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(2.949 produtos)
- Antibiótico(918 produtos)
- Antifecção(23 produtos)
- DHFR(32 produtos)
- Síntese de DNA/RNA(706 produtos)
- HBV(176 produtos)
- HIV Protease(447 produtos)
- HSV(91 produtos)
- Integrase(2 produtos)
- Ribossomo(13 produtos)
Exibir 2 mais subcategorias
Foram encontrados 5832 produtos de "Microbiologia/Virologia"
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Zika virus-IN-2
CAS:<p>Zika virus-IN-2 (Compd 3) is a Zika virus inhibitor (EC 50= 7.4 μM).</p>Fórmula:C24H23N3O3Cor e Forma:SolidPeso molecular:401.46Antimalarial agent 10
CAS:<p>Compound 17b, an amino alcohol-quinoline, targets Pf3D7 (IC50: 14.9 nM) and PfW2 (IC50: 11 nM) with selectivity index >770.</p>Fórmula:C23H22F6N2O2Cor e Forma:SolidPeso molecular:472.42WRNA10
CAS:<p>WRNA10 is a potent binding agent for HIV-1TAR RNA (IC50: 10 μM, CC50: 40 μM).</p>Fórmula:C25H32N4O4Cor e Forma:SolidPeso molecular:452.55Lagociclovir valactate
CAS:<p>Lagociclovir valactate is a prodrug of Lagociclovir . Lagociclovir valactate is an orally active anti- HBV agent [1] .</p>Fórmula:C18H25FN6O6Cor e Forma:SolidPeso molecular:440.43AZ-27
CAS:<p>AZ-27 is a respiratory syncytial virus inhibitor which differentially inhibits different polymerase activities at the promoter.</p>Fórmula:C36H35N5O4SCor e Forma:SolidPeso molecular:633.76Micronomicin
CAS:<p>Micronomicin (Gentamicin C2b) is an antibiotic exhibiting antibacterial and bactericidal capacity.</p>Fórmula:C20H41N5O7Pureza:97.05% - 99.79%Cor e Forma:SolidPeso molecular:463.57T145
CAS:<p>T145 halts key bacteria growth at sub μg/ml, deters resistance, and may enhance drug lifespan.</p>Fórmula:C18H16N2O5Pureza:98%Cor e Forma:SolidPeso molecular:340.33Ulonivirine
CAS:<p>Ulonivirine is an orally active non-nucleoside reverse transcriptase inhibitor that exhibits high antiviral activity and can be used to study HIV-1 infection.</p>Fórmula:C18H8ClF6N5O3Cor e Forma:SolidPeso molecular:491.73Antifungal agent 77
CAS:<p>Antifungal agent 77 (Compound 13h) exhibits not only antifungal properties, but also effective insecticidal activity against Mythimna separata, Helicoverpa</p>Fórmula:C21H18FN5O2Cor e Forma:SolidPeso molecular:391.4Anti-Trypanosoma cruzi agent-3
CAS:<p>Anti-Trypanosoma cruzi agent-3 is an antiprotozoal agent.</p>Fórmula:C29H29N3O6SCor e Forma:SolidPeso molecular:547.62Elastase LasB-IN-1
CAS:<p>Elastase LasB-IN-1 (Compound 4b), a potent and selective inhibitor of elastase LasB, exhibits antibacterial activity and has been determined to possess an IC50</p>Fórmula:C13H17F3NO4PCor e Forma:SolidPeso molecular:339.25Mpro 61
CAS:<p>Mpro 61 is a potent non-covalent inhibitor of SARS-CoV-2 main protease.</p>Fórmula:C28H19Cl2FN4O4Cor e Forma:SolidPeso molecular:565.38BMS-561390
CAS:<p>BMS-561390, a reverse transcriptase inhibitor, is used potentially for the treatment of HIV infection.</p>Fórmula:C14H12ClF3N2OCor e Forma:SolidPeso molecular:316.71ISPA-28
CAS:<p>ISPA-28: reversible PSAC antagonist via direct CLAG3 binding.</p>Fórmula:C21H24N6O3Cor e Forma:SolidPeso molecular:408.45β-Lactamase-IN-2
CAS:<p>β-Lactamase-IN-2 is an inhibitor of β-Lactamase with anti-microbial and anti-bacterial effects.</p>Fórmula:C11H9FO3Pureza:99.52%Cor e Forma:SolidPeso molecular:208.19RSV604 (R enantiomer)
CAS:<p>RSV604 R enantiomer is the R-enantiomer of RSV604. RSV604 is a respiratory syncytial virus (RSV) replication inhibitor.</p>Fórmula:C22H17FN4O2Pureza:98%Cor e Forma:SolidPeso molecular:388.39Ravidasvir HCl
CAS:<p>Ravidasvir, also known as PPI-668 and ASC16, is a second-generation, orally active, potent and selective HCV NS5A protein inhibitor.</p>Fórmula:C42H52Cl2N8O6Cor e Forma:SolidPeso molecular:835.828BMY-43748
CAS:<p>BMY-43748 is an antibacterial compound with great in vitro and in vivo antibacterial activity.</p>Fórmula:C20H17F3N4O3Pureza:98%Cor e Forma:SolidPeso molecular:418.37Anti-MRSA agent 5
CAS:<p>Potent anti-MRSA compound, MIC50: 0.38 μg/mL, minimal hERG activity (IC50: 40 μM), low toxicity, and resistance unlikely.</p>Fórmula:C25H22N4O4Cor e Forma:SolidPeso molecular:442.47RNA polymerase II-IN-1
CAS:<p>RNA polymerase II-IN-1 (19iv), an amatoxin, inhibits Pol II at 36.66 nM IC50, is more toxic to cancer cells, less to normal cells than α-Amanitin.</p>Fórmula:C38H53N11O12SPureza:98%Cor e Forma:SolidPeso molecular:887.964-Hydroxy-2-methylbenzenesulfonic acid ammonium
CAS:<p>4-Hydroxy-2-methylbenzene ammonium: Policresulen impurity, inhibits NS2B/NS3 protease (IC50: 0.48 μg/mL), hinders DENV2 in BHK-21 cells (IC50: 4.99 μg/mL).</p>Fórmula:C7H11NO4SPureza:98%Cor e Forma:SolidPeso molecular:205.23NS5A-IN-3
CAS:<p>NS5A-IN-3 is a potent NS5A inhibitor with high efficacy against HCV 1b, good activity on 3a, and strong metabolic stability; superior to daclatasvir.</p>Fórmula:C44H44N6O8Pureza:98%Cor e Forma:SolidPeso molecular:784.86UCB7362
CAS:<p>UCB7362 (GLXC-26743) is an orally available and potent plasmepsin X (PMX) inhibitor with anti-malarial activity.UCB7362 inhibits parasite reproduction.</p>Fórmula:C25H26ClN5O3Pureza:97.67%Cor e Forma:SolidPeso molecular:479.96Antileishmanial agent-17
CAS:<p>Antileishmanial agent-17, a coumarin hybrid, exhibits potent antileishmanial activity (IC50 <0.78 μM) while proving non-toxic to normal VERO cells.</p>Fórmula:C27H37N5O5Pureza:98%Cor e Forma:SolidPeso molecular:511.61Antibacterial agent 93
