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(3.389 produtos)
- Antibiótico(941 produtos)
- Antifecção(27 produtos)
- DHFR(30 produtos)
- Síntese de DNA/RNA(803 produtos)
- HBV(185 produtos)
- HIV Protease(507 produtos)
- HSV(99 produtos)
- Integrase(2 produtos)
- Ribossomo(6 produtos)
Exibir 2 mais subcategorias
Foram encontrados 6402 produtos de "Microbiologia/Virologia"
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Altersolanol A
CAS:Altersolanol A (Stemphylin; NSC 173943) demonstrates effective antimicrobial properties, inhibiting the growth of Bacillus subtilis and Pseudomonas aeruginosa with a minimum inhibitory concentration (MIC) ranging from 25-100 μg/mL. Additionally, it shows no phytotoxic effects on Taxus at a concentration of 4 μg/μL.Fórmula:C16H16O8Cor e Forma:SolidPeso molecular:336.29PqsR-IN-1
PqsR-IN-1, potent PqsR inhibitor, curbs pyocyanin in Pseudomonas aeruginosa with low cytotoxicity.Fórmula:C17H18ClN3OSCor e Forma:SolidPeso molecular:347.86MIV-150
CAS:MIV-150 is a nonnucleoside inhibitor of reverse transcriptase (NNRT). MIV-150 also blocking HIV-1 and HIV-2 infections (EC50<1 nM against HIV-1/HIV-2MN).Fórmula:C19H17FN4O3Pureza:98%Cor e Forma:SolidPeso molecular:368.367-APRA
CAS:7-APRA is a semisynthetic intermediate of the cephalosporin class of antibiotics. It exhibits antibacterial activity and is primarily used in the synthesis of other cephalosporin antibiotics, such as Cefaclor and Cefprozil.Fórmula:C10H12N2O3SPeso molecular:240.28MT0703
CAS:MT0703 is a cephalosporin antibiotic featuring an aminothiazolylglycyl moiety with a 1,5-dihydroxy-4-pyridinone-2-carbonyl group, displaying potent activity against Pseudomonas species.Fórmula:C26H25N7O9S3Cor e Forma:SolidPeso molecular:675.71(-)-15-Deoxyspergualin
CAS:(-)-15-Deoxyspergualin is a potent antitumor agent that demonstrates significant inhibition against mouse leukemia L-1210.Fórmula:C17H37N7O3Cor e Forma:SolidPeso molecular:387.52Lamivudine, (+/-)-trans-
CAS:Lamivudine, a drug for HIV-1 and HBV, inhibits reverse transcriptase and resembles zalcitabine.Fórmula:C8H11N3O3SPureza:98%Cor e Forma:SolidPeso molecular:229.26Chitin synthase inhibitor 11
Potent CHS inhibitor with an IC50 of 0.10 mM; exhibits broad-spectrum antifungal properties.Fórmula:C24H24N4O8Cor e Forma:SolidPeso molecular:496.47DXR-IN-3
CAS:DXR-IN-3 is an anti-Toxoplasma DXR inhibitor. It exhibits in vitro activity against the TgDXR enzyme, with an IC50 value of 0.62 μM and a Ki value of 0.19 μM. Furthermore, DXR-IN-3 can inhibit the proliferation of Toxoplasma, displaying an IC50 value of 5.46 μM.Fórmula:C10H12Cl2NO5PSCor e Forma:SolidPeso molecular:360.15RAD51-IN-6
CAS:RAD51-IN-6, a potent RAD51 gene inhibitor, may help research mitochondrial disorders. (WO2021164746A1, cmpd 23)Fórmula:C27H40N3O5PSCor e Forma:SolidPeso molecular:549.66LpxA-IN-1
CAS:LpxA-IN-1, a novel UDP-N-acetylglucosamine acyltransferase (LpxA) inhibitor exhibiting potent activity (IC 50 2 nM), effectively targets Pseudomonas aeruginosaFórmula:C21H11D7F3N5O3Cor e Forma:SolidPeso molecular:452.44bc1 Complex-IN-1
CAS:Bc1 Complex-IN-1 (compound 12g) is a potent inhibitor of the bc1 complex, demonstrating fungicidal properties against cucumber downy mildew (CDM).Fórmula:C16H22N6O5S2Cor e Forma:SolidPeso molecular:442.513RdRP-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:419.43Polθ-IN-7
CAS:Polθ-IN-7 (example 12) is an inhibitor of DNA polymerase θ (Polθ) with a Ki of 1.27 nM.Fórmula:C28H35F3N6O2Cor e Forma:SolidPeso molecular:544.612MtMetAP1-IN-1
MtMetAP1-IN-1 is an inhibitor of methionine aminopeptidase 1 ( MetAP1 ). MtMetAP1-IN-1 shows antimycobacterial activity.Fórmula:C15H10BrN5O2SCor e Forma:SolidPeso molecular:404.24Antitubercular agent-13
Compound 3d: antitubercular, MIC 0.007 μg/mL vs MTB H37Rv, 1.851 μg/mL vs MDR-MTB 16833, metabolically unstable.Fórmula:C18H18N4O5Cor e Forma:SolidPeso molecular:370.36Squalamine lactate
CAS:Squalamine lactate is an aminosterol compound discovered in the tissues of the dogfish shark, with antimicrobial activity.Fórmula:C37H71N3O8SPureza:98%Cor e Forma:SolidPeso molecular:718.04Antimalarial agent 2
Antimalarial agent 2 is an orally active, novel antimalarial agent that exhibits rapid in vitro killing effects.Fórmula:C27H25N3O5Cor e Forma:SolidPeso molecular:471.517,17-Ethylendioxyandrost-5-en-3β-ol
CAS:17,17-Ethylendioxyandrost-5-en-3β-ol, with an EC 50 of 629 μM, acts as an inhibitor of HSV-1. This compound is applicable in research studies focusing on viral infections.Fórmula:C21H32O3Cor e Forma:SolidPeso molecular:332.48HIV-1-IN-86
CAS:HIV-1-IN-86 (compound 6m) is an HIV-1 inhibitor with an EC50 of 0.77 μM, exhibiting antiviral activity.Fórmula:C20H17N3O7SCor e Forma:SolidPeso molecular:443.43
