Microbiology/Virology
Microbiology and virology inhibitors are compounds that target microorganisms, including bacteria, viruses, and fungi, disrupting their growth, replication, or survival. These inhibitors are essential for studying microbial pathogenesis, understanding resistance mechanisms, and developing new antimicrobial and antiviral therapies. Inhibitors in this category are used to combat infectious diseases, explore microbial ecology, and investigate host-pathogen interactions. At CymitQuimica, we provide a broad selection of high-quality microbiology and virology inhibitors to support your research in infectious diseases, microbiology, and virology.
Subcategories of "Microbiology/Virology"
- Antibacterial(3,423 products)
- Antibiotic(947 products)
- Antifection(27 products)
- DHFR(30 products)
- DNA/RNA Synthesis(808 products)
- HBV(187 products)
- HIV Protease(507 products)
- HSV(99 products)
- Integrase(2 products)
- Ribosome(5 products)
Show 2 more subcategories
Found 6444 products of "Microbiology/Virology"
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Antimalarial agent 46
CAS:Antimalarial agent 46 (Compound 42a) is a compound with antimalarial activity, effective in inhibiting P. falciparum lines.Formula:C21H17Cl3N4OColor and Shape:SolidMolecular weight:447.75WRN inhibitor 15
WRN inhibitor 15 (Compound 9) is a WRN inhibitor with antitumor properties, displaying IC50 values of 37.9, 40.2, and 46.6 μM in PC3, LNCaP, and HeLa cells, respectively, making it suitable for prostate cancer research.Formula:C16H13F2N3OColor and Shape:SolidMolecular weight:301.292-Acetylthiophene thiosemicarbazone
CAS:2-Acetylthiophene thiosemicarbazone is an antimicrobial agent against a wide range of gram-negative and gram-positive bacteri and fungi.Formula:C7H9N3S2Color and Shape:SolidMolecular weight:199.3SARS-CoV-2-IN-52
CAS:SARS-CoV-2-IN-52 (Compound 5) is an inhibitor of SARS-CoV-2 with a pIC50 of 0.3187.Formula:C20H16N6OColor and Shape:SolidMolecular weight:356.38AV5124
CAS:AV5124 is a prodrug of AV5116 and acts as an orally active inhibitor of influenza virus cap-dependent endonuclease (CEN).Formula:C25H21F2N3O7S2Color and Shape:SolidMolecular weight:577.58Fosetyl-aluminum
CAS:Fosetyl-aluminum is a systemic fungicide that controls downy mildews and Phytophthora diseases, used on a variety of crops including fruits and vegetables。Formula:C6H18AlO9P3Purity:99.52%Color and Shape:SolidMolecular weight:354.1Moenomycin Complex
CAS:Moenomycin complex is a mixture of moenomycins A, A12, C1, C3 and C4, which are antibiotics from several Streptomyces that directly inhibit bacterial PGTs.
