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"
Ordenar por
Pureza (%)
0
100
|
0
|
50
|
90
|
95
|
100
Anti-parasitic agent 3
CAS:<p>Anti-parasitic agent 3 is an anti-parasitic agent active against drug-resistant parasites.</p>Fórmula:C21H22FN5O3Pureza:98%Cor e Forma:SolidPeso molecular:411.43SARS-CoV-2 nsp13-IN-6
CAS:<p>nsp13-IN-6 inhibits SARS-CoV-2 nsp13, targeting ssDNA+ATPase (IC50: 27 μM) and ssDNA-ATPase (IC50: 33 μM) for COVID-19 research.</p>Fórmula:C21H19N5O3SCor e Forma:SolidPeso molecular:421.47Antifungal agent 33
CAS:<p>Antifungal 33 (4e) strongly inhibits Candida albicans. MIC: 16 μg/ml; IC50: 0.19 μg/ml.</p>Fórmula:C21H14ClN5O3Cor e Forma:SolidPeso molecular:419.82DHX9-IN-1
CAS:<p>DHX9-IN-1 is a potent ATP-dependent RNA helicase A (DHX9) inhibitor, exhibiting an IC50 of 9.45 nM and demonstrating antitumor activity [1].</p>Fórmula:C21H21F2N5O3SCor e Forma:SolidPeso molecular:461.49BMS-433771 free base
CAS:<p>BMS-433771, a novel inhibitor of respiratory syncytial virus (RSV), binds the RSV F glycoprotein and inhibits membrane fusion.</p>Fórmula:C21H23N5O2Cor e Forma:SolidPeso molecular:377.44Amorolfine
CAS:<p>Amorolfine is available in the nail lacquer and can be used to treat fungal nail infections.</p>Fórmula:C21H35NOCor e Forma:White To Off-White Crystalline PowderPeso molecular:317.517Braco-19 trihydrochloride
CAS:<p>BRACO19 3HCl inhibits telomerase, blocking its capping function, and prevents HAdV viral replication.</p>Fórmula:C35H46Cl3N7O2Pureza:98.74%Cor e Forma:SolidPeso molecular:703.14MMV666693
CAS:<p>MMV666693 is a selective allosteric Plasmodium Kinesin-5 inhibitor.</p>Fórmula:C18H15NO4Cor e Forma:SolidPeso molecular:309.32Exalamide
CAS:<p>Exalamide (2-(Hexyloxy)benzamide) is an aromatic amide with antifungal activity used in the study of dermatophytes.</p>Fórmula:C13H19NO2Pureza:99.61%Cor e Forma:White PowderPeso molecular:221.3PknB-IN-2
CAS:<p>PknB-IN-2 (Compound 10) is an inhibitor of Mycobacterium tuberculosis protein kinase B (PknB) (IC50: 12.1 μM).</p>Fórmula:C28H32N2O4Cor e Forma:SolidPeso molecular:460.56Antileishmanial agent-12
CAS:<p>Compound 5a: potent anti-leishmanial, IC50 - L. brazilensis 14.9μM, L. infantum 21.3μM; antiprotozoal against T. cruzi 9.3μM.</p>Fórmula:C25H21N3O4Cor e Forma:SolidPeso molecular:427.45TBI-166
CAS:<p>TBI-166, an oral riminophenazine, treats tuberculosis with fewer side effects than Clofazimine.</p>Fórmula:C32H30F3N5O3Cor e Forma:SolidPeso molecular:589.61BA38017
CAS:<p>BA38017 is a potent assembly modulator of HBV core protein that inhibits the replication of HBV (EC50 = 0.20 μM) [1].</p>Fórmula:C15H11ClFNO3Cor e Forma:SolidPeso molecular:307.7SARS-CoV-2 3CLpro-IN-1
CAS:<p>SARS-CoV-2 3CLpro-IN-1 is a potent inhibitor of the key enzyme 3CL pro in coronaviruses, promising for antiviral drug R&D.</p>Fórmula:C27H30ClN3O3SCor e Forma:SolidPeso molecular:512.06S.pombe lumazine synthase-IN-1
CAS:<p>S.pombe lumazine synthase-IN-1 inhibits lumazine synthases: Ki of 243μM for S.pombe, 9.6μM for M.tuberculosis.</p>Fórmula:C14H13N3O6Cor e Forma:SolidPeso molecular:319.27HIV-1 inhibitor-20
CAS:<p>HIV-1 inhibitor-20 is a potent HIV-1 inhibitor.</p>Fórmula:C19H11ClF3N3O2Cor e Forma:SolidPeso molecular:405.76SARS-CoV MPro-IN-2
CAS:<p>SARS-CoV MPro-IN-2, a potent SARS-CoV-2 main protease inhibitor (IC50: 72.07 nM), may aid COVID-19 research.</p>Fórmula:C13H10O4Cor e Forma:SolidPeso molecular:230.22DENV-IN-9
CAS:<p>DENV-IN-9 is a DENV2 inhibitor with an EC 50 of 0.88 μM .</p>Fórmula:C15H9BrO5Cor e Forma:SolidPeso molecular:349.13Antibacterial agent 115
CAS:<p>Antibacterial agent 115 is an antibacterial and anti-inflammatory agent that is active when taken orally.</p>Fórmula:C35H48N2O3Cor e Forma:SolidPeso molecular:544.77SARS-CoV MPro-IN-1
CAS:<p>MProinhibitor 11b blocks SARS-CoV-2 main protease (IC50=0.04 μM), cuts viral yield and RNA in Vero E6 cells (EC50=0.72 μM).</p>Fórmula:C25H25FN4O4Cor e Forma:SolidPeso molecular:464.495-Dehydroepisterol
CAS:<p>5-Dehydroepisterol, an anti-fungal episterol form, made by C-5 sterol desaturase, turns into 24-methylenecholesterol.</p>Fórmula:C28H44OPureza:98%Cor e Forma:SolidPeso molecular:396.65Chaetoglobosin C
CAS:<p>Chaetoglobosin C (Compound 4), an anthraquinone-chromone derivative of Chaetomium globosum KMITL-N0802, exhibits anti-tuberculosis activity [1].</p>Fórmula:C32H36N2O5Cor e Forma:SolidPeso molecular:528.64HIV-1 inhibitor-38
CAS:<p>HIV-1 inhibitor-38, or Compound 91, shows promise as a strong latency reversing agent against HIV-1.</p>Fórmula:C15H13Cl3N6Cor e Forma:SolidPeso molecular:383.66HBV-IN-22
CAS:<p>HBV-IN-22 (Compound LC5f) is an HBV DNA replication inhibitor that acts on both wild-type HBV (IC50: 0.71 μM) and drug-resistant HBV (IC50: 0.84 μM).</p>Fórmula:C26H29N3O2S2Cor e Forma:SolidPeso molecular:479.66Thiambutosine
CAS:<p>Thiambutosine exhibits inhibitory activity against Mycobacterium leprae and mushroom tyrosinase, making it suitable for infection studies.</p>Fórmula:C19H25N3OSPureza:99.95%Cor e Forma:SolidPeso molecular:343.49Saperconazole
