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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Dermaseptin-S3
CAS:<p>Dermaseptin-S3 is an antimicrobial peptide originating from frog skin with activity against filamentous fungi [1].</p>Fórmula:C138H240N38O35SCor e Forma:SolidPeso molecular:3023.68Dactimicin sulfate
CAS:<p>Dactimicin is a new aminoglycoside. It also has in vitro activity, post-antibiotic effect, and interaction with other antibiotics.</p>Fórmula:C18H40N6O14S2Cor e Forma:SolidPeso molecular:628.67SARS-CoV-2-IN-11
CAS:<p>SARS-CoV-2-IN-11, potent non-toxic 3CLpro inhibitor, has IC50 of 0.17 nM and EC50 of 1.45 nM; promising for specific SARS-CoV-2 antivirals.</p>Fórmula:C27H39F2N3NaO8SCor e Forma:SolidPeso molecular:626.67Antiparasitic agent-14
<p>Antiparasitic agent-14: potent, cytotoxic, inhibits trypomastigote and amastigote growth.</p>Fórmula:C19H20N4OSCor e Forma:SolidPeso molecular:352.45Influenza A NP(366-374) Strain A/PR/8/35
CAS:<p>This peptide is an H2-Db-restricted epitope from the Influenza A/PR/8/34 nucleoprotein.</p>Fórmula:C38H63N11O18S2Pureza:98%Cor e Forma:SolidPeso molecular:1026.1Picoxystrobin
CAS:<p>Picoxystrobin, a strobilurin fungicide, halts mitochondrial respiration in plants by blocking electron transfer.</p>Fórmula:C18H16F3NO4Cor e Forma:SolidPeso molecular:367.32WJM280
<p>WJM280 is an orally active antimalarial compound with an EC50 of 0.04 μM against the parasite P. falciparum 3D7.</p>Fórmula:C22H25F3N2OCor e Forma:SolidPeso molecular:390.44PAT-LM1
<p>PAT-LM1 is a human monoclonal antibody that targets NRB54/NONO. It is applicable in the study of hematological malignancies.</p>Cor e Forma:Odour LiquidHinnuliquinone
CAS:Hinnuliquinone is an anti-HIV agent.Fórmula:C32H30N2O4Pureza:98%Cor e Forma:SolidPeso molecular:506.59SARS-CoV-2 3CLpro-IN-26
<p>SARS-CoV-2 3CLpro-IN-26 (Compound (S,R)-4y) is a conformational inhibitor of SARS-CoV-2 3CLpro with an IC50 of 0.43 μM. It demonstrates good cellular permeability, being able to effectively cross the cell membrane following co-incubation with Vero-E6 cells.</p>Fórmula:C24H18Cl3N3O3Cor e Forma:SolidPeso molecular:502.78BRD-9327
<p>BRD-9327 is an EfpA inhibitor that binds to the external vestibule, yet it does not entirely block the substrate's path to the outside, suggesting it may inhibit the movement necessary for the transporter's alternative pathway. BRD-9327 is applicable in tuberculosis research.</p>Cor e Forma:Odour SolidsPLA2 inhibitor 2
<p>sPLA2 inhibitor 2 (compound 6a) is an sPLA2 inhibitor with an IC50 value of 0.0475 μM, making it valuable for diabetes research.</p>Fórmula:C20H18N6O4S2Cor e Forma:SolidPeso molecular:470.52Cytochalasin A
CAS:<p>Cytochalasin A, a cell-penetrating fungal toxin, blocks HIV-1 protease (IC50 = 3 μM) and hinders actin and microtubule assembly. It's an antibiotic.</p>Fórmula:C29H35NO5Pureza:98%Cor e Forma:White Crystalline PowderPeso molecular:477.59Antileishmanial agent-33
<p>Antileishmanial agent-33 (4e) is a hybrid compound of grandisin and machilin G, demonstrating moderate activity against promastigotes with an IC50 of 38.1 μM. In studies of cutaneous leishmaniasis (CL), Antileishmanial agent-33 (4e) has shown potential as an antileishmanial agent.</p>Cor e Forma:Odour SolidAntifungal agent 51
CAS:<p>Antifungal 51 (5c) is effective against C. albicans, C. parapsilosis, C. tropicalis with MIC < 0.063 μg/mL; low cell toxicity, non-carcinogenic.</p>Fórmula:C18H16FN5OSCor e Forma:SolidPeso molecular:369.42Chartreusin
CAS:<p>Chartreusin is an antibiotic. It also has anticancer activity.</p>Fórmula:C32H32O14Pureza:98%Cor e Forma:SolidPeso molecular:640.59Sofosbuvir impurity H