<p>Antibacterial agent 93: potent aaRS inhibitor; effective against certain gram-positive and negative bacteria.</p>Fórmula:C29H28Cl3N5O4Cor e Forma:SolidPeso molecular:616.92LS-BF1
CAS:<p>LS-BF1: Stable, low-toxic antimicrobial peptide targeting ESKAPE pathogens via cell membrane disruption, effective in mouse infection model.</p>Fórmula:C107H166N28O15Cor e Forma:SolidPeso molecular:2084.64CPFX2090
CAS:<p>CPFX2090, a cephalosporin antibacterial compound.</p>Fórmula:C28H28ClNO6Pureza:98%Cor e Forma:SolidPeso molecular:509.98XZ426
CAS:<p>XZ426 is a potent integrase strand transfer inhibitor with anti- HIV activity .</p>Fórmula:C22H24F2N4O4Cor e Forma:SolidPeso molecular:446.45BMS-433771 dihydrochloride hydrate
CAS:<p>BMS-433771 dihydrochloride hydrate is a potent oral RSV inhibitor, affects groups A & B, with a 20 nM EC50, used in respiratory disease research.</p>Fórmula:C21H27Cl2N5O3Cor e Forma:SolidPeso molecular:468.38BDM91270
CAS:<p>BDM91270 (compound 29) serves as an inhibitor of the E.</p>Fórmula:C17H21Cl3N4O2Cor e Forma:SolidPeso molecular:419.73PYR01
CAS:<p>PYR01 is a potent nonnucleoside reverse transcriptase inhibitor of HIV-1 and concurrently acts as a targeted activator to eliminate cells expressing HIV-1 [1].</p>Fórmula:C21H13F7N4O3Cor e Forma:SolidPeso molecular:502.34Flurofamide
CAS:<p>Flurofamide is an effective bacterial urease inhibitor and has potential in the treatment of infected urinary calculi.</p>Fórmula:C7H9FN3O2PPureza:96.01% - 98%Cor e Forma:SolidPeso molecular:217.14Antiviral agent 43
CAS:<p>Antiviral agent 43 (compound 16) serves as a potent, orally active inhibitor of influenza A virus entry, demonstrating efficacy by inhibiting the replication of the influenza A strains VH04-H5N1 and PR8-H1N1 with EC50 values of 240 nM and 72 nM, respectively [1].</p>Fórmula:C17H22ClF3N2OCor e Forma:SolidPeso molecular:362.82BRL44385
CAS:<p>BRL44385 is an effective and selective inhibitor of the replication of HSV-1 and HSV2, Epstein-Barr virus (EBV), and varicella-zoster virus (VZV).</p>Fórmula:C8H11N5O3Pureza:98%Cor e Forma:SolidPeso molecular:225.2MF 5137
CAS:<p>MF 5137 is an effective antimicrobial agent.</p>Fórmula:C23H23N3O3Pureza:98%Cor e Forma:SolidPeso molecular:389.45Pencitabine
CAS:<p>Pen is an oral cancer drug that blocks DNA synthesis by inhibiting key enzymes and integrating into DNA.</p>Fórmula:C15H20F3N3O6Cor e Forma:SolidPeso molecular:395.33β-Lactamase-IN-8
CAS:<p>β-Lactamase-IN-8 (compound 20) is a potent and oral bioavailable broad-spectrum cyclic boronate β-lactamase inhibitor that can be used for researching</p>Fórmula:C10H14BNO4SCor e Forma:SolidPeso molecular:255.1L-696229
CAS:<p>L-696229: specific HIV-1 RT inhibitor, blocks viral spread in various cells.</p>Fórmula:C17H18N2O2Pureza:98%Cor e Forma:SolidPeso molecular:282.34Y18501
CAS:<p>Y18501, an oxysterol-binding protein (OSBPI) inhibitor structurally akin to Oxathiapiprolin, demonstrates potent inhibition against Phytophthora spp.</p>Fórmula:C27H26F2N6O2SCor e Forma:SolidPeso molecular:536.6JTK-853
CAS:<p>JTK-853: novel non-nucleoside HCV polymerase inhibitor with strong antiviral activity (EC50: 0.38 μM genotype 1a, 0.035 μM 1b).</p>Fórmula:C28H23F7N6O4S2Pureza:98%Cor e Forma:SolidPeso molecular:704.64VT-1598
CAS:<p>VT-1598 is a novel, selective, orally active fungal CYP51 inhibitor. VT-1598 exhibits antifungal effects against Candida albicans.</p>Fórmula:C31H20F4N6O2Cor e Forma:SolidPeso molecular:584.52APX2039
CAS:<p>APX2039 is an orally active fungal Gwt1 enzyme inhibitor and a prodrug of the novel Gwt2096 inhibitor APX1.APX2039 exhibits potent anti-Kryptococcal activity</p>Fórmula:C20H15FN4O2Pureza:98.72% - 99.07%Cor e Forma:SolidPeso molecular:362.36Fosalvudine tidoxil
CAS:<p>Fosalvudine tidoxil, a nucleoside reverse transcriptase inhibitor, is used potentially for the treatment of HIV infection.</p>Fórmula:C35H64FN2O8PSPureza:98%Cor e Forma:SolidPeso molecular:722.93Antibiofilm agent-1
CAS:<p>Antibiofilm Agent-1, as detailed in WO2017011725A1 (compound 17) [1], serves as an antibacterial agent effective against Gram-positive pathogens.</p>Fórmula:C11H5Br2Cl2NO2Cor e Forma:SolidPeso molecular:413.88PTC725
CAS:<p>PTC725 is a selective HCV 1b replicons inhibitor. It has been shown to target the nonstructural protein 4B.</p>Fórmula:C23H18F4N6O2SPureza:98%Cor e Forma:SolidPeso molecular:518.49MC-VC-PAB-Cyclohexanediamine-Thailanstatin A
CAS:<p>MC-VC-PAB-Cyclohexanediamine-Thailanstatin A is a spliceostatin analog and a drug-linker conjugate for antibody-drug conjugates (ADC), comprising the cytotoxic</p>Fórmula:C63H91N9O16Pureza:98%Cor e Forma:SolidPeso molecular:1230.45HIV-1 inhibitor-3
CAS:<p>HIV-1 inhibitor-3 is an HIV infection inhibitor.</p>Fórmula:C9H10F2N2O5Pureza:98%Cor e Forma:SolidPeso molecular:264.18SARS-CoV-2 3CLpro-IN-2
CAS:<p>SARS-CoV-2 3CLpro-IN-2 is a potent inhibitor of the 3CL protease pair and has shown research potential for SARS-CoV-2 disease.</p>Fórmula:C21H18F5N5O4Cor e Forma:SolidPeso molecular:499.39Hinokinin
CAS:<p>Hinokinin (Cubebinolide), a bioactive lignan, exhibits a broad spectrum of pharmacological activities.</p>Fórmula:C20H18O6Cor e Forma:SolidPeso molecular:354.35UNC2170 maleate
