Microbiologie/Virologie
Les inhibiteurs en microbiologie et virologie sont des composés qui ciblent les microorganismes, y compris les bactéries, les virus et les champignons, perturbant leur croissance, leur réplication ou leur survie. Ces inhibiteurs sont essentiels pour étudier la pathogénie microbienne, comprendre les mécanismes de résistance et développer de nouvelles thérapies antimicrobiennes et antivirales. Les inhibiteurs de cette catégorie sont utilisés pour combattre les maladies infectieuses, explorer l'écologie microbienne et étudier les interactions hôte-pathogène. Chez CymitQuimica, nous offrons une large sélection d'inhibiteurs de haute qualité en microbiologie et virologie pour soutenir vos recherches en maladies infectieuses, microbiologie et virologie.
Sous-catégories appartenant à la catégorie "Microbiologie/Virologie"
- Antibactérien(2.968 produits)
- Antibiotique(922 produits)
- Antifection(23 produits)
- DHFR(33 produits)
- Synthèse ADN/ARN(711 produits)
- VHB(177 produits)
- Protéase du VIH(451 produits)
- HSV(91 produits)
- Intégrase(2 produits)
- Ribosome(13 produits)
Affichez 2 plus de sous-catégories
5863 produits trouvés pour "Microbiologie/Virologie"
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Fenbutatin oxide
CAS :<p>Fenbutatin oxide is an organometallic insecticide chemical. It mainly used in agricultural practices to kill ticks and mites.</p>Formule :C60H78OSn2Degré de pureté :98%Couleur et forme :White Crytalline Powder Fenbutatin Oxide Is A White Crystalline Solid With A Mild OdorMasse moléculaire :1052.68A2315A
CAS :<p>A2315A is an antibiotic.</p>Formule :C26H37N3O7Couleur et forme :SolidMasse moléculaire :503.59ent-Heronamide C
<p>Ent-Heronamide C possesses antifungal properties and is utilized as a probe for analyzing the mode of action of heronamide C [1].</p>Formule :C29H41NO3Couleur et forme :SolidMasse moléculaire :451.64AcrAP2
<p>AcrAP2 is an antimicrobial peptide found in the venom of the Arabian scorpion (Androctonus crassicauda). It exhibits inhibitory effects on Gram-positive bacteria and yeast while generally showing no activity against Gram-negative bacteria. The cationic-enhanced analogue of AcrAP2 (AcrAP2a) has demonstrated significant antiproliferative effects on certain human cancer cell lines at low concentrations. AcrAP2 holds potential for research in antibacterial and antitumor applications.</p>Formule :C95H149N21O22Masse moléculaire :1936.11861Ivermectin B1a monosaccharide
CAS :<p>Ivermectin B1a monosaccharide, a hydrolysis product, inhibits nematode larvae and detects ivermectin resistance.</p>Formule :C41H62O11Couleur et forme :SolidMasse moléculaire :730.936Demethyl bleomycin A2
CAS :<p>Demethyl bleomycin A2 is a Bleomycin congener. The DNA cleavage of demethyl bleomycin A2 is insensitive to the presence of 5-Methylcytidine [1] .</p>Formule :C54H81N17O21S3Couleur et forme :SolidMasse moléculaire :1400.52Fobrepodacin
CAS :<p>Fobrepodacin (SPR720) is an orally active and potent phosphate prodrug of SPR719 (VXc-486). Fobrepodacin has potent bactericidal activities in vivo.</p>Formule :C21H26FN6O6PCouleur et forme :SolidMasse moléculaire :508.44pBD-1 TFA (206367-33-1 free base)
pBD-1 TFA is an endogenous and constitutively expressed antimicrobial peptide (AMP) from porcine tissues, has antimicrobial activities and contributes toFormule :C312H544F3N91O75S11Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :7180DENV ligand 2
