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(2.949 produtos)
- Antibiótico(919 produtos)
- Antifecção(23 produtos)
- DHFR(32 produtos)
- Síntese de DNA/RNA(707 produtos)
- HBV(176 produtos)
- HIV Protease(447 produtos)
- HSV(91 produtos)
- Integrase(2 produtos)
- Ribossomo(13 produtos)
Exibir 2 mais subcategorias
Foram encontrados 5832 produtos de "Microbiologia/Virologia"
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PC190723
CAS:<p>PC190723 is an inhibitor of the bacterial cytosolic protein FtsZ with antimicrobial activity against Staphylococcus spp.</p>Fórmula:C14H8ClF2N3O2SPureza:97.64%Cor e Forma:SolidPeso molecular:355.75ITX-4520
CAS:<p>ITX-4520 novel highly potent, orally bioavailable inhibitor of hepatitis C virus (HCV) entry.</p>Fórmula:C24H23F2N3OSCor e Forma:SolidPeso molecular:439.52Ornidazole 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:201.18Vif-A3G Inhibitor N.41
CAS:<p>Vif-A3G Inhibitor N.41 is a HIV-1 inhibitor-targeting drug. It causes Vif-dependent degradation of human APOBEC3G, thereby inhibiting the Vif-A3G interaction.</p>Fórmula:C15H14N2O2Pureza:98%Cor e Forma:SolidPeso molecular:254.28Deaminase inhibitor-1
CAS:<p>Deaminase inhibitor-1 is an APOBEC3G DNA Deaminase inhibitor with an IC 50 value of 18.9 μM [1].</p>Fórmula:C11H12BrN3OSCor e Forma:SolidPeso molecular:314.2LpxH-IN-AZ1
CAS:<p>LpxH-IN-AZ1: Strong LpxH inhibitor, antimicrobial; IC50 0.36 μM against Klebsiella pneumoniae.</p>Fórmula:C21H22F3N3O3SPureza:99.82%Cor e Forma:SolidPeso molecular:453.48RIG-1 modulator 1
CAS:<p>RIG-1 modulator 1 is useful for the treatment of viral infections including influenza virus, HBV, HCV and HIV.</p>Fórmula:C14H17N5OS2Pureza:98%Cor e Forma:SolidPeso molecular:335.45Miloxacin
CAS:<p>Miloxacin is an antibiotic active against gram-negative bacteria.</p>Fórmula:C12H9NO6Pureza:98%Cor e Forma:SolidPeso molecular:263.20RO-9187
CAS:<p>RO-9187 is an effective HCV virus replication inhibitor(IC50: 171 nM).</p>Fórmula:C9H12N6O5Pureza:98%Cor e Forma:SolidPeso molecular:284.23HBV-IN-14
CAS:<p>HBV-IN-14: a pyridinopyrimidinone, potent cccDNA inhibitor for HBV study (patent WO2021190502A1, comp 5).</p>Fórmula:C22H21ClN2O5Cor e Forma:SolidPeso molecular:428.87Antibacterial agent 126
<p>Antibacterial agent 126 combats biofilm, disrupts membranes, and boosts ROS/RNS to prevent drug resistance.</p>Fórmula:C21H24NO6PCor e Forma:SolidPeso molecular:417.39HIV-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:337.78BI-10
CAS:<p>BI-10, paired with fluconazole, hinders fungal growth, increases ROS, decreases MMP, and changes membrane permeability.</p>Fórmula:C23H17BrN2OCor e Forma:SolidPeso molecular:417.3MMV666810
CAS:<p>MMV666810 is a potent 2-aminopyrazine, effective against asexual parasites at 5.94 nM and 3.3x more selective for late-stage gametocytes.</p>Fórmula:C23H21F3N4O2Cor e Forma:SolidPeso molecular:442.43SSAA09E1
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:199.3CP-320626
CAS:<p>CP-320626 is an effective human liver glycogen phosphorylase (GP) inhibitor with cholesterol-lowering activity, used in type 2 diabetes research.</p>Fórmula:C23H23ClFN3O3Pureza:98.06%Cor e Forma:SolidPeso molecular:443.9Fozivudine tidoxil
CAS:<p>Fozivudine tidoxil, a reverse transcriptase inhibitor, is used potentially for the treatment of HIV infection.</p>Fórmula:C35H64N5O8PSCor e Forma:SolidPeso molecular:745.95HIV-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:609.26MK436
CAS:<p>MK436 is a therapeutic agent and an antigenic animal drug that is effective in the treatment of Trypanosoma cruzonii infection.</p>Fórmula:C11H14N4O3Cor e Forma:SolidPeso molecular:250.25RSV-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:385.57F-17
CAS:<p>F-17 inhibits biofilm, elastase, pyocyanin, and motility, binds to LasR/PqsR, and is non-cytotoxic.</p>Fórmula:C17H15BrO4Cor e Forma:SolidPeso molecular:363.2FabH-IN-1
CAS:<p>FabH-IN-1, a broad-spectrum antibiotic and antioxidant, inhibits bacterial FabH enzyme.</p>Fórmula:C17H16N2OSCor e Forma:SolidPeso molecular:296.39FR900098 (sodium salt)
CAS:<p>FR900098, a fosmidomycin derivative, has potent antimalarial effects, targeting DOXP reductoisomerase and eradicating P. vinckei in mice at >10 mg/kg.</p>Fórmula:C5H12NNaO5PCor e Forma:SolidPeso molecular:220.117HIV-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:357.83Cap-dependent endonuclease-IN-3
CAS:<p>Cap-dependent endonuclease-IN-3 inhibits CEN, promising for studying influenza A/B. (Patent WO2019141179A1, compound III-2)</p>Fórmula:C29H25F2N3O7SCor e Forma:SolidPeso molecular:597.59Influenza virus-IN-1
CAS:<p>Influenza virus-IN-1, a potent anti-influenza A compound, has CC50 >200 μM, EC50 2.46 μM, and inhibits PAN endonuclease (EC50 312.36 nM).</p>Fórmula:C16H17NO5Cor e Forma:SolidPeso molecular:303.31Isobellidifolin
CAS:<p>Isobellidifolin, a xanthone compound, serves as a free radical scavenger and antioxidant. It exhibits a potent antifungal effect.</p>Fórmula:C14H10O6Cor e Forma:SolidPeso molecular:274.23DMJ-I-228
