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(2.966 produtos)
- Antibiótico(922 produtos)
- Antifecção(23 produtos)
- DHFR(33 produtos)
- Síntese de DNA/RNA(710 produtos)
- HBV(177 produtos)
- HIV Protease(450 produtos)
- HSV(91 produtos)
- Integrase(2 produtos)
- Ribossomo(13 produtos)
Exibir 2 mais subcategorias
Foram encontrados 5858 produtos de "Microbiologia/Virologia"
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Amythiamicin D
CAS:<p>Amythiamicin D is a thiopeptide antibiotic that effectively inhibits the growth of various Gram-positive bacteria, but it is ineffective against Gram-negative bacteria such as Escherichia coli.</p>Fórmula:C43H42N12O7S6Cor e Forma:SolidPeso molecular:1031.26Arylomycin B1
CAS:<p>Arylomycin B1 is a lipid hexapeptide antibiotic (antibiotic) effective against Gram-positive bacteria.</p>Fórmula:C41H57N7O13Cor e Forma:SolidPeso molecular:855.93Lorutengitide
CAS:<p>Lorutengitide is a transcription-regulating peptide with antiproliferative activity.</p>Fórmula:C30H50N8O12Cor e Forma:SolidPeso molecular:714.764SARS-CoV-2 3CLpro-IN-19
<p>SARS-CoV-2 3CLpro-IN-19 (Compound C5a), a non-covalent, non-peptide inhibitor of the SARS-CoV-2 3CLpro enzyme, exhibits potent in vitro activity with an IC50 of</p>Fórmula:C24H22ClN3O2SPureza:98%Cor e Forma:SolidPeso molecular:451.97wrwyar-NH2 TFA
<p>wrwyar-NH2 (TFA) serves as the control peptide for wrwycr-NH2.</p>Cor e Forma:Odour SolidArylomycin A4
CAS:<p>Arylomycin A4 is a lipopeptide antibiotic (antibiotic) effective against Gram-positive bacteria.</p>Fórmula:C43H62N6O11Cor e Forma:SolidPeso molecular:838.986E07 aptamer
<p>SARS-CoV-2 nsp14-IN-4 (Compound 12q) is a selective inhibitor of the SARS-CoV-2 nsp14 methyltransferase with an IC50 of 19 ± 2.5 nM.</p>Pureza:98%Cor e Forma:Odour SolidNPD-2975
<p>NPD-2975 (compound 30) is an orally active antitrypanosomal agent effective against Human African Trypanosomiasis (HAT), demonstrating acceptable metabolic</p>Fórmula:C14H13FN4OPureza:98%Cor e Forma:SolidPeso molecular:272.28HOE 33187-O-CONH-PEG4-phenol-thiophenone-NHPh-COOEt
CAS:<p>HOE 33187-O-CONH-PEG4-phenol-thiophenone-NHPh-COOEt inhibits pre-miR-21 RNA, potential for cancer research.</p>Fórmula:C57H62N8O10SCor e Forma:SolidPeso molecular:1051.21Pezadeftide
CAS:<p>Pezadeftide, a potent antifungal peptide, readily penetrates fungal cells, eliciting an immediate mitochondrial response that leads to hyperpolarization of the</p>Pureza:98%Cor e Forma:SolidRO7196472
CAS:RO7196472 is a potent macrocyclic peptide antibiotic that selectively inhibits the activity of Acinetobacter strains. It targets the lipopolysaccharide (LPS) binding site on the inner membrane's LptB2FG complex, inhibiting lipopolysaccharide transport and thereby suppressing the activity of Acinetobacter strains.Fórmula:C41H49ClN10O3SCor e Forma:SolidPeso molecular:797.41SARS-CoV-2 nsp14-IN-4
<p>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-19</p>Fórmula:C31H27N7O6SPureza:98%Cor e Forma:SolidPeso molecular:625.65Antitrypanosomal 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:889.21SARS-CoV-2-IN-30 disodium
<p>SARS-CoV-2-IN-30 disodium: antiviral diphosphate ester, IC50 0.6/6.9 μM against virus/spike transduction, disrupts liposomal membranes (EC50 6.9 μM).</p>Fórmula:C60H50Na2O8P2Cor e Forma:SolidPeso molecular:1006.96Antileishmanial agent-19
<p>Compound F27 (Antileishmanial agent-19) is an antileishmanial compound effective against L.</p>Fórmula:C22H18N4O3Pureza:98%Cor e Forma:SolidPeso molecular:386.4MPI60
<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:441.52Chevalone B
CAS:<p>Chevalone B, a meroterpenoid from E. chevalieri fungus, is cytotoxic with IC50s: KB cells 2.9 μg/ml, NCI-H187 9.8 μg/ml.</p>Fórmula:C28H40O5Cor e Forma:SolidPeso molecular:456.61Wulfenioidin 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:328.45Thrazarine
CAS:<p>Thrazarine is a new antitumor antibiotic agent produced by Streptomyces coerulescens MH802-fF5.</p>Fórmula:C7H11N3O5Pureza:98%Cor e Forma:SolidPeso molecular:217.18HBV-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:412.84MptpB-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:479.54HSV-gB2 (498-505)
CAS:This is the immunodominant epitope gB-8p from herpes simplex virus (HSV) glycoprotein B (gB), amino acids 498 to 505.Fórmula:C41H67N11O13Pureza:98%Cor e Forma:SolidPeso molecular:922.04SARS-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 Solid10-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:434.39NSC89641
