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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AQ 148
CAS:<p>AQ 148 is a potent competitive inhibitor of HIV-1 PR.</p>Fórmula:C30H37N3O4Cor e Forma:SolidPeso molecular:503.63Netzahualcoyone
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:416.3Neoarsphenamine
CAS:<p>Neoarsphenamine is an antisyphilitic still used for infections occasionally.</p>Fórmula:C13H14As2N2NaO4SPureza:98%Cor e Forma:SolidPeso molecular:467.16Taribavirin
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:243.22S 863390
CAS:<p>S 863390 is a renin inhibitor.</p>Fórmula:C37H52N6O4Pureza:98%Cor e Forma:SolidPeso molecular:644.85Antiparasitic agent-9
CAS:<p>Antiparasitic agent-9 (compound 47) - orally active with high efficacy against human parasites.</p>Fórmula:C18H20N6O2SCor e Forma:SolidPeso molecular:384.46Nucleoside-Analog-2
CAS:<p>Nucleoside-Analog-2 is a 4'-Azidocytidine analogue, used to against Hepatitis C virus (HCV) replication.</p>Fórmula:C9H11N5O6Pureza:98%Cor e Forma:SolidPeso molecular:285.21Deoxypheganomycin D
CAS:<p>Deoxypheganomycin D is a specific mycobacteria inhibitor.</p>Fórmula:C30H47N9O11Pureza:98%Cor e Forma:SolidPeso molecular:709.75PSI-7409 tetrasodium
CAS:<p>PSI-7409 tetrasodium, a sofosbuvir metabolite, inhibits GT 1b, 2a, 3a, 4a NS5B polymerases with IC50s of 1.6, 2.8, 0.7, 2.6 μM.</p>Fórmula:C10H16FN2Na4O14P3Pureza:98%Cor e Forma:SolidPeso molecular:592.117BMVC2
CAS:<p>BMVC2 (o-BMVC), a carbazole derivative of BMVC, is a G-quadruplex (G4) stabilizer.</p>Fórmula:C28H25I2N3Cor e Forma:SolidPeso molecular:657.33PXYC1
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:254.27Bivittoside A
CAS:<p>Bivittoside A is a non-sulfated hexoside analog obtained from Bovine sea cucumber with antifungal activity and potential antitumor activity.</p>Fórmula:C41H66O12Pureza:98%Cor e Forma:SolidPeso molecular:750.96FabH-IN-1
CAS:<p>FabH-IN-1, a broad-spectrum antibiotic and antioxidant, inhibits bacterial FabH enzyme.</p>Fórmula:C17H16N2OSCor e Forma:SolidPeso molecular:296.39Acyclovir alaninate
CAS:<p>Acyclovir alanine is a pro-drug of Acyclovir. Acyclovir works by decreasing the production of DNA of the virus and it shows very low cytotoxicity.</p>Fórmula:C11H16N6O4Cor e Forma:SolidPeso molecular:296.28RSV-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:385.57L-708906
CAS:<p>L-708906 is the Human Immunodeficiency Virus Type 1 inhibitor.</p>Fórmula:C24H20O6Pureza:98%Cor e Forma:SolidPeso molecular:404.41BPH-651
CAS:<p>BPH-651 is a CrtM inhibitor.</p>Fórmula:C19H21NOCor e Forma:SolidPeso molecular:279.38Antibacterial agent 101
CAS:<p>Antibacterial agent 101 exhibited antibacterial and antifungal effects (MIC=4-32 μg/mL).</p>Fórmula:C28H29BrN2OCor e Forma:SolidPeso molecular:489.45PXYD4
CAS:<p>PXYD4 antagonizes RpsA, key in Mtb translocation, binding RpsA-CTD (Kd 3.24 μM) & RpsA-CTD Δ438A (Kd 1.64 μM).</p>Fórmula:C25H21NO5Cor e Forma:SolidPeso molecular:415.44HIV-1 inhibitor-34
CAS:<p>HIV-1 inhibitor-34 (5q): potent, selective; EC50: 6.4 nM; MT-4 CC50: 16 μM; useful in AIDS research.</p>Fórmula:C26H27N7OCor e Forma:SolidPeso molecular:453.54Lascufloxacin HCl
CAS:<p>Lascufloxacin (KRP-AM-1977) is a strong antibiotic, most effective against gram-positive bacteria, with limited cross-resistance.</p>Fórmula:C21H25ClF3N3O4Pureza:98%Cor e Forma:SolidPeso molecular:475.89Antifungal agent 36
CAS:<p>Antifungal agent 36 is a potent anti-fungal agent that shows anti-fungal activity for Basidiomycetes [1].</p>Fórmula:C14H21NO2Cor e Forma:SolidPeso molecular:235.32BMH-23
CAS:<p>BMH-23 is an RNA polymerase I inhibitor that acts by causing nucleolar stress and showing potent anticancer activity across many tumor types.</p>Fórmula:C15H15N3Pureza:98%Cor e Forma:SolidPeso molecular:237.3Ornidazole diol
CAS:<p>Ornidazole diol is a diol produced through ornidazole rapidly hydrolyzing in basic solutions.</p>Fórmula:C7H11N3O4Pureza:98%Cor e Forma:SolidPeso molecular:201.18WRR-483
CAS:<p>WRR-483, a cysteine protease inhibitor similar to K-11777, has trypanocidal properties and potential against Chagas' disease.</p>Fórmula:C29H41N7O4SCor e Forma:SolidPeso molecular:583.75ST7612AA1
