
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(3.153 produtos)
- Antibiótico(932 produtos)
- Antifecção(24 produtos)
- DHFR(34 produtos)
- Síntese de DNA/RNA(774 produtos)
- HBV(182 produtos)
- HIV Protease(477 produtos)
- HSV(94 produtos)
- Integrase(2 produtos)
- Ribossomo(13 produtos)
Exibir 2 mais subcategorias
Foram encontrados 6158 produtos de "Microbiologia/Virologia"
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1-O-Methylemodin
CAS:1-O-Methylemodin, a natural product isolated from Zopfiella longicaudata, exhibits antifungal activity [1].Fórmula:C16H12O5Cor e Forma:SolidPeso molecular:284.26Orfamide A
CAS:Orfamide A, a lipopeptide biosurfactant isolated from P. protegens, exhibits multifaceted bioactivity. With an LC50 of 34.5 μg/ml, it significantly increases mortality in adult green peach aphids. Additionally, at a concentration of 50 μM, Orfamide A inhibits appressoria formation in M. oryzae isolates and decreases the prevalence of sporulating blast lesions in M. oryzae-infected plants. Furthermore, it demonstrates efficacy against T. b. brucei, with an IC50 value of 6 µM.Fórmula:C64H114N10O17Cor e Forma:SolidPeso molecular:1295.67HPV16 E7 (86-93)
CAS:HPV16 E7 oncoprotein fragment (amino acids 86-93) binds strongly to HLA-A*0201; may aid in cervical cancer vaccine development.Fórmula:C37H66N8O10SPureza:98%Cor e Forma:SolidPeso molecular:815.03CEF1, Influenza Matrix Protein M1 (58-66)
CAS:CEF1, M1 (58-66) epitope from influenza A; GILGFVFTL is HLA-A2-restricted.Fórmula:C49H75N9O11Pureza:98%Cor e Forma:SolidPeso molecular:966.17Lienomycin
CAS:Lienomycin is a pentaene macrolide antitumor antibiotic generated by Actinomyces vendargensis Struyk et Stheeman. It has inonphore-like action.Fórmula:C67H107NO18Pureza:98%Cor e Forma:SolidPeso molecular:1214.58216,16-dimethyl Prostaglandin A1
CAS:16,16-dimethyl Prostaglandin A1 is a useful organic compound for research related to life sciences.Fórmula:C22H36O4Cor e Forma:SolidPeso molecular:364.5265'-O-DMT-ibu-dC
CAS:<p>5'-O-DMT-ibu-dC can be used in the synthesis of oligodeoxyribonucleotides.</p>Fórmula:C34H37N3O7Cor e Forma:SolidPeso molecular:599.67Biotin protein ligase-IN-1
<p>Biotin protein ligase-IN-1 (Compound Bio-9) is an inhibitor of biotin protein ligase (BPL) with a Kd of 7 nM. This compound exhibits antimicrobial activity, with minimum inhibitory concentration (MIC) values of 0.2 μM against Staphylococcus aureus (including MRSA and MSSA) and 20 μM against Mycobacterium tuberculosis.</p>Fórmula:C19H27N10NaO7S2Cor e Forma:SolidPeso molecular:594.6RSV L-protein-6
<p>RSVL-protein-6 (Compound 19a) is an inhibitor of respiratory syncytial virus (RSV) polymerase, with an IC50 of 13 nM in an SPA primer extension-based enzymatic assay. It is capable of inhibiting RSV replication in HeLa cells.</p>Fórmula:C29H39ClN4O3Cor e Forma:SolidPeso molecular:527.098Isepamicin
CAS:Isepamicin (Sch 21420) is a strong aminoglycoside antibiotic, effective on Enterobacteriaceae and staphylococci, less so on other bacteria.Fórmula:C22H43N5O12Cor e Forma:SolidPeso molecular:569.60SARS-CoV-2 Mpro-IN-38
