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"
Ordenar por
Pureza (%)
0
100
|
0
|
50
|
90
|
95
|
100
Verazine
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:397.64Antifungal 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:416.42Berkeleylactone E
CAS:<p>Berkeleylactone E, a macrolide antibiotic [1], exhibits antimicrobial properties.</p>Fórmula:C20H32O7Cor e Forma:SolidPeso molecular:384.469HCV-IN-44
CAS:<p>HCV-IN-44 (compound 28) is an inhibitor of the HCV NS5B protein, efficacious in suppressing HCV virus replication and useful for researching HCV infection [1].</p>Fórmula:C24H26FN3O5SCor e Forma:SolidPeso molecular:487.54KNI-272
CAS:<p>Kynostatin-272 is a HIV protease inhibitor. KNI-272 blocked the maturation of viral particles.</p>Fórmula:C33H41N5O6S2Cor e Forma:SolidPeso molecular:667.84DU-34569 Maleate
CAS:<p>DU-34569 Maleate, an antiviral agent, acts against influenza A, parainfluenza Sendai, coxsackie A21, and rhinovirus.</p>Fórmula:C18H27NO4Pureza:98%Cor e Forma:SolidPeso molecular:321.41Antifungal agent 49
CAS:<p>Antifungal agent 49 (Example 112) exhibits activity against Cryptococcus neoformans, demonstrating a minimum inhibitory concentration (MIC) of 49 μM [1].</p>Fórmula:C15H12O4Cor e Forma:SolidPeso molecular:256.25SARS-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:394.33NCI-B16
CAS:<p>NCI-B16 is a small-molecule RNA binder that inhibits HCV (hepatitis C virus) replication [1].</p>Fórmula:C27H26N8O4Cor e Forma:SolidPeso molecular:526.55L 687908
CAS:<p>L 687908 is a potent inhibitor of hydroxyethylene-containing HIV protease.</p>Fórmula:C40H51N5O5Pureza:98%Cor e Forma:SolidPeso molecular:681.86CDD-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:553.65Antibiofilm agent-9
CAS:<p>Antibiofilm agent-9 (Compound 4), a derivative of pyrrolnitrin, exhibits antimicrobial activity. It inhibits Bacillus anthracis with a Minimum Inhibitory Concentration (MIC) of 0.031 μg/mL. The compound demonstrates significant antibiofilm activity, achieving an inhibition rate of 84% after 24 hours at a concentration of 8.0 μg/mL. Additionally, Antibiofilm agent-9 shows favorable pharmacokinetic properties in mouse models.</p>Fórmula:C11H5BrCl2FNO2Cor e Forma:SolidPeso molecular:352.97L 694746
CAS:<p>L 694746 is an inhibitor of HIV-1 protease.</p>Fórmula:C35H42N2O8Pureza:98%Cor e Forma:SolidPeso molecular:618.72D1N8
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:395.8LY 173013
CAS:LY 173013 is a bicyclic pyrazolidinone, it has antibacterial properties.Fórmula:C15H16N6O7SPureza:98%Cor e Forma:SolidPeso molecular:424.39SLU-10482
CAS:<p>SLU-10482, an antiparasitic agent, effectively reduces C.</p>Fórmula:C18H16F4N6OCor e Forma:SolidPeso molecular:408.35AS-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:467.6Gusperimus trihydrochloride
CAS:Gusperimus trihydrochloride is a derivative of the antitumor antibiotic spergualin with immunosuppressant activity.Fórmula:C17H40Cl3N7O3Pureza:98%Cor e Forma:SolidPeso molecular:496.9Tuberculosis 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:344.323-Cyanovinylcarbazole phosphoramidite
CAS:<p>3-Cyanovinylcarbazole phosphoramidite: an antiviral, hinders viral DNA synthesis, modifies ribonucleotides.</p>Fórmula:C50H53N4O6PCor e Forma:SolidPeso molecular:836.95Phenethicillin sodium
CAS:<p>Phenethicillin sodium (α-Phenoxyethylpenicillin) is a penicillin-class antibiotic that exhibits antimicrobial activity [1].</p>Fórmula:C17H19N2NaO5SCor e Forma:SolidPeso molecular:386.4APX2039
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:362.36Antifungal 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:262.28Pencitabine
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:395.33R 87366
CAS:R 87366 is used as a water-soluble HIV protease inhibitor.Fórmula:C32H39N7O6Pureza:98%Cor e Forma:SolidPeso molecular:617.7CcpA-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:1557.5Lagociclovir 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:440.43HBV-IN-13
