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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Emoquine-1
<p>Emoquine-1 is a potent orally active antimalarial agent effective against various drug-resistant Plasmodium strains, including artemisinin-resistant dormant parasites. It demonstrates efficacy against proliferative malignant Plasmodium with an IC50 value ranging from 20 to 55 nM. Emoquine-1 holds potential for treating Plasmodium strains resistant to artemisinin combination therapy (ACT), with the capability to eradicate persistent parasites.</p>Fórmula:C30H28ClN3O6Cor e Forma:SolidPeso molecular:562.013LASSBio-1985
<p>LASSBio-1985 is an inhibitor of NHLd (nucleoside hydrolase of Leishmania donovani), with a Ki of 79 μM and an IC50 of 84.6 μM. It exhibits selective toxicity against Leishmania parasites without affecting mammals, showing potential for research in infectious disease treatment.</p>Fórmula:C18H22N2O7Cor e Forma:SolidPeso molecular:378.38CpNMT-IN-1
<p>CpNMT-IN-1 (Compound 11e) is an inhibitor of N-myristoyltransferase (CpNMT) with an IC50 value of 2.5 μM. It also inhibits the growth of microsporidia, demonstrating an EC50 value of 6.9 μM.</p>Fórmula:C25H25ClN4O4SCor e Forma:SolidPeso molecular:513.008NDM-1 inhibitor-8
<p>NDM-1 inhibitor-8 (Compound 18b) is a covalent inhibitor of New Delhi metallo-β-lactamase-1 (NDM-1), with an IC50 of 7.03 μM. It effectively inhibits resistant bacterial strains and demonstrates synergistic antibacterial effects when used in combination with Meropenem. In mouse models, NDM-1 inhibitor-8 exhibits anti-infective activity.</p>Fórmula:C28H23Cl2N3O4SSeCor e Forma:SolidPeso molecular:647.43AAP4
<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:488.8112-Butyl-1,2-benzisothiazolin-3-one
CAS:<p>2-Butyl-1,2-benzisothiazolin-3-one is an orally available antimicrobial agent with antimicrobial activity commonly used in the pharmaceutical profession and</p>Fórmula:C11H13NOSPureza:98.34%Cor e Forma:SolidPeso molecular:207.29HBV-IN-37
CAS:<p>HBV-IN-37, an HBV inhibitor with 10 μM EC50, may treat hepatitis B.</p>Fórmula:C23H22ClN3O2SPureza:98%Cor e Forma:SolidPeso molecular:439.96RNA recruiter 2
<p>RNA recruiter 2 serves as a QSOX1mRNA ligand. This compound functions as a target RNA ligand (RIBOTAC's target RNA ligand) and aids in developing RIBOTAC RNA degraders with antitumor activity. Additionally, RNA recruiter 2 is utilized in the synthesis of F1-RIBOTAC.</p>Fórmula:C20H16FNO4SCor e Forma:SolidPeso molecular:385.409DNA Gyrase-IN-15
<p>DNA Gyrase-IN-15 (Compound 11) is an antibacterial agent that inhibits both DHPS and DNA gyrase, with IC50 values of 1.73 and 0.07 µM, respectively. It shows antimicrobial activity against Enterococcus faecium (MIC of 15.62 µg/mL), Acinetobacter baumannii, Enterobacter (MIC of 7.81 µg/mL), Pseudomonas aeruginosa, Klebsiella pneumoniae, and Staphylococcus aureus. Additionally, DNA Gyrase-IN-15 exhibits antibiofilm activity against Enterococcus faecium.</p>Fórmula:C31H26N4O4S2Cor e Forma:SolidPeso molecular:582.693RNase L ligand 1
<p>RNase L ligand 1 (Compound F1-COOH) serves as a ligand for RNase L and is utilized in the synthesis of F1-RIBOTAC.</p>Fórmula:C21H21Cl2NO3Cor e Forma:SolidPeso molecular:406.302Lipofermata
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:360.23Acetyl-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:444.47Modoflaner
