Microbiologia/Virologia
Os inibidores de microbiologia e virologia são compostos que têm como alvo microrganismos, incluindo bactérias, vírus e fungos, interrompendo seu crescimento, replicação ou sobrevivência. Esses inibidores são essenciais para estudar a patogênese microbiana, entender os mecanismos de resistência e desenvolver novas terapias antimicrobianas e antivirais. Os inibidores nessa categoria são usados para combater doenças infecciosas, explorar a ecologia microbiana e investigar as interações hospedeiro-patógeno. Na CymitQuimica, oferecemos uma ampla seleção de inibidores de alta qualidade para microbiologia e virologia para apoiar sua pesquisa em doenças infecciosas, microbiologia e virologia.
Subcategorias de "Microbiologia/Virologia"
- Antibacteriano(2.968 produtos)
- Antibiótico(922 produtos)
- Antifecção(23 produtos)
- DHFR(33 produtos)
- Síntese de DNA/RNA(711 produtos)
- HBV(177 produtos)
- HIV Protease(451 produtos)
- HSV(91 produtos)
- Integrase(2 produtos)
- Ribossomo(13 produtos)
Exibir 2 mais subcategorias
Foram encontrados 5863 produtos de "Microbiologia/Virologia"
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Diazaborine
CAS:<p>Diazaborine disrupts large ribosome formation by inhibiting rRNA maturation and AAA-ATPase Drg1, leading to rapid protein redistribution.</p>Fórmula:C14H13BN2O3SPureza:98%Cor e Forma:SolidPeso molecular:300.14Mycobactin-IN-2
CAS:<p>Mycobactin-IN-2 inhibits mycobactin production by targeting salicyl-AMP ligase (MbtA), a crucial enzyme in its pathway.</p>Fórmula:C15H13BrN2OCor e Forma:SolidPeso molecular:317.18DHDPS-IN-1
CAS:<p>DHDPS-IN-1 (compound 8), a DHDPS inhibitor with 39 μM IC50, has potential in antibacterial and herbicidal applications.</p>Fórmula:C13H11NO5SCor e Forma:SolidPeso molecular:293.3WRR-483
CAS:<p>WRR-483, a cysteine protease inhibitor similar to K-11777, has trypanocidal properties and potential against Chagas' disease.</p>Fórmula:C29H41N7O4SCor e Forma:SolidPeso molecular:583.75(R,R)-BAY-Y 3118
CAS:<p>(R,R)-BAY-Y 3118, the R-enantiomer of BAY-Y 3118, exhibits weak bactericidal activity.</p>Fórmula:C20H21ClFN3O3Cor e Forma:SolidPeso molecular:405.85L-Eflornithine
CAS:<p>L-Eflornithine: irreversible ODC inhibitor, KD 1.3±0.3 μM, Kinact 0.15±0.03 min-1, enantiomer of Eflornithine.</p>Fórmula:C6H12F2N2O2Pureza:98%Cor e Forma:SolidPeso molecular:182.17SDH-IN-5
CAS:<p>SDH-IN-5 (compound 7d), a potent inhibitor of succinate dehydrogenase (SDH) with an IC50 of 3.293 μM, additionally demonstrates antifungal efficacy, exhibiting</p>Fórmula:C16H19F2N3O2Cor e Forma:SolidPeso molecular:323.34BMH-22
CAS:<p>BMH-22 is an RNA polymerase I inhibitor that acts by causing nucleolar stress and showing potent anticancer activity across many tumor types.</p>Fórmula:C16H17N3Cor e Forma:SolidPeso molecular:251.33Triaziquone
CAS:<p>Triaziquone is an alkylating agent that can react with DNA to form intrastrand crosslinks.</p>Fórmula:C12H13N3O2Cor e Forma:SolidPeso molecular:231.25BPH-1218
CAS:BPH-1218 is a SQS inhibitor.Fórmula:C15H30N2O6P2Pureza:98%Cor e Forma:SolidPeso molecular:396.36(S)-Tedizolid
CAS:<p>(S)-Tedizolid is the S-enantiomer of Tedizolid. Tedizolid is a novel oxazolidinone with activity against Gram-positive pathogens.</p>Fórmula:C17H15FN6O3Pureza:98%Cor e Forma:SolidPeso molecular:370.34KDU731
