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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Covidcil-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:294.31BPH-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:366.8M2 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:317.43Biclotymol
CAS:<p>Biclotymol is used in the study about infectious oropharyngeal diseases.</p>Fórmula:C21H26Cl2O2Pureza:98.56%Cor e Forma:SolidPeso molecular:381.34BA38017
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:307.7NSC666715
CAS:<p>NSC666715 is the strand-displacement activity of DNA polymerase inhibitor.</p>Fórmula:C15H13Cl2N5O2S2Pureza:98%Cor e Forma:SolidPeso molecular:430.3318BIOder
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:210.62PPQ-581
CAS:<p>PPQ-581 is an anti-flu drug that blocks RNP trafficking and stops virus replication, preventing cell damage.</p>Fórmula:C25H24FN3O3Cor e Forma:SolidPeso molecular:433.47X77
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:459.58HIV-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:494.88Tuberculosis 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:563.69Ceftibuten
CAS:<p>Ceftibuten is a third-generation cephalosporin antibiotic.</p>Fórmula:C15H14N4O6S2Pureza:98%Cor e Forma:SolidPeso molecular:410.42Metallo-β-lactamase-IN-4
CAS:<p>Metallo-β-lactamase-IN-4 (compound 40) is a potent inhibitor of metallo-β-lactamases (MBL) with IC 50 values of 0.5 μM, 2.1 μM, and 3.3 μM for VIM-1, NDM-1 and</p>Fórmula:C10H14N4O3S2Cor e Forma:SolidPeso molecular:302.37FLDP-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:479.61HBV-IN-6
CAS:<p>HBV-IN-6 is a potent inhibitor of HBV (EC50: 44 nM).</p>Fórmula:C23H21ClFN3O5S2Cor e Forma:SolidPeso molecular:538.01Clevudine 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:500.16KIN1400
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:449.47CL-55
CAS:<p>CL-55 is a novel inhibitor of T3SS.</p>Fórmula:C19H17F2N3O4SCor e Forma:SolidPeso molecular:421.42Linogliride
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:286.37HCV-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:502.09SARS-CoV-2-IN-15
CAS:<p>SARS-CoV-2-IN-15, a stable niclosamide analogue, enhances bioavailability and half-life, with potent antiviral activity (IC50: 0.49 μM).</p>Fórmula:C14H9ClF3NO2Cor e Forma:SolidPeso molecular:315.67LpxC-IN-9
CAS:<p>LpxC-IN-9 (compound 19) is a potent inhibitor of LpxC and exhibits antibacterial and hypotensive activity.</p>Fórmula:C23H25N5O3SCor e Forma:SolidPeso molecular:451.54Antibacterial agent 104
CAS:<p>Antibacterial agent 104 is an effective antibacterial agent with significant antibacterial effects in vitro and good anti-MRSA effects in vivo.</p>Fórmula:C28H39NO4SCor e Forma:SolidPeso molecular:485.68SARS-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:450.94Cap-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:389.45HSV-1/HSV-2-IN-1
CAS:<p>HSV-1/HSV-2-IN-1 inhibits HSV-1, HSV-2, and cowpox virus with EC50 values of 7.6, 7.6, 4, and 12 μM, respectively.</p>Fórmula:C18H14F4N4OSCor e Forma:SolidPeso molecular:410.39Erythromycin Gluceptate
CAS:<p>Erythromycin Gluceptate is an inhibitor of protein translation and mammalian mRNA splicing. It inhibits growth of gram negative and gram positiove bacteria.</p>Fórmula:C44H81NO21Cor e Forma:SolidPeso molecular:960.11Thiambutosine
CAS:<p>Thiambutosine exhibits inhibitory activity against Mycobacterium leprae and mushroom tyrosinase, making it suitable for infection studies.</p>Fórmula:C19H25N3OSPureza:99.95%Cor e Forma:SolidPeso molecular:343.49HBV-IN-22