CAS:<p>DMJ-I-228 is a specific inhibitor of HIV-1 entry through interaction with the Env spike by virtue of the incorporation of a guandinium group.</p>Fórmula:C19H19ClFN5O4Cor e Forma:SolidPeso molecular:435.84Sitamaquine tosylate
CAS:<p>Sitamaquine: antileishmanial, targets L. donovani species, EC50 = 9.5-19.8 μM, inhibits mitochondrial complex II, induces apoptosis in promastigotes.</p>Fórmula:C28H41N3O4SCor e Forma:SolidPeso molecular:515.71Antimalarial agent 11
CAS:<p>Antimalarial compound 1: Spirocyclic chromane, EC50 - D6: 1.48 μM, ARC08-022: 1.81 μM.</p>Fórmula:C25H25F2NO3Cor e Forma:SolidPeso molecular:425.47SARS-CoV-2 3CLpro-IN-7
CAS:<p>SARS-CoV-2 3CLpro-IN-7 is a reversible covalent inhibitor of the SARS-CoV-2 3CL protease, exhibiting an inhibitory concentration (IC50) value of 1.4 µM.</p>Fórmula:C24H17ClN2O6Cor e Forma:SolidPeso molecular:464.85DHQZ 36
CAS:<p>DHQZ 36: retrograde trafficking inhibitor, anti-parasite, stops Leishmania amazonensis (EC50: 13.63 μM).</p>Fórmula:C21H18F2N2OSPureza:98%Cor e Forma:SolidPeso molecular:384.44Halofantrine, (-)-
CAS:<p>Halofantrine, (-)- is an antimalarial agent.</p>Fórmula:C26H30Cl2F3NOCor e Forma:SolidPeso molecular:500.42Cap-dependent endonuclease-IN-21
CAS:<p>Cap-dependent endonuclease-IN-21 inhibits CEN and flu virus replication, potential against influenza A. (From patent WO2021233302A1, compound 8B/8A)</p>Fórmula:C26H23F2N3O7Cor e Forma:SolidPeso molecular:527.47Purfalcamine
CAS:<p>Purfalcamine, a selective PfCDPK1 inhibitor effective against malaria, has IC50 of 17 nM and EC50 of 230 nM; halts parasites at schizont stage.</p>Fórmula:C29H33FN8OCor e Forma:SolidPeso molecular:528.62Inarigivir
CAS:<p>Inarigivir (ORI-9020) is a dinucleotide that can significantly reduce liver HBV DNA.</p>Fórmula:C20H26N7O10PSPureza:98%Cor e Forma:SolidPeso molecular:587.5RmlA-IN-1
CAS:<p>RmlA-IN-1 inhibits RmlA enzyme with 0.073 μM IC50, affecting l-Rhamnose synthesis and bacterial wall permeability.</p>Fórmula:C18H18N4O4SCor e Forma:SolidPeso molecular:386.42Antifungal agent 32
CAS:<p>Antifungal 32 (1a) strongly inhibits Candida albicans growth, filamentation, biofilm, and adhesion.</p>Fórmula:C25H28N2OCor e Forma:SolidPeso molecular:372.5HCV-IN-33
CAS:<p>HCV-IN-33 (Compound (S)-3i) is an inhibitor of HCV entry.</p>Fórmula:C31H36ClN5Cor e Forma:SolidPeso molecular:514.1HIV-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:541.09SP187
CAS:<p>SP187 (MON-DNJ) is a host-targeted iminosugar. It has anti-filovirus infection activity.SP187 is used for therapeutic use against influenza and dengue viruses.</p>Fórmula:C16H33NO5Pureza:99.18%Cor e Forma:SolidPeso molecular:319.44BPH-1358
CAS:<p>BPH-1358 (NSC-50460) inhibits FPPS and UPPS (IC50: 1.8 μM, 110 nM), active against S. aureus (MIC ~250 ng/mL).</p>Fórmula:C32H30Cl2N6O2Pureza:99.74%Cor e Forma:SolidPeso molecular:601.53Mtb-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:381.53SQ109
CAS:<p>SQ109 (NSC-722041) is an effective inhibitor of the trypomastigote form of the parasite (IC50 = 50 nM). SQ109 is an antitubercular agent and targets MmpL3.</p>Fórmula:C22H38N2Pureza:99.70% - 99.91%Cor e Forma:SolidPeso molecular:330.55Mt KARI-IN-4
CAS:<p>Mt KARI-IN-4 inhibits Mtb KARI with Ki of 5.48μM, has MIC of 0.78μM against H37Rv, and IC50 >72μg/mL, low cytotoxicity.</p>Fórmula:C13H8FN5O3S2Cor e Forma:SolidPeso molecular:365.36GA-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:619.76Mt 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:410.45RMI 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:370.44Stampidine
CAS:<p>Stampidine prevents HIV-1, effective against resistant strains at subnanomolar levels.</p>Fórmula:C20H23BrN3O8PPureza:98%Cor e Forma:SolidPeso molecular:544.29DLC27-14
CAS:<p>DLC27-14 is an HIV-1 Nef specific protein disorder catalyzer.</p>Fórmula:C25H25NO4Cor e Forma:SolidPeso molecular:403.47Neuraminidase-IN-8
CAS:<p>Neuraminidase-IN-8 (Compound 6d) is a powerful inhibitor of neuraminidase, exhibiting a low half-maximal inhibitory concentration (IC50) of 0.027 μM and</p>Fórmula:C18H16FN3O3SCor e Forma:SolidPeso molecular:373.4Neuraminidase-IN-3
CAS:<p>Neuraminidase-IN-3 inhibits flu NA: H1N1 IC50=0.73nM, H5N1=0.26nM, H5N8=0.63nM.</p>Fórmula:C27H32N2O4SCor e Forma:SolidPeso molecular:480.62Benzoxonium chloride
CAS:<p>Benzoxonium chloride used in Thio-Ben for cutaneous leishmaniasis treatment with cryotherapy.</p>Fórmula:C23H42ClNO2Cor e Forma:SolidPeso molecular:400.04SJ-3366
CAS:<p>SJ3366 is a unique and highly potent nonnucleoside reverse transcriptase human immunodeficiency virus type 1 and HIV-2 inhibitor.</p>Fórmula:C21H24N2O3Cor e Forma:SolidPeso molecular:352.43F8-S40
CAS:<p>F8-S40 is a SARS-CoV-2 main protease inhibitor (IC 50 = 10.88 μM) [1].</p>Fórmula:C13H11N3O3SCor e Forma:SolidPeso molecular:289.31CAY10784