CAS:<p>53BP1-binding protein 1 (53BP1) engages with dimethylated lysine 20 on histone 4 (H4K20me2) through its tandem tudor domains within a homodimer configuration, crucial for the DNA damage response. UNC2170, a micromolar 53BP1 ligand, selectively interacts with this site, demonstrating at least 17-fold preference for 53BP1 over similar proteins. This interaction occurs in a pocket formed by the 53BP1's tudor domains. Moreover, UNC2170 acts as an antagonist to 53BP1 in cellular lysates, effectively inhibiting class switch recombination, a process dependent on the functional 53BP1 tudor domain, thus confirming its cellular activity.</p>Fórmula:C14H21BrN2OC4H4O4Cor e Forma:SolidPeso molecular:429.314'-Acetyl-chrysomycin B
CAS:<p>4'-Acetyl-chrysomycin B, a 4'-acetylated analog of chrysomycin B, exhibits anti-Gram-positive bacterial and antimicrobial activities [1].</p>Fórmula:C29H30O10Cor e Forma:SolidPeso molecular:538.54GlcNAcstatin
CAS:<p>GlcNAcstatin, a selective glucoimidazole-based inhibitor of bacterial O-GlcNAcase, exhibits a K_i value of 4.6 pM and demonstrates a specificity that is 100,000</p>Fórmula:C20H27N3O4Cor e Forma:SolidPeso molecular:373.45AVG-233
CAS:<p>AVG-233 is an RNA-dependent RNA polymerase (RdRp) inhibitor with antiviral activity for the study of respiratory syncytial virus infections.</p>Fórmula:C26H22ClN5O3Pureza:99%Cor e Forma:SolidPeso molecular:487.94Antituberculosis agent-1
CAS:<p>Antituberculosis Agent-1 (Compound 8a) is an effective antituberculosis agent, demonstrating a minimum inhibitory concentration (MIC) of 3.84 μg/mL against</p>Fórmula:C21H21NO4Cor e Forma:SolidPeso molecular:351.4GSK-2485852
CAS:<p>GSK-2485852, a NS5B inhibitor, is used potentially for treatment of HCV infection.</p>Fórmula:C27H25BF2N2O6SCor e Forma:SolidPeso molecular:554.37Disoxaril
CAS:<p>Disoxaril (BRN 3626820, WIN 51711), an anti-picornavirus, blocks enterovirus by targeting VP1; boosts poliovirus inhibition with Ambioxime, Bioxazole.</p>Fórmula:C20H26N2O3Cor e Forma:SolidPeso molecular:342.43DHX9-IN-4
CAS:<p>DHX9-IN-4 is an ATP-dependent RNA helicase DHX9 inhibitor used in cancer research.</p>Fórmula:C21H22ClN5O4S2Pureza:98.12%Cor e Forma:SolidPeso molecular:508.01β-Gal-NONOate
CAS:<p>Beta-gal-nonoate, a β-galactosidase dependent nitric oxide (NO) donor, releases NO upon activation by β-galactosidase. It exhibits bactericidal activity, thus serving as an effective bactericide [1].</p>Fórmula:C10H19N3O7Cor e Forma:SolidPeso molecular:293.27Inz-5
CAS:<p>Inz-5 is a fungal-selective inhibitor of mitochondrial cytochrome bc1. Inz-5 impairs fungal virulence. It also prevents the evolution of drug resistance.</p>Fórmula:C18H14F4N6Cor e Forma:SolidPeso molecular:390.34Antifungal agent 50
CAS:<p>Antifungal agent 50 exhibits minimum inhibitory concentrations (MICs) ranging from less than 0.063 to 1 μg/mL [1].</p>Fórmula:C25H20ClN5O2SCor e Forma:SolidPeso molecular:489.98Zevotrelvir
CAS:<p>Zevotrelvir (Compound 52) serves as an inhibitor of coronavirus, demonstrating IC50 values below 0.1 μM for 229E hCoV protease and below 0.1 mM for SARS-CoV-3C-</p>Fórmula:C28H26F3N5O3Pureza:98%Cor e Forma:SolidPeso molecular:537.53Antibacterial agent 159
CAS:<p>Compound 6d (Antibacterial agent 159) is an antibiotic effective against impetigo and Clostridium difficile infection (CDI), with no observed recurrence for CDI</p>Fórmula:C51H50N16O10S6Pureza:98%Cor e Forma:SolidPeso molecular:1239.43ZIKV-IN-1
CAS:<p>ZIKV-IN-1 blocks Zika virus effectively (EC50: 2.8 μM, EC90: 6.8 μM), targets the RdRp domain, and is low-toxic.</p>Fórmula:C21H18BrF2N3O3Cor e Forma:SolidPeso molecular:478.29R 87366
CAS:<p>R 87366 is used as a water-soluble HIV protease inhibitor.</p>Fórmula:C32H39N7O6Pureza:98%Cor e Forma:SolidPeso molecular:617.7HBV-IN-13
CAS:<p>HBV-IN-12 is a potent inhibitor of hepatitis B surface antigen (HBsAg).</p>Fórmula:C22H25NO7Cor e Forma:SolidPeso molecular:415.44SARS-CoV-2-IN-62
CAS:<p>SARS-CoV-2-IN-62 (Compound R3b) effectively inhibits SARS-CoV-2 replication in Vero E6 and Calu-3 cells, demonstrating low cytotoxicity and EC50 values of 2.97</p>Fórmula:C17H21N3O3SePureza:98%Cor e Forma:SolidPeso molecular:394.33CDD-1819
CAS:<p>CDD-1819, a non-covalent and non-peptide compound, serves as a potent SARS-CoV-2 Mpro inhibitor, exhibiting a K i value of 5 nM.</p>Fórmula:C35H31N5O2Pureza:98%Cor e Forma:SolidPeso molecular:553.65D1N8
CAS:<p>D1N8 is a potent inhibitor of the SARS-CoV-2 3CL protease, displaying an IC50 value of 0.44 μM and a CC50 value of greater than 20 μM.</p>Fórmula:C19H14ClN5O3Pureza:98%Cor e Forma:SolidPeso molecular:395.8Cyclic HPMPC
CAS:<p>Cyclic HPMPC: Potent antiviral, raises O2 in mice with lethal vaccinia, lowers guinea pig CMV replication.</p>Fórmula:C8H12N3O5PCor e Forma:SolidPeso molecular:261.17SARS-CoV-2-IN-63
CAS:<p>SARS-CoV-2-IN-63 (Compound R3e) serves as an inhibitor of SARS-CoV-2 replication, demonstrating low cytotoxicity.</p>Fórmula:C20H21N3O3SePureza:98%Cor e Forma:SolidPeso molecular:430.36Eugenitin
CAS:<p>Eugenitin, a polyketide from Mycoleptodiscus indicus, exhibits inhibitory activity against Leishmania major with an LD50 of 39.9 μM and demonstrates low</p>Fórmula:C12H12O4Pureza:98%Cor e Forma:SolidPeso molecular:220.22Tuberculosis inhibitor 12
CAS:<p>Tuberculosis Inhibitor 12, an oxadiazole derivative, effectively inhibits Mycobacterium tuberculosis, demonstrating inhibition rates of 82% and 78% at a</p>Fórmula:C15H9FN4O3SCor e Forma:SolidPeso molecular:344.32SARS-CoV-2-IN-59