CAS:<p>Saperconazole is a broad-spectrum antifungal triazole (MIC90: 0.19 mg/L).</p>Fórmula:C35H38F2N8O4Pureza:98%Cor e Forma:SolidPeso molecular:672.72Bunamidine hydrochloride
CAS:<p>Bunamidine hydrochloride is a veterinary anthelmintic that acts against Echinococcus granulosus and Tapeworm.</p>Fórmula:C25H39ClN2OCor e Forma:SolidPeso molecular:419.05Erythromycin Gluceptate
CAS:<p>Erythromycin Gluceptate is an inhibitor of protein translation and mammalian mRNA splicing. It inhibits growth of gram negative and gram positiove bacteria.</p>Fórmula:C44H81NO21Cor e Forma:SolidPeso molecular:960.11SARS-CoV-2 3CLpro-IN-3
CAS:<p>SARS-CoV-2 3CLpro-IN-3 is a SARS CoV-2 3CLpro inhibitor that exhibits antiviral, antibacterial, and antifungal effects.</p>Fórmula:C23H21BrN6O2SCor e Forma:SolidPeso molecular:525.42Cap-dependent endonuclease-IN-26
CAS:<p>Cap-dependent endonuclease-IN-26 inhibits CEN (IC50: 286 nM), has broad antiviral effects on influenza A/B.</p>Fórmula:C23H23N3O3Cor e Forma:SolidPeso molecular:389.45Zelpolib
CAS:<p>Zelpolib is a specific inhibitor of DNA polymerase δ (Pol δ), inhibiting DNA replication. antiproliferative.</p>Fórmula:C22H21N3O5S2Pureza:98.79%Cor e Forma:SolidPeso molecular:471.55Antibacterial agent 123
CAS:<p>Antibacterial Agent 123 (Compound 111) serves as an effective membrane-disrupting agent targeting antibiotic-resistant Gram-positive bacteria [1].</p>Fórmula:C17H8F9N3OCor e Forma:SolidPeso molecular:441.25UIAA-II-232
CAS:<p>UIAA-II-232 (compound 19b) is a potent inhibitor of DNA gyrase catalytic (IC 50= 3.5 μM).</p>Fórmula:C20H24FN5O3Cor e Forma:SolidPeso molecular:401.43SARS-CoV-2 3CLpro-IN-4
CAS:<p>SARS-CoV-2 3CLpro-IN-4 (Compound 5g) is a multifunctional inhibitor of SARS CoV-2 3CLpro, exhibiting antiviral, antibacterial, and antifungal activities.</p>Fórmula:C22H19ClN6OSCor e Forma:SolidPeso molecular:450.94Berteroin
CAS:<p>Berteroin, found in cruciferous veggies like rucola and mustard, may act as an antioxidant, reducing inflammation and androgen receptors in cancer.</p>Fórmula:C7H13NS2Cor e Forma:SolidPeso molecular:175.31HI-236
CAS:<p>HI-236 is used as a non-nucleoside HIV-1 reverse-transcriptase inhibitor.</p>Fórmula:C16H18BrN3O2SPureza:98%Cor e Forma:SolidPeso molecular:396.3CBR-6672
CAS:<p>CBR-6672, a potent anti-tuberculosis agent; type II NADH dehydrogenase inhibitor; MIC: 0.14 μM.</p>Fórmula:C17H20FN3O2SCor e Forma:SolidPeso molecular:349.42As-358
CAS:<p>As-358 has inhibitory effects against Ebola virus (IC50 = 47.5 μM) and Marburg virus (IC50 = 3.7 μM) [1].</p>Fórmula:C18H31NO2Cor e Forma:SolidPeso molecular:293.4413(S)-HpOTrE
CAS:<p>13(S)-HpOTrE, a fatty acid from soy LO-2 action on α-linolenic acid, forms in soybeans (9:1 ratio). It generates plant defense signals against pests.</p>Fórmula:C18H30O4Cor e Forma:SolidPeso molecular:310.43Antifungal agent 30
CAS:<p>Potent antifungal, works against Candida albicans (MIC: 0.03 μg/mL) & Aspergillus fumigatus (MIC: 0.5 μg/mL) via CYP51 interactions.</p>Fórmula:C18H14Cl2F2N2SeCor e Forma:SolidPeso molecular:446.18InhA-IN-4
CAS:<p>InhA-IN-4 (TU14) is a Mycobacterium tuberculosis InhA (enoyl ACP reductase) inhibitor for the study of Mycobacterium tuberculosis infection.</p>Fórmula:C14H12BrN3O2SPureza:>99.99%Cor e Forma:SolidPeso molecular:366.23Antofloxacin Hydrochloride
CAS:<p>Antofloxacin Hydrochloride: Fluoroquinolone for AECB, AP, cystitis, folliculitis treatment.</p>Fórmula:C18H22ClFN4O4Pureza:98%Cor e Forma:SolidPeso molecular:412.84Linogliride
CAS:<p>Linogliride: a guanidine derivative, inhibits insulin release, and enhances glucose tolerance by blocking ATP-sensitive K+ channels in pancreatic beta cells.</p>Fórmula:C16H22N4OPureza:98%Cor e Forma:SolidPeso molecular:286.37KIN1400
CAS:<p>KIN1400 activates IRF3, boosts antiviral immunity, stimulates IFNbeta, and inhibits WNV, DV, and HCV.</p>Fórmula:C24H17F2N3O2SPureza:98%Cor e Forma:SolidPeso molecular:449.47Anthrarobin
CAS:<p>Anthrarobin is an antipsoriatic.</p>Fórmula:C14H10O3Pureza:98%Cor e Forma:SolidPeso molecular:226.23Clevudine triphosphate
CAS:<p>Clevudine triphosphate is a TTP analog that is able to inhibit protein priming independently of the deoxynucleoside triphosphate substrate.</p>Fórmula:C10H16FN2O14P3Pureza:98%Cor e Forma:SolidPeso molecular:500.16Influenza virus-IN-2
CAS:<p>Influenza virus-IN-2 (compound 19) has anti-influenza A virus activities that is a potent inhibitor of influenza virus with an CC 50 of 150.85 μM and EC 50 of 2</p>Fórmula:C17H17NO5Cor e Forma:SolidPeso molecular:315.32ATD-3169
CAS:<p>ATD-3169 is a ROS generator with antibacterial activity.</p>Fórmula:C15H14O3Pureza:98%Cor e Forma:SolidPeso molecular:242.27A3N19
CAS:<p>A3N19 is a potent inhibitor of HIV-1 non-nucleoside reverse transcriptase and is able to act on HIV-1 IIIB (EC50: 3.28 nM).</p>Fórmula:C31H31N9O2SCor e Forma:SolidPeso molecular:593.7TbPTR1 inhibitor 1