CAS:<p>CAY10784(STAT3-IN-17) is a STAT3 inhibitor with antiproliferative and antitumor activities. CAY10784 showed antibacterial activity against Clostridium difficile</p>Fórmula:C11H6F3N3O3SPureza:99.74%Cor e Forma:SolidPeso molecular:317.24BPH-1086
CAS:<p>BPH-1086 inhibits IspH, which with RPS1 binds mRNA or integrates into bacterial ribosomes.</p>Fórmula:C4H8O7P2Cor e Forma:SolidPeso molecular:230.05Globosuxanthone A
CAS:<p>Globosuxanthone A: a dihydroxanthenone with anticancer and antifungal properties (MIC: F. graminearum 4, F. solani 8, B. cinerea 16 μg/mL).</p>Fórmula:C15H12O7Cor e Forma:SolidPeso molecular:304.25HIV-1 inhibitor-46
CAS:<p>HIV-1 inhibitor-46, compound 13d, is a potent non-nucleoside reverse transcriptase inhibitor with an EC50 of 1.425 μM, useful in AIDS research.</p>Fórmula:C24H21ClN4OSCor e Forma:SolidPeso molecular:448.97SARS-CoV-2-IN-12
CAS:<p>SARS-CoV-2-IN-12: strong 3C-like protease inhibitor; prevents viral replication; Ki=32.1 pM; useful in COVID-19 research.</p>Fórmula:C32H42F3N5O9Cor e Forma:SolidPeso molecular:697.7EGFR/HER2/TS-IN-2
CAS:<p>EGFR/HER2/TS-IN-2: Strong EGFR, HER2 & TS inhibitor; EGFR IC50=0.173μM, HER2 IC50=0.125μM, TS IC50=1.12μM; kills MDA-MB-231 cells (IC50=1.69μM).</p>Fórmula:C26H21N7OS2Cor e Forma:SolidPeso molecular:511.62Cap-dependent endonuclease-IN-16
CAS:<p>Cap-dependent endonuclease-IN-16, a pyridone derivative, inhibits CEN, showing promise for flu research.</p>Fórmula:C28H25F2N3O7SCor e Forma:SolidPeso molecular:585.58Metallo-β-lactamase-IN-7
CAS:<p>Metallo-β-lactamase-IN-7 is a potent inhibitor of VIM -Type metallo-β-lactamase with IC 50 s of 0.019 μM, 13.64 μM, 0.38 μM for VIM-2, VIM-1 and VIM-5,</p>Fórmula:C12H10N4O2SCor e Forma:SolidPeso molecular:274.3Antimicrobial agent-3
CAS:<p>Antimicrobial agent-3 (Compound U10) is an antimicrobial agent that is used against bacterial, fungal, and tubercular infections [1].</p>Fórmula:C14H11N3OSCor e Forma:SolidPeso molecular:269.32Sudoterb HCl
CAS:<p>Sudoterb has anti-tubercular activity.</p>Fórmula:C29H30Cl2F3N5OPureza:98%Cor e Forma:SolidPeso molecular:592.48Bulaquine
CAS:<p>Bulaquine, a 8-aminoquinoline derivative, targets liver stage of P. falciparum and dormant P. vivax/ovale.</p>Fórmula:C21H27N3O3Cor e Forma:SolidPeso molecular:369.46Beaucage reagent
CAS:<p>Beaucage reagent, which is found to be effective in causing DNA cleavage.</p>Fórmula:C7H4O3S2Pureza:98.50%Cor e Forma:White To Off-White PowderPeso molecular:200.23RYL-552S
CAS:<p>RYL-552S is a drug-resistant strain of Plasmodium falciparum that effectively kills the asexual blood stage of the parasite in vitro.</p>Fórmula:C24H17F4NOSCor e Forma:SolidPeso molecular:443.46Antiviral agent 18
CAS:<p>Compound 5, an antiviral agent, effectively targets murine norovirus, with potential in infectious disease and oncology research.</p>Fórmula:C11H13ClN4O4Cor e Forma:SolidPeso molecular:300.7PD 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:468.86Pirlindole free base
CAS:<p>Pirlindole is a reversible inhibitor of monoamine oxidase A (RIMA). It is structurally and pharmacologically related to metralindole.</p>Fórmula:C15H18N2Cor e Forma:SolidPeso molecular:226.32INSCoV-614(1B)
CAS:<p>INSCoV-614(1B), a potent Mpro inhibitor, may help fight SARS-CoV-2, per patent WO2021219089A1.</p>Fórmula:C23H21ClF3N5O3Cor e Forma:SolidPeso molecular:507.89HIV-1 inhibitor-56
CAS:<p>HIV-1 inhibitor-56 (compound 12126065) is a potent non-nucleoside reverse transcriptase inhibitor with significant antiviral activity against wild-type HIV-1,</p>Fórmula:C22H14ClN7O2SCor e Forma:SolidPeso molecular:475.91Tromantadine
CAS:<p>Tromantadine is an amantadine derivative with antiherpetic activity (inhibits HSV-1 and HSV-2 replication).</p>Fórmula:C16H28N2O2Pureza:98%Cor e Forma:SolidPeso molecular:280.413'-Deoxyuridine-5'-triphosphate
CAS:<p>3'-dUTP, a nucleotide analogue, competitively inhibits RNA polymerases I & II, with a Ki of 2.0 µM.</p>Fórmula:C9H15N2O14P3Cor e Forma:SolidPeso molecular:468.14Epsiprantel
CAS:<p>Epsiprantel is an orally active antiparasitic drug that inhibits various tapeworms, including Echinococcus granulosus (granular echinococcus), in dogs.</p>Fórmula:C20H26N2O2Pureza:98.09%Cor e Forma:SolidPeso molecular:326.43BK 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:494.88Neuraminidase-IN-13
CAS:<p>Neuraminidase-IN-13 (Compound 10), a neuraminidase inhibitor exhibiting antiviral activity, demonstrates significant inhibition of NDV infection in Vero cells</p>Fórmula:C13H13F7N4O7Pureza:98%Cor e Forma:SolidPeso molecular:470.25Antimalarial agent 24
CAS:<p>Compound 24 (Compound 7), an in vitro antimalarial agent, demonstrates inhibitory activity against the Plasmodium falciparum W2 strain with an IC50 of 0.81 μM</p>Fórmula:C20H16N4O2Pureza:98%Cor e Forma:SolidPeso molecular:344.37SARS-CoV-2 nsp14-IN-3
CAS:<p>SARS-CoV-2 nsp14-IN-3 (4975) is a potent inhibitor targeting the N7-Methyltransferase activity of SARS-CoV-2 nonstructural protein 14 (Nsp14), with an IC50</p>Fórmula:C17H17N3O3SPureza:98%Cor e Forma:SolidPeso molecular:343.4SARS-CoV-2-IN-41
