Microbiologia/Virologia
Gli inibitori in microbiologia e virologia sono composti che bersagliano microrganismi, inclusi batteri, virus e funghi, interrompendo la loro crescita, replicazione o sopravvivenza. Questi inibitori sono essenziali per studiare la patogenesi microbica, comprendere i meccanismi di resistenza e sviluppare nuove terapie antimicrobiche e antivirali. Gli inibitori in questa categoria vengono utilizzati per combattere le malattie infettive, esplorare l'ecologia microbica e studiare le interazioni ospite-patogeno. Presso CymitQuimica, offriamo un'ampia selezione di inibitori di alta qualità in microbiologia e virologia per supportare la tua ricerca in malattie infettive, microbiologia e virologia.
Sottocategorie di "Microbiologia/Virologia"
- Antibatterico(2.968 prodotti)
- Antibiotico(922 prodotti)
- Antinfettivo(23 prodotti)
- DHFR(33 prodotti)
- Sintesi del DNA/RNA(711 prodotti)
- HBV(177 prodotti)
- Proteasi HIV(451 prodotti)
- HSV(91 prodotti)
- Integrasi(2 prodotti)
- Ribosoma(13 prodotti)
Mostrare 2 più sottocategorie
Trovati 5863 prodotti di "Microbiologia/Virologia"
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Antitubercular agent 34
CAS:<p>Compound 42g: potent antitubercular, MIC 90 of 1.25 µg/mL, resists liver metabolism.</p>Formula:C19H14N4O2SColore e forma:SolidPeso molecolare:362.41AFK-108
CAS:<p>AFK-108 is a fungicide agent.</p>Formula:C21H26Cl2N2OPurezza:98%Colore e forma:SolidPeso molecolare:393.35PXYC13
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:C15H15N5O2SColore e forma:SolidPeso molecolare:329.38A3N19
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:C31H31N9O2SColore e forma:SolidPeso molecolare:593.7ATD-3169
CAS:<p>ATD-3169 is a ROS generator with antibacterial activity.</p>Formula:C15H14O3Purezza:98%Colore e forma:SolidPeso molecolare: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:C7H13NS2Colore e forma:SolidPeso molecolare:175.31Lagociclovir
CAS:<p>Lagociclovir (MIV-210), a nucleoside analogue antiviral, treats HBV by inhibiting its replication in liver cancer cells.</p>Formula:C10H12FN5O3Purezza:99.18% - 99.33%Colore e forma:SolidPeso molecolare:269.23Antimicrobial agent-4
CAS:<p>Antimicrobial agent-4 (6a) has potent activity against pathogens; binds target enzyme with 10.0 kcal/mol affinity.</p>Formula:C22H16ClN5O2SColore e forma:SolidPeso molecolare:449.91MurA-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:C27H23ClN2O5SColore e forma:SolidPeso molecolare:523Antileishmanial agent-8
CAS:<p>Compound 18: Antileishmanial, IC50=5.64 μM for L. donovani, low toxicity in L-6 cells, IC50=73.9 μM.</p>Formula:C18H16O4Colore e forma:SolidPeso molecolare:296.32GAK inhibitor 2
CAS:<p>GAK inhibitor 2, IC50: 0.024μM, strongly blocks GAK; potent against dengue virus, EC50: 1.049μM.</p>Formula:C20H23N3O3SColore e forma:SolidPeso molecolare:385.48SARS-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:C17H20N2O2Colore e forma:SolidPeso molecolare:284.35Tromantadine
CAS:Tromantadine is an amantadine derivative with antiherpetic activity (inhibits HSV-1 and HSV-2 replication).Formula:C16H28N2O2Purezza:98%Colore e forma:SolidPeso molecolare:280.41Epsiprantel
CAS:<p>Epsiprantel is an orally active antiparasitic drug that inhibits various tapeworms, including Echinococcus granulosus (granular echinococcus), in dogs.</p>Formula:C20H26N2O2Purezza:98.09%Colore e forma:SolidPeso molecolare:326.43HIV-1 inhibitor-9
CAS:<p>HIV-1 inhibitor-9 potently blocks WT and NNRTI-resistant HIV strains at low nanomolar levels.</p>Formula:C24H21N5OColore e forma:SolidPeso molecolare:395.462-Keto-D-galactose
CAS:<p>2-Keto-D-galactose inhibits DNA synthesis and inhibits the proliferation of in vitro grown Ehrlich ascites tumor cells.</p>Formula:C6H10O6Purezza:98%Colore e forma:SolidPeso molecolare:178.14Salifluor
CAS:<p>Salifluor is a broad spectrum antimicrobial agent that has been investigated for its abilities to inhibit dental plaque formation.</p>Formula:C22H24F3NO3Colore e forma:SolidPeso molecolare:407.43MmpL3-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:C27H30N2Colore e forma:SolidPeso molecolare:382.54Penciclovir Sodium
CAS:antiviral drugFormula:C10H14N5NaO3Purezza:98%Colore e forma:SolidPeso molecolare:275.2396GS-9256
CAS:<p>GS-9256 is a selective inhibitor of the HCV NS3 protease, exhibiting favorable pharmacokinetic properties and antiviral activity [1].</p>Formula:C46H56ClF2N6O8PSPurezza:98%Colore e forma:SolidPeso molecolare:957.46Antimalarial 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:C20H16N4O2Purezza:98%Colore e forma:SolidPeso molecolare:344.37BA-53038B