CAS:<p>Modoflaner is an antiparasitic (veterinary use).</p>Fórmula:C23H10F12IN3O2Pureza:98.78%Cor e Forma:SolidPeso molecular:715.23Ac-rC Phosphoramidite
CAS:<p>Ac-rC Phosphoramidite can modify phosphodisulfide oligonucleotides.</p>Fórmula:C47H64N5O9PSiPureza:98.29%Cor e Forma:SolidPeso molecular:902.1sPLA2 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:470.52SARS-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:502.78SARS-CoV-2 3CLpro-IN-27
<p>SARS-CoV-2 3CLpro-IN-27 (Compound 9H) is an inhibitor of SARS-CoV-2 3CLpro, demonstrating an IC50 of 21 nM. It also exhibits robust anti-replicase activity against SARS-CoV-2, with an EC50 of 5 nM.</p>Fórmula:C29H27F4N5O4Cor e Forma:SolidPeso molecular:585.55SARS-CoV-2-IN-101
<p>SARS-CoV-2-IN-101 (compound 10O) is an effective orally active inhibitor of SARS-CoV-2 with an EC50 value of 0.64 µM against HCoV-229E. This compound exhibits cytotoxicity and can reduce the expression levels of HCoV-229E N protein and RNA. Additionally, SARS-CoV-2-IN-101 has broad-spectrum antiviral activity against coronaviruses.</p>Fórmula:C22H23N5O3Cor e Forma:SolidPeso molecular:405.45Streptolydigin
CAS:<p>Streptolydigin inhibits RNA synthesis by binding to RNA polymerase and does not inhibit eukaryotic RNA polymerases.</p>Fórmula:C32H44N2O9Pureza:98%Cor e Forma:SolidPeso molecular:600.70Dodecamethylpentasiloxane
CAS:<p>Dodecamethylpentasiloxane can be used as a bed bug insecticide. Dodecamethylpentasiloxane is a component of siloxane and can be used as silicone oil.</p>Fórmula:C12H36O4Si5Pureza:97.43%Cor e Forma:SolidPeso molecular:384.84Paclobutrazol
CAS:<p>Paclobutrazol ((R,R)-paclobutrazol) is a triazole-containing plant growth retardant that is known to inhibit the biosynthesis of gibberellins.1,2It also has</p>Fórmula:C15H20ClN3OPureza:99.23%Cor e Forma:Off-White To Beige SolidPeso molecular:293.79Ledipasvir D-tartrate
CAS:<p>Ledipasvir D-tartrate (GS-5885 D-tartrate) is an HCV NS5A inhibitor that suppresses viral overphosphorylation and replication</p>Fórmula:C53H60F2N8O12Pureza:99.83%Cor e Forma:SolidPeso molecular:1039.09Leu-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:230.3Tipranavir
CAS:<p>Tipranavir is a protease inhibitor that inhibits HIV-1 resistant to more than 1 protease inhibitor .Tipranavir effectively inhibits HIV-1 protease enzyme</p>Fórmula:C31H33F3N2O5SPureza:99.85%Cor e Forma:White SolidPeso molecular:602.66R-1479
CAS:<p>R-1479 (4'-Azidocytidine) is an RdRp inhibitor with an IC50 value of 1.28 μM for HCV RNA replication in the HCV subgenomic replicon system.</p>Fórmula:C9H12N6O5Pureza:98.11% - 99.95%Cor e Forma:SolidPeso molecular:284.23LAH4 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:2839.51Azlocillin sodium salt
CAS:<p>Azlocillin sodium, an acylampicillin, is a broad-spectrum antibiotics</p>Fórmula:C20H22N5NaO6SPureza:97.63% - 98.302%Cor e Forma:SolidPeso molecular:483.47Sofosbuvir impurity N
CAS:<p>Sofosbuvir impurity N is an diastereoisomer of Sofosbuvir.Sofosbuvir is an HCV RNA replication inhibitor, with potent anti-hepatitis C virus activity.</p>Fórmula:C20H25FN3O9PPureza:98%Cor e Forma:SolidPeso molecular:501.404WAY-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:294.3Antitubercular agent-41
CAS:<p>Antitubercular agent-41是一种抗菌剂。</p>Fórmula:C23H20FN3O3Pureza:99.78%Cor e Forma:SoildPeso molecular:405.42Bac8c