CAS:<p>SARS-CoV-2-IN-41 (compound 2) is a potent inhibitor of SARS-CoV-2 3CL protease, exhibiting an IC50 of 0.022 µM and demonstrating antiviral efficacy [1].</p>Fórmula:C22H30F3N5O4S2Pureza:98%Cor e Forma:SolidPeso molecular:549.63Succinate dehydrogenase-IN-1
CAS:<p>Succinate dehydrogenase-IN-1 (Compound 34) acts as an inhibitor of succinate dehydrogenase (SDH), exhibiting an IC50 value of 0.94 μM and a KD of 22.4 μM. This compound also demonstrates antifungal activity, with EC50 values against Rhizoctonia solani, Sclerotinia sclerotiorum, Monilinia fructicola, and Botrytis cinerea measured at 0.04 μM, 1.13 μM, 1.61 μM, and 1.21 μM, respectively.</p>Fórmula:C20H13F6N3OCor e Forma:SolidPeso molecular:425.33HIV-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:357.62CM03
CAS:<p>CM03 is a cell-selective G-quadruplex ligand with anti-cancer activity, stabilizing G4 genes, useful in pancreatic cancer research.</p>Fórmula:C34H44N6O6Pureza:98.65%Cor e Forma:SolidPeso molecular:632.75Sulfasymazine
CAS:Sulfasymazine is a sulfonamide drug.Fórmula:C13H17N5O2SPureza:98%Cor e Forma:SolidPeso molecular:307.37TBT1
CAS:<p>TBT1 is a first-gen MsbA ATPase activator and LPS transport blocker in Acinetobacter, EC50 at 13 μM.</p>Fórmula:C16H14ClNO3SPureza:99.27%Cor e Forma:SolidPeso molecular:335.81MAC13243 HCl
CAS:<p>MAC13243 HCl inhibits LolA chaperone, targeting Gram-negative bacteria as a specific antimicrobial agent.</p>Fórmula:C20H25Cl2N3O2SPureza:98.42%Cor e Forma:SolidPeso molecular:442.4TH1217
CAS:<p>TH1217: potent dCTPase inhibitor, IC50=47 nM; boosts cytidine analogues in leukemia, may affect COVID-19.</p>Fórmula:C20H17BCl2N4O6Pureza:99.3%Cor e Forma:SolidPeso molecular:491.09ME1111
CAS:<p>ME1111, a succinate dehydrogenase inhibitor of Trichophyton species, serves as an antifungal agent effective against dermatophytes.</p>Fórmula:C12H14N2OPureza:99.45%Cor e Forma:SolidPeso molecular:202.25Uprifosbuvir
CAS:<p>Uprifosbuvir is an inhibitor of uridine nucleotide analog HCV NS5B polymerase.</p>Fórmula:C22H29ClN3O9PPureza:99.73% - >99.99%Cor e Forma:SolidPeso molecular:545.91BILB-1941
CAS:<p>BILB-1941 (BILB-1941ZW) is an inhibitor of HCV NS5B polymerase and can be used in studies about HCV infection.</p>Fórmula:C34H34N4O4Pureza:99.51% - 99.65%Cor e Forma:SolidPeso molecular:562.66SARS-CoV-2 3CLpro-IN-16
CAS:<p>SARS-CoV-2 3CLpro-IN-16 is a covalent SARS-CoV-2 3CLpro inhibitor that inhibits 3CLpro activity by forming a covalent bond with Cys145.</p>Fórmula:C17H14N2OSPureza:99.50%Cor e Forma:SolidPeso molecular:294.37Setrobuvir
CAS:<p>Setrobuvir (ANA-598) is an orally active non-nucleoside HCV NS5B polymerase inhibitor with inhibitory effects on de novo RNA synthesis and primer extension with</p>Fórmula:C25H25FN4O6S2Pureza:98.92% - >99.99%Cor e Forma:SolidPeso molecular:560.62ZIM
CAS:<p>ZIM, from 4-Aminoantipyrine, induces DNA and chromosomal damage, cell death, and phagocytosis, with potential in cancer therapy.</p>Fórmula:C20H19N3O3Pureza:99.85%Cor e Forma:SolidPeso molecular:349.38ABMA
CAS:<p>ABMA is a broad-spectrum inhibitor shielding cells from viruses, bacteria, and parasites, acting in late endosomes.</p>Fórmula:C18H24BrNOPureza:99.866%Cor e Forma:SolidPeso molecular:350.29anti-TB agent 1
CAS:<p>anti-TB agent 1 is a potent and orally active anti-tuberculosis agent (MICs: < 2 nM against the Mtb strains H37Rv, rRMP and rINH).</p>Fórmula:C23H19F3N4O3Pureza:99.73%Cor e Forma:SolidPeso molecular:456.42Nortopixantrone HCl
CAS:<p>Nortopixantrone HCl (BBR 3438) is a novel 9-azacyclonopyrazole that shows antitumor activity in a human prostate cancer model.</p>Fórmula:C20H26Cl2N6O2Pureza:99.08% - 99.74%Cor e Forma:SolidPeso molecular:453.36Sivelestat sodium tetrahydrate
CAS:<p>Sivelestat sodium tetrahydrate (ONO5046 sodium tetrahydrate) is a competitive inhibitor of human neutrophil elastase, with an IC50 of 44 nM and a Ki of 200 nM.</p>Fórmula:C20H29N2NaO11SPureza:99.68%Cor e Forma:SolidPeso molecular:528.51VP-4604
CAS:<p>VP-4604: potent anti-MRSA, inhibits S. aureus growth (MIC 4-8 μg/mL), >95% effective against MRSA.</p>Fórmula:C11H14N2O4SPureza:99.76%Cor e Forma:SolidPeso molecular:270.3Mtb-IN-2
CAS:<p>Mtb-IN-2 is a Mycobacterium tuberculosis (Mtb) compound with antimicrobial activity and low toxicity for the study of tuberculosis.</p>Fórmula:C17H12N2O4Pureza:99.27%Cor e Forma:SolidPeso molecular:308.29116-9e
CAS:<p>116-9e (MAL2-11B) is an Hsp70 chaperone DNAJA1 inhibitor with antiviral properties, inhibits SV40 replication, and can be used to study cancer drug resistance.</p>Fórmula:C31H32N2O5Pureza:99.55%Cor e Forma:SolidPeso molecular:512.6Clofoctol
CAS:<p>Clofoctol is a bacteriostatic antibiotic with activity against Gram-positive bacteria, used in the treatment of upper and lower respiratory tract infections.</p>Fórmula:C21H26Cl2OPureza:98% - 99.87%Cor e Forma:SolidPeso molecular:365.34Cytembena
