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(2.959 produtos)
- Antibiótico(921 produtos)
- Antifecção(23 produtos)
- DHFR(33 produtos)
- Síntese de DNA/RNA(708 produtos)
- HBV(176 produtos)
- HIV Protease(449 produtos)
- HSV(91 produtos)
- Integrase(2 produtos)
- Ribossomo(13 produtos)
Exibir 2 mais subcategorias
Foram encontrados 5843 produtos de "Microbiologia/Virologia"
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C16G2
CAS:<p>C16G2 is a Specific Targeted Antimicrobial Peptide (STAMP) that selectively targets the cariogenic oral pathogen Streptococcus mutans. This compound operates by recognizing and disrupting the bacterial cell membrane, leading to small molecule leakage and the loss of membrane potential, which results in bacterial death. Unlike broad-spectrum antimicrobial peptides, C16G2 exhibits higher selectivity and efficacy against Streptococcus mutans.</p>Fórmula:C190H310N58O42Cor e Forma:SolidPeso molecular:4078.93SCR7
CAS:<p>SCR7, a specific DNA Ligase IV inhibitor, blocks nonhomologous end-joining (NHEJ).</p>Fórmula:C18H14N4OSPureza:98%Cor e Forma:SolidPeso molecular:334.4Ile-AMS TFA
<p>Ile-AMS TFA exhibits activity against P. falciparum, with an ABSIC50 value of 1.19 nM.</p>Fórmula:C18H27F3N8O8SCor e Forma:SolidPeso molecular:572.52Libevitug
<p>Libevitug is a humanized IgG1λ2 antibody targeting HBV, with HumanIgG1lambda2, Isotype Control as its corresponding isotype control.</p>Cor e Forma:Odour LiquidMTH1 ligand 1
CAS:<p>MTH1 ligand 1 functions as a target protein ligand for MTH1, and is utilized in the synthesis of PROTACaTAG 2139.</p>Fórmula:C23H18N4O3Cor e Forma:SolidPeso molecular:398.41N-Demethylvancomycin
CAS:<p>N-Demethylvancomycin is a glycopeptide antibiotic that can be extracted from Nocardia orientalis and exhibits activity against various strains of Staphylococcus aureus and Staphylococcus epidermidis. It is utilized in research related to infections.</p>Fórmula:C65H73Cl2N9O24Cor e Forma:SolidPeso molecular:1435.23Apidaecin IB
CAS:<p>Apidaecin IB is an insect antimicrobial peptide, with MIC values of 8 μM for E. coli (O18K1H7, ML35 and ATCC 25922).</p>Fórmula:C95H150N32O23Pureza:98%Cor e Forma:SolidPeso molecular:2108.446GS-443902
CAS:<p>Remdesivir triphosphate (GS-443902) inhibits RSV/HCV RdRp with IC50s: 1.1/5 µM.</p>Fórmula:C12H16N5O13P3Pureza:98%Cor e Forma:SolidPeso molecular:531.2T2AA
CAS:<p>T2AA (4-[4-[(2S)-2-amino-3-hydroxypropyl]-2,6-diiodophenoxy]phenol) is an inhibitor of proliferating cell nuclear antigen (PCNA) with IC50 of 1 μM for PCNA/PIP-</p>Fórmula:C15H15I2NO3Pureza:99.53%Cor e Forma:SolidPeso molecular:511.09DMT-dU-CE Phosphoramidite
CAS:<p>DMT-dU-CE Phosphoramidite is a nucleoside molecule commonly used for the synthesis and sequencing of DNA.</p>Fórmula:C39H47N4O8PPureza:99.55%Cor e Forma:SolidPeso molecular:730.79NCGC00029283
CAS:<p>NCGC00029283 is a potent inhibitor of Werner syndrome helicase-nuclease (WRN), displaying inhibitory activity against WRN helicase with an IC 50 value of 2.3 μM</p>Fórmula:C18H12FN3O3Pureza:99.84%Cor e Forma:SolidPeso molecular:337.3N2-Acetylaciclovir
CAS:<p>N2-Acetylaciclovir (Aciclovir EP Impurity F) is a derivative of the antiviral compound Aciclovir, which has selective T-cell immunotoxicity.</p>Fórmula:C10H13N5O4Pureza:98.2%Cor e Forma:SolidPeso molecular:267.24Neamine tetrahydrochloride
CAS:<p>Neamine tetrahydrochloride has antimicrobial and neuroprotective activities and inhibits the growth of pancreatic cancer cells.</p>Fórmula:C12H30Cl4N4O6Pureza:98.98% - 99.09%Cor e Forma:SolidPeso molecular:468.2Vaborbactam ammonium salt
<p>Vaborbactam ammonium salt is a β-lactamase inhibitor that restores carbapenem activity against KPC-producing strains.</p>Fórmula:C12H19BN2O5SPureza:97.36%Cor e Forma:SoildPeso molecular:314.17Saframycin S
