor and Shape:SolidMolecular weight:250.14HBV-IN-6
CAS:<p>HBV-IN-6 is a potent inhibitor of HBV (EC50: 44 nM).</p>Formula:C23H21ClFN3O5S2Color and Shape:SolidMolecular weight:538.01Abimtrelvir
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:656.83FtsZ-IN-1
CAS:<p>FtsZ-IN-1: potent quinoline-based FtsZ inhibitor; targets Gram-positive bacteria, minimal hemolysis, resists drug resistance.</p>Formula:C26H32IN3Color and Shape:SolidMolecular weight:513.467Derquantel
CAS:<p>nicotinic acetylcholine receptor antagonist</p>Formula:C28H37N3O4Purity:98%Color and Shape:SolidMolecular weight:479.61FLDP-5
CAS:<p>FLDP-5: BBB-penetrant curcuminoid, induces ROS, DNA damage, S phase arrest, suppresses tumors in LN-18 cells.</p>Formula:C21H21NO5Color and Shape:SolidMolecular weight:367.4RSV/IAV-IN-1
CAS:<p>RSV/IAV-IN-1, a dual inhibitor of RSV/IAV, is less toxic than Ribavirin and holds research potential for RSV/IAV infections.</p>Formula:C18H17ClN2O2SColor and Shape:SolidMolecular weight:360.86EGFR/HER2/TS-IN-2
CAS:<p>EGFR/HER2/TS-IN-2: Strong EGFR, HER2 & TS inhibitor; EGFR IC50=0.173μM, HER2 IC50=0.125μM, TS IC50=1.12μM; kills MDA-MB-231 cells (IC50=1.69μM).</p>Formula:C26H21N7OS2Color and Shape:SolidMolecular weight:511.62Cap-dependent endonuclease-IN-16
CAS:<p>Cap-dependent endonuclease-IN-16, a pyridone derivative, inhibits CEN, showing promise for flu research.</p>Formula:C28H25F2N3O7SColor and Shape:SolidMolecular weight:585.58MtInhA-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:396.32BK 218
CAS:<p>BK 218: New cephalosporin, treats S. pneumoniae, H. influenzae, M. catarrhalis; less effective on penicillin-resistant strains; oral/IV use.</p>Formula:C15H14ClN7NaO5S2Color and Shape:SolidMolecular weight:494.88HIV-1 inhibitor-37
CAS:<p>HIV-1 inhibitor-37, a potent HIV-1 suppressant, shows promise as a novel latent reactivator.</p>Formula:C14H11Cl3N4OColor and Shape:SolidMolecular weight:357.62RIG-1 modulator 1
CAS:<p>RIG-1 modulator 1 is useful for the treatment of viral infections including influenza virus, HBV, HCV and HIV.</p>Formula:C14H17N5OS2Purity:98%Color and Shape:SolidMolecular weight:335.45Metallo-β-lactamase-IN-7
CAS:<p>Metallo-β-lactamase-IN-7 is a potent inhibitor of VIM -Type metallo-β-lactamase with IC 50 s of 0.019 μM, 13.64 μM, 0.38 μM for VIM-2, VIM-1 and VIM-5,</p>Formula:C12H10N4O2SColor and Shape:SolidMolecular weight:274.3Antimicrobial agent-3
CAS:<p>Antimicrobial agent-3 (Compound U10) is an antimicrobial agent that is used against bacterial, fungal, and tubercular infections [1].</p>Formula:C14H11N3OSColor and Shape:SolidMolecular weight:269.32Anti-infective agent 2
CAS:<p>Compound 3k is antiprotozoal/antimycobacterial, with IC50s: P. falciparum 0.07 μM, T. brucei 2.20 μM; MIC: M. smegmatis 32 μg/mL.</p>Formula:C15H8ClNO2Color and Shape:SolidMolecular weight:269.68KFU-127
<p>KFU-127: broad-spectrum antimicrobial; targets bacterial/fungal biofilms; toxic to eukaryotic cells.</p>Formula:C34H43BrN2O3Color and Shape:SolidMolecular weight:607.62Ipconazole [ISO]
CAS:<p>Ipconazole, a cyclopentanol with 1,2,4-triazolylmethyl, 4-chlorobenzyl & isopropyl groups, is a fungicide that targets seed diseases.</p>Formula:C18H24ClN3OColor and Shape:SolidMolecular weight:333.86MmpL3-IN-2
CAS:<p>MmpL3-IN-2, an inhibitor targeting MmpL3, exhibits low cytotoxicity and moderate metabolic stability, making it suitable for tuberculosis research [1].</p>Formula:C27H30N2Color and Shape:SolidMolecular weight:382.54HIV-1 inhibitor-22
CAS:<p>HIV-1 inhibitor-22 effectively blocks HIV-1 RT (IC50=3.63 μM) with low cytotoxicity (CC50 > 227 μM).</p>Formula:C30H26N6O3SColor and Shape:SolidMolecular weight:550.63Bulaquine
CAS:<p>Bulaquine, a 8-aminoquinoline derivative, targets liver stage of P. falciparum and dormant P. vivax/ovale.</p>Formula:C21H27N3O3Color and Shape:SolidMolecular weight:369.46Beaucage reagent
CAS:<p>Beaucage reagent, which is found to be effective in causing DNA cleavage.</p>Formula:C7H4O3S2Purity:98.50%Color and Shape:White To Off-White PowderMolecular weight:200.23(S)-Tedizolid
CAS:<p>(S)-Tedizolid is the S-enantiomer of Tedizolid. Tedizolid is a novel oxazolidinone with activity against Gram-positive pathogens.</p>Formula:C17H15FN6O3Purity:98%Color and Shape:SolidMolecular weight:370.34BPH-1218
CAS:<p>BPH-1218 is a SQS inhibitor.</p>Formula:C15H30N2O6P2Purity:98%Color and Shape:SolidMolecular weight:396.36
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