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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Antiparasitic agent-5
CAS:<p>Compound 8h: Antiparasitic, selective against L. infantum (IC50: 2.50 μM); cytotoxic to HepG2 cells (CC50: 6.78 μM).</p>Fórmula:C20H16ClN3O3Cor e Forma:SolidPeso molecular:381.81Antimycobacterial 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:502.73Riodoxol
CAS:<p>Riodoxol is an antiviral agent that effectively affects the reproduction and maturation of viruses.</p>Fórmula:C6H3I3O2Cor e Forma:SolidPeso molecular:487.8JNJ-2408068
CAS:<p>JNJ-2408068 inhibits RSV with EC50 of 2.1 nM; blocks fusion (EC50=0.9 nM) by targeting F protein.</p>Fórmula:C22H30N6OPureza:98%Cor e Forma:SolidPeso molecular:394.51BO3482
CAS:<p>BO3482 is an antimicrobial compound and can inhibit the growth of methicillin-resistant Staphylococci (MIC90: 6.25 mg/mL).</p>Fórmula:C14H20N2NaO5S2Pureza:98%Cor e Forma:SolidPeso molecular:383.43SC-58272
CAS:<p>SC-58272 is an inhibitor of N-myristoyltransferase (Nmt), a target for anti-fungal and anti-viral therapy.</p>Fórmula:C33H52N6O4Pureza:98%Cor e Forma:SolidPeso molecular:596.8FR-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:198.17GCA-186
CAS:<p>GCA-186 is an effective non-nucleoside HIV-1 reverse transcriptase inhibitor.</p>Fórmula:C19H26N2O3Pureza:98%Cor e Forma:SolidPeso molecular:330.42GSK3494245
CAS:<p>GSK3494245: potent, selective oral proteasome inhibitor targeting WTL.donovani with an IC50 of 0.16 μM; safe, affects human proteasome too.</p>Fórmula:C21H23FN6O2Cor e Forma:SolidPeso molecular:410.44Synucleozid
CAS:<p>Synucleozid is a potent the SNCA mRNA inhibitor that encodes α-synuclein protein (IC50=1.5 μM), has the potential for the investigation of Parkinson’s disease.</p>Fórmula:C22H20N6Pureza:98%Cor e Forma:SolidPeso molecular:368.43Amorolfine
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:309.32Chaetoglobosin 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:528.64Saperconazole
CAS:<p>Saperconazole is a broad-spectrum antifungal triazole (MIC90: 0.19 mg/L).</p>Fórmula:C35H38F2N8O4Pureza:98%Cor e Forma:SolidPeso molecular:672.72Antibacterial 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:441.25SARS-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:450.94Linogliride
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:449.47Clevudine 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:500.163CPLro-IN-1
CAS:<p>Compound A17, an oral SARS-CoV-2 3CLpro inhibitor (IC50: 5.65 μM), targets key COVID-19 replication protein.</p>Fórmula:C29H25NO3Cor e Forma:SolidPeso molecular:435.51Ceftibuten
CAS:<p>Ceftibuten is a third-generation cephalosporin antibiotic.</p>Fórmula:C15H14N4O6S2Pureza:98%Cor e Forma:SolidPeso molecular:410.42BPIC
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:452.46JMI-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:337.42Tuberculosis 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:563.6918BIOder
CAS:18BIOder is a neuroprotective inhibitor of GSK-3β, highly selectively inhibiting HIV-1. It is the second generation derivative of 6BIO.Fórmula:C9H7ClN2O2Pureza:98%Cor e Forma:SolidPeso molecular:210.62NSC666715