CAS:<p>HBV-IN-12 is a potent inhibitor of hepatitis B surface antigen (HBsAg).</p>Fórmula:C22H25NO7Cor e Forma:SolidPeso molecular:415.44Antitrypanosomal agent 14
CAS:Antitrypanosomal agent 14 (Compound 1), a potent T.Fórmula:C14H23N3OSPureza:98%Cor e Forma:SolidPeso molecular:281.42Vinclozolin M2
CAS:<p>Vinclozolin M2, an active metabolite of vinclozolin, is generated through successive esterase activity and decarboxylation in C. elegans, as well as decarboxylation in human liver microsomes. It functions as an antagonist to the mineralocorticoid (IC50= 1,400 nM) and androgen receptors (IC50= 0.17 nM), demonstrated in reporter assays with MCF-7 cells. This compound is exclusively sold for research and analytical purposes, tailored for controlled laboratory use, and is not available in bulk sizes.</p>Fórmula:C11H11Cl2NO2Cor e Forma:SolidPeso molecular:260.1TH-Z145
CAS:<p>TH-Z145 is a potent FPPS inhibitor for the study of myeloma and lung cancer.</p>Fórmula:C16H28O7P2Pureza:98.29%Cor e Forma:SolidPeso molecular:394.34Roseoflavin
CAS:<p>Roseoflavin, a chemical analog of FMN and riboflavin that has antimicrobial activity, can directly bind to FMN riboswitch aptamers and downregulate the</p>Fórmula:C18H23N5O6Pureza:99.81% - 99.89%Cor e Forma:SolidPeso molecular:405.412-Dodecanol
CAS:<p>2-Dodecanol suppresses both hyphal development and SIR2 gene expression in Candida albicans [1].</p>Fórmula:C12H26OCor e Forma:SolidPeso molecular:186.33OfChi-h-IN-2
CAS:<p>OfChi-h-IN-2 (compound TQ19) is a potent inhibitor of OfChi-h, exhibiting a K i of 0.33 μM, and significantly impairs the growth and development of Ostrinia</p>Fórmula:C25H28ClN5O3Pureza:98%Cor e Forma:SolidPeso molecular:481.98SIMR3030
CAS:<p>SIMR3030, a potent inhibitor of SARS-CoV-2 PLpro, possesses an IC50 of 0.0399 µg/mL and demonstrates antiviral activity by diminishing the expression of SARS-</p>Fórmula:C27H29N3O2Pureza:98%Cor e Forma:SolidPeso molecular:427.54Debrisoquin
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:175.23Tuberculosis inhibitor 7
CAS:<p>Tuberculosis inhibitor 7 (compound 2d), a 3-methoxy-2-phenylimidazo[1,2-b]pyridazine derivative, exhibits potent activity against Mycobacterium tuberculosis and</p>Fórmula:C21H18FN3O2SCor e Forma:SolidPeso molecular:395.45PYR01
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:502.34H3B-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:548.46AZ-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:633.76MK-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:475.62COH1
CAS:<p>COH1 is a ribonucleotide reductase (RR) inhibitor utilized in research pertaining to cancer, mitochondrial diseases, and neurodegenerative disorders [1].</p>Fórmula:C11H10N2O3SPureza:98%Cor e Forma:SolidPeso molecular:250.27MAC13772
CAS:<p>MAC13772 is a potent inhibitor of the enzyme BioA with an IC50 of 250 nM thereby inhibiting biotin biosynthesis. MAC13772 exhibits antibacterial activity.</p>Fórmula:C8H9N3O3SPureza:98.7%Cor e Forma:SolidPeso molecular:227.24BAY-Y 3118
CAS:BAY-Y 3118, a new chlorofluoroquinolone, has antimicrobial activity.Fórmula:C20H21ClFN3O3Cor e Forma:SolidPeso molecular:405.85UNC-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:313.23Ipflufenoquin
CAS:<p>Ipflufenoquin, an insecticide, effectively combats primary apple scab infections. Its application is optimal between the stages of half an inch of green and fruit set [1].</p>Fórmula:C19H16F3NO2Cor e Forma:SolidPeso molecular:347.33BDM91270
CAS:<p>BDM91270 (compound 29) serves as an inhibitor of the E.</p>Fórmula:C17H21Cl3N4O2Cor e Forma:SolidPeso molecular:419.73Cyclic 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:261.17Antiparasitic 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:351.37HEC72702
