
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(2.949 produtos)
- Antibiótico(918 produtos)
- Antifecção(23 produtos)
- DHFR(32 produtos)
- Síntese de DNA/RNA(706 produtos)
- HBV(176 produtos)
- HIV Protease(447 produtos)
- HSV(91 produtos)
- Integrase(2 produtos)
- Ribossomo(13 produtos)
Exibir 2 mais subcategorias
Foram encontrados 5832 produtos de "Microbiologia/Virologia"
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Mram 8
CAS:<p>Mram 8, a cyclotide isolated from Viola philippica of the Violaceae family [1], exhibits a characteristic cyclic peptide structure.</p>Fórmula:C132H208N36O39S6Cor e Forma:SolidPeso molecular:3115.672-Benzylaniline
CAS:<p>2-Benzylaniline is a potential Cytochrome P450 2B6 inhibitor with an IC50 value of 4.36 μM.</p>Fórmula:C13H13NPureza:99.77%Cor e Forma:SolidPeso molecular:183.25Altromycin F
CAS:<p>Altromycin F is a new pluramycin-like antibiotic.</p>Fórmula:C47H59NO17Cor e Forma:SolidPeso molecular:909.97Ticarcillin free base
CAS:<p>Ticarcillin disodium is an antibiotic derived from penicillin. It is similar to Carbenicillin in action.</p>Fórmula:C15H16N2O6S2Pureza:98%Cor e Forma:SolidPeso molecular:384.42Almurtide
CAS:<p>Almurtide: Muramyl dipeptide derivative with anti-inflammatory, anti-tumor properties, protects mice from Pseudomonas and Candida infections.</p>Fórmula:C18H30N4O11Cor e Forma:SolidPeso molecular:478.45A 25794
CAS:<p>A 25794 is an antibiotic with possible antidepressant properties.</p>Fórmula:C17H21NO4Pureza:98%Cor e Forma:SolidPeso molecular:303.358Bikaverin
CAS:<p>Bikaverin: A red fungal pigment with antibiotic effects on protozoa/fungi and antitumor properties.</p>Fórmula:C20H14O8Pureza:98%Cor e Forma:SolidPeso molecular:382.32Arylomycin B7
CAS:<p>Arylomycin B7 is a lipohexapeptide antibiotic (antibiotic) that specifically targets Gram-positive bacteria.</p>Fórmula:C45H65N7O13Cor e Forma:SolidPeso molecular:912.037IBU-DC Phosphoramidite
CAS:<p>IBU-DC Phosphoramidite is used for synthesis of oligonucleotides.</p>Fórmula:C43H54N5O8PCor e Forma:SolidPeso molecular:799.906SARS-CoV-2-IN-28
<p>SARS-CoV-2-IN-28: two-armed diphosphate ester, C7 alkyl, molecular tweezers. Antiviral IC50: 0.4μM/1.0μM. Disrupts membranes, EC50: 4.4μM.</p>Fórmula:C56H60O8P2Cor e Forma:SolidPeso molecular:923.02Telomycin
CAS:<p>elomycin is a cyclic depsipeptide antibiotic with activity against Gram-positive bacteria.</p>Fórmula:C59H77N13O19Pureza:98%Cor e Forma:SolidPeso molecular:1272.337Succinate dehydrogenase-IN-7
<p>Succinate dehydrogenase-IN-7 (Compound 2f) is a succinate dehydrogenase inhibitor with an IC50 value of 2.51 μM and exhibits bactericidal properties.</p>Fórmula:C11H5Cl2F3N2O2SCor e Forma:SolidPeso molecular:357.14CA inhibitor 1
CAS:<p>CA inhibitor 1 (GS-6207 analog) is a potent inhibitor of the HIV capsid.</p>Fórmula:C41H36ClF8N7O5S2Pureza:98%Cor e Forma:SolidPeso molecular:958.34Dermaseptin-S2
CAS:<p>Dermaseptin-S2, an antimicrobial peptide sourced from frog skin, exhibits activity against filamentous fungi [1].</p>Fórmula:C155H255N43O43S2Cor e Forma:SolidPeso molecular:3473.08Antibacterial agent 39
CAS:<p>Antibacterial agent 39 boosts Ceftazidime's efficacy by lowering its MIC.</p>Fórmula:C9H11N5NaO7SCor e Forma:SolidPeso molecular:356.26JM 1397
CAS:<p>JM 1397 is a bioactive chemical.</p>Fórmula:C16H18O2OsCor e Forma:SolidPeso molecular:432.54sPLA2 inhibitor 2
<p>sPLA2 inhibitor 2 (compound 6a) is an sPLA2 inhibitor with an IC50 value of 0.0475 μM, making it valuable for diabetes research.</p>Fórmula:C20H18N6O4S2Cor e Forma:SolidPeso molecular:470.521-O-Methylemodin
CAS:<p>1-O-Methylemodin, a natural product isolated from Zopfiella longicaudata, exhibits antifungal activity [1].</p>Fórmula:C16H12O5Cor e Forma:SolidPeso molecular:284.26Arylomycin A3
CAS:<p>Arylomycin A3 is a lipopeptide antibiotic (antibiotic) effective against Gram-positive bacteria.</p>Fórmula:C42H60N6O11Cor e Forma:SolidPeso molecular:824.959Antimalarial agent 17
