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(3.127 produtos)
- Antibiótico(928 produtos)
- Antifecção(24 produtos)
- DHFR(34 produtos)
- Síntese de DNA/RNA(763 produtos)
- HBV(181 produtos)
- HIV Protease(474 produtos)
- HSV(94 produtos)
- Integrase(2 produtos)
- Ribossomo(13 produtos)
Exibir 2 mais subcategorias
Foram encontrados 6126 produtos de "Microbiologia/Virologia"
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Antibacterial agent 114
CAS:<p>Compound 1: Potent antibacterial, MIC 625-1250μM for P.aeruginosa to S.aureus.</p>Fórmula:C19H14N4OCor e Forma:SolidPeso molecular:314.34Acaterin
CAS:Acaterin, an inhibitor of acyl-CoA: cholesterol acyltransferase (ACAT), inhibits synthesis of cholesteryl ester in macrophage J774.Fórmula:C13H22O3Cor e Forma:SolidPeso molecular:226.31Benthiavalicarb isopropyl
CAS:Benthiavalicarb isopropyl is a fungicide, specifically targeting downy mildew and blight.Fórmula:C18H24FN3O3SPureza:98%Cor e Forma:SolidPeso molecular:381.465-Et-ddU
CAS:5-Et-ddU: A pyrimidine nucleoside with anti-HIV-1 activity in human blood cells.Fórmula:C11H16N2O4Pureza:98%Cor e Forma:SolidPeso molecular:240.26BMS-199945
CAS:BMS-199945 is an Influenza H1N1 Virus inhibitor.Fórmula:C18H27NO2Pureza:98%Cor e Forma:SolidPeso molecular:289.41DSM74
CAS:DSM74 is a metabolically stable dihydroorotate dehydrogenase inhibitor that has antimalarial activity.Fórmula:C13H10F3N5Pureza:98%Cor e Forma:SolidPeso molecular:293.25ZINC04177596
CAS:ZINC04177596 is a novel Nef Protein Inhibitor with anti-HIV activity.Fórmula:C22H16N6O4Cor e Forma:SolidPeso molecular:428.4Aminoanfol
CAS:Aminoanfol is an antifolic acid agent.Fórmula:C18H18N8O5Pureza:98%Cor e Forma:SolidPeso molecular:426.39CID21480113
CAS:CID21480113, an antibacterial agent, is effective in treating dapsone resistant leprosy.Fórmula:C12H10FNO2SPureza:98%Cor e Forma:SolidPeso molecular:251.28Anti-infective agent 1
CAS:Compound 3a: potent, selective antiprotozoal/antimycobacterial. IC50: P. falciparum 10.95 μM, T. brucei 0.06 μM. MIC against M. smegmatis: 8 μg/mL.Fórmula:C16H10O2Cor e Forma:SolidPeso molecular:234.25Goitrin
CAS:<p>Goitrin, from glucosinolate reactions, blocks thyroid peroxidase and iodine use, and fights H1N1.</p>Fórmula:C5H7NOSCor e Forma:SolidPeso molecular:129.18SMR000071098
CAS:SMR000071098 is an inhibitor of Fe-S cluster-dependent aconitase. SMR000071098 interacts with Suf proteins to inhibit iron-sulfur (Fe-S) cluster assembly.Fórmula:C17H12N2O2Cor e Forma:SolidPeso molecular:276.29BDM31827
CAS:BDM31827 is an EthR inhibitor.Fórmula:C22H18N2O3SPureza:98%Cor e Forma:SolidPeso molecular:390.45FMDP
CAS:FMDP is a glucosamine-6-phosphate synthase inhibitor.Fórmula:C8H12N2O5Pureza:98%Cor e Forma:SolidPeso molecular:216.19Isometamidium chloride
CAS:Isometamidium chloride is an antiprotozoal agent. It is also used in veterinary medicine.Fórmula:C28H26ClN7Pureza:98%Cor e Forma:SolidPeso molecular:496.01Fozivudine tidoxil