CAS:KDU731: oral drug for Cryptosporidium-induced diarrhea, safe PI4K inhibitor (IC50: 25 nM), effective in vitro/in vivo.Fórmula:C22H16N6O2Pureza:98%Cor e Forma:SolidPeso molecular:396.4A110
CAS:A110 is a potent and selective IMPDHs inhibitor. It binds to the NAD(+) cofactor site and forms a ternary complex with IMP.Fórmula:C19H15ClN4O2Pureza:98%Cor e Forma:SolidPeso molecular:366.8HIV-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>Fórmula:C30H26N6O3SCor e Forma:SolidPeso molecular:550.63ST7612AA1
CAS:<p>ST7612AA1: potent, oral HDAC inhibitor; reactivates HIV-1 latency; shows antitumor effects; may study malaria.</p>Fórmula:C20H27N3O4SPureza:99.71%Cor e Forma:SolidPeso molecular:405.51Ipconazole [ISO]
CAS:<p>Ipconazole, a cyclopentanol with 1,2,4-triazolylmethyl, 4-chlorobenzyl & isopropyl groups, is a fungicide that targets seed diseases.</p>Fórmula:C18H24ClN3OCor e Forma:SolidPeso molecular:333.86KFU-127
<p>KFU-127: broad-spectrum antimicrobial; targets bacterial/fungal biofilms; toxic to eukaryotic cells.</p>Fórmula:C34H43BrN2O3Cor e Forma:SolidPeso molecular:607.62SARS-CoV-2-IN-19
CAS:<p>"SARS-CoV-2-IN-19: potent SARS-CoV-2 decapping enzyme inhibitor, EC50 8.8 μM, potential for HCoV outbreaks."</p>Fórmula:C33H38N2O6Cor e Forma:SolidPeso molecular:558.66HIV-1 inhibitor-37
CAS:<p>HIV-1 inhibitor-37, a potent HIV-1 suppressant, shows promise as a novel latent reactivator.</p>Fórmula:C14H11Cl3N4OCor e Forma:SolidPeso molecular:357.62BK 218
CAS:<p>BK 218: New cephalosporin, treats S. pneumoniae, H. influenzae, M. catarrhalis; less effective on penicillin-resistant strains; oral/IV use.</p>Fórmula:C15H14ClN7NaO5S2Cor e Forma:SolidPeso molecular:494.88YXL-13
CAS:<p>YXL-13 suppresses Pseudomonas aeruginosa, hampers virulence and biofilms, and reduces drug resistance with an IC50 of 3.686 μM.</p>Fórmula:C13H15BrN2O4Cor e Forma:SolidPeso molecular:343.17Metallo-β-lactamase-IN-4
CAS:<p>Metallo-β-lactamase-IN-4 (compound 40) is a potent inhibitor of metallo-β-lactamases (MBL) with IC 50 values of 0.5 μM, 2.1 μM, and 3.3 μM for VIM-1, NDM-1 and</p>Fórmula:C10H14N4O3S2Cor e Forma:SolidPeso molecular:302.37FLDP-5
CAS:<p>FLDP-5: BBB-penetrant curcuminoid, induces ROS, DNA damage, S phase arrest, suppresses tumors in LN-18 cells.</p>Fórmula:C21H21NO5Cor e Forma:SolidPeso molecular:367.4Derquantel
CAS:<p>nicotinic acetylcholine receptor antagonist</p>Fórmula:C28H37N3O4Pureza:98%Cor e Forma:SolidPeso molecular:479.61HBV-IN-6
CAS:<p>HBV-IN-6 is a potent inhibitor of HBV (EC50: 44 nM).</p>Fórmula:C23H21ClFN3O5S2Cor e Forma:SolidPeso molecular:538.01Metallo-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>Fórmula:C9H9Cl2NOSCor e Forma:SolidPeso molecular:250.14PD 140248
CAS:<p>PD 140248, a broad-spectrum 7-pyrrolidinyl fluoronaphthyridines, has been demonstrated to have excellent in vitro activity against gram-positive organisms.</p>Fórmula:C21H20ClF3N4O3Cor e Forma:SolidPeso molecular:468.86Benzoxonium chloride
CAS:<p>Benzoxonium chloride used in Thio-Ben for cutaneous leishmaniasis treatment with cryotherapy.</p>Fórmula:C23H42ClNO2Cor e Forma:SolidPeso molecular:400.04CL-55