SARS-CoV-2 Mpro-IN-38 (2-5a) is an inhibitor of SARS-CoV‑2 Mpro with an IC50 value of 0.0435 μM.Cor e Forma:Odour SolidAntiviral agent 66
<p>Antiviralagent 66 (Compound 60) serves as an inhibitor of filoviruses (Filovirus), effectively suppressing pseudoviruses of Ebola, Marburg, Zaire, Sudan, Bundibugyo, Reston, and Tai Forest, with EC50 values of 0.16, 2.24, 0.16, 0.89, 0.21, 0.21, and 0.11 μM, respectively.</p>Fórmula:C27H29F3N4O3Cor e Forma:SolidPeso molecular:514.539HA Peptide TFA
HA Peptide (TFA): 9-amino acid sequence from influenza HA, used in protein isolation and detection.Fórmula:C55H68F3N9O19Cor e Forma:SolidPeso molecular:1216.19Gallichrome
CAS:<p>Gallichrome: an active peptide that interacts with siderophore hydroxamate; used in iron uptake research in gram-positive/negative bacteria.</p>Fórmula:C27H42GaN9O12Cor e Forma:SolidPeso molecular:754.40Galloyl-bis-HHDP glucose
Galloyl-bis-HHDP glucose (HeT), an ellagitannin, exhibits phytoprotective effects against Pseudomonas viridiflava [1].Fórmula:C42H30O25Cor e Forma:SolidPeso molecular:934.67Isogarcinol
CAS:Isogarcinol, a Garcinia-derived immunosuppressant, inhibits T-cell proliferation and exhibits anti-inflammatory and anticancer properties.Fórmula:C38H50O6Cor e Forma:SolidPeso molecular:602.8Anti gram-positive/negative bacteria agent 1
Anti gram-positive/negative bacteria agent 1 is an antibiotic linked with a synthetic MECAM-based siderophore, serving as a conjugate aimed at combating gram-Fórmula:C67H68N10O21SCor e Forma:SolidPeso molecular:1381.38XT-2 peptide
CAS:<p>XT-2 peptide, an antimicrobial agent sourced from the skin secretions of Xenopus tropicalis, exhibits potent activity against E.</p>Fórmula:C118H193N31O31SCor e Forma:SolidPeso molecular:2574.05Pyrazine-2-carbaldehyde
CAS:<p>Pyrazine-2-carbaldehyde inhibits nicotinamidase in Mycobacterium tuberculosis and can be used for tuberculosis research</p>Fórmula:C5H4N2OPureza:99.67%Cor e Forma:SolidPeso molecular:108.1Antibacterial agent 33
CAS:<p>Antibacterial Agent 33 boosts Ceftazidime's efficacy by lowering its MIC.</p>Fórmula:C12H17N5O6SCor e Forma:SolidPeso molecular:359.36ML267
CAS:ML267 (4-(3-chloro-5-(trifluoromethyl)pyridin-2-yl)-N-(4-methoxypyridin-2-yl)piperazine-1-carbothioamide trifluoroacetate) is a potent inhibitor of bacterialFórmula:C19H18ClF6N5O3SPureza:97.85%Cor e Forma:SolidPeso molecular:545.89Antibacterial agent 272
<p>Antibacterialagent 272 (Compound Z22) is a potential antibacterial agent that targets the DNA and DNA-topoisomerase II (DNA-Topo II) complex. It exhibits strong antibacterial activity, with a minimum inhibitory concentration (MIC) of 1 μg/mL against Staphylococcus aureus 25923 and 29213, 2 μg/mL against Staphylococcus epidermidis 12228, 2-4 μg/mL against Enterococcus faecalis, and 4 μg/mL against Pseudomonas aeruginosa 9027 and 27853. Antibacterialagent 272 binds by intercalating between DNA base pairs, disrupting the normal function of bacterial DNA, and is suitable for research into bacterial infectious diseases.</p>Cor e Forma:Odour SolidLaccase-IN-5