CAS:<p>NSC666715 is the strand-displacement activity of DNA polymerase inhibitor.</p>Fórmula:C15H13Cl2N5O2S2Pureza:98%Cor e Forma:SolidPeso molecular:430.33BA38017
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:307.7Biclotymol
CAS:<p>Biclotymol is used in the study about infectious oropharyngeal diseases.</p>Fórmula:C21H26Cl2O2Pureza:98.56%Cor e Forma:SolidPeso molecular:381.34M2 ion channel blocker
CAS:<p>M2 ion channel blocker ,Antiviral agent, is capable of inhibiting and blocking the activity of M2 ion channel.</p>Fórmula:C18H27N3O2Pureza:98%Cor e Forma:SolidPeso molecular:317.43Covidcil-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:294.31HCV-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:515.64Ditalimfos
CAS:<p>Ditalimfos is a fungicide.</p>Fórmula:C12H14NO4PSCor e Forma:SolidPeso molecular:299.28Pafuramidine maleate
CAS:<p>Pafuramidine is an orally bioavailable prodrug of formamidine which was developed for the treatment of human African trypanosomiasis.</p>Fórmula:C24H24N4O7Pureza:98%Cor e Forma:SolidPeso molecular:480.16GNF6702
CAS:<p>GNF6702 inhibits kinetoplastid proteasome, treating leishmaniasis, Chagas, and trypanosomiasis in mice.</p>Fórmula:C22H16FN7O2Cor e Forma:SolidPeso molecular:429.41Enviroxime
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:358.41MAC173979
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:380.36Mab 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:293.28CK-2-68
CAS:<p>CK-2-68 is a potent inhibitor of PfNDH2.</p>Fórmula:C24H17ClF3NO2Pureza:98%Cor e Forma:SolidPeso molecular:443.85GNF179 (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:245.3Synthalin sulfate
CAS:<p>Synthalin sulfate is a NMDA receptor antagonist.</p>Fórmula:C12H30N6O4SPureza:98%Cor e Forma:SolidPeso molecular:354.47Antitubercular 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:558.5Acibenzolar-S-methyl
CAS:<p>Acibenzolar-S-methyl, a fungicide, boosts plant defenses by upregulating W-box genes like CAD1, NPR1, PR2.</p>Fórmula:C8H6N2OS2Pureza:99.64% - 99.86%Cor e Forma:Beige Fine PowderPeso molecular:210.28Oxaquin
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:706.58Nucleoside-Analog-1
CAS:<p>Nucleoside-Analog-1 is a 4′-Azidocytidine analogue, used to against Hepatitis C virus replication.</p>Fórmula:C9H9N5O5Pureza:98%Cor e Forma:SolidPeso molecular:267.2Acoziborole
CAS:<p>Acoziborole (SCYX-7158), a benzoxaborole derivative, is a novel, safe HAT agent with a MIC of 0.6 µg/mL against T. b. brucei S427.</p>Fórmula:C17H14BF4NO3Cor e Forma:SolidPeso molecular:367.1Sisapronil
CAS:<p>Sisapronil is a member of the phenylpyrazole class of antiparasitics.</p>Fórmula:C15H6Cl2F8N4Cor e Forma:SolidPeso molecular:465.13SARS-CoV-2 nsp13-IN-4
CAS:<p>Potent SARS-CoV-2 nsp13-IN-4 selectively inhibits nsp13 helicase with 57 μM IC50, offering antiviral effects.</p>Fórmula:C20H15BrN4OCor e Forma:SolidPeso molecular:407.26HIV-1 inhibitor-49
<p>HIV-1 inhibitor-49, an oral HEPT analog, has strong pharmacokinetics, potent reverse transcriptase inhibition (IC50=30nM), and is safe in mice.</p>Fórmula:C21H18F2N2O3SCor e Forma:SolidPeso molecular:416.44Antibacterial agent 72