CAS:<p>CL-55 is a novel inhibitor of T3SS.</p>Fórmula:C19H17F2N3O4SCor e Forma:SolidPeso molecular:421.42HCV-IN-36
CAS:<p>HCV-IN-36: oral HCV inhibitor, EC50 0.016 μM, CC50 8.78 μM, potent antiviral.</p>Fórmula:C30H36ClN5Cor e Forma:SolidPeso molecular:502.09SARS-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>Fórmula:C14H9ClF3NO2Cor e Forma:SolidPeso molecular:315.67LpxC-IN-9
CAS:<p>LpxC-IN-9 (compound 19) is a potent inhibitor of LpxC and exhibits antibacterial and hypotensive activity.</p>Fórmula:C23H25N5O3SCor e Forma:SolidPeso molecular:451.54Antibacterial 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>Fórmula:C28H39NO4SCor e Forma:SolidPeso molecular:485.68PXYC12
CAS:<p>PXYC12 inhibits Mtb RpsA, key in trans-translation; binds RpsA-CTD (Kd 2.67μM) and RpsA-CTD Δ438A (Kd 4.67μM).</p>Fórmula:C15H15N5O2SCor e Forma:SolidPeso molecular:329.38Tenofovir maleate
CAS:<p>Tenofovir Disoproxil Fumarate is a nucleotide reverse transcriptase inhibitor used in the treatment of HIV and chronic Hepatitis B.</p>Fórmula:C13H18N5O8PCor e Forma:SolidPeso molecular:403.28HBV-IN-21
CAS:<p>HBV-IN-21 inhibits HBV DNA replication (IC50: 2.2 μM) and binds HBV capsid protein well (KD: 60.0 μM).</p>Fórmula:C17H17FN4OS2Cor e Forma:SolidPeso molecular:376.47MMV676584
CAS:<p>MMV676584 has anti-tuberculosis avtivity. MMV676584 is a novel drug candidate for eumycetoma .</p>Fórmula:C12H8ClFN2OS2Cor e Forma:SolidPeso molecular:314.79HSV-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>Fórmula:C18H14F4N4OSCor e Forma:SolidPeso molecular:410.39ANT431
CAS:<p>ANT431 is a novel metallo-β-lactamase inhibitor for the treatment of carbapenem-resistant enterobacteriaceae infections</p>Fórmula:C9H7N3O4S2Cor e Forma:SolidPeso molecular:285.3CAY10760
CAS:<p>CAY10760 inhibits RAD51-BRCA2 interaction (EC50=19 μM), reduces homologous recombination by 54%, and hinders BxPC-3/Capan-1 cancer cell proliferation.</p>Fórmula:C28H24ClN3O3Cor e Forma:SolidPeso molecular:485.96Stampidine
CAS:<p>Stampidine prevents HIV-1, effective against resistant strains at subnanomolar levels.</p>Fórmula:C20H23BrN3O8PPureza:98%Cor e Forma:SolidPeso molecular:544.29Antileishmanial agent-3
CAS:<p>Antileishmanial agent-3 (Compound 13) effectively inhibits the growth of Leishmania major [1].</p>Fórmula:C14H13ClN6O4Cor e Forma:SolidPeso molecular:364.74Antiparasitic agent-2
CAS:<p>Compound 8a: potent against L. infantum (IC50=7.28μM) & T. cruzi (IC50=2.30μM); mildly toxic to HepG2 (CC50=26.79μM).</p>Fórmula:C20H17N3O3Cor e Forma:SolidPeso molecular:347.37GA-O-06
<p>GA-O-06: 18β-Glycyrrhetinic acid derivative with powerful antimicrobial effects on Gram-positive bacteria and anti-inflammatory properties.</p>Fórmula:C37H46FNO6Cor e Forma:SolidPeso molecular:619.76HBV-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>Fórmula:C22H19ClO5SCor e Forma:SolidPeso molecular:430.9Influenza virus-IN-1
CAS:<p>Influenza virus-IN-1, a potent anti-influenza A compound, has CC50 >200 μM, EC50 2.46 μM, and inhibits PAN endonuclease (EC50 312.36 nM).</p>Fórmula:C16H17NO5Cor e Forma:SolidPeso molecular:303.31MMV666810