Laccase-IN-5 (Compound 2b) is an inhibitor of laccase with an IC50 of 0.82 μM. It enhances cell membrane permeability, restricts mycelial growth, disrupts cell walls, and induces oxidative stress responses. Laccase-IN-5 exhibits antifungal activity against various plant pathogenic fungi and oomycetes, effectively inhibiting B. dothidea with an EC50 of 0.96 mg/L.Fórmula:C16H17FN2OCor e Forma:SolidPeso molecular:272.317Enduracidin B
CAS:<p>Enduracidin B, a polypeptide antibiotic, is a prominent constituent of Enduracidin. This antibiotic is synthesized by Streptomyces fungicides.</p>Fórmula:C108H140Cl2N26O31Cor e Forma:SolidPeso molecular:2369.36Xinjiachalcone A
CAS:<p>Xinjiachalcone A, from Glycyrrhiza inflata, kills H. pylori effectively (MIC: 12.5-50 μM, 17 strains).</p>Fórmula:C21H22O4Pureza:98%Cor e Forma:SolidPeso molecular:338.4SDH-IN-8
SDH-IN-8 (compound G40) is a potent inhibitor of succinate dehydrogenase (SDH), demonstrating an IC50 value of 27 nM against porcine SDH and exhibits fungicidalFórmula:C18H14Cl3F4N3OCor e Forma:SolidPeso molecular:470.68Clostomycin B2
CAS:<p>Clostomycin B2 is a bioactive chemical.</p>Fórmula:C52H74Cl2O18Cor e Forma:SolidPeso molecular:1058.05Antibacterial agent 43
CAS:Antibacterial agent 43 from patent WO2013030735A1 shows strong activity against infections and has research potential.Fórmula:C12H11N4NaO7SCor e Forma:SolidPeso molecular:378.29Voriconazole N-oxide
CAS:Voriconazole N-oxide, a key metabolite of voriconazole, results from oxidation by CYP3A4 and CYP2C19.Fórmula:C16H14F3N5O2Cor e Forma:SolidPeso molecular:365.316Quorum sensing-IN-10
<p>Quorum sensing-IN-10 (10p) is an antimicrobial adjuvant that significantly inhibits the virulence, biofilm formation, and motility of Pseudomonas aeruginosa, while exhibiting low toxicity. It is applicable for research related to drug-resistant Pseudomonas aeruginosa infections.</p>Fórmula:C16H18FN3O4S2Cor e Forma:SolidPeso molecular:399.07228Gepotidacin S enantiomer
Gepotidacin S enantiomer is an S enantionmer of gepotidacin.Fórmula:C24H28N6O3Pureza:98%Cor e Forma:SolidPeso molecular:448.52Carbazole
CAS:<p>Carbazole belongs to the class of carbazole-based organic compounds. Carbazole can form novel DNA small groove complexes, inhibiting the synthesis of new DNA or RNA.</p>Fórmula:C12H9NPureza:99.82%Cor e Forma:SolidPeso molecular:167.211VRC01LS
<p>VRC01LS is a humanized monoclonal antibody inhibitor that targets the CD4 binding site of the HIV-1 envelope glycoprotein (Env). By blocking the interaction between HIV-1 and the host cell's CD4 receptor, VRC01LS inhibits viral entry. It holds potential for research in HIV-1 infection.</p>Cor e Forma:Odour LiquidFlomoxef
CAS:Flomoxef is an antibiotic in oxacephem group and has excellent activity against various gram-positive bacteria.Fórmula:C15H18F2N6O7S2Pureza:98%Cor e Forma:SolidPeso molecular:496.47(S)-Dinotefuran