CAS:<p>HEC72702: New HBV capsid inhibitor, from GLS4. No CYP1A2, CYP3A4, CYP2B6 induction at 10μM.</p>Fórmula:C24H26BrFN4O5SCor e Forma:SolidPeso molecular:581.45Japonilure
CAS:<p>Japonilure is an agent of insecticide and pheromone.</p>Fórmula:C14H24O2Pureza:98%Cor e Forma:SolidPeso molecular:224.34Antifungal agent 66
CAS:<p>Antifungal agent 66 (compound 10) exhibits broad-spectrum antifungal activity against seven phytopathogenic fungal mycelia and significant inhibitory effects on</p>Fórmula:C19H25ClO6Cor e Forma:SolidPeso molecular:384.85NSC309401
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:304.35WRN inhibitor 5
CAS:<p>WRN Inhibitor 5 (Example 157), a cyclic vinyl sulfone-based compound, serves as an inhibitor of Werner Syndrome ATP-dependent helicase enzyme (WRN).</p>Fórmula:C23H20N2O6SCor e Forma:SolidPeso molecular:452.48N-(3-Oxobutanoyl)-L-homoserine lactone
CAS:<p>N-(3-Oxobutanoyl)-L-homoserine lactone (3-oxo-C4-HSL) serves as an autoregulator for carbapenem antibiotic biosynthesis in Erwinia carotovora ATCC 39048 and induces the expression of rhiI in R. leguminosarum [1].</p>Fórmula:C8H11NO4Cor e Forma:SolidPeso molecular:185.18N-Acetylpurinomycin
CAS:<p>N-Acetylpurinomycin is a selective agonist of CB2 receptor.</p>Fórmula:C24H31N7O6Cor e Forma:SolidPeso molecular:513.55Antibacterial compound 2
CAS:<p>Antibacterial compound 2 is a potent antimicrobial agent effective against many human veterinary pathogens, inhibiting multi-drug resistant staphylococci,</p>Fórmula:C22H30FN5O6Pureza:90.4%Cor e Forma:SolidPeso molecular:479.5DMP 323
CAS:DMP 323 is a potent inhibitor of HIV-1 protease.Fórmula:C35H38N2O5Pureza:98%Cor e Forma:SolidPeso molecular:566.69Capravirine
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:451.37APX001
CAS:<p>APX001 is a prodrug of APX-001A. APX001 is the first-in-class inhibitor of the fungal protein Gwt1.</p>Fórmula:C22H21N4O6PPureza:98%Cor e Forma:SolidPeso molecular:468.4SARS-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:285.32BMS-433771 dihydrochloride hydrate
CAS:BMS-433771 dihydrochloride hydrate is a potent oral RSV inhibitor, affects groups A & B, with a 20 nM EC50, used in respiratory disease research.Fórmula:C21H27Cl2N5O3Cor e Forma:SolidPeso molecular:468.38Cefteram
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:479.49Koshidacin B
CAS:<p>Koshidacin B, a cyclic tetrapeptide, inhibits malaria strains FCR3/K1 (IC50: 0.89/0.83 μM), showing promise for antiplasmodial research.</p>Fórmula:C28H40N4O7Cor e Forma:SolidPeso molecular:544.64Votoplam
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:419.48RSV 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:556.65Bio-AMS
CAS:<p>Bio-AMS is a potent inhibitor of bacterial biotin protein ligase, exhibiting selective activity against Mycobacterium tuberculosis (Mtb) and disrupting fatty</p>Fórmula:C20H29N9O7S2Cor e Forma:SolidPeso molecular:571.63AB-836
CAS:<p>AB-836, an orally active hepatitis B virus (HBV) capsid inhibitor, hampers viral replication by engaging with the HBV core protein.</p>Fórmula:C20H15F3N4O2Cor e Forma:SolidPeso molecular:400.35Urease-IN-6
CAS:<p>Urease-IN-6, a potent Urease inhibitor, exhibits an IC50 value of 14.2 μM and is utilized in the research of peptic and gastric ulcers [1].</p>Fórmula:C18H19N3OSCor e Forma:SolidPeso molecular:325.43(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:412.52Pinokalant
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:712.83UNC2170 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:429.31Teropavimab
CAS:<p>Teropavimab (3BNC117-LS), an antibody, is utilized in the research of HIV infection [1].</p>Cor e Forma:Liquid9-Deazaguanine
CAS:<p>9-Deazaguanine is a nucleoside analogue exhibiting inhibitory activity against bovine purine nucleoside phosphorylase (PNP).</p>Fórmula:C6H6N4OPureza:98%Cor e Forma:SolidPeso molecular:150.14N,O-Diacetyltyramine