CAS:<p>HBV-IN-22 (Compound LC5f) is an HBV DNA replication inhibitor that acts on both wild-type HBV (IC50: 0.71 μM) and drug-resistant HBV (IC50: 0.84 μM).</p>Fórmula:C26H29N3O2S2Cor e Forma:SolidPeso molecular:479.66Antileishmanial agent-3
CAS:<p>Antileishmanial agent-3 (Compound 13) effectively inhibits the growth of Leishmania major [1].</p>Fórmula:C14H13ClN6O4Cor e Forma:SolidPeso molecular:364.74Chaetoglobosin 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:528.64HBV-IN-32
CAS:<p>HBV-IN-32 is a strong cccDNA inhibitor with an IC50 of 0.14 µM against HBsAg, also halting cell growth.</p>Fórmula:C22H19ClO5SCor e Forma:SolidPeso molecular:430.95-Dehydroepisterol
CAS:<p>5-Dehydroepisterol, an anti-fungal episterol form, made by C-5 sterol desaturase, turns into 24-methylenecholesterol.</p>Fórmula:C28H44OPureza:98%Cor e Forma:SolidPeso molecular:396.65HIV-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:427.43DENV-IN-9
CAS:<p>DENV-IN-9 is a DENV2 inhibitor with an EC 50 of 0.88 μM .</p>Fórmula:C15H9BrO5Cor e Forma:SolidPeso molecular:349.13SARS-CoV MPro-IN-2
CAS:<p>SARS-CoV MPro-IN-2, a potent SARS-CoV-2 main protease inhibitor (IC50: 72.07 nM), may aid COVID-19 research.</p>Fórmula:C13H10O4Cor e Forma:SolidPeso molecular:230.22Edelfosine
CAS:<p>inhibits phosphatidylinositol phospholipase C</p>Fórmula:C27H58NO6PPureza:98%Cor e Forma:SolidPeso molecular:523.73MMV666693
CAS:<p>MMV666693 is a selective allosteric Plasmodium Kinesin-5 inhibitor.</p>Fórmula:C18H15NO4Cor e Forma:SolidPeso molecular:309.32Braco-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:703.14Phosphoglycolohydroxamic 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:461.85Amorolfine
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:317.517BMS-433771 free base
CAS:<p>BMS-433771, a novel inhibitor of respiratory syncytial virus (RSV), binds the RSV F glycoprotein and inhibits membrane fusion.</p>Fórmula:C21H23N5O2Cor e Forma:SolidPeso molecular:377.44SARS-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:293.43Anti-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:411.43Synucleozid
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:368.43pUL89 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:446.78PD 113270
CAS:<p>PD 113,270 is an analog of the fermentation products fostriecin with antitumor activity in vitro and in vivo.</p>Fórmula:C19H27O8PCor e Forma:SolidPeso molecular:414.39GSK3494245
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:410.44Debneyol
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:404.39FR-182024
CAS:<p>FR-182024 is a novel cephem derivative, it has potent anti-Helicobacter pylori activity.</p>Fórmula:C18H16N4O4S3Cor e Forma:SolidPeso molecular:448.54Antileishmanial agent-7
CAS:<p>Compound 23: Strong against Leishmania, IC50: 6.89 μM (L. donovani), 259 μM (L-6).</p>Fórmula:C20H18O8Cor e Forma:SolidPeso molecular:386.35GCA-186
CAS:<p>GCA-186 is an effective non-nucleoside HIV-1 reverse transcriptase inhibitor.</p>Fórmula:C19H26N2O3Pureza:98%Cor e Forma:SolidPeso molecular:330.42IMB-26
CAS:<p>IMB-26 is an HCV inhibitor (EC50: 2.1 μM) and has shown potent anti-HCV effects.</p>Fórmula:C20H23BrN2O6Cor e Forma:SolidPeso molecular:467.31Penamecillin
CAS:<p>Penamecillin (Wy 20788) is an orally active antibacterial agent.</p>Fórmula:C19H22N2O6SCor e Forma:SolidPeso molecular:406.45Antitubercular agent-37
CAS:<p>Antitubercular Agent-37 exhibits antimycobacterial properties and functions as an antibacterial agent with an MIC (minimum inhibitory concentration) value of 0.</p>Fórmula:C22H22N8O2Cor e Forma:SolidPeso molecular:430.46FR-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:198.17Quinuronium 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:455.51Acyclovir monophosphate