CAS:<p>SARS-CoV-2-IN-59 (compound E07), an imidazoline derivative, is a non-peptide small molecule that inhibits SARS-CoV-2 by targeting its main protease (Mpro).</p>Fórmula:C10H9N3Pureza:98%Cor e Forma:SolidPeso molecular:171.2H3B-968
CAS:<p>H3B-968 is a potent inhibitor of Werner syndrome protein (WRN) with an IC50 of approximately 10 nM, effectively targeting its helicase, ATPase, and exonuclease</p>Fórmula:C22H18F6N4O4SPureza:98%Cor e Forma:SolidPeso molecular:548.46JNJ4796
CAS:<p>JNJ4796 is an oral fusion inhibitor that neutralizes influenza A group 1 by blocking HA-mediated fusion, mimicking bnAbs.</p>Fórmula:C28H27N9O3Pureza:98%Cor e Forma:SolidPeso molecular:537.57HBV-IN-41
CAS:<p>HBV-IN-41 (compound 45) is a potent, orally active inhibitor of Hepatitis B Virus (HBV), exhibiting an EC50 value of 0.027μM [1].</p>Fórmula:C18H19ClFN5O3Pureza:98%Cor e Forma:SolidPeso molecular:407.83GSK-625433
CAS:<p>GSK-625433: Homochiral inhibitor blocks HCV genotypes 1a/1b polymerase.</p>Fórmula:C26H32N4O5SCor e Forma:SolidPeso molecular:512.62NSC 288387
CAS:<p>NSC 288387, a pan-flavivirus MTase inhibitor, binds to the SAM-binding pocket and effectively inhibits Zika virus (ZIKV) with an IC50 of 0.2 μM, also preventing</p>Fórmula:C19H16N4O3Pureza:98%Cor e Forma:SolidPeso molecular:348.36DB-766
CAS:<p>DB-766: Chagas' treatment candidate with potent, selective trypanocidal action. IC50: 60 nM (bloodstream), 25 nM (intracellular). Promising new lead.</p>Fórmula:C34H34N6O3Cor e Forma:SolidPeso molecular:574.67RSV L-protein-IN-2
CAS:<p>RSV L-protein-IN-2 (Compound A), a noncompetitive inhibitor of the RSV polymerase (IC50: 4.5 μM), exhibits antiviral activity against long RSV strains (EC50: 1.</p>Fórmula:C32H36N4O5Pureza:98%Cor e Forma:SolidPeso molecular:556.65Votoplam
CAS:<p>Votoplam functions as a gene splicing modulator, employed in the inhibition of Huntington's disease [1].</p>Fórmula:C21H25N9OPureza:98%Cor e Forma:SolidPeso molecular:419.48Laninamivir Octanoate Monohydrate
CAS:<p>Laninamivir Octanoate Monohydrate is a neuraminidase inhibitor.</p>Fórmula:C21H38N4O9Pureza:98%Cor e Forma:SolidPeso molecular:490.55Levofuraltadone
CAS:<p>Levofuraltadone is an antiprotozoal and antibacterial agent.</p>Fórmula:C13H16N4O6Pureza:98%Cor e Forma:SolidPeso molecular:324.29BVDU 5′-Triphosphate
CAS:<p>BVDU 5′-Triphosphate is an antiviral agent labeled with 5′-Triphosphate that specifically targets viral DNA polymerase.</p>Fórmula:C11H16BrN2O14P3Pureza:98%Cor e Forma:SolidPeso molecular:573.08Arbemnifosbuvir
CAS:<p>Arbemnifosbuvir, a drug interfering with the nidovirus DdRp-associated nucleotidyltransferase (NiRAN) domain of non-structural protein 12 (nsp12), is utilized</p>Fórmula:C24H33FN7O7PPureza:98%Cor e Forma:SolidPeso molecular:581.53Cyclopropavir
CAS:<p>Cyclopropavir (Filociclovir; MBX-400) is a broad-spectrum anti-herpes drug effective against CMV and HHV-6/8 (EC50: 0.7-8 μM).</p>Fórmula:C11H13N5O3Pureza:98%Cor e Forma:SolidPeso molecular:263.25CDD-1845
CAS:<p>CDD-1845, a non-covalent, non-peptide inhibitor, exhibits potent inhibition of SARS-CoV-2 M^pro with a K_i value of 3 nM.</p>Fórmula:C34H31N5O2Pureza:98%Cor e Forma:SolidPeso molecular:541.64SARS-CoV-2-IN-44
CAS:<p>SARS-CoV-2-IN-44, an inhibitor of SARS-CoV-2, effectively suppresses viral replication with an EC50 value of 0.6μM and exhibits negligible cytotoxicity in Calu-</p>Fórmula:C18H16O5Pureza:98%Cor e Forma:SolidPeso molecular:312.32IR415
CAS:<p>IR415 selectively interacts with Hepatitis B virus X protein (HBx, Kd = 2 nM) and blocks HBV-mediated RNAi suppression, reverses the inhibitory effect of HBx</p>Fórmula:C13H14F2N4SPureza:99.85%Cor e Forma:SolidPeso molecular:296.34LY 173013
CAS:<p>LY 173013 is a bicyclic pyrazolidinone, it has antibacterial properties.</p>Fórmula:C15H16N6O7SPureza:98%Cor e Forma:SolidPeso molecular:424.39ddUTP
CAS:<p>ddUTP (2′,3′-Dideoxyuridine-5′-triphosphate) serves as a selective inhibitor of HIV and AMV reverse transcriptases with Ki values of 0.05 µM for HIV and 1 µM</p>Fórmula:C9H15N2O13P3Pureza:98%Cor e Forma:SolidPeso molecular:448.111L-697661
CAS:<p>L-697661, a reverse transcriptase inhibitor, is used potentially for the treatment of HIV infection.</p>Fórmula:C16H15Cl2N3O2Cor e Forma:SolidPeso molecular:352.22A 74704
CAS:<p>A 74704 is a pseudo C2-symmetric inhibitor of HIV-1 protease and its diester analog.</p>Fórmula:C43H52N4O7Pureza:98%Cor e Forma:SolidPeso molecular:736.9Indinavir, threo-
CAS:<p>Indinavir, threo- is a protease inhibitor utilized as a component of highly active antiretroviral treatment to HIV/AIDS.</p>Fórmula:C36H47N5O4Pureza:98%Cor e Forma:SolidPeso molecular:613.79N-Acetylpurinomycin
CAS:<p>N-Acetylpurinomycin is a selective agonist of CB2 receptor.</p>Fórmula:C24H31N7O6Cor e Forma:SolidPeso molecular:513.55DDD85646
CAS:<p>DDD85646 is an inhibitor of T. brucei N-myristoyltransferase with a Ki of 1.44 nM, an IC50 of 2 nM and an EC50 of 2 nM. The IC50 of hNMT is 4 nM.</p>Fórmula:C21H24Cl2N6O2SPureza:97.8% - 99.76%Cor e Forma:SolidPeso molecular:495.43AB131
CAS:<p>AB131, an inhibitor of MSMEG 6649 and Rv2172c (KD values of 0.16 and 0.02 μM, respectively), enhances the antimycobacterial efficacy of the antitubercular agent</p>Fórmula:C21H19NO6SCor e Forma:SolidPeso molecular:413.44Galidesivir hydrochloride
CAS:<p>Galidesivir hydrochloride is an inhibitor of viral RNA-dependent RNA polymerase (RdRp). It inhibits SARS-CoV-2 by tightly binding to its RdRp.</p>Fórmula:C11H16ClN5O3Pureza:98%Cor e Forma:SolidPeso molecular:301.73G4/HDAC-IN-1