CAS:BA-53038B is an HBV core protein allosteric modulator (CpAM), binding to the HAP pocket and modulating HBV capsid assembly in a distinct manner (EC50: 3.32 μM).Formula:C14H16ClNOColore e forma:SolidPeso molecolare:249.74Antiparasitic agent-18
CAS:<p>Antiparasitic agent-18 (compound 3a) exhibits potent and selective antiprotozoal activity, demonstrating effective inhibition of T.</p>Formula:C25H21N7OPurezza:98%Colore e forma:SolidPeso molecolare:435.48Tropesin
CAS:<p>Tropesin is a non-steroidal anti-inflammatory agent (NSAIA) that has inhibitory effects on the growth of Xylaria green.</p>Formula:C28H24ClNO6Colore e forma:SolidPeso molecolare:505.95MptpB-IN-1
CAS:<p>MptpB-IN-1: orally active, potent MptpB inhibitor; reduces drug-resistant tuberculosis.</p>Formula:C17H11Cl2NO4Colore e forma:SolidPeso molecolare:364.18β-Lactamase-IN-1
CAS:β-Lactamase-IN-1 (4-(1,3-dihydroxypropan-2-yl)-6-methoxypyrido[2,3-b]pyrazin-3-one) is a β-Lactamase inhibitor and targets the infection of NeisseriaFormula:C11H13N3O4Purezza:99.89%Colore e forma:SolidPeso molecolare:251.24Werner syndrome RecQ helicase-IN-4
CAS:<p>Werner syndrome RecQ helicase-IN-4 is a WRN inhibitor with anticancer and anti-proliferative activity, used in colorectal and gastric cancer research.</p>Formula:C32H33F3N8O5Purezza:98.27%Colore e forma:SolidPeso molecolare:666.65HIV-1 inhibitor-53
CAS:<p>HIV-1 Inhibitor-53 targets HIV-1 protease (IC50: 1.93 nM) and reverse transcriptase (IC50: 2.35 μM), aiding AIDS research.</p>Formula:C30H34N2O8SPurezza:98%Colore e forma:SolidPeso molecolare:582.66HIV-1 protease-IN-5
CAS:<p>HIV-1 protease-IN-5 is an HIV-1 protease inhibitor (IC50: 1.64 nM). HIV-1 protease-IN-5 exhibits significant effects on wild-type and DRV-resistant HIV-1.</p>Formula:C27H29F3N2O7SColore e forma:SolidPeso molecolare:582.59Chelator 1a
CAS:<p>Chelator 1a has antifungal activity, inhibiting Aspergillus and Candida, and can be used to study fungal infections and cancer.</p>Formula:C16H12BrN3OSColore e forma:SolidPeso molecolare:374.26Chitin synthase inhibitor 2
CAS:<p>Chitin synthase inhibitor 2 (2b) has an IC50 of 0.09 mM, K i 0.12 mM, shows in vitro antimicrobial activity and boosts fluconazole/polyoxin B.</p>Formula:C20H19N3O3Colore e forma:SolidPeso molecolare:349.38Metallo-β-lactamase-IN-8
CAS:<p>Metallo-β-lactamase-IN-8 (compound 17) is a potent, reversible and competitive broad-spectrum metallo-β-lactamases (MβLs) inhibitor with antibacterial activity.</p>Formula:C13H11ClN2O4SColore e forma:SolidPeso molecolare:326.76DPC-963
CAS:<p>DPC-963 is a RNA-directed DNA polymerase inhibitor.</p>Formula:C14H9F5N2OColore e forma:SolidPeso molecolare:316.23SARS-CoV-2 nsp3-IN-2
CAS:<p>SARS-CoV-2 nsp3-IN-2: Mac1 inhibitor, IC50=180μM, hinders virus replication.</p>Formula:C10H12N4O2Colore e forma:SolidPeso molecolare:220.23VP-4509
CAS:<p>VP-4509: Anti-MRSA, MIC 49.3 μM; combats Pseudomonas aeruginosa.</p>Formula:C14H16N2O5SColore e forma:SolidPeso molecolare:324.35Fozivudine tidoxil
CAS:<p>Fozivudine tidoxil, a reverse transcriptase inhibitor, is used potentially for the treatment of HIV infection.</p>Formula:C35H64N5O8PSColore e forma:SolidPeso molecolare:745.95Antiparasitic agent-9
CAS:<p>Antiparasitic agent-9 (compound 47) - orally active with high efficacy against human parasites.</p>Formula:C18H20N6O2SColore e forma:SolidPeso molecolare:384.46SMR000071098
CAS:<p>SMR000071098 is an inhibitor of Fe-S cluster-dependent aconitase. SMR000071098 interacts with Suf proteins to inhibit iron-sulfur (Fe-S) cluster assembly.</p>Formula:C17H12N2O2Colore e forma:SolidPeso molecolare:276.29Taribavirin hydrochloride
CAS:<p>Taribavirin HCl: oral drug targeting HCV in liver, spares red blood cells, aims to reduce anemia risk.</p>Formula:C8H14ClN5O4Purezza:98%Colore e forma:SolidPeso molecolare:279.68Goitrin
CAS:<p>Goitrin, from glucosinolate reactions, blocks thyroid peroxidase and iodine use, and fights H1N1.</p>Formula:C5H7NOSColore e forma:SolidPeso molecolare:129.18Anti-infective agent 1
CAS:<p>Compound 3a: potent, selective antiprotozoal/antimycobacterial. IC50: P. falciparum 10.95 μM, T. brucei 0.06 μM. MIC against M. smegmatis: 8 μg/mL.</p>Formula:C16H10O2Colore e forma:SolidPeso molecolare:234.25ZINC04177596
CAS:<p>ZINC04177596 is a novel Nef Protein Inhibitor with anti-HIV activity.</p>Formula:C22H16N6O4Colore e forma:SolidPeso molecolare:428.4D-Xylofuranose, 1,2,3,5-tetraacetate