CAS:<p>ST7612AA1: potent, oral HDAC inhibitor; reactivates HIV-1 latency; shows antitumor effects; may study malaria.</p>Fórmula:C20H27N3O4SPureza:99.71%Cor e Forma:SolidPeso molecular:405.51Tromantadine hydrochloride
CAS:<p>Tromantadine hydrochloride is an amantadine derivative with antiherpetic activity (inhibits HSV-1 and HSV-2 replication).</p>Fórmula:C16H29ClN2O2Pureza:98%Cor e Forma:SolidPeso molecular:316.87HIV-1 inhibitor-37
CAS:<p>HIV-1 inhibitor-37, a potent HIV-1 suppressant, shows promise as a novel latent reactivator.</p>Fórmula:C14H11Cl3N4OCor e Forma:SolidPeso molecular:357.62BK 218
CAS:<p>BK 218: New cephalosporin, treats S. pneumoniae, H. influenzae, M. catarrhalis; less effective on penicillin-resistant strains; oral/IV use.</p>Fórmula:C15H14ClN7NaO5S2Cor e Forma:SolidPeso molecular:494.88FLDP-5
CAS:<p>FLDP-5: BBB-penetrant curcuminoid, induces ROS, DNA damage, S phase arrest, suppresses tumors in LN-18 cells.</p>Fórmula:C21H21NO5Cor e Forma:SolidPeso molecular:367.4Derquantel
CAS:<p>nicotinic acetylcholine receptor antagonist</p>Fórmula:C28H37N3O4Pureza:98%Cor e Forma:SolidPeso molecular:479.61RO-9187
CAS:<p>RO-9187 is an effective HCV virus replication inhibitor(IC50: 171 nM).</p>Fórmula:C9H12N6O5Pureza:98%Cor e Forma:SolidPeso molecular:284.23PD 140248
CAS:<p>PD 140248, a broad-spectrum 7-pyrrolidinyl fluoronaphthyridines, has been demonstrated to have excellent in vitro activity against gram-positive organisms.</p>Fórmula:C21H20ClF3N4O3Cor e Forma:SolidPeso molecular:468.86Benzoxonium chloride
CAS:<p>Benzoxonium chloride used in Thio-Ben for cutaneous leishmaniasis treatment with cryotherapy.</p>Fórmula:C23H42ClNO2Cor e Forma:SolidPeso molecular:400.04AFK-108
CAS:<p>AFK-108 is a fungicide agent.</p>Fórmula:C21H26Cl2N2OPureza:98%Cor e Forma:SolidPeso molecular:393.35Stampidine
CAS:<p>Stampidine prevents HIV-1, effective against resistant strains at subnanomolar levels.</p>Fórmula:C20H23BrN3O8PPureza:98%Cor e Forma:SolidPeso molecular:544.29GA-O-06
<p>GA-O-06: 18β-Glycyrrhetinic acid derivative with powerful antimicrobial effects on Gram-positive bacteria and anti-inflammatory properties.</p>Fórmula:C37H46FNO6Cor e Forma:SolidPeso molecular:619.76HIV-1 inhibitor-50
CAS:<p>HIV-1 inhibitor-50 is a non-nucleoside reverse transcriptase inhibitor (NNRTI) that targets HIV-1 reverse transcriptase (IC50 = 50 nM).</p>Fórmula:C24H18FN5O2Cor e Forma:SolidPeso molecular:427.43Phosphoglycolohydroxamic acid
CAS:<p>Phosphoglycolohydroxamic acid inhibits aldolase/triose-phosphate isomerase; used in antibacterial/antifungal research.</p>Fórmula:C2H6NO6PCor e Forma:SolidPeso molecular:171.05AB-506
CAS:<p>AB-506: Oral HBV replication blocker, targets core protein, hinders pgRNA encapsidation, for CHB study.</p>Fórmula:C21H18ClF2N5O3Cor e Forma:SolidPeso molecular:461.85Antituberculosis agent-2
CAS:<p>Compound 8d: treats MDR and sensitive tuberculosis, low toxicity, good oral bioavailability, stable in humans/mice; MIC: 0.454-1.757 μg/mL.</p>Fórmula:C19H17NO4Cor e Forma:SolidPeso molecular:323.34Debneyol
CAS:<p>Debneyol exhibits more potent fungicidal activity than validamycin.</p>Fórmula:C15H26O2Cor e Forma:SolidPeso molecular:238.37cp028
CAS:<p>cp028 inhibits pre-mRNA splicing in vitro.</p>Fórmula:C23H17FN2O4Cor e Forma:SolidPeso molecular:404.39Dealanylalahopcin
CAS:<p>Dealanylalahopcin is a procollagen prolyl-4-hydroxylase inhibitor.</p>Fórmula:C6H10N2O5Cor e Forma:SolidPeso molecular:190.15Quinuronium Sulfate
CAS:<p>Quinuronium sulfate treats Babesia in calves; doesn't stop carrier state; may lead to hepatic fat degeneration, not GSH depletion.</p>Fórmula:C22H23N4O5SCor e Forma:SolidPeso molecular:455.51Fungicide4
CAS:<p>Fungicide4 exhibits the high activity against the P. infestans strain.</p>Fórmula:C14H11N3OCor e Forma:SolidPeso molecular:237.26Ceftobiprole medocaril sodium
CAS:<p>Ceftobiprole medocaril sodium (BAL5788) is a prodrug of broad-spectrum cephalosporin active against MRSA, VRSA, and resistant streptococci.</p>Fórmula:C26H25N8NaO11S2Cor e Forma:SolidPeso molecular:712.64(3R,4R)-A2-32-01
CAS:<p>(3R,4R)-A2-32-01 is the (R,R)-enantiomer of A2-32-01 and has potential antibacterial activity.</p>Fórmula:C19H27NO2Pureza:98.19%Cor e Forma:SolidPeso molecular:301.42Antitubercular agent-12