CAS:<p>Acyclovir monophosphate, a strong anti-HSV agent, inhibits viral DNA polymerase, blocking DNA synthesis and chain elongation.</p>Fórmula:C8H12N5O6PCor e Forma:SolidPeso molecular:305.18Aranotin
CAS:<p>Aranotin, from Arachniotus aureus, inhibits RNA viruses by blocking RNA polymerase.</p>Fórmula:C20H18N2O7S2Cor e Forma:SolidPeso molecular:462.5Metallo-β-lactamase-IN-3
CAS:<p>Metallo-β-lactamase-IN-3 (compound 35) is a potent metallo-β-lactamases (MBL) inhibitor that has the potential to restore the activity of current β-lactam</p>Fórmula:C10H11NO3SCor e Forma:SolidPeso molecular:225.26MptpB-IN-1
CAS:<p>MptpB-IN-1: orally active, potent MptpB inhibitor; reduces drug-resistant tuberculosis.</p>Fórmula:C17H11Cl2NO4Cor e Forma:SolidPeso molecular:364.18JFN05510
CAS:<p>Compound: 3'-O-tert-BDMS-5'-O-DMT-N2-IBG 2'-CE phosphoramidite; has anticancer properties and activates enzymes.</p>Fórmula:C50H68N7O9PSiCor e Forma:SolidPeso molecular:970.18SC-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:596.8Sudoterb HCl
CAS:<p>Sudoterb has anti-tubercular activity.</p>Fórmula:C29H30Cl2F3N5OPureza:98%Cor e Forma:SolidPeso molecular:592.48PknB-IN-1
CAS:<p>PknB-IN-1 inhibits PknB (IC50: 14.4 μM), has anti-mycobacterial effects (MIC: 6.2 μg/mL) against M. tuberculosis H37Rv.</p>Fórmula:C25H30N2O2Cor e Forma:SolidPeso molecular:390.52Salifluor
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:407.43B07 hydrochloride
CAS:<p>B07 hydrochloride is a CCR5 antagonist-based inhibitor of HIV-1 entry.</p>Fórmula:C29H38ClFN4O2Pureza:98%Cor e Forma:SolidPeso molecular:529.09HIV-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:395.465,10-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:377.4BO3482
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:383.43Anti-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:300.38MMV688845
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:353.37HIV-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:242.28DPC-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:314.69Antibacterial agent 124
CAS:<p>Antibacterial agent 124 inhibits Sa ProRS with an IC50 of 0.18 μM.</p>Fórmula:C16H17ClFN3O2Cor e Forma:SolidPeso molecular:337.78GRL-1720
CAS:<p>GRL-1720 is a SARS-CoV-2 Protease inhibitor (IC50 = 320 nM). GRL-1720 contains an indoline which targets the SARS-CoV-2 main protease (Mpro)</p>Fórmula:C14H11ClN2O2Cor e Forma:SolidPeso molecular:274.7HBV-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:401.64AN11251
CAS:<p>AN11251: oral anti-Wolbachia, treats onchocerciasis & lymphatic filariasis, EC50=1.5nM (LDW1), 15nM (C6/36).</p>Fórmula:C29H38BFO7Pureza:98%Cor e Forma:SolidPeso molecular:528.42Antitrypanosomal 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:353.45BHBM
CAS:<p>BHBM, an acylhydrazone antifungal, halts C. neoformans growth (MIC80 = 1 μg/ml) by blocking glucosylceramide synthesis.</p>Fórmula:C15H13BrN2O2Cor e Forma:SolidPeso molecular:333.18Anti-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:535.62JNJ-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:394.51SSAA09E1
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:199.3Thiamphenicol 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:582.59Metallo-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:220.23Antifungal agent 33
CAS:<p>Antifungal 33 (4e) strongly inhibits Candida albicans. MIC: 16 μg/ml; IC50: 0.19 μg/ml.</p>Fórmula:C21H14ClN5O3Cor e Forma:SolidPeso molecular:419.82Riodoxol