<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:522.38Lenapenem
CAS:<p>Lenapenem is a broad-spectrum, carbapenem antibiotic with bactericidal activity by weakens the bacterial cell wall and leads to lytic cell death.</p>Fórmula:C18H29N3O5SCor e Forma:SolidPeso molecular:399.51Simaravibart
<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 LiquidCephalonium
CAS:<p>Cephalonium (Cefalonium) is a first-generation cephalosporin antibiotic.</p>Fórmula:C20H18N4O5S2Pureza:98.17%Cor e Forma:SolidPeso molecular:458.51Anticancer agent 140
<p>Compound 140 (Compd 3) exhibits potential anticancer and antiparasitic activities [1].</p>Fórmula:C20H26N2OPureza:98%Cor e Forma:SolidPeso molecular:310.43SARS-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:456.46Antileishmanial 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-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:493.53SARS-CoV-2 3CLpro-IN-25
<p>SARS-CoV-2 3CLpro-IN-25 (compound 56) effectively inhibits the SARS-CoV-2 3CLpro enzyme, exhibiting an IC50 value of 70 nM, and demonstrates cellular antiviral activity with an EC50 of 3.1 μM.</p>Fórmula:C17H14N2O3SCor e Forma:SolidPeso molecular:326.375'-O-DMTr-N4-Fmoc-5-Me-dC-phosphoramidite
CAS:<p>5'-O-DMTr-N4-Fmoc-5-Me-dC-phosphoramidite is a Nucleoside Phosphoramidite.</p>Fórmula:C55H60N5O9PCor e Forma:SolidPeso molecular:966.07EDTA, Disodium Salt, Dihydrate
CAS:<p>EDTA disodium dihydrate chelates metals, inhibits proteases, and aids in protein purification; doesn't affect cellulase.</p>Fórmula:C10H18N2Na2O10Pureza:99.97%Cor e Forma:SolidPeso molecular:372.24Lumefantrine-d18
CAS:<p>Lumefantrine D18 is an antimalarial drug, and is the deuterium labeled Lumefantrine.</p>Fórmula:C30H32Cl3NOPureza:98%Cor e Forma:SolidPeso molecular:547.055'-DMTr-dA(Bz)-Methyl phosphonamidite
CAS:<p>5'-DMTr-dA(Bz)-Methyl phosphonamidite is a Nucleoside Derivative - phosphonamidite.</p>Fórmula:C45H51N6O6PCor e Forma:SolidPeso molecular:802.9N-Butanoyl-DL-homoserine lactone
CAS:N-Butanoyl-DL-homoserine lactone aptamers blocks qurom sensing and inhibits biofilm formation in Pseudomonas aeruginosa.Fórmula:C8H13NO3Pureza:98%Cor e Forma:SolidPeso molecular:171.19Cephalexin hydrochloride
CAS:<p>Cefalexin hydrochloride is a cephalosporin antibiotic.</p>Fórmula:C16H18ClN3O4SPureza:98%Cor e Forma:SolidPeso molecular:383.85RNase L-IN-1
<p>RNase L-IN-1 is an RNase L inhibitor with potential anticancer activity and inhibits viral replication.</p>Fórmula:C27H35FN6O3SPureza:98.55%Cor e Forma:SolidPeso molecular:542.67Torcitabine
CAS:<p>Torcitabine is useful against the hepatitis B virus.</p>Fórmula:C9H13N3O4Cor e Forma:SolidPeso molecular:227.22Sulfadiazine-d4
CAS:<p>Sulfadiazine D4 is a deuterium labeled Sulfadiazine. Sulfadiazine used for the treatment of toxoplasmosis.</p>Fórmula:C10H10N4O2SPureza:98%Cor e Forma:SolidPeso molecular:254.34-(tert-Butyl)-benzhydroxamic Acid
CAS:4-t-Butyl-benzhydroxamic Acid: PqsR antagonist, IC50 of 12.5 μM (E. coli), 23.6 μM (P. aeruginosa), lowers pyocyanin with IC50 87.2 μM.Fórmula:C11H15NO2Cor e Forma:SolidPeso molecular:193.24Sulfathiazole-d4
CAS:<p>Sulfathiazole D4 is a deuterium labeled Sulfathiazole. Sulfathiazole used as a short-acting sulfonamide antibiotic.</p>Fórmula:C9H9N3O2S2Pureza:98%Cor e Forma:SolidPeso molecular:259.34Acetyllovastatin
CAS:Acetyllovastatin inhibits acetylcholinesterase (IC50: 79 μg/mL), has antifungal properties, and hinders cancer cell growth.Fórmula:C26H38O6Cor e Forma:SolidPeso molecular:446.58Stilbamidine dihydrochloride
CAS:<p>Stilbamidine dihydrochloride blocks nerve signals, studied by tracking its distribution in rat organs post-injection.</p>Fórmula:C16H18Cl2N4Pureza:98%Cor e Forma:SolidPeso molecular:337.25H-Lys-Trp-Lys-OH
CAS:<p>H-Lys-Trp-Lys-OH is a small molecule peptide that shows antibacterial and antiviral activities.</p>Fórmula:C23H36N6O4Cor e Forma:SolidPeso molecular:460.57DMTr-LNA-G(iBu)-3'-CED-phosphoramidite
CAS:<p>Nucleoside Derivatives - LNA-related nucleosides; Nucleoside Phosphoramidites</p>Fórmula:C45H54N7O9PCor e Forma:SolidPeso molecular:867.93DMTr-TNA-5MeU-amidite
CAS:<p>DMTr-TNA-5MeU-amidite is a Nucleoside Phosphoramidite.</p>Fórmula:C39H47N4O8PCor e Forma:SolidPeso molecular:730.799-Propenyladenine
CAS:9-Propenyladenine is a mutagenic impurity in tenofovir disoproxil fumarate.Fórmula:C8H9N5Cor e Forma:SolidPeso molecular:175.19