CAS:<p>Antibacterial agent 72 has an antibacterial effect by selectively acting on bacterial membranes.</p>Fórmula:C19H21BrN4SCor e Forma:SolidPeso molecular:417.37Influenza virus-IN-3
CAS:<p>Influenza virus-IN-3 inhibits H5N1, H5N2, H5N6, H5N8 with low toxicity; targets neuraminidase.</p>Fórmula:C25H32N2O4SCor e Forma:SolidPeso molecular:456.6Antiviral agent 20
CAS:<p>Antiviral agent 20 (Compound 17b) is a selective inhibitor of Zika virus (EC50: 4.5 μM) and exhibits low cytotoxicity.</p>Fórmula:C31H35Cl2NO6Cor e Forma:SolidPeso molecular:588.52Apricitabine
CAS:<p>Apricitabine (SPD754) is a highly selective and orally active HIV-1 reverse transcriptase inhibitor (Ki=0.08 μM), the (-) enantiomer of 2′-deoxy-3′-oxy-4′-</p>Fórmula:C8H11N3O3SPureza:99.45%Cor e Forma:SolidPeso molecular:229.26Antimalarial agent 8
CAS:<p>Compound 7e: novel oral antimalarial, effective against P. falciparum in vitro and in vivo (40 mg/kg).</p>Fórmula:C22H21Cl3N4OCor e Forma:SolidPeso molecular:463.79Antibacterial agent 98
CAS:<p>Compound g37, an oral antibacterial, inhibits Gyrase B ATPase and S. aureus DNA super-helix without causing MRSA resistance.</p>Fórmula:C17H13N5O3S2Cor e Forma:SolidPeso molecular:399.45Besifloxacin
CAS:<p>Besifloxacin is the fourth generation of fluoroquinolones, which can be used to treat bacterial conjunctivitis</p>Fórmula:C19H21ClFN3O3Pureza:98%Cor e Forma:SolidPeso molecular:393.84FadD32 Inhibitor-1
CAS:<p>FadD32 inhibitor -1 has anti-tuberculosis activity and is an effective FadD32 inhibitor.</p>Fórmula:C24H20ClN3OPureza:98%Cor e Forma:SolidPeso molecular:401.89SARS-CoV-2 Mpro-IN-5
<p>SARS-CoV-2 Mpro-IN-5: inhibits Mpro (IC50=1800nM) & CatL (IC50=145nM), antiviral, hinders replication in hACE2 A549 cells (IC50=14.7nM).</p>Fórmula:C34H43FN4O7Cor e Forma:SolidPeso molecular:638.73PC170942 Sodium
CAS:<p>PC170942 Sodium is a water-soluble bacterial cytokinesis inhibitor that acts by inhibiting FtsZ.</p>Fórmula:C24H24ClNO2SPureza:98%Cor e Forma:SolidPeso molecular:425.97BMVC
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:472.83HI-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:396.3TbPTR1 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:399.45BA-53038B
CAS:<p>BA-53038B is an HBV core protein allosteric modulator (CpAM), binding to the HAP pocket and modulating HBV capsid assembly in a distinct manner (EC50: 3.32 μM).</p>Fórmula:C14H16ClNOCor e Forma:SolidPeso molecular:249.74Xenalamine
CAS:<p>Xenalamine is a synthetic compound of antiviral.</p>Fórmula:C23H21NO4Pureza:98%Cor e Forma:SolidPeso molecular:375.42Antifungal agent 35
CAS:<p>Antifungal agent 35 is an effective antifungal agent that potentiates the antifungal activity of fluconazole against C. albicans.</p>Fórmula:C26H27BrN4O4Cor e Forma:SolidPeso molecular:539.42MDRTB-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:274.32S-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:545.42Netzahualcoyone
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:416.3Taribavirin
