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(3.385 produtos)
- Antibiótico(940 produtos)
- Antifecção(27 produtos)
- DHFR(30 produtos)
- Síntese de DNA/RNA(802 produtos)
- HBV(185 produtos)
- HIV Protease(506 produtos)
- HSV(99 produtos)
- Integrase(2 produtos)
- Ribossomo(6 produtos)
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Foram encontrados 6394 produtos de "Microbiologia/Virologia"
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LmNADK1-IN-1
LmNADK1-IN-1 (MC1) inhibits L. monocytogenes NADK1, K_i 54 nM, useful in bacterial infection research.
Fórmula:C27H33N13O9SCor e Forma:SolidPeso molecular:715.7LL-37, acetylated,amidated
LL-37 peptide: acetylated at N-terminus, amidated at C-terminus; crucial in initial infection defense.Fórmula:C207H343N61O53Pureza:98%Cor e Forma:SolidPeso molecular:4534.4Arbekacin
CAS:Arbekacin is an aminoglycoside antibiotic.Fórmula:C22H44N6O10Pureza:98%Cor e Forma:SolidPeso molecular:552.63MK-6169
CAS:MK-6169 is an effective Pan-Genotype Hepatitis C Virus NS5A inhibitor. It also has Optimized Activity against Common Resistance-Associated Substitutions.Fórmula:C54H62FN9O8SPureza:98%Cor e Forma:SolidPeso molecular:1016.2Brilacidin
CAS:Brilacidin is a nonpeptidic anti-infective in a new class of defensin mimetics used for the research of eye infections.Fórmula:C40H50F6N14O6Pureza:98%Cor e Forma:SolidPeso molecular:936.91Carbazomycin A
CAS:Carbazomycin A: antimicrobial, antifungal, and cytotoxic; MIC 12.5-25 μg/ml; IC50 18.4-32.6 μg/ml.Fórmula:C16H17NO2Cor e Forma:SolidPeso molecular:255.31HBV-IN-36
HBV-IN-36 (also known as compound 42) is a hepatitis B virus (HBV) inhibitor with an IC50 of 2 μM, exhibiting anti-HBV activity characterized by an EC50 of 0.58Fórmula:C21H18ClFN4O2Pureza:98%Cor e Forma:SolidPeso molecular:412.84NNRT-IN-6
NNRT-IN-6 (Compound 13a) is a non-nucleoside reverse transcriptase inhibitor (NNRT) used to inhibit HIV-1 reverse transcriptase (HIV-1RT), with an IC50 of 0.41 μM. It effectively suppresses both wild-type HIV-1 and mutants L100I, K103N, Y181C, Y188L, E138K, F227L/V106A, and RES056, with an EC50 range of 6.2-250 nM.Fórmula:C32H31N9O3SCor e Forma:SolidPeso molecular:621.71MptpB-IN-2
MptpB-IN-2 (compound 20), a selective inhibitor for mycobacterium tuberculosis protein tyrosine phosphatase B (MptpB), exhibits half maximal inhibitoryFórmula:C23H20F3NO3S2Pureza:98%Cor e Forma:SolidPeso molecular:479.54SARS-CoV-2-IN-65
SARS-CoV-2-IN-65 (compound 2f (81)) is a potent, orally active reversible inhibitor of SARS-CoV-2 entry, primarily obstructing the RBD:ACE2 interaction andPureza:98%Cor e Forma:Odour SolidNv-CATH
Nv-CATH, an antibacterial peptide derived from frogs, exhibits broad-spectrum activity against both gram-positive and gram-negative bacteria, and significantlyFórmula:C142H243N49O39S3Cor e Forma:SolidPeso molecular:3356.95EFdA-TP
CAS:EFdA-TP: potent HIV-1 RT inhibitor; acts via immediate/delayed chain termination (ICT/DCT) and multiple pathways.Fórmula:C12H15FN5O12P3Cor e Forma:SolidPeso molecular:533.19510-Hydroxyaloin A
CAS:Hydroxyaloin A (10-10-Hydroxyaloin A) is a potent inhibitor of SARS-CoV-2, demonstrating significant efficacy in binding to the active site of the SARS-CoV-2Fórmula:C21H22O10Pureza:98%Cor e Forma:SolidPeso molecular:434.39NSC89641
NSC89641 demonstrates potent inhibition of MERS-CoV M^pro, achieving an IC_50 value of less than 3.5 µM.Fórmula:C19H18N6O12Pureza:98%Cor e Forma:SolidPeso molecular:522.38Anticancer agent 140
Compound 140 (Compd 3) exhibits potential anticancer and antiparasitic activities [1].Fórmula:C20H26N2OPureza:98%Cor e Forma:SolidPeso molecular:310.43SARS-CoV-2-IN-53
ARS-CoV-2-IN-53 (Compd 5d) exhibits an inhibitory effect on SARS-CoV-2 replication, with an effective concentration (EC50) value of 14.3 μM, and demonstratesFórmula:C23H18F2N2O4SPureza:98%Cor e Forma:SolidPeso molecular:456.46(S)-1-(4-Hydroxyphenyl)ethane-1,2-diol
CAS:(S)-1-(4-Hydroxyphenyl)ethane-1,2-diol, from Angelica sinensis, inhibits Aeromonas hydrophila and acts as an anticoagulant and antibiotic.Fórmula:C8H10O3Cor e Forma:SolidPeso molecular:154.16SARS-CoV-2-IN-109
SARS-CoV-2-IN-109 (compound 50) is an inhibitor targeting SARS-CoV, demonstrating in vivo anti-infection activity. It interferes with the interaction between the SARS-CoV-2 Spike receptor-binding domain (RBD) and the human receptor angiotensin-converting enzyme 2 (ACE2) with an EC50 of 26.5 μM, effectively blocking SARS-CoV-2 entry into VeroE6 cells (ECS50=17.0 μM). The compound has a CC50 greater than 100 μM in VeroE6 cells.Fórmula:C34H26N2O2Cor e Forma:SolidPeso molecular:494.58Antibacterial agent 42
CAS:Antibacterial Agent 42 boosts Ceftazidime's efficacy by lowering its MIC.Fórmula:C11H11N5NaO7SCor e Forma:SolidPeso molecular:380.29Antileishmanial agent-21
Antileishmanial agent-21 (compound 4e) functions as an inhibitor of Leishmania pteridine reductase 1 (Lm-PTR1), employing an anti-folate mechanism.Fórmula:C21H16N2O3Pureza:98%Cor e Forma:SolidPeso molecular:344.36