<p>Sofosbuvir impurity H, an diastereoisomer of Sofosbuvir, is the impurity of Sofosbuvir.</p>Fórmula:C29H33FN3O10PPureza:98%Cor e Forma:SolidPeso molecular:633.565'-O-TBDMS-dA
CAS:<p>5’-O-TBDMS-dA is a modified nucleoside and can be used to synthesize DNA or RNA.</p>Fórmula:C16H27N5O3SiCor e Forma:SolidPeso molecular:365.509Maximin 15
<p>Maximin 15, an antimicrobial peptide originating from toad brain, exhibits activity against Staphylococcus aureus, Escherichia coli, and Bacillus subtilis, with</p>Fórmula:C121H211N33O34Cor e Forma:SolidPeso molecular:2672.17N-3-oxo-pentanoyl-L-Homoserine lactone
CAS:<p>N-3-oxo-pentanoyl-L-Homoserine lactone is a quorum sensing inhibitor for E. coli at 230 nM and activates V. fischeri luminescence at 20-200 nM.</p>Fórmula:C9H13NO4Cor e Forma:SolidPeso molecular:199.206KU13
CAS:<p>KU13 is an inhibitor of non-tuberculous mycobacteria (NTM), demonstrating minimum inhibitory concentrations (MIC) of 0.032-8 μg/mL against Mycobacterium and 2 μg/mL against E. coli. It is applicable in research focused on anti-infective treatments.</p>Fórmula:C58H92N6O17Cor e Forma:SolidPeso molecular:1145.38Ristocetin
CAS:<p>Ristocetin, an antibiotic from Amycolatopsis lurida, treated staph infections but was discontinued due to causing thrombocytopenia.</p>Fórmula:C95H110N8O44Pureza:98%Cor e Forma:SolidPeso molecular:2067.937Capoamycin
CAS:<p>Capoamycin is an insotatracine antibiotic investigated for anti tumor properties.</p>Fórmula:C35H38O10Pureza:98%Cor e Forma:SolidPeso molecular:618.679RK 1441B
CAS:<p>RK 1441B is a bacteriophage antibiotic related to neothramycin.</p>Fórmula:C13H14N2O5Pureza:98%Cor e Forma:SolidPeso molecular:278.26Acetyl-binankadsurin A
CAS:<p>Acetyl-binankadsurin A (compound 5), a lignan obtained from Kadsura longipedunculata, exhibits weak inhibitory effects on HIV-1 protease, demonstrating an IC50</p>Fórmula:C24H28O8Pureza:98%Cor e Forma:SolidPeso molecular:444.47Lipofermata
CAS:<p>Lipofermata is a fatty acid transport protein (FATP) inhibitor that prevents lipid transport to melanoma cells and reduces melanoma growth and invasion.</p>Fórmula:C15H10BrN3OSPureza:99.22% - 99.57%Cor e Forma:SolidPeso molecular:360.23ICeD-2
<p>ICeD-2 triggers death in HIV-1 infected cells, requires HIV protease, inhibits DPP8/9, and stabilizes DPP9 in PBMCs.</p>Fórmula:C20H29N3OCor e Forma:SolidPeso molecular:327.46Cefotiam hydrochloride
CAS:<p>Cefotiam hydrochloride is a third-gen cephalosporin that disrupts bacterial cell wall synthesis by inhibiting PBPs.</p>Fórmula:C18H23N9O4S3·2HClPureza:98.23%Cor e Forma:SolidPeso molecular:598.60Anticancer agent 262
<p>Anticanceragent 262 (compound 3h) is a DNA-intercalating antineoplastic agent with an IC50 value of 5.7 µM against A549 cancer cells.</p>Fórmula:C26H31N3OCor e Forma:SolidPeso molecular:401.544Ipomoeassin F
CAS:<p>Ipomoeassin F: Selective inhibitor of ER protein translocation, targeting Sec61α, blocks SARS-CoV-2 protein movement.</p>Fórmula:C44H62O15Cor e Forma:SolidPeso molecular:830.95RSV L-protein-6
<p>RSVL-protein-6 (Compound 19a) is an inhibitor of respiratory syncytial virus (RSV) polymerase, with an IC50 of 13 nM in an SPA primer extension-based enzymatic assay. It is capable of inhibiting RSV replication in HeLa cells.</p>Fórmula:C29H39ClN4O3Cor e Forma:SolidPeso molecular:527.098Cefotetan disodium
CAS:<p>Cefotetan Sodium: a 2nd-gen cephamycin antibiotic effective against various aerobic/anaerobic, gram+/- bacteria, inhibits cell wall synthesis.</p>Fórmula:C17H15N7Na2O8S4Cor e Forma:SolidPeso molecular:619.57WYFA-15