CAS:Fozivudine tidoxil, a reverse transcriptase inhibitor, is used potentially for the treatment of HIV infection.Fórmula:C35H64N5O8PSCor e Forma:SolidPeso molecular:745.95HEPT
CAS:HEPT is a non-nucleoside inhibitor of HIV-1 reverse transcription.Fórmula:C14H16N2O4SPureza:98%Cor e Forma:SolidPeso molecular:308.35L-Ristosamine nucleoside
CAS:<p>L-Ristosamine nucleoside shows antiviral activity.</p>Fórmula:C21H21N3O7Cor e Forma:SolidPeso molecular:427.41Acrisorcin
CAS:Acrisorcin is a topical anti-infective typically used as a fungicide.Fórmula:C25H28N2O2Pureza:98%Cor e Forma:SolidPeso molecular:388.5BMY-27709
CAS:<p>BMY-27709 inhibits influenza growth (IC50: 3-8 μM, A/WSN/33), targets H1/H2 subtypes via hemagglutinin, ineffective against H3/B Lee/40.</p>Fórmula:C17H24ClN3O2Pureza:98.37% - 98.55%Cor e Forma:SolidPeso molecular:337.84ML372
CAS:ML372 is a potent and selective SMN Modulator (EC50 = 12 nM, 325% increase inSMN2) with good potency, pharmacokinetics, tolerance, and CNS penetration.Fórmula:C18H20N2O4SCor e Forma:SolidPeso molecular:360.43PPT
CAS:PPT is a modulator of water-heme interactions of CYP2C9d and CYP125A1 in low-spin P450 complexes.Fórmula:C11H13N3Pureza:98%Cor e Forma:SolidPeso molecular:187.24KSK-120
CAS:KSK-120 is a potent Chlamydia trachomatis inhibitor, it targets the glucose-6-phosphate (G-6P) metabolism pathway of Chlamydia trachomatis.Fórmula:C28H22N2O2SCor e Forma:SolidPeso molecular:450.55Suberosol
CAS:Suberosol possesses anti-HIV replication activity.Fórmula:C31H50O2Pureza:98%Cor e Forma:SolidPeso molecular:454.73Tedizolid phosphate disodium salt
CAS:Tedizolid phosphate: novel prodrug antibiotic targeting MRSA, VRE, and other Gram-positive bacteria.Fórmula:C17H16FN6Na2O6PPureza:98%Cor e Forma:SolidPeso molecular:496.3032-Mc-1,4-NHQ
CAS:2-Mc-1,4-NHQ, an inhibitor of the Cdc42-PBD interaction, blocks the association of Cdc42 with the PBD.Fórmula:C12H10O3Pureza:98%Cor e Forma:SolidPeso molecular:202.21DVR-23
CAS:DVR-23 is a potent inhibitor of HBV virus.Fórmula:C17H17F3N2O3SCor e Forma:SolidPeso molecular:386.39Picoplatin
CAS:Picoplatin, an anti-cancer agent overcoming platinum resistance, alkylates DNA to block replication, transcription, and induce apoptosis.Fórmula:C6H10Cl2N2PtPureza:98%Cor e Forma:SolidPeso molecular:376.14Amphotalide
CAS:<p>Amphotalide is an anthelminthic agent.</p>Fórmula:C19H20N2O3Pureza:98%Cor e Forma:SolidPeso molecular:324.37JX040
CAS:JX040 inhibits enterovirus replication, strong against non-polio strains, weak on polioviruses.Fórmula:C19H17N5OSCor e Forma:SolidPeso molecular:363.44Brecanavir
CAS:Brecanavir is a tyrosyl-based arylsulfonamide, high affinity, protease inhibitor (PI) for the treatment of human immunodeficiency virus type 1.Fórmula:C33H41N3O10S2Cor e Forma:SolidPeso molecular:703.82HHL-6
CAS:HHL-6 is a c-Fos and BDNF protein expression modulator.Fórmula:C19H26N2O3Cor e Forma:SolidPeso molecular:330.42BAS00127538