CAS:<p>Antimalarial agent 17 doubles as a herbicide, inhibiting photosystem II with effectiveness akin to market herbicides.</p>Fórmula:C19H21ClN2O3SCor e Forma:SolidPeso molecular:392.9Arylomycin B4
CAS:<p>Arylomycin B4 is a lipidic hexapeptide antibiotic (antibiotic) targeting Gram-positive bacteria.</p>Fórmula:C43H61N7O13Cor e Forma:SolidPeso molecular:883.9843′-Omethyl-5′-hydroxydiplacone
CAS:<p>3′-Omethyl-5′-hydroxydiplacone (compound 2), a C-6-geranylflavonoid isolated from the ethanol extract of Paulownia tomentosa fruits, exhibits antibacterial</p>Fórmula:C26H30O7Cor e Forma:SolidPeso molecular:454.51MMV674850
CAS:<p>MMV674850: IC50 asexual parasites 2.7-4.5 nM; early gametocytes 4.5 ± 3.6 nM, late 28.7 ± 0.2 nM.</p>Fórmula:C23H20N2O4S2Cor e Forma:SolidPeso molecular:452.55Adipic dihydrazide
CAS:<p>Adipic dihydrazide (ADH) is a dihydrazide a bifunctional cross-linking agent for water-in-oil emulsions and a curing agent for epoxy resins.</p>Fórmula:C6H14N4O2Pureza:99.84%Cor e Forma:SolidPeso molecular:174.20SARS-CoV-2 Mpro-IN-27
<p>SARS-CoV-2 Mpro-IN-27 (Compound 4h) is an effective inhibitor of SARS-CoV-2 Mpro.</p>Fórmula:C22H16N4OCor e Forma:SolidPeso molecular:352.39CW-2
<p>CW-2 is a PARP1 PROTAC degrader known for its potent antiproliferative effects against MDA-MB-231 cells (IC50 = 0.72 μM) and cisplatin-resistant cells (A549/CDDP: IC50 = 3.52 μM). It exhibits synergistic antitumor activity and enhanced membrane permeability. CW-2 exerts its antitumor effects by inducing DNA damage, disrupting DNA repair, and triggering mitochondrial-dependent apoptosis (apoptosis).</p>Fórmula:C43H42Cl2FN11O10PtCor e Forma:SolidPeso molecular:1156.21251Arylomycin B1
CAS:<p>Arylomycin B1 is a lipid hexapeptide antibiotic (antibiotic) effective against Gram-positive bacteria.</p>Fórmula:C41H57N7O13Cor e Forma:SolidPeso molecular:855.93GP(33-41)
CAS:<p>GP(33-41) is a 9-amino acid lymphocytic choriomeningitis virus epitope; it increases H-2Db on RMA-S at 344 nM SC50 and activates P14 TCR-mouse CD8 T cells.</p>Fórmula:CTFKNVYPureza:98%Cor e Forma:SolidPeso molecular:226.98Frequentin
CAS:<p>Frequentin, an antibiotic from P. frequentans, combats bacteria and fungi; MICs: 200 µg/ml for B. subtilis, 300 for S. aureus.</p>Fórmula:C14H20O4Cor e Forma:SolidPeso molecular:252.31Sofosbuvir impurity J
CAS:<p>Sofosbuvir impurity J is an diastereoisomer of Sofosbuvir.Sofosbuvir is an HCV RNA replication inhibitor, with potent anti-hepatitis C virus activity.</p>Fórmula:C22H30FN4O8PPureza:98%Cor e Forma:SolidPeso molecular:528.47Enfuvirtide
CAS:<p>Enfuvirtide (INN) is an HIV fusion inhibitor, the first of a class of antiretroviral drugs used in combination therapy for the treatment of HIV-1 infection.</p>Fórmula:C204H301N51O64Pureza:98%Cor e Forma:White To Off-White Amorphous SolidPeso molecular:4491.945Eflornithine hydrochloride
CAS:<p>Eflornithine HCl treats African sleeping sickness and curbs female facial hair growth by blocking ornithine decarboxylase.</p>Fórmula:C6H13ClF2N2O2Cor e Forma:SolidPeso molecular:218.63S2H97
<p>S2H97 is a neutralizing antibody that broadly protects against viruses such as neococcal pneumonia and SARS under clade B of coronavirus B.</p>Pureza:98.8% (SDS-PAGE); 98.5% (SEC-HPLC) - 98.8% (SDS-PAGE); 98.5% (SEC-HPLC)Cor e Forma:Odour LiquidRSM01
<p>RSM01 is a fully human IgG1 monoclonal antibody that targets a site in the pre-F region of RSV with a YTE half-life prolongation mutation.</p>Pureza:97.5% (SDS-PAGE); 99.5% (SEC-HPLC) - 97.5% (SDS-PAGE); 99.5% (SEC-HPLC)Cor e Forma:Odour LiquidDalbavancin hydrochloride
CAS:<p>Dalbavancin HCl (MDL-63397 HCl), a semi-synthetic antibiotic, targets Gram-positive bacteria with low MICs for S. aureus and B. anthracis.</p>Fórmula:C88H101Cl3N10O28Cor e Forma:SolidPeso molecular:1853.15Atrovenetin