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:488.44Reverse 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:343.45Rovafovir Etalafenamide
CAS:<p>Rovafovir Etalafenamide is a prodrug of anti-HIV nucleoside phosphonate.</p>Fórmula:C21H24FN6O6PPureza:98%Cor e Forma:SolidPeso molecular:506.42D-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:279.68RNPA1000
CAS:<p>RNPA1000 is an attractive antimicrobial development candidate and RnpA inhibitor.</p>Fórmula:C23H18BrN3O3Pureza:98%Cor e Forma:SolidPeso molecular:464.31VP-4509
CAS:<p>VP-4509: Anti-MRSA, MIC 49.3 μM; combats Pseudomonas aeruginosa.</p>Fórmula:C14H16N2O5SCor e Forma:SolidPeso molecular:324.35PXYC1
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:254.27Antibacterial 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:411.36HIV-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:566.63RSV-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:385.57AN7973
CAS:<p>AN7973 inhibits Cryptosporidium, blocks parasites, orally active, safe, stable, good PK.</p>Fórmula:C19H17BClN3O3Cor e Forma:SolidPeso molecular:381.62Vibunazole
CAS:<p>Vibunazole is an antifungal agent.</p>Fórmula:C15H20ClN3O2Cor e Forma:SolidPeso molecular:309.79Piperic acid
CAS:<p>Piperic acid is a powerful antioxidant and has potent antibacterial properties</p>Fórmula:C12H10O4Cor e Forma:SolidPeso molecular:218.21JMI-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:336.39Megazol
CAS:<p>Megazol treats protozoan infections like Chagas and sleeping sickness; it's a potent nitroimidazole drug.</p>Fórmula:C6H6N6O2SPureza:98%Cor e Forma:SolidPeso molecular:226.22MMV687807
CAS:<p>MMV687807: potent anthelmintic, IC50 0.15 μM, CC50 1.69 μM against T. gondii.</p>Fórmula:C15H8ClF6NO2Cor e Forma:SolidPeso molecular:383.67Antiparasitic agent-6
CAS:<p>Compound 5b: antiparasitic against L. infantum (IC50 = 3.89 μM), cytotoxic to HepG2 cells (CC50 = 13.64 μM).</p>Fórmula:C19H15N3O3Cor e Forma:SolidPeso molecular:333.34BAY-707
CAS:<p>BAY-707: tolerable in mice, no anticancer efficacy; potent, selective MTH1 inhibitor, IC50 = 2.3 nM; good PK profile.</p>Fórmula:C15H20N4O2Pureza:98%Cor e Forma:SolidPeso molecular:288.34Furalaxyl
CAS:<p>Furalaxyl is an fungicide of acyl amino chiral.</p>Fórmula:C17H19NO4Cor e Forma:SolidPeso molecular:301.34ASN03576800
CAS:<p>ASN03576800 is an inhibitor of the VP40 matrix protein.</p>Fórmula:C11H11NO6SPureza:99.76%Cor e Forma:SolidPeso molecular:285.27WRR-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:583.75BMH-22
CAS:<p>BMH-22 is an RNA polymerase I inhibitor that acts by causing nucleolar stress and showing potent anticancer activity across many tumor types.</p>Fórmula:C16H17N3Cor e Forma:SolidPeso molecular:251.33BPH-1218
CAS:<p>BPH-1218 is a SQS inhibitor.</p>Fórmula:C15H30N2O6P2Pureza:98%Cor e Forma:SolidPeso molecular:396.36HIV-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:550.63Ipconazole [ISO]
CAS:<p>Ipconazole, a cyclopentanol with 1,2,4-triazolylmethyl, 4-chlorobenzyl & isopropyl groups, is a fungicide that targets seed diseases.</p>Fórmula:C18H24ClN3OCor e Forma:SolidPeso molecular:333.86KFU-127