<p>DENV ligand 2 is a ligand for the DENV E protein. It is used in the synthesis of the PROTAC degrader ZXH-8-004 and serves as the active form of DENV ligand 1.</p>Formule :C19H12F6N4O4Masse moléculaire :474.07627Cyclacillin
CAS :Cyclacillin (Wy-4508), an oral aminopenicillin, fights many gram-positive/negative bacteria.Formule :C15H23N3O4SCouleur et forme :SolidMasse moléculaire :341.43Nornidulin
CAS :Nornidulin, a depsidone from A. nidulans, fights various bacteria, fungi, MRSA (MIC=2 μg/ml), and has larvicidal (LC50=1.7 μg/ml) and cytotoxic properties.Formule :C19H15Cl3O5Couleur et forme :SolidMasse moléculaire :429.67LBM-415
CAS :<p>LBM-415 is a peptide deformylase (PDF) inhibitor.</p>Formule :C18H25FN4O5Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :396.41Antimicrobial agent-26
<p>Antimicrobial agent-26 is a powerful antimicrobial that has demonstrated the ability to counteract antibiotic resistance in vitro [1].</p>Couleur et forme :Odour Solidβ-Cedrene
CAS :<p>β-Cedrene ((+)-β-Cedrene), a sesquiterpene isolated from both Centaurea kotschyi var. kotschyi and Centaurea kotschyi var. decumbens, exhibits a broad range of biological activities, including antibacterial, anti-inflammatory, antispasmodic, tonic, diuretic, sedative, insecticidal, and antifungal properties. Additionally, β-Cedrene acts as a potent competitive inhibitor of the CYP2B6-mediated bupropion hydroxylase activity, demonstrating a K i value of 1.6 μM [1] [2].</p>Formule :C15H24Couleur et forme :SolidMasse moléculaire :204.35Apramycin (Nebramycin II)
CAS :<p>Apramycin: a veterinary aminoglycoside antibiotic, blocks translocation, binds to eukaryotic/bacterial RNA despite differing key residues.</p>Formule :C21H41N5O11Couleur et forme :SolidMasse moléculaire :539.58A-39183A
CAS :A-39183A, from Streptomyces NRRL 12049, targets penicillin-resistant S. aureus & S. faecalis (MICs 32 μg/ml), plus other anaerobes (MICs 16-128 μg/ml).Formule :C34H30O10Couleur et forme :SolidMasse moléculaire :598.604Aureothricin
CAS :<p>Aureothricin: DTP antibiotic from Streptomyces, broad-spectrum, inhibits HUVEC adhesion to vitronectin.</p>Formule :C9H10N2O2S2Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :242.32Antibacterial agent 128
<p>Antibacterial 128, a siderophore-Ciprofloxacin blend with cleavable linker, targets P. aeruginosa and B. pseudomallei.</p>Formule :C26H25FN4O9Couleur et forme :SolidMasse moléculaire :556.5RNA polymerase II-IN-2
<p>RNA Pol II-IN-2 (20iii) strongly inhibits Pol II (Ki=9.5 nM), is more toxic to CHO/HEK293 than α-amanitin.</p>Formule :C41H58N10O12SCouleur et forme :SolidMasse moléculaire :915.022'-Deoxy-2'-fluoroadenosine 5'-triphosphate tetralithium
<p>2'-Deoxy-2'-fluoroadenosine 5'-triphosphate tetralithium, an ATP analog, exhibits robust mixed-type inhibition of poly(AU) synthesis.</p>Formule :C10H11FLi4N5O12P3Couleur et forme :SolidMasse moléculaire :532.9Anguinomycin A
CAS :<p>Anguinomycin A, an antibiotic from Streptomyces, is like leptomycin B, kills mouse leukemia cells, and fights lung cancer in mice.</p>Formule :C31H44O6Couleur et forme :SolidMasse moléculaire :512.6875'-O-DMT-ibu-dC
CAS :<p>5'-O-DMT-ibu-dC can be used in the synthesis of oligodeoxyribonucleotides.</p>Formule :C34H37N3O7Couleur et forme :SolidMasse moléculaire :599.67SARS-CoV-2-IN-98