Formula:C66H101N4O31PColor and Shape:SolidMolecular weight:1477.505AB-161
CAS:AB-161 is an orally active destabilizer of HBV RNA and an inhibitor of PAPD5/7, primarily targeting the liver. It treats hepatitis B virus (HBV) infection by reducing hepatitis B surface antigen (HBsAg) levels, exhibiting an EC50 value of 2.2 nM for HBsAg. AB-161 is applicable in HBV infection research.Formula:C21H21F2N3O5Color and Shape:SolidMolecular weight:433.41MCG-02
MCG-02 is an inhibitor of cruzain (CRZ) and cathepsin L-like protease (CATL), capable of inhibiting CRZ in Trypanosoma cruzi and CATL in Trypanosoma brucei, with IC50 values of 0.2 μM and 0.02 μM, respectively.Formula:C13H13N3O2SColor and Shape:SolidMolecular weight:275.33IAV replication-IN-1
CAS:IAV replication-IN-1 (compound 3h) can reduce the upregulation of inflammatory factors and apoptosis caused by IAV infection and alleviate lung damage resulting from IAV infection.Formula:C23H22N2O5S2Color and Shape:SolidMolecular weight:470.56Ap4dT
CAS:Ap4dT serves as an inhibitor of human adenylate kinase isozyme 1 (hAK1), effectively suppressing the synthesis of ATP and ADP, with IC50 values of 42 μM and 38 μM, respectively.Formula:C20H41N11O20P4Color and Shape:SolidMolecular weight:879.5Se2h
Se2h is a cruzain inhibitor exhibiting potent activity against intracellular amastigotes of Trypanosoma cruzi (EC50< 1 μM, SI> 10), with an inhibitory effect on cruzain of IC50< 100 nM (SI> 5.55). Compared to Benznidazole and cruzain inhibitor K777, Se2h shows superior selectivity and inhibition while its selenazole structure reduces selenium-related toxicity. Se2h demonstrates antiparasitic activity and holds promise for Chagas disease research.Formula:C12H13ClN4O2SeColor and Shape:SolidMolecular weight:359.67Antileishmanial agent-31
CAS:Antileishmanial agent-31 (Compound p1) is a pyrazole derivative exhibiting antileishmanial activity with an IC50 of 35.53 μg/mL. Furthermore, Antileishmanial agent-31 demonstrates high stability and is applicable in studies focused on leishmaniasis treatment.Formula:C11H11ClN2Color and Shape:SolidMolecular weight:206.67CpCDPK1/TgCDPK1-IN-2
CAS:CpCDPK1/TgCDPK1-IN-2 is a dual inhibitor of CpCDPK1 and TgCDPK1 with IC50 values of 12 and 5 nM for CpCDPK1 and TgCDPK1, respectively.CpCDPK1/TgCDPK1-IN-2 can
Formula:C20H21N5OPurity:99.12%Color and Shape:SoildMolecular weight:347.41ACHE-IN-38
CAS:ACHE-IN-38, an Acetylcholinesterase inhibitor, can be used to synthesize compounds with anti-inflammatory activity.Formula:C17H23NO3Purity:99.78%Color and Shape:SolidMolecular weight:289.37Durlobactam Triethylamine
Durlobactam Triethylamine inhibits A, C, D β-lactamases and possesses antifungal properties.Formula:C14H26N4O6SPurity:97.39%Color and Shape:SoildMolecular weight:378.44Adenoregulin
CAS:Adenoregulin (Dermaseptin b2), an antimicrobial peptide antibiotic, exhibits efficacy against both Gram-negative and Gram-positive bacteria, as well as yeastFormula:C142H242N40O42Purity:98%Color and Shape:SolidMolecular weight:3181.68HBA(111-142)
HBA(111-142), a C-terminal 32-mer fragment of alpha-hemoglobin, exhibits antibacterial activity against the ESKAPE panel of pathogens, forms amyloid fibrils,Formula:C157H247N41O45Purity:98%Color and Shape:SolidMolecular weight:3428.89NS2B-NS3pro-IN-1
NS2B-NS3pro-IN-1, a potent Zika Virus NS2B-NS3 protease inhibitor, exhibits an EC50 of 50 μM and is significant in the ZIKV replication cycle [1].Purity:98%Color and Shape:Odour SolidAntileishmanial agent-20
Antileishmanial agent-20 exhibits selectivity against the Leishmania parasite, with IC50 values of 2.8 μM for L.Formula:C15H16N4O3Purity:98%Color and Shape:SolidMolecular weight:300.31SARS-CoV-2-IN-64
SARS-CoV-2-IN-64 (compound 9), derived from chenodeoxycholic acid, serves as a potent inhibitor of the SARS-CoV-2 spike glycoprotein [1].Purity:98%Color and Shape:Odour SolidMajoranaquinone
CAS:Majoranaquinone demonstrates potent antibacterial activity against four Staphylococcus strains, one Moraxella strain, and one Enterococcus strain.