CAS:<p>1,2,3,5-Tetra-O-acetyl-D-xylofuranose is a starting material for the synthesis of nucleosides.</p>Formula:C13H18O9Colore e forma:SolidPeso molecolare:318.28Rovafovir Etalafenamide
CAS:<p>Rovafovir Etalafenamide is a prodrug of anti-HIV nucleoside phosphonate.</p>Formula:C21H24FN6O6PPurezza:98%Colore e forma:SolidPeso molecolare:506.42Trovirdine hydrochloride
CAS:<p>Trovirdine hydrochloride is a reverse transcriptase inhibitor.</p>Formula:C13H14BrClN4SPurezza:98%Colore e forma:SolidPeso molecolare:373.7Exeporfinium chloride
CAS:Exeporfinium chloride(XF-73) is an antimicrobial agent that can weaken bacterial cell walls.Formula:C44H50Cl2N6O2Colore e forma:SolidPeso molecolare:765.81Pyrisoxazole
CAS:<p>Pyrisoxazole is a novel fungicide inhibitor of Sterol 14α-demethylase.</p>Formula:C16H17ClN2OColore e forma:SolidPeso molecolare:288.77SARS-CoV-2 nsp13-IN-6
CAS:<p>nsp13-IN-6 inhibits SARS-CoV-2 nsp13, targeting ssDNA+ATPase (IC50: 27 μM) and ssDNA-ATPase (IC50: 33 μM) for COVID-19 research.</p>Formula:C21H19N5O3SColore e forma:SolidPeso molecolare:421.47Reverse transcriptase-IN-4
<p>Reverse transcriptase-IN-4: potent, selective NNRT inhibitor; EC50 = 0.053 μM for HIV-1, 0.26 μM for E138K mutant.</p>Formula:C17H21N5OSColore e forma:SolidPeso molecolare:343.453-Fucosyllactose
CAS:<p>3-Fucosyllactose, a key fucosylated oligosaccharide in human milk, offers prebiotic and immune benefits.</p>Formula:C18H32O15Colore e forma:SolidPeso molecolare:488.44Antimalarial agent 20
CAS:<p>Antimalarial agent 20, exhibiting potent efficacy with an IC50 value of 0.6 nM against the P.</p>Formula:C31H38N4O3Colore e forma:SolidPeso molecolare:514.66Bunamidine hydrochloride
CAS:<p>Bunamidine hydrochloride is a veterinary anthelmintic that acts against Echinococcus granulosus and Tapeworm.</p>Formula:C25H39ClN2OColore e forma:SolidPeso molecolare: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:C23H21BrN6O2SColore e forma:SolidPeso molecolare:525.42MK436
CAS:<p>MK436 is a therapeutic agent and an antigenic animal drug that is effective in the treatment of Trypanosoma cruzonii infection.</p>Formula:C11H14N4O3Colore e forma:SolidPeso molecolare:250.25S-F24
CAS:<p>S-F24 is a broad-spectrum antifungal agent that demonstrates potent inhibition of CYP3A4, with an IC50 of 0.4 μM.</p>Formula:C25H27BrF2N6OColore e forma:SolidPeso molecolare:545.42MDRTB-IN-1
CAS:<p>MDRTB-IN-1 (5aα) is an antibiotic which is against Mycobacterium tuberculosis H37Rv(MIC90 :10.5 μM).</p>Formula:C15H18N2O3Purezza:98%Colore e forma:SolidPeso molecolare:274.32F-17
CAS:<p>F-17 inhibits biofilm, elastase, pyocyanin, and motility, binds to LasR/PqsR, and is non-cytotoxic.</p>Formula:C17H15BrO4Colore e forma:SolidPeso molecolare:363.2CBR-6672
CAS:<p>CBR-6672, a potent anti-tuberculosis agent; type II NADH dehydrogenase inhibitor; MIC: 0.14 μM.</p>Formula:C17H20FN3O2SColore e forma:SolidPeso molecolare:349.42Antitubercular agent-24
CAS:<p>Compound 1: Antitubercular, fights M. tuberculosis H37Rv, IC50 - extracellular 0.83 μM, intracellular 0.17 μM.</p>Formula:C18H19N3O2S2Colore e forma:SolidPeso molecolare:373.49Adenallene
CAS:<p>Adenallene inhibits replication and cytopathic effects of HIV in vitro.</p>Formula:C9H9N5OPurezza:98%Colore e forma:SolidPeso molecolare:203.2FR900098 (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:C5H12NNaO5PColore e forma:SolidPeso molecolare:220.117MurA-IN-2
CAS:<p>MurA-IN-2: potent MurA inhibitor, IC50 of 39μM, chloroacetamide with aliphatic amine; has antibacterial properties.</p>Formula:C12H20ClNOColore e forma:SolidPeso molecolare:229.75HadAB-IN-1
CAS:<p>HadAB-IN-1: potent TB research chemical; IC50 = 0.03μM; inhibits HadAB, affecting Mtb mycolic acid synthesis.</p>Formula:C19H17BrClN3O3SColore e forma:SolidPeso molecolare:482.78DDD100097
CAS:<p>DDD100097 is a N-myristoyltransferase inhibitor with potential inhibitory effects on Trypanosoma brucei, which can be used to study neurological disorders.</p>Formula:C22H30Cl2F2N4O2SPurezza:98.89%Colore e forma:SolidPeso molecolare:523.47Antibacterial agent 67
CAS:<p>Antibacterial agent 67 blocks succinate dehydrogenase more effectively than haloperidol, with IC50 of 0.03 μM vs 4.40 μM.</p>Formula:C24H15F6N5OColore e forma:SolidPeso molecolare:503.4HIV-1 protease-IN-1
CAS:<p>HIV-1 protease-IN-1, potent HIV inhibitor; IC50=90pM, fights B/C-HIV strains with EC50=89-13.59/8.23nM.</p>Formula:C25H35N3O6SColore e forma:SolidPeso molecolare:505.63TbPTR1 inhibitor 1
CAS:<p>TbPTR1 inhibitor 1 effectively targets kinetochore PTR1 with IC50 <0.1 nM, EC50 0.66 μM against Trypanosoma brucei.</p>Formula:C22H21N7OColore e forma:SolidPeso molecolare:399.45BTZ-N3