<p>SARS-CoV-2-IN-98 (compound 38) is a SARS-CoV-2 inhibitor with a dissociation constant (Kd) of 0.73 μM, utilized in research on COVID-19.</p>Couleur et forme :Odour SolidPMAP-23
CAS :<p>PMAP-23 is an antimicrobial peptide (AMP) with biological activity, derived from porcine myeloid cells.</p>Formule :C140H230N44O27Couleur et forme :SolidMasse moléculaire :2961.6Glycoprotein (276-286)
CAS :<p>Known Db-restricted peptide of lymphocytic choriomeningitis virus (LCMV).</p>Formule :C46H70N12O17SDegré de pureté :98%Couleur et forme :SolidMasse moléculaire :1095.18VIR-7229
<p>VIR-7229 is a human IgG1 monoclonal antibody that targets the Receptor-Binding Domain (RBD) of the Spike glycoprotein. It exhibits antiviral activity by competing with ACE2 for binding and inducing the shedding of the S1 protein. VIR-7229 is applicable for research on SARS-CoV-2 infections. Recommended isotype control: Human IgG1 kappa, Isotype Control.</p>Couleur et forme :Odour LiquidTAPI 2
CAS :<p>ADAM-17 inhibitor with Ki of 120 nM, enhances 5-FU lethality in cancer stem cells, prevents TNF-α release.</p>Formule :C19H37N5O5Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :415.54Isariin B
CAS :<p>Isariin B is a new cyclodepsipeptide isolated from the entomopathogenic fungus Beauveria felina.</p>Formule :C30H53N5O7Couleur et forme :SolidMasse moléculaire :595.77SARS-CoV-2-IN-23 disodium
<p>SARS-CoV-2-IN-23 disodium is an antiviral diphosphate ester, inhibiting SARS-CoV-2 at 8.2μM and its spike at 2.6μM, while disrupting membranes at 4.4μM.</p>Formule :C52H50Na2O8P2Couleur et forme :SolidMasse moléculaire :910.88A 83016A
CAS :<p>A 83016A is a kinamycin-type antibiotic.</p>Formule :C28H28N2O10Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :552.536Spectinamide 1599
CAS :<p>Spectinamide-1599 is a combination partner for anti-tuberculosis therapy.</p>Formule :C21H31ClN4O7Couleur et forme :SolidMasse moléculaire :486.95L 754394
CAS :<p>L 754394 is an effective and specific inhibitor of the HIV-1 protease.</p>Formule :C38H47N5O5Couleur et forme :SolidMasse moléculaire :653.81Influenza HA (126-138)
CAS :<p>Influenza HA (126-138), a peptide from the virus's HA protein, induces apoptosis in T-cells.</p>Formule :C52H81N19O22Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :1324.31Cefoperazone dihydrate
CAS :<p>Cefoperazone dihydrate, a semi-synthetic cephalosporin, exhibits a wide range of antibacterial properties.</p>Formule :C25H27N9O8S2Couleur et forme :SolidMasse moléculaire :645.67Ropidoxuridine
CAS :<p>Ropidoxuridine (IPdR), a novel oral prodrug, is a halogenated thymidine analogue that may sensitize human tumors.</p>Formule :C9H11IN2O4Degré de pureté :97.07%Couleur et forme :SolidMasse moléculaire :338.1Antibacterial agent 256
CAS :Antibacterialagent 256 (Compound C09) is an inhibitor of Type I signal peptidase (SPase I). It targets Gram-positive bacteria, effectively inhibiting S. aureus ATCC 29213, E. faecium QF31, E. faecalis SF23-1, and S. suis P1/7, with MIC values ranging from 1-16 μg/mL. In cancer cells HEp-2 and Caco-2, Antibacterialagent 256 exhibits cytotoxicity with CC50 values of 14.65 μg/mL and 21.93 μg/mL, respectively. Additionally, it shows hemolytic activity on mouse red blood cells with an HC50 of 13.29 μg/mL and can improve MRSA skin infections in mouse models.Formule :C27H19ClF3NO2SCouleur et forme :SolidMasse moléculaire :513.96Cytochalasin R
