
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)
Exibir 2 mais subcategorias
Foram encontrados 5842 produtos de "Microbiologia/Virologia"
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SARS-CoV-2 Mpro-IN-27
<p>SARS-CoV-2 Mpro-IN-27 (Compound 4h) is an effective inhibitor of SARS-CoV-2 Mpro.</p>Fórmula:C22H16N4OCor e Forma:SolidPeso molecular:352.39Deoxyfusapyrone
CAS:<p>Deoxyfusapyrone, an antifungal α-pyrone, combats C. neoformans and Aspergillus species; ineffective against yeast and B. megaterium.</p>Fórmula:C34H54O8Cor e Forma:SolidPeso molecular:590.79Toonaciliatin M
<p>Toonaciliatin M is a useful organic compound for research related to life sciences and the catalog number is T123902.</p>Fórmula:C20H32O3Cor e Forma:SolidPeso molecular:320.473Tropodithietic acid
CAS:<p>Tropodithietic acid, a sulfur-based antibiotic from Phaeobacter inhibens, targets many bacteria types.</p>Fórmula:C8H4O3S2Pureza:98%Cor e Forma:SolidPeso molecular:212.25Mpro/PLPro-IN-2
<p>Mpro/PLPro-IN-2 (Compound 22l) is a non-covalent competitive dual inhibitor of SARS-CoV-2's papain-like protease and main protease, exhibiting a Ki of 0.2 μM for the papain-like protease and 1.1 μM for the main protease. Mpro/PLPro-IN-2 is applicable in research related to anti-SARS-CoV-2 efforts.</p>Cor e Forma:Odour SolidWAY-299017
CAS:<p>WAY-299017 is a potent and selective UPPS inhibitor for the treatment of bacterial infections.</p>Fórmula:C17H14N2O3Pureza:97.01%Cor e Forma:SolidPeso molecular:294.32'-(2-Nitrobenzyl)-ATP trisodium
<p>2'-(2-Nitrobenzyl)-ATP trisodium is an rATP analogue that acts as a transcription terminator. It inhibits T7 RNA polymerase from continuing RNA chain extension.</p>Fórmula:C17H18N6Na3O15P3Cor e Forma:SolidPeso molecular:707.97361Mtb-IN-5
<p>Mtb-IN-5 (compound (-)17j) is an isoxazole exhibiting anti-Mycobacterium tuberculosis (Mtb) activity.</p>Fórmula:C24H24N2O4SCor e Forma:SolidPeso molecular:436.52Oxiran-2-ylmethanol
CAS:<p>Oxiran-2-ylmethanol exhibits antibacterial activity against Escherichia coli and can be used in related research in the field of life sciences.</p>Fórmula:C3H6O2Cor e Forma:SolidPeso molecular:74.08Antimicrobial agent-24
<p>Compound E8 (Antimicrobial agent-24) is a hydrazide with broad-spectrum fungicidal properties, disrupting the plasma membrane's functionality and inducing</p>Fórmula:C19H17F2N3O3Cor e Forma:SolidPeso molecular:373.35Dehydropipernonaline
CAS:<p>Dehydropipernonaline is a useful organic compound for research related to life sciences. The catalog number is T126447 and the CAS number is 107584-38-3.</p>Fórmula:C21H25NO3Cor e Forma:SolidPeso molecular:339.4351-(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:273.33SARS-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>Fórmula:C52H50Na2O8P2Cor e Forma:SolidPeso molecular:910.88LAH4 acetate
<p>LAH4 acetate is the α-helical structure of the designed amphoteric peptide antibiotic, which is capable of complexing DNA, associating with the cell surface</p>Fórmula:C134H232N38O29Pureza:98.41%Cor e Forma:SoildPeso molecular:2839.511,6-Digalloylglucose
CAS:<p>1,6-Digalloylglucose is a useful organic compound for research related to life sciences. The catalog number is T125261 and the CAS number is 23363-08-8.</p>Fórmula:C20H20O14Cor e Forma:SolidPeso molecular:484.366Antiviral agent 25