CAS:<p>TbPTR1 inhibitor 1 effectively targets kinetochore PTR1 with IC50 <0.1 nM, EC50 0.66 μM against Trypanosoma brucei.</p>Fórmula:C22H21N7OCor e Forma:SolidPeso molecular:399.45SARS-CoV-2 nsp13-IN-2
CAS:<p>SARS-CoV-2 nsp13-IN-2 (Compound C2) is a small molecule inhibitor of SARS-CoV-2 non-structural protein 13 (nsp13) that acts on nsp13 ssDNA+ATPase (IC50: 42 μM).</p>Fórmula:C20H18N6OS2Cor e Forma:SolidPeso molecular:422.53Enviroxime
CAS:<p>Enviroxime(LY 122772, NSC 346230) is an anti-infective and anti-disease agent. Enviroxime targets the 3A coding region of rhinovirus and poliovirus.</p>Fórmula:C17H18N4O3SCor e Forma:SolidPeso molecular:358.41DDD100097
CAS:<p>DDD100097 is a N-myristoyltransferase inhibitor with potential inhibitory effects on Trypanosoma brucei, which can be used to study neurological disorders.</p>Fórmula:C22H30Cl2F2N4O2SPureza:98.89%Cor e Forma:SolidPeso molecular:523.47PXYC13
CAS:<p>PXYC13 inhibits Mtb RpsA essential for trans-translation with Kd of 7.61 μM; less effective on RpsA-CTD Δ438A (Kd 8.50 μM).</p>Fórmula:C15H15N5O2SCor e Forma:SolidPeso molecular:329.38B 669
CAS:<p>B 669 has antibacterial activity.</p>Fórmula:C30H28N4Cor e Forma:SolidPeso molecular:444.57HIV-1 inhibitor-45
CAS:<p>HIV-1 inhibitor-45 is a potent inhibitor of HIV-1 RNase H (IC50: 0.067 μM) and has antiviral effects.</p>Fórmula:C23H24N4O8SCor e Forma:SolidPeso molecular:516.52Pterophyllin 2
CAS:<p>Pterophyllin 2 is an agent of natural antifungal. It also against postharvest fruit pathogenic fungi.</p>Fórmula:C15H12O3Pureza:98%Cor e Forma:SolidPeso molecular:240.25IACS-4759
CAS:<p>IACS-4759 is a novel potent and selective MTH1 inhibitor with excellent cell permeability and good metabolic stability in microsomes.</p>Fórmula:C10H17N3O2Cor e Forma:SolidPeso molecular:211.26SARS-CoV-2-IN-31
CAS:<p>SARS-CoV-2-IN-31: COVID-19 inhibitor, IC50: 28.84-38.36 μM, useful in cancer studies.</p>Fórmula:C29H28N4O2Cor e Forma:SolidPeso molecular:464.56Antimycobacterial agent-3
CAS:<p>Antimycobacterial agent-3: low toxicity, fights MTB H37Rv and drug-resistant strains (MIC 0.029-0.110 μM).</p>Fórmula:C21H15F6N5O4SCor e Forma:SolidPeso molecular:547.43Xenalamine
CAS:<p>Xenalamine is a synthetic compound of antiviral.</p>Fórmula:C23H21NO4Pureza:98%Cor e Forma:SolidPeso molecular:375.42Adenallene
CAS:<p>Adenallene inhibits replication and cytopathic effects of HIV in vitro.</p>Fórmula:C9H9N5OPureza:98%Cor e Forma:SolidPeso molecular:203.2Antitubercular agent-27
CAS:<p>Antitubercular agent-27: IC50=3.2 μM, MIC=7.8 μM, IC90=7.0 μM; effective against resistant Mycobacterium tuberculosis, low toxicity.</p>Fórmula:C14H8BrN3O3Cor e Forma:SolidPeso molecular:346.14Antitubercular agent-24
CAS:<p>Compound 1: Antitubercular, fights M. tuberculosis H37Rv, IC50 - extracellular 0.83 μM, intracellular 0.17 μM.</p>Fórmula:C18H19N3O2S2Cor e Forma:SolidPeso molecular:373.49MDRTB-IN-1
CAS:<p>MDRTB-IN-1 (5aα) is an antibiotic which is against Mycobacterium tuberculosis H37Rv(MIC90 :10.5 μM).</p>Fórmula:C15H18N2O3Pureza:98%Cor e Forma:SolidPeso molecular:274.32AQ 148
CAS:<p>AQ 148 is a potent competitive inhibitor of HIV-1 PR.</p>Fórmula:C30H37N3O4Cor e Forma:SolidPeso molecular:503.63RyRs activator 1
CAS:<p>RyRs activator 1 triggers ranibulin receptors; 100% larvicidal at 0.5 mg/L, 90% at 0.01 mg/L.</p>Fórmula:C21H14ClF3N6O4Cor e Forma:SolidPeso molecular:506.82Fumaramidmycin
CAS:<p>Fumaramidmycin is an antibiotic that is produced by Streptomyces kurssanovii NR-7GG1.</p>Fórmula:C12H12N2O3Pureza:98%Cor e Forma:SolidPeso molecular:232.24Netzahualcoyone
CAS:<p>Netzahualcoyone inhibited the respiration of intact cells of B. subtilis but had no effect on the respiration of E. coli.</p>Fórmula:C30H36O6Pureza:98%Cor e Forma:SolidPeso molecular:492.6Albitiazolium bromide
CAS:<p>Albitiazolium bromide is an antimalarial compound disrupting phosphatidylcholine biosynthesis in Plasmodium, transported via NPP and cation carriers.</p>Fórmula:C24H42BrN2O2S2Pureza:99.743%Cor e Forma:SolidPeso molecular:534.64HIV-1 integrase inhibitor 9
CAS:<p>HIV-1 integrase inhibitor 9 (compound 8a) is a potent inhibitor of HIV-1 RNase H (IC50: 12.3 μM) and has antiviral effects.</p>Fórmula:C18H12N2O10Cor e Forma:SolidPeso molecular:416.3Mtb-cyt-bd oxidase-IN-4
<p>Mtb-cyt-bd oxidase inhibitor; IC50=0.25μM; MIC=8μM against Mycobacterium tuberculosis; for TB research.</p>Fórmula:C25H32FNOCor e Forma:SolidPeso molecular:381.53Taribavirin
CAS:<p>Taribavirin: oral drug targeting HCV in liver, spares RBCs to reduce risk of anemia.</p>Fórmula:C8H13N5O4Pureza:98%Cor e Forma:SolidPeso molecular:243.223-Fucosyllactose
CAS:<p>3-Fucosyllactose, a key fucosylated oligosaccharide in human milk, offers prebiotic and immune benefits.</p>Fórmula:C18H32O15Cor e Forma:SolidPeso molecular:488.44FPI-1602
CAS:<p>FPI-1602 is a β-lactamase inhibitor with strong antimicrobial activity against Pseudomonas aeruginosa, Escherichia coli, and Enterobacter species [1].</p>Fórmula:C11H17N5O7SCor e Forma:SolidPeso molecular:363.35Cgp 53820