<p>KFU-127: broad-spectrum antimicrobial; targets bacterial/fungal biofilms; toxic to eukaryotic cells.</p>Fórmula:C34H43BrN2O3Cor e Forma:SolidPeso molecular:607.62HIV-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:494.88YXL-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:343.17HBV-IN-6
CAS:<p>HBV-IN-6 is a potent inhibitor of HBV (EC50: 44 nM).</p>Fórmula:C23H21ClFN3O5S2Cor e Forma:SolidPeso molecular:538.01Metallo-β-lactamase-IN-2
CAS:<p>Metallo-β-lactamase-IN-4 (compound 40) is a potent metallo-β-lactamases (MBL) inhibitor with IC 50 values of 0.1 μM for VIM-1, 1.3 μM for NDM-1 and 5.0 μM for</p>Fórmula:C9H9Cl2NOSCor e Forma:SolidPeso molecular:250.14CL-55
CAS:<p>CL-55 is a novel inhibitor of T3SS.</p>Fórmula:C19H17F2N3O4SCor e Forma:SolidPeso molecular:421.42HCV-IN-36
CAS:<p>HCV-IN-36: oral HCV inhibitor, EC50 0.016 μM, CC50 8.78 μM, potent antiviral.</p>Fórmula:C30H36ClN5Cor e Forma:SolidPeso molecular:502.09Stampidine
CAS:<p>Stampidine prevents HIV-1, effective against resistant strains at subnanomolar levels.</p>Fórmula:C20H23BrN3O8PPureza:98%Cor e Forma:SolidPeso molecular:544.29Antileishmanial agent-3
CAS:<p>Antileishmanial agent-3 (Compound 13) effectively inhibits the growth of Leishmania major [1].</p>Fórmula:C14H13ClN6O4Cor e Forma:SolidPeso molecular:364.74Influenza 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:303.31MMV666810
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:442.43Deaminase 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:314.2Edelfosine
CAS:<p>inhibits phosphatidylinositol phospholipase C</p>Fórmula:C27H58NO6PPureza:98%Cor e Forma:SolidPeso molecular:523.73Antimycobacterial agent-1
CAS:<p>Compound 33: antimycobacterial, MIC 1 μg/ml vs M. tuberculosis H37Ra, low toxicity (IC50 143.2 μg/ml in Vero cells).</p>Fórmula:C18H12N4O5SCor e Forma:SolidPeso molecular:396.38Phosphoglycolohydroxamic 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:461.85SARS-CoV-2 3CLpro-IN-6
CAS:<p>SARS-CoV-2 3CLpro-IN-6: reversible inhibitor for COVID-19 3CL protease, IC50 4.9 μM, useful in research.</p>Fórmula:C22H15NO7Cor e Forma:SolidPeso molecular:405.36Diamthazole
CAS:<p>Diamthazole (Dimazole) is an antifungal agent that can be used in the infection research[1].</p>Fórmula:C15H23N3OSCor e Forma:SolidPeso molecular:293.43pUL89 Endonuclease-IN-1
CAS:<p>Compound 13d: potent pUL89 endonuclease inhibitor, IC50 0.88 μM, anti-HCMV activity.</p>Fórmula:C10H8N2O4SCor e Forma:SolidPeso molecular:252.25SARS-CoV-2 Mpro-IN-6
CAS:<p>SARS-CoV-2 Mpro-IN-6: irreversible Mpro inhibitor, IC50 0.18 μM, selective; doesn't block cathepsins B/F/K/L or caspase 3.</p>Fórmula:C18H18Cl3N3O2SCor e Forma:SolidPeso molecular:446.78Dealanylalahopcin
CAS:<p>Dealanylalahopcin is a procollagen prolyl-4-hydroxylase inhibitor.</p>Fórmula:C6H10N2O5Cor e Forma:SolidPeso molecular:190.15(5S,8R)-HBV-IN-10
CAS:<p>'(5S,8R)-HBV-IN-10 is an EC50 0.1-1 μM HBsAg inhibitor, isomer of compound 6 from patent WO2021204258A1.</p>Fórmula:C23H24FN7OCor e Forma:SolidPeso molecular:433.48Mtb-cyt-bd oxidase-IN-3
<p>Mtb-cyt-bd oxidase-IN-3 inhibits M. tuberculosis growth, IC50 0.36 μM, MIC 32 μM, for TB research.</p>Fórmula:C26H35NO2Cor e Forma:SolidPeso molecular:393.56Aranotin