CAS:<p>Compound 6g, non-peptide inhibitor of SARS-CoV-2 3CL pro/PL pro, IC50: 0.118/0.448 µM, EC50: 7.249 µM, strong antiviral.</p>Fórmula:C15H12FN3SCor e Forma:SolidPeso molecular:285.34Valanimycin
CAS:<p>Valanimycin is a biochemical.</p>Fórmula:C7H12N2O3Cor e Forma:SolidPeso molecular:172.181233B
CAS:<p>1233B is a secondary metabolite from filamentous fungus, Fusarium sp. RK97-94 [1] .</p>Fórmula:C18H30O6Cor e Forma:SolidPeso molecular:342.434-Methoxycoumarine
CAS:<p>4-Methoxycoumarine has antitumour effects.</p>Fórmula:C10H8O3Pureza:99.64%Cor e Forma:SolidPeso molecular:176.17Micrococcin P1
CAS:<p>Micrococcin P1 is a macrocyclic peptide antibiotic and is a potent hepatitis C virus (HCV) inhibitor(EC50 range of 0.1-0.5 μM)</p>Fórmula:C48H49N13O9S6Pureza:98%Cor e Forma:SolidPeso molecular:1144.36Tetromycin B
CAS:<p>Tetromycin B was isolated from Streptomyces axinellae Pol001T cultivated from the Mediterranean sponge Axinella polypoides.</p>Fórmula:C34H46O5Cor e Forma:SolidPeso molecular:534.737Magainin 1
CAS:<p>Magainin 1 is an antimicrobial and amphipathic peptide isolated from the skin of Xenopus laevis.</p>Fórmula:C112H177N29O28SPureza:98%Cor e Forma:SolidPeso molecular:2409.85Guignardone K
CAS:<p>Guignardone K, a meroterpene compound extracted from solid cultures of the endophytic fungus Guignardia sp., exhibits antifungal activity [1].</p>Fórmula:C17H24O6Cor e Forma:SolidPeso molecular:324.37PD 124895
CAS:<p>PD 124895 is an antitumor antibiotic isolated from the fermentation broth of Streptomyces sp.</p>Fórmula:C32H46O7Pureza:98%Cor e Forma:SolidPeso molecular:542.70Thiotropocin
CAS:<p>Thiotropocin is an antibiotic.</p>Fórmula:C8H4O3S2Cor e Forma:SolidPeso molecular:212.25Amprolium
CAS:<p>Amprolium is a veterinary coccidiostat that interferes with THIAMINE metabolism.</p>Fórmula:C14H19N4·ClPureza:98%Cor e Forma:SolidPeso molecular:278.79Tebipenem pivoxil hydrochloride
CAS:<p>Tebipenem pivoxil HCl: oral antibiotic that targets PBPs to block bacterial cell wall synthesis.</p>Fórmula:C22H32ClN3O6S2Cor e Forma:SolidPeso molecular:534.09RSV-IN-2
CAS:<p>RSV-IN-2, a dual inhibitor for wild-type/mutant RSV fusion proteins, has EC50 of 0.27 nM (wild-type) and 0.70 nM (D486N mutant).</p>Fórmula:C27H31ClN6O4Cor e Forma:SolidPeso molecular:539.03DNA gyrase B-IN-2
<p>DNA gyrase B-IN-2 (Compound E), a 2-aminobenzothiazole derivative, serves as a potent inhibitor of DNA gyrase B with substantial efficacy against ESKAPE</p>Fórmula:C18H18Cl2N4O4SCor e Forma:SolidPeso molecular:457.33Tilatamig samrotecan
<p>Tilatamig samrotecan (AZD9592) is an antibody-drug conjugate (ADC) designed to deliver a topoisomerase I inhibitor (TOP1i). It targets epidermal growth factor receptor (EGFR) and c-MET and demonstrates antitumor activity. The compound induces DNA double-strand breaks, elevates pRAD50 and γH2AX expression, and inhibits the growth of non-small cell lung cancer.</p>Cor e Forma:Odour SolidCox B-IN-1
<p>CoxB-IN-1 (7a) exhibits antiviral activity against Coxsackie B virus (CoxB). This compound demonstrates dual functionality by inhibiting both virus adsorption and replication. Additionally, CoxB-IN-1 (7a) shows significant potential as an inhibitor of the Coxsackie virus 3C protease.</p>Fórmula:C38H32N10O2S2Cor e Forma:SolidPeso molecular:724.856Laidlomycin phenylcarbamate