CAS:<p>N,O-Diacetyltyramine, isolated from the actinomycete Pseudonocardia endophytica VUK-10, exhibits both antibacterial activity against Gram-positive and Gram-negative bacteria, alongside fungi, and demonstrates cytotoxicity towards MDA-MB-231, HeLa, MCF-7, and OAW-42 cells [1].</p>Fórmula:C12H15NO3Cor e Forma:SolidPeso molecular:221.25SPR38
<p>SPR38: SARS-CoV-2 protease inhibitor with Ki 0.260 μM; also blocks hCatL (Ki 1.92 μM) and hCatB (Ki 11.1 μM).</p>Fórmula:C24H33N3O5Cor e Forma:SolidPeso molecular:443.54FR194738 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:439.65Cladosporin
CAS:<p>Cladosporin, from Cladosporium cladosporioid fungus, halts dermatophyte growth on agar at 75 μg/mL.</p>Fórmula:C16H20O5Cor e Forma:SolidPeso molecular:292.33WQ 2743
CAS:<p>WQ 2743 is a potent agent of antimicrobial.</p>Fórmula:C19H15BrF3N5O3Pureza:98%Cor e Forma:SolidPeso molecular:498.25VT-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:584.52AG 85
CAS:<p>AG 85 is a major secretion protein of Mycobacterium tuberculosis.</p>Fórmula:C27H22N4O3SCor e Forma:SolidPeso molecular:482.55KY386
CAS:<p>KY386 is a potent and selective DHX33 helicase inhibitor with an IC50 value of 19 nM.</p>Fórmula:C21H19N5O2SCor e Forma:SolidPeso molecular:405.478-NH2-ATP tetrasodium
CAS:<p>8-NH2-ATP tetrasodium, an inactive ATP variant, originates from 8-NH2-Ado tetrasodium, which triggers the apoptosis-associated cleavage of poly (ADP-ribose) polymerase [1] [2].</p>Fórmula:C10H13N6Na4O13P3Cor e Forma:SolidPeso molecular:610.12BRL44385
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:225.2Cap-dependent endonuclease-IN-13
CAS:<p>Cap-dependent endonuclease-IN-13 is a potent inhibitor of cap-dependent endonuclease (CEN) and shows research potential against influenza virus infection (</p>Fórmula:C25H20F2N4O4SCor e Forma:SolidPeso molecular:510.51SA09-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:364.03Valtorcitabine 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:399.27BILR-355
CAS:<p>BILR-355 is a reverse transcriptase inhibitor.</p>Fórmula:C25H23N5O3Pureza:98%Cor e Forma:SolidPeso molecular:441.48Variculanol
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:372.58Inz-5
CAS:Inz-5 is a fungal-selective inhibitor of mitochondrial cytochrome bc1. Inz-5 impairs fungal virulence. It also prevents the evolution of drug resistance.Fórmula:C18H14F4N6Cor e Forma:SolidPeso molecular:390.34SARS-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:430.36Zika virus-IN-1
CAS:<p>Zika virus-IN-1 is an inhibitor of Zika virus (EC50: 1.56 μM).</p>Fórmula:C30H37N3O3SiCor e Forma:SolidPeso molecular:515.72Dihydroaltenuene B
CAS:<p>Dihydroaltenuene B inhibits mushroom tyrosinase (IC50: 38.33µM) and binds His244, Met280, Gly281 via hydrogen bonds.</p>Fórmula:C15H18O6Cor e Forma:SolidPeso molecular:294.3HBV-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:407.83ThrRS-IN-3
<p>ThrRS-IN-3: Potent inhibitor of Salmonella enterica ThrRS, IC50 = 19 nM, Kd = 34 nM, with antibacterial effects.</p>Fórmula:C31H30Cl2N6O5Cor e Forma:SolidPeso molecular:637.51Valnemulin
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:564.83Zoxamide
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:336.64Antibacterial agent 135
CAS:<p>Antibacterial Agent 135 (example 7) effectively inhibits various bacteria, including P.</p>Fórmula:C11H15N5O6SCor e Forma:SolidPeso molecular:345.336-Chloro-7-deazapurine-β-D-riboside
CAS:6-Chloro-7-deazapurine-β-D-riboside shows antifungal activity.Fórmula:C11H12ClN3O4Pureza:98.26%Cor e Forma:SolidPeso molecular:285.68SARS-CoV-2/MERS Mpro-IN-1
<p>SARS-CoV-2/MERS Mpro-IN-1 is a potent inhibitor of the main proteases in SARS-CoV-2 and MERS, exhibiting IC50 values of 0.10 and 0.06 µM, respectively.</p>Fórmula:C30H36N4O7Cor e Forma:SolidPeso molecular:564.63