CAS:<p>Riodoxol is an antiviral agent that effectively affects the reproduction and maturation of viruses.</p>Fórmula:C6H3I3O2Cor e Forma:SolidPeso molecular:487.8Diethofencarb
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:360.43Antimycobacterial 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:502.73MtTMPK-IN-4
CAS:<p>MtTMPK-IN-4, a para-piperidine, blocks MtTMPK in tuberculosis with 6.1 μM IC50 and also inhibits tyrosinase.</p>Fórmula:C23H25N3O3Cor e Forma:SolidPeso molecular:391.46SMR000071098
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:429.52Antiparasitic 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:381.81Chitin 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:609.26Endochin
CAS:<p>Endochin is an experimental antimalarial. Endochin and analogues thereof are causal prophylactic and potent erythrocytic stage agents in avian models.</p>Fórmula:C18H25NO2Pureza:98%Cor e Forma:SolidPeso molecular:287.4Pyrisoxazole
CAS:<p>Pyrisoxazole is a novel fungicide inhibitor of Sterol 14α-demethylase.</p>Fórmula:C16H17ClN2OCor e Forma:SolidPeso molecular:288.77Antileishmanial agent-10
CAS:<p>Antileishmanial agent-10 (Compound 7h) is an antiprotozoal agent.</p>Fórmula:C25H41NO2SCor e Forma:SolidPeso molecular:419.66TBI-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:512.06Kayahope
CAS:<p>Kayahope is a novel antifungals.</p>Fórmula:C15H14ClNO3SPureza:98%Cor e Forma:SolidPeso molecular:323.79Bunamidine 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:525.42MK436
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:250.25L-573655
CAS:<p>L-573655, an antibacterial agents, targets lipid A biosynthesis in gram-negative bacteria.</p>Fórmula:C10H10N2O3Pureza:98%Cor e Forma:SolidPeso molecular:206.2F-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:363.2FR900098 (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:220.117HBV-IN-9
CAS:<p>HBV-IN-9 inhibits HBsAg (IC50: 10 nM) and HBV DNA replication (IC50: 0.15 nM) per WO2018001952A1.</p>Fórmula:C22H24FN7OCor e Forma:SolidPeso molecular:421.47HIV-1 inhibitor-24
CAS:<p>HIV-1 inhibitor-24 (S-12a) blocks HIV reverse transcription effectively (IC50: 9.5 nM), low toxicity, well-tolerated in mice, good heart safety.</p>Fórmula:C26H19N5O2Cor e Forma:SolidPeso molecular:433.46Acetarsone
CAS:<p>Acetarsone is an antiinfective agent. Acetarsone also inhibits protozoa growth.</p>Fórmula:C8H10AsNO5Cor e Forma:SolidPeso molecular:275.09HadAB-IN-1
CAS:<p>HadAB-IN-1: potent TB research chemical; IC50 = 0.03μM; inhibits HadAB, affecting Mtb mycolic acid synthesis.</p>Fórmula:C19H17BrClN3O3SCor e Forma:SolidPeso molecular:482.78DSHS00884
CAS:<p>DSHS00884 is a potent inhibitor of human papillomavirus E6 (IC50: 10 μM).</p>Fórmula:C12H12N4O2S2Cor e Forma:SolidPeso molecular:308.38Antibacterial agent 67
CAS:<p>Antibacterial agent 67 blocks succinate dehydrogenase more effectively than haloperidol, with IC50 of 0.03 μM vs 4.40 μM.</p>Fórmula:C24H15F6N5OCor e Forma:SolidPeso molecular:503.4Leu-AMS
CAS:<p>Leu-AMS, a leucine analogue with 22.34 nM IC50, inhibits LRS and bacterial growth without affecting mTORC1.</p>Fórmula:C16H25N7O7SPureza:98%Cor e Forma:SolidPeso molecular:459.48HIV-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:427.4BMS-986094
CAS:<p>INX 08189 is an RNA-directed RNA polymerase (NS5B) inhibitor.</p>Fórmula:C30H39N6O9PCor e Forma:SolidPeso molecular:658.64SARS-CoV-2-IN-16
CAS:<p>SARS-CoV-2-IN-16 strongly inhibits NPro, with EC50 of 3.69 μM and Kd of 7.82 μM, suggesting effective binding and antiviral properties.</p>Fórmula:C17H20N2O2Cor e Forma:SolidPeso molecular:284.35Texaline
CAS:<p>Texaline is an agent of the antitubercular.</p>Fórmula:C15H10N2O3Pureza:98%Cor e Forma:SolidPeso molecular:266.25SS148