CAS:<p>CGP 53820 is a pseudosymmetric inhibitor of HIV-1 Protease.</p>Fórmula:C31H51N5O5Cor e Forma:SolidPeso molecular:573.77(-)-Pinocembrin
CAS:<p>(-)-Pinocembrin: Anti-tuberculosis (IC50: 1.11 mg/mL dormant, 1.21 mg/mL active), antiproliferative (IC50: 1.88-11 mg/mL on various cell lines).</p>Fórmula:C15H12O4Cor e Forma:SolidPeso molecular:256.25Reverse transcriptase-IN-4
<p>Reverse transcriptase-IN-4: potent, selective NNRT inhibitor; EC50 = 0.053 μM for HIV-1, 0.26 μM for E138K mutant.</p>Fórmula:C17H21N5OSCor e Forma:SolidPeso molecular:343.45Chitin synthase inhibitor 4
CAS:<p>Chitin synthase inhibitor 4: a CHS inhibitor with antimicrobial properties, potential fungicide.</p>Fórmula:C20H15FN4OPureza:99.74%Cor e Forma:SolidPeso molecular:346.36RO5464466
CAS:<p>RO5464466 is an inhibitor of influenza A virus (H1N1) fusion.</p>Fórmula:C16H26N2O3SCor e Forma:SolidPeso molecular:326.45Rovafovir Etalafenamide
CAS:<p>Rovafovir Etalafenamide is a prodrug of anti-HIV nucleoside phosphonate.</p>Fórmula:C21H24FN6O6PPureza:98%Cor e Forma:SolidPeso molecular:506.42NSC666715
CAS:<p>NSC666715 is the strand-displacement activity of DNA polymerase inhibitor.</p>Fórmula:C15H13Cl2N5O2S2Pureza:98%Cor e Forma:SolidPeso molecular:430.33D-Xylofuranose, 1,2,3,5-tetraacetate
CAS:<p>1,2,3,5-Tetra-O-acetyl-D-xylofuranose is a starting material for the synthesis of nucleosides.</p>Fórmula:C13H18O9Cor e Forma:SolidPeso molecular:318.28Taribavirin hydrochloride
CAS:<p>Taribavirin HCl: oral drug targeting HCV in liver, spares red blood cells, aims to reduce anemia risk.</p>Fórmula:C8H14ClN5O4Pureza:98%Cor e Forma:SolidPeso molecular:279.68SARS-CoV-IN-2
CAS:<p>SARS-CoV-IN-2 is an effective SARS-CoV replication inhibitor</p>Fórmula:C24H26ClFeN3OPureza:98%Cor e Forma:SolidPeso molecular:463.78PPQ-581
CAS:<p>PPQ-581 is an anti-flu drug that blocks RNP trafficking and stops virus replication, preventing cell damage.</p>Fórmula:C25H24FN3O3Cor e Forma:SolidPeso molecular:433.47Antiparasitic agent-9
CAS:<p>Antiparasitic agent-9 (compound 47) - orally active with high efficacy against human parasites.</p>Fórmula:C18H20N6O2SCor e Forma:SolidPeso molecular:384.46HIV-1 inhibitor-48
CAS:<p>HIV-1 inhibitor-48 is a novel non-nucleoside reverse transcriptase inhibitor (NNRTI) and exhibits anti-HIV-1 activity .</p>Fórmula:C19H16BrN5Cor e Forma:SolidPeso molecular:394.27SARS-CoV-2-IN-16
CAS:<p>SARS-CoV-2-IN-16 strongly inhibits NPro, with EC50 of 3.69 μM and Kd of 7.82 μM, suggesting effective binding and antiviral properties.</p>Fórmula:C17H20N2O2Cor e Forma:SolidPeso molecular:284.35HIV-1 inhibitor-35
CAS:<p>HIV-1 inhibitor-35, potent against HIV (EC50: 80 nM LTR, 70 nM CMV), also suppresses HepG2 cells (CC50: 40 nM), may reverse HIV-1 latency.</p>Fórmula:C13H12Cl3N5OSCor e Forma:SolidPeso molecular:392.69Antistaphylococcal agent 1
CAS:<p>Antistaphylococcal agent 1 is an antistaphylococcal therapeutic agent.</p>Fórmula:C22H16N6O2Cor e Forma:SolidPeso molecular:396.4Antifungal agent 69
CAS:<p>Antifungal agent 69 (compound 13), a eugenol-imidazole derivative, demonstrates targeted activity against Candida albicans with a minimum inhibitory</p>Fórmula:C23H23ClN2O4Cor e Forma:SolidPeso molecular:426.89Enisamium iodide
CAS:<p>Enisamium iodide is used as an antiviral agent.</p>Fórmula:C14H15IN2OCor e Forma:SolidPeso molecular:354.19Antiviral agent 19
CAS:<p>Antiviral agent 19 (Compound 3) is a selective inhibitor of Zika virus (EC50: 1.3 μM) with low cytotoxicity.</p>Fórmula:C29H35NO5Cor e Forma:SolidPeso molecular:477.59VP-4509
CAS:<p>VP-4509: Anti-MRSA, MIC 49.3 μM; combats Pseudomonas aeruginosa.</p>Fórmula:C14H16N2O5SCor e Forma:SolidPeso molecular:324.35Antibacterial agent 64
CAS:<p>Potent antibacterial, YycG inhibitor with 6.1 µM IC50. Synergistic with ampicillin against biofilm bacteria.</p>Fórmula:C29H20ClN3O6S2Cor e Forma:SolidPeso molecular:606.07SSF-109
CAS:<p>SSF-109 is a broad-spectrum fungicide, has protective activity against plant disease.</p>Fórmula:C15H18ClN3OPureza:98%Cor e Forma:SolidPeso molecular:291.78Vebufloxacin
CAS:<p>Vebufloxacin (OPC-7251) shows potent antibacterial activity against gram-positive and -negative bacteria, including Staphylococcus aureus and Pseudomonas</p>Fórmula:C19H22FN3O3Pureza:98%Cor e Forma:SolidPeso molecular:359.39Helioxanthin 8-1
CAS:<p>Helioxanthin 8-1, an analogue of helioxanthin, exhibits significant in vitro anti-HBV/HCV/HSV-1/HIV activity with EC50 of >5/10/1.4/15 μM.</p>Fórmula:C20H12N2O6Pureza:98%Cor e Forma:SolidPeso molecular:376.32Urease-IN-5
<p>Urease-IN-5: urease inhibitor, IC50 1.473 µM, low cytotoxicity, IC50 17.78 µg/mL on P. vulgaris.</p>Fórmula:C16H20N2O3SCor e Forma:SolidPeso molecular:320.41MAC173979
CAS:<p>MAC173979 inhibits E. coli de novo PABA biosynthesis and growth.</p>Fórmula:C9H5Cl2NO3Pureza:98%Cor e Forma:SolidPeso molecular:246.05SARS-CoV-2-IN-17