CAS:<p>Cytembena is a cytostatic and a carcinogenic compound that may increase the incidence of fibroadenomas.Cytembena broadly inhibits DNA biosynthesis.</p>Fórmula:C11H8BrNaO4Pureza:99.35%Cor e Forma:White PowderPeso molecular:307.07NITD-916
CAS:<p>NITD-916: oral Mycobacterium InhA inhibitor (IC50: 570 nM), lipophilic 4-hydroxy-2-pyridone with antituberculosis action.</p>Fórmula:C20H25NO2Pureza:99.01% - 99.78%Cor e Forma:SolidPeso molecular:311.42RP-6685
CAS:<p>RP-6685 is a potent, selective DNA Polθ inhibitor with strong oral efficacy, an IC50 of 5.8 nM, and marked antitumor effects in mice.</p>Fórmula:C22H14F7N5OPureza:99.65%Cor e Forma:SoildPeso molecular:497.37PLpro/RBD-IN-1
CAS:<p>PLpro/RBD-IN-1 is a dual inhibitor of SARS-CoV-2 PLpro and the spiking protein RBD, and is considered for use in the study of viral infections.</p>Fórmula:C13H10N4OPureza:99.90%Cor e Forma:SolidPeso molecular:238.24Antimalarial agent 30
CAS:<p>Antimalarial agent 30 has anti-Plasmodium berghei liver stage parasite activity and antimalarial activity for the study of malarial infections.</p>Fórmula:C18H11F3N2Pureza:99.83% - 99.90%Cor e Forma:SolidPeso molecular:312.29Trofosfamide
CAS:<p>Trofosfamide is a derivative of oxazaphosphorine with antineoplastic potency.</p>Fórmula:C9H18Cl3N2O2PPureza:98.5% - >99.99%Cor e Forma:SolidPeso molecular:323.58N-phenylacetyl-L-Homoserine lactone
CAS:<p>N-phenylacetyl-L-Homoserine lactone attenuates the group sensing of the pathogen Acinetobacter baumannii and can be used to study bacterial infections.</p>Fórmula:C12H13NO3Pureza:98.99%Cor e Forma:SolidPeso molecular:219.24DDRI-18
CAS:<p>DDRI-18 is an inhibitor that regulates the DNA damage response, has anticancer activity, and inhibits non-homologous end-joining (NHEJ) DNA repair.</p>Fórmula:C26H20N6Pureza:98%Cor e Forma:SolidPeso molecular:416.48ClpB-IN-1
CAS:<p>ClpB-IN-1 is a potential antimicrobial agent.ClpB-IN-1 is a potent ClpB inhibitor.</p>Fórmula:C14H10N2O2S2Pureza:98.68%Cor e Forma:SolidPeso molecular:302.37QPX7728-OH disodium
CAS:<p>QPX7728 disodium (Xeruborbactam disodium) is a cyclic boronate inhibitor of many serine and metal-β-lactamases, exhibiting antibacterial activity.</p>Fórmula:C10H8BFNa2O5Pureza:>99.99%Cor e Forma:SolidPeso molecular:283.96ERCC1-XPF-IN-2
CAS:<p>ERCC1-XPF-IN-2: Nucleotide repair active, boosts cisplatin, inhibits ERCC1-XPF (IC50: 0.6 μM).</p>Fórmula:C15H13Cl2NO3Pureza:98.21%Cor e Forma:SolidPeso molecular:326.17Tivicilovir
CAS:<p>Tivicilovir (AM188) is a hepatitis B virus inhibitor. tiviclovir is a guanine-related acyclic 2'-deoxyguanine analogue with anti-herpesvirus activity.</p>Fórmula:C9H13N5O3Pureza:99.94%Cor e Forma:SolidPeso molecular:239.23BB-78485
CAS:<p>BB-78485 is an inhibitor of LpxC metalloenzymes with antibacterial activity. BB-78485 can be used for the study of Gram-negative bacterial infections.</p>Fórmula:C23H20N2O4SPureza:99.49%Cor e Forma:SolidPeso molecular:420.48Trimetozine
CAS:<p>Trimetozine (Sedoxazine) is a sedative that has been marketed in Europe since 1959. It has mild tranquilizing effects and has been used to treat anxiety.</p>Fórmula:C14H19NO5Pureza:99.83%Cor e Forma:SolidPeso molecular:281.3Morinidazole
CAS:<p>Morinidazole has antibacterial properties for researching anaerobic infections like appendicitis and PID.</p>Fórmula:C11H18N4O4Pureza:98.92% - 99.82%Cor e Forma:SolidPeso molecular:270.29Flutrimazole
CAS:<p>Flutrimazole: a dual-action imidazole with anti-inflammatory and antifungal effects; ideal for topical use due to limited skin penetration.</p>Fórmula:C22H16F2N2Pureza:98.56%Cor e Forma:SolidPeso molecular:346.37Sovaprevir
CAS:<p>Sovaprevir is a non-structural 3 (NS3) protease inhibitor with antiviral activity for the treatment of HCV infection.</p>Fórmula:C43H53N5O8SPureza:99.11%Cor e Forma:SolidPeso molecular:799.97Flaviviruses-IN-2
CAS:<p>Flaviviruses-IN-2 is a potent flaviviruses inhibitor. Flaviviruses-IN-2 reduces West Nile virus (WNV) protease activity and inhibits WNV by 56%.</p>Fórmula:C21H20N2O3SPureza:99.68%Cor e Forma:SoildPeso molecular:380.46BDCRB
<p>BDCRB disrupts HCMV DNA maturation by altering terminase cleavage, extending packaging 30 kb until second site.</p>Fórmula:C12H11BrCl2N2O4Pureza:99.41% - 99.43%Cor e Forma:SoildPeso molecular:398.04NS1-IN-1
CAS:<p>NS1-IN-1: Potent NS1 inhibitor, antiviral, reduces viral proteins by inhibiting mTORC1 via TSC1-TSC2, limits replication.</p>Fórmula:C23H26N2O4Pureza:98.71%Cor e Forma:SolidPeso molecular:394.46PI-55
CAS:<p>PI-55 is a cytokinin receptor blocker similar to BAP, disrupting BAP's receptor binding and increasing parasite aggression.</p>Fórmula:C13H13N5OPureza:98.59%Cor e Forma:SolidPeso molecular:255.28Pramiconazole
CAS:Pramiconazole (R126638), an oral antifungal, treats dermatophyte and yeast infections in seborrheic dermatitis.Fórmula:C35H39F2N7O4Pureza:98.1% - 98.59%Cor e Forma:SolidPeso molecular:659.73β-Glucuronidase-IN-1
CAS:<p>β-Glucuronidase-IN-1 is an E.</p>Fórmula:C23H27N3O3SPureza:98.05%Cor e Forma:SolidPeso molecular:425.54AP-C5
