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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Du011
CAS:<p>Du011 is a biogenesis inhibitor of the E.</p>Fórmula:C20H15F2NO4SCor e Forma:SolidPeso molecular:403.4UNC2170 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:429.31GSK3839919A
CAS:<p>GSK3839919A is a potent allosteric inhibitor of HIV-1 integrase [1].</p>Fórmula:C36H46ClN3O3Cor e Forma:SolidPeso molecular:604.22(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:412.52Bio-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:571.63VT-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:584.52Capravirine
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:451.37BRL44385
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:225.2DDD85646
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:495.43DHFR-IN-10
CAS:<p>DHFR-IN-10 (compound 4c) is a potent inhibitor of dihydrofolate reductase (DHFR), displaying an inhibition concentration half-maximum (IC50) of 4.21 μM against</p>Fórmula:C20H14BrN3S3Cor e Forma:SolidPeso molecular:472.44NCI-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:526.55Daldinone A
CAS:<p>Daldinone A (Compound 4), isolated from Nigrospora oryzae, exhibits antibacterial properties, specifically demonstrating antimicrobial potential against P. aeruginosa [1].</p>Fórmula:C20H16O5Cor e Forma:SolidPeso molecular:336.34Antitrypanosomal agent 14
CAS:<p>Antitrypanosomal agent 14 (Compound 1), a potent T.</p>Fórmula:C14H23N3OSPureza:98%Cor e Forma:SolidPeso molecular:281.42Mtb-IN-4
CAS:<p>Mtb-IN-4 (compound 17h) is a non-toxic isoxazole that exhibits anti-Mycobacterium tuberculosis (Mtb) activity, with an IC50 value of 0.70 μM.</p>Fórmula:C24H18N2O4SCor e Forma:SolidPeso molecular:430.48Pinokalant
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:712.83Hinokinin
CAS:<p>Hinokinin (Cubebinolide), a bioactive lignan, exhibits a broad spectrum of pharmacological activities.</p>Fórmula:C20H18O6Cor e Forma:SolidPeso molecular:354.35SARS-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:499.39Variculanol
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:372.58Tuberculosis 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:377.46Icofungipen
CAS:<p>Icofungipen is an oral antifungals with active against Candida species.</p>Fórmula:C7H11NO2Pureza:98%Cor e Forma:SolidPeso molecular:141.17HIV-1 inhibitor-3
CAS:<p>HIV-1 inhibitor-3 is an HIV infection inhibitor.</p>Fórmula:C9H10F2N2O5Pureza:98%Cor e Forma:SolidPeso molecular:264.18DQn-1
CAS:<p>DQn-1, a potent antifolate, demonstrates efficacy against Mycobacterium tuberculosis (Mtb) with an MIC 90 of 0.03 µM.</p>Fórmula:C16H14ClN5O2Cor e Forma:SolidPeso molecular:343.77OfChi-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:427.54Fosalvudine 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:722.93MF 5137
CAS:<p>MF 5137 is an effective antimicrobial agent.</p>Fórmula:C23H23N3O3Pureza:98%Cor e Forma:SolidPeso molecular:389.45WRN inhibitor 3
CAS:<p>WRN Inhibitor 3 (example 110), a cyclic vinyl sulfone-based compound, serves as an inhibitor of the Werner Syndrome ATP-dependent helicase enzyme (WRN).</p>Fórmula:C20H20N2O5SCor e Forma:SolidPeso molecular:400.45WRN inhibitor 4
CAS:<p>WRN Inhibitor 4 (Example 107), a cyclic vinyl sulfone-based compound, serves as an inhibitor of the Werner Syndrome ATP-dependent helicase enzyme (WRN).</p>Fórmula:C16H14N2O5SCor e Forma:SolidPeso molecular:346.36MC-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:1230.45PTC725
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:518.49COH1
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:250.27Oxynitidine
CAS:<p>Oxynitidine, an HBV inhibitor (ID50 = 30.8 µg/mL), effectively suppresses HBV DNA replication and may be utilized in viral infection research [1].</p>Fórmula:C21H17NO5Pureza:98%Cor e Forma:SolidPeso molecular:363.36Antifungal agent 26
CAS:<p>Pradimicin A derivative 26 exhibits antifungal, antiviral, and antiparasitic properties by attaching to d-mannose (Man)-rich glycans in pathogenic organisms [1</p>Fórmula:C40H45N3O18Cor e Forma:SolidPeso molecular:855.79TH-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:394.34Diazoketone methotrexate
CAS:<p>Diazoketone methotrexate is an analog of methotrexate with potential antitumor activity.</p>Fórmula:C21H22N10O4Cor e Forma:SolidPeso molecular:478.46Antibacterial 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:356.39Indinavir, 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:613.795-DACTHF
CAS:<p>5,11-methenyltetrahydrohomofolate blocks GAR & AIR transformylase; used as an anti-purine drug.</p>Fórmula:C19H24N6O6Pureza:98%Cor e Forma:SolidPeso molecular:432.43Alteconazole
CAS:<p>Alteconazole is an antifungal drug.</p>Fórmula:C17H12Cl3N3OPureza:98%Cor e Forma:SolidPeso molecular:380.66Cladosporin
CAS:<p>Cladosporin, from Cladosporium cladosporioid fungus, halts dermatophyte growth on agar at 75 μg/mL.</p>Fórmula:C16H20O5Cor e Forma:SolidPeso molecular:292.33Antiproliferative 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:434.57NIK-250
CAS:<p>NIK-250 is a P-glycoprotein inhibitor. NIK250 could reverse multidrug resistance in human glioma cells.</p>Fórmula:C26H25N3O4S2Cor e Forma:SolidPeso molecular:507.62NS5A-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:807.89Azaconazole
CAS:<p>Azaconazole, an agricultural fungicide, is used for controlling powdery mildew on crops and bean rust.</p>Fórmula:C12H11Cl2N3O2Cor e Forma:SolidPeso molecular:300.14SARS-CoV-2-IN-43
CAS:<p>Compound 8h, also known as SARS-CoV-2-IN-43, is a powerful inhibitor effective in obstructing the replication of SARS-CoV-2, exhibiting significant antiviral</p>Fórmula:C16H12O3Pureza:98%Cor e Forma:SolidPeso molecular:252.26RNA 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:887.96(S)-Mosnodenvir
CAS:<p>(S)-Mosnodenvir, a pan-serotype dengue antiviral agent, exhibits picomolar to low nanomolar in vitro activity with a high barrier to resistance and is</p>Fórmula:C26H22ClF3N2O6SPureza:98%Cor e Forma:SolidPeso molecular:582.98Vaborbactam
CAS:<p>Vaborbactam (RPX7009) is a β-lactamase inhibitor that is often used in conjunction with meropenem to study pneumonia and CRE infections.</p>Fórmula:C12H16BNO5SPureza:97.29%Cor e Forma:SolidPeso molecular:297.14Loflucarban
CAS:<p>Loflucarban (Fluonilid) is an antimycotic compoud.</p>Fórmula:C13H9Cl2FN2SPureza:98.08% - 98.15%Cor e Forma:SolidPeso molecular:315.19BVDU 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:573.08