CAS:<p>SARS-CoV-2-IN-17 inhibits NPro effectively, with EC50 of 2.18 μM and Kd of 7.82 μM, showing strong anti-viral properties.</p>Fórmula:C19H19F3N2O3Cor e Forma:SolidPeso molecular:380.36Sulfamethomidine
CAS:<p>Sulfamethomidine has antibacterial activity [1].</p>Fórmula:C12H14N4O3SCor e Forma:SolidPeso molecular:294.33Fenpropimorph
CAS:<p>Fenpropimorph is used as a small molecule fungicide.</p>Fórmula:C20H33NOCor e Forma:SolidPeso molecular:303.48Mab Aspartate Decarboxylase-IN-1
CAS:<p>Mab Aspartate Decarboxylase-IN-1 is a potent inhibitor of aspartate decarboxylase (PanD) (IC50 = 56.3 μM) with antibacterial activity [1].</p>Fórmula:C16H11N3O3Cor e Forma:SolidPeso molecular:293.28Pam 1392
CAS:<p>Pam 1392 is a chemotherapeutic agent.</p>Fórmula:C15H13Cl2N5Cor e Forma:SolidPeso molecular:334.2Antiparasitic agent-4
CAS:<p>Compound 4q: Antiparasitic; IC50: 8.51 μM (L. infantum), 2.20 μM (T. cruzi); HepG2 cytotoxicity: CC50 18.97 μM.</p>Fórmula:C16H13N3O2Cor e Forma:SolidPeso molecular:279.29P163-0892
CAS:<p>P163-0892: potent, specific antifungal for Cryptococcus; moderate blood-brain barrier penetration.</p>Fórmula:C19H20N2O3SCor e Forma:SolidPeso molecular:356.44HBV-IN-16
CAS:<p>HBV-IN-16, a quinoline derivative, inhibits HBV cccDNA, key for viral replication (from patent WO2019121357A1).</p>Fórmula:C22H20ClNO4Cor e Forma:SolidPeso molecular:397.85Chlorhexidine-d8 HCl
CAS:<p>Chlorhexidine-d8: internal standard for GC/LC-MS, antimicrobial, inhibits MRSA/MSSA/MRSP/MSSP, affects E. faecium/C. albicans, destabilizes cell walls.</p>Fórmula:C22H24D8Cl4N10Cor e Forma:SolidPeso molecular:586.4168Mycobacterial Zmp1-IN-1
<p>Zmp1-IN-1: An inhibitor of mycobacterial Zmp1 with dose-dependent anti-tuberculosis effects.</p>Fórmula:C26H27N3O7SCor e Forma:SolidPeso molecular:525.57Cefmenoxime
CAS:<p>Cefmenoxime: IV/IM cephalosporin antibiotic, resists beta-lactamase, targets Enterobacteriaceae, gram-positive/negative bacteria.</p>Fórmula:C16H17N9O5S3Pureza:98%Cor e Forma:Almost White Or Almost Yellow Crystalline PowderPeso molecular:511.558(R)-Gyramide A hydrochloride
CAS:<p>(R)-Gyramide A HCl inhibits DNA gyrase in bacteria (IC50: 875 μM), with MIC 10-80 μM against P. aeruginosa & E. coli, sparing topoisomerase IV.</p>Fórmula:C21H28ClFN2O3SCor e Forma:SolidPeso molecular:442.97BiPNQ
CAS:<p>BiPNQ is a Trypanosoma cruzi inhibitor. Trypanosoma cruzi is the etiological agent of Chagas disease (American trypanosomiasis).</p>Fórmula:C16H12N6OCor e Forma:SolidPeso molecular:304.31Mpro/PLpro-IN-1
CAS:<p>Compound 29 inhibits SARS-CoV-2 Mpro (IC50:1.72μM) & PLpro (IC50:0.67μM) proteases effectively.</p>Fórmula:C25H27ClN4O3Cor e Forma:SolidPeso molecular:466.96PXYC1
CAS:<p>PXYC1 binds Mtb RpsA-CTD (Kd 0.81 μM) & RpsA-CTD Δ438A (Kd 0.31 μM), hindering trans-translation.</p>Fórmula:C9H10N4O3SCor e Forma:SolidPeso molecular:254.27HBV-IN-4
CAS:<p>HBV-IN-4, a phthalazinone, inhibits HBV DNA replication orally (IC50: 14 nM), encouraging genome-free capsids with strong anti-HBV effects.</p>Fórmula:C24H19ClFN5O3Cor e Forma:SolidPeso molecular:479.89Quinfamide
CAS:<p>Quinfamide is a compound with the potential to treat tropical parasitic infections such as Amoebiasis and Helminthiasis.</p>Fórmula:C16H13Cl2NO4Pureza:99.92%Cor e Forma:SolidPeso molecular:354.18DprE1-IN-1
CAS:<p>DprE1-IN-1: Potent, oral DprE1 inhibitor; stable in hepatocytes, low toxicity, anti-bacilli in macrophages, -1.29 log10 CFU.</p>Fórmula:C19H21N3O6S2Cor e Forma:SolidPeso molecular:451.52Mt KARI-IN-5
CAS:<p>Mt KARI-IN-5 inhibits MtbKARI with Ki 4.72 μM, has MIC 1.56 μM against MtbH37Rv, and is low in cytotoxicity with IC50 >64 μg/mL in HEK.</p>Fórmula:C14H10N4O5S3Cor e Forma:SolidPeso molecular:410.45X77
CAS:<p>X77, a non-covalent inhibitor of SARS-CoV-2 main protease, binds with 0.057 μM affinity.</p>Fórmula:C27H33N5O2Cor e Forma:SolidPeso molecular:459.58Antibacterial agent 48
CAS:<p>Antibacterial agent 48 is an antimicrobial agent that reduces the MIC of the antimicrobial agent Ceftazidime.</p>Fórmula:C13H18N5NaO7SCor e Forma:SolidPeso molecular:411.36AIC-292
CAS:<p>AIC-292 is a potent, tolerable reverse transcriptase inhibitor active against various HIV-1 strains, including NNRTI-resistant K103N, G190A, Y181C.</p>Fórmula:C19H12Cl2F2N4O2Cor e Forma:SolidPeso molecular:437.23RMI 10874
CAS:<p>RMI 10874 is a tilorone analogue. Tilorone is an orally bioavailable antiviral agent.</p>Fórmula:C21H26N2O4Pureza:98%Cor e Forma:SolidPeso molecular:370.4415(S)-HpETE
CAS:<p>15(S)-HpETE is a product of arachidonic acid formed in the 15-lipoxygenase pathway and inhibits angiogenesis.</p>Fórmula:C20H32O4Cor e Forma:SolidPeso molecular:336.47FabH-IN-1
CAS:<p>FabH-IN-1, a broad-spectrum antibiotic and antioxidant, inhibits bacterial FabH enzyme.</p>Fórmula:C17H16N2OSCor e Forma:SolidPeso molecular:296.39Crisnatol mesylate
CAS:<p>Crisnatol, a potent and selective DNA intercalator, has potential anticancer activity.</p>Fórmula:C24H27NO5SCor e Forma:SolidPeso molecular:441.54CTP Synthetase-IN-1