Formula:C14H10O4Purity:98%Color and Shape:SolidMolecular weight:242.23Taq DNA polymerase
CAS:Taq DNA polymerase is a thermostable enzyme utilized in polymerase chain reactions (PCR) to amplify DNA sequences [1].Purity:98%Color and Shape:SolidDihydrodehydrodiconiferyl alcohol 9-O-β-D-xylopyranoside
CAS:Dihydrodehydrodiconiferyl alcohol 9-O-β-D-xylopyranoside serves as an anti-hepatitis B virus (anti-HBV) agent, effectively inhibiting the secretion of HBVFormula:C25H32O10Purity:98%Color and Shape:SolidMolecular weight:492.52DNA polymerase-IN-2
DNA polymerase-IN-2 (Compd 3c), a coumarin derivative, demonstrates inhibitory activity towards Taq DNA polymerase, with an IC50 value of 48.25 μM, and holdsFormula:C14H12O5SPurity:98%Color and Shape:SolidMolecular weight:292.31Gramicidin B
CAS:Gramicidin B is a nonribosomal peptide with antibiotic properties [1].Formula:C97H139N19O17Purity:98%Color and Shape:SolidMolecular weight:1843.26HBV-IN-35
Compound HBV-IN-35 (Compound 88) serves as an HBV inhibitor and exhibits anti-HBV activity in both mouse and human hepatocytes with EC50 values of 100 nM andFormula:C22H23F5N4OPurity:98%Color and Shape:SolidMolecular weight:454.44Anti-Influenza agent 5
Anti-Influenza agent 5 (Compound IIB-2), a chalcone-like derivative, serves as an influenza nuclear export inhibitor.Purity:98%Color and Shape:Odour SolidUrumin
CAS:Urumin, a compound with antiviral properties, inhibits human influenza A virus growth, particularly the PR8 strain, with an inhibitory concentration (IC 50) ofFormula:C129H198N42O35S2Purity:98%Color and Shape:SolidMolecular weight:2961.34Funiculosin
CAS:Funiculosin, a neutral lipophilic antibiotic, demonstrates inhibitory effects against both DNA and RNA viruses, in addition to possessing antifungal properties.Formula:C27H41NO7Purity:98%Color and Shape:SolidMolecular weight:491.62SARS-CoV-2-IN-54
SARS-CoV-2-IN-54 (Compound 2), a SARS-CoV-2 inhibitor, exhibits antiviral activity by impeding the virus in Vero E6 cells with an inhibitory concentration (IC50Formula:C63H59N11O16S3Purity:98%Color and Shape:SolidMolecular weight:1322.4β-Herpesvirus protease-IN-1
β-Herpesvirus protease-IN-1 (compound 19) serves as an inhibitor of β-herpesvirus protease, exhibiting IC50 values of 2.5 μM for HCMVPro and 0.33 μM for HHV6ProPurity:98%Color and Shape:Odour SolidSARS-CoV-2 3CLpro-IN-17
Compound 3h, also known as SARS-CoV-2 3CLpro-IN-17, is a selective inhibitor of the SARS-CoV-2 3CL protease, demonstrating an IC50 of 0.322 μM [1].Formula:C16H9N3OS2Purity:98%Color and Shape:SolidMolecular weight:323.39RdRP-IN-6
RdRP-IN-6 (compound 27) is an inhibitor of RNA-dependent RNA polymerase (RdRp), exhibiting an IC90 value of 14.1 μM.