CAS:<p>Bac8c is an antimicrobial peptide exhibiting potent activity against both Gram-negative and Gram-positive bacteria. The minimum inhibitory concentrations (MIC) of Bac8c for S. aureus, MRSA, S. epidermidis, E. coli, and P. aeruginosa are 2, 8, 4, 4, and 4 μg/mL, respectively.</p>Fórmula:C57H90N20O8Cor e Forma:SolidPeso molecular:1183.45C16G2
CAS:<p>C16G2 is a Specific Targeted Antimicrobial Peptide (STAMP) that selectively targets the cariogenic oral pathogen Streptococcus mutans. This compound operates by recognizing and disrupting the bacterial cell membrane, leading to small molecule leakage and the loss of membrane potential, which results in bacterial death. Unlike broad-spectrum antimicrobial peptides, C16G2 exhibits higher selectivity and efficacy against Streptococcus mutans.</p>Fórmula:C190H310N58O42Cor e Forma:SolidPeso molecular:4078.93Ile-AMS TFA
<p>Ile-AMS TFA exhibits activity against P. falciparum, with an ABSIC50 value of 1.19 nM.</p>Fórmula:C18H27F3N8O8SCor e Forma:SolidPeso molecular:572.52Libevitug
<p>Libevitug is a humanized IgG1λ2 antibody targeting HBV, with HumanIgG1lambda2, Isotype Control as its corresponding isotype control.</p>Cor e Forma:Odour LiquidTQL-1055
CAS:<p>TQL-1055 is a semi-synthetic analog of the saponin adjuvant QS-21, utilized as an adjuvant in preventive vaccines. It demonstrates potent adjuvant activity with influenza antigens and shows good tolerability when combined with an acellular pertussis vaccine (aP), enhancing anti-pertussis toxin (PT) antibody responses in mice and rabbits. TQL-1055 holds promise for research into chronic Hepatitis B.</p>Fórmula:C59H95NO20Cor e Forma:SolidPeso molecular:1138.38MTH1 ligand 1
CAS:<p>MTH1 ligand 1 functions as a target protein ligand for MTH1, and is utilized in the synthesis of PROTACaTAG 2139.</p>Fórmula:C23H18N4O3Cor e Forma:SolidPeso molecular:398.41N-Demethylvancomycin
CAS:<p>N-Demethylvancomycin is a glycopeptide antibiotic that can be extracted from Nocardia orientalis and exhibits activity against various strains of Staphylococcus aureus and Staphylococcus epidermidis. It is utilized in research related to infections.</p>Fórmula:C65H73Cl2N9O24Cor e Forma:SolidPeso molecular:1435.23Apidaecin IB
CAS:<p>Apidaecin IB is an insect antimicrobial peptide, with MIC values of 8 μM for E. coli (O18K1H7, ML35 and ATCC 25922).</p>Fórmula:C95H150N32O23Pureza:98%Cor e Forma:SolidPeso molecular:2108.446T2AA
CAS:<p>T2AA (4-[4-[(2S)-2-amino-3-hydroxypropyl]-2,6-diiodophenoxy]phenol) is an inhibitor of proliferating cell nuclear antigen (PCNA) with IC50 of 1 μM for PCNA/PIP-</p>Fórmula:C15H15I2NO3Pureza:99.53%Cor e Forma:SolidPeso molecular:511.09DMT-dU-CE Phosphoramidite
CAS:<p>DMT-dU-CE Phosphoramidite is a nucleoside molecule commonly used for the synthesis and sequencing of DNA.</p>Fórmula:C39H47N4O8PPureza:99.55%Cor e Forma:SolidPeso molecular:730.79NCGC00029283
CAS:<p>NCGC00029283 is a potent inhibitor of Werner syndrome helicase-nuclease (WRN), displaying inhibitory activity against WRN helicase with an IC 50 value of 2.3 μM</p>Fórmula:C18H12FN3O3Pureza:99.84%Cor e Forma:SolidPeso molecular:337.3ART812
CAS:<p>ART812 is an orally active inhibitor of DNA polymerase Polθ, possessing an IC50 value of 7.6 nM.</p>Fórmula:C19H16ClF4N3O4Pureza:99.07%Cor e Forma:SolidPeso molecular:461.79Cefoxitin sodium
CAS:<p>Cefoxitin sodium (Betacef) is a semisynthetic cephamycin antibiotic resistant to beta-lactamase.</p>Fórmula:C16H16N3NaO7S2Pureza:99.19%Cor e Forma:White To Almost White PowderPeso molecular:449.43N2-Acetylaciclovir