CAS:<p>Saframycin S, an antibiotic featuring a Racemomycin group, demonstrates inhibitory effects against Ehrlich ascites tumor. The LD50 value of Saframycin S in ddY mice is 3.2 mg/kg (i.p.).</p>Fórmula:C28H31N3O9Cor e Forma:SolidPeso molecular:553.56WRN inhibitor 15
<p>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.</p>Fórmula:C16H13F2N3OCor e Forma:SolidPeso molecular:301.292-Acetylthiophene thiosemicarbazone
CAS:<p>2-Acetylthiophene thiosemicarbazone is an antimicrobial agent against a wide range of gram-negative and gram-positive bacteri and fungi.</p>Fórmula:C7H9N3S2Cor e Forma:SolidPeso molecular:199.3SARS-CoV-2-IN-52
CAS:<p>SARS-CoV-2-IN-52 (Compound 5) is an inhibitor of SARS-CoV-2 with a pIC50 of 0.3187.</p>Fórmula:C20H16N6OCor e Forma:SolidPeso molecular:356.38AV5124
CAS:<p>AV5124 is a prodrug of AV5116 and acts as an orally active inhibitor of influenza virus cap-dependent endonuclease (CEN).</p>Fórmula:C25H21F2N3O7S2Cor e Forma:SolidPeso molecular:577.58Jun13728
<p>Jun13728 is a potent and covalent inhibitor of the SARS-CoV-2 papain-like protease, with an IC50 value of 0.1 μM. This compound is applicable for antiviral research related to SARS-CoV-2.</p>Fórmula:C34H36F2N8O4Cor e Forma:SolidPeso molecular:658.7Anti-Trypanosoma cruzi agent-6
<p>Anti-Trypanosoma cruzi agent-6 (Compound 8) exhibits inhibitory activity against Trypanosoma cruzi. It effectively suppresses the epimastigote, trypomastigote, and amastigote forms of T. cruzi, with IC50 values of 24.7 µM, 1.8 µM, and 1.6 µM, respectively.</p>Fórmula:C19H20N2O5Cor e Forma:SolidPeso molecular:356.37Cordysinin C/D
CAS:<p>Cordysinin C/D (compound 9) is a potential antimalarial agent that effectively inhibits the Plasmodium falciparum 3D7 strain.</p>Fórmula:C13H12N2OCor e Forma:SolidPeso molecular:212.25CpCDPK1/TgCDPK1-IN-2
CAS:<p>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</p>Fórmula:C20H21N5OPureza:99.12%Cor e Forma:SoildPeso molecular:347.41Adenoregulin
CAS:<p>Adenoregulin (Dermaseptin b2), an antimicrobial peptide antibiotic, exhibits efficacy against both Gram-negative and Gram-positive bacteria, as well as yeast</p>Fórmula:C142H242N40O42Pureza:98%Cor e Forma:SolidPeso molecular:3181.68HBA(111-142)
<p>HBA(111-142), a C-terminal 32-mer fragment of alpha-hemoglobin, exhibits antibacterial activity against the ESKAPE panel of pathogens, forms amyloid fibrils,</p>Fórmula:C157H247N41O45Pureza:98%Cor e Forma:SolidPeso molecular:3428.89NS2B-NS3pro-IN-1
<p>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].</p>Pureza:98%Cor e Forma:Odour SolidAntileishmanial agent-20
<p>Antileishmanial agent-20 exhibits selectivity against the Leishmania parasite, with IC50 values of 2.8 μM for L.</p>Fórmula:C15H16N4O3Pureza:98%Cor e Forma:SolidPeso molecular:300.31SARS-CoV-2-IN-64
<p>SARS-CoV-2-IN-64 (compound 9), derived from chenodeoxycholic acid, serves as a potent inhibitor of the SARS-CoV-2 spike glycoprotein [1].</p>Pureza:98%Cor e Forma:Odour SolidMajoranaquinone
CAS:<p>Majoranaquinone demonstrates potent antibacterial activity against four Staphylococcus strains, one Moraxella strain, and one Enterococcus strain.</p>Fórmula:C14H10O4Pureza:98%Cor e Forma:SolidPeso molecular:242.23HA-IN-1
<p>HA-IN-1 (compound 5g), a high-affinity Hemagglutinin (HA) ligand, targets the trypsin cleavage site of HA to inhibit HA-mediated membrane fusion and decrease</p>Fórmula:C42H35NO6Pureza:98%Cor e Forma:SolidPeso molecular:649.73Citrullinated LL-37 3cit
<p>Citrullinated LL-37 3cit is a host defense peptide with potent immunomodulatory and antimicrobial properties, demonstrating direct antiviral activity against</p>Fórmula:C205H337N57O56Pureza:98%Cor e Forma:SolidPeso molecular:4496.22Z-L(D-Val)G-CHN2