CAS:BAS00127538 is an Lipid II inhibitor.Fórmula:C31H28BF4NOCor e Forma:SolidPeso molecular:517.37TDR32570
CAS:TDR32570 is an antimalarial agent.Fórmula:C22H21F3N2O3Pureza:98%Cor e Forma:SolidPeso molecular:418.41Antitubercular agent-32
CAS:Antitubercular agent-32, a Benzothiazinone, inhibits DprE1 in tuberculosis, stable and water-soluble, IC50: 3.9 μM.Fórmula:C22H28N4O5S2Cor e Forma:SolidPeso molecular:492.61Diethofencarb
CAS:Diethofencarb: a fungicide effective against Botrytis cinerea and resistant Botryis strains.Fórmula:C14H21NO4Cor e Forma:SolidPeso molecular:267.32Ianthelliformisamine A TFA
CAS:Ianthelliformisamine A TFA, an antibiotic enhancer, is used to against resistant Gram-negative bacteria.Fórmula:C24H34Br2F6N4O6Pureza:98%Cor e Forma:SolidPeso molecular:748.356Iprovalicarb
CAS:Iprovalicarb is a fungicide aimed at oomycetes.Fórmula:C18H28N2O3Pureza:98%Cor e Forma:SolidPeso molecular:320.43Linatine
CAS:Linatine is used as a bacterial inhibitor.Fórmula:C10H17N3O5Pureza:98%Cor e Forma:SolidPeso molecular:259.26HIPP
CAS:HIPP is a highly selective inhibitor of antineoplastic CtBP.Fórmula:C9H9NO3Cor e Forma:SolidPeso molecular:179.17NDM-1 inhibitor-2
CAS:NDM-1 inhibitor-2 is an inhibitor of new delhi metallo-β-lactamase-1 (NDM-1).Fórmula:C9H9BrN4SPureza:98%Cor e Forma:SolidPeso molecular:285.16ZP7
CAS:ZP7 is a HIV-1 replication inhibitor.Fórmula:C15H9Br2ClN4OS2Pureza:98%Cor e Forma:SolidPeso molecular:520.65APA-APA-MPO
CAS:APA-APA-MPO is a PCAF bromodomain/Tat-AcK50 association inhibitor.Fórmula:C12H25Cl2N5OPureza:98%Cor e Forma:SolidPeso molecular:326.27Ingenol 3-Hexanoate
CAS:Ingenol 3-Hexanoate is a novel potent reactivator of latent HIV-1.Fórmula:C26H38O6Pureza:98%Cor e Forma:SolidPeso molecular:446.58SARS-CoV-2 nsp3-IN-2
CAS:SARS-CoV-2 nsp3-IN-2: Mac1 inhibitor, IC50=180μM, hinders virus replication.Fórmula:C10H12N4O2Cor e Forma:SolidPeso molecular:220.23DPC-963
CAS:DPC-963 is a RNA-directed DNA polymerase inhibitor.Fórmula:C14H9F5N2OCor e Forma:SolidPeso molecular:316.23BAY39-5493
CAS:BAY39-5493 is a hepatitis B virus inhibitor and possess antiviral activity in vitro and in vivo.Fórmula:C17H15ClFN3O2SCor e Forma:SolidPeso molecular:379.84Metallo-β-lactamase-IN-8
CAS:Metallo-β-lactamase-IN-8 (compound 17) is a potent, reversible and competitive broad-spectrum metallo-β-lactamases (MβLs) inhibitor with antibacterial activity.Fórmula:C13H11ClN2O4SCor e Forma:SolidPeso molecular:326.76Phenethicillin potassium
CAS:Phenethicillin potassium is a potassium salt form of phenethicillin with antibacterial activity.Fórmula:C17H20KN2O5SPureza:98%Cor e Forma:SolidPeso molecular:403.51GSK729
CAS:GSK729 is a novel potent EchA6 inhibitor.Fórmula:C16H16F3N3O2Pureza:98%Cor e Forma:SolidPeso molecular:339.31Tunicamine
CAS:Tunicamine is a reversible polyprenol-phosphate inhibitor.Fórmula:C11H21NO9Pureza:98%Cor e Forma:SolidPeso molecular:311.29DA-7867