CAS:<p>Laidlomycin phenylcarbamate is a semi-synthetic polyether antibiotic.</p>Fórmula:C44H67NO13Cor e Forma:SolidPeso molecular:818.014Trypacidin
CAS:<p>Trypacidin, from A. fumigatus, kills B. subtilis, M. bovis, T. cruzi, T. gondii, and induces A549 cell lysis; boosts mouse survival in T. gondii model.</p>Fórmula:C18H16O7Cor e Forma:SolidPeso molecular:344.319Repromicin
CAS:<p>Repromicin is a chemical compound whose derivatives have strong antibacterial characteristics.</p>Fórmula:C31H51NO8Pureza:98%Cor e Forma:SolidPeso molecular:565.74Brilacidin tetrahydrochloride
CAS:<p>Brilacidin tetrahydrochloride is a synthetic antibiotic effective against multiple bacteria with MIC90 values ranging from 1 to 8 μg/mL.</p>Fórmula:C40H54Cl4F6N14O6Cor e Forma:SolidPeso molecular:1082.75SARS-CoV-2-IN-25
<p>SARS-CoV-2-IN-25 (CP026): Strong inhibitor of spike-driven entry with IC50 at 1.6 μM, affects enveloped viruses, liposomes.</p>Fórmula:C58H48O8P2Cor e Forma:SolidPeso molecular:934.94Rivabazumab pegol
CAS:<p>Rivabazumab pegol, a pegylated Fab antibody targeting the PcrV protein, is utilized in phase II studies for chronic Pseudomonas aeruginosa infections [1].</p>Cor e Forma:LiquidAldgamycin G
CAS:<p>Aldgamycin G is a Macrolide antibiotic against Gram-positive bacteria isolated from Streptomyces avidinii.</p>Fórmula:C37H56O15Cor e Forma:SolidPeso molecular:740.83ZHAWOC25153
<p>ZHAWOC25153 (Compound 17o) is an inhibitor of the SARS-CoV-2 papain-like protease (PLpro) with an IC50 of 7 μM. It demonstrates antiviral properties and is applicable for research in the field of anti-infective studies.</p>Fórmula:C32H33FN2O6Cor e Forma:SolidPeso molecular:560.613AT-9010 tetrasodium
CAS:<p>AT-9010 tetrasodium, from AT-527, inhibits NiRAN essential for viral replication and stops SARS-CoV-2 spread.</p>Fórmula:C11H13FN5Na4O13P3Cor e Forma:SolidPeso molecular:627.13Peptide T
CAS:<p>Peptide T, an HIV-1 derived octapeptide, may inhibit gp120 binding to CD4 and cytokines, and affect VIP receptors.</p>Fórmula:C35H55N9O16Pureza:98%Cor e Forma:SolidPeso molecular:857.86Wulfenioidin H
<p>Wulfenioidin H (Compound 5), a diterpenoid, demonstrates anti-Zika virus (ZIKV) activity by inhibiting the expression of the ZIKV envelope (E) protein,</p>Fórmula:C21H28O3Cor e Forma:SolidPeso molecular:328.45Magnesium silicate
CAS:<p>Mg silicate (MgO & SiO2) used in antacids, deodorizing, decolorizing & as antifungal.</p>Fórmula:MgO3SiCor e Forma:SolidPeso molecular:100.39SPR206 acetate
CAS:<p>SPR206 acetate, a polymyxin analog, fights Gram-negative and MDR bacteria, with MICs of 0.125 mg/L against P. aeruginosa and A. baumannii.</p>Fórmula:C52H82ClN15O12·xC2H4O2Cor e Forma:SolidIndoline
CAS:<p>Compound PDK0239, with CAS No. 496-15-1, is a fragment molecule that serves as an important scaffold for molecular linking, expansion, and modification. Compound PDK0239 provides a structural basis and research tool for the design and screening of novel drug candidates, and is commonly used in drug discovery, drug synthesis, and related research.</p>Fórmula:C8H9NCor e Forma:Clear To Yellow LiquidPeso molecular:119.16Mezlocillin
CAS:<p>Meloxicillin: a liver-excreted penicillin effective against Gram-negative and some Gram-positive bacteria; treats biliary infections.</p>Fórmula:C21H25N5O8S2Cor e Forma:SolidPeso molecular:539.58Antifungal agent 53