<p>Z-L(D-Val)G-CHN2, an isoform of Z-LVG-CHN2, serves as a cell-permeable and irreversible inhibitor of cysteine proteinase.</p>Fórmula:C22H31N5O5Pureza:98%Cor e Forma:SolidPeso molecular:445.51Antimalarial agent 31
<p>Compound 31 (compound 7k) is an orally active inhibitor of Plasmodium falciparum aspartic protease, plasmepsin X (PMX), with antimalarial properties [1].</p>Fórmula:C36H47N3O4Pureza:98%Cor e Forma:SolidPeso molecular:585.78Antitrypanosomal agent 17
<p>Compound 17 (Compd 7a) exhibits potent antiamastigote activity, demonstrated by its IC50 value of 0.03 μM against the T. congolense strain IL3000 [1].</p>Pureza:98%Cor e Forma:Odour SolidSARS-CoV-2-IN-42
<p>SARS-CoV-2-IN-42 (Compound 8q) effectively inhibits SARS-CoV-2 replication with an EC50 value of 0.4 μM and demonstrates no significant toxicity to the host</p>Fórmula:C20H20O7Pureza:98%Cor e Forma:SolidPeso molecular:372.37SARS-CoV-2-IN-67
<p>SARS-CoV-2-IN-67 (Compound 16), a derivative of vitamin K, exhibits anti-SARS-CoV-2 properties, with an effective concentration (EC50) of 64.8 μM in VeroE6/</p>Pureza:98%Cor e Forma:Odour SolidSARS-CoV-2-IN-50
<p>SARS-CoV-2-IN-50 (Compound X77C) is a potent inhibitor of the SARS-CoV-2 main protease (M^pro), exhibiting high affinity for the enzyme's catalytic site [1].</p>Fórmula:C26H28FN5O4Pureza:98%Cor e Forma:SolidPeso molecular:493.53Antileishmanial agent-21
<p>Antileishmanial agent-21 (compound 4e) functions as an inhibitor of Leishmania pteridine reductase 1 (Lm-PTR1), employing an anti-folate mechanism.</p>Fórmula:C21H16N2O3Pureza:98%Cor e Forma:SolidPeso molecular:344.36SARS-CoV-2-IN-53
<p>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 demonstrates</p>Fórmula:C23H18F2N2O4SPureza:98%Cor e Forma:SolidPeso molecular:456.46Anticancer agent 140
<p>Compound 140 (Compd 3) exhibits potential anticancer and antiparasitic activities [1].</p>Fórmula:C20H26N2OPureza:98%Cor e Forma:SolidPeso molecular:310.43Simaravibart
<p>Simaravibart (MAD-0004J08), an IgG1κ monoclonal antibody, specifically targets the receptor-binding domain of the SARS-CoV-2 spike (S) glycoprotein [1].</p>Pureza:98%Cor e Forma:Odour LiquidNSC89641
<p>NSC89641 demonstrates potent inhibition of MERS-CoV M^pro, achieving an IC_50 value of less than 3.5 µM.</p>Fórmula:C19H18N6O12Pureza:98%Cor e Forma:SolidPeso molecular:522.3810-Hydroxyaloin A
CAS:<p>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-2</p>Fórmula:C21H22O10Pureza:98%Cor e Forma:SolidPeso molecular:434.39SARS-CoV-2-IN-65
<p>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 and</p>Pureza:98%Cor e Forma:Odour SolidMptpB-IN-2
<p>MptpB-IN-2 (compound 20), a selective inhibitor for mycobacterium tuberculosis protein tyrosine phosphatase B (MptpB), exhibits half maximal inhibitory</p>Fórmula:C23H20F3NO3S2Pureza:98%Cor e Forma:SolidPeso molecular:479.54HBV-IN-36
<p>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 0.58</p>Fórmula:C21H18ClFN4O2Pureza:98%Cor e Forma:SolidPeso molecular:412.84Wulfenioidin F
<p>Wulfenioidin F, a diterpenoid isolated from the whole plant of Orthosiphon wulfenioides, exhibits anti-Zika virus (ZIKV) activity with an EC50 of 8.07 μM and</p>Fórmula:C21H28O3Pureza:98%Cor e Forma:SolidPeso molecular:328.45MPI60
<p>MPI60 is a potent inhibitor of SARS-CoV-2 main protease (M^pro) exhibiting high antiviral efficacy, low cellular cytotoxicity, and considerable in vitro</p>Fórmula:C24H31N3O5Pureza:98%Cor e Forma:SolidPeso molecular:441.52Antileishmanial agent-19
<p>Compound F27 (Antileishmanial agent-19) is an antileishmanial compound effective against L.</p>Fórmula:C22H18N4O3Pureza:98%Cor e Forma:SolidPeso molecular:386.4Antitrypanosomal agent 13
<p>Compound 4b (antitrypanosomal agent 13) is a potent antitrypanosomal with notable trypanocidal and cytotoxic activities, exhibiting GI50 values of 0.18 μM</p>Fórmula:C47H81N2NaO10SPureza:98%Cor e Forma:SolidPeso molecular:889.21