Formula:C41H67N8O7PSi2Purity:98%Color and Shape:SolidMolecular weight:871.16Lugdunin
CAS:Lugdunin is an antibiotic peptide that disrupts membrane potential in bacteria, demonstrating activity against Gram-positive species including S.Formula:C40H62N8O6SPurity:98%Color and Shape:SolidMolecular weight:783.04Antitrypanosomal agent 16
Antitrypanosomal agent 16 functions as a potent trypanocide, exhibiting an inhibitory concentration 50 (IC50) of 0.04μM against the T.Purity:98%Color and Shape:Odour SolidAurein 3.1
CAS:Aurein 3.1 is an antibiotic antimicrobial peptide, whereas Aurein 2.6 demonstrates activity against Gram-positive bacteria, exhibiting minimum inhibitoryFormula:C81H136N22O20Purity:98%Color and Shape:SolidMolecular weight:1738.08SARS-CoV-2-IN-61
SARS-CoV-2-IN-61 (compound 8i) is a potent inhibitor of the SARS-CoV-2 PLpro, exhibiting an IC50 of 16 µM and demonstrating antiviral activities [1].Formula:C26H30N2O2Purity:98%Color and Shape:SolidMolecular weight:402.53SARS-CoV-2 Mpro-IN-10
SARS-CoV-2 Mpro-IN-10 (27h) is a potent inhibitor of the Mpro enzyme, exhibiting IC50 and EC50 values of 10.9 nM and 43.6 nM, respectively.Formula:C28H30F4N4O4Purity:98%Color and Shape:SolidMolecular weight:562.56Poly(A) polymerase
CAS:Poly(A) polymerase enzymatically adds a polyadenosine tail of 20-200 adenine bases to the 3' end of RNA, a process that involves integrating ATP as AMP.Purity:98%Color and Shape:SolidMAT-POS-e194df51-1
MAT-POS-e194df51-1 is an orally active, non-covalent, non-peptide inhibitor of the SARS-CoV-2 main protease (M^pro) with an IC_50 of 37nM.Purity:98%Color and Shape:Odour SolidDihydrodehydrodiconiferyl alcohol 9-O-α-L-rhamnopyranoside
CAS:Dihydrodehydrodiconiferyl alcohol 9-O-α-L-rhamnopyranoside (Compound 1), a lignan with anti-HBV activity, exhibits selectivity by targeting the HBV surfaceFormula:C26H34O10Purity:98%Color and Shape:SolidMolecular weight:506.54MTase-IN-1
MTase-IN-1 (compound 26), a potent and selective inhibitor of coronavirus nsp14 N7-methyltransferases, exhibits an IC50 of 0.72 nM.Formula:C31H29N7O6SPurity:98%Color and Shape:SolidMolecular weight:627.67H-Arg-OtBu dihydrochloride
CAS:H-Arg-OtBu (dihydrochloride) is a membrane-targeting antimicrobial that engages the negatively charged bacterial membrane through electrostatic and hydrophobicFormula:C10H24Cl2N4O2Purity:98%Color and Shape:SolidMolecular weight:303.23HBV-IN-40
HBV-IN-40 (Compound 11826096), with an IC50 of 0.7 µM, serves as a potent HBV inhibitor and exhibits antiviral activity [1].Formula:C29H55Cl4N11Purity:98%Color and Shape:SolidMolecular weight:699.63MPI60
MPI60 is a potent inhibitor of SARS-CoV-2 main protease (M^pro) exhibiting high antiviral efficacy, low cellular cytotoxicity, and considerable in vitroFormula:C24H31N3O5Purity:98%Color and Shape:SolidMolecular weight:441.52Antileishmanial agent-19
Compound F27 (Antileishmanial agent-19) is an antileishmanial compound effective against L.Formula:C22H18N4O3Purity:98%Color and Shape:SolidMolecular weight:386.4Antitrypanosomal agent 13
Compound 4b (antitrypanosomal agent 13) is a potent antitrypanosomal with notable trypanocidal and cytotoxic activities, exhibiting GI50 values of 0.18 μMFormula:C47H81N2NaO10SPurity:98%Color and Shape:SolidMolecular weight:889.21SARS-CoV-2 nsp14-IN-4
SARS-CoV-2 nsp14-IN-4 (Compound 12q), a non-cytotoxic and cell-permeable inhibitor of SARS-CoV-2 nsp14 methyltransferase (IC50 = 19 nM), is employed in COVID-19Formula:C31H27N7O6SPurity:98%Color and Shape:SolidMolecular weight:625.65Pezadeftide
CAS:Pezadeftide, a potent antifungal peptide, readily penetrates fungal cells, eliciting an immediate mitochondrial response that leads to hyperpolarization of thePurity:98%Color and Shape:Solid