CAS:<p>N2-Acetylaciclovir (Aciclovir EP Impurity F) is a derivative of the antiviral compound Aciclovir, which has selective T-cell immunotoxicity.</p>Fórmula:C10H13N5O4Pureza:98.2%Cor e Forma:SolidPeso molecular:267.24Cefonicid sodium
CAS:<p>Cefonicid sodium is a broad-spectrum cephalosporin antibiotic that inhibits bacterial cell wall formation.Cost-effective and quality-assured.</p>Fórmula:C18H16N6Na2O8S3Pureza:98.61%Cor e Forma:White Or Off-White Crystalline PowderPeso molecular:586.53Thanatin acetate
Thanatin acetate is a cationic peptide with antimicrobial activity, inhibiting bacterial and fungal growth.Fórmula:C105H181N35O29S3Pureza:99.65%Cor e Forma:SolidPeso molecular:2493.97Cymal-6
CAS:<p>Cymal-6 (Cyclohexyl-hexyl-β-D-maltoside) is a TEM-1 β-lactamase inhibitor and a glycoside surfactant.</p>Fórmula:C24H44O11Cor e Forma:SolidPeso molecular:508.6Vaborbactam ammonium salt
<p>Vaborbactam ammonium salt is a β-lactamase inhibitor that restores carbapenem activity against KPC-producing strains.</p>Fórmula:C12H19BN2O5SPureza:97.36%Cor e Forma:SoildPeso molecular:314.17Quilseconazole Formic acid(1340593-70-5 Free base)
<p>Quilseconazole Formic acid is a selective inhibitor of fungal Cyp51 with potent activities against Cryptococcus neoformans and Cryptococcus gattii.</p>Fórmula:C23H16F7N5O4Pureza:99.56% - 99.84%Cor e Forma:SoildPeso molecular:559.39Tetrazolast
CAS:<p>Tetrazolast has anticancer activity and may have antifungal activity.</p>Fórmula:C10H6N8Pureza:99.06%Cor e Forma:SolidPeso molecular:238.21Obafluorin
CAS:<p>Obafluorin is a β-lactone antibiotic produced by fluorescent Pseudomonas ATCC 39502, with broad-spectrum antibacterial activity.</p>Fórmula:C17H14N2O7Cor e Forma:SolidPeso molecular:358.3Tetramycin
CAS:<p>Tetramycin (Tetramycin A) is a macrolide antibiotic isolated from Streptomyces hygrospinosus var. Beijingensis, a new and highly effective polyene antibiotic.</p>Fórmula:C35H53NO13Pureza:95.28%Cor e Forma:SolidPeso molecular:695.79Methylclonazepam
CAS:<p>Methylclonazepam is a benzodiazepine with anxiolytic properties. It inhibits the uptake of 5-hydroxytryptamine by Schistosoma mansoni, and its derivatives exhibit anti-Schistosoma mansoni activity.</p>Fórmula:C16H12ClN3O3Cor e Forma:SolidPeso molecular:329.74Antimalarial agent 46
CAS:<p>Antimalarial agent 46 (Compound 42a) is a compound with antimalarial activity, effective in inhibiting P. falciparum lines.</p>Fórmula:C21H17Cl3N4OCor e Forma:SolidPeso molecular:447.75WRN inhibitor 15
<p>WRN inhibitor 15 (Compound 9) is a WRN inhibitor with antitumor properties, displaying IC50 values of 37.9, 40.2, and 46.6 μM in PC3, LNCaP, and HeLa cells, respectively, making it suitable for prostate cancer research.</p>Fórmula:C16H13F2N3OCor e Forma:SolidPeso molecular:301.292-Acetylthiophene thiosemicarbazone
CAS:<p>2-Acetylthiophene thiosemicarbazone is an antimicrobial agent against a wide range of gram-negative and gram-positive bacteri and fungi.</p>Fórmula:C7H9N3S2Cor e Forma:SolidPeso molecular:199.3SARS-CoV-2-IN-52
CAS:<p>SARS-CoV-2-IN-52 (Compound 5) is an inhibitor of SARS-CoV-2 with a pIC50 of 0.3187.</p>Fórmula:C20H16N6OCor e Forma:SolidPeso molecular:356.38AV5124