CAS:<p>Antifungal 53 inhibits Candida CYP51, blocks biofilms, and is safe.</p>Fórmula:C18H15Cl3N2SeCor e Forma:SolidPeso molecular:444.64RNA binder 1
<p>RNA binder 1 (Compound 4b) is an RNA-binding agent capable of crossing the blood-brain barrier. It selectively binds to the G-quadruplex structure of the G4C2 repeat sequence RNA of the C9orf72 gene. This compound significantly reduces levels of the toxic polypeptides poly(GA) and poly(GP) in cells derived from amyotrophic lateral sclerosis (ALS) patients, while it has no significant impact on the antisense polypeptide poly(PR), demonstrating selectivity for sense RNA. RNA binder 1 is useful for studying ALS and frontotemporal dementia (FTD).</p>Fórmula:C22H20N10S2Cor e Forma:SolidPeso molecular:488.13138Septamycin
CAS:<p>Septamycin is a polycyclic, polyether, monocarboxylic acid antibiotic. Septamycin is isolated from strain of Streptomyces albus.</p>Fórmula:C48H82O16Cor e Forma:SolidPeso molecular:915.168Carumonam
CAS:<p>Carumonam, an antibiotic, could enhance the reactivity of Escherichia coli with mono- and polyclonal antisera to rough Escherichia coli J5.</p>Fórmula:C12H14N6O10S2Pureza:98%Cor e Forma:SolidPeso molecular:466.40[(Cys(Bzl)84,Glu(OBzl)85)]CD4 (81-92)
CAS:[(Cys(Bzl)84, Glu(OBzl)85)]CD4 (81-92) is a selective HIV-1 inhibitor that blocks the interaction between HIV-1 and CD4 molecules, thereby inhibiting viral infection and cell fusion. At a concentration of 25 μM, it can completely prevent fusion formation [1].Fórmula:C76H108N14O26SCor e Forma:SolidPeso molecular:1665.81DMT-5Me-dC(Bz)-CE Phosphoramidite
CAS:<p>DMT-5Me-dC(Bz)-CE Phosphoramidite aids in crafting LNAs for better fluorescent probes.</p>Fórmula:C47H54N5O8PCor e Forma:SolidPeso molecular:847.93(-)-Rabdosiin
CAS:<p>(-)-Rabdosiin, identified as a novel phenolic marker in Symphytum officinale L., exhibits antioxidant, neuroprotective, and anti-HIV activities [1].</p>Fórmula:C36H30O16Cor e Forma:SolidPeso molecular:718.61ATV03
<p>ATV03 is an antiviral agent exhibiting potent activity against both type A and type B influenza viruses. It inhibits the type A (H3N2) and type B influenza viruses with EC50 values of 0.78 nM and 2.02 nM, respectively. The mechanism of action of ATV03 involves the inhibition of the polymerase acidic protein (PA) and RNA-dependent RNA polymerase (RdRp), as well as the disruption of nucleoprotein, thereby exerting its antiviral effects against influenza.</p>Fórmula:C24H20FN3O5Cor e Forma:SolidPeso molecular:449.43MRV03-037
CAS:<p>MRV03-037 inhibits ClbP, blocking colibactin's genotoxic impact on cells, and stops gut bacterial genotoxin production.</p>Fórmula:C9H19BN2O4Cor e Forma:SolidPeso molecular:230.07PD 116779
CAS:<p>PD 116779 is a new antitumor antibiotic in the class os benz[a]anthraquinone.</p>Fórmula:C19H14O6Cor e Forma:SolidPeso molecular:338.315SARS-CoV-2 Mpro-IN-43
<p>SARS-CoV-2 Mpro-IN-43 (Compound 1) is an inhibitor of the coronavirus main protease (Mpro) with an IC50 of 72 μM. It exerts its antiviral effects by interacting non-covalently with the key residues at the Mpro active site. This compound exhibits moderate to low cytotoxicity with CC50 values of 13.24, 41.02, and 42.26 µM in HaCaT, HEK293T, and HepG2 cells, respectively. SARS-CoV-2 Mpro-IN-43 is applicable for SARS-CoV-2 research.</p>Fórmula:C32H41F3N2O4S2Cor e Forma:SolidPeso molecular:638.24598LMW peptide
