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(2.957 produtos)
- Antibiótico(920 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)
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Foram encontrados 5842 produtos de "Microbiologia/Virologia"
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SARS-CoV-2-IN-30
<p>SARS-CoV-2-IN-30: two-armed diphosphate benzene, antiviral IC50 0.6/6.9μM, disrupts membranes EC50 6.9μM.</p>Fórmula:C60H52O8P2Cor e Forma:SolidPeso molecular:963Griseoluteic acid
CAS:<p>Griseoluteic acid is a breakdown product of griseolutein A and B. Griseoluteic acid is a phenazine antibiotic and is originally isolated from S. griseoluteus.</p>Fórmula:C15H12N2O4Pureza:98%Cor e Forma:SolidPeso molecular:284.27Antiangiogenic agent 8
<p>Antiangiogenic agent 8 (Compound 3m) functions as both an antibacterial agent and an antiangiogenic compound. It shows minimum inhibitory concentrations (MIC) of 16, 8, 4, 16, and 8 μg/mL against E. coli, P. aeruginosa, B. subtilis, S. aureus, and C. glabrata, respectively, with minimum bactericidal concentrations (MBC) ranging from 32 to 64 μg/mL. This compound holds potential for applications in infection control and cardiovascular disease research.</p>Fórmula:C23H20ClNOSCor e Forma:SolidPeso molecular:393.929Antimalarial agent 42
<p>Compound 42 (Compound 2), an antimalarial agent, effectively inhibits Plasmodium falciparum during the asexual blood stages (IC 50 <0.5μM) and gametocytes (IC 50 is 0.14 μM).</p>Fórmula:C24H42N2Cor e Forma:SolidPeso molecular:358.6HDAC-IN-85
<p>HDAC-IN-85 (Compound 1) is an HDAC inhibitor capable of crossing the blood-brain barrier. It exhibits inhibitory effects on brain tumor cell lines and can induce acetylation, resulting in DNA double-strand breaks and promoting RAD51 ubiquitination, which disrupts the DNA repair process. HDAC-IN-85 is applicable in studies of glioblastoma.</p>Fórmula:C24H27FN4O5Cor e Forma:SolidPeso molecular:470.49Ikarugamycin
CAS:<p>Ikarugamycin, an antibiotic, is an inhibitor of clathrin-mediated endocytosis (CME).</p>Fórmula:C29H38N2O4Pureza:98%Cor e Forma:SolidPeso molecular:478.62CCOE-5
<p>CCOE-5 is a chalcone derivative with antimalarial activity, exhibiting an IC50 of 1.4 μg/mL against P. falciparum (3D7) and an IC50 of less than 5 μg/mL against P. falciparum (INDO). CCOE-5 shows potential for research in the anti-infective domain.</p>Fórmula:C34H31NO6Cor e Forma:SolidPeso molecular:549.61SARS-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:1006.96HIV-1 inhibitor-81
<p>HIV-1inhibitor-81 (Compound 14g) is an HIV-1 protease inhibitor with a Ki of 1.6 nM. This compound exhibits antiviral activity against HIV-1, with an EC50 value of 250 nM.</p>Fórmula:C32H44N2O8SCor e Forma:SolidPeso molecular:616.77Talaromycesone A
CAS:<p>Talaromycesone A, from Talaromyces, fights S. epidermidis & MRSA (IC50: 3.7 & 5.48 μM), inhibits AChE (IC50: 7.49 μM).</p>Fórmula:C29H24O11Cor e Forma:SolidPeso molecular:548.59-AMN
<p>9-AMN is an inhibitor of the SARS-CoV-2 papain-like protease (SARS-CoV-2 PLpro), effectively reducing its deubiquitinating (DUB) activity and protease activity, with IC50 values of 4.55 µM and 4.15 µM, respectively. Additionally, 9-AMN suppresses the replication of the SARS-CoV variants Delta and Omicron in Calu-3 cells, with IC50 values of 1.04 µM and 2.35 µM, respectively.</p>Fórmula:C23H28N4O7Cor e Forma:SolidPeso molecular:472.49Antiparasitic agent-24
<p>Antiparasitic agent-24 (Compound 14a) is an antiparasitic compound with EC50 values of 0.005 μM for L. maj, 0.069 μM for L. don, 0.82 μM for T. brucei, and 4.1 μM for T. cruzi.</p>Fórmula:C23H22ClN7O2SCor e Forma:SolidPeso molecular:495.98Magnesium silicate
CAS:<p>Mg silicate (MgO & SiO2) used in antacids, deodorizing, decolorizing & as antifungal.</p>Fórmula:MgO3SiCor e Forma:SolidPeso molecular:100.39Diaporthein 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>Fórmula:C20H28O6Cor e Forma:SolidPeso molecular:364.432,2-Dithiobis(Benzothiazole)