CAS:<p>Compound 2c, an effective antitubercular, MIC 1.439 μg/mL, low toxicity with CC50 57.34 μg/mL.</p>Fórmula:C13H7BrN4O5Cor e Forma:SolidPeso molecular:379.124-Piperidinecarboxamide
CAS:<p>4-Piperidinecarboxamide is a mycobacterial aspartyl-tRNA synthetase (AspS) inhibitor and a potential anti-tuberculosis (TB) agent [1].</p>Fórmula:C16H15Cl2N3O2SCor e Forma:SolidPeso molecular:384.28HCV-IN-35
CAS:<p>HCV-IN-35 is a potent inhibitor of HCV and shows potential for infectious disease research.</p>Fórmula:C30H36ClN5Cor e Forma:SolidPeso molecular:502.09PC58538
CAS:<p>PC58538 is an inhibitor of FtsZ protein, a important role in the division machinery of bacterial cells.</p>Fórmula:C24H25NO3Cor e Forma:SolidPeso molecular:375.46HIV-1 inhibitor-47
CAS:<p>HIV-1 Inhibitor-47 blocks Vif-APOBEC3G interaction, has 14.33 μM IC50, and may yield antianxiety and antipsychotic derivatives.</p>Fórmula:C12H14N6Cor e Forma:SolidPeso molecular:242.28Antibacterial agent 124
CAS:<p>Antibacterial agent 124 inhibits Sa ProRS with an IC50 of 0.18 μM.</p>Fórmula:C16H17ClFN3O2Cor e Forma:SolidPeso molecular:337.78HBV-IN-15
CAS:<p>HBV-IN-15, a flavone derivative, is a potent cccDNA inhibitor, potentially aiding HBV research.</p>Fórmula:C24H23ClO6Cor e Forma:SolidPeso molecular:442.89Antileishmanial agent-13
CAS:<p>Antileishmanial agent-13, a quinoline-isatin hybrid, targets L. Major with IC50s of 0.604 μM (promastigote) and 0.508 μM (amastigote).</p>Fórmula:C17H10BrClN4OCor e Forma:SolidPeso molecular:401.64Symetine
CAS:<p>Symetine（L 16726） is a small molecule compound with antiparasitic activity that can be used to study amoebic liver abscesses in guinea pigs.</p>Fórmula:C30H48N2O2Pureza:99.79%Cor e Forma:SolidPeso molecular:468.71Ametoctradin
CAS:<p>Ametoctradin is a Qo-site inhibitor of mitochondrial respiratory complex III and is used in the study of oomycete diseases.</p>Fórmula:C15H25N5Pureza:99.65%Cor e Forma:SolidPeso molecular:275.39SSAA09E1
CAS:<p>SSAA09E1 blocks SARS-CoV entry, lowers ACE2-mediated HEK293T cell infection (EC50 = 6.7 μM), and inhibits cathepsin L (IC50 = 5.33 μM).</p>Fórmula:C7H9N3S2Cor e Forma:SolidPeso molecular:199.3CID 5951923
CAS:<p>CID 5951923 is an inhibitor of KLF5 transcription factor with an IC50 of 603 nM.</p>Fórmula:C16H18N2O7SPureza:99.95%Cor e Forma:SolidPeso molecular:382.39CRK12-IN-2
CAS:<p>CRK12-IN-2, a potent CRK12 inhibitor, has EC50 of 3.2 nM for T. congolense and 0.08 nM for T. vivax; treats trypanosomiasis in animals.</p>Fórmula:C23H33F2N5O3S2Pureza:99.26% - 99.70%Cor e Forma:SolidPeso molecular:529.67FBA-IN-1
CAS:<p>FBA-IN-1 (2a11) is the first covalent, allosteric CaFBA inhibitor, effective against Azole-resistant strains with a MIC 80 of 1 μg/mL.</p>Fórmula:C15H13NOSePureza:98.79%Cor e Forma:SolidPeso molecular:302.23Enocitabine
CAS:<p>Enocitabine is a nucleoside analog.</p>Fórmula:C31H55N3O6Pureza:97.22%Cor e Forma:SolidPeso molecular:565.78Rustmicin
CAS:<p>Rustmicin is a 14-membered macrolide identified as an inhibitor of plant pathogenic fungi.</p>Fórmula:C21H32O6Cor e Forma:SolidPeso molecular:380.48Alalevonadifloxacin HCl
CAS:<p>Alalevonadifloxacin HCl is a novel l-alanine ester prodrug of levonadifloxacin.</p>Fórmula:C22H27ClFN3O5Pureza:98%Cor e Forma:SolidPeso molecular:467.92Dextrorotation nimorazole phosphate ester
CAS:<p>Dextrorotation nimorazole phosphate ester: new, efficient, well-tolerated antibacterial and antiparasitic fourth-gen nitroimidazole.</p>Fórmula:C11H19N4O7PCor e Forma:SolidPeso molecular:350.26TCMDC-125457
CAS:<p>TCMDC-125457 aids calcium redistribution and treats artemisinin-resistant parasites with artesunate, not affecting heme crystallization.</p>Fórmula:C19H18ClN5O3Cor e Forma:SolidPeso molecular:399.83MTH1-IN-2
CAS:<p>MTH1-IN-2 is an inhibitor of MutT homolog 1 (MTH1), with anti-tumor activity.</p>Fórmula:C24H27N3O5SPureza:98%Cor e Forma:SolidPeso molecular:469.55Tenofovir diphosphate
CAS:<p>TFV-DP inhibits DNA polymerases, mimics dATP, and is used by HIV-1's reverse transcriptase.</p>Fórmula:C9H16N5O10P3Cor e Forma:SolidPeso molecular:447.17HIV-1 integrase inhibitor 4
CAS:<p>HIV-1 integrase inhibitor 4 is an HIV-1 integrase strand transfer (INST) inhibitor (IC50: 3.7 nM).</p>Fórmula:C24H20F2N4O5SPureza:98%Cor e Forma:SolidPeso molecular:514.5HIV-1 inhibitor-29