CAS :<p>Cytochalasin R (compound 17), an analogue of cytochalasin, is derived from the endophytic fungus Phomopsis sp.</p>Formule :C28H39NO5Couleur et forme :SolidMasse moléculaire :469.61Trypanothione synthetase-IN-3
CAS :<p>Trypanothione synthetase-IN-3: noncompetitive TryS inhibitor, Ki: 0.8 μM, useful in parasite research.</p>Formule :C68H54O43Couleur et forme :SolidMasse moléculaire :1559.13Diaporthein B
CAS :<p>Diaporthein B, a potent pimarane diterpene, inhibits M. tuberculosis (MIC: 3.1 μg/mL) and combats colon cancer cells (IC50: 1.5-3 μM/L).</p>Formule :C20H28O6Couleur et forme :SolidMasse moléculaire :364.43AL-611
CAS :<p>AL-611 is an HCV NS5B polymerase inhibitor ( EC 50 = 5 nM).</p>Formule :C25H33F2N6O8PCouleur et forme :SolidMasse moléculaire :614.5444-Methoxycoumarine
CAS :<p>4-Methoxycoumarine has antitumour effects.</p>Formule :C10H8O3Degré de pureté :99.64%Couleur et forme :SolidMasse moléculaire :176.17Tetromycin B
CAS :<p>Tetromycin B was isolated from Streptomyces axinellae Pol001T cultivated from the Mediterranean sponge Axinella polypoides.</p>Formule :C34H46O5Couleur et forme :SolidMasse moléculaire :534.737CMV pp65 (415-429)
CAS :CMVpp65 (415-429) is a CEF control peptide derived from cytomegalovirus (CMV).Formule :C38H67N13O13SCouleur et forme :SolidMasse moléculaire :946.08Thio-ITP
CAS :<p>Thio-ITP (6-Thioinosine 5'-triphosphate) inhibits RNA polymerases I & II with Ki of 40.9 & 38.0 μM.</p>Formule :C10H15N4O13P3SCouleur et forme :SolidMasse moléculaire :524.23Sordarin sodium
CAS :<p>Sordarin, from S. araneosa, inhibits fungal EF-2 protein synthesis; effective against C. albicans with varying potency on other species.</p>Formule :C27H40NaO8Couleur et forme :SolidMasse moléculaire :515.599RK 1441B
CAS :<p>RK 1441B is a bacteriophage antibiotic related to neothramycin.</p>Formule :C13H14N2O5Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :278.26MPD2
<p>MPD2 is a PROTAC compound based on a Cereblon-binding ligand that degrades the main protease MPro of SARS-CoV-2. In 293T cells, it effectively reduces MPro protein levels with a DC50 of 296 nM and shows time-dependent activity. MPD2 exhibits strong antiviral properties against various SARS-CoV-2 strains and has increased potency against Nirmatrelvir-resistant variants. It holds potential for researching SARS-CoV-2 diseases.</p>Formule :C51H68N6O13Masse moléculaire :972.48444MBL-IN-2
MBL-IN-2 ((2R, 2R')-5αC) is a Metallo-β-lactamase (MBL) inhibitor that effectively inhibits New Delhi Metallo-β-lactamase-1 (NDM-1) with an IC50 of 0.3 μM. MBL-IN-2 ((2R, 2R')-5αC) can be used in research on resistance to β-lactam antibiotics.Formule :C9H12F3NO3SMasse moléculaire :271.049Orfamide A
CAS :<p>Orfamide A, a lipopeptide biosurfactant isolated from P. protegens, exhibits multifaceted bioactivity. With an LC50 of 34.5 μg/ml, it significantly increases mortality in adult green peach aphids. Additionally, at a concentration of 50 μM, Orfamide A inhibits appressoria formation in M. oryzae isolates and decreases the prevalence of sporulating blast lesions in M. oryzae-infected plants. Furthermore, it demonstrates efficacy against T. b. brucei, with an IC50 value of 6 µM.</p>Formule :C64H114N10O17Couleur et forme :SolidMasse moléculaire :1295.67BNM-III-170
CAS :<p>BNM-III-170 is able to inhibit HIV-1 viral entry into target cells.</p>Formule :C25H26ClF7N6O6Couleur et forme :SolidMasse moléculaire :674.96