CAS:<p>LMW peptide, an antimicrobial peptide, exhibits activity against both Gram-positive and Gram-negative bacteria, including B.</p>Fórmula:C75H121N21O20S2Cor e Forma:SolidPeso molecular:1701.02Maximin 49
<p>Maximin 49, an antimicrobial peptide, exhibits antibacterial activity against S.</p>Fórmula:C120H209N33O33Cor e Forma:SolidPeso molecular:2642.14MtbHU-IN-1
CAS:<p>MtbHU-IN-1 is a Mycobacterium tuberculosis nucleoid-associated protein HU (MtbHU)inhibitor(binding to WT MtbHU with a Kd of 98 nM).</p>Fórmula:C44H36N4O12S2Pureza:98%Cor e Forma:SolidPeso molecular:876.91Acetyl-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:444.47L2P4
<p>L2P4 is a peptide-based fluorescent probe targeting EBNA1 that inhibits the homodimerization of EBNA1 and selectively suppresses the growth of EBV+ tumors. Exhibiting cytotoxicity in EBV-positive C666-1 cells, L2P4 has an LC50 of 46.4 μM.</p>Fórmula:C93H139N25O16S2Cor e Forma:SolidPeso molecular:1927.39Bivittoside B
CAS:<p>Bivittoside B is a non-sulfated hexoside analog obtained from Bovine sea cucumber with antifungal activity and potential antitumor activity.</p>Fórmula:C54H88O22Pureza:98%Cor e Forma:SolidPeso molecular:1089.276RNA splicing modulator 3
CAS:<p>RNA Splicing Modulator 3 (Compound 236) is an effective RNA splicing modulator, exhibiting an AC50 value of less than 100 nM [1].</p>Fórmula:C19H20N6OSCor e Forma:SolidPeso molecular:380.47Ditercalinium chloride
CAS:<p>Ditercalinium chloride, an anticancer agent, inhibits human DNA polymerase gamma activity and can deplete mitochondrial DNA in both mouse and human cells. Additionally, Ditercalinium chloride is a potential ligand against the COMMD10-AP3S1 fusion protein [1] [2].</p>Fórmula:C46H50Cl2N6O2Cor e Forma:SolidPeso molecular:789.83Cyclopetide 1
CAS:<p>Cyclopeptide 1 (Compound 1) is an antimicrobial peptide exhibiting moderate efficacy in inhibiting B.</p>Fórmula:C20H28N4O8Cor e Forma:SolidPeso molecular:452.46POLRMT-IN-1
<p>POLRMT-IN-1 (compound S7) is an inhibitor of POLRMT, specifically utilized in cancer-related research.</p>Cor e Forma:Odour SolidAmp1EP9
<p>Amp1EP9: antimicrobial peptide, non-toxic, combats multidrug-resistant bacteria.</p>Fórmula:C90H173N21O16Cor e Forma:SolidPeso molecular:1805.47SARS-CoV-2 Mpro-IN-39
<p>SARS-CoV-2 Mpro-IN-39 (Compound 9d) is an inhibitor of the SARS-CoV-2 main protease (Mpro) with an IC50 value of 5.94 µM. It inhibits the replication of SARS-CoV-2 in Vero cells with an EC50 value of 9.33 µM, and has a cytotoxicity CC50 value of 289.63 µM. This compound is applicable in COVID-19 related research.</p>Cor e Forma:Odour SolidBING
CAS:<p>BING is an antimicrobial peptide isolated from Japanese medaka fish. It exhibits broad-spectrum toxicity against pathogenic bacteria, including resistant strains. BING disrupts the periplasmic peptidyl-prolyl isomerase in Gram-negative bacteria and reduces RNA levels of cpxR, which plays a crucial role in the development of antibiotic resistance.</p>Fórmula:C67H125N21O15Cor e Forma:SolidPeso molecular:1464.84Leu-Val
CAS:<p>Leu-Val (L-leucyl-L-valine) is a novel potent dipeptide with antibacterial and antimalarial activity.</p>Fórmula:C11H22N2O3Pureza:97.72%Cor e Forma:SolidPeso molecular:230.3Naphthalene