CAS:<p>AP-C5 inhibits cGKII with a Pic50 of 7.2, useful in diarrheal disease research.</p>Fórmula:C16H13N5Pureza:99.82%Cor e Forma:SolidPeso molecular:275.31GSK2556286
CAS:<p>GSK2556286 (GSK286) is an oral Mycobacterium tuberculosis inhibitor effective against MDR, XDR, and DS strains with an IC50 of 0.07 μM.</p>Fórmula:C18H23N3O3Pureza:98.17% - 99.59%Cor e Forma:SolidPeso molecular:329.39B220
CAS:<p>B220, an antiviral agent, inhibits the growth of HSV-1, HSV-2, and human cytomegalovirus (CMV).</p>Fórmula:C20H22N4Pureza:99.61% - 99.9%Cor e Forma:SolidPeso molecular:318.42Anticancer agent 73
CAS:<p>Anticancer agent 73 inhibits TRBP, disrupting TRBP-Dicer, and hinders HCC growth and spread by altering HCC miRNA and protein expression.</p>Fórmula:C14H15NO4Pureza:99.19%Cor e Forma:SolidPeso molecular:261.27N6-Allyladenosine
CAS:<p>N6-allyladenosine is an RNA labeling probe that acts through metabolic and enzyme - assisted approaches.</p>Fórmula:C13H17N5O4Pureza:99.85% - 99.90%Cor e Forma:SolidPeso molecular:307.31Carnidazole
CAS:<p>Carnidazole (ME-108) shows antiprotozoal activity and can be used in studies about the treatment of Trichomonas infection.</p>Fórmula:C8H12N4O3SPureza:99.81%Cor e Forma:SolidPeso molecular:244.27SARS-CoV-2 Mpro-IN-2
CAS:<p>SARS-CoV-2 MPro-IN-2, selective non-covalent inhibitor, IC50 0.40 μM, low toxicity, anti-COVID-19 with EC50 1.1 μM.</p>Fórmula:C22H20Cl2N4O2SPureza:99.87% - 99.97%Cor e Forma:SolidPeso molecular:475.39Brotianide
CAS:<p>Brotianide (BAY-VA4059) has anthelmintic activity and is highly potent against liver fluke and gastric fluke infestations and can be used to treat acute,</p>Fórmula:C15H10Br2ClNO2SPureza:97.44% - 98.12%Cor e Forma:SolidPeso molecular:463.57Talviraline
CAS:<p>Talviraline (Bay 10-8979) is an RNA-induced DNA polymerase inhibitor.Talviraline is a potent inhibitor of HIV-1-induced cell killing and HIV-1 replication in a</p>Fórmula:C15H20N2O3S2Pureza:99.82%Cor e Forma:SolidPeso molecular:340.46JCP174
CAS:<p>JCP174 is a depalmitoylase inhibitor that enhances Toxoplasma host-cell invasion by targeting TgPPT1.</p>Fórmula:C12H12ClNO3Pureza:97.05%Cor e Forma:SolidPeso molecular:253.68D-I03
CAS:<p>D-I03 is a selective RAD52 inhibitor with a Kd of 25.8 µM.</p>Fórmula:C23H36N6SPureza:99.65%Cor e Forma:SolidPeso molecular:428.64Isatin-β-thiosemicarbazone
CAS:<p>Isatin-β-thiosemicarbazone is a potent inhibitor of herpes simplex virus (HSV).</p>Fórmula:C9H8N4OSPureza:98.23%Cor e Forma:SolidPeso molecular:220.25BAY-43-9695
CAS:<p>BAY-43-9695 is a non-nucleoside compound with anti-human cytomegalovirus (HCMV) activity. It is the major metabolite of BAY-38-4766.</p>Fórmula:C22H25N3O4SPureza:99.50% - 99.65%Cor e Forma:SolidPeso molecular:427.526-Hydroxy-DOPA
CAS:<p>6-Hydroxy-DOPA is an allosteric inhibitor of RAD52, it inhibits proliferation of BRCA-deficient cancer cells in vitro and also inhibits APE1.</p>Fórmula:C9H11NO5Pureza:97.78% - 97.95%Cor e Forma:SolidPeso molecular:213.19SMN-C2
CAS:<p>SMN-C2, a SMN2 gene splicing regulator, is an RNA-binding ligand that regulates pre-mRNA splicing and has potential for studying spinal muscular atrophy.</p>Fórmula:C24H27N5O2Pureza:99.14%Cor e Forma:SolidPeso molecular:417.5MtUng-IN-1
CAS:<p>MtUng-IN-1 acts as an inhibitor of Mycobacterium uracil DNA glycosylase (MtUng).MtUng-IN-1 is indicated for use in cancer and infectious disease research.</p>Fórmula:C14H12N2O6Pureza:99.88%Cor e Forma:SolidPeso molecular:304.25TTP-8307
CAS:<p>TTP-8307 is an antiviral compound that inhibits the replication of rhinoviruses and enteroviruses and is used in the study of viral infections.</p>Fórmula:C27H21FN4OPureza:98.95%Cor e Forma:SolidPeso molecular:436.482'-C-Methyladenosine
CAS:<p>2'-C-Methyladenosine from C. renalis inhibits HCV, NS5B RNA synthesis (IC50: 0.3, 1.9µM), and LRV1 in L. guyanensis, L. braziliensis.</p>Fórmula:C11H15N5O4Pureza:99.85%Cor e Forma:SolidPeso molecular:281.27BMS-929075
CAS:<p>BMS-929075 is an orally active HCV NS5B replicase (HCV NS5B replicase) palm site variant inhibitor with potency, high oral bioavailability and pharmacokinetic</p>Fórmula:C31H24F2N4O3Pureza:98.44% - 99.94%Cor e Forma:SolidPeso molecular:538.54Bersacapavir
CAS:<p>Bersacapavir (JNJ-56136379) is an in vitro modulator of hepatitis B virus capsid assembly that inhibits HBV replication.</p>Fórmula:C16H14F4N4O3SPureza:98.53%Cor e Forma:SolidPeso molecular:418.37NIOCH 14
CAS:<p>NIOCH 14 is an orally available antiviral compound that inhibits exocorticoviruses, poxviruses, and smallpox viruses.</p>Fórmula:C19H17F3N2O4Pureza:98%Cor e Forma:SolidPeso molecular:394.35Bithionol sulfoxide
CAS:<p>Bithionol sulfoxide (Bithionoloxide) is a compound with inhibitory effects against parasites, inhibiting Fasciola hepatica and Schistosoma mansoni.</p>Fórmula:C12H6Cl4O3SPureza:98.76%Cor e Forma:Off White To Tinch Pink Crystalline PowderPeso molecular:372.05JPD447