CAS:<p>BTZ-N3 is an effective and selective anti-tuberculosis drug candidate.</p>Formula:C17H16F3N5O3SColore e forma:SolidPeso molecolare:427.42-Hydroxydocosanoic acid
CAS:<p>2-Hydroxydocosanoic acid exhibits antioxidant, cholinesterase inhibitory, and antimicrobial properties [1].</p>Formula:C22H44O3Colore e forma:SolidPeso molecolare: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:C14H12BrN5OColore e forma:SolidPeso molecolare:346.18Salazopyridazine
CAS:<p>Salazopyridazine is an antibacterial agent that inhibits ulcerative colitis. salazopyridazine can be used in the study of rheumatic diseases.</p>Formula:C18H15N5O6SColore e forma:SolidPeso molecolare:429.41VEC-5
CAS:<p>VEC-5: an HIV-1 inhibitor, outperforms RN18 by better binding with Vif in studies.</p>Formula:C29H21NO4Purezza:98%Colore e forma:SolidPeso molecolare:447.48P516-0475
CAS:<p>P516-0475, a novel inducer, enhances Streptococcus quorum sensing by blocking PepO, stabilizing SHP pheromones.</p>Formula:C15H17N5O3Colore e forma:SolidPeso molecolare:315.33HI-236
CAS:<p>HI-236 is used as a non-nucleoside HIV-1 reverse-transcriptase inhibitor.</p>Formula:C16H18BrN3O2SPurezza:98%Colore e forma:SolidPeso molecolare:396.3HIV-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:C15H13Cl3N6Colore e forma:SolidPeso molecolare:383.66Cefepime chloride
CAS:<p>Cefepime chloride, a broad-spectrum cephalosporin, combats Gram-positive/negative bacteria and can induce neurotoxicity.</p>Formula:C19H25ClN6O5S2Colore e forma:SolidPeso molecolare:517.02Pyribencarb
CAS:<p>Pyribencarb, a benzylcarbamate-type fungicide, exhibits broad-spectrum activity against various plant pathogenic fungi.</p>Formula:C18H20ClN3O3Purezza:99.75%Colore e forma:SolidPeso molecolare:361.82SARS-CoV MPro-IN-1
CAS:<p>MProinhibitor 11b blocks SARS-CoV-2 main protease (IC50=0.04 μM), cuts viral yield and RNA in Vero E6 cells (EC50=0.72 μM).</p>Formula:C25H25FN4O4Colore e forma:SolidPeso molecolare:464.49Antibacterial agent 97
CAS:<p>Antibacterial agent 97 is potent; MIC: 16 μg/mL for E. coli and S. aureus.</p>Formula:C19H23N5SColore e forma:SolidPeso molecolare:353.48Bofumustine
CAS:<p>Bofumustine is a chloroethyl nitrosourea with anti tumor properties.</p>Formula:C18H21ClN4O9Colore e forma:SolidPeso molecolare:472.83HIV-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:C19H20ClN3O2Colore e forma:SolidPeso molecolare:357.83Lupulon
CAS:<p>Lupulon has a role as an apoptosis inducer, antimicrobial agent, angiogenesis inhibitor, and antineoplastic agent.</p>Formula:C26H38O4Colore e forma:SolidPeso molecolare:414.583CPLro-IN-2
CAS:<p>3CPLro-IN-2: Potent oral SARS-CoV-2 3CLpro inhibitor, IC50: 1.55 μM, Ki: 6.09 μM, targets vital COVID-19 protein.</p>Formula:C32H24BrNO2Colore e forma:SolidPeso molecolare:534.44BMVC
CAS:<p>BMVC is a potent G-quadruplex (G4) stabilizer and a selective telomerase inhibitor (IC50: ~0.2 μM) with anticancer activities.</p>Formula:C28H25I2N3Colore e forma:SolidPeso molecolare:657.33PC170942 Sodium
CAS:<p>PC170942 Sodium is a water-soluble bacterial cytokinesis inhibitor that acts by inhibiting FtsZ.</p>Formula:C24H24ClNO2SPurezza:98%Colore e forma:SolidPeso molecolare:425.97Antitubercular agent-26
CAS:<p>Compound 32: oral antitubercular, acts on M. tuberculosis, IC50 ~0.50μM, stable, low cardiotoxicity, non-genotoxic.</p>Formula:C22H23N5O3S2Colore e forma:SolidPeso molecolare:469.58RD3-0028
CAS:<p>RD3-0028 is a potent and selective RSV replication inhibitor(EC50 of 4.5 μM).</p>Formula:C8H8S2Purezza:98%Colore e forma:SolidPeso molecolare:168.28SARS-CoV-2 Mpro-IN-5
<p>SARS-CoV-2 Mpro-IN-5: inhibits Mpro (IC50=1800nM) & CatL (IC50=145nM), antiviral, hinders replication in hACE2 A549 cells (IC50=14.7nM).</p>Formula:C34H43FN4O7Colore e forma:SolidPeso molecolare:638.73Cap-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:C29H25F2N3O7SColore e forma:SolidPeso molecolare:597.59RSV-IN-4
CAS:<p>RSV-IN-4 is a dual inhibitor for RSV and IAV with an EC50 of 11.76 μM.</p>Formula:C18H18N2O2SColore e forma:SolidPeso molecolare:326.41RyRs 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:C21H14ClF3N6O4Colore e forma:SolidPeso molecolare:506.82FadD32 Inhibitor-1
CAS:<p>FadD32 inhibitor -1 has anti-tuberculosis activity and is an effective FadD32 inhibitor.</p>Formula:C24H20ClN3OPurezza:98%Colore e forma:SolidPeso molecolare:401.89SARS-CoV-2-IN-18
