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(2,959 products)
- Antibiotic(921 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 5843 products of "Microbiology/Virology"
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IMB-26
CAS:<p>IMB-26 is an HCV inhibitor (EC50: 2.1 μM) and has shown potent anti-HCV effects.</p>Formula:C20H23BrN2O6Color and Shape:SolidMolecular weight:467.31Diamthazole hydrochloride
CAS:<p>Diamthazole (Dimazole) hydrochloride, an antifungal agent, is utilized in infection research.</p>Formula:C15H24ClN3OSColor and Shape:SolidMolecular weight:329.89Antitubercular agent-37
CAS:<p>Antitubercular Agent-37 exhibits antimycobacterial properties and functions as an antibacterial agent with an MIC (minimum inhibitory concentration) value of 0.</p>Formula:C22H22N8O2Color and Shape:SolidMolecular weight:430.46FR-198248
CAS:<p>FR-198248, a new anti-influenza agent, shows antiinfluenza virus activity in Madin-Darby canine kidney (MDCK) cells in vitro.</p>Formula:C9H10O5Color and Shape:SolidMolecular weight:198.172-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:346.18SARS-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:284.35Salazopyridazine
CAS:<p>Salazopyridazine is an antibacterial agent that inhibits ulcerative colitis. salazopyridazine can be used in the study of rheumatic diseases.</p>Formula:C18H15N5O6SColor and Shape:SolidMolecular weight:429.41VEC-5
CAS:<p>VEC-5: an HIV-1 inhibitor, outperforms RN18 by better binding with Vif in studies.</p>Formula:C29H21NO4Purity:98%Color and Shape:SolidMolecular weight:447.48P516-0475
CAS:<p>P516-0475, a novel inducer, enhances Streptococcus quorum sensing by blocking PepO, stabilizing SHP pheromones.</p>Formula:C15H17N5O3Color and Shape:SolidMolecular weight:315.33HIV-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:383.66Cefepime 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:517.02JFN05510
CAS:<p>Compound: 3'-O-tert-BDMS-5'-O-DMT-N2-IBG 2'-CE phosphoramidite; has anticancer properties and activates enzymes.</p>Formula:C50H68N7O9PSiColor and Shape:SolidMolecular weight:970.18SC-58272
CAS:<p>SC-58272 is an inhibitor of N-myristoyltransferase (Nmt), a target for anti-fungal and anti-viral therapy.</p>Formula:C33H52N6O4Purity:98%Color and Shape:SolidMolecular weight:596.8Antibacterial agent 97
CAS:<p>Antibacterial agent 97 is potent; MIC: 16 μg/mL for E. coli and S. aureus.</p>Formula:C19H23N5SColor and Shape:SolidMolecular weight:353.48HIV-1 inhibitor-30
CAS:<p>HIV-1 inhibitor-30 (10i) targets RT enzyme, EC50=40nM, IC50=80nM. Effective against seven NNRTI-resistant HIV-1 strains.</p>Formula:C19H20ClN3O2Color and Shape:SolidMolecular weight:357.83B07 hydrochloride
CAS:<p>B07 hydrochloride is a CCR5 antagonist-based inhibitor of HIV-1 entry.</p>Formula:C29H38ClFN4O2Purity:98%Color and Shape:SolidMolecular weight:529.09BO3482
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:383.43Antitubercular 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:469.58Antitubercular 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:316.36Cap-dependent endonuclease-IN-3
CAS:<p>Cap-dependent endonuclease-IN-3 inhibits CEN, promising for studying influenza A/B. (Patent WO2019141179A1, compound III-2)</p>Formula:C29H25F2N3O7SColor and Shape:SolidMolecular weight:597.59DPC-961
CAS:<p>DPC-961, a reverse transcriptase inhibitor, is used potentially for the treatment of HIV infection.</p>Formula:C14H10ClF3N2OColor and Shape:SolidMolecular weight:314.69SARS-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:464.56AN11251