CAS:<p>CTP Synthetase-IN-1 is a cytidine 5'-triphosphate synthetase (CTPS) inhibitor with antitumor activity for the study of arthritis and rheumatoid arthritis.</p>Fórmula:C20H19F3N6O3S2Pureza:98.11% - 99.18%Cor e Forma:SolidPeso molecular:512.53DprE1-IN-4
CAS:<p>DprE1-IN-4: Potent DprE1 inhibitor (IC50: 0.90 μg/mL), good pharmacokinetics, kills TB bacteria in mice.</p>Fórmula:C20H21N3O5SCor e Forma:SolidPeso molecular:415.46Cefepime chloride
CAS:<p>Cefepime chloride, a broad-spectrum cephalosporin, combats Gram-positive/negative bacteria and can induce neurotoxicity.</p>Fórmula:C19H25ClN6O5S2Cor e Forma:SolidPeso molecular:517.02CRK12-IN-1
CAS:<p>CRK12-IN-1: strong inhibitor of CRK12, kills T.b. brucei & T. congolense (EC50s: 1.3 & 18 nM).</p>Fórmula:C20H26F2N4O3S2Pureza:99.72%Cor e Forma:SolidPeso molecular:472.57TH-Z93
CAS:<p>TH-Z93 is a potent FPPS inhibitor (IC50:90 nM) and a lipophilic bisphosphonate.</p>Fórmula:C12H22N2O7P2Pureza:98.37%Cor e Forma:SolidPeso molecular:368.26Vapendavir diphosphate
CAS:<p>Vapendavir diphosphate binds enterovirus capsids, inhibiting EV71 replication effectively (EC50: 0.5-1.4 μM).</p>Fórmula:C21H32N4O11P2Pureza:98.75% - 98.75%Cor e Forma:SolidPeso molecular:578.45CRS400393
CAS:<p>CRS400393: Anti-tuberculosis drug, MIC - M. abs.: 0.03μg/mL, M. avium: 2μg/mL, M. intracellulare: ≤0.12 μg/mL, M. tuberculosis: ≤0.12 μg/mL.</p>Fórmula:C18H20Cl2N2OSPureza:98%Cor e Forma:SolidPeso molecular:383.34DuP 105
CAS:<p>DuP 105 is an oral oxazolidinone, a novel synthetic antimicrobial compound effective against gram-positive bacteria.</p>Fórmula:C13H16N2O4SPureza:99.82%Cor e Forma:SolidPeso molecular:296.34HIV-1 inhibitor-23
CAS:<p>HIV-1 inhibitor-23 suppresses HIV reverse transcriptase, effective on wild-type (EC50: 24.9 nM) and K103N mutant (EC50: 10.4 nM), with in vitro stability.</p>Fórmula:C30H26N6O4SCor e Forma:SolidPeso molecular:566.63OYYF-175
CAS:<p>OYYF-175: potent antimicrobial antifolate; targets multi-drug resistant Gram-Negative bacteria; DHFR inhibitor with 2.36 nM IC50 against E. coli.</p>Fórmula:C17H14FN5Cor e Forma:SolidPeso molecular:307.33ThrRS-IN-1
CAS:<p>ThrRS-IN-1 inhibits Salmonella ThrRS with IC50 1.4μM, Kd 1.36μM, targets tRNA/L-threonine sites, has strong antibacterial effects.</p>Fórmula:C16H18Cl2N4O3Cor e Forma:SolidPeso molecular:385.25Urease-IN-4
<p>Urease-IN-4 inhibits urease (IC50: 1.64 µM), targets P. vulgaris (IC50: 15.27 µg/mL), and is low in cytotoxicity.</p>Fórmula:C16H20N2O3SCor e Forma:SolidPeso molecular:320.41Covidcil-19
CAS:<p>Covidcil-19 targets SARS-CoV-2 FSE with 11 nM affinity, cuts frameshifting, and lowers infectivity sharply.</p>Fórmula:C16H14N4O2Cor e Forma:SolidPeso molecular:294.31Tuberculosis inhibitor 1
CAS:<p>Tuberculosis inhibitor 1 is a potent and non-cytotoxic inhibitor of trypanosoma brucei growth (EC50: 5 nM).</p>Fórmula:C34H37N5O3Pureza:98%Cor e Forma:SolidPeso molecular:563.69cis-ccc_R08
CAS:<p>cis-ccc_R08 infection . cis-ccc_R08 is a cccDNA (covalently closed circular DNA) inhibitor .</p>Fórmula:C22H19ClO6Cor e Forma:SolidPeso molecular:414.84JMI-105
CAS:<p>JMI-105, a potent antimalarial, inhibits PfFP-2; IC50: 8.8/14.3 μM for CQ S/R strains; reduces murine P. berghei parasitemia, extends survival.</p>Fórmula:C20H23N3O2Cor e Forma:SolidPeso molecular:337.42RSV-IN-6
CAS:<p>RSV-IN-6, or Compound 53, inhibits RSV by targeting M2-1; EC50: 4.4 μM (RSV-A), 1.3 μM (RSV-B).</p>Fórmula:C19H19N3S3Cor e Forma:SolidPeso molecular:385.57Antitubercular agent 34
CAS:<p>Compound 42g: potent antitubercular, MIC 90 of 1.25 µg/mL, resists liver metabolism.</p>Fórmula:C19H14N4O2SCor e Forma:SolidPeso molecular:362.41BPIC
CAS:<p>BPIC is an agent of anti-tumor that acts by inhibiting inflammation and scavenging free radicals.</p>Fórmula:C27H20N2O5Cor e Forma:SolidPeso molecular:452.464-((4-((4-Aminophenyl)sulfonyl)phenyl)amino)-4-oxobutanoic acid
CAS:<p>4-((4-((4-Aminophenyl)sulfonyl)phenyl)amino)-4-oxobutanoic acid is a sulfonamide compound that can be used as an anti infective agent [1].</p>Fórmula:C16H16N2O5SCor e Forma:SolidPeso molecular:348.37Polyketide synthase 13-IN-2
CAS:<p>Comp 42 is a potent PKS13 inhibitor in M. tuberculosis with MIC of 0.25 μg/mL.</p>Fórmula:C22H21NO5Cor e Forma:SolidPeso molecular:379.41Cap-dependent endonuclease-IN-19
CAS:<p>Cap-dependent endonuclease-IN-19, a spirocyclic pyridinone, strongly inhibits influenza A virus RNA polymerase.</p>Fórmula:C28H31N3O4Cor e Forma:SolidPeso molecular:473.56NVP018
CAS:<p>NVP018 (BC 556) inhibits HBV, HCV, HIV-1 replication, barely affects drug transporters, and resists HCV/HIV-1 resistance development.</p>Fórmula:C45H62FN5O11Cor e Forma:SolidPeso molecular:868Antibacterial agent 67
CAS:<p>Antibacterial agent 67 blocks succinate dehydrogenase more effectively than haloperidol, with IC50 of 0.03 μM vs 4.40 μM.</p>Fórmula:C24H15F6N5OCor e Forma:SolidPeso molecular:503.4CBL 0100 free base
