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(3.365 produtos)
- Antibiótico(937 produtos)
- Antifecção(27 produtos)
- DHFR(30 produtos)
- Síntese de DNA/RNA(799 produtos)
- HBV(182 produtos)
- HIV Protease(496 produtos)
- HSV(99 produtos)
- Integrase(2 produtos)
- Ribossomo(10 produtos)
Exibir 2 mais subcategorias
Foram encontrados 6326 produtos de "Microbiologia/Virologia"
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MTase-IN-1
MTase-IN-1 (compound 26), a potent and selective inhibitor of coronavirus nsp14 N7-methyltransferases, exhibits an IC50 of 0.72 nM.Fórmula:C31H29N7O6SPureza:98%Cor e Forma:SolidPeso molecular:627.67(±)-Emodin bianthrone
CAS:(±)-Emodin bianthrone (compound 10), a naturally occurring substance, demonstrates antimalarial, antitubercular, and antifungal properties [1].Fórmula:C30H22O8Pureza:98%Cor e Forma:SolidPeso molecular:510.49Moloney murine leukemia virus RT
Moloney murine leukemia virus reverse transcriptase (MMLV RT) is a monomeric replicative polymerase intrinsic to the retrovirus life cycle [1].Pureza:98%Cor e Forma:Odour Solid7-51A
7-51A is an effective inhibitor of the PB2 subunit of the influenza RNA-dependent RNA polymerase (RdRP), with a dissociation constant (K_D) of 1.64 nM asPureza:98%Cor e Forma:Odour SolidPlutavimab
CAS:Plutavimab is a humanized IgG1-κ monoclonal antibody targeting the receptor binding domain (RBD) of the SARS-CoV-2 spike (S) glycoprotein [1] [2].Pureza:98%Cor e Forma:LiquidCalpain inhibitor V
CAS:Calpain Inhibitor V (Mu-Val-HPh-FMK) is a cell-permeable, irreversible calpain inhibitor with demonstrated anti-chlamydial activity [1].Fórmula:C21H30FN3O4Pureza:98%Cor e Forma:SolidPeso molecular:407.48Aurein 2.3
CAS:Aurein 2.3, an antibiotic antimicrobial peptide, partially inhibits E. coli ATPase activity and suppresses cell growth [1] [2].Fórmula:C76H131N19O19Pureza:98%Cor e Forma:SolidPeso molecular:1614.976-C-Methylquercetin-3,4'-dimethyl ether
6-C-Methylquercetin-3,4'-dimethyl ether is a flavonol derivative extracted from Bauhinia thonningii Schum leaves, displaying antibacterial effects on Gram-Fórmula:C18H16O7Pureza:98%Cor e Forma:SolidPeso molecular:344.32Antileishmanial agent-22
Antileishmanial agent-22 (compound 15b) serves as an antiparasitic and antibacterial, exhibiting activities against Leishmania (IC50 = 0.408 μM), malaria, andFórmula:C29H26Cl2N4O3Pureza:98%Cor e Forma:SolidPeso molecular:549.45D-4-77
D-4-77 is a potent inhibitor of SARS-CoV-2 Mpro, exhibiting an IC 50 of 0.95 μM, and possesses antiviral activity with an EC 50 of 0.49 μM.Fórmula:C23H34BrN3O5Pureza:98%Cor e Forma:SolidPeso molecular:512.44BMAP-28
CAS:BMAP-28, an antibiotic peptide, induces cell death by triggering the mitochondrial permeability transition pore and serves as a research tool in the study ofFórmula:C145H250N44O29Pureza:98%Cor e Forma:SolidPeso molecular:3073.81Cangorinine E-1
CAS:Cangorinine E-1 (compound 11), a dihydroagarofuran sesquiterpenoid derivative, exhibits weak inhibitory effects on herpes simplex virus type II (HSV) [1].
Fórmula:C43H49NO18Pureza:98%Cor e Forma:SolidPeso molecular:867.85Acryl42-10
Acryl42-10 serves as a covalent inhibitor for the SARS-CoV-2 Nsp14 N7-Methyltransferase, exhibiting an inhibition concentration (IC50) of 7 μM [1].Fórmula:C20H24ClN3O4Pureza:98%Cor e Forma:SolidPeso molecular:405.88SARS-CoV-2 Mpro-IN-7
SARS-CoV-2 Mpro-IN-7 (compound 6g) effectively inhibits SARS-CoV-2 main protease (Mpro) with an IC50 value of 8.8 μM and exhibits a cytotoxic concentration (Fórmula:C33H34Br2N3O5PPureza:98%Cor e Forma:SolidPeso molecular:743.42Xenopsin precursor fragment
CAS:Xenopsin precursor fragment, an antimicrobial peptide, exhibits both antibacterial/antifungal activity at concentrations ranging from 10 to 500 μg/mL and anti-Fórmula:C123H211N33O32Pureza:98%Cor e Forma:SolidPeso molecular:2664.19Z795161988
Z795161988 functions as an inhibitor targeting the SARS-CoV-2 Nsp14 N7-Methyltransferase, exhibiting an inhibitory concentration (IC50) of 2.2 μM [1].Fórmula:C16H12BrN3O4Pureza:98%Cor e Forma:SolidPeso molecular:390.19Antimalarial agent 33
Antimalarial agent 33 (compound 5g) exhibits antiplasmodial activity targeting both erythrocytic and hepatic stages of Plasmodium, with an effectivePureza:98%Cor e Forma:Odour SolidUNC9512
UNC9512 is a potent antagonist of the methyl-lysine reader protein 53BP1, which can be utilized to investigate the function of 53BP1 in DNA repair, gene editingFórmula:C31H34N6O3Pureza:98%Cor e Forma:SolidPeso molecular:538.64SARS-CoV-2-IN-49
SARS-CoV-2-IN-49 acts as an irreversible covalent inhibitor targeting the main protease of SARS-CoV-2 [1].Fórmula:C29H34FN5O4Pureza:98%Cor e Forma:SolidPeso molecular:535.61Cefuzonam
CAS:Cefazolin is a novel cephalosporin with anti-inflammatory activity and may be used in studies of respiratory tract infections and hepatobiliary infections.Fórmula:C16H15N7O5S4Pureza:97.79% - 99.60%Cor e Forma:SolidPeso molecular:513.59