CAS:<p>SS148 inhibits nsp14/nsp16 MTase, selective vs human MTases; promising for potent, selective coronavirus MTase inhibitors.</p>Fórmula:C16H20N6O5SCor e Forma:SolidPeso molecular:408.43Antibacterial agent 121
CAS:<p>Antibacterial agent 121 exhibits anti-TB and anti-inflammatory properties.</p>Fórmula:C18H22N2O3SCor e Forma:SolidPeso molecular:346.44Cyclophilin inhibitor 3
CAS:<p>Cyclophilin inhibitor 3 (compound 7c), a potent inhibitor of cyclophilin A (CypA), exhibited potent anti-HCV effects with an EC50 value of 4.2 μM.</p>Fórmula:C34H38N4O6Cor e Forma:SolidPeso molecular:598.69Antileishmanial 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:296.32Kumbicin C
CAS:<p>Kumbicin C inhibits the growth of NS-1 mouse myeloma cells (IC50 = 0.74 μg/ml) and the growth of the Gram-positive bacteria B. subtilis (MIC = 1.6 μg/ml).</p>Fórmula:C28H24N2O3Cor e Forma:SolidPeso molecular:436.5HIV-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:357.83Lascufloxacin
CAS:<p>Lascufloxacin: potent, oral fluoroquinolone antibiotic for respiratory infections, effective against quinolone-resistant strains.</p>Fórmula:C21H24F3N3O4Pureza:98%Cor e Forma:SolidPeso molecular:439.43MAC-0547630
CAS:<p>MAC-0547630 potent and selective inhibitor of UppS.</p>Fórmula:C19H21FN4Pureza:98%Cor e Forma:SolidPeso molecular:324.4RSV-IN-3
CAS:<p>RSV-IN-3 is a dual RSV/IAV inhibitor with an EC50 of 32.70 μM against RSV.</p>Fórmula:C16H12Cl2N2OSCor e Forma:SolidPeso molecular:351.25RD3-0028
CAS:<p>RD3-0028 is a potent and selective RSV replication inhibitor(EC50 of 4.5 μM).</p>Fórmula:C8H8S2Pureza:98%Cor e Forma:SolidPeso molecular:168.28Berteroin
CAS:<p>Berteroin, found in cruciferous veggies like rucola and mustard, may act as an antioxidant, reducing inflammation and androgen receptors in cancer.</p>Fórmula:C7H13NS2Cor e Forma:SolidPeso molecular:175.31ATD-3169
CAS:<p>ATD-3169 is a ROS generator with antibacterial activity.</p>Fórmula:C15H14O3Pureza:98%Cor e Forma:SolidPeso molecular:242.27A3N19
CAS:<p>A3N19 is a potent inhibitor of HIV-1 non-nucleoside reverse transcriptase and is able to act on HIV-1 IIIB (EC50: 3.28 nM).</p>Fórmula:C31H31N9O2SCor e Forma:SolidPeso molecular:593.7PXYC13
CAS:<p>PXYC13 inhibits Mtb RpsA essential for trans-translation with Kd of 7.61 μM; less effective on RpsA-CTD Δ438A (Kd 8.50 μM).</p>Fórmula:C15H15N5O2SCor e Forma:SolidPeso molecular:329.38RyRs activator 1
CAS:<p>RyRs activator 1 triggers ranibulin receptors; 100% larvicidal at 0.5 mg/L, 90% at 0.01 mg/L.</p>Fórmula:C21H14ClF3N6O4Cor e Forma:SolidPeso molecular:506.82trans-ccc_R08
CAS:<p>trans-ccc_R08: potent cccDNA inhibitor, IC50 0.08 µM, may help research HBV.</p>Fórmula:C22H19ClO6Cor e Forma:SolidPeso molecular:414.84Urease-IN-5
<p>Urease-IN-5: urease inhibitor, IC50 1.473 µM, low cytotoxicity, IC50 17.78 µg/mL on P. vulgaris.</p>Fórmula:C16H20N2O3SCor e Forma:SolidPeso molecular:320.41HBV-IN-16
CAS:<p>HBV-IN-16, a quinoline derivative, inhibits HBV cccDNA, key for viral replication (from patent WO2019121357A1).</p>Fórmula:C22H20ClNO4Cor e Forma:SolidPeso molecular:397.85LEDGIN6
CAS:<p>HIV-1 integrase inhibitor 2 is used for the treatment of human immunodeficiency virus (HIV) infection.</p>Fórmula:C21H20ClNO2Cor e Forma:SolidPeso molecular:353.84Crisnatol mesylate
CAS:<p>Crisnatol, a potent and selective DNA intercalator, has potential anticancer activity.</p>Fórmula:C24H27NO5SCor e Forma:SolidPeso molecular:441.54Isobellidifolin
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:435.84SARS-CoV-2-IN-20
