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(2.966 produtos)
- Antibiótico(922 produtos)
- Antifecção(23 produtos)
- DHFR(33 produtos)
- Síntese de DNA/RNA(710 produtos)
- HBV(177 produtos)
- HIV Protease(450 produtos)
- HSV(91 produtos)
- Integrase(2 produtos)
- Ribossomo(13 produtos)
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Foram encontrados 5858 produtos de "Microbiologia/Virologia"
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28-O-Imidazolyl-azepano-betulin
SARS-CoV-2-IN-70 (compound 6) is an effective inhibitor of SARS-CoV-2, with an IC50 value of 3.2 μM.Fórmula:C34H53N3O2Peso molecular:535.41378Antibacterial agent 138
<p>Antibacterial agent 138 effectively targets multi-drug resistant bacteria by inhibiting protein synthesis.</p>Fórmula:C34H52INO4SCor e Forma:SolidPeso molecular:697.75Gramicidin A TFA
<p>Gramicidin A (TFA) is a peptide component of Gramicidin, an antibiotic mixture originally isolated from B. brevis. It is a highly hydrophobic channel-forming ion carrier that creates monovalent cation-permeable channels in artificial membranes. Additionally, Gramicidin A (TFA) induces the degradation of hypoxia-inducible factor 1α (HIF-1α).</p>Fórmula:C99H140N20O17·xC2HF3O2Antibiotic PF 1052
CAS:<p>PF 1052: Phoma fungal metabolite, combats S. aureus, S. parvulus, C. perfringens, hinders neutrophil migration.</p>Fórmula:C26H39NO4Cor e Forma:SolidPeso molecular:429.601Sirpefenicol
CAS:<p>Sirpefenicol (ZTS-00007928), a phenicol antibacterial for treating animal bacterial infections.</p>Fórmula:C17H18F3N3O3SCor e Forma:SolidPeso molecular:401.4Maximin 32
<p>Maximin 32, an antimicrobial peptide originating from toad brain, exhibits activity against Staphylococcus aureus and Escherichia coli, with minimum inhibitory</p>Fórmula:C121H208N34O33Cor e Forma:SolidPeso molecular:2667.15Mpro ligand 1
<p>Mpro ligand 1 is the target protein ligand for PROTACSARS-CoV-2 Mpro degrader-3. It is the active form of Mpro ligand 2.</p>Fórmula:C22H32N3NaO9SPeso molecular:537.1757Antibacterial agent 176
<p>Antibacterialagent 176 (Compound 6f) is a potent PqsR antagonist. It effectively inhibits Pseudomonas aeruginosa (P. aeruginosa CF), demonstrating significant suppression of pyocyanin and 2-alkyl-4(1H)-quinolone production.</p>Fórmula:C21H23ClN4O2Peso molecular:398.15095LL-BM123α
CAS:<p>LL-BM123α is a basic antibiotic isolated from Nocardia species and exhibits moderate activity against Gram-negative bacteria.</p>Fórmula:C30H53N9O17Peso molecular:811.79CC 1014
CAS:CC 1014 is a polypeptide antibiotic isolated from Penicillium lilacinum that inhibits phosphorylation of ADP, Mg ATPase.Fórmula:C62H111N11O13Pureza:98%Cor e Forma:SolidPeso molecular:1218.634SARS-CoV-2 Mpro-IN-17
SARS-CoV-2 Mpro-IN-17 (compound S5-28) is an orally active, non-covalent inhibitor of SARS-CoV-2 Mpro, with an EC50 value of 1.35 μM. It is applicable for research related to COVID-19.Fórmula:C20H19BrClN3O2Peso molecular:447.03492UCK2 Inhibitor-3
CAS:<p>UCK2 Inhibitor-3 blocks UCK2 (IC50: 16.6μM) and DNA polymerases eta/kappa (IC50s: 56μM/16μM), aiding uridine salvage in certain cells.</p>Fórmula:C19H13BrFN5O2SCor e Forma:SolidPeso molecular:474.31SARS-CoV-2-IN-11
CAS:<p>SARS-CoV-2-IN-11, potent non-toxic 3CLpro inhibitor, has IC50 of 0.17 nM and EC50 of 1.45 nM; promising for specific SARS-CoV-2 antivirals.</p>Fórmula:C27H39F2N3NaO8SCor e Forma:SolidPeso molecular:626.67Chalcomycin
CAS:Chalcomycin is a macrolide antibiotic effective against Gram-positive Staphylococcus aureus and Streptococcus pyogenes. It protects mice from infections caused by various Staphylococcus and Streptococcus strains and exhibits no significant toxicity (LD50>2500 mg/kg).Fórmula:C35H56O14Peso molecular:700.36701Clindamycin palmitate hydrochloride
CAS:Clindamycin palmitate hydrochloride (Clindamycin palmitate HCl) is the hydrochloride salt of clindamycin and palmitate, a lincosamide antibiotic.Fórmula:C34H63ClN2O6S·HClPureza:98%Cor e Forma:SolidPeso molecular:699.85Urease-IN-18
<p>Urease-IN-18 (compound 13a) is a non-competitive urease inhibitor with an IC50 value of 1.6 μM. Urease plays a role in maintaining an alkaline environment that supports the survival and proliferation of certain pathogens within the host.</p>Fórmula:C30H27N5O5Cor e Forma:SolidPeso molecular:537.566BRD1401
<p>BRD1401 is a small molecule that targets the outer membrane protein OprH. It disrupts the interaction between OprH and LPS and can increase membrane fluidity.</p>Fórmula:C17H17N5O3Peso molecular:339.13314SDZ 283-910
CAS:<p>SDZ 283-910 is used as a statine-derived inhibitor.</p>Fórmula:C46H59N5O9Pureza:98%Cor e Forma:SolidPeso molecular:826.004Dactimicin sulfate
CAS:<p>Dactimicin is a new aminoglycoside. It also has in vitro activity, post-antibiotic effect, and interaction with other antibiotics.</p>Fórmula:C18H40N6O14S2Cor e Forma:SolidPeso molecular:628.67
