
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(3.296 productos)
- Antibiótico(937 productos)
- Antifección(26 productos)
- DHFR(34 productos)
- Síntesis de ADN / ARN(793 productos)
- HBV(188 productos)
- Proteasa del VIH(506 productos)
- HSV(96 productos)
- Integrasa(2 productos)
- Ribosoma(13 productos)
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Se han encontrado 6367 productos de "Microbiología / Virología"
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FGI-106
CAS:FGI-106 combats Ebola, Rift Valley, Dengue Fever, HCV, and HIV-1; EC50s range from 100-900 nM.Fórmula:C28H38N6Pureza:98%Forma y color:SolidPeso molecular:458.6420S 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:421.83Gougerotin
CAS:Gougerotin is an inhibitor of protein synthesis.Fórmula:C16H25N7O8Forma y color:SolidPeso molecular:443.41VNI
CAS:VNI is an effective inhibitor of CYP51. It suppresses sterol synthesis in Trypanosoma cruzi, exhibiting anti-Trypanosoma cruzi activity.Fórmula:C26H19Cl2N5O2Forma y color:SolidPeso molecular:504.37(S)-ZG197
(S)-ZG197 is a compound that acts as a highly selective activator of the Staphylococcus aureus Caseinolytic Protease P (Sa ClpP), demonstrating efficacy at aFórmula:C28H35F3N4O3Forma y color:SolidPeso molecular:532.6TAN-1057C
CAS:TAN-1057C is a potent antibiotic with antimicrobial activity against both Gram-negative and Gram-positive bacteria, including Methicillin-resistant Staphylococcus aureus (MRSA).Fórmula:C13H25N9O3Forma y color:SolidPeso molecular:355.42,5-Di-tert-butyl-1,4-benzoquinone
CAS:2,5-Di-tert-butyl-1,4-benzoquinone is a potent antibacterial agent found primarily in marine Streptomyces sp. VITVSK1, effective against emerging antibiotic resistance. Additionally, it serves as a powerful inhibitor of RNA polymerase.Fórmula:C14H20O2Forma y color:SolidPeso molecular:220.31SARS-CoV-2 Mpro-IN-34
SARS-CoV-2 Mpro-IN-34 (Compound 26) acts as an inhibitor of SARS-CoV-2 Mpro with an IC50 of 6 nM. It also inhibits OC43 Mpro, demonstrating an IC50 of 33 nM. Furthermore, this compound exhibits antiviral activity in Vero E6 cells infected with SARS-CoV-2, with an EC50 of 0.103 μM.Fórmula:C30H37Cl2N5O3Forma y color:SolidPeso molecular:586.55Cefamandole lithium
CAS:Cefamandole (lithium), a second-generation broad-spectrum cephalosporin antibiotic, exhibits antimicrobial activity. Upon metabolism in the body, it releases free NMTT, which can lead to hypoprothrombinemia.Fórmula:C18H17LiN6O5S2Forma y color:SolidPeso molecular:468.44Cilastatin ammonium salt
CAS:Cilastatin ammonium salt is an antibiotic that is particularly effective against Gram-positive cocci, with a half-life of 3-4 hours.Fórmula:C16H29N3O5SForma y color:SolidPeso molecular:375.48RAD51-IN-6
CAS:RAD51-IN-6, a potent RAD51 gene inhibitor, may help research mitochondrial disorders. (WO2021164746A1, cmpd 23)Fórmula:C27H40N3O5PSForma y color:SolidPeso molecular:549.66CYP2C19-IN-1
CYP2C19-IN-1: potent CYP2C19 inhibitor, non-genotoxic, non-hepatotoxic, blocks RdRP (Ki: 6.16 μM), useful for ZIKV research.Fórmula:C26H26N2O6SForma y color:SolidPeso molecular:494.56Mt KARI-IN-1
Mt KARI-IN-1 inhibits Mtb KARI with a 3.06 μM Ki, targeting tuberculosis.Fórmula:C14H11N5O4S2Forma y color:SolidPeso molecular:377.4Gallinamide A
CAS:Gallinamide A is a potent inhibitor of cathepsin L with an IC 50 value of 17.6 pM.Fórmula:C31H52N4O7Forma y color:SolidPeso molecular:592.77Antifungal agent 42
Antifungal 42 blocks biofilm formation and inhibits C.albicans' CYP51.Fórmula:C22H20Cl2N4Se2Forma y color:SolidPeso molecular:569.25Chitinase-IN-4
Chitinase-IN-4 (compound 8f) is a potent and selective inhibitor of OfChi-h with an IC50 value of 0.1 μM and good insecticidal activity.Fórmula:C21H24ClN7Forma y color:SolidPeso molecular:409.92HC2210
CAS:HC2210 exhibits antibacterial effects against Mycobacterium abscessus (Mab) with an EC50 of 0.72 µM. It modulates the expression of Mab genes associated with oxidative stress and lipid metabolism. HC2210 is applicable for studies on Mab infections.Fórmula:C17H18N4O9Forma y color:SolidPeso molecular:422.35MetRS-IN-1
CAS:MetRS-IN-1 (Compound 27) is an inhibitor of E. coli methionyl-tRNA synthetase (MetRS) with an IC50 value of 237 nM [1].Fórmula:C15H13N3O4SForma y color:SolidPeso molecular:331.35Antibacterial agent 79
Antibacterial agent 79 is an antibacterial agent.Fórmula:C18H27N3O2S3Forma y color:SolidPeso molecular:413.628-Deazafolic acid
CAS:8-Deazafolic acid inhibits folate-dependent bacteria S. faecium & L. casei, and fights lymphoid leukemia L1210 in mice.Fórmula:C20H20N6O6Pureza:98%Forma y color:SolidPeso molecular:440.41