<p>G4/HDAC-IN-1, a G4/HDAC dual inhibitor, IC50 1.1 µM, blocks TNBC growth, useful in cancer research.</p>Fórmula:C36H49ClFN7O4Cor e Forma:SolidPeso molecular:698.27MK-3281
CAS:<p>MK-3281: Oral, potent HCV NS5B inhibitor with promising properties and efficacy in replication trials, suitable for clinical use.</p>Fórmula:C29H37N3O3Cor e Forma:SolidPeso molecular:475.62Capravirine
CAS:<p>Capravirine, a non-nucleoside reverse transcriptase inhibitor, is used potentially for the treatment of HIV infection.</p>Fórmula:C20H20Cl2N4O2SPureza:98%Cor e Forma:SolidPeso molecular:451.37Mirincamycin HCl
CAS:<p>Mirincamycin HCl is a close analog of the drug clindamycin used for the treatment of Plasmodium falciparum blood stages.</p>Fórmula:C19H36Cl2N2O5SPureza:98%Cor e Forma:SolidPeso molecular:475.47SA09-Cu
CAS:<p>SA09-Cu is a potent, noncompetitive inhibitor of NDM-1, with an IC50 of 9.6 nM.</p>Fórmula:C8H16CuN2O2S4Cor e Forma:SolidPeso molecular:364.03SARS-CoV-2-IN-69
CAS:<p>SARS-CoV-2-IN-69 (Compound 7E) is a potent, non-covalent inhibitor of the SARS-CoV-2 main protease (M^pro) with an EC50 of 7.4 μM and also inhibits the papain-</p>Fórmula:C15H11NO3SPureza:98%Cor e Forma:SolidPeso molecular:285.32Antimalarial agent 15
CAS:<p>Antimalarial agent 15 halts Plasmodium falciparum growth with a 20 nM IC50.</p>Fórmula:C29H30N2O6Cor e Forma:SolidPeso molecular:502.56FX-06
CAS:<p>FX-06 (Fibrin-derived peptide Bβ15-42) is a peptide derived from the fibrin Bbeta chain.</p>Fórmula:C133H216N44O38Cor e Forma:SolidPeso molecular:3039.41I-A09
CAS:<p>I-A09 is a noncompetitive mPTPB inhibitor.</p>Fórmula:C29H25N5O6Pureza:98%Cor e Forma:SolidPeso molecular:539.54Berlopentin
CAS:<p>Berlopentin is splenopentin analog used to treat HIV-positive patients. It also has immunostimulatory properties.</p>Fórmula:C35H55N9O11Cor e Forma:SolidPeso molecular:777.86AS-2077715
CAS:<p>AS-2077715, an antifungal agent, exhibits inhibitory activity against Trichophyton species and is derived from the fermentation broth of Capnodium sp. 339855. It is utilized in the study of fungal infections [1].</p>Fórmula:C25H41NO7Cor e Forma:SolidPeso molecular:467.6Beclabuvir HCl
CAS:<p>Beclabuvir (BMS-791325) is an HCV inhibitor targeting NS5B polymerase with sub-28 nM potency for genotypes 1, 3, 4, 5.</p>Fórmula:C36H46ClN5O5SCor e Forma:SolidPeso molecular:696.3(E)-LHF-535
CAS:<p>(E)-LHF-535, an E-isomer antiviral, EC50 <1 μM vs Lassa/Machupo/Junin, 1-10 μM vs VSVg.</p>Fórmula:C27H28N2O2Pureza:98%Cor e Forma:SolidPeso molecular:412.52SLU-10482
CAS:<p>SLU-10482, an antiparasitic agent, effectively reduces C.</p>Fórmula:C18H16F4N6OCor e Forma:SolidPeso molecular:408.35FIKK9.1-IN-1
CAS:<p>FIKK9.1-IN-1 (Compound 1), an antimalarial agent (IC50: 2.68 μg/mL), serves as a FIKK9.1 inhibitor by interacting with the ATP-binding residues within FIKK9.1,</p>Fórmula:C22H22N2SePureza:98%Cor e Forma:SolidPeso molecular:393.38HCV-IN-43
CAS:<p>HCV-IN-43 (compound 2), an HCV NS5B protein inhibitor, efficiently inhibits HCV virus replication and is utilized in the study of HCV infection [1].</p>Fórmula:C26H26FN3O5SCor e Forma:SolidPeso molecular:511.57HBV-IN-30
CAS:<p>HBV-IN-30, a flavone derivative, inhibits cccDNA in HBV research.</p>Fórmula:C22H18BrClO6Cor e Forma:SolidPeso molecular:493.73Antibacterial agent 158
CAS:<p>Compound 158 (6c), a Micrococcin analogue, serves as an antibacterial agent effective against impetigo and Clostridium difficile infection (CDI) [1].</p>Fórmula:C54H61N15O8S6Cor e Forma:SolidPeso molecular:1240.55Emtricitabine triphosphate tetrasodium salt
CAS:<p>Emtricitabine triphosphate tetrasodium salt is the tetrasodium salt form of the phosphorylated anabolite (-)-Emtricitabine triphosphate, an active nucleoside</p>Fórmula:C8H9FN3Na4O12P3SPureza:98%Cor e Forma:SolidPeso molecular:575.11FAICAR
CAS:<p>FAICAR (5-Formamidoimidazole-4-carboxamide ribotide), a purine nucleotide, plays a crucial role in metabolic processes.</p>Fórmula:C10H15N4O9PCor e Forma:SolidPeso molecular:366.22Fervenulin
CAS:<p>Fervenulin, from Streptomyces sp. CMU-MH021, halts egg hatch (MIC: 30 μg/mL) and kills J2 larvae (MIC: 120 μg/mL) of M. incognita.</p>Fórmula:C7H7N5O2Pureza:99.75%Cor e Forma:SolidPeso molecular:193.16Cochliodone A
CAS:<p>Cochliodone A, a bioactive compound isolated from the deep-sea fungus Chaetomium sp., exhibits both antibacterial and anticancer properties.</p>Fórmula:C34H38O12Cor e Forma:SolidPeso molecular:638.66Pinokalant
CAS:<p>Pinokalant (LOE-908) is a novel non-selective cation channel inhibitor.Pinokalant significantly reduces cortical infarct volume in in vivo experiments, improves</p>Fórmula:C41H48N2O9Pureza:98.04%Cor e Forma:SolidPeso molecular:712.83SARS-CoV-2 3CLpro-IN-5
CAS:<p>SARS-CoV-2 3CLpro-IN-5 is a covalent inhibitor targeting the 3C-like protease (3CLpro), exhibiting potent inhibitory activity with an IC50 of 3.8 nM and</p>Fórmula:C22H26ClF2N5O4Pureza:98%Cor e Forma:SolidPeso molecular:497.92GS-6620
CAS:<p>GS-6620 is a HCV nonstructural protein 5B (NS5B) inhibitor.</p>Fórmula:C29H37N6O9PCor e Forma:SolidPeso molecular:644.61Valnemulin
CAS:<p>Valnemulin, a broad-spectrum pleuromutilin antibiotic, targets peptidyl transferase within the 50S ribosomal subunit, effectively used in veterinary medicine to address swine diseases such as B. hyodysenteriae and M. hyopneumoniae.</p>Fórmula:C31H52N2O5SCor e Forma:SolidPeso molecular:564.83Aranciamycin