CAS:<p>AN11251: oral anti-Wolbachia, treats onchocerciasis & lymphatic filariasis, EC50=1.5nM (LDW1), 15nM (C6/36).</p>Formula:C29H38BFO7Purity:98%Color and Shape:SolidMolecular weight:528.42RyRs activator 1
CAS:<p>RyRs activator 1 triggers ranibulin receptors; 100% larvicidal at 0.5 mg/L, 90% at 0.01 mg/L.</p>Formula:C21H14ClF3N6O4Color and Shape:SolidMolecular weight:506.82Crisnatol mesylate
CAS:<p>Crisnatol, a potent and selective DNA intercalator, has potential anticancer activity.</p>Formula:C24H27NO5SColor and Shape:SolidMolecular weight:441.54Anti-MRSA agent 1
CAS:<p>Anti-MRSA agent 1 is an MRSA inhibitor with an MIC value of 0.5 μg/mL and is effective in alleviating the effects of MRSA resistance.</p>Formula:C26H29N7O4SColor and Shape:SolidMolecular weight:535.62JNJ-2408068
CAS:<p>JNJ-2408068 inhibits RSV with EC50 of 2.1 nM; blocks fusion (EC50=0.9 nM) by targeting F protein.</p>Formula:C22H30N6OPurity:98%Color and Shape:SolidMolecular weight:394.51Antitubercular 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:362.41Marasmic acid
CAS:<p>Marasmic acid is a bioactive antifungal.</p>Formula:C15H18O4Color and Shape:SolidMolecular weight:262.3EV-A71-IN-1
CAS:<p>EV-A71-IN-1: potent EV-A71 capsid inhibitor, EC50 0.27 μM, disrupts VP1/hSCARB2 interaction, broad-spectrum antiviral, non-toxic to human cells.</p>Formula:C21H15N5SColor and Shape:SolidMolecular weight:369.44Werner syndrome RecQ helicase-IN-3
CAS:<p>Potent WRN inhibitor, Werner syndrome RecQ helicase-IN-3, is orally active with 0.06 µM IC50; exhibits antiproliferative and anticancer effects.</p>Formula:C31H30ClF3N8O5Color and Shape:SolidMolecular weight:687.07Riodoxol
CAS:<p>Riodoxol is an antiviral agent that effectively affects the reproduction and maturation of viruses.</p>Formula:C6H3I3O2Color and Shape:SolidMolecular weight:487.8Floxacrine
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:413.28Antibacterial agent 122
CAS:<p>Thiourea derivative 122 is a low-toxicity antibacterial used in tuberculosis research with anti-mycobacterial properties.</p>Formula:C15H14N2O3SColor and Shape:SolidMolecular weight:302.35Cadrofloxacin
CAS:<p>Cadrofloxacin (Caderofloxacin, CS-940) is a novel fluoroquinolone antimicrobial agent.</p>Formula:C19H20F3N3O4Color and Shape:SolidMolecular weight:411.38TDRL-X80
CAS:<p>TDRL-X80 inhibits XPA DNA binding; effective on single, double, and cisplatin-damaged DNA; IC50: 18-29 μM (FP), 21-39 μM (ELISA).</p>Formula:C23H15ClN2O6Color and Shape:SolidMolecular weight:450.83Antimycobacterial agent-2
CAS:<p>Antimycobacterial agent-2 has MIC99 0.8 μM vs M.tb H37Rv; cytotoxic with IC50 48.1 μM on CHO cells.</p>Formula:C31H50O5Color and Shape:SolidMolecular weight:502.73Antitubercular 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:516.58Metallo-β-lactamase-IN-6
CAS:<p>Metallo-β-lactamase-IN-6 is a highly effective inhibitor of VIM-Type metallo-β-lactamase, demonstrating IC 50 values of 0.56 μM, 29.50 μM, and 5.78 μM for VIM-2</p>Formula:C10H9N3O2Color and Shape:SolidMolecular weight:203.2gp120-IN-2
CAS:<p>gp120-IN-2 is a potent HIV-1 inhibitor (IC50 = 7.5 μM) with low cytotoxicity (CC50 = 112.93 μM).</p>Formula:C15H18N2O5Color and Shape:SolidMolecular weight:306.31Mt KARI-IN-2
CAS:<p>Mt KARI-IN-2, an inhibitor for Mtb KARI (Ki: 2.02 μM) and Mtb H37Rv (MIC: 0.78 μM), has low cytotoxicity (HEK IC50: >86 μg/mL).</p>Formula:C14H11N5O4S2Color and Shape:SolidMolecular weight:377.4MtTMPK-IN-4
CAS:<p>MtTMPK-IN-4, a para-piperidine, blocks MtTMPK in tuberculosis with 6.1 μM IC50 and also inhibits tyrosinase.</p>Formula:C23H25N3O3Color and Shape:SolidMolecular weight:391.46A 80987