CAS:<p>2,2-Dithiobis(Benzothiazole) inhibits MAPK8 and Pseudomonas aeruginosa and is commonly used as an accelerator in rubber and plastic synthesis.</p>Fórmula:C14H8N2S4Pureza:99.33%Cor e Forma:SolidPeso molecular:332.49Nusinersen
CAS:<p>Nusinersen (nusinersen) is a antisense oligonucleotide (ASO) for the treatment of pediatric and adult spinal muscular atrophy (SMA) and increases SMN proteinss.</p>Pureza:98.62%Cor e Forma:Solid5'-O-DMT-PAC-dA
CAS:<p>5’-O-DMT-PAC-dA can be used in the synthesis of oligoribonucleotides[1].</p>Fórmula:C39H37N5O7Cor e Forma:SolidPeso molecular:687.74Doramectin monosaccharide
CAS:<p>Doramectin monosaccharide, an anthelmintic breakdown product, forms by acid hydrolysis of doramectin.</p>Fórmula:C43H62O11Cor e Forma:SolidPeso molecular:754.953'-Deoxyuridine-5'-triphosphate trisodium
<p>3'-dUTP trisodium, a nucleotide analogue, inhibits RNA polymerases I/II and UTP integration into RNA (Ki=2.0 μM).</p>Fórmula:C9H12N2Na3O14P3Cor e Forma:SoildPeso molecular:534.08Spm viii
CAS:<p>Spm viii is a derivative of the nucleoside antibiotic spicamycin that has antitumor activity.</p>Fórmula:C26H43N7O7Pureza:98%Cor e Forma:SolidPeso molecular:565.66AB-343
<p>AB-343 is a selective covalent inhibitor of SARS-CoV-2 Mpro with an IC50 of 8 nM and a Ki of 2.8 nM. It effectively inhibits the main protease of SARS-CoV-2 and several other coronaviruses and is active against some resistant variants. AB-343 can be utilized in research related to diseases associated with coronavirus infections.</p>Fórmula:C26H34F5N5O4Cor e Forma:SolidPeso molecular:575.57Kievitone
CAS:<p>Kievitone, an isoflavanone from Phaseolus vulgaris, has antifungal and antitumor properties.</p>Fórmula:C20H20O6Cor e Forma:SolidPeso molecular:356.37Myristoyl glutamic acid sodium
CAS:<p>Myristoyl glutamic acid sodium, a surfactant in amino acid cleansers, has mild antibacterial properties and cleanses the skin surface of excess oil and dirt.</p>Fórmula:C19H34NNaO5Pureza:99.91%Cor e Forma:SolidPeso molecular:379.47HR-568
<p>HR-568 displays broad-spectrum anti-enterovirus activity. It inhibits enterovirus strains EV-A71, E30, and CVA24 in MRC-5 cells, with EC50 values of 1.53 μM, 0.4 μM, and 1.22 μM, respectively. HR-568 targets the hydrophobic pocket on enterovirus capsid proteins, thereby hindering viral replication.</p>Fórmula:C24H18N4SCor e Forma:SolidPeso molecular:394.49Rugulosin
CAS:<p>Rugulosin (RUG) is a bis-anthraquinoid pigment produced by fungi.</p>Fórmula:C30H22O10Cor e Forma:SolidPeso molecular:542.496RdRP-IN-8
<p>RdRP-IN-8 (compound 45) is an antiviral agent targeting influenza viruses. It inhibits the viral RNA-dependent RNA polymerase (RdRP) activity by disrupting the heterodimerization of the PA and PB1 subunits, with an IC50 value of 0.13 μM.</p>Fórmula:C23H21N3O6SCor e Forma:SolidPeso molecular:467.49Lankacidinol
CAS:<p>Lankacidinol is an antibiotic that has antitumor and immunosuppressive activities.</p>Fórmula:C25H35NO7Pureza:98%Cor e Forma:SolidPeso molecular:461.55Rolusafine
CAS:<p>Rolusafine is an antifungal agent [1] .</p>Fórmula:C19H18N2O2Cor e Forma:SolidPeso molecular:306.36Nitroxynil
CAS:<p>Nitroxynil is an anthelmintic for adult/immature parasites, mainly used in Fasciola hepatica studies.</p>Fórmula:C7H3IN2O3Pureza:99.76%Cor e Forma:SolidPeso molecular:290.01Loloatin B 10
CAS:<p>Loloatin B 10 is a bioactive chemical.</p>Fórmula:C67H85N13O14Pureza:98%Cor e Forma:SolidPeso molecular:1296.494HIV-1 inhibitor-80
<p>HIV-1inhibitor-80 (compound M44) is an HIV-1 inhibitor with an EC50 of 5-148 nM. It demonstrates excellent metabolic stability and low cytotoxicity in human plasma and liver microsomes.</p>Fórmula:C26H19N7OCor e Forma:SolidPeso molecular:445.475BNM-III-170