CAS:<p>SARS-CoV-2-IN-18 (Compound 26) is a potent inhibitor of SARS-CoV-2 3C-like protease (IC50 = 45 nM) [1].</p>Formula:C20H14N2O3Colore e forma:SolidPeso molecolare:330.34Urease-IN-5
<p>Urease-IN-5: urease inhibitor, IC50 1.473 µM, low cytotoxicity, IC50 17.78 µg/mL on P. vulgaris.</p>Formula:C16H20N2O3SColore e forma:SolidPeso molecolare:320.41HBV-IN-16
CAS:<p>HBV-IN-16, a quinoline derivative, inhibits HBV cccDNA, key for viral replication (from patent WO2019121357A1).</p>Formula:C22H20ClNO4Colore e forma:SolidPeso molecolare:397.85Dihydropteroate synthase-IN-1
CAS:<p>"Dihydropteroate synthase-IN-1 (5g) inhibits DHPS and cytochrome P450, useful as radiographic diagnostic material."</p>Formula:C19H23N5O4S2Colore e forma:SolidPeso molecolare:449.55Crisnatol mesylate
CAS:<p>Crisnatol, a potent and selective DNA intercalator, has potential anticancer activity.</p>Formula:C24H27NO5SColore e forma:SolidPeso molecolare:441.54Isobellidifolin
CAS:<p>Isobellidifolin, a xanthone compound, serves as a free radical scavenger and antioxidant. It exhibits a potent antifungal effect.</p>Formula:C14H10O6Colore e forma:SolidPeso molecolare: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:C19H19ClFN5O4Colore e forma:SolidPeso molecolare:435.84Floxacrine
CAS:<p>Floxacrine is drug candidate for chemoprophylaxis of malaria.</p>Formula:C20H13ClF3NO3Purezza:98%Colore e forma:SolidPeso molecolare: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:C20H27NOColore e forma:SolidPeso molecolare:297.43Antitrypanosomal agent 10
<p>Antitrypanosomal agent 10, an antitrypanosomal compound, effectively inhibits Trypanosoma cruzi with an IC50 of 0.28 μM.</p>Formula:C17H9F6N5OColore e forma:SolidPeso molecolare:413.28Antibacterial agent 122
CAS:<p>Thiourea derivative 122 is a low-toxicity antibacterial used in tuberculosis research with anti-mycobacterial properties.</p>Formula:C15H14N2O3SColore e forma:SolidPeso molecolare:302.35Cadrofloxacin
CAS:<p>Cadrofloxacin (Caderofloxacin, CS-940) is a novel fluoroquinolone antimicrobial agent.</p>Formula:C19H20F3N3O4Colore e forma:SolidPeso molecolare:411.38Sitamaquine 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:C28H41N3O4SColore e forma:SolidPeso molecolare:515.71Antimalarial agent 11
CAS:<p>Antimalarial compound 1: Spirocyclic chromane, EC50 - D6: 1.48 μM, ARC08-022: 1.81 μM.</p>Formula:C25H25F2NO3Colore e forma:SolidPeso molecolare: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:C24H17ClN2O6Colore e forma:SolidPeso molecolare:464.85DHQZ 36
CAS:<p>DHQZ 36: retrograde trafficking inhibitor, anti-parasite, stops Leishmania amazonensis (EC50: 13.63 μM).</p>Formula:C21H18F2N2OSPurezza:98%Colore e forma:SolidPeso molecolare:384.44gp120-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:C15H18N2O5Colore e forma:SolidPeso molecolare:306.31Antifungal agent 68
CAS:<p>Antifungal agent 68 (compound 10) effectively combats fungal infections caused by Candida and Cryptococcus gattii through the inhibition of ergosterol</p>Formula:C23H27ClN2O3Colore e forma:SolidPeso molecolare:414.93Laburnetin
CAS:<p>Laburnetin: an isoflavone antibacterial, combats fungi/S. vesicarium, boosts MRSA methicillin susceptibility, used in pest control.</p>Formula:C20H18O6Colore e forma:SolidPeso molecolare:354.35Antibacterial agent 98
CAS:<p>Compound g37, an oral antibacterial, inhibits Gyrase B ATPase and S. aureus DNA super-helix without causing MRSA resistance.</p>Formula:C17H13N5O3S2Colore e forma:SolidPeso molecolare:399.45Antimalarial agent 8
CAS:<p>Compound 7e: novel oral antimalarial, effective against P. falciparum in vitro and in vivo (40 mg/kg).</p>Formula:C22H21Cl3N4OColore e forma:SolidPeso molecolare:463.79Antibacterial agent 105
CAS:<p>Compound 17, a phenanthrolinic quinolone, fights M. tuberculosis (MIC 90: 2.64 μM) and various bacteria (MIC 90: 0.70-44.70 μM).</p>Formula:C14H9N3O5Colore e forma:SolidPeso molecolare:299.24PqsR/LasR-IN-3
CAS:<p>PqsR/LasR-IN-3 (Compound 7a) inhibits hERG with the IC 50 of 109.01 μM which is also a PqsR and LasR systems inhibitor in P. aeruginosa [1].</p>Formula:C14H17NO5SColore e forma:SolidPeso molecolare:311.35Apricitabine
CAS:<p>Apricitabine (SPD754) is a highly selective and orally active HIV-1 reverse transcriptase inhibitor (Ki=0.08 μM), the (-) enantiomer of 2′-deoxy-3′-oxy-4′-</p>Formula:C8H11N3O3SPurezza:99.45%Colore e forma:SolidPeso molecolare:229.26Antiviral agent 20
CAS:<p>Antiviral agent 20 (Compound 17b) is a selective inhibitor of Zika virus (EC50: 4.5 μM) and exhibits low cytotoxicity.</p>Formula:C31H35Cl2NO6Colore e forma:SolidPeso molecolare:588.52MPO