CAS:<p>A 80987 is an inhibitor of HIV-1 protease.</p>Formula:C37H43N5O6Color and Shape:SolidMolecular weight:653.77Antiparasitic agent-5
CAS:<p>Compound 8h: Antiparasitic, selective against L. infantum (IC50: 2.50 μM); cytotoxic to HepG2 cells (CC50: 6.78 μM).</p>Formula:C20H16ClN3O3Color and Shape:SolidMolecular weight:381.81Endochin
CAS:<p>Endochin is an experimental antimalarial. Endochin and analogues thereof are causal prophylactic and potent erythrocytic stage agents in avian models.</p>Formula:C18H25NO2Purity:98%Color and Shape:SolidMolecular weight:287.4GW-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:410.25Antileishmanial agent-10
CAS:<p>Antileishmanial agent-10 (Compound 7h) is an antiprotozoal agent.</p>Formula:C25H41NO2SColor and Shape:SolidMolecular weight:419.66Neuraminidase-IN-9
CAS:<p>Neuraminidase-IN-9 inhibits flu virus neuraminidase H5N1 (IC50: 0.12 μM), H5N2 (IC50: 0.049 μM), H5N6 (IC50: 0.16 μM).</p>Formula:C24H33BrN6O3Color and Shape:SolidMolecular weight:533.46Purfalcamine
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:528.62HIV-1 inhibitor-45
CAS:<p>HIV-1 inhibitor-45 is a potent inhibitor of HIV-1 RNase H (IC50: 0.067 μM) and has antiviral effects.</p>Formula:C23H24N4O8SColor and Shape:SolidMolecular weight:516.52HIV-IN-5
CAS:<p>HIV-IN-5 (5r) inhibits HIV-1 with 0.16 μM IC50, targeting NNIBP as a NNRTI.</p>Formula:C30H24N2O8SColor and Shape:SolidMolecular weight:572.59Metallo-β-lactamase-IN-9
CAS:<p>Metallo-β-lactamase-IN-9 (Compound 23) serves as a broad-spectrum inhibitor of metallo-beta-lactamases (MBL), exhibiting inhibition constants (IC50) of 35 nM</p>Formula:C13H12N6O3SColor and Shape:SolidMolecular weight:332.34Kayahope
CAS:<p>Kayahope is a novel antifungals.</p>Formula:C15H14ClNO3SPurity:98%Color and Shape:SolidMolecular weight:323.79Antiviral 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:454.53L-573655
CAS:<p>L-573655, an antibacterial agents, targets lipid A biosynthesis in gram-negative bacteria.</p>Formula:C10H10N2O3Purity:98%Color and Shape:SolidMolecular weight:206.2CB 3717
CAS:<p>CB 3717 is an enzyme inhibitor, antineoplastic agent, folic acid antagonist.</p>Formula:C24H23N5O6Color and Shape:SolidMolecular weight:477.47Antifungal agent 37
CAS:<p>Antifungal agent 37 is a heterocyclic disulfide that exhibits antifungal activity [1].</p>Formula:C7H10N2S2Color and Shape:SolidMolecular weight:186.3HBV-IN-9
CAS:<p>HBV-IN-9 inhibits HBsAg (IC50: 10 nM) and HBV DNA replication (IC50: 0.15 nM) per WO2018001952A1.</p>Formula:C22H24FN7OColor and Shape:SolidMolecular weight:421.47HIV-1 inhibitor-24
CAS:<p>HIV-1 inhibitor-24 (S-12a) blocks HIV reverse transcription effectively (IC50: 9.5 nM), low toxicity, well-tolerated in mice, good heart safety.</p>Formula:C26H19N5O2Color and Shape:SolidMolecular weight:433.46Acetarsone
CAS:<p>Acetarsone is an antiinfective agent. Acetarsone also inhibits protozoa growth.</p>Formula:C8H10AsNO5Color and Shape:SolidMolecular weight:275.09DSHS00884
CAS:DSHS00884 is a potent inhibitor of human papillomavirus E6 (IC50: 10 μM).Formula:C12H12N4O2S2Color and Shape:SolidMolecular weight:308.38Leu-AMS
CAS:<p>Leu-AMS, a leucine analogue with 22.34 nM IC50, inhibits LRS and bacterial growth without affecting mTORC1.</p>Formula:C16H25N7O7SPurity:98%Color and Shape:SolidMolecular weight:459.48Antitubercular agent-27
CAS:<p>Antitubercular agent-27: IC50=3.2 μM, MIC=7.8 μM, IC90=7.0 μM; effective against resistant Mycobacterium tuberculosis, low toxicity.</p>Formula:C14H8BrN3O3Color and Shape:SolidMolecular weight:346.14Norstictic acid