CAS:DA-7867, an oxazolidinone, has lower MIC(≤0.25 μg/ml) against aerobic gram-positive bacteria than linezolid, with MIC(90) at 0.125 μg/ml.Fórmula:C19H18FN7O3Cor e Forma:SolidPeso molecular:411.39LP10
CAS:LP10 is a reverse type I inhibitor of Mycobacterium tuberculosis CYP125A1 and a Potent type II inhibitor of Trypanosoma cruzi CYP51.Fórmula:C24H28N4O2Cor e Forma:SolidPeso molecular:404.5Chitin synthase inhibitor 2
CAS:Chitin synthase inhibitor 2 (2b) has an IC50 of 0.09 mM, K i 0.12 mM, shows in vitro antimicrobial activity and boosts fluconazole/polyoxin B.Fórmula:C20H19N3O3Cor e Forma:SolidPeso molecular:349.38HIV-1 protease-IN-5
CAS:HIV-1 protease-IN-5 is an HIV-1 protease inhibitor (IC50: 1.64 nM). HIV-1 protease-IN-5 exhibits significant effects on wild-type and DRV-resistant HIV-1.Fórmula:C27H29F3N2O7SCor e Forma:SolidPeso molecular:582.59TachypleginA-2
CAS:TachypleginA-2 is a parasite motility and invasion inhibitor.Fórmula:C22H23NOPureza:98%Cor e Forma:SolidPeso molecular:317.42BM 21.1298
CAS:<p>BM 21.1298 is a inhibition of HIV-1 reverse transcriptase.</p>Fórmula:C16H13NOSPureza:98%Cor e Forma:SolidPeso molecular:267.35Antibacterial agent 65
CAS:Antibacterial agent 65 is a potential antimicrobial agent and antioxidant agent.Fórmula:C17H16O3Cor e Forma:SolidPeso molecular:268.31Gyramide A
CAS:Gyramide A is an inhibitor of bacterial DNA gyrase. It shows antimicrobial activity and inhibits bacterial cell division.Fórmula:C21H27FN2O3SPureza:98%Cor e Forma:SolidPeso molecular:406.51Guineesine
CAS:Guineesine is an Acyl-CoA. It acts by inhibiting cholesterol acyltransferase.Fórmula:C24H33NO3Pureza:98%Cor e Forma:SolidPeso molecular:383.52Rolicyprine
CAS:Rolicyprine is an antidepressant.Fórmula:C14H16N2O2Pureza:98%Cor e Forma:SolidPeso molecular:244.29HIV-1 inhibitor-53
CAS:HIV-1 Inhibitor-53 targets HIV-1 protease (IC50: 1.93 nM) and reverse transcriptase (IC50: 2.35 μM), aiding AIDS research.Fórmula:C30H34N2O8SPureza:98%Cor e Forma:SolidPeso molecular:582.66HBV-IN-10
CAS:HBV-IN-10, an isomer of compound 6, inhibits HBsAg with EC50 between 0.1-1 μM (Patent WO2021204258A1).Fórmula:C23H24FN7OCor e Forma:SolidPeso molecular:433.48Netzahualcoyonol
CAS:Netzahualcoyonol has antibacterial/cytotoxic effects; isolated with tingenone as active compounds.Fórmula:C30H38O5Pureza:98%Cor e Forma:SolidPeso molecular:478.62Levovirin valinate HCl
CAS:Levovirin valinate HCl is a valine ester prodrug of levovirin as a new investigational drug for the therapy of the hepatitis C virus.Fórmula:C13H22ClN5O6Pureza:98%Cor e Forma:SolidPeso molecular:379.8Caspofungin
CAS:Caspofungin is a cyclic lipopeptide echinocandin and beta-(1,3)-D-glucan synthase inhibitor that is used to treat internal or systemic mycoses.Fórmula:C52H88N10O15Cor e Forma:SolidPeso molecular:1093.31Azosulfamide
CAS:Azosulfamide is an azo compound with similar antibacterial effect as sulfanilamide.Fórmula:C18H16N4Na2O10S3Cor e Forma:SolidPeso molecular:590.5Mollugogenol A