CAS:<p>HIV-1 inhibitor-29: Blocks HIV-1 IIIB (EC50: 2.18μM), resists F227L/V106A (EC50: 0.974μM), low toxicity (CC50: 211μM), for AIDS research.</p>Fórmula:C30H36N6O5Cor e Forma:SolidPeso molecular:560.64(-)-5′-Noraristeromycin
CAS:<p>(-)-5′-Noraristeromycin is an antiviral agent.</p>Fórmula:C10H13N5O3Cor e Forma:SolidPeso molecular:251.24LY 186826
CAS:<p>LY 186826 is an antibacterial agent with bicyclic pyrazolidinone properties.</p>Fórmula:C15H16N6O6SPureza:98%Cor e Forma:SolidPeso molecular:408.39360A iodide
CAS:<p>360A iodide is a selective stabilizer of G-quadruplex and inhibits telomerase activity (IC50: 300 nM in TRAP-G4 assay).</p>Fórmula:C27H23I2N5O2Pureza:98%Cor e Forma:SolidPeso molecular:703.31Sakyomicin A
CAS:<p>Sakyomicin A is an inhibitor of reverse transcriptase.</p>Fórmula:C25H26O10Cor e Forma:SolidPeso molecular:486.47Antifungal agent 2
CAS:<p>Antifungal agent 2 suppresses growth of Cryptococcus, Candida, Aspergillus at ≥0.5 μg/mL.</p>Fórmula:C19H11Br2F3N4O2Pureza:98%Cor e Forma:SolidPeso molecular:544.12Phen-DC3
CAS:<p>Phen-DC3 is a G-quadruplex (G4) specific ligand which can inhibit FANCJ and DinG helicases (IC50s of 65±6 and 50±10 nM, respectively).</p>Fórmula:C34H26N6O2Pureza:98%Cor e Forma:SolidPeso molecular:550.61OX11
CAS:<p>OX11 is a selective inhibitor of S. pneumoniae, P. aeruginosa and E. coli bacteria.</p>Fórmula:C17H10Cl2N4O3S2Cor e Forma:SolidPeso molecular:453.32LmCPB-IN-1
CAS:<p>LmCPB-IN-1, compound 35, is a reversible inhibitor of LmCPB with strong binding (pKi 9.7).</p>Fórmula:C18H30N6O2Cor e Forma:SolidPeso molecular:362.47Flomoxef sodium
CAS:<p>Flomoxef sodium, an antibiotic belonging to the oxacephem group, exhibits excellent activity against a broad spectrum of Gram-positive bacteria.</p>Fórmula:C15H17F2N6NaO7S2Pureza:97.88%Cor e Forma:SolidPeso molecular:518.44BPH-1358 free base
CAS:<p>BPH-1358 inhibits UPPS (IC50: 110 nM) and FPPS (IC50: 1.8 µM), effective against S. aureus (MIC ~250 ng/mL).</p>Fórmula:C32H28N6O2Pureza:98%Cor e Forma:SolidPeso molecular:528.6Antitrypanosomal agent 8
CAS:<p>Antitrypanosomal agent 8 (compound 3b) showed a strong antitrypanosomal effect against Trypanosoma brucei (IC50: 0.79 μM). The IC50 value was 80.95 μM.</p>Fórmula:C23H19N5O2SCor e Forma:SolidPeso molecular:429.49TMC310911
CAS:<p>TMC310911 is an oral HIV-1 protease inhibitor with an EC50 of 2.2-14.2 nM, effective against various HIV-1 strains.</p>Fórmula:C38H53N5O7S2Pureza:98%Cor e Forma:SolidPeso molecular:755.99Nifuroxime
CAS:<p>Nifuroxime, an anti-infective agent, is utilized in researching fungal infections.</p>Fórmula:C5H4N2O4Cor e Forma:SolidPeso molecular:156.1HBV-IN-19
CAS:<p>HBV-IN19 suppresses HBV, cutting HBsAg output, useful for chronic HBV study.</p>Fórmula:C24H30N2O6Cor e Forma:SolidPeso molecular:442.5Methenamine mandelate
CAS:<p>Methenamine mandelate-loaded nanoparticles can induce DNA damage and apoptosis of cancer cells.</p>Fórmula:C14H20N4O3Cor e Forma:SolidPeso molecular:292.33Neuraminidase-IN-10
CAS:<p>Neuraminidase-IN-10 inhibits flu virus strains H1N1, H5N1, and H5N8 with IC50 values of 2.6, 5.1, and 1.65 nM respectively.</p>Fórmula:C26H34N2O5SCor e Forma:SolidPeso molecular:486.62Penflufen
CAS:<p>Penflufen, a broad-spectrum succinate dehydrogenase inhibitor (SDHI), serves effectively as a fungicide.</p>Fórmula:C18H24FN3OCor e Forma:SolidPeso molecular:317.4Viral 2C protein inhibitor 1
CAS:<p>Potent 2C protein inhibitor 6aw targets various enteroviruses with low toxicity, EC50: 0.1-3.6μM.</p>Fórmula:C19H18FN3OCor e Forma:SolidPeso molecular:323.36BMS-986094
CAS:<p>INX 08189 is an RNA-directed RNA polymerase (NS5B) inhibitor.</p>Fórmula:C30H39N6O9PCor e Forma:SolidPeso molecular:658.64Antimycobacterial agent-2
CAS:<p>Antimycobacterial agent-2 has MIC99 0.8 μM vs M.tb H37Rv; cytotoxic with IC50 48.1 μM on CHO cells.</p>Fórmula:C31H50O5Cor e Forma:SolidPeso molecular:502.73Anti-MRSA agent 1
CAS:<p>Anti-MRSA agent 1 is an MRSA inhibitor with an MIC value of 0.5 μg/mL and is effective in alleviating the effects of MRSA resistance.</p>Fórmula:C26H29N7O4SCor e Forma:SolidPeso molecular:535.62DPC-961
CAS:<p>DPC-961, a reverse transcriptase inhibitor, is used potentially for the treatment of HIV infection.</p>Fórmula:C14H10ClF3N2OCor e Forma:SolidPeso molecular:314.69FR-198248