CAS:<p>Aranotin, from Arachniotus aureus, inhibits RNA viruses by blocking RNA polymerase.</p>Fórmula:C20H18N2O7S2Cor e Forma:SolidPeso molecular:462.5Sudoterb HCl
CAS:<p>Sudoterb has anti-tubercular activity.</p>Fórmula:C29H30Cl2F3N5OPureza:98%Cor e Forma:SolidPeso molecular:592.48Tropesin
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:505.954-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:375.465,10-Dideazaaminopterin
CAS:<p>5,10-Dideazaaminopterin is an antileukemic drug.</p>Fórmula:C21H22N6O5Pureza:98%Cor e Forma:SolidPeso molecular:438.44(+)-Dihydrocalanolide A
CAS:<p>DHCal A (NSC 678323) is an oral nonnucleoside Reverse Transcriptase inhibitor for HIV research.</p>Fórmula:C22H28O5Cor e Forma:SolidPeso molecular:372.45HPV18-IN-1
CAS:<p>HPV18-IN-1, potent cervical cancer inhibitor, blocks E7-Rb-E2F pathway and DNA methylation.</p>Fórmula:C14H10N4OSCor e Forma:SolidPeso molecular:282.32(S)-Enzaplatovir
CAS:<p>(S)-Enzaplatovir, an S-enantiomer with antiviral properties, has an EC50 of 56 nM against RSV.</p>Fórmula:C20H19N5O3Cor e Forma:SolidPeso molecular:377.4Anti-inflammatory agent 14
CAS:<p>Anti-inflammatory agent 14 (compound 28) has a MIC 50 of 2 μM for Mtb H37Rv. Anti-inflammatory agent 14 is also an anti-inflammatory agent [1].</p>Fórmula:C16H16N2O2SCor e Forma:SolidPeso molecular:300.38BioA-IN-13
CAS:<p>BioA-IN-13 is a highly effective inhibitor of the Mycobacterium tuberculosis BioA enzyme, displaying potent cell permeability and whole-cell activity [1].</p>Fórmula:C19H16N2O4SCor e Forma:SolidPeso molecular:368.41Antiparasitic agent-7
CAS:<p>Compound 5d, antiparasitic for L. infantum, IC50 of 2.85μM; cytotoxic to HepG2 cells, CC50 of 10.61μM.</p>Fórmula:C18H15N3O5Cor e Forma:SolidPeso molecular:353.33Pomotrelvir
CAS:<p>Pomotrelvir (PBI-0451) is an oral SARS-CoV-2 3CL protease inhibitor with antiviral properties for COVID-19 research.</p>Fórmula:C23H26ClN5O3Cor e Forma:SolidPeso molecular:455.94HBV-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:401.64Antitrypanosomal agent 7
CAS:<p>Compound 18c, an antitrypanosomal, is twice as potent as Nifurtimox against T. brucei (IC50: 0.71 μM), with favorable ADME and AT-DNA binding affinity.</p>Fórmula:C23H29N5O2Cor e Forma:SolidPeso molecular:407.51Antitrypanosomal agent 9
CAS:<p>Agent 9 inhibits T. b. brucei (IC50: 1.15 μM), used in HAT research.</p>Fórmula:C22H27NO3Cor e Forma:SolidPeso molecular:353.45Pyrrofolic acid
CAS:<p>Pyrrofolic acid shows high anti-folate biological activity for S. faecalis.</p>Fórmula:C23H21N7O7Pureza:98%Cor e Forma:SolidPeso molecular:507.46Thiamphenicol glycinate hydrochloride
CAS:<p>Thiamphenicol glycinate hydrochloride is a broad-spectrum antibacterial agent utilized in research on respiratory tract infections.</p>Fórmula:C14H19Cl3N2O6SCor e Forma:SolidPeso molecular:449.73Caspofungin
CAS:<p>Caspofungin is a cyclic lipopeptide echinocandin and beta-(1,3)-D-glucan synthase inhibitor that is used to treat internal or systemic mycoses.</p>Fórmula:C52H88N10O15Cor e Forma:SolidPeso molecular:1093.31HBV-IN-10