CAS:<p>SARS-CoV-2-IN-20 inhibits virus effectively with 6.5 μM EC50, promising for disease research.</p>Fórmula:C24H30N2O2Cor e Forma:SolidPeso molecular:378.51NS2B/NS3-IN-6
CAS:<p>Compound 1a: DENV/ZIKV NS2B/NS3 protease inhibitor; IC50: ZIKV 2.23 μM, DENV 25.2 μM.</p>Fórmula:C19H19N3O5S2Cor e Forma:SolidPeso molecular:433.5CGP 53353
CAS:<p>CGP 53353 (DAPH-7) is a PKC inhibitor with inhibitory effects on PKCβII and PKCβI and can be used to study atherosclerosis.</p>Fórmula:C20H13F2N3O2Pureza:98.11%Cor e Forma:SolidPeso molecular:365.33Viral 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:323.36SPR41
<p>SPR41 inhibits SARS-CoV-2 main protease (K i : 0.184µM) and is antiviral with some cytotoxicity.</p>Fórmula:C27H37N3O5Cor e Forma:SolidPeso molecular:483.6C16-K-cBB1
<p>C16-K-cBB1: potent, selective MRSA killer; MIC 1µg/mL, low hemolysis, works in 120 min at 12.5µg/mL.</p>Fórmula:C33H58ClN5O5SCor e Forma:SolidPeso molecular:672.36UGM-IN-3
CAS:<p>UGM-IN-3 inhibits UGM (Kd=66 μM) and M. tuberculosis growth (MIC=6.2 μg/mL).</p>Fórmula:C18H16INO2Cor e Forma:SolidPeso molecular:405.23Antitubercular 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:203.2Mt KARI-IN-2
CAS:<p>Mt KARI-IN-2, an inhibitor for Mtb KARI (Ki: 2.02 μM) and Mtb H37Rv (MIC: 0.78 μM), has low cytotoxicity (HEK IC50: >86 μg/mL).</p>Fórmula:C14H11N5O4S2Cor e Forma:SolidPeso molecular:377.4Antifungal 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:414.93Penflufen
CAS:<p>Penflufen, a broad-spectrum succinate dehydrogenase inhibitor (SDHI), serves effectively as a fungicide.</p>Fórmula:C18H24FN3OCor e Forma:SolidPeso molecular:317.4A 80987
CAS:<p>A 80987 is an inhibitor of HIV-1 protease.</p>Fórmula:C37H43N5O6Cor e Forma:SolidPeso molecular:653.77MK-4965
CAS:<p>MK-4965 is a new type of non-nucleoside reverse transcriptase inhibitor with antiviral activity.</p>Fórmula:C20H13Cl2N5O2Cor e Forma:SolidPeso molecular:426.26GW-695634
CAS:<p>GW-695634, a non-nucleoside reverse transcriptase inhibitor, is used potentially for the treatment of HIV infection.</p>Fórmula:C26H21Cl2N3O6SCor e Forma:SolidPeso molecular:574.43HIV-1 inhibitor-31
CAS:<p>HIV-1 inhibitor-31 (compound 4) is a potent inhibitor of HIV-1. HIV-1 inhibitor-31 can be used in the study of AIDS.</p>Fórmula:C21H13Cl2N3O2Cor e Forma:SolidPeso molecular:410.25FWM-3
CAS:<p>FWM-3 is a potent SARS-CoV-2 NSP13 helicase inhibitor [1].</p>Fórmula:C16H16N6O2SCor e Forma:SolidPeso molecular:356.4Neuraminidase-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:533.46Neuraminidase-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:486.62S-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:436.03Inz-4
CAS:<p>Inz-4 is a fungal-selective inhibitor of mitochondrial cytochrome bc1.</p>Fórmula:C18H14F4N2O2Cor e Forma:SolidPeso molecular:366.31VIM-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:436.23Chlorfenson
CAS:<p>Chlorfenson is used to treat onychomycosis as the primary indication.</p>Fórmula:C12H8Cl2O3SCor e Forma:SolidPeso molecular:303.16Antiviral agent 23
CAS:<p>Antiviral agent 23 targets EV71 with 94 nM EC50 and suppresses METTL3/14, useful in infection research.</p>Fórmula:C18H21N5O4Cor e Forma:SolidPeso molecular:371.39Tolindate
CAS:<p>Tolindate, a potent PXR agonist, demonstrates antifungal activity and possesses an EC50 value of 8.3 µM.</p>Fórmula:C18H19NOSCor e Forma:SolidPeso molecular:297.41PF-46396
CAS:<p>PF-46396 is a HIV maturation inhibitor and can be used against HIV-1 clade B and C.</p>Fórmula:C27H29F3N2OCor e Forma:SolidPeso molecular:454.53Antistaphylococcal agent 2
CAS:<p>Antistaphylococcal agent 2 is an anti-staphylococcal therapeutic agent.</p>Fórmula:C23H21N5O5Cor e Forma:SolidPeso molecular:447.44