CAS:<p>FR-198248, a new anti-influenza agent, shows antiinfluenza virus activity in Madin-Darby canine kidney (MDCK) cells in vitro.</p>Fórmula:C9H10O5Cor e Forma:SolidPeso molecular:198.17Anti-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:411.43Chaetoglobosin 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:528.64Cap-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:389.45Antofloxacin Hydrochloride
CAS:<p>Antofloxacin Hydrochloride: Fluoroquinolone for AECB, AP, cystitis, folliculitis treatment.</p>Fórmula:C18H22ClFN4O4Pureza:98%Cor e Forma:SolidPeso molecular:412.84Fosdevirine
CAS:<p>Fosdevirine (GSK2248761), a non-nucleoside reverse transcriptase (NNRTI) inhibitor with anti-HIV activity, is used in the study of neurological related diseases</p>Fórmula:C20H17ClN3O3PPureza:99.92%Cor e Forma:SolidPeso molecular:413.79Ceftibuten
CAS:<p>Ceftibuten is a third-generation cephalosporin antibiotic.</p>Fórmula:C15H14N4O6S2Pureza:98%Cor e Forma:SolidPeso molecular:410.42X77
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:459.58Valnivudine
CAS:<p>Valnivudine, oral BCNA antiviral, targets herpes zoster; transforms into CF-1743 in body.</p>Fórmula:C27H35N3O6Pureza:98%Cor e Forma:SolidPeso molecular:497.58Antimycobacterial 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:547.43Antibacterial 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:544.77Fumaramidmycin
CAS:<p>Fumaramidmycin is an antibiotic that is produced by Streptomyces kurssanovii NR-7GG1.</p>Fórmula:C12H12N2O3Pureza:98%Cor e Forma:SolidPeso molecular:232.24SARS-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:380.36Mab 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:293.28DprE1-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:451.52AIC-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:437.23GNF179 (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:245.3Oxaquin
CAS:<p>Oxaquin, a water-soluble injectable prodrug, converts to active MCB3681 post-IV to fight Gram-positive bacteria.</p>Fórmula:C31H33F2N4O11PPureza:98%Cor e Forma:SolidPeso molecular:706.58L 739594
CAS:<p>L 739594 is an inhibitor of HIV-1 protease.</p>Fórmula:C31H47N3O6Pureza:98%Cor e Forma:SolidPeso molecular:557.72HIV-1 inhibitor-28
CAS:<p>HIV-1 inhibitor-28: potent, selective, EC50=58 nM, low MT-4 cell toxicity (CC50=38.6 μM), valuable in AIDS research.</p>Fórmula:C26H32N6O3SCor e Forma:SolidPeso molecular:508.649-OxoOTrE
CAS:<p>9-OxoOTrE, made by oxidizing 9-HpOTrE, has antimicrobial effects on plant pathogens like bacteria and fungi.</p>Fórmula:C18H28O3Cor e Forma:SolidPeso molecular:292.41Grepafloxacin Hydrochloride
CAS:<p>Grepafloxacin Hydrochloride is an antimicrobial agent, oral broad-spectrum fluoroquinolone. It is used to treat bacterial infections.</p>Fórmula:C19H23ClFN3O3Cor e Forma:SolidPeso molecular:395.86MPO
CAS:<p>MPO (5-(4'-Methoxyphenyl)-oxazole) is a hatch and growth of Caenorhabditis Elegans inhibitor.</p>Fórmula:C10H9NO2Pureza:99.86%Cor e Forma:SolidPeso molecular:175.18GlyRS-IN-1
CAS:<p>GlyRS-IN-1 is an inhibitor of glycyl-tRNA synthase (GlyRS). It can inhibit the growth of bacteria.</p>Fórmula:C12H17N7O7SCor e Forma:SolidPeso molecular:403.37SARS-CoV-2-IN-18
CAS:<p>SARS-CoV-2-IN-18 (Compound 26) is a potent inhibitor of SARS-CoV-2 3C-like protease (IC50 = 45 nM) [1].</p>Fórmula:C20H14N2O3Cor e Forma:SolidPeso molecular:330.34BMVC
CAS:<p>BMVC is a potent G-quadruplex (G4) stabilizer and a selective telomerase inhibitor (IC50: ~0.2 μM) with anticancer activities.</p>Fórmula:C28H25I2N3Cor e Forma:SolidPeso molecular:657.33Bofumustine
CAS:<p>Bofumustine is a chloroethyl nitrosourea with anti tumor properties.</p>Fórmula:C18H21ClN4O9Cor e Forma:SolidPeso molecular:472.83TbPTR1 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:399.45Xenalamine
CAS:<p>Xenalamine is a synthetic compound of antiviral.</p>Fórmula:C23H21NO4Pureza:98%Cor e Forma:SolidPeso molecular:375.42S-F24
CAS:<p>S-F24 is a broad-spectrum antifungal agent that demonstrates potent inhibition of CYP3A4, with an IC50 of 0.4 μM.</p>Fórmula:C25H27BrF2N6OCor e Forma:SolidPeso molecular:545.42SARS-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:463.78Sulfamethomidine