CAS:<p>Atrovenetin is an antibiotic found in Penicillium species (antibiotic). It exhibits inhibitory activity against Bacillus subtilis and Staphylococcus aureus. Atrovenetin is also a potent antioxidant.</p>Fórmula:C19H18O6Cor e Forma:SolidPeso molecular:342.343Antitrypanosomal agent 23
<p>Antitrypanosomal agent 23 is an antiparasitic compound effective against intracellular amastigotes of Trypanosoma cruzi in LLC-MK2 and C2C12 cells, demonstrating activity with IC50 values of 0.10 and 0.11 μM, respectively. It also acts as a weak inhibitor of recombinant Trypanosoma cruzi sialyltransferase (TcTS) with an IC50 of 1.1 mM.</p>Fórmula:C14H16N4O7Cor e Forma:SolidPeso molecular:352.1019Tuberculosis inhibitor 9
<p>Tuberculosis inhibitor 9 (compound 3d), a 3-methoxy-2-phenylimidazo[1,2-b]pyridazine derivative, exhibits potent activity against Mycobacterium tuberculosis and</p>Fórmula:C21H18F2N4OCor e Forma:SolidPeso molecular:380.39αGalCer-RBD
<p>αGalCer-RBD, a conjugate of the potent invariant natural killer T cell (iNKT) agonist α-Galactosylceramide (αGalCer) and the receptor-binding domain (RBD),</p>Fórmula:C60H118N4O14Cor e Forma:SolidPeso molecular:1119.6N-Demethylansamitocin P-3
CAS:<p>N-Demethylansamitocin P-3, an ansamycin antibiotic derivative with antitumor properties, is synthesized by S. minutiscleroticus IFO 13361.</p>Fórmula:C31H41ClN2O9Cor e Forma:SolidPeso molecular:621.12ATV03
<p>ATV03 is an antiviral agent exhibiting potent activity against both type A and type B influenza viruses. It inhibits the type A (H3N2) and type B influenza viruses with EC50 values of 0.78 nM and 2.02 nM, respectively. The mechanism of action of ATV03 involves the inhibition of the polymerase acidic protein (PA) and RNA-dependent RNA polymerase (RdRp), as well as the disruption of nucleoprotein, thereby exerting its antiviral effects against influenza.</p>Fórmula:C24H20FN3O5Cor e Forma:SolidPeso molecular:449.435'-O-TBDMS-Bz-dA
CAS:<p>5’-O-TBDMS-Bz-dA is a nucleoside with protective and modification effects.</p>Fórmula:C23H31N5O4SiCor e Forma:SolidPeso molecular:469.617TNM001
<p>TNM001 is an anti-RSV fully humanized monoclonal antibody for the study of lower respiratory tract disease due to RSV infection.</p>Pureza:99% (SDS-PAGE); 99.6% (SEC-HPLC) - 99% (SDS-PAGE); 99.6% (SEC-HPLC)Cor e Forma:Odour LiquidAnti-IAV agent 1
<p>Anti-IAV agent 1 -1a: Orally active, fights influenza A. IC50: 0.03μM for H1N1, 0.06μM for resistant strains.</p>Fórmula:C28H28FN9O3Cor e Forma:SolidPeso molecular:557.58(R)-Eucomol
CAS:<p>(R)-Eucomol, a flavonoid derivative, exhibits slight antibacterial properties and demonstrates cytotoxic activity against KB and P-388 cells [1].</p>Fórmula:C17H16O6Cor e Forma:SolidPeso molecular:316.31Viomycin
CAS:<p>Viomycin: tuberactinomycin antibiotic, halts prokaryotic protein synthesis and group I intron splicing, arrests bacterial ribosomes.</p>Fórmula:C25H43N13O10Pureza:98%Cor e Forma:SolidPeso molecular:685.69Enduracidin
CAS:<p>Enduracidin (Enramycin) is a polypeptide antibiotic produced by Streptomyces fungicides.</p>Cor e Forma:SolidSaccharothrixin F
<p>Saccharothrixin F, an extensively oxygenated variant within the saccharothrixin class, exhibits antibacterial and anti-inflammatory properties.</p>Fórmula:C20H18O6Cor e Forma:SolidPeso molecular:354.35Antimicrobial agent-40
<p>Antimicrobial agent-40 exhibits antibacterial activity against fungi, Gram-negative, and Gram-positive bacteria. It also shows anticancer properties, displaying significant cytotoxicity towards MCF-7 cells with an IC50 of 33.52 μM.</p>Fórmula:C18H19ClFN5SCor e Forma:SolidPeso molecular:391.10337Albocycline
CAS:<p>Albocycline, a macrolide antibiotic from S. bruneogriseus MCRL-0129, targets staph including resistant strains.</p>Fórmula:C18H28O4Pureza:98%Cor e Forma:SolidPeso molecular:308.41

