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(2.966 produtos)
- Antibiótico(922 produtos)
- Antifecção(23 produtos)
- DHFR(33 produtos)
- Síntese de DNA/RNA(710 produtos)
- HBV(177 produtos)
- HIV Protease(450 produtos)
- HSV(91 produtos)
- Integrase(2 produtos)
- Ribossomo(13 produtos)
Exibir 2 mais subcategorias
Foram encontrados 5858 produtos de "Microbiologia/Virologia"
Ordenar por
Pureza (%)
0
100
|
0
|
50
|
90
|
95
|
100
(S)-Tenofovir
CAS:<p>(S)-Tenofovir ((S)-PMPA) is the less active S-enantiomer of Tenofovir which is a nucleotide reverse transcriptase inhibitor.</p>Fórmula:C9H14N5O4PPureza:99.9%Cor e Forma:SolidPeso molecular:287.21Halofuginone
CAS:<p>Halofuginone (RU-19110) inhibits prolyl-tRNA synthetase (Ki=18.3 nM), down-regulates Smad3, and blocks TGF-β at 10 ng/ml.</p>Fórmula:C16H17BrClN3O3Pureza:99.53%Cor e Forma:Off-White SolidPeso molecular:414.68Norvancomycin hydrochloride
CAS:<p>Norvancomycin hydrochloride (Desmethyl-vancomycin hydrochloride) is used as a treatment for endocarditis, osteomyelitis, pneumonia, sepsis, or soft tissue</p>Fórmula:C65H74Cl3N9O24Pureza:95.29% - 99.02%Cor e Forma:SolidPeso molecular:1471.693,4-Dihydroxybenzylamine hydrobromide
CAS:<p>3,4-Dihydroxybenzylamine hydrobromide inhibits DNA polymerase and melanoma growth, varying with tyrosinase activity.</p>Fórmula:C7H10BrNO2Pureza:98.49%Cor e Forma:Light Beige Crystalline PowderPeso molecular:220.06Codon readthrough inducer 1
CAS:Codon readthrough inducer 1 contains pyrimidine bases and shows good readthrough activity.Fórmula:C15H11N3O5Pureza:98%Cor e Forma:SolidPeso molecular:313.26Tromantadine
CAS:Tromantadine is an amantadine derivative with antiherpetic activity (inhibits HSV-1 and HSV-2 replication).Fórmula:C16H28N2O2Pureza:98%Cor e Forma:SolidPeso molecular:280.412,3-Dehydro-2-Deoxy-N-Acetylneuraminic Acid
CAS:<p>2,3-Dehydro-2-Deoxy-N-Acetylneuraminic Acid is a pan-sialidase (neuraminidase, NEU) inhibitor with inhibitory activity and against various influenza viruses.</p>Fórmula:C11H17NO8Cor e Forma:SolidPeso molecular:291.26GS-9256
CAS:<p>GS-9256 is a selective inhibitor of the HCV NS3 protease, exhibiting favorable pharmacokinetic properties and antiviral activity [1].</p>Fórmula:C46H56ClF2N6O8PSPureza:98%Cor e Forma:SolidPeso molecular:957.46CM03
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:632.75Afabicin
CAS:<p>Afabicin is an antibiotic targeting Staphylococcus aureus. treat acute bacterial skin and skin structure infections.the prodrug of Debio1452.</p>Fórmula:C23H24N3O7PPureza:98%Cor e Forma:SolidPeso molecular:485.43TNK-6123
CAS:TNK-6123 is an emivirine analog. TNK-6123 has improved activity against drug-resistant HIV mutants.Fórmula:C16H26N2O3SPureza:98%Cor e Forma:SolidPeso molecular:326.45SSJ-183
CAS:<p>SSJ-183 is a low-toxicity and orally available and anti-malarial drug with an IC50 = 7.6 nM against P. falciparum and no lethality at doses up to 2000 mg/kg po.</p>Fórmula:C25