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:303.48Antifungal agent 74
CAS:<p>Antifungal agent 74 (compound 3c), is a potent substance that exhibits excellent fungicidal activity against C.</p>Fórmula:C4HCl3N4SCor e Forma:SolidPeso molecular:243.5Olanexidine Hydrochloride semihydrate
CAS:<p>Olanexidine is a monobiguanide compound with the activity of bactericidal.</p>Fórmula:C17H31Cl4N5OPureza:98%Cor e Forma:SolidPeso molecular:463.27Bentysrepinine
CAS:<p>Bentysrepinine, a novel anti-HBV agent, inhibits DNA-HBV and cccDNA activities for the treatment of hepatitis B virus (HBV)-infected hepatitis.</p>Fórmula:C29H35N3O4Pureza:98%Cor e Forma:SolidPeso molecular:489.61MMV687807
CAS:<p>MMV687807: potent anthelmintic, IC50 0.15 μM, CC50 1.69 μM against T. gondii.</p>Fórmula:C15H8ClF6NO2Cor e Forma:SolidPeso molecular:383.67GA-O-02
<p>GA-O-02, an 18β-Glycyrrhetinic acid derivative, inhibits NO/cytokines and fights Gram-positive bacteria; potent anti-inflammatory/antimicrobial.</p>Fórmula:C37H46ClNO6Cor e Forma:SolidPeso molecular:636.22SDH-IN-5
CAS:<p>SDH-IN-5 (compound 7d), a potent inhibitor of succinate dehydrogenase (SDH) with an IC50 of 3.293 μM, additionally demonstrates antifungal efficacy, exhibiting</p>Fórmula:C16H19F2N3O2Cor e Forma:SolidPeso molecular:323.34BPH-1218
CAS:<p>BPH-1218 is a SQS inhibitor.</p>Fórmula:C15H30N2O6P2Pureza:98%Cor e Forma:SolidPeso molecular:396.36KDU731
CAS:<p>KDU731: oral drug for Cryptosporidium-induced diarrhea, safe PI4K inhibitor (IC50: 25 nM), effective in vitro/in vivo.</p>Fórmula:C22H16N6O2Pureza:98%Cor e Forma:SolidPeso molecular:396.4A110
CAS:<p>A110 is a potent and selective IMPDHs inhibitor. It binds to the NAD(+) cofactor site and forms a ternary complex with IMP.</p>Fórmula:C19H15ClN4O2Pureza:98%Cor e Forma:SolidPeso molecular:366.8HIV-1 inhibitor-22
CAS:<p>HIV-1 inhibitor-22 effectively blocks HIV-1 RT (IC50=3.63 μM) with low cytotoxicity (CC50 > 227 μM).</p>Fórmula:C30H26N6O3SCor e Forma:SolidPeso molecular:550.63YXL-13
CAS:<p>YXL-13 suppresses Pseudomonas aeruginosa, hampers virulence and biofilms, and reduces drug resistance with an IC50 of 3.686 μM.</p>Fórmula:C13H15BrN2O4Cor e Forma:SolidPeso molecular:343.17PXYC12
CAS:<p>PXYC12 inhibits Mtb RpsA, key in trans-translation; binds RpsA-CTD (Kd 2.67μM) and RpsA-CTD Δ438A (Kd 4.67μM).</p>Fórmula:C15H15N5O2SCor e Forma:SolidPeso molecular:329.38Tenofovir maleate
CAS:<p>Tenofovir Disoproxil Fumarate is a nucleotide reverse transcriptase inhibitor used in the treatment of HIV and chronic Hepatitis B.</p>Fórmula:C13H18N5O8PCor e Forma:SolidPeso molecular:403.28HBV-IN-21
CAS:<p>HBV-IN-21 inhibits HBV DNA replication (IC50: 2.2 μM) and binds HBV capsid protein well (KD: 60.0 μM).</p>Fórmula:C17H17FN4OS2Cor e Forma:SolidPeso molecular:376.47MMV676584
CAS:<p>MMV676584 has anti-tuberculosis avtivity. MMV676584 is a novel drug candidate for eumycetoma .</p>Fórmula:C12H8ClFN2OS2Cor e Forma:SolidPeso molecular:314.79ANT431
CAS:<p>ANT431 is a novel metallo-β-lactamase inhibitor for the treatment of carbapenem-resistant enterobacteriaceae infections</p>Fórmula:C9H7N3O4S2Cor e Forma:SolidPeso molecular:285.3CAY10760
CAS:<p>CAY10760 inhibits RAD51-BRCA2 interaction (EC50=19 μM), reduces homologous recombination by 54%, and hinders BxPC-3/Capan-1 cancer cell proliferation.</p>Fórmula:C28H24ClN3O3Cor e Forma:SolidPeso molecular:485.96Antiparasitic agent-2
CAS:<p>Compound 8a: potent against L. infantum (IC50=7.28μM) & T. cruzi (IC50=2.30μM); mildly toxic to HepG2 (CC50=26.79μM).</p>Fórmula:C20H17N3O3Cor e Forma:SolidPeso molecular:347.37W13
CAS:<p>W13 is a potent inhibitor of MsbA and is an ATPase stimulator (EC50: 5.5 μM).</p>Fórmula:C30H34N4O3Cor e Forma:SolidPeso molecular:498.62Penamecillin
CAS:<p>Penamecillin (Wy 20788) is an orally active antibacterial agent.</p>Fórmula:C19H22N2O6SCor e Forma:SolidPeso molecular:406.45Antibacterial agent 74
CAS:<p>Antibacterial agent 74 (compound 36) has anti-Salmonella activity [1].</p>Fórmula:C16H20N2O3Cor e Forma:SolidPeso molecular:288.34Antifungal agent 70
CAS:<p>Antifungal Agent 70 (Compound 13), a dihydroeugenol-imidazole, exhibits efficacy against multi-resistant Candida auris with a minimum inhibitory concentration (</p>Fórmula:C23H25ClN2O4Cor e Forma:SolidPeso molecular:428.91Tropesin