CAS:<p>BNM-III-170 is able to inhibit HIV-1 viral entry into target cells.</p>Fórmula:C25H26ClF7N6O6Cor e Forma:SolidPeso molecular:674.96Aurodox
CAS:<p>Aurodox is a biochemical.</p>Fórmula:C44H62N2O12Cor e Forma:SolidPeso molecular:810.97Chevalone 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:456.61Malolactomycin C
CAS:<p>Malolactomycin C (compound 1) is a macrocyclic lactone antifungal antibiotic isolated from the Streptomyces strain KP-3144. It effectively inhibits Botrytis cinerea (gray mold), thereby controlling various plant diseases, including gray mold infections.</p>Fórmula:C62H109N3O20Cor e Forma:SolidPeso molecular:1216.54Antifungal agent 14
CAS:<p>Antifungal 14: potent, broad-spectrum, low-minimum inhibitory concentration.</p>Fórmula:C18H19N7O3Cor e Forma:SolidPeso molecular:381.396Aldgamycin E
CAS:<p>Aldgamycin E is a neutral macrolide antibiotic agent from culture filtrates of Streptomyces lavendulae. Methanolysis produces methyl algarosides A & B.</p>Fórmula:C37H58O15Pureza:98%Cor e Forma:SolidPeso molecular:742.856Anti-MRSA agent 4
<p>Compound 7a: potent, selective MRSA growth inhibitor; MIC ≤ 0.26 µM; non-cytotoxic, non-hemolytic.</p>Fórmula:C48H68F6N4O8Cor e Forma:SolidPeso molecular:943.07CC 1014
CAS:<p>CC 1014 is a polypeptide antibiotic isolated from Penicillium lilacinum that inhibits phosphorylation of ADP, Mg ATPase.</p>Fórmula:C62H111N11O13Pureza:98%Cor e Forma:SolidPeso molecular:1218.634Junceellolide C
CAS:<p>Junceellolide C: transcription inhibitor of cccDNA, curbs HBV DNA replication, EC50 of 5.19 & 3.52μM in HepAD38 cells, potent anti-HBV.</p>Fórmula:C26H33ClO10Cor e Forma:SolidPeso molecular:540.99Antileishmanial agent-30
<p>Compound 17k, also known as Antileishmanial agent-30, effectively inhibits Leishmania with an IC50 of 0.2 μM for L. donovani. It exhibits a CC50 of >100 μM and an SI of >500, indicating significant selectivity and potency.</p>Fórmula:C23H21N5O2Cor e Forma:SolidPeso molecular:399.45Tomopenem
CAS:<p>Tomopenem is a penem antibiotic.</p>Fórmula:C23H35N7O6SPureza:98%Cor e Forma:SolidPeso molecular:537.635'-O-DMT-N4-Bz-2'-F-dC
CAS:<p>5’-O-DMT-N4-Bz-2’-F-dC is a nucleoside with protective and modification effects.</p>Fórmula:C37H34FN3O7Cor e Forma:SolidPeso molecular:651.68Antifungal agent 78
<p>Antifungal agent 78 (compound 25am) exhibits potent activity, with an EC50 of 13.46 μM against Fusarium graminearum [1].</p>Fórmula:C18H12F2N2O2Cor e Forma:SolidPeso molecular:326.3Altromycin E
CAS:<p>Altromycin E is a new pluramycin-like antibiotic.</p>Fórmula:C46H57NO17Pureza:98%Cor e Forma:SolidPeso molecular:895.952Longistyline A
CAS:<p>Natural stilbene Longistyline A from Cajanus cajan leaves; antimicrobial against MRSA, MIC 1.56 μg/mL; neuroprotective.</p>Fórmula:C20H22O2Cor e Forma:SolidPeso molecular:294.39Octaethylene glycol monododecyl ether
CAS:<p>Octaethylene glycol monododecyl ether (C12E8) is a non-ionic surfactant and detergent, for assisting LOX activity assays and membrane protein extraction.</p>Fórmula:C28H58O9Pureza:97.30%Cor e Forma:SolidPeso molecular:538.7512R-LOX-IN-2
CAS:<p>12R-LOX-IN-2 is a 12R-LOX inhibitor that inhibits the hyperproliferation of psoriatic cells and can be used in the study of psoriasis and other skin diseases.</p>Fórmula:C19H13NOPureza:99.84%Cor e Forma:SolidPeso molecular:271.31IDR-1018 acetate
<p>IDR-1018 acetate is an innate defense regulator conjugate with a minimum inhibitory concentration (MIC) of 16 μg/mL against MRSA USA300 LAC, MRSA SAP 0017, and S. epidermidis ATCC14990. It serves a role in the synthesis of V-IDR1018 (vancomycin-innate defense regulator conjugate).</p>Fórmula:C71H126N26O12·xC2H4O2Cor e Forma:SolidLAH4
<p>Amphipathic peptide LAH4 forms a-helix, binds phospholipid membranes, and shows in vitro transfection on par with commercial reagents.</p>Fórmula:C132H228N38O27Pureza:98%Cor e Forma:SolidPeso molecular:2779.53