CAS:<p>Aranciamycin (Compound 1), an anthracycline antibiotic, exhibits collagenase inhibitory activity (IC50 3.7*10^-7 M) and can inhibit DNA synthesis in tumor cells</p>Fórmula:C27H28O12Cor e Forma:SolidPeso molecular:544.5Glycolithocholic acid 3-sulfate disodium
CAS:<p>Glycolithocholic acid 3-sulfate (disodium) demonstrates inhibitory effects on in vitro HIV-1 replication and has potential applications in HIV infection and</p>Fórmula:C26H41NNa2O7SCor e Forma:SolidPeso molecular:557.65Quorum Sensing-IN-2
CAS:<p>Quorum Sensing-IN-2 (compound 23e) is a quorum sensing inhibitor that curtails bacterial pathogenicity without impeding growth.</p>Fórmula:C19H13F2NO3Cor e Forma:SolidPeso molecular:341.31Azaconazole
CAS:<p>Azaconazole, an agricultural fungicide, is used for controlling powdery mildew on crops and bean rust.</p>Fórmula:C12H11Cl2N3O2Cor e Forma:SolidPeso molecular:300.14Antiparasitic agent-8
CAS:<p>Antiparasitic agent-8 (Compound 9) exhibits potent antiparasitic activity against Hymenolepis nana, while demonstrating low levels of cytotoxicity [1].</p>Fórmula:C17H22FN3O4Cor e Forma:SolidPeso molecular:351.37Antileishmanial agent-16
CAS:<p>Antileishmanial agent-16 (compound 14c), an anti-Leishmania agent, exhibits potent activity against Leishmania major promastigotes (IC50 = 0.59 µM) and</p>Fórmula:C27H37N5O4Pureza:98%Cor e Forma:SolidPeso molecular:495.61Pyrethrin II
CAS:<p>Pyrethrin II, an active insecticidal component of pyrethrins, is a biogenic insecticide derived from Chrysanthemum cinerariifolium [1].</p>Fórmula:C22H28O5Cor e Forma:SolidPeso molecular:372.45Isotianil
CAS:<p>Isotianil is a plant defense inducer that activates typical plant defense responses without direct antimicrobial effects, serving as a plant protection agent</p>Fórmula:C11H5Cl2N3OSCor e Forma:SolidPeso molecular:298.15AG 85
CAS:<p>AG 85 is a major secretion protein of Mycobacterium tuberculosis.</p>Fórmula:C27H22N4O3SCor e Forma:SolidPeso molecular:482.55EDI048
CAS:<p>EDI048, also known as compound 1.16, is an orally active inhibitor of Cryptosporidium PI4K, utilized in the study of cryptosporidiosis [1].</p>Fórmula:C25H21ClN4O4Pureza:98%Cor e Forma:SolidPeso molecular:476.91Debrisoquin
CAS:<p>Debrisoquin (Isocaramidine) is a TMPRSS2 inhibitor that prevents SARS-CoV-2 from entering human lung cells through TMPRSS2-dependent pathways, exhibiting an</p>Fórmula:C10H13N3Pureza:98%Cor e Forma:SolidPeso molecular:175.23IpOHA
CAS:<p>IpOHA is a potent inhibitor of plant KARI and functions as an antimycobacterial agent, demonstrating a K_i value of 97.7 nM against Mycobacterium tuberculosis (</p>Fórmula:C5H9NO4Cor e Forma:SolidPeso molecular:147.13SARS-CoV-2 3CLpro-IN-15
CAS:<p>SARS-CoV-2 3CLpro-IN-15 (compound a), a beta-nitrostyrene derivative, acts as an inhibitor of the SARS-CoV-2 3CL protease (3CLpro), effectively inhibiting viral</p>Fórmula:C8H6N2O4Pureza:98%Cor e Forma:SolidPeso molecular:194.14ZINC03129319
CAS:<p>ZINC03129319 is an inhibitor of dengue virus (DENV) NS2B-NS3 protease.</p>Fórmula:C24H14N2O6S2Pureza:90%Cor e Forma:SolidPeso molecular:490.51Annamycin
CAS:<p>Annamycin, a semi-synthetic doxorubicin derivative, binds DNA, blocks topoisomerase II, and evades MDR, inhibiting DNA/RNA/protein synthesis.</p>Fórmula:C26H25IO11Cor e Forma:SolidPeso molecular:640.37SHR5133
CAS:<p>SHR5133 is a potent, orally active regulator of HBV capsid assembly that reduces HBV DNA (EC50: 26.6 nM).</p>Fórmula:C19H18F4N6O2Cor e Forma:SolidPeso molecular:438.38Palinavir
CAS:<p>Palinavir is an antiviral, it inhibits HIV-1 protease.</p>Fórmula:C41H52N6O5Pureza:98%Cor e Forma:SolidPeso molecular:708.89Tobevibart
CAS:<p>Tobevibart, an IgG1-lambda humanized monoclonal antibody targeting the hepatitis B virus (HBV) surface envelope protein, exhibits antiviral activity [1].</p>Pureza:98%Cor e Forma:LiquidDespropylene gatifloxacin
CAS:<p>Despropylene gatifloxacin, a metabolite of AM-1155, exhibits potent antibacterial activity and has favorable pharmacokinetics [1].</p>Fórmula:C16H18FN3O4Cor e Forma:SolidPeso molecular:335.33Amoxicillin-clavulanate potassium
CAS:<p>Amoxicillin-clavulanate potassium is an orally administered antibiotic and combination agent indicated for various bacterial infections.</p>Fórmula:C24H27KN4O10SPureza:98%Cor e Forma:SolidPeso molecular:602.66Cefteram
CAS:<p>Cefteram (T-2525), an orally active ester of the cephalosporin class, is the free acid form of Cefteram pivoxil.</p>Fórmula:C16H17N9O5S2Cor e Forma:SolidPeso molecular:479.49Valtorcitabine dihydrochloride
CAS:<p>Valtorcitabine dihydrochloride, a DNA polymerase inhibitor, is used potentially for the treatment of HBV infection.</p>Fórmula:C14H24Cl2N4O5Cor e Forma:SolidPeso molecular:399.27MsbA-IN-6
CAS:<p>MsbA-IN-6: potent antibiotic, hinders MsbA in gram-negative bacteria, kills E. coli, effective on drug-resistant strains.</p>Fórmula:C24H20Cl2N4OPureza:98%Cor e Forma:SolidPeso molecular:451.35GSK3839919A
CAS:<p>GSK3839919A is a potent allosteric inhibitor of HIV-1 integrase [1].</p>Fórmula:C36H46ClN3O3Cor e Forma:SolidPeso molecular:604.22CcpA-IN-1
CAS:<p>CcpA-IN-1 is a Staphylococcus aureus antibiotic exhibiting significant bactericidal activity (MICs=460 nM) [1].</p>Fórmula:C77H82F12N8OP3RuPureza:98%Cor e Forma:SolidPeso molecular:1557.5Japonilure