CAS:<p>Tropesin is a non-steroidal anti-inflammatory agent (NSAIA) that has inhibitory effects on the growth of Xylaria green.</p>Fórmula:C28H24ClNO6Cor e Forma:SolidPeso molecular:505.95Salifluor
CAS:<p>Salifluor is a broad spectrum antimicrobial agent that has been investigated for its abilities to inhibit dental plaque formation.</p>Fórmula:C22H24F3NO3Cor e Forma:SolidPeso molecular:407.43HIV-1 inhibitor-9
CAS:<p>HIV-1 inhibitor-9 potently blocks WT and NNRTI-resistant HIV strains at low nanomolar levels.</p>Fórmula:C24H21N5OCor e Forma:SolidPeso molecular:395.46MMV688845
CAS:<p>MMV688845: NTM RNA polymerase inhibitor, kills Mycobacterium abscessus, and fights TB.</p>Fórmula:C24H25N3O3SCor e Forma:SolidPeso molecular:435.54TLC3407-3786
CAS:<p>MMV665916: Antimalarial quinazolinedione, effective against P. falciparum (EC50 = 0.4 µM), high selectivity (SI > 250).</p>Fórmula:C19H19N3O4Cor e Forma:SolidPeso molecular:353.37L 870810
CAS:<p>L 870810 is a small-molecule inhibitor of HIV-1 integrase with potent antiviral activity in cell culture and good pharmacokinetic properties.</p>Fórmula:C20H19FN4O4SCor e Forma:SolidPeso molecular:430.45Mtb-cyt-bd oxidase-IN-7
<p>Mtb-cyt-bd oxidase-IN-7 inhibits Cyt-bd with 4.17 μM affinity and has anti-tuberculosis properties.</p>Fórmula:C18H14F3NO2Cor e Forma:SolidPeso molecular:333.3Pyrrofolic acid
CAS:<p>Pyrrofolic acid shows high anti-folate biological activity for S. faecalis.</p>Fórmula:C23H21N7O7Pureza:98%Cor e Forma:SolidPeso molecular:507.46Metallo-β-lactamase-IN-8
CAS:<p>Metallo-β-lactamase-IN-8 (compound 17) is a potent, reversible and competitive broad-spectrum metallo-β-lactamases (MβLs) inhibitor with antibacterial activity.</p>Fórmula:C13H11ClN2O4SCor e Forma:SolidPeso molecular:326.76DPC-963
CAS:<p>DPC-963 is a RNA-directed DNA polymerase inhibitor.</p>Fórmula:C14H9F5N2OCor e Forma:SolidPeso molecular:316.23SARS-CoV-2 nsp3-IN-2
CAS:<p>SARS-CoV-2 nsp3-IN-2: Mac1 inhibitor, IC50=180μM, hinders virus replication.</p>Fórmula:C10H12N4O2Cor e Forma:SolidPeso molecular:220.23Diethofencarb
CAS:<p>Diethofencarb: a fungicide effective against Botrytis cinerea and resistant Botryis strains.</p>Fórmula:C14H21NO4Cor e Forma:SolidPeso molecular:267.32Antitubercular agent-32
CAS:<p>Antitubercular agent-32, a Benzothiazinone, inhibits DprE1 in tuberculosis, stable and water-soluble, IC50: 3.9 μM.</p>Fórmula:C22H28N4O5S2Cor e Forma:SolidPeso molecular:492.61Brecanavir
CAS:<p>Brecanavir is a tyrosyl-based arylsulfonamide, high affinity, protease inhibitor (PI) for the treatment of human immunodeficiency virus type 1.</p>Fórmula:C33H41N3O10S2Cor e Forma:SolidPeso molecular:703.82ML372
CAS:<p>ML372 is a potent and selective SMN Modulator (EC50 = 12 nM, 325% increase inSMN2) with good potency, pharmacokinetics, tolerance, and CNS penetration.</p>Fórmula:C18H20N2O4SCor e Forma:SolidPeso molecular:360.43HIV-1 inhibitor-42
CAS:<p>HIV-1 inhibitor-42 (5b) strongly blocks HIV-1 (IC50: 0.06μM) and its RT RNA/DNA polymerases (IC50: 0.518/0.072μM).</p>Fórmula:C22H20N2O5SCor e Forma:SolidPeso molecular:424.47SARS-CoV-2 nsp13-IN-3
CAS:<p>SARS-CoV-2 nsp13-IN-3 (Compound C3) is a small molecule inhibitor of SARS-CoV-2 non-structural protein 13 (nsp13) that acts on nsp13 ssDNA+ATPase (IC50: 32 μM).</p>Fórmula:C24H27N7OCor e Forma:SolidPeso molecular:429.52Chitin synthase inhibitor 10
CAS:<p>Chitin Synthase Inhibitor 10: potent antifungal with 0.11 mM IC50, effective against resistant C. albicans and C. neoformans. Used in IFI research.</p>Fórmula:C24H23Br2N3O6Cor e Forma:SolidPeso molecular:609.26UIAA-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:401.43Antifungal 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:446.18Anthrarobin
CAS:<p>Anthrarobin is an antipsoriatic.</p>Fórmula:C14H10O3Pureza:98%Cor e Forma:SolidPeso molecular:226.23HIV-1 protease-IN-1
CAS:<p>HIV-1 protease-IN-1, potent HIV inhibitor; IC50=90pM, fights B/C-HIV strains with EC50=89-13.59/8.23nM.</p>Fórmula:C25H35N3O6SCor e Forma:SolidPeso molecular:505.63BTZ-N3
CAS:<p>BTZ-N3 is an effective and selective anti-tuberculosis drug candidate.</p>Fórmula:C17H16F3N5O3SCor e Forma:SolidPeso molecular:427.4Antileishmanial 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:296.32HIV-1 inhibitor-30
