Microbiología / Virología
Los inhibidores en microbiología y virología son compuestos que se dirigen a microorganismos, incluyendo bacterias, virus y hongos, interrumpiendo su crecimiento, replicación o supervivencia. Estos inhibidores son esenciales para estudiar la patogénesis microbiana, comprender los mecanismos de resistencia y desarrollar nuevas terapias antimicrobianas y antivirales. Los inhibidores en esta categoría se utilizan para combatir enfermedades infecciosas, explorar la ecología microbiana e investigar las interacciones huésped-patógeno. En CymitQuimica, ofrecemos una amplia selección de inhibidores de alta calidad en microbiología y virología para apoyar su investigación en enfermedades infecciosas, microbiología y virología.
Subcategorías de "Microbiología / Virología"
- Antibacteriano(3.334 productos)
- Antibiótico(937 productos)
- Antifección(26 productos)
- DHFR(32 productos)
- Síntesis de ADN / ARN(796 productos)
- HBV(189 productos)
- Proteasa del VIH(507 productos)
- HSV(96 productos)
- Integrasa(2 productos)
- Ribosoma(11 productos)
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Se han encontrado 6383 productos de "Microbiología / Virología"
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And1 degrader 1
CAS:And1 degrader 1 (Compound A15) is a degrader of acidic nucleoplasmic DNA-binding protein 1 (And1) that notably induces degradation of And1 in NSCLC cells. When combined with Olaparib (1 μM), And1 degrader 1 at a concentration of 5 μM effectively inhibits proliferation in A549 and H460 cells. This compound is applicable in cancer research studies.Fórmula:C26H27Cl2N3OForma y color:SolidPeso molecular:468.4220S Proteasome-IN-4
CAS:20S Proteasome-IN-4: brain-penetrant, parasite-specific, oral, inhibits T.b. brucei proteasome (IC50: 6.3nM), for HAT research.Fórmula:C20H18ClF2N3O3Forma y color:SolidPeso molecular:421.83Epiderstatin
CAS:Epiderstatin is isolated from Streptomyces pulveraceus subsp. epiderstagenes; inhibits mitogenic activity of epidermal growth factor.Fórmula:C15H20N2O4Forma y color:SolidPeso molecular:292.33Antifungal agent 113
CAS:Antifungalagent 113 (compound 9a) serves as an effective antifungal and antibacterial agent. It exhibits strong inhibitory activity against both S. aureus and methicillin-resistant S. aureus.Fórmula:C23H20O5Forma y color:SolidPeso molecular:376.40HCV-IN-40
CAS:HCV-IN-39 is a potent oral drug inhibiting HCV, effective on GT1a (EC50: 0.259μM), GT1b (EC50: 0.434μM), GT1b CES1 (EC50: 0.069μM) replicons.Fórmula:C21H26BrFN3O9PForma y color:SolidPeso molecular:594.32LasR 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:C20H15F3N2O3Forma y color:SolidPeso molecular:388.34PRRSV-IN-1
CAS:PRRSV-IN-1 (Compound 4s) acts as an inhibitor of the nsp4 protease of PRRSV. It has an EC50 value of 0.45 μM against PRRSV, binds to the nsp4 protease with a Kd of 29.24 pM, and exhibits an IC50 value of 80.36 pM for nsp4 protease inhibition. PRRSV-IN-1 is applicable in antiviral infection research.Fórmula:C19H18BrNO3Forma y color:SolidPeso molecular:388.255WRN inhibitor 7
CAS:<p>WRN inhibitor 7 (Compound h6), a potent inhibitor of Werner syndrome helicase, demonstrates effective suppression of WRN's helicase and ATPase activities with IC50 values of 9.8 μM and 15.8 μM, respectively. This compound is utilized in the study of microsatellite instable (MSI) cancers [1].</p>Fórmula:C27H23N3O6Forma y color:SolidPeso molecular:485.49Chitin synthase inhibitor 5