CAS:MPO (5-(4'-Methoxyphenyl)-oxazole) is a hatch and growth of Caenorhabditis Elegans inhibitor.Formula:C10H9NO2Purezza:99.86%Colore e forma:SolidPeso molecolare:175.18Antitrypanosomal agent 11
<p>Antitrypanosomal Agent 11 is a chemical compound effective against Trypanosoma cruzi, exhibiting an inhibition concentration (IC 50) of 0.23 μM.</p>Formula:C16H10F6N6OColore e forma:SolidPeso molecolare:416.28Antibacterial agent 95
CAS:<p>Antibacterial 95, a quinoline-derived antituberculotic, shows 0.3 μM MIC against Mycobacterium tuberculosis H37Rv and inhibits its growth in macrophages.</p>Formula:C19H16ClNO3Colore e forma:SolidPeso molecolare:341.79Influenza virus-IN-3
CAS:<p>Influenza virus-IN-3 inhibits H5N1, H5N2, H5N6, H5N8 with low toxicity; targets neuraminidase.</p>Formula:C25H32N2O4SColore e forma:SolidPeso molecolare:456.6Antibacterial agent 19
CAS:<p>Antibacterial agent 19 targets K. pneumoniae and multi-resistant S. aureus with MICs: 0.022 and 0.045 mg/mL.</p>Formula:C16H16F2N2O4Colore e forma:SolidPeso molecolare:338.31Purfalcamine
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:C29H33FN8OColore e forma:SolidPeso molecolare:528.62RHI002-Me
CAS:<p>RHI002-Me is a methylated derivative of RHI002, a selective inhibitor of human RNaseH2.</p>Formula:C18H19N3O2S2Purezza:98%Colore e forma:SolidPeso molecolare:373.49Antibacterial agent 72
CAS:<p>Antibacterial agent 72 has an antibacterial effect by selectively acting on bacterial membranes.</p>Formula:C19H21BrN4SColore e forma:SolidPeso molecolare:417.37HIV-1 inhibitor-49
<p>HIV-1 inhibitor-49, an oral HEPT analog, has strong pharmacokinetics, potent reverse transcriptase inhibition (IC50=30nM), and is safe in mice.</p>Formula:C21H18F2N2O3SColore e forma:SolidPeso molecolare:416.44Grepafloxacin Hydrochloride
CAS:<p>Grepafloxacin Hydrochloride is an antimicrobial agent, oral broad-spectrum fluoroquinolone. It is used to treat bacterial infections.</p>Formula:C19H23ClFN3O3Colore e forma:SolidPeso molecolare:395.86CAY10784
CAS:<p>CAY10784(STAT3-IN-17) is a STAT3 inhibitor with antiproliferative and antitumor activities. CAY10784 showed antibacterial activity against Clostridium difficile</p>Formula:C11H6F3N3O3SPurezza:99.74%Colore e forma:SolidPeso molecolare:317.24HIV-IN-5
CAS:<p>HIV-IN-5 (5r) inhibits HIV-1 with 0.16 μM IC50, targeting NNIBP as a NNRTI.</p>Formula:C30H24N2O8SColore e forma:SolidPeso molecolare: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:C13H12N6O3SColore e forma:SolidPeso molecolare:332.34Antibacterial agent 106
CAS:<p>Compound 106 is an orally active antibacterial with biofilm-fighting properties, kills 99.7% of MRSA in macrophages.</p>Formula:C20H24N6SColore e forma:SolidPeso molecolare:380.51Antiviral agent 23
CAS:<p>Antiviral agent 23 targets EV71 with 94 nM EC50 and suppresses METTL3/14, useful in infection research.</p>Formula:C18H21N5O4Colore e forma:SolidPeso molecolare:371.39Tolindate
CAS:<p>Tolindate, a potent PXR agonist, demonstrates antifungal activity and possesses an EC50 value of 8.3 µM.</p>Formula:C18H19NOSColore e forma:SolidPeso molecolare: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:C27H29F3N2OColore e forma:SolidPeso molecolare:454.53APOBEC3G-IN-1
CAS:<p>APOBEC3G-IN-1 (MN136.0185) is a targeted APOBEC3G inhibitor with anti-HIV activity for the study of infectious diseases and cancer.</p>Formula:C15H11NO3Purezza:96.54%Colore e forma:SolidPeso molecolare:253.259-OxoOTrE
CAS:<p>9-OxoOTrE, made by oxidizing 9-HpOTrE, has antimicrobial effects on plant pathogens like bacteria and fungi.</p>Formula:C18H28O3Colore e forma:SolidPeso molecolare:292.41Antistaphylococcal agent 2
CAS:<p>Antistaphylococcal agent 2 is an anti-staphylococcal therapeutic agent.</p>Formula:C23H21N5O5Colore e forma:SolidPeso molecolare:447.44Sch 25393
CAS:Sch 25393 is an antibacterial agent in vitro.Formula:C12H14F3NO4SPurezza:98%Colore e forma:SolidPeso molecolare:325.3SARS-CoV-2 nsp13-IN-4
CAS:<p>Potent SARS-CoV-2 nsp13-IN-4 selectively inhibits nsp13 helicase with 57 μM IC50, offering antiviral effects.</p>Formula:C20H15BrN4OColore e forma:SolidPeso molecolare:407.26GSK983
CAS:<p>GSK983 inhibits DHODH to halt cell growth and dengue virus replication, acting as a broad-spectrum antiviral.</p>Formula:C18H16ClN3OPurezza:98%Colore e forma:SolidPeso molecolare:325.79HIV-1 inhibitor-28
CAS:<p>HIV-1 inhibitor-28: potent, selective, EC50=58 nM, low MT-4 cell toxicity (CC50=38.6 μM), valuable in AIDS research.</p>Formula:C26H32N6O3SColore e forma:SolidPeso molecolare:508.64Zidebactam sodium salt