CAS:<p>Norstictic acid: a potent, selective transcription regulator with anticancer, antioxidant, and antimicrobial properties.</p>Formula:C18H12O9Color and Shape:SolidMolecular weight:372.28Antimicrobial agent-6
<p>Antimicrobial agent-6: MIC 4-8 μg/mL for gram+ & gram- bacteria, anti-inflammatory.</p>Formula:C40H64N16Color and Shape:SolidMolecular weight:769.04BMS-986094
CAS:<p>INX 08189 is an RNA-directed RNA polymerase (NS5B) inhibitor.</p>Formula:C30H39N6O9PColor and Shape:SolidMolecular weight:658.64Texaline
CAS:<p>Texaline is an agent of the antitubercular.</p>Formula:C15H10N2O3Purity:98%Color and Shape:SolidMolecular weight:266.25SS148
CAS:<p>SS148 inhibits nsp14/nsp16 MTase, selective vs human MTases; promising for potent, selective coronavirus MTase inhibitors.</p>Formula:C16H20N6O5SColor and Shape:SolidMolecular weight:408.43Antimicrobial 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:506.04Cyclophilin inhibitor 3
CAS:<p>Cyclophilin inhibitor 3 (compound 7c), a potent inhibitor of cyclophilin A (CypA), exhibited potent anti-HCV effects with an EC50 value of 4.2 μM.</p>Formula:C34H38N4O6Color and Shape:SolidMolecular weight:598.69Efavirenz, (R)-
CAS:<p>Efavirenz, (R)- is an antiviral agent and a nonnucleoside HIV-1 reverse transcriptase inhibitor.</p>Formula:C14H9ClF3NO2Color and Shape:SolidMolecular weight:315.67Kumbicin C
CAS:<p>Kumbicin C inhibits the growth of NS-1 mouse myeloma cells (IC50 = 0.74 μg/ml) and the growth of the Gram-positive bacteria B. subtilis (MIC = 1.6 μg/ml).</p>Formula:C28H24N2O3Color and Shape:SolidMolecular weight:436.5HBV-IN-7
CAS:<p>HBV-IN-6 is a potent inhibitor of HBV (EC50: 5 nM).</p>Formula:C18H17ClFN3O5S2Color and Shape:SolidMolecular weight:473.93HIV-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:392.69Mt KARI-IN-4
CAS:<p>Mt KARI-IN-4 inhibits Mtb KARI with Ki of 5.48μM, has MIC of 0.78μM against H37Rv, and IC50 >72μg/mL, low cytotoxicity.</p>Formula:C13H8FN5O3S2Color and Shape:SolidMolecular weight:365.36DHMB
CAS:<p>DHMB (2,3-Dihydroxy-4-Methoxybenzaldehyde) exerts protective effects on intestinal epithelial cells. DHMB exhibits anti-inflammatory and antifungal capacity.</p>Formula:C8H8O4Purity:99.57%Color and Shape:SolidMolecular weight:168.15Lascufloxacin
CAS:<p>Lascufloxacin: potent, oral fluoroquinolone antibiotic for respiratory infections, effective against quinolone-resistant strains.</p>Formula:C21H24F3N3O4Purity:98%Color and Shape:SolidMolecular weight:439.43MAC-0547630
CAS:<p>MAC-0547630 potent and selective inhibitor of UppS.</p>Formula:C19H21FN4Purity:98%Color and Shape:SolidMolecular weight:324.4RSV-IN-3
CAS:<p>RSV-IN-3 is a dual RSV/IAV inhibitor with an EC50 of 32.70 μM against RSV.</p>Formula:C16H12Cl2N2OSColor and Shape:SolidMolecular weight:351.25Influenza 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:418.5P163-0892
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:525.57DprE1-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:415.46OYYF-175
CAS:<p>OYYF-175: potent antimicrobial antifolate; targets multi-drug resistant Gram-Negative bacteria; DHFR inhibitor with 2.36 nM IC50 against E. coli.</p>Formula:C17H14FN5Color and Shape:SolidMolecular weight:307.33trans-ccc_R08
CAS:<p>trans-ccc_R08: potent cccDNA inhibitor, IC50 0.08 µM, may help research HBV.</p>Formula:C22H19ClO6Color and Shape:SolidMolecular weight:414.84Soporidine
CAS:<p>Soporidine, a strigolactone antagonist, blocks AtHTL, hindering SL signaling and seed germination.</p>Formula:C27H30F3NO3Purity:98%Color and Shape:SolidMolecular weight:473.53