CAS:Mollugogenol A: a Gammacerane saponin from Mollugo pentaphylla with antifungal and spermatocidal properties; damages sperm membrane.Fórmula:C30H52O4Cor e Forma:SolidPeso molecular:476.73BMS-663749 lysine
CAS:BMS-663749 lysine is used as a phosphonooxymethyl prodrug 4 for HIV-1 attachment inhibitor.Fórmula:C29H39N6O11PPureza:98%Cor e Forma:SolidPeso molecular:678.63Thiamphenicol glycinate hydrochloride
CAS:Thiamphenicol glycinate hydrochloride is a broad-spectrum antibacterial agent utilized in research on respiratory tract infections.Fórmula:C14H19Cl3N2O6SCor e Forma:SolidPeso molecular:449.73Sortin2
CAS:Sortin2 is a sorting inhibitor that acts upstream from the morphological marker of lateral root primordium formation, the mitotic activity.Fórmula:C16H12ClNO5S3Pureza:98%Cor e Forma:SolidPeso molecular:429.92Tolciclate
CAS:Tolciclate is an agent of antifungal medication.Fórmula:C20H21NOSPureza:98%Cor e Forma:SolidPeso molecular:323.45D4DAP
CAS:D4DAP is an inhibitor of HIV virus replication.Fórmula:C10H12N6O2Pureza:98%Cor e Forma:SolidPeso molecular:248.24Anti-infective agent 3
CAS:Antiprotozoal and antimycobacterial compound 3l; IC50: P. falciparum 0.47 μM, T. brucei 0.13 μM; MIC against M. smegmatis 4 μg/mL.Fórmula:C14H7ClN2O2Cor e Forma:SolidPeso molecular:270.67Iodiconazole
CAS:Iodiconazole, an azole antifungal, is used potentially for the treatment of fungal infection.Fórmula:C19H19F2IN4OPureza:98%Cor e Forma:SolidPeso molecular:484.28HIV-1 inhibitor-32
CAS:HIV-1 inhibitor-32 is a potent inhibitor of HIV-1 that acts on wild-type HIV (IC50: 34 nM) and can be used in AIDS research.Fórmula:C26H29N5O3SCor e Forma:SolidPeso molecular:491.61SSAA09E1
CAS:SSAA09E1 blocks SARS-CoV entry, lowers ACE2-mediated HEK293T cell infection (EC50 = 6.7 μM), and inhibits cathepsin L (IC50 = 5.33 μM).Fórmula:C7H9N3S2Cor e Forma:SolidPeso molecular:199.3TachypleginA
CAS:TachypleginA is a parasite motility and invasion inhibitor.Fórmula:C22H21F2NOPureza:98%Cor e Forma:SolidPeso molecular:353.4Pyrrofolic acid
CAS:Pyrrofolic acid shows high anti-folate biological activity for S. faecalis.Fórmula:C23H21N7O7Pureza:98%Cor e Forma:SolidPeso molecular:507.46Aconiazide
CAS:<p>Aconiazide is a prodrug of anti-tuberculosis.</p>Fórmula:C15H13N3O4Pureza:98%Cor e Forma:SolidPeso molecular:299.28BHBM
CAS:BHBM, an acylhydrazone antifungal, halts C. neoformans growth (MIC80 = 1 μg/ml) by blocking glucosylceramide synthesis.Fórmula:C15H13BrN2O2Cor e Forma:SolidPeso molecular:333.18BI-10
CAS:BI-10, paired with fluconazole, hinders fungal growth, increases ROS, decreases MMP, and changes membrane permeability.Fórmula:C23H17BrN2OCor e Forma:SolidPeso molecular:417.3Flaviviruses-Inhibitor-I
CAS:Flaviviruses-Inhibitor-I is several viruses belonging to the family of Flaviviridae inhibitor.Fórmula:C17H17N3O3SPureza:98%Cor e Forma:SolidPeso molecular:343.4Antitrypanosomal agent 9
