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(3.365 produtos)
- Antibiótico(937 produtos)
- Antifecção(27 produtos)
- DHFR(30 produtos)
- Síntese de DNA/RNA(799 produtos)
- HBV(182 produtos)
- HIV Protease(496 produtos)
- HSV(99 produtos)
- Integrase(2 produtos)
- Ribossomo(10 produtos)
Exibir 2 mais subcategorias
Foram encontrados 6326 produtos de "Microbiologia/Virologia"
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10(R)-hydroxy Stearic Acid
CAS:10(R)-hydroxy Stearic acid is a hydroxy fatty acid resulting from the hydroxylation of oleic acid, produced by gut microbiota.Fórmula:C18H36O3Cor e Forma:SolidPeso molecular:300.48MK-3402
CAS:MK-3402 is a metallo-beta-lactamase inhibitor. MK-3402can be used in the research of bacteria .Fórmula:C15H19N9O5S2Cor e Forma:SolidPeso molecular:469.50HIV-1 inhibitor-82
CAS:HIV-1inhibitor-82 (Compound L14) is a small molecule inhibitor of HIV-1 entry with oral bioavailability, exhibiting an IC50 value of 0.39 μM. It holds potential for research in combating HIV-1 infection.Fórmula:C37H37ClN2O6S2Cor e Forma:SolidPeso molecular:705.28DHX9-IN-9
CAS:DHX9-IN-9 (509) acts as an inhibitor of the RNA helicase DHX9, demonstrating an EC50 of 0.0177 μM in DHX9 cellular target engagement, primarily utilized in cancer research [1].Fórmula:C21H21ClFN5O3S2Cor e Forma:SolidPeso molecular:510Plevitrexed
CAS:Plevitrexed, an oral TS inhibitor (Ki: 0.44 nM), targets α-folate receptor & reduced folate carrier, treats gastric cancer.Fórmula:C26H25FN8O4Pureza:98%Cor e Forma:SolidPeso molecular:532.53Tenellin
CAS:Tenellin is a fungal metabolite that inhibits Mg2+-, Ca2+-, and Na+/K+-ATPase activities in erythrocytes. Tenellin is cytotoxic to Sf9 and Sf21 insect cells.Fórmula:C21H23NO5Cor e Forma:SolidPeso molecular:369.41Cephalosporin C
CAS:Cephalosporin C exhibits relatively weak resistance to Gram-positive and Gram-negative bacteria. It is stable against penicillinase, but can be decomposed by cephalosporinase. When hydrolyzed to remove its side chain, it yields 7-amino-cefenoic acid (7-ACA), which is an essential raw material for the production of semisynthetic cephalosporins.
Fórmula:C16H21N3O8SCor e Forma:SolidPeso molecular:415.418Tetrahydrouridine dihydrate
THU dihydrate, a potent CDA inhibitor, outperforms cytidine by blocking the enzyme's active site.Fórmula:C9H20N2O8Cor e Forma:SolidPeso molecular:284.26LasR antagonist 1
CAS:LasR antagonist 1 (Compound 7), with an IC50 of 0.4 μM, is an effective antagonist of LasR that modulates quorum sensing (QS) in the opportunistic pathogen Pseudomonas aeruginosa [1].Fórmula:C20H15F3N2O3Cor e Forma:SolidPeso molecular:388.34TBAJ-5307
CAS:TBAJ-5307 is a broad-spectrum anti-non-tuberculous mycobacteria inhibitor that targets the FO-domain of the engine, preventing rotation and proton-translocation. TBAJ-5307 inhibits non-tuberculous mycobacteria in vitro and in vivo [1].Fórmula:C30H35BrN4O6Cor e Forma:SolidPeso molecular:627.53Neuraminidase-IN-4
Neuraminidase-IN-4 inhibits neuraminidase (EC50: 1.59 μM) and has strong anti-H5N1 activity.Fórmula:C21H20N2O6SCor e Forma:SolidPeso molecular:428.46RdRP-IN-5
CAS:RdRP-IN-5 (compound 20), a potent inhibitor of the influenza virus RNA-dependent RNA polymerase (RdRP), has potential application in influenza research [1].Fórmula:C23H21N3O5Pureza:98%Cor e Forma:SolidPeso molecular:419.43Elongation factor P-IN-1
EFP-IN-1: potent β-lysine derivative, inhibits EFP, slows E. coli growth.Fórmula:C14H31N3O2Cor e Forma:SolidPeso molecular:273.41SARS-CoV-2 Mpro-IN-25
CAS:SARS-CoV-2 Mpro-IN-25 (Compound 3a) is a protease inhibitor for SARS-CoV-2, exhibiting an IC50 value of 0.26 μM. It demonstrates antiviral activity and is useful for research in the field of pneumonia.Fórmula:C13H10FNO4Cor e Forma:SolidPeso molecular:263.22Antitumor agent-74
Antitumor agent-74, a quinazoline derivative, inhibits DNA, arrests cell cycle, and induces apoptosis with agent-75.Fórmula:C26H23FN6Cor e Forma:SolidPeso molecular:438.5PROTAC eDHFR Degrader-2
CAS:PROTACeDHFR Degrader-2 (compound 7b) is an effective degrader targeting Escherichia coli dihydrofolate reductase (eDHFR), capable of reliably degrading eDHFR-tagged proteins.Fórmula:C34H40N8O9Peso molecular:704.73RSV-IN-7
CAS:RSV-IN-7 (example 253) is a RSV inhibitor ( EC 50 : < 0.4 μΜ) .Fórmula:C27H22F3N7O3Cor e Forma:SolidPeso molecular:549.50GRL-190-21
CAS:GRL-190-21 (compound 5e), an inhibitor of SARS-Cov-2-Mpro, shows potent antiviral activity, with a K_i of 0.04 nM and an EC_50 of 0.26 μM in VeroE6 cells. It significantly reduces the infectivity, replication, and cytopathic effect of SARS-CoV-2 without notable toxicity [1].
Fórmula:C24H34F3N5O4Cor e Forma:SolidPeso molecular:513.55Antifungal agent 16
Antifungal agent 16 has antimicrobial activity comparable to that of ciprofloxacin and has higher antifungal activity than fluconazole.Fórmula:C27H21N5O2SCor e Forma:SolidPeso molecular:479.55NEU-1017
CAS:NEU-1017 serves as a broad-spectrum antiparasitic compound, effectively inhibiting T. brucei, L. major, and P. falciparum with EC50 values of 210 nM, 240 nM, and 3 nM, respectively.Fórmula:C33H31ClFN5O3SCor e Forma:SolidPeso molecular:632.147