<p>WYFA-15 is an inhibitor of sphingomyelin synthase 1 (SMS1) that has been shown to protect mice from lethal SFTSV infection and reduce the replication and pathogenicity of SARS-CoV-2. WYFA-15 is applicable for antiviral research.</p>Fórmula:C22H16Cl2N2OCor e Forma:SolidPeso molecular:395.281PhoPS
<p>PhoPS is a photoactivatable β-lactamase inhibitor. Upon exposure to light, PhoPS releases the active β-lactamase inhibitor Sulbactam. This compound is capable of inhibiting the synthesis of bacterial cell walls and the formation of biofilms in Escherichia coli, thereby exhibiting antibacterial activity.</p>Fórmula:C42H57N5O17SCor e Forma:SolidPeso molecular:935.99Samandarone
CAS:<p>Samandarone is a major alkaloid from the European fire salamander (Salamandra salamandra terrestris).</p>Fórmula:C19H29NO2Cor e Forma:SolidPeso molecular:303.441-(4-AMinophenyl)-5,6-dihydro-3-(4-Morpholinyl)-2(1h)-pyridinone
CAS:<p>Antifungal 1-(4-AMinophenyl)-2(1h)-pyridinone inhibits Candida, Aspergillus, Pseudomonas, and Staphylococcus.</p>Fórmula:C15H19N3O2Pureza:99.79%Cor e Forma:SolidPeso molecular:273.33Ro 09-1428
CAS:<p>Ro 09-1428, a parenteral cephalosporin, has high antipseudomonal activity.</p>Fórmula:C31H31N11O10S3Cor e Forma:SolidPeso molecular:813.84RS 49676
CAS:<p>RS 49676 is an N-substituted imidazole.</p>Fórmula:C25H28ClN3O5Cor e Forma:SolidPeso molecular:485.96SID-852843
CAS:<p>SID-852843, WNV NS2B-NS3 protease inhibitor, IC50: 0.105 μM, useful in viral infection studies.</p>Fórmula:C17H15N3O5SPureza:97.19%Cor e Forma:SolidPeso molecular:373.38SARS-CoV-2-IN-29
<p>SARS-CoV-2-IN-29: diphosphate ester, benzene, molecular tweezers; IC50: 1.5-1.6 μM; disrupts membranes, EC50: 3.0 μM. Antiviral.</p>Fórmula:C58H48O8P2Cor e Forma:SolidPeso molecular:934.94Himastatin
CAS:<p>Himastatin, an antitumor antibiotic from S. hygroscopicus, is a dimeric cyclohexadepsipeptide with piperazic acid and a unique aromatic core.</p>Fórmula:C72H104N14O20Cor e Forma:SolidPeso molecular:1485.68CI-39
CAS:<p>CI-39, an NNRTI with EC50 of 3.40 µM, inhibits HIV-1 reverse transcriptase and RNase H, with CC50 >30 µM.</p>Fórmula:C19H18N2O4Cor e Forma:SolidPeso molecular:338.36L 685818
CAS:<p>L 685818 is the C18-hydroxy, C21-ethyl of FK-506 analog.</p>Fórmula:C43H69NO13Cor e Forma:SolidPeso molecular:808.019Janthitrem G
CAS:<p>Janthitrem G is a type of naphthopyran. Janthitrem G is obtained from Penicillium janthinellum. Tremorgenic mycotoxi.</p>Fórmula:C39H51NO6Cor e Forma:SolidPeso molecular:629.838HIV-IN-2
CAS:<p>HIV-IN-2 (Compound 100) is a potent inhibitor of HIV, showing potential for research into HIV infection [1].</p>Fórmula:C34H27ClF7N9O3SCor e Forma:SolidPeso molecular:810.14Paldimycin B
CAS:<p>Paldimycin B is a semi-synthetic antibiotic.</p>Fórmula:C43H62N4O23S3Pureza:98%Cor e Forma:SolidPeso molecular:1099.15Cladospirone bisepoxide
CAS:<p>Cladospirone bisepoxide, a fungal metabolite, is a selective antibiotic that also hinders L. sativum germination.</p>Fórmula:C20H14O7Cor e Forma:SolidPeso molecular:366.32Amphotericin B methyl ester hydrochloride
CAS:<p>Amphotericin B methyl ester hydrochloride, an antifungal and anti-HIV cholesterol binder, is a methyl ester of Amphotericin B.</p>Fórmula:C48H76ClNO17Cor e Forma:SolidPeso molecular:974.57Cletoquine
CAS:<p>Cletoquine, Hydroxychloroquine's active metabolite, fights CHIKV, has antimalarial properties, and may treat autoimmune diseases.</p>Fórmula:C16H22ClN3OPureza:99.95% - 99.98%Cor e Forma:SolidPeso molecular:307.82AAP4
<p>AAP4 is a potent inhibitor of OfChi-h and OfHex1, exhibiting Ki values of 29.3 nM and 4.9 μM, respectively. It also demonstrates insecticidal activity against the lepidopteran pest Ostrinia furnacalis.</p>Fórmula:C21H23BrClN7Cor e Forma:SolidPeso molecular:488.811