CAS:<p>HBV-IN-10, an isomer of compound 6, inhibits HBsAg with EC50 between 0.1-1 μM (Patent WO2021204258A1).</p>Fórmula:C23H24FN7OCor e Forma:SolidPeso molecular:433.48HIV-1 inhibitor-53
CAS:<p>HIV-1 Inhibitor-53 targets HIV-1 protease (IC50: 1.93 nM) and reverse transcriptase (IC50: 2.35 μM), aiding AIDS research.</p>Fórmula:C30H34N2O8SPureza:98%Cor e Forma:SolidPeso molecular:582.66Antibacterial agent 65
CAS:<p>Antibacterial agent 65 is a potential antimicrobial agent and antioxidant agent.</p>Fórmula:C17H16O3Cor e Forma:SolidPeso molecular:268.31HIV-1 protease-IN-5
CAS:<p>HIV-1 protease-IN-5 is an HIV-1 protease inhibitor (IC50: 1.64 nM). HIV-1 protease-IN-5 exhibits significant effects on wild-type and DRV-resistant HIV-1.</p>Fórmula:C27H29F3N2O7SCor e Forma:SolidPeso molecular:582.59Diethofencarb
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:360.43SMR000071098
CAS:<p>SMR000071098 is an inhibitor of Fe-S cluster-dependent aconitase. SMR000071098 interacts with Suf proteins to inhibit iron-sulfur (Fe-S) cluster assembly.</p>Fórmula:C17H12N2O2Cor e Forma:SolidPeso molecular:276.29Goitrin
CAS:<p>Goitrin, from glucosinolate reactions, blocks thyroid peroxidase and iodine use, and fights H1N1.</p>Fórmula:C5H7NOSCor e Forma:SolidPeso molecular:129.18Anti-infective agent 1
CAS:<p>Compound 3a: potent, selective antiprotozoal/antimycobacterial. IC50: P. falciparum 10.95 μM, T. brucei 0.06 μM. MIC against M. smegmatis: 8 μg/mL.</p>Fórmula:C16H10O2Cor e Forma:SolidPeso molecular:234.25ZINC04177596
CAS:<p>ZINC04177596 is a novel Nef Protein Inhibitor with anti-HIV activity.</p>Fórmula:C22H16N6O4Cor e Forma:SolidPeso molecular:428.4HIV-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:609.26SARS-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:421.47TBI-166
CAS:<p>TBI-166, an oral riminophenazine, treats tuberculosis with fewer side effects than Clofazimine.</p>Fórmula:C32H30F3N5O3Cor e Forma:SolidPeso molecular:589.61SARS-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:512.06Bunamidine hydrochloride
CAS:<p>Bunamidine hydrochloride is a veterinary anthelmintic that acts against Echinococcus granulosus and Tapeworm.</p>Fórmula:C25H39ClN2OCor e Forma:SolidPeso molecular:419.05SARS-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:525.42FR900098 (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:220.117MurA-IN-2
CAS:<p>MurA-IN-2: potent MurA inhibitor, IC50 of 39μM, chloroacetamide with aliphatic amine; has antibacterial properties.</p>Fórmula:C12H20ClNOCor e Forma:SolidPeso molecular:229.75HIV-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:427.4Antibacterial agent 121
CAS:<p>Antibacterial agent 121 exhibits anti-TB and anti-inflammatory properties.</p>Fórmula:C18H22N2O3SCor e Forma:SolidPeso molecular:346.44Antibacterial agent 97
CAS:<p>Antibacterial agent 97 is potent; MIC: 16 μg/mL for E. coli and S. aureus.</p>Fórmula:C19H23N5SCor e Forma:SolidPeso molecular:353.48Antitubercular agent-14
CAS:<p>Antitubercular agent-14 (Compound 1) shows antitubercular activity. The MIC value of Antitubercular agent-14 against M. tuberculosis is 0.3 μg/mL [1].</p>Fórmula:C20H27ClN2Cor e Forma:SolidPeso molecular:330.89Anticandidal agent-1