CAS:<p>Japonilure is an agent of insecticide and pheromone.</p>Fórmula:C14H24O2Pureza:98%Cor e Forma:SolidPeso molecular:224.34L 694746
CAS:<p>L 694746 is an inhibitor of HIV-1 protease.</p>Fórmula:C35H42N2O8Pureza:98%Cor e Forma:SolidPeso molecular:618.72HCoV-OC43-IN-1
CAS:<p>HCoV-OC43-IN-1 (Compound IV-16) serves as an inhibitor of the coronavirus HCoV-OC43, exhibiting antiviral efficacy with an EC50 of 90 nM.</p>Fórmula:C23H22F6N4O2Pureza:98%Cor e Forma:SolidPeso molecular:500.44HIV-1 inhibitor-10
CAS:<p>HIV-1 inhibitor-10 is a nanomolar HIV-1 maturation inhibitor.</p>Fórmula:C39H54O6Cor e Forma:SolidPeso molecular:618.84HOE961
CAS:<p>HOE961, a diacetate ester prodrug of S2242, is an oral anti-orthopoxvirus agent effective against cowpox.</p>Fórmula:C13H17N5O5Cor e Forma:SolidPeso molecular:323.3FR194738 free base
CAS:<p>FR194738 free base inhibits squalene epoxidase activity in HepG2 cell homogenates with an IC50 of 9.8 nM. </p>Fórmula:C27H37NO2SPureza:99.13%Cor e Forma:SolidPeso molecular:439.65EHNA hydrochloride
CAS:<p>EHNA hydrochloride is a PDE2 and ADA inhibitor with anticancer activity, increasing intracellular adenosine concentration in a treatment time-dependent manner.</p>Fórmula:C14H24ClN5OPureza:98%Cor e Forma:SolidPeso molecular:313.83Antibacterial agent 154
CAS:<p>Antibacterial Agent 154 (Compound 7), a Fluoroquinolone derivative, exhibits broad-spectrum efficacy against both Gram-positive and Gram-negative bacteria when</p>Fórmula:C25H28ClFN4O5Cor e Forma:SolidPeso molecular:518.97Ibuzatrelvir
CAS:<p>Ibuzatrelvir (PF-07817883) is an antiviral compound designed to inhibit the SARS-CoV-2 3CL protease, and is utilized in the treatment of COVID-19 [1].</p>Fórmula:C21H30F3N5O5Pureza:98%Cor e Forma:SolidPeso molecular:489.49Icofungipen
CAS:<p>Icofungipen is an oral antifungals with active against Candida species.</p>Fórmula:C7H11NO2Pureza:98%Cor e Forma:SolidPeso molecular:141.17Antifungal agent 48
CAS:<p>Antifungal agent 48 (Example 308), active against Cryptococcus neoformans, exhibits a minimum inhibitory concentration (MIC) value of 11 μM [1].</p>Fórmula:C13H10O4SCor e Forma:SolidPeso molecular:262.28Variculanol
CAS:<p>Variculanol, a compound with antimicrobial, anticancer, and anti-HCV NS3/4A protease properties, is derived from the marine fungus Aspergillus versicolor [1].</p>Fórmula:C25H40O2Cor e Forma:SolidPeso molecular:372.58RSV L-protein-IN-4
CAS:<p>RSV L-protein-IN-4 (Compound C) is a noncompetitive inhibitor of the RSV polymerase with an IC50 of 0.88 μM.</p>Fórmula:C32H35N5O6Pureza:98%Cor e Forma:SolidPeso molecular:585.651,8-Dichloroanthraquinone
CAS:<p>1,8-Dichloroanthraquinone, a derivative of anthraquinone, effectively inhibits sulfide production in sulfate-reducing bacteria [1].</p>Fórmula:C14H6Cl2O2Cor e Forma:SolidPeso molecular:277.1Tirfipiravir
CAS:<p>Tirapiravir is an antiviral nucleoside analog that exhibits activity against both the novel coronavirus and influenza virus [1].</p>Fórmula:C14H17N3O8Pureza:98%Cor e Forma:SolidPeso molecular:355.3U 89360E
CAS:<p>U 89360E is a peptidic inhibitor.</p>Fórmula:C28H52N8O6Pureza:98%Cor e Forma:SolidPeso molecular:596.76Antibacterial agent 94
CAS:<p>Compound 5b, an antibacterial, effectively targets MRSA and disrupts bacterial membranes and PG synthesis.</p>Fórmula:C21H21FO4Cor e Forma:SolidPeso molecular:356.39UNC-2170
CAS:<p>UNC-2170 (UNC2170 Maleate) is the methyl-lysine binding protein, 53BP1 ligand.</p>Fórmula:C14H21BrN2OPureza:97.44%Cor e Forma:SolidPeso molecular:313.23SARS-CoV-2-IN-66
CAS:<p>SARS-CoV-2-IN-66 (1), a derivative of vitamin K, functions as an inhibitor of SARS-CoV-2, exhibiting an effective concentration (EC50) of 70.8 μM in VeroE6/</p>Fórmula:C28H30O2Pureza:98%Cor e Forma:SolidPeso molecular:398.54Bavtavirine
CAS:<p>Bavtavirine is a non-nucleoside reverse HIV-1 transcriptase inhibitor (NNRTIs),inhibits HIV replication by preventing the transcription of viral RNA into DNA.</p>Fórmula:C26H20N6Pureza:97.2%Cor e Forma:SolidPeso molecular:416.48Methyl 3,4-dimethoxycinnamate
CAS:<p>Methyl 3,4-dimethoxycinnamate impedes uredospore germination and concurrently inhibits global DNA methylation in Hep3B cells [1] [2].</p>Fórmula:C12H14O4Cor e Forma:SolidPeso molecular:222.24Antiproliferative agent-18
CAS:<p>Compound 5k (Antiproliferative Agent-18) is an antiproliferative agent that exhibits moderate antibacterial and antifungal activities [1].</p>Fórmula:C26H27FN2OSCor e Forma:SolidPeso molecular:434.57Antibacterial agent 91
<p>Antibacterial 91: Inhibits aaRS, IC50 2.10μM vs. S. enterica ThrRS, has antibacterial properties. [1]</p>Fórmula:C33H31BrClN5O4Cor e Forma:SolidPeso molecular:676.99Phenethicillin sodium
CAS:<p>Phenethicillin sodium (α-Phenoxyethylpenicillin) is a penicillin-class antibiotic that exhibits antimicrobial activity [1].</p>Fórmula:C17H19N2NaO5SCor e Forma:SolidPeso molecular:386.4NS5A-IN-2
CAS:<p>NS5A-IN-2, a potent inhibitor, is highly effective against HCV 1b and shows increased activity for GT 3a with good metabolic stability.</p>Fórmula:C46H45N7O7Pureza:98%Cor e Forma:SolidPeso molecular:807.89Antibacterial compound 1
CAS:<p>Antibacterial compound 1 is an antibacterial compound.</p>Fórmula:C14H16FN3O4Pureza:98%Cor e Forma:SolidPeso molecular:309.29DHX9-IN-6
CAS:<p>DHX9-IN-6 is a highly effective ATP-dependent RNA helicase A (DHX9) inhibitor, used in cancer research.</p>Fórmula:C23H18ClFN4O4S2Pureza:99.71%Cor e Forma:SolidPeso molecular:533Zoxamide