CAS:<p>HIV-1 inhibitor-30 (10i) targets RT enzyme, EC50=40nM, IC50=80nM. Effective against seven NNRTI-resistant HIV-1 strains.</p>Fórmula:C19H20ClN3O2Cor e Forma:SolidPeso molecular:357.83LabMol-301
CAS:<p>LabMol-301 blocks NS5 RdRp/NS2B-NS3pro (IC50: 0.8/7.4µM), protects cells from ZIKV death.</p>Fórmula:C18H16N6Cor e Forma:SolidPeso molecular:316.36SARS-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:464.56PXYD3
CAS:<p>PXYD3 inhibits RpsA-CTD (Kd: 5.66 μM) & RpsA-CTD Δ438A (Kd: 6.91 μM) crucial in Mtb translocation.</p>Fórmula:C25H21NO5Cor e Forma:SolidPeso molecular:415.44Marasmic acid
CAS:<p>Marasmic acid is a bioactive antifungal.</p>Fórmula:C15H18O4Cor e Forma:SolidPeso molecular:262.3EV-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:369.44Werner 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:687.07gp120-IN-2
CAS:<p>gp120-IN-2 is a potent HIV-1 inhibitor (IC50 = 7.5 μM) with low cytotoxicity (CC50 = 112.93 μM).</p>Fórmula:C15H18N2O5Cor e Forma:SolidPeso molecular:306.31Antifungal agent 68
CAS:<p>Antifungal agent 68 (compound 10) effectively combats fungal infections caused by Candida and Cryptococcus gattii through the inhibition of ergosterol</p>Fórmula:C23H27ClN2O3Cor e Forma:SolidPeso molecular:414.93A 80987
CAS:<p>A 80987 is an inhibitor of HIV-1 protease.</p>Fórmula:C37H43N5O6Cor e Forma:SolidPeso molecular:653.77Antibacterial agent 105
CAS:<p>Compound 17, a phenanthrolinic quinolone, fights M. tuberculosis (MIC 90: 2.64 μM) and various bacteria (MIC 90: 0.70-44.70 μM).</p>Fórmula:C14H9N3O5Cor e Forma:SolidPeso molecular:299.24PqsR/LasR-IN-3
CAS:<p>PqsR/LasR-IN-3 (Compound 7a) inhibits hERG with the IC 50 of 109.01 μM which is also a PqsR and LasR systems inhibitor in P. aeruginosa [1].</p>Fórmula:C14H17NO5SCor e Forma:SolidPeso molecular:311.35Neuraminidase-IN-9
CAS:<p>Neuraminidase-IN-9 inhibits flu virus neuraminidase H5N1 (IC50: 0.12 μM), H5N2 (IC50: 0.049 μM), H5N6 (IC50: 0.16 μM).</p>Fórmula:C24H33BrN6O3Cor e Forma:SolidPeso molecular:533.46DC07090 Dihydrochloride
CAS:<p>DC07090 Dihydrochloride is a potent inhibitor of human enterovirus 71 3C protease.</p>Fórmula:C18H16Cl2N4OCor e Forma:SolidPeso molecular:375.25FabG1-IN-1
CAS:<p>FabG1-IN-1 (Compound 29) is a potent inhibitor of MabA (FabG1) (IC50: 38 μM).</p>Fórmula:C14H8Cl2INO3Cor e Forma:SolidPeso molecular:436.03VIM-2-IN-1
CAS:<p>VIM-2-IN-1 (compound 1dj) is a β-lactamase inhibitor with antibacterial activity. IC50: 48 μM) and New Delhi Metal (NDM-1) (IC50: 231 μM).</p>Fórmula:C12H13IN4O4SCor e Forma:SolidPeso molecular:436.23HIV-1 inhibitor-39
CAS:<p>HIV-1 inhibitor-39: blocks HIV-1, anti-RT (IC50=15.75 μM), toxic to MT-4 cells (CC50=112.9 μM).</p>Fórmula:C20H17ClN4O4S4Cor e Forma:SolidPeso molecular:541.09Antimicrobial agent-1
CAS:<p>Antimicrobial Agent-1 (compound 6C) shows strong activity (MIC = 2 μg/mL) against TolC mutant E.</p>Fórmula:C22H21N3O2SCor e Forma:SolidPeso molecular:391.49As-358 hydrochloride
CAS:<p>As-358 (hydrochloride) shows well in vivo safety as well as inhibits Ebola virus and Marburg virus with IC 50 values of 9.1 μM and 18.1 μM [1].</p>Fórmula:C18H32ClNO2Cor e Forma:SolidPeso molecular:329.91Antiviral agent 9
<p>Antiviral agent 9: EC50 0.006 nM vs HIV-1, 300x more selective than TAF.</p>Fórmula:C38H50N7O8PCor e Forma:SolidPeso molecular:763.82ERCC1-XPF-IN-1
CAS:<p>ERCC1-XPF-IN-1: potent ERCC1-XPF inhibitor (IC50: 0.49 μM), hampers CPD removal, boosts UV toxicity, hinders DNA repair.</p>Fórmula:C28H32ClN5O2Cor e Forma:SolidPeso molecular:506.04HIV-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:394.27HIV-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:392.69Vebufloxacin
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:359.39Antifungal agent 22
CAS:<p>Orally active antifungal D16 (IC50: 0.5 μg/mL) passes blood-brain barrier, stable, low toxicity, targets C. neoformansH99 cells.</p>Fórmula:C21H26Cl3NOSCor e Forma:SolidPeso molecular:446.86Antitubercular agent-28
CAS:<p>Antitubercular agent-28 targets resistant Mycobacterium tuberculosis; MIC: 4.5 μM, IC50: 1.5 μM, IC90: 2.5 μM; low cytotoxicity.</p>Fórmula:C17H14N4O2Cor e Forma:SolidPeso molecular:306.32