CAS:Agent 9 inhibits T. b. brucei (IC50: 1.15 μM), used in HAT research.Fórmula:C22H27NO3Cor e Forma:SolidPeso molecular:353.45NPD9948
CAS:NPD9948 is a competitive inhibitor of MTH1.Fórmula:C13H14N6Cor e Forma:SolidPeso molecular:254.29Antitrypanosomal agent 7
CAS:Compound 18c, an antitrypanosomal, is twice as potent as Nifurtimox against T. brucei (IC50: 0.71 μM), with favorable ADME and AT-DNA binding affinity.Fórmula:C23H29N5O2Cor e Forma:SolidPeso molecular:407.51Zimet 38-74
CAS:Zimet 38-74 is an agent of antiviral.Fórmula:C27H28N4O2SPureza:98%Cor e Forma:SolidPeso molecular:472.6HBV-IN-29
CAS:HBV-IN-29 (ex8), a flavone derivative, inhibits cccDNA in HBV research.Fórmula:C22H19ClO6Cor e Forma:SolidPeso molecular:414.84Mtb-cyt-bd oxidase-IN-7
Mtb-cyt-bd oxidase-IN-7 inhibits Cyt-bd with 4.17 μM affinity and has anti-tuberculosis properties.Fórmula:C18H14F3NO2Cor e Forma:SolidPeso molecular:333.3L 870810
CAS:L 870810 is a small-molecule inhibitor of HIV-1 integrase with potent antiviral activity in cell culture and good pharmacokinetic properties.Fórmula:C20H19FN4O4SCor e Forma:SolidPeso molecular:430.45Antileishmanial agent-13
CAS:Antileishmanial agent-13, a quinoline-isatin hybrid, targets L. Major with IC50s of 0.604 μM (promastigote) and 0.508 μM (amastigote).Fórmula:C17H10BrClN4OCor e Forma:SolidPeso molecular:401.64HBV-IN-15
CAS:HBV-IN-15, a flavone derivative, is a potent cccDNA inhibitor, potentially aiding HBV research.Fórmula:C24H23ClO6Cor e Forma:SolidPeso molecular:442.89GRL-1720
CAS:GRL-1720 is a SARS-CoV-2 Protease inhibitor (IC50 = 320 nM). GRL-1720 contains an indoline which targets the SARS-CoV-2 main protease (Mpro)Fórmula:C14H11ClN2O2Cor e Forma:SolidPeso molecular:274.7Antibacterial agent 124
CAS:Antibacterial agent 124 inhibits Sa ProRS with an IC50 of 0.18 μM.Fórmula:C16H17ClFN3O2Cor e Forma:SolidPeso molecular:337.78HIV-1 inhibitor-47
CAS:<p>HIV-1 Inhibitor-47 blocks Vif-APOBEC3G interaction, has 14.33 μM IC50, and may yield antianxiety and antipsychotic derivatives.</p>Fórmula:C12H14N6Cor e Forma:SolidPeso molecular:242.28Ceforanide lysine
CAS:Ceforanide lysine is an Anti-Infective.Fórmula:C26H35N9O8S2Pureza:98%Cor e Forma:SolidPeso molecular:665.74Pomotrelvir
CAS:<p>Pomotrelvir (PBI-0451) is an oral SARS-CoV-2 3CL protease inhibitor with antiviral properties for COVID-19 research.</p>Fórmula:C23H26ClN5O3Cor e Forma:SolidPeso molecular:455.94Antiparasitic agent-7
CAS:<p>Compound 5d, antiparasitic for L. infantum, IC50 of 2.85μM; cytotoxic to HepG2 cells, CC50 of 10.61μM.</p>Fórmula:C18H15N3O5Cor e Forma:SolidPeso molecular:353.33Codon readthrough inducer 1
CAS:Codon readthrough inducer 1 contains pyrimidine bases and shows good readthrough activity.Fórmula:C15H11N3O5Pureza:98%Cor e Forma:SolidPeso molecular:313.26BPH-652
CAS:BPH-652 is an S. aureus dehydrosqualene synthase (CrtM) inhibitor (Ki: 1.5 nM; IC50: 100-300 nM for S. aureus pigment formation).Fórmula:C16H19K3O7PSPureza:98%Cor e Forma:SolidPeso molecular:503.65