CAS:<p>AV5124 is a prodrug of AV5116 and acts as an orally active inhibitor of influenza virus cap-dependent endonuclease (CEN).</p>Fórmula:C25H21F2N3O7S2Cor e Forma:SolidPeso molecular:577.58Extracellular Death Factor TFA
<p>Extracellular death factor TFA (EDF TFA) is a linear pentapeptide that communicating cells produce and release, which activates the cell death pathway.</p>Pureza:98.77%Cor e Forma:Odour SolidDestomycin A
CAS:<p>Destomycin A, an aminoglycoside antibiotic, exhibits activity against bacterial (Gram-positive and Gram-negative), antifungal, and anthelmintic agents. It inhibits peptide synthesis in Escherichia coli cells and stimulates adenylate cyclase in animal tissues.</p>Fórmula:C20H37N3O13Cor e Forma:SolidPeso molecular:527.52AB-161
CAS:<p>AB-161 is an orally active destabilizer of HBV RNA and an inhibitor of PAPD5/7, primarily targeting the liver. It treats hepatitis B virus (HBV) infection by reducing hepatitis B surface antigen (HBsAg) levels, exhibiting an EC50 value of 2.2 nM for HBsAg. AB-161 is applicable in HBV infection research.</p>Fórmula:C21H21F2N3O5Cor e Forma:SolidPeso molecular:433.41MCG-02
<p>MCG-02 is an inhibitor of cruzain (CRZ) and cathepsin L-like protease (CATL), capable of inhibiting CRZ in Trypanosoma cruzi and CATL in Trypanosoma brucei, with IC50 values of 0.2 μM and 0.02 μM, respectively.</p>Fórmula:C13H13N3O2SCor e Forma:SolidPeso molecular:275.33IAV replication-IN-1
CAS:<p>IAV replication-IN-1 (compound 3h) can reduce the upregulation of inflammatory factors and apoptosis caused by IAV infection and alleviate lung damage resulting from IAV infection.</p>Fórmula:C23H22N2O5S2Cor e Forma:SolidPeso molecular:470.56MAPI
CAS:<p>MAPI is an irreversible peptidyl 3C cysteine protease (SV3CP) inhibitor. By covalently attaching its C-terminal Michael acceptor moiety to the active site thiol of SV3CP Cys 139, MAPI inhibits SV3CP. It shows potential for use in the study of norovirus infections.</p>Fórmula:C36H53N7O11Cor e Forma:SolidPeso molecular:759.85WRN inhibitor 14
<p>WRN inhibitor 14 (compound S35) is an orally administered WRN inhibitor with anticancer properties. It effectively suppresses tumor growth in the SW48 xenograft model in BALB/c nude mice.</p>Fórmula:C35H40F4N10O5Cor e Forma:SolidPeso molecular:756.75Antileishmanial agent-31
CAS:<p>Antileishmanial agent-31 (Compound p1) is a pyrazole derivative exhibiting antileishmanial activity with an IC50 of 35.53 μg/mL. Furthermore, Antileishmanial agent-31 demonstrates high stability and is applicable in studies focused on leishmaniasis treatment.</p>Fórmula:C11H11ClN2Cor e Forma:SolidPeso molecular:206.67ACHE-IN-38
CAS:<p>ACHE-IN-38, an Acetylcholinesterase inhibitor, can be used to synthesize compounds with anti-inflammatory activity.</p>Fórmula:C17H23NO3Pureza:99.52%Cor e Forma:SolidPeso molecular:289.37Durlobactam Triethylamine
<p>Durlobactam Triethylamine inhibits A, C, D β-lactamases and possesses antifungal properties.</p>Fórmula:C14H26N4O6SPureza:97.39%Cor e Forma:SoildPeso molecular:378.44Antiviral agent 36
Antiviral agent 36 (compound 27), a potent inhibitor of both dengue (DENV) and Zika (ZIKV) viruses, demonstrates replication inhibition with EC50 values of 100Fórmula:C30H32N4O3Pureza:98%Cor e Forma:SolidPeso molecular:496.6Antiparasitic agent-20
<p>Antiparasitic Agent-20 (Compound 1p) exhibits broad-spectrum activity as a parasitic inhibitor, demonstrating efficacy against T.</p>Pureza:98%Cor e Forma:Odour SolidMelimine
