
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(919 produtos)
- Antifecção(23 produtos)
- DHFR(32 produtos)
- Síntese de DNA/RNA(707 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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Cefetamet pivoxyl
CAS:<p>Cefetamet pivoxyl, a cephalosporin antibiotic, effectively inhibits 355 enteropathogens, including Gram-negative bacteria (ausgenommen Pseudomonas aeruginosa) and Legionella pneumophila [1].</p>Fórmula:C20H25N5O7S2Pureza:98%Cor e Forma:SolidPeso molecular:511.57Sulfamonomethoxine sodium
CAS:<p>Sulfamonomethoxine sodium is a long-acting sulfonamide antibacterial agent utilized in blood kinetic studies; it inhibits dihydropteroate synthetase, thereby blocking folic acid synthesis [1].</p>Fórmula:C11H11N4NaO3SPureza:98%Cor e Forma:SolidPeso molecular:302.29Pulcherriminic acid
CAS:<p>Pulcherriminic acid, a cyclic dipeptide, chelates Fe3+, forms pulcherrimin, and has antimicrobial properties used in food, agriculture, and medicine.</p>Fórmula:C12H20N2O4Cor e Forma:SolidPeso molecular:256.30Antiviral agent 5
CAS:<p>Antiviral agent 5 is a crucial intermediate utilized in the development of antiviral agents that specifically target 3C and 3CL proteases, which includes the SARS-CoV-2 M pro enzyme.</p>Fórmula:C18H30N2O7Cor e Forma:SolidPeso molecular:386.445BMS-378806
<p>BMS-378806 is an HIV inhibitor with EC50: 0.85-26.5nM for various strains.</p>Fórmula:C22H22N4O4Pureza:98%Cor e Forma:SolidPeso molecular:406.43Bacampicillin hydrochloride
CAS:<p>Bacampicillin hydrochloride is an improved oral bioavailability penicillin antibiotic which is a prodrug of ampicillin.</p>Fórmula:C21H28ClN3O7SPureza:98%Cor e Forma:SolidPeso molecular:501.982-Mercaptopyridine N-oxide sodium
CAS:<p>2-Mercaptopyridine N-oxide sodium is a useful organic compound for research related to life sciences. The catalog number is T66776 and the CAS number is 3811-73-2.</p>Fórmula:C5H4NNaOSCor e Forma:SolidPeso molecular:149.14FtsZ-IN-10
CAS:<p>Compound GK02084(SC) may have activity against the GTP site of Bs‐FtsZ.</p>Fórmula:C15H13ClN2O4SPureza:98%Cor e Forma:SolidPeso molecular:352.79N-Butylthiophosphoric triamide
CAS:<p>N-Butylthiophosphoric triamide is a useful organic compound for research related to life sciences. The catalog number is T65336 and the CAS number is 94317-64-3.</p>Fórmula:C4H14N3PSCor e Forma:SolidPeso molecular:167.21Rhizocticin A
CAS:<p>Rhizocticin A is a potential inhibitor of threonine synthase.</p>Fórmula:C11H22N5O6PPureza:98%Cor e Forma:SolidPeso molecular:351.3Darobactin
CAS:<p>Darobactin is an antibiotic effective against critical Gram-negative pathogens, demonstrating activity both in vitro and in animal infection models [1].</p>Fórmula:C47H55N11O12Pureza:98%Cor e Forma:SolidPeso molecular:966.01Tetraconazole
CAS:<p>Tetraconazole is an agent of pesticides.</p>Fórmula:C13H11Cl2F4N3OCor e Forma:Liquid ViscousPeso molecular:372.14l-Atabrine dihydrochloride
CAS:<p>l-Atabrine dihydrochloride displays antiprion activity. l-Atabrine dihydrochloride is a less active enantiomer of quinacrine.</p>Fórmula:C23H31Cl2N3OPureza:98%Cor e Forma:SolidPeso molecular:436.425'-O-TBDMS-dT
CAS:<p>5’-O-TBDMS-dT is a nucleoside with protective and modification effects.</p>Fórmula:C16H28N2O5SiCor e Forma:SolidPeso molecular:356.49Phosalacine
CAS:<p>Phosalacine, isolated from Kitasatosporia phosalacinea, is a new herbicidal antibiotic that contains phosphinothricin.</p>Fórmula:C14H28N3O6PPureza:98%Cor e Forma:SolidPeso molecular:365.367Ramifenazone
CAS:<p>Ramifenazone is a drug of nonsteroidal anti-inflammatory.</p>Fórmula:C14H19N3OPureza:98%Cor e Forma:SolidPeso molecular:245.32Golgicide A-2