CAS:<p>Naphthalene is the simplest polycyclic aromatic hydrocarbon (PAH) and a major component of coal tar, serving as an insect repellent in camphor balls</p>Fórmula:C10H8Pureza:99.94%Cor e Forma:SolidPeso molecular:128.17Pyrrocidine A
CAS:Pyrrocidine A, an antibiotic known for its antibacterial properties, can be isolated from LL-Cyan426.Fórmula:C31H37NO4Cor e Forma:SolidPeso molecular:487.63Farobin A
CAS:<p>Farobin A, a natural compound, exhibits antibacterial, antioxidant, and anti-inflammatory properties. It is effective against Streptococcus mutans ATCC 25175 and Streptococcus sobrinus ATCC 33478. Additionally, Farobin A demonstrates anti-inflammatory activity by targeting cytokine IL-6 and TNF-α [1].</p>Fórmula:C27H30O14Cor e Forma:SolidPeso molecular:578.52PF-1163B
CAS:<p>PF-1163B, from Penicillium sp. II, is an antifungal that blocks ERG synthesis (IC50: 34 ng/ml) and targets Candida albicans without harming mammalian cells.</p>Fórmula:C27H43NO5Cor e Forma:SolidPeso molecular:461.63Macropin
CAS:<p>Macropin (MAC-1 peptide) is an antimicrobial peptide found in the venom of the solitary bee Macropis fulvipes. It exhibits antibacterial properties against both Gram-positive and Gram-negative bacteria, demonstrates inhibitory effects on fungi, and possesses moderate hemolytic activity on human red blood cells. Macropin is utilized in research for anti-infective therapies.</p>Fórmula:C68H121N17O13SCor e Forma:SolidPeso molecular:1416.86ML188 enantiomer
CAS:<p>16-(S)-ML188 is a inhibitor of HKU4-CoV 3CLpro, showing effective enzyme inhibition and antiviral activity.</p>Fórmula:C26H31N3O3Cor e Forma:SolidPeso molecular:433.54Linearmycin B
CAS:<p>Linearmycin B, a polyene antibiotic from Streptomyces, causes B. subtilis lysis in Streptomyces Mg1 extract.</p>Fórmula:C66H103NO16Cor e Forma:SolidPeso molecular:1166.541CEF1, Influenza Matrix Protein M1 (58-66)
CAS:<p>CEF1, M1 (58-66) epitope from influenza A; GILGFVFTL is HLA-A2-restricted.</p>Fórmula:C49H75N9O11Pureza:98%Cor e Forma:SolidPeso molecular:966.17Furaltadone L-tartrate
CAS:<p>Furaltadone L-tartrate, a nitrofuran, may help study Salmonella enteritidis in chickens; it's an antibacterial agent against staphylococci.</p>Fórmula:C17H22N4O12Cor e Forma:SolidPeso molecular:474.38HYNIC-UBI29-41
CAS:<p>HYNIC-UBI29-41 is composed of the bifunctional chelator HYNIC and the antimicrobial peptide UBI 29-41. It retains the antimicrobial properties of UBI 29-41, showing strong affinity for both Gram-positive and Gram-negative bacteria. When labeled with the radioactive element Technetium (99mTc), HYNIC-UBI29-41 can be used as an imaging agent for detecting bacterial infections in mouse models.</p>Fórmula:C74H126N34O19SCor e Forma:SolidPeso molecular:1828.07Anthracen-1-Amine
CAS:<p>Anthracen-1-amine exhibits inhibitory activity against Escherichia coli.</p>Fórmula:C14H11NPureza:99.70%Cor e Forma:SolidPeso molecular:193.24Lankacyclinone C
<p>Lankacyclinone C, a congener of lankacidin C devoid of the δ-lactone moiety, exhibits antitumor activity.</p>Fórmula:C24H33NO5Cor e Forma:SolidPeso molecular:415.52Yl 704 A1
CAS:<p>Yl 704 A1 is a primary component of macrolide antibiotic YL-704 from Streptomyces platensis subsp. malvinus.</p>Fórmula:C43H71NO15Pureza:98%Cor e Forma:SolidPeso molecular:842.033TAT peptide