CAS:Zidebactam sodium salt is a potent inhibitor of β-lactamase, and also is an inhibitor of penicillin-binding protein2 (PBP2)(IC50 of 0.26 μg/mL).Formula:C13H21N5NaO7SPurezza:98%Colore e forma:SolidPeso molecolare:414.39B 669
CAS:<p>B 669 has antibacterial activity.</p>Formula:C30H28N4Colore e forma:SolidPeso molecolare:444.57L 739594
CAS:<p>L 739594 is an inhibitor of HIV-1 protease.</p>Formula:C31H47N3O6Purezza:98%Colore e forma:SolidPeso molecolare:557.72IACS-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:C10H17N3O2Colore e forma:SolidPeso molecolare:211.26Antitubercular 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:C14H8BrN3O3Colore e forma:SolidPeso molecolare:346.14Norstictic acid
CAS:<p>Norstictic acid: a potent, selective transcription regulator with anticancer, antioxidant, and antimicrobial properties.</p>Formula:C18H12O9Colore e forma:SolidPeso molecolare:372.28Antimicrobial agent-6
<p>Antimicrobial agent-6: MIC 4-8 μg/mL for gram+ & gram- bacteria, anti-inflammatory.</p>Formula:C40H64N16Colore e forma:SolidPeso molecolare:769.04Mtb-cyt-bd oxidase-IN-4
<p>Mtb-cyt-bd oxidase inhibitor; IC50=0.25μM; MIC=8μM against Mycobacterium tuberculosis; for TB research.</p>Formula:C25H32FNOColore e forma:SolidPeso molecolare:381.53G0507
CAS:G0507, a potent pyrrolopyrimidinedione, blocks E. coli growth by activating σE stress and targeting LolCDE ABC Transporter.Formula:C18H15N3O3SColore e forma:SolidPeso molecolare:353.39(-)-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:C15H12O4Colore e forma:SolidPeso molecolare:256.25RO5464466
CAS:<p>RO5464466 is an inhibitor of influenza A virus (H1N1) fusion.</p>Formula:C16H26N2O3SColore e forma:SolidPeso molecolare:326.45Sisapronil
CAS:<p>Sisapronil is a member of the phenylpyrazole class of antiparasitics.</p>Formula:C15H6Cl2F8N4Colore e forma:SolidPeso molecolare:465.13Acoziborole
CAS: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.Formula:C17H14BF4NO3Colore e forma:SolidPeso molecolare:367.1HIV-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:C19H16BrN5Colore e forma:SolidPeso molecolare: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:C13H12Cl3N5OSColore e forma:SolidPeso molecolare:392.69Nucleoside-Analog-1
CAS:Nucleoside-Analog-1 is a 4′-Azidocytidine analogue, used to against Hepatitis C virus replication.Formula:C9H9N5O5Purezza:98%Colore e forma:SolidPeso molecolare:267.2Oxaquin
CAS:<p>Oxaquin, a water-soluble injectable prodrug, converts to active MCB3681 post-IV to fight Gram-positive bacteria.</p>Formula:C31H33F2N4O11PPurezza:98%Colore e forma:SolidPeso molecolare:706.58Mt 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:C13H8FN5O3S2Colore e forma:SolidPeso molecolare:365.36Furalazine
CAS:<p>Furalazine: antimicrobial, treats cholera, more effective than chloramphenicol in shortening stool culture positivity.</p>Formula:C9H7N5O3Purezza:98%Colore e forma:SolidPeso molecolare:233.18VU0420373
CAS:<p>VU0420373 activates HssRS at EC50 10.7 μM, induces heme synthesis, toxic to S. aureus.</p>Formula:C15H11FN2OColore e forma:SolidPeso molecolare:254.26CWHM-1008
CAS:CWHM-1008: Oral antimalarial, EC50 - 46 nM (3D7 strain), 21 nM (Dd2 resistant).Formula:C22H26F3N3OColore e forma:SolidPeso molecolare:405.46Antifungal 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:C21H26Cl3NOSColore e forma:SolidPeso molecolare:446.86Acibenzolar-S-methyl
CAS:<p>Acibenzolar-S-methyl, a fungicide, boosts plant defenses by upregulating W-box genes like CAD1, NPR1, PR2.</p>Formula:C8H6N2OS2Purezza:99.64% - 99.86%Colore e forma:Beige Fine PowderPeso molecolare:210.28Antitubercular 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:C17H14N4O2Colore e forma:SolidPeso molecolare: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:C20H21N3O5SColore e forma:SolidPeso molecolare: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:C17H14FN5Colore e forma:SolidPeso molecolare:307.33Soporidine
CAS:<p>Soporidine, a strigolactone antagonist, blocks AtHTL, hindering SL signaling and seed germination.</p>Formula:C27H30F3NO3Purezza:98%Colore e forma:SolidPeso molecolare:473.53Antitubercular 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:C24H20F6N4O3SColore e forma:SolidPeso molecolare:558.5DLC27-14
CAS:<p>DLC27-14 is an HIV-1 Nef specific protein disorder catalyzer.</p>Formula:C25H25NO4Colore e forma:SolidPeso molecolare:403.47Neuraminidase-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:C18H16FN3O3SColore e forma:SolidPeso molecolare:373.4Neuraminidase-IN-3