CAS:(S)-Dinotefuran, a neonicotinoid, more toxic to bees than its R-isomer, targets α8 nAChR.Fórmula:C7H14N4O3Cor e Forma:SolidPeso molecular:202.21Thailanstatin C
CAS:Thailanstatin C from Burkholderia thailandensis blocks pre-mRNA splicing, IC50 6.84 μM.Fórmula:C30H46ClNO9Cor e Forma:SolidPeso molecular:600.15β-Lactamase-IN-5
CAS:<p>β-Lactamase-IN-5, a β-lactamase inhibitor isolated from compound 720, holds significant potential for studying bacterial infections.</p>Fórmula:C11H17N5O6SCor e Forma:SolidPeso molecular:347.35Kapurimycin A3
CAS:Kapurimycin A3 is an antitumor antibiotics.Fórmula:C27H24O9Cor e Forma:SolidPeso molecular:492.47Ophiobolin B
CAS:Ophiobolin B is a sesterterpene Helminthosporium oryzae metabolite, inhibits proton extrusion from maize coleoptiles.Fórmula:C25H38O4Pureza:98%Cor e Forma:SolidPeso molecular:402.57CysHHC10
CAS:CysHHC10 is a synthetic antimicrobial peptide (AMP), and exhibits strong anti-microbial properties against both Gram-positive and Gram-negative bacteria.Fórmula:C77H107N23O10SPureza:98%Cor e Forma:SolidPeso molecular:1546.89Insecticidal agent 4
Compound IA-8, an aryl isoxazoline derivative, exhibits insecticidal efficacy against M. separate [1].Fórmula:C21H14Cl2F4N4O2Cor e Forma:SolidPeso molecular:501.26FtsZ-IN-8
FtsZ-IN-8: Strong FtsZ inhibitor, blocks bacterial cell division, low resistance risk, minimal toxicity to mammalian cells.Fórmula:C27H28BrN3O2Cor e Forma:SolidPeso molecular:506.43Choline Iodide
CAS:<p>Choline Iodide has antibacterial activity against Leishmania panamensis and inhibitor of Acetylcholinesterase, degenerative neurological diseases.</p>Fórmula:C5H14INOCor e Forma:SolidPeso molecular:231.08SARS-CoV-2 Mpro-IN-30
SARS-CoV-2 Mpro-IN-30 (compound L2) is a SARS-CoV-2 Mpro inhibitor with an IC50 value of 9.1 nM.Cor e Forma:Odour SolidDienone B
CAS:<p>Dienone B is a cytotoxic secondary metabolite from tyrosine as isolated from the sponges Verongia aerophoba &amp; Aplysina aerophoba.</p>Fórmula:C8H7Br2NO3Cor e Forma:SolidPeso molecular:324.95Sibeprenlimab
CAS:<p>Sibeprenlimab (VIS649) is a humanized IgG 2 monoclonal antibody that suppresses APRIL.</p>Pureza:100% (SEC-HPLC) - > 95%Cor e Forma:LiquidPeso molecular:146.36 kDaAntibiotic LB 10517
CAS:Antibiotic LB 10517 is a catechol-substituted cephalosporin with a broad spectrum of antibacterial.Fórmula:C27H25N9NaO9S2Pureza:98%Cor e Forma:SolidPeso molecular:706.666'-Hydroxy-3,4,2',3',4'-pentamethoxychalcone
CAS:<p>6'-Hydroxy-3,4,2',3',4'-pentamethoxychalcone is an alkenylphenol from Piper obliquum with antiinflammatory and antibacterial activities.</p>Fórmula:C20H22O7Pureza:98%Cor e Forma:SolidPeso molecular:374.38Metallo-β-lactamase-IN-11
Metallo-β-lactamase-IN-11 (compound 5f), a potent inhibitor of Metallo-β-lactamases (MBLs), demonstrates efficacy against the bacterial metallophyllactamaseFórmula:C31H23N3OCor e Forma:SolidPeso molecular:453.53Leucinostatin (mixture of A&B)
<p>Leucinostatin, a mixture of components A and B, constitutes the primary elements of a unique nonapeptide complex synthesized by Paecilomyces lilacinus,</p>Cor e Forma:Odour Solid