<p>TAT peptide, a CPP, delivers molecules into cells by traversing membrane barriers using aa49-57 of TAT protein.</p>Fórmula:C65H124N34O15Pureza:98%Cor e Forma:SolidPeso molecular:1621.91BAL-30072
CAS:<p>BAL30072: Antibiotic effective against MDR Acinetobacter (4 μg/mL) and P. aeruginosa (8 μg/mL); a monocyclic beta-lactam.</p>Fórmula:C16H18N6O10S2Pureza:98%Cor e Forma:SolidPeso molecular:518.47XJ5
<p>XJ5 is a non-nucleoside covalent inhibitor of Nsp12 (IC50=0.12 μM), which is a non-structural protein 12 of the virus. XJ5 has the potential to become an antiviral inhibitor for SARS-CoV-2.</p>Fórmula:C23H27BrCl2N6O4Cor e Forma:SolidPeso molecular:602.308V-C6-Bg-PhCl TFA
<p>V–C6–Bg-PhCl TFA (compound 5e) is a biguanide-vancomycin conjugate with broad-spectrum antibacterial activity. It effectively eradicates biofilm-forming Gram-negative and Gram-positive bacteria.</p>Cor e Forma:Odour SolidLuminamicin
CAS:<p>Luminamicin is active against anaerobic bacteria, especially Clostridium sp.; isolated from actinomycete strain OMR-59.</p>Fórmula:C32H38O12Cor e Forma:SolidPeso molecular:614.644Potassium clavulanate cellulose
<p>Potassium clavulanate cellulose is a mixture of potassium clavulanate and cellulose, is an inhibitor of beta-lactamase.</p>Fórmula:C8H9NO5K·(C6H10O5)nPureza:98%Cor e Forma:SolidProteasome-IN-6
<p>Proteasome-IN-6 (Compound J-80) inhibits the β5 catalytic subunit of the Trypanosoma brucei 20S proteasome, effectively blocking T. b. brucei, T. b. gambiense, and T. b. rhodesiense with EC50 values of 157 nM, 220 nM, and 156 nM, respectively. Additionally, Proteasome-IN-6 has demonstrated antitrypanosomal activity in a mouse model.</p>Fórmula:C35H45F3N4O6Cor e Forma:SolidPeso molecular:674.75LpxC-IN-5
CAS:<p>LpxC-IN-5: potent non-hydroxamate LpxC enzyme inhibitor, IC50=20 nM, antibacterial, with MICs for E. coli, P. aeruginosa, K. pneumoniae at 16, 4, 64, 4 μg/mL.</p>Fórmula:C21H24N4O5Cor e Forma:SolidPeso molecular:412.446α-Cembrenediol
<p>α-Cembrenediol is a useful organic compound for research related to life sciences and the catalog number is T124625.</p>Fórmula:C20H34O2Cor e Forma:SolidPeso molecular:306.49Astodrimer
CAS:<p>Astodrimer: large (~3-4 nm, ~16.5 kDa), negative dendrimer with broad-spectrum antiviral, virucidal, and antibacterial properties.</p>Cor e Forma:SolidLysozyme chloride
CAS:<p>Lysozyme chloride: enzyme that kills gram-positive bacteria; used in HIV, emphysema research.</p>Cor e Forma:SolidA-315675
CAS:<p>A-315675 is a neuramidase inhibitor with anti-infuenza activity.</p>Fórmula:C17H30N2O4Cor e Forma:SolidPeso molecular:326.43m-Chloramphenicol
CAS:<p>m-Chloramphenicol, an impurity, hinders bacterial protein synthesis as a potent broad-spectrum antibiotic.</p>Fórmula:C11H12Cl2N2O5Cor e Forma:SolidPeso molecular:323.13Pseudin-2
CAS:<p>Pseudin-2, an AMP from Pseudis paradoxa, inhibits Gram-negative bacterial growth.</p>Fórmula:C122H202N36O32Cor e Forma:SolidPeso molecular:2685.13Spiroxamine
CAS:<p>Spiroxamine: fungicide targeting δ-wine pathogens.</p>Fórmula:C18H35NO2Pureza:99.67%Cor e Forma:SolidPeso molecular:297.48Neuraminidase-IN-16
<p>Neuraminidase-IN-16 (43b) inhibits H5N1, H5N8, H1N1, H3N2, H5N1-H274Y, H1N1-H274Y neuraminidases; IC50: 0.031-10.08 μM.</p>Fórmula:C26H35FN2O4Cor e Forma:SolidPeso molecular:458.57