CAS:<p>CBL0100 is an inhibitor of viral transcriptional elongation, blocking both HIV-1 replication and reactivation.</p>Fórmula:C24H26N2O2Pureza:98.18% - 98.86%Cor e Forma:SolidPeso molecular:374.48Penconazole
CAS:<p>Penconazole is a broad-spectrum and highly effective triazole antifungal agent that acts by inhibiting fungal sterol biosynthesis. Penconazole induces oxidative stress in rat brain and cerebellum tissues and inhibits AChE activity.</p>Fórmula:C13H15Cl2N3Pureza:98.68%Cor e Forma:White PowderPeso molecular:284.18Enocitabine
CAS:<p>Enocitabine is a nucleoside analog.</p>Fórmula:C31H55N3O6Pureza:97.22%Cor e Forma:SolidPeso molecular:565.78Sarafloxacin
CAS:<p>Sarafloxacin (A56620) has antibacterial activities against Gram-positive and Gram-negative bacteria.</p>Fórmula:C20H17F2N3O3Pureza:98.07% - 98.94%Cor e Forma:SolidPeso molecular:385.36Marasmic acid
CAS:<p>Marasmic acid is a bioactive antifungal.</p>Fórmula:C15H18O4Cor e Forma:SolidPeso molecular:262.3α-Artemether
CAS:<p>alpha-Artemether is a Quinghaosu derivative with antifungal and antimalarial activity.</p>Fórmula:C16H26O5Pureza:98%Cor e Forma:SolidPeso molecular:298.37Valnivudine
CAS:<p>Valnivudine, oral BCNA antiviral, targets herpes zoster; transforms into CF-1743 in body.</p>Fórmula:C27H35N3O6Pureza:98%Cor e Forma:SolidPeso molecular:497.58CK-2-68
CAS:<p>CK-2-68 is a potent inhibitor of PfNDH2.</p>Fórmula:C24H17ClF3NO2Pureza:98%Cor e Forma:SolidPeso molecular:443.85EV-A71-IN-1
CAS:<p>EV-A71-IN-1: potent EV-A71 capsid inhibitor, EC50 0.27 μM, disrupts VP1/hSCARB2 interaction, broad-spectrum antiviral, non-toxic to human cells.</p>Fórmula:C21H15N5SCor e Forma:SolidPeso molecular:369.44BMS-585248
CAS:<p>BMS-585248 is a highly effective HIV-1 adhesion inhibitor that targets the viral envelope protein gp120.</p>Fórmula:C22H18FN7O3Cor e Forma:SolidPeso molecular:447.42GNF179 (Metabolite)
CAS:<p>GNF179 metabolite is a potent (4.8 nM vs. W2 strain) derivative of 8,8-dimethyl IP with strong in vitro stability and oral bioavailability.</p>Fórmula:C14H16FN3Pureza:98%Cor e Forma:SolidPeso molecular:245.3Cap-dependent endonuclease-IN-8
CAS:<p>Cap-dependent endonuclease-IN-8, from CN111410661A (I-196), inhibits CENs, halting orthomyxovirus replication, like influenza A/B/C.</p>Fórmula:C29H23F2N3O6SCor e Forma:SolidPeso molecular:579.57SARS-CoV-IN-1
CAS:<p>SARS-CoV-IN-1 is an effective SARS-CoV replication inhibitor(EC50 of 4.9 μM in Vero cells).</p>Fórmula:C23H24ClFeN3OPureza:98%Cor e Forma:SolidPeso molecular:449.76MmpL3-IN-3
CAS:<p>MmpL3-IN-3 (Compound 12), an MmpL3 inhibitor, exhibits potent anti-tuberculosis activity with a minimum inhibitory concentration (MIC) of 0.1 μM against H37Rv</p>Fórmula:C26H33ClN2SiCor e Forma:SolidPeso molecular:437.09Werner syndrome RecQ helicase-IN-3
CAS:<p>Potent WRN inhibitor, Werner syndrome RecQ helicase-IN-3, is orally active with 0.06 µM IC50; exhibits antiproliferative and anticancer effects.</p>Fórmula:C31H30ClF3N8O5Cor e Forma:SolidPeso molecular:687.07Floxacrine
CAS:<p>Floxacrine is drug candidate for chemoprophylaxis of malaria.</p>Fórmula:C20H13ClF3NO3Pureza:98%Cor e Forma:SolidPeso molecular:407.77F594-1001
CAS:<p>F594-1001 (compound 6) serves as a potent, highly selective inhibitor of SARS-CoV-2 Mac1-ADP-ribose, displaying IC 50 values of 8.5 μM, 68 μM, and 45 μM in AS, FP, and FRET assays, respectively. It binds directly to SARS-CoV-2 Mac1 and demonstrates dose-dependent inhibition of Mac1 ADP-ribosylhydrolase activity.</p>Fórmula:C23H28ClN3O4Cor e Forma:SolidPeso molecular:445.94Bederocin
CAS:<p>Bederocin (REP8839), a METS inhibitor, has strong activity against S. aureus, S. pyogenes, and Gram-positive bacteria.</p>Fórmula:C20H21BrFN3OSPureza:98%Cor e Forma:SolidPeso molecular:450.37Vibunazole
CAS:<p>Vibunazole is an antifungal agent.</p>Fórmula:C15H20ClN3O2Cor e Forma:SolidPeso molecular:309.79HCV-IN-37
CAS:<p>HCV-IN-37: potent HCV inhibitor, stable in rat plasma post-oral dose (15 mg/kg), blocks virus entry phase.</p>Fórmula:C31H35F2N5Cor e Forma:SolidPeso molecular:515.64Afabicin disodium
CAS:<p>Afabicin (Debio 1450), a Debio1452 precursor, targets Staphylococcus by inhibiting lipid synthesis.</p>Fórmula:C23H22N3Na2O7PCor e Forma:SolidPeso molecular:529.396Mtb-cyt-bd oxidase-IN-6
CAS:<p>Mtb-cyt-bd oxidase-IN-6, a potent inhibitor of Mycobacterium tuberculosis (Mtb) cytochrome bd (cyt-bd) oxidase (MtbCyt-bd Oxidase), exhibits an inhibitory</p>Fórmula:C20H27NOCor e Forma:SolidPeso molecular:297.43Antitrypanosomal agent 2
CAS:<p>Antitrypanosomal agent 2 shows potent and specific antiparasite activities against Trypanosoma brucei.</p>Fórmula:C17H13N5O3Pureza:99.2%Cor e Forma:SolidPeso molecular:335.32ACH-806
CAS:<p>ACH-806 is an NS4A antagonist. It can inhibit Hepatitis C Virus (HCV) replication with an EC50 of 14 nM.</p>Fórmula:C19H20F3N3O2SPureza:98%Cor e Forma:SolidPeso molecular:411.44Antimicrobial Compound 1