<p>Melimine, a hybrid antimicrobial peptide derived from Melittin and Protamine, exhibits broad-spectrum activity against various microorganisms, including</p>Fórmula:C158H290N74O35Pureza:98%Cor e Forma:SolidPeso molecular:3786.47Taq DNA polymerase
CAS:<p>Taq DNA polymerase is a thermostable enzyme utilized in polymerase chain reactions (PCR) to amplify DNA sequences [1].</p>Pureza:98%Cor e Forma:SolidDihydrodehydrodiconiferyl alcohol 9-O-β-D-xylopyranoside
CAS:<p>Dihydrodehydrodiconiferyl alcohol 9-O-β-D-xylopyranoside serves as an anti-hepatitis B virus (anti-HBV) agent, effectively inhibiting the secretion of HBV</p>Fórmula:C25H32O10Pureza:98%Cor e Forma:SolidPeso molecular:492.52DNA polymerase-IN-2
DNA polymerase-IN-2 (Compd 3c), a coumarin derivative, demonstrates inhibitory activity towards Taq DNA polymerase, with an IC50 value of 48.25 μM, and holdsFórmula:C14H12O5SPureza:98%Cor e Forma:SolidPeso molecular:292.31Gramicidin B
CAS:<p>Gramicidin B is a nonribosomal peptide with antibiotic properties [1].</p>Fórmula:C97H139N19O17Pureza:98%Cor e Forma:SolidPeso molecular:1843.26HBV-IN-35
<p>Compound HBV-IN-35 (Compound 88) serves as an HBV inhibitor and exhibits anti-HBV activity in both mouse and human hepatocytes with EC50 values of 100 nM and</p>Fórmula:C22H23F5N4OPureza:98%Cor e Forma:SolidPeso molecular:454.44Anti-Influenza agent 5
<p>Anti-Influenza agent 5 (Compound IIB-2), a chalcone-like derivative, serves as an influenza nuclear export inhibitor.</p>Pureza:98%Cor e Forma:Odour SolidUrumin
CAS:<p>Urumin, a compound with antiviral properties, inhibits human influenza A virus growth, particularly the PR8 strain, with an inhibitory concentration (IC 50) of</p>Fórmula:C129H198N42O35S2Pureza:98%Cor e Forma:SolidPeso molecular:2961.34Funiculosin
CAS:<p>Funiculosin, a neutral lipophilic antibiotic, demonstrates inhibitory effects against both DNA and RNA viruses, in addition to possessing antifungal properties.</p>Fórmula:C27H41NO7Pureza:98%Cor e Forma:SolidPeso molecular:491.62GRL-1720 TFA
<p>GRL-1720 TFA is a potent SARS-CoV-2 Mpro inhibitor, demonstrating anti-SARS-CoV-2 activity with an EC50 of 15 μM [1].</p>Pureza:98%Cor e Forma:Odour SolidAurein 2.6
CAS:<p>Aurein 2.6, an antibiotic antimicrobial peptide, exhibits activity against various Gram-positive bacteria with minimum inhibitory concentrations (MIC) of 25, 25</p>Fórmula:C77H133N19O19Pureza:98%Cor e Forma:SolidPeso molecular:1629Aurein 5.2
CAS:<p>Aurein 5.2 is an antibiotic antimicrobial peptide [1].</p>Fórmula:C110H194N28O32SPureza:98%Cor e Forma:SolidPeso molecular:2452.95Dermcidin-1L (human)
CAS:<p>Dermcidin-1L (human), an antibiotic peptide secreted by sweat glands, exhibits antimicrobial activity and is utilized in the research of inflammatory skin</p>Fórmula:C210H359N57O71Pureza:98%Cor e Forma:SolidPeso molecular:4818.44Cysteine protease inhibitor-3
<p>Cysteine protease inhibitor-3 (Compound 15), a cysteine protease inhibitor, exhibits anti-plasmodial activity, effectively inhibiting Pf3D7 (IC50 = 0.74 μM),</p>Fórmula:C26H22ClF2N3OPureza:98%Cor e Forma:SolidPeso molecular:465.92HAT-IN-8
<p>HAT-IN-8 (Compound 38), a blood-brain barrier-permeable inhibitor of Trypanosoma brucei with an EC50 of 0.18 μM, is utilized in the study of Human African</p>Fórmula:C14H15F2N3O2SPureza:98%Cor e Forma:SolidPeso molecular:327.35SARS-CoV-2-IN-56