CAS:<p>Neuraminidase-IN-3 inhibits flu NA: H1N1 IC50=0.73nM, H5N1=0.26nM, H5N8=0.63nM.</p>Formula:C27H32N2O4SColore e forma:SolidPeso molecolare:480.62Afabicin disodium
CAS:<p>Afabicin (Debio 1450), a Debio1452 precursor, targets Staphylococcus by inhibiting lipid synthesis.</p>Formula:C23H22N3Na2O7PColore e forma:SolidPeso molecolare:529.396Synthalin sulfate
CAS:<p>Synthalin sulfate is a NMDA receptor antagonist.</p>Formula:C12H30N6O4SPurezza:98%Colore e forma:SolidPeso molecolare:354.47Vps34-IN-2
CAS: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).Formula:C18H25F3N4O3Purezza:98%Colore e forma:SolidPeso molecolare:402.41EP39
<p>EP39 is a potent HIV-1 inhibitor, stabilizing the SP1 domain's helix and blocking virus maturation.</p>Formula:C38H62N2O5Colore e forma:SolidPeso molecolare:626.91Posaconazole hydrate
CAS:<p>Posaconazole: broad-spectrum antifungal, second-gen triazole, strong C14α demethylase inhibitor (IC50: 0.25 nM).</p>Formula:C37H44F2N8O5Purezza:98%Colore e forma:SolidPeso molecolare:718.79MmpL3-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:C26H33ClN2SiColore e forma:SolidPeso molecolare:437.09SARS-CoV-IN-1
CAS:SARS-CoV-IN-1 is an effective SARS-CoV replication inhibitor(EC50 of 4.9 μM in Vero cells).Formula:C23H24ClFeN3OPurezza:98%Colore e forma:SolidPeso molecolare:449.76Cap-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:C29H23F2N3O6SColore e forma:SolidPeso molecolare:579.57SARS-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:C30H30N4O5Colore e forma:SolidPeso molecolare:526.58Robenidine
CAS:<p>Robenidine, an anticoccidial guanidine, is used as an additive in rabbit fodder.</p>Formula:C15H13Cl2N5Purezza:98%Colore e forma:SolidPeso molecolare:334.2GNF179 (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:C14H16FN3Purezza:98%Colore e forma:SolidPeso molecolare:245.3BMS-585248
CAS:<p>BMS-585248 is a highly effective HIV-1 adhesion inhibitor that targets the viral envelope protein gp120.</p>Formula:C22H18FN7O3Colore e forma:SolidPeso molecolare:447.42CK-2-68
CAS:<p>CK-2-68 is a potent inhibitor of PfNDH2.</p>Formula:C24H17ClF3NO2Purezza:98%Colore e forma:SolidPeso molecolare:443.85SJ-3366
CAS:<p>SJ3366 is a unique and highly potent nonnucleoside reverse transcriptase human immunodeficiency virus type 1 and HIV-2 inhibitor.</p>Formula:C21H24N2O3Colore e forma:SolidPeso molecolare:352.43Phenosulfazole
CAS:<p>Phenosulfazole is a potent antiviral agent which has the potential for the research of poliomyelitis virus [1].</p>Formula:C9H8N2O3S2Colore e forma:SolidPeso molecolare:256.3NEU617
CAS:<p>NEU617 is an inhibitor of the growth of protozoan parasites, against T. brucei bloodstream proliferation.</p>Formula:C31H26ClFN4O2Colore e forma:SolidPeso molecolare:541.02Pralurbactam
CAS:<p>Pralurbactam is a β-Lactamase inhibitor utilized in the research of bacterial infections.</p>Formula:C10H18N6O8SColore e forma:SolidPeso molecolare:382.35TH-Z93
CAS:<p>TH-Z93 is a potent FPPS inhibitor (IC50:90 nM) and a lipophilic bisphosphonate.</p>Formula:C12H22N2O7P2Purezza:98.37%Colore e forma:SolidPeso molecolare:368.26AIC-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:C19H12Cl2F2N4O2Colore e forma:SolidPeso molecolare:437.23Cylindrospermopsin
CAS:<p>Cylindrospermopsin: a toxic cyanobacterial uracil derivative, disrupts protein/glutathione synthesis in hepatocytes, and is genotoxic.</p>Formula:C15H21N5O7SColore e forma:SolidPeso molecolare: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:C17H21N5O3Colore e forma:SolidPeso molecolare: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:C39H55N6O8PColore e forma:SolidPeso molecolare:766.86HCV-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:C31H36ClN5Colore e forma:SolidPeso molecolare:514.1DprE1-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:C19H21N3O6S2Colore e forma:SolidPeso molecolare:451.52Dabequin
CAS:<p>Dabequin is a derivative of aminoquinoline. It is said to have pharmacological activity against Plasmodium fukiparum.</p>Formula:C19H29N3O8P2Colore e forma:SolidPeso molecolare:489.4MMV024101
CAS:<p>MMV024101: PI4K inhibitor, P. falciparum NF54 IC50 543 nM, poor solubility (<5 μM), fast mouse liver clearance.</p>Formula:C16H12N6O2SColore e forma:SolidPeso molecolare:352.37SARS-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:C30H38N4O5Colore e forma:SolidPeso molecolare:534.65pUL89 Endonuclease-IN-2
CAS:<p>pUL89 Endonuclease-IN-2 inhibits HCMV with a 3.0 μM IC50, showing potent antiviral effects.</p>Formula:C17H12F3N3O3SColore e forma:SolidPeso molecolare:395.36