CAS:<p>Zoxamide (RH-7281) is an oomycete-specific fungicide that impedes nuclear division in Phytophthora capsici germlings and disrupts the microtubule cytoskeleton [</p>Fórmula:C14H16Cl3NO2Cor e Forma:SolidPeso molecular:336.64Verazine
CAS:<p>(-)-Verazine is an antifungal agent isolated from the dried roots and rhizome of Veratrum maackii Regel, which induces DNA damage in the cerebellum and cerebral</p>Fórmula:C27H43NOCor e Forma:SolidPeso molecular:397.64GSK3532795
CAS:<p>GSK3532795: potent oral HIV-1 maturation inhibitor; EC50: 1.9-13 nM for various strains.</p>Fórmula:C42H62N2O4SPureza:98%Cor e Forma:SolidPeso molecular:691.02HBV-IN-8
CAS:<p>HBV-IN-6 is a potent inhibitor of HBV (EC50: 287.9 nM).</p>Fórmula:C21H25ClFN5O5S2Cor e Forma:SolidPeso molecular:546.04Ro 31-8588
CAS:<p>Talviraline (HBY 097) inhibits HIV-1 replication and reduces cell death in various cells and immune cells.</p>Fórmula:C33H56N4O5Cor e Forma:SolidPeso molecular:588.82Fenpropidin
CAS:<p>Fenpropidin (Ro-12-3049), a fungicide, is a specific inhibitor of sterol 14-reductase and biosynthesis.</p>Fórmula:C19H31NPureza:98.58% - 99.54%Cor e Forma:SolidPeso molecular:273.46HIV-1 integrase inhibitor 3
CAS:<p>HIV-1 integrase inhibitor 3 is an HIV-1 integrase strand transfer (INST) inhibitor (IC50: 2.7 nM).</p>Fórmula:C21H22F2N4O4Pureza:98%Cor e Forma:SolidPeso molecular:432.42LtaS-IN-1
CAS:<p>LtaS-IN-1 inhibits LTA synthesis in MDR E. faecium; alters cell walls; MIC: 0.5-64 μg/mL for 28 Enterococcus strains.</p>Fórmula:C24H17N3O5Pureza:93.44%Cor e Forma:SolidPeso molecular:427.41Myxopyronin A
CAS:<p>Myxopyronin A is an inhibitor of bacterial RNA polymerase.</p>Fórmula:C23H31NO6Pureza:98%Cor e Forma:SolidPeso molecular:417.5Phylloflavan
CAS:<p>Phylloflavan, an antileishmanial compound, exhibits an intracellular half maximal effective concentration (EC50) of 3.2 nM in RAW 264.7 cells and inhibits the</p>Fórmula:C26H26O10Pureza:98%Cor e Forma:SolidPeso molecular:498.48L-742001 Hydrochloride
CAS:<p>L-742001 Hydrochloride is an RNA polymerase inhibitor.</p>Fórmula:C23H25Cl2NO4Cor e Forma:SolidPeso molecular:450.36Caerulomycin A
CAS:<p>Caerulomycin A (Caerulomycin) (Cerulomycin; Caerulomycin) is an antifungal compound.</p>Fórmula:C12H11N3O2Pureza:99.28%Cor e Forma:SolidPeso molecular:229.23EBOV-IN-1
CAS:<p>EBOV-IN-1 is an adamantane dipeptide piperazine inhibitor of Ebola virus (EBOV) that inhibits EBOV infection and suppresses pseudotypic EBOV infection.</p>Fórmula:C34H43N3O5Pureza:98.62% - 98.92%Cor e Forma:SolidPeso molecular:573.72HIV-IN-8
CAS:<p>HIV-IN-8 (Compound 9) acts as an HIV inhibitor, suppressing HIV replication with an effective concentration (EC50) of 13 μg/mL [1].</p>Fórmula:C36H30O16Cor e Forma:SolidPeso molecular:718.613-Cyanovinylcarbazole phosphoramidite
CAS:<p>3-Cyanovinylcarbazole phosphoramidite: an antiviral, hinders viral DNA synthesis, modifies ribonucleotides.</p>Fórmula:C50H53N4O6PCor e Forma:SolidPeso molecular:836.95Tuberculosis inhibitor 6
CAS:<p>Tuberculosis inhibitor 6 (compound 2c), a 3-methoxy-2-phenylimidazo[1,2-b]pyridazine derivative, is highly active against Mycobacterium tuberculosis (MIC 90 of</p>Fórmula:C21H19N3O2SCor e Forma:SolidPeso molecular:377.46Dup-721
CAS:<p>DuP-721: broad-spectrum, oral antibiotic targeting various bacteria, including M. tuberculosis.</p>Fórmula:C14H16N2O4Pureza:99.84%Cor e Forma:SolidPeso molecular:276.29NSC309401
CAS:<p>NSC309401 is an E. coli dihydrofolate reductase inhibitor, displaying potency with an IC50 value of 189 nM and a dissociation constant (KD) of 14.57 nM [1].</p>Fórmula:C17H16N6Cor e Forma:SolidPeso molecular:304.35Galidesivir dihydrochloride
CAS:<p>Galidesivir inhibits RdRP; has broad antiviral effects on various RNA viruses; effective against Ebola, Marburg in animals.</p>Fórmula:C11H17Cl2N5O3Cor e Forma:SolidPeso molecular:338.19MPI8
CAS:<p>MPI8 is a SARS-CoV-2 Protease inhibitor (IC50 = 105 nM).</p>Fórmula:C32H48N4O7Cor e Forma:SolidPeso molecular:600.75ZINC475239213
CAS:<p>ZINC475239213 acts as an inhibitor targeting the SARS-CoV-2 Nsp14 N7-Methyltransferase with an IC50 value of 20 μM [1].</p>Fórmula:C21H15N5O2Pureza:98%Cor e Forma:SolidPeso molecular:369.38(-)-Neplanocin A
CAS:<p>S-Adenosylhomocysteine (SAH) hydrolase is responsible for the reversible hydrolysis of SAH into adenosine and homocysteine. Inhibition of this enzyme leads to the accumulation of SAH within cells, thereby increasing the SAH to S-adenosylmethionine (SAM) ratio and subsequently inhibiting SAM-dependent methyltransferases. (−)-Neplanocin A, a potent and irreversible inhibitor of SAH hydrolase (Ki= 8.39 nM), exhibits significant antitumor activity against mouse leukemia L1210 cells and holds broad-spectrum antiviral properties. Its efficacy notably surpasses that of the reversible inhibitor 3-deazaneplanocin, especially in combating vesicular stomatitis, evidencing a higher potency with ID50 values of 0.07 μg/ml for Neplanocin A versus 0.3 μg/ml for 3-deazaneplanocin.</p>Fórmula:C11H13N5O3Cor e Forma:SolidPeso molecular:263.3Antifungal agent 24
CAS:<p>Antifungal agent 24 (Compound 6) is an antifungal agent that inhibits Candida albicans (MIC: 0.03 μg/ml).</p>Fórmula:C24H18F2N4OCor e Forma:SolidPeso molecular:416.42Loflucarban
CAS:<p>Loflucarban (Fluonilid) is an antimycotic compoud.</p>Fórmula:C13H9Cl2FN2SPureza:98.08% - 98.15%Cor e Forma:SolidPeso molecular:315.19