CAS:<p>MMV666810 is a potent 2-aminopyrazine, effective against asexual parasites at 5.94 nM and 3.3x more selective for late-stage gametocytes.</p>Fórmula:C23H21F3N4O2Cor e Forma:SolidPeso molecular:442.43Deaminase inhibitor-1
CAS:<p>Deaminase inhibitor-1 is an APOBEC3G DNA Deaminase inhibitor with an IC 50 value of 18.9 μM [1].</p>Fórmula:C11H12BrN3OSCor e Forma:SolidPeso molecular:314.2HIV-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>Fórmula:C24H18FN5O2Cor e Forma:SolidPeso molecular:427.43Edelfosine
CAS:<p>inhibits phosphatidylinositol phospholipase C</p>Fórmula:C27H58NO6PPureza:98%Cor e Forma:SolidPeso molecular:523.73Antimycobacterial 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>Fórmula:C18H12N4O5SCor e Forma:SolidPeso molecular:396.38Phosphoglycolohydroxamic acid
CAS:<p>Phosphoglycolohydroxamic acid inhibits aldolase/triose-phosphate isomerase; used in antibacterial/antifungal research.</p>Fórmula:C2H6NO6PCor e Forma:SolidPeso molecular:171.05AB-506
CAS:<p>AB-506: Oral HBV replication blocker, targets core protein, hinders pgRNA encapsidation, for CHB study.</p>Fórmula:C21H18ClF2N5O3Cor e Forma:SolidPeso molecular:461.85SARS-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>Fórmula:C22H15NO7Cor e Forma:SolidPeso molecular:405.36Antituberculosis agent-2
CAS:<p>Compound 8d: treats MDR and sensitive tuberculosis, low toxicity, good oral bioavailability, stable in humans/mice; MIC: 0.454-1.757 μg/mL.</p>Fórmula:C19H17NO4Cor e Forma:SolidPeso molecular:323.34Diamthazole
CAS:<p>Diamthazole (Dimazole) is an antifungal agent that can be used in the infection research[1].</p>Fórmula:C15H23N3OSCor e Forma:SolidPeso molecular:293.43pUL89 Endonuclease-IN-1
CAS:<p>Compound 13d: potent pUL89 endonuclease inhibitor, IC50 0.88 μM, anti-HCMV activity.</p>Fórmula:C10H8N2O4SCor e Forma:SolidPeso molecular:252.25SARS-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>Fórmula:C18H18Cl3N3O2SCor e Forma:SolidPeso molecular:446.78W13
CAS:<p>W13 is a potent inhibitor of MsbA and is an ATPase stimulator (EC50: 5.5 μM).</p>Fórmula:C30H34N4O3Cor e Forma:SolidPeso molecular:498.62Debneyol
CAS:<p>Debneyol exhibits more potent fungicidal activity than validamycin.</p>Fórmula:C15H26O2Cor e Forma:SolidPeso molecular:238.37cp028
CAS:<p>cp028 inhibits pre-mRNA splicing in vitro.</p>Fórmula:C23H17FN2O4Cor e Forma:SolidPeso molecular:404.39FR-182024
CAS:<p>FR-182024 is a novel cephem derivative, it has potent anti-Helicobacter pylori activity.</p>Fórmula:C18H16N4O4S3Cor e Forma:SolidPeso molecular:448.54Dealanylalahopcin
CAS:<p>Dealanylalahopcin is a procollagen prolyl-4-hydroxylase inhibitor.</p>Fórmula:C6H10N2O5Cor e Forma:SolidPeso molecular:190.15Penamecillin
CAS:<p>Penamecillin (Wy 20788) is an orally active antibacterial agent.</p>Fórmula:C19H22N2O6SCor e Forma:SolidPeso molecular:406.45(5S,8R)-HBV-IN-10
CAS:<p>'(5S,8R)-HBV-IN-10 is an EC50 0.1-1 μM HBsAg inhibitor, isomer of compound 6 from patent WO2021204258A1.</p>Fórmula:C23H24FN7OCor e Forma:SolidPeso molecular:433.48Mtb-cyt-bd oxidase-IN-3
<p>Mtb-cyt-bd oxidase-IN-3 inhibits M. tuberculosis growth, IC50 0.36 μM, MIC 32 μM, for TB research.</p>Fórmula:C26H35NO2Cor e Forma:SolidPeso molecular:393.56Quinuronium Sulfate