CAS:<p>Antimicrobial Compound 1: Alkyl pyridinium, 12C tail, 4-carboxyl head, effective against B. subtilis & E. coli.</p>Fórmula:C18H30BrNO2Pureza:>99.99%Cor e Forma:SolidPeso molecular:372.34Datelliptium chloride
CAS:<p>Datelliptium chloride is a DNA-intercalating agent derived from ellipticine. Datelliptium chloride shows anti-tumor activities.</p>Fórmula:C23H28ClN3OPureza:98%Cor e Forma:SolidPeso molecular:397.94Piperic acid
CAS:<p>Piperic acid is a powerful antioxidant and has potent antibacterial properties</p>Fórmula:C12H10O4Cor e Forma:SolidPeso molecular:218.21Ceftibuten
CAS:<p>Ceftibuten is a third-generation cephalosporin antibiotic.</p>Fórmula:C15H14N4O6S2Pureza:98%Cor e Forma:SolidPeso molecular:410.42EP39
<p>EP39 is a potent HIV-1 inhibitor, stabilizing the SP1 domain's helix and blocking virus maturation.</p>Fórmula:C38H62N2O5Cor e Forma:SolidPeso molecular:626.91WCK-4234 sodium
CAS:<p>WCK-4234 sodium inhibits β-lactamase A, C, D & OXA carbapenemases, useful against MDR infections.</p>Fórmula:C7H8N3NaO5SPureza:97.01%Cor e Forma:SolidPeso molecular:269.21Sulfaethoxypyridazine
CAS:<p>Sulfaethoxypyridazine is a antibacterial agent that can induce cataracts in rats and dogs.</p>Fórmula:C12H14N4O3SPureza:99.91%Cor e Forma:SolidPeso molecular:294.33Posaconazole hydrate
CAS:<p>Posaconazole: broad-spectrum antifungal, second-gen triazole, strong C14α demethylase inhibitor (IC50: 0.25 nM).</p>Fórmula:C37H44F2N8O5Pureza:98%Cor e Forma:SolidPeso molecular:718.79Vps34-IN-2
CAS:<p>Vps34-IN-2 is a potent and selective Vps34 inhibitor (IC50s: 2 and 82 nM on the Vps34 enzymatic assay and the GFP-FYVE cellular assay, respectively).</p>Fórmula:C18H25F3N4O3Pureza:98%Cor e Forma:SolidPeso molecular:402.41DVR-01
CAS:<p>DVR-01 is an HBV capsid inhibitor and can be used in studies about the treatment of Hepatitis B virus (HBV) infection and related conditions.</p>Fórmula:C20H23ClN2O3SPureza:99.95%Cor e Forma:SolidPeso molecular:406.93Antiviral agent 10
CAS:<p>Antiviral agent 10 effectively inhibits the respiratory syncytial virus (RSV) [1], serving as a potent anti-viral compound.</p>Fórmula:C22H24N2O5Cor e Forma:SolidPeso molecular:396.44Finafloxacin hydrochloride
CAS:<p>"Finafloxacin is a fluoroquinolone antimicrobial agent optimized for maximum effectiveness in mildly acidic conditions."</p>Fórmula:C20H20ClFN4O4Cor e Forma:SolidPeso molecular:434.853-Chlorogentisyl alcohol
CAS:<p>3-Chlorogentisyl alcohol: E. coli β-glucuronidase inhibitor (IC50=0.74µM, Ki=0.58µM), antiproliferative, for anti-cancer/inflammatory research.</p>Fórmula:C7H7ClO3Cor e Forma:SolidPeso molecular:174.58Thiarabine
CAS:<p>Thiarabine displays effective anti-tumor activity. It also inhibition of DNA synthesis.</p>Fórmula:C9H13N3O4SPureza:98%Cor e Forma:SolidPeso molecular:259.28Antitrypanosomal agent 10
<p>Antitrypanosomal agent 10, an antitrypanosomal compound, effectively inhibits Trypanosoma cruzi with an IC50 of 0.28 μM.</p>Fórmula:C17H9F6N5OCor e Forma:SolidPeso molecular:413.28SCH-43478
CAS:SCH-43478 is a non-nucleoside agent of antiviral. It has an effective and selective activity against herpes simplex virus type 2 (HSV-2).Fórmula:C12H10ClN3OPureza:98%Cor e Forma:SolidPeso molecular:247.68Synthalin sulfate
CAS:<p>Synthalin sulfate is a NMDA receptor antagonist.</p>Fórmula:C12H30N6O4SPureza:98%Cor e Forma:SolidPeso molecular:354.47Adafosbuvir PM
CAS:<p>Adafosbuvir PM (AL-335 PM) is a small molecule NS5B inhibitor that can be used to study chronic hepatitis C.</p>Fórmula:C10H13FN2O6Pureza:97.08%Cor e Forma:SolidPeso molecular:276.22Lexithromycin
CAS:<p>Lexithromycin is an erythromycin A derivative. It has antibacterial activity.</p>Fórmula:C38H70N2O13Pureza:98%Cor e Forma:SolidPeso molecular:762.97Antitubercular agent-19
CAS:<p>Antitubercular agent-19: effective against MTB H37Rv/MDR strains (MIC <0.016μg/ml), low cytotoxicity, high acute toxicity in BALB/c mice.</p>Fórmula:C24H20F6N4O3SCor e Forma:SolidPeso molecular:558.5Pyribencarb
CAS:<p>Pyribencarb, a benzylcarbamate-type fungicide, exhibits broad-spectrum activity against various plant pathogenic fungi.</p>Fórmula:C18H20ClN3O3Pureza:99.75%Cor e Forma:SolidPeso molecular:361.82Influenza A virus-IN-4
CAS:<p>Influenza A virus-IN-4 (23b), a potent neuraminidase inhibitor derived from Oseltamivir, effectively targets influenza viruses.</p>Fórmula:C19H28N4O4Cor e Forma:SolidPeso molecular:376.45JMI-346
CAS:<p>JMI-346: Anti-malarial, inhibits P. falciparum (CQS, CQR), IC50: 13 μM (3D7), 33 μM (RKL-9), targets PfFP-2 protease.</p>Fórmula:C19H20N4O2Cor e Forma:SolidPeso molecular:336.39Antileishmanial agent-8
CAS:<p>Compound 18: Antileishmanial, IC50=5.64 μM for L. donovani, low toxicity in L-6 cells, IC50=73.9 μM.</p>Fórmula:C18H16O4Cor e Forma:SolidPeso molecular:296.32Chelator 1a
CAS:<p>Chelator 1a has antifungal activity, inhibiting Aspergillus and Candida, and can be used to study fungal infections and cancer.</p>Fórmula:C16H12BrN3OSCor e Forma:SolidPeso molecular:374.26