<p>SARS-CoV-2-IN-56 (Compound 63) is a SARS-CoV-2 inhibitor with antiviral activity, demonstrating inhibition of the virus in Vero E6 cells with an IC50 of 0.7 μM</p>Fórmula:C70H72N12O19S3Pureza:98%Cor e Forma:SolidPeso molecular:1481.58H-Arg-OtBu dihydrochloride
CAS:<p>H-Arg-OtBu (dihydrochloride) is a membrane-targeting antimicrobial that engages the negatively charged bacterial membrane through electrostatic and hydrophobic</p>Fórmula:C10H24Cl2N4O2Pureza:98%Cor e Forma:SolidPeso molecular:303.23HBV-IN-40
<p>HBV-IN-40 (Compound 11826096), with an IC50 of 0.7 µM, serves as a potent HBV inhibitor and exhibits antiviral activity [1].</p>Fórmula:C29H55Cl4N11Pureza:98%Cor e Forma:SolidPeso molecular:699.63Crexavibart
CAS:<p>Crexavibart (BMS-986413; C-144-LS), an IgG1 λ2 antibody, specifically targets the receptor-binding domain of the SARS-CoV-2 spike (S) glycoprotein [1].</p>Pureza:98%Cor e Forma:LiquidAntitrypanosomal agent 12
<p>Antitrypanosomal agent 12, a C20-phenylthiourea, exhibits trypanocidal and cytotoxic activities, demonstrating antitrypanosomal activity with GI50 values of 0.</p>Fórmula:C49H77N2NaO10SPureza:98%Cor e Forma:SolidPeso molecular:909.2SARS-CoV-2-IN-55
<p>SARS-CoV-2-IN-55 (compound 65) is an inhibitor of SARS-CoV-2 exhibiting low cytotoxicity, characterized by an IC50 of 0.3 μM, effectuated through direct</p>Fórmula:C138H136N22O32S6Pureza:98%Cor e Forma:SolidPeso molecular:2807.07Clovibactin
CAS:<p>Clovibactin, a novel antibiotic, effectively eradicates drug-resistant bacterial pathogens and demonstrates no discernible resistance.</p>Fórmula:C43H70N10O11Pureza:98%Cor e Forma:SolidPeso molecular:903.08Antiparasitic agent-17
<p>Antiparasitic Agent-17 (compound 5u), an orally active antiparasitic, demonstrates inhibition against both Chloroquine-sensitive (Pf3D7) and Chloroquine-</p>Fórmula:C32H30N2O4Pureza:98%Cor e Forma:SolidPeso molecular:506.59Defensin HNP-3 human
CAS:<p>Defensin HNP-3 human, a cytotoxic antibiotic peptide referred to as "defensin," exhibits inhibitory effects on Staphylococcus aureus, Pseudomonas aeruginosa,</p>Fórmula:C151H222N44O40S6Pureza:98%Cor e Forma:SolidPeso molecular:3486.04SARS-CoV-2-IN-60
<p>SARS-CoV-2-IN-60 (compound 5a) is a specific, irreversible inhibitor of SARS-CoV-2 nsp16-nsp10 methyltransferase, competing with S-adenosylmethionine (SAM) and</p>Fórmula:C13H7Cl2F3N2OPureza:98%Cor e Forma:SolidPeso molecular:335.11SARS-CoV-2 3CLpro-IN-18
<p>SARS-CoV-2 3CLpro-IN-18 (Compound 3C) is a covalent inhibitor of SARS-CoV-2 3CLpro with an IC50 of 0.478 μM.</p>Fórmula:C17H13ClN2OSPureza:98%Cor e Forma:SolidPeso molecular:328.82(±)-Emodin bianthrone
CAS:<p>(±)-Emodin bianthrone (compound 10), a naturally occurring substance, demonstrates antimalarial, antitubercular, and antifungal properties [1].</p>Fórmula:C30H22O8Pureza:98%Cor e Forma:SolidPeso molecular:510.49Moloney murine leukemia virus RT
<p>Moloney murine leukemia virus reverse transcriptase (MMLV RT) is a monomeric replicative polymerase intrinsic to the retrovirus life cycle [1].</p>Pureza:98%Cor e Forma:Odour Solid7-51A
<p>7-51A is an effective inhibitor of the PB2 subunit of the influenza RNA-dependent RNA polymerase (RdRP), with a dissociation constant (K_D) of 1.64 nM as</p>Pureza:98%Cor e Forma:Odour SolidPlutavimab
CAS:<p>Plutavimab is a humanized IgG1-κ monoclonal antibody targeting the receptor binding domain (RBD) of the SARS-CoV-2 spike (S) glycoprotein [1] [2].</p>Pureza:98%Cor e Forma:Liquid