CAS:<p>Quinuronium sulfate treats Babesia in calves; doesn't stop carrier state; may lead to hepatic fat degeneration, not GSH depletion.</p>Fórmula:C22H23N4O5SCor e Forma:SolidPeso molecular:455.51Antibacterial agent 74
CAS:<p>Antibacterial agent 74 (compound 36) has anti-Salmonella activity [1].</p>Fórmula:C16H20N2O3Cor e Forma:SolidPeso molecular:288.34Acyclovir monophosphate
CAS:<p>Acyclovir monophosphate, a strong anti-HSV agent, inhibits viral DNA polymerase, blocking DNA synthesis and chain elongation.</p>Fórmula:C8H12N5O6PCor e Forma:SolidPeso molecular:305.18Aranotin
CAS:<p>Aranotin, from Arachniotus aureus, inhibits RNA viruses by blocking RNA polymerase.</p>Fórmula:C20H18N2O7S2Cor e Forma:SolidPeso molecular:462.5Fungicide4
CAS:<p>Fungicide4 exhibits the high activity against the P. infestans strain.</p>Fórmula:C14H11N3OCor e Forma:SolidPeso molecular:237.26Antifungal agent 70
CAS:<p>Antifungal Agent 70 (Compound 13), a dihydroeugenol-imidazole, exhibits efficacy against multi-resistant Candida auris with a minimum inhibitory concentration (</p>Fórmula:C23H25ClN2O4Cor e Forma:SolidPeso molecular:428.91Metallo-β-lactamase-IN-3
CAS:<p>Metallo-β-lactamase-IN-3 (compound 35) is a potent metallo-β-lactamases (MBL) inhibitor that has the potential to restore the activity of current β-lactam</p>Fórmula:C10H11NO3SCor e Forma:SolidPeso molecular:225.26MptpB-IN-1
CAS:<p>MptpB-IN-1: orally active, potent MptpB inhibitor; reduces drug-resistant tuberculosis.</p>Fórmula:C17H11Cl2NO4Cor e Forma:SolidPeso molecular:364.18Ceftobiprole medocaril sodium
CAS:<p>Ceftobiprole medocaril sodium (BAL5788) is a prodrug of broad-spectrum cephalosporin active against MRSA, VRSA, and resistant streptococci.</p>Fórmula:C26H25N8NaO11S2Cor e Forma:SolidPeso molecular:712.64Sudoterb HCl
CAS:<p>Sudoterb has anti-tubercular activity.</p>Fórmula:C29H30Cl2F3N5OPureza:98%Cor e Forma:SolidPeso molecular:592.48PknB-IN-1
CAS:<p>PknB-IN-1 inhibits PknB (IC50: 14.4 μM), has anti-mycobacterial effects (MIC: 6.2 μg/mL) against M. tuberculosis H37Rv.</p>Fórmula:C25H30N2O2Cor e Forma:SolidPeso molecular:390.52Tropesin
CAS:<p>Tropesin is a non-steroidal anti-inflammatory agent (NSAIA) that has inhibitory effects on the growth of Xylaria green.</p>Fórmula:C28H24ClNO6Cor e Forma:SolidPeso molecular:505.95Antitubercular agent-12
CAS:<p>Compound 2c, an effective antitubercular, MIC 1.439 μg/mL, low toxicity with CC50 57.34 μg/mL.</p>Fórmula:C13H7BrN4O5Cor e Forma:SolidPeso molecular:379.124-Piperidinecarboxamide
CAS:<p>4-Piperidinecarboxamide is a mycobacterial aspartyl-tRNA synthetase (AspS) inhibitor and a potential anti-tuberculosis (TB) agent [1].</p>Fórmula:C16H15Cl2N3O2SCor e Forma:SolidPeso molecular:384.28HCV-IN-35
CAS:<p>HCV-IN-35 is a potent inhibitor of HCV and shows potential for infectious disease research.</p>Fórmula:C30H36ClN5Cor e Forma:SolidPeso molecular:502.09PC58538
CAS:<p>PC58538 is an inhibitor of FtsZ protein, a important role in the division machinery of bacterial cells.</p>Fórmula:C24H25NO3Cor e Forma:SolidPeso molecular:375.46Salifluor
CAS:<p>Salifluor is a broad spectrum antimicrobial agent that has been investigated for its abilities to inhibit dental plaque formation.</p>Fórmula:C22H24F3NO3Cor e Forma:SolidPeso molecular:407.43HIV-1 inhibitor-9