Calpain Inhibitor-2, lipophilic, inhibits calpain; shows anti-proliferative effects on melanoma, PC-3 cells; blocks 80% DU-145 cell invasion.Fórmula:C23H22BrN3O5Forma y color:SolidPeso molecular:500.34HldA/E-IN-1
CAS:HldA/E-IN-1 (compound 8) is a dual inhibitor of HldA/E, exhibiting IC50 values of 17.2 μM and 67.8 μM, respectively. This compound is utilized in research on antibacterial infections.Fórmula:C8H17FO13P2Forma y color:SolidPeso molecular:402.16Neuraminidase-IN-18
CAS:Neuraminidase-IN-18 (compound N5), a novel polyheterocyclic neuraminidase (NA) inhibitor, demonstrates significant inhibitory activity against H5N1 NA, with an IC 50 of 0.14 μM against the wild-type H5N1 NA and 0.27 μM against the H5N1-H274Y mutant NA. This compound effectively binds to NAs, inhibiting influenza virus replication at the cellular level [1].Fórmula:C22H18FN3O3SForma y color:SolidPeso molecular:423.46HIV-1 inhibitor-17
HIV-1 inhibitor-18 blocks HIV-1 capsid, acts on NL4-3 strain (EC50: 2.57 μM), has low cytotoxicity (MT-4 CC50: >8.55).Fórmula:C32H32N4O5SForma y color:SolidPeso molecular:584.69Pyriftalid
CAS:Pyriftalid is a novel insecticide known for its potent inhibitory activity against a variety of pests. It is widely utilized in agriculture to effectively manage crop pests, thereby enhancing both the yield and quality of crops. Additionally, research is exploring the use of Pyriftalid in boosting plant resistance to pests and diseases.Fórmula:C15H14N2O4SForma y color:SolidPeso molecular:318.35SARS-CoV-2-IN-102
CAS:SARS-CoV-2-IN-102 (example 58) is an inhibitor of the SARS-CoV papain-like protease (SARS-CoVPLpro), demonstrating an IC50 of less than 100 nM.Fórmula:C29H34F2N6O2Forma y color:SolidPeso molecular:536.62Isazofos
CAS:Isazofos is a broad-spectrum organophosphate insecticide and nematicide effective in controlling a variety of lawn pests, such as nematodes (Radopholus similis). It also demonstrates efficacy in managing rice gall midge.Fórmula:C9H17ClN3O3PSForma y color:SolidPeso molecular:313.74FG-2101
CAS:FG-2101 is a selective, orally active non-hydroxamate LpxC inhibitor with an IC50 of approximately 1 nM. It demonstrates exceptional selectivity over other bacterial and human metalloproteases. FG-2101 is useful for studying infections caused by Gram-negative bacteria, including resistant strains.Fórmula:C30H32N5O6PForma y color:SolidPeso molecular:589.579Antibacterial agent 77
Antibacterial agent 77 (compound 12) is an antibacterial agent [1].Fórmula:C22H27N3OSForma y color:SolidPeso molecular:381.53GSK-3036656 free base
CAS:GSK656 (GSK3036656) inhibits Mtb LeuRS with IC50 of 0.20 μM, promising for tuberculosis treatment.Fórmula:C10H13BClNO4Forma y color:SolidPeso molecular:257.48N6-Benzoyl-2'-deoxyadenosine monohydrate
CAS:N6-Benzoyl-2'-deoxyadenosine monohydrate is a nucleoside analogue that helps diagnose bacterial infections by binding to double-stranded DNA and altering its structure, which can subsequently be detected using electrophoresis.Fórmula:C17H19N5O5Forma y color:SolidPeso molecular:373.363SARS-CoV-2 PLpro-IN-1
CAS:SARS-CoV-2 PLpro-IN-1 (Compound 85) is a non-covalent competitive inhibitor of SARS-CoV-2 PLpro with an IC50 value of 15.06 μM and a Ki value of 22.93 μM. It inhibits the proliferation of Vero cells, exhibiting an IC50 of 7.47 μM.Fórmula:C18H19N5OForma y color:SolidPeso molecular:321.376