CAS:<p>Compound C2 is a broad-spectrum anticandidal, blocking biofilm and filament growth with MIC50 of 13.51μg/mL (C. glabrata) and 8.65μg/mL (C. albicans).</p>Fórmula:C19H22O5Cor e Forma:SolidPeso molecular:330.38LabMol-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:316.36Cap-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:597.59SARS-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:415.44Isobellidifolin
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:435.84Marasmic 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:687.07Antibacterial agent 122
CAS:<p>Thiourea derivative 122 is a low-toxicity antibacterial used in tuberculosis research with anti-mycobacterial properties.</p>Fórmula:C15H14N2O3SCor e Forma:SolidPeso molecular:302.35Cadrofloxacin
CAS:<p>Cadrofloxacin (Caderofloxacin, CS-940) is a novel fluoroquinolone antimicrobial agent.</p>Fórmula:C19H20F3N3O4Cor e Forma:SolidPeso molecular:411.38Antitubercular agent-18
CAS:<p>Antitubercular agent-18 (9a) MIC: 2 μg/ml for H37Rv, Spec 192, 210; 128 μg/ml for Spec 800. Selective antimycobacterial.</p>Fórmula:C14H12BrN5OCor e Forma:SolidPeso molecular:346.18F8-S43-S3
CAS:<p>F8-S43-S3 is a SARS-CoV-2 main protease inhibitor (IC 50 = 9.69 μM) [1].</p>Fórmula:C12H10N4O3SCor e Forma:SolidPeso molecular:290.3Antimalarial agent 16
CAS:<p>Antimalarial agent 16 is a parasite inhibitor that exhibits antimalarial effects and inhibits the growth of Plasmodium falciparum with an IC50 value of 2.0 nM.</p>Fórmula:C30H32N2O6Cor e Forma:SolidPeso molecular:516.58Metallo-β-lactamase-IN-6
CAS:<p>Metallo-β-lactamase-IN-6 is a highly effective inhibitor of VIM-Type metallo-β-lactamase, demonstrating IC 50 values of 0.56 μM, 29.50 μM, and 5.78 μM for VIM-2</p>Fórmula:C10H9N3O2Cor e Forma:SolidPeso molecular:203.2Antifungal 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:414.93Halofantrine, (-)-
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:527.47Antibacterial 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:311.35Antitrypanosomal agent 11
<p>Antitrypanosomal Agent 11 is a chemical compound effective against Trypanosoma cruzi, exhibiting an inhibition concentration (IC 50) of 0.23 μM.</p>Fórmula:C16H10F6N6OCor e Forma:SolidPeso molecular:416.28Antibacterial agent 95
CAS:<p>Antibacterial 95, a quinoline-derived antituberculotic, shows 0.3 μM MIC against Mycobacterium tuberculosis H37Rv and inhibits its growth in macrophages.</p>Fórmula:C19H16ClNO3Cor e Forma:SolidPeso molecular:341.79Antibacterial agent 19
CAS:<p>Antibacterial agent 19 targets K. pneumoniae and multi-resistant S. aureus with MICs: 0.022 and 0.045 mg/mL.</p>Fórmula:C16H16F2N2O4Cor e Forma:SolidPeso molecular:338.31S-1360
CAS:<p>S-1360 is an inhibitor of HIV-1 integrase.</p>Fórmula:C16H12FN3O3Pureza:98%Cor e Forma:SolidPeso molecular:313.28Antitumor agent-85
<p>Antitumor agent-85 stabilizes G4-DNA with potent anti-tumor effects.</p>Fórmula:C24H33N7Cor e Forma:SolidPeso molecular:419.57DC07090 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:436.23
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