CAS:<p>HIV-1 inhibitor-9 potently blocks WT and NNRTI-resistant HIV strains at low nanomolar levels.</p>Fórmula:C24H21N5OCor e Forma:SolidPeso molecular:395.465,10-Dideazaaminopterin
CAS:<p>5,10-Dideazaaminopterin is an antileukemic drug.</p>Fórmula:C21H22N6O5Pureza:98%Cor e Forma:SolidPeso molecular:438.44(+)-Dihydrocalanolide A
CAS:<p>DHCal A (NSC 678323) is an oral nonnucleoside Reverse Transcriptase inhibitor for HIV research.</p>Fórmula:C22H28O5Cor e Forma:SolidPeso molecular:372.45HPV18-IN-1
CAS:<p>HPV18-IN-1, potent cervical cancer inhibitor, blocks E7-Rb-E2F pathway and DNA methylation.</p>Fórmula:C14H10N4OSCor e Forma:SolidPeso molecular:282.32(S)-Enzaplatovir
CAS:<p>(S)-Enzaplatovir, an S-enantiomer with antiviral properties, has an EC50 of 56 nM against RSV.</p>Fórmula:C20H19N5O3Cor e Forma:SolidPeso molecular:377.4HBV-IN-14
CAS:<p>HBV-IN-14: a pyridinopyrimidinone, potent cccDNA inhibitor for HBV study (patent WO2021190502A1, comp 5).</p>Fórmula:C22H21ClN2O5Cor e Forma:SolidPeso molecular:428.87Antibacterial agent 126
<p>Antibacterial agent 126 combats biofilm, disrupts membranes, and boosts ROS/RNS to prevent drug resistance.</p>Fórmula:C21H24NO6PCor e Forma:SolidPeso molecular:417.39Anti-inflammatory agent 14
CAS:<p>Anti-inflammatory agent 14 (compound 28) has a MIC 50 of 2 μM for Mtb H37Rv. Anti-inflammatory agent 14 is also an anti-inflammatory agent [1].</p>Fórmula:C16H16N2O2SCor e Forma:SolidPeso molecular:300.38MMV688845
CAS:<p>MMV688845: NTM RNA polymerase inhibitor, kills Mycobacterium abscessus, and fights TB.</p>Fórmula:C24H25N3O3SCor e Forma:SolidPeso molecular:435.54TLC3407-3786
CAS:<p>MMV665916: Antimalarial quinazolinedione, effective against P. falciparum (EC50 = 0.4 µM), high selectivity (SI > 250).</p>Fórmula:C19H19N3O4Cor e Forma:SolidPeso molecular:353.37BioA-IN-13
CAS:<p>BioA-IN-13 is a highly effective inhibitor of the Mycobacterium tuberculosis BioA enzyme, displaying potent cell permeability and whole-cell activity [1].</p>Fórmula:C19H16N2O4SCor e Forma:SolidPeso molecular:368.41Antiparasitic agent-7
CAS:<p>Compound 5d, antiparasitic for L. infantum, IC50 of 2.85μM; cytotoxic to HepG2 cells, CC50 of 10.61μM.</p>Fórmula:C18H15N3O5Cor e Forma:SolidPeso molecular:353.33Pomotrelvir
CAS:<p>Pomotrelvir (PBI-0451) is an oral SARS-CoV-2 3CL protease inhibitor with antiviral properties for COVID-19 research.</p>Fórmula:C23H26ClN5O3Cor e Forma:SolidPeso molecular:455.94HIV-1 inhibitor-47
CAS:<p>HIV-1 Inhibitor-47 blocks Vif-APOBEC3G interaction, has 14.33 μM IC50, and may yield antianxiety and antipsychotic derivatives.</p>Fórmula:C12H14N6Cor e Forma:SolidPeso molecular:242.28Antibacterial agent 124
CAS:<p>Antibacterial agent 124 inhibits Sa ProRS with an IC50 of 0.18 μM.</p>Fórmula:C16H17ClFN3O2Cor e Forma:SolidPeso molecular:337.78GRL-1720
CAS:<p>GRL-1720 is a SARS-CoV-2 Protease inhibitor (IC50 = 320 nM). GRL-1720 contains an indoline which targets the SARS-CoV-2 main protease (Mpro)</p>Fórmula:C14H11ClN2O2Cor e Forma:SolidPeso molecular:274.7HBV-IN-15
CAS:<p>HBV-IN-15, a flavone derivative, is a potent cccDNA inhibitor, potentially aiding HBV research.</p>Fórmula:C24H23ClO6Cor e Forma:SolidPeso molecular:442.89
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