CAS:<p>JPD447, a derivative of MAC-0547630, represents a new class of UppS inhibitors designed to enhance the efficacy of β-lactam antibiotics.</p>Fórmula:C20H23FN4Pureza:99.69%Cor e Forma:SolidPeso molecular:338.42Isothiafludine
CAS:<p>Isothiafludine is a HBV virus inhibitor that dramatically reduces the HBV DNA level in cells.</p>Fórmula:C18H18FN3OS2Pureza:99.71%Cor e Forma:SolidPeso molecular:375.48Galocitabine
CAS:<p>Galocitabine (Neofrutulon), a thymidylate synthase inhibitor, is used potentially for the treatment of cancer.</p>Fórmula:C19H22FN3O8Pureza:99.89%Cor e Forma:SolidPeso molecular:439.39N-(2-Hydroxypropyl)methacrylamide
CAS:<p>N-(2-Hydroxypropyl)methacrylamide is used in the synthesis of copolymers for the targeted delivery of antileishmanial agents in Visceral leishmaniasis.</p>Fórmula:C7H13NO2Pureza:99.87%Cor e Forma:SolidPeso molecular:143.18Quorum Sensing-IN-3
CAS:<p>Quorum Sensing-IN-3 (QS-IN-1) inhibits bacterial community sensing, which can inhibit information exchange between bacteria and inhibit biofilm formation.</p>Fórmula:C14H10N2OSPureza:99.58%Cor e Forma:SolidPeso molecular:254.31Tenofovir alafenamide fumarate
CAS:<p>Tenofovir alafenamide fumarate (GS-7340) is an oral anti-HIV drug that prevents infection.</p>Fórmula:C25H33N6O9PPureza:99.95%Cor e Forma:SolidPeso molecular:592.54CCR-11
CAS:<p>CCR-11 is a bypassed tannin derivative with antimicrobial activity that inhibits bacterial proliferation and can be used in the study of breast cancer.</p>Fórmula:C15H8F3NO2S2Pureza:98%Cor e Forma:SolidPeso molecular:355.35CHD1Li 6.11
CAS:<p>CHD1Li 6.11 inhibits CHD1L protein (IC50: 3.3 µM), shrinks CRC tumors in vivo, and is orally active.</p>Fórmula:C21H22BrN5OSPureza:99.04%Cor e Forma:SolidPeso molecular:472.4SQ609
CAS:<p>SQ609 is a dipiperidine-based drug candidate with notable in vitro anti-tuberculosis effects in mouse macrophages.</p>Fórmula:C22H38N2OPureza:99.84%Cor e Forma:SolidPeso molecular:346.55Isatoribine
CAS:<p>Isatoribine(ANA245) free base is a potent TLR7 receptor agonist with anti-hepatitis C virus infection activity for the study of HCV infection.</p>Fórmula:C10H12N4O6SPureza:98.99% - 99.75%Cor e Forma:SolidPeso molecular:316.29Caracemide
CAS:<p>Caracemide (NSC-253272) inhibits the enzyme ribonucleotide reductase of Escherichia coli. Caracemide can be used in anticancer studies.</p>Fórmula:C6H11N3O4Pureza:99.8%Cor e Forma:SolidPeso molecular:189.17GSK572A
CAS:<p>GSK572A is a novel and potent potent inhibitor of EchA6, which can be used to treat tuberculosis.</p>Fórmula:C22H21F4N5OPureza:98.97%Cor e Forma:SolidPeso molecular:447.43Molnupiravir
CAS:<p>Molnupiravir (EIDD-2801) is an isopropyl ester prodrug of the ribonucleoside analog EIDD-1931 with oral bioavailability.Cost-effective and quality-assured.</p>Fórmula:C13H19N3O7Pureza:99.81% - 99.98%Cor e Forma:SolidPeso molecular:329.31Azidamfenicol
CAS:<p>Azidamfenicol inhibits ribosomal peptidyltransferase with a Ki of 22 µM. Azidamfenicol is a broad-spectrum chloramphenicol-like antibiotic.</p>Fórmula:C11H13N5O5Pureza:99.61%Cor e Forma:SolidPeso molecular:295.25Quinupristin
CAS:<p>Quinupristin, a macrolide-lincosamide-streptogramin antibiotic, inhibits protein synthesis in bacteria.</p>Fórmula:C53H67N9O10SPureza:98.05% - 98.16%Cor e Forma:SolidPeso molecular:1022.22Artelinic acid
CAS:<p>Artelinic acid is an artemisinin analog with antimalarial activity and is used for the treatment of multi-drug resistant strains of Plasmodium falciparum.</p>Fórmula:C23H30O7Pureza:97.49% - 97.69%Cor e Forma:SolidPeso molecular:418.48MK-8325
CAS:<p>MK-8325 is a potent and orally available HCV NS5A inhibitor with replicative activity against a wide range of genotypes.MK-8325 has demonstrated bioavailability</p>Fórmula:C43H54Cl2F2N8O6SiPureza:>99.99%Cor e Forma:SolidPeso molecular:915.93Besifovir PM
<p>Besifovir PM (LB80331 PM) is an analogue of Besifovir, a novel orally available acyclic nucleotide phosphonate for the treatment of chronic hepatitis B</p>Fórmula:C11H15N5OPureza:98.48% - 99.90%Cor e Forma:SoildPeso molecular:233.27Chlamydia pneumoniae-IN-1
CAS:<p>Chlamydia pneumoniae-IN-1 (compound 55), a benzimidazole derivative, exhibits potent antibacterial activity, inhibiting 99% of C.</p>Fórmula:C19H15N3OSPureza:97.71%Cor e Forma:SolidPeso molecular:333.41MP265
CAS:<p>MP265 disrupts the MreB cytoskeleton and has antiproliferative effects.</p>Fórmula:C8H10Cl2N2SPureza:99.55%Cor e Forma:SolidPeso molecular:237.15Enzaplatovir
CAS:<p>Enzaplatovir is an inhibitor of Respiratory Syncytial Virus (RSV), can be used as a viral fusion protein inhibitor.</p>Fórmula:C20H19N5O3Pureza:98.54% - 99.72%Cor e Forma:SolidPeso molecular:377.4Ferroquine
CAS:<p>Ferroquine, a ferrocenyl variant of Chloroquine, exhibits antimalarial properties through oxidative stress induction, destroying Plasmodium membranes.</p>Fórmula:C23H24ClFeN3Pureza:99.97%Cor e Forma:SolidPeso molecular:433.76Rilopirox
CAS:<p>Rilopirox is a synthetic fungicidal antimycotic with hydrophobic characteristics.</p>Fórmula:C19H16ClNO4Pureza:99.17% - 99.72%Cor e Forma:SolidPeso molecular:357.79Niridazole