CAS:<p>GCA-2 is a potent enantiomer of GCA, selectively and efficiently kills An. stephensi larvae, useful for dengue research.</p>Fórmula:C17H14F2N2Cor e Forma:SolidPeso molecular:284.31Loviride
CAS:<p>Loviride, a reverse transcriptase inhibitor with IC50 of 0.3 μM, blocks HIV-1/2 and SIV in MT-4 cells.</p>Fórmula:C17H16Cl2N2O2Cor e Forma:SolidPeso molecular:351.23Ref: TM-T15776
Produto descontinuadoTP0586532
CAS:<p>TP0586532 is effective against carbapenem-resistant Klebsiella pneumoniae and does not pose a cardiovascular risk.</p>Fórmula:C26H28N4O4Pureza:98%Cor e Forma:SolidPeso molecular:460.52Oxindole
CAS:<p>Oxindole (Indolin-2-one) is an aromatic heterocyclic building block. 2-indolinone derivatives have become lead compounds in the research of kinase inhibitors.Oxindole structure has been used in receptor tyrosine kinases (RTKs) inhibitors such as SU4984 and intedanib, the RTK family represents an important therapeutic target for anti-cancer drug development.</p>Fórmula:C8H7NOPureza:99.34%Cor e Forma:Off-White Crystalline PowderPeso molecular:133.15HBV-IN-34
CAS:<p>HBV-IN-34 (compound 17i) is a potent inhibitor of HBsAg production, demonstrating remarkable in vitro anti-HBV efficacy with EC50 values of 0.018 μM for HBV DNA</p>Fórmula:C21H19F2N7Pureza:98%Cor e Forma:SolidPeso molecular:407.42Ref: TM-T79469
Produto descontinuadoHIV-1 integrase inhibitor
CAS:<p>Hiv-1 integrase inhibitor is an effective anti-HIV drug.</p>Fórmula:C11H9N3O4Pureza:98%Cor e Forma:SolidPeso molecular:247.21Pritelivir mesylate
CAS:<p>Pritelivir mesylate is active against herpes simplex virus types 1 and 2 (IC50: 0.02 μM against HSV1-2). Pritelivir mesylate is an inhibitor of the viral helicase-primase complex. Pritelivir mesylate shows antiviral activity in vitro and in animal models </p>Fórmula:C19H22N4O6S3Pureza:98%Cor e Forma:SolidPeso molecular:498.6DprE1-IN-8
CAS:<p>DprE1-IN-8 is a potent inhibitor of DprE1, exhibiting an IC50 of less than 0.75 μM.</p>Fórmula:C19H12F3N5O4SPureza:98%Cor e Forma:SolidPeso molecular:463.39Ref: TM-T79628
Produto descontinuadoPKUMDL-LTQ-301
CAS:PKUMDL-LTQ-301 is a potent inhibitor of HipA toxin. PKUMDL-LTQ-301 also inhibits E. coli persistence.Fórmula:C30H28N2O4Pureza:98%Cor e Forma:SolidPeso molecular:480.55d-Atabrine dihydrochloride
CAS:<p>d-Atabrine hydrochloride is the active enantiomer of quinacrine and has anti-pr virus activity.</p>Fórmula:C23H31Cl2N3OPureza:98%Cor e Forma:SolidPeso molecular:436.42MitoE10
CAS:<p>MitoE10 is an effective mitochondrial targeting antioxidant.</p>Fórmula:C42H55O5PSCor e Forma:SolidPeso molecular:702.92SARS-CoV-2-IN-68
CAS:<p>SARS-CoV-2-IN-68 (compound 6C) is a covalent inhibitor of both SARS-CoV-2 PLpro and Mpro, exhibiting potent antiviral properties by targeting the Zn-finger</p>Fórmula:C14H12N2OSePureza:98%Cor e Forma:SolidPeso molecular:303.22HBV-IN-38
CAS:<p>HBV-IN-38 (Example 193), an HBV DNA inhibitor with an EC50 value of ≤100 nM, serves as a research tool for investigating viral infections [1].</p>Fórmula:C18H16F3N5O4S2Pureza:98%Cor e Forma:SolidPeso molecular:487.48Yhhu6669
CAS:<p>Yhhu6669 is an anti-HBV agent that suppresses viral DNA and replication by promoting DNA-free capsid assembly, effectively reducing HBV DNA and HBcAg levels in</p>Fórmula:C29H28ClFN6O3Pureza:98%Cor e Forma:SolidPeso molecular:563.02Ref: TM-T78756
Produto descontinuadoInsecticidal agent 6
CAS:<p>Compound Im (Insecticidal agent 6) is a potent inhibitor of insect ryanodine receptors (RyRs), exhibiting an EC50 of 0.6308 µM against S.</p>Fórmula:C19H14BrCl2N5O4Pureza:98%Cor e Forma:SolidPeso molecular:527.16Cap-dependent endonuclease-IN-9
CAS:<p>Cap-dependent endonuclease-IN-9, a strong influenza inhibitor, shows low toxicity, good pharmacokinetics, and dynamic action.</p>Fórmula:C29H22F2N4O7SPureza:98%Cor e Forma:SolidPeso molecular:608.57Ref: TM-T72125
Produto descontinuado