CAS:<p>Niridazole (Ambilhar) is an antiparasitic compound belonging to nitroimidazoles.</p>Fórmula:C6H6N4O3SPureza:98.26% - 99.55%Cor e Forma:Yellow Crystals From Dimethylformamide/Methanol SolidPeso molecular:214.2Bofutrelvir
CAS:<p>MProinhibitor 11a: SARS-CoV-2 MPro blocker, IC50=0.053μM; cuts viral yield/RNA in Vero E6 cells, EC50=0.53μM, effective 1.85-50μM.</p>Fórmula:C25H32N4O4Pureza:99.92% - >99.99%Cor e Forma:SolidPeso molecular:452.55SARS-CoV-2-IN-13
CAS:<p>SARS-CoV-2-IN-13, a stable niclosamide analogue, enhances oral bioavailability and inhibits SARS-CoV-2 (IC50: 0.057 μM).</p>Fórmula:C13H8Cl2N2O4Pureza:98.54%Cor e Forma:SolidPeso molecular:327.12SARS-CoV-2-IN-38
CAS:<p>SARS-CoV-2-IN-38, also known as compound 24, is an inhibitor of SARS-CoV-2 that demonstrates favorable oral bioavailability in mice, with an absorption fraction</p>Fórmula:C18H14ClF4NO4Pureza:99.37%Cor e Forma:SolidPeso molecular:419.76UCT943
CAS:<p>UCT943 is an inhibitor of Plasmodium falciparum PI4K (IC50 = 23 nM).</p>Fórmula:C22H20F3N5OPureza:99.87%Cor e Forma:SolidPeso molecular:427.42SARS-CoV-2-IN-14
CAS:<p>SARS-CoV-2-IN-14 is a potent and oral inhibitor of SARS-CoV-2 (IC50:0.39 μM), which is an analogue of niclosamide.</p>Fórmula:C13H9Cl2NO2Pureza:99.78%Cor e Forma:SolidPeso molecular:282.12BTA-9881
CAS:<p>BTA-9881 is a novel RSV fusion inhibitor with oral activity and antiviral activity for the study of respiratory syncytial virus infections.</p>Fórmula:C21H15ClN4O2Pureza:99.78% - 99.92%Cor e Forma:SolidPeso molecular:390.82Urease Inhibitor 07
CAS:<p>Urease Inhibitor 07 is an isosubstituted metalloproteinase inhibitor with potential activity against Mycobacterium tuberculosis strain H37Rv.</p>Fórmula:C7H5N3OSPureza:99.65%Cor e Forma:SolidPeso molecular:179.2Antimicrobial photosensitizer-1
CAS:<p>Photosensitizer-1 shows promise in treating infections, effective against S. aureus in mouse wounds.</p>Fórmula:C19H19BF2I3N3Cor e Forma:SolidPeso molecular:718.9Indinavir, threo-
CAS:<p>Indinavir, threo- is a protease inhibitor utilized as a component of highly active antiretroviral treatment to HIV/AIDS.</p>Fórmula:C36H47N5O4Pureza:98%Cor e Forma:SolidPeso molecular:613.79Brevicompanine B
CAS:<p>Brevicompanine B: fungal metabolite, regulates plant growth/circadian rhythm, inhibits Arabidopsis roots, affects gene transcription, anti-P. falciparum.</p>Fórmula:C22H29N3O2Cor e Forma:SolidPeso molecular:367.48AVG-233
CAS:<p>AVG-233 is an RNA-dependent RNA polymerase (RdRp) inhibitor with antiviral activity for the study of respiratory syncytial virus infections.</p>Fórmula:C26H22ClN5O3Pureza:99%Cor e Forma:SolidPeso molecular:487.94Aminoacyl tRNA synthetase-IN-1
CAS:<p>Aminoacyl tRNA synthetase-IN-1 is an inhibitor of bacterial aminoacyl tRNA synthetase (aaRS).</p>Fórmula:C16H25N7O7SPureza:98%Cor e Forma:SolidPeso molecular:459.48L-696229
CAS:<p>L-696229: specific HIV-1 RT inhibitor, blocks viral spread in various cells.</p>Fórmula:C17H18N2O2Pureza:98%Cor e Forma:SolidPeso molecular:282.34β-Lactamase-IN-8
CAS:<p>β-Lactamase-IN-8 (compound 20) is a potent and oral bioavailable broad-spectrum cyclic boronate β-lactamase inhibitor that can be used for researching</p>Fórmula:C10H14BNO4SCor e Forma:SolidPeso molecular:255.1CPFX2090
CAS:<p>CPFX2090, a cephalosporin antibacterial compound.</p>Fórmula:C28H28ClNO6Pureza:98%Cor e Forma:SolidPeso molecular:509.98FIKK9.1-IN-1
CAS:<p>FIKK9.1-IN-1 (Compound 1), an antimalarial agent (IC50: 2.68 μg/mL), serves as a FIKK9.1 inhibitor by interacting with the ATP-binding residues within FIKK9.1,</p>Fórmula:C22H22N2SePureza:98%Cor e Forma:SolidPeso molecular:393.38Tirfipiravir
CAS:<p>Tirapiravir is an antiviral nucleoside analog that exhibits activity against both the novel coronavirus and influenza virus [1].</p>Fórmula:C14H17N3O8Pureza:98%Cor e Forma:SolidPeso molecular:355.3Alteconazole
CAS:<p>Alteconazole is an antifungal drug.</p>Fórmula:C17H12Cl3N3OPureza:98%Cor e Forma:SolidPeso molecular:380.66Limocrocin
CAS:<p>Limocrocin is an inhibitor of reverse transcriptase.</p>Fórmula:C26H26N2O6Pureza:98%Cor e Forma:SolidPeso molecular:462.49Oxynitidine
CAS:<p>Oxynitidine, an HBV inhibitor (ID50 = 30.8 µg/mL), effectively suppresses HBV DNA replication and may be utilized in viral infection research [1].</p>Fórmula:C21H17NO5Pureza:98%Cor e Forma:SolidPeso molecular:363.36BMS-561390
CAS:<p>BMS-561390, a reverse transcriptase inhibitor, is used potentially for the treatment of HIV infection.</p>Fórmula:C14H12ClF3N2OCor e Forma:SolidPeso molecular:316.71L-742001 Hydrochloride
CAS:<p>L-742001 Hydrochloride is an RNA polymerase inhibitor.</p>Fórmula:C23H25Cl2NO4Cor e Forma:SolidPeso molecular:450.363,4'-Dihydroxyflavone
CAS:<p>3,4'-Dihydroxyflavone (3,4'-DHF) is an oral active flavonoid. 3,4'-Dihydroxyflavone (3,4'-DHF) shows antiviral activity against Influenza A virus.</p>Fórmula:C15H10O4Pureza:98.33%Cor e Forma:SolidPeso molecular:254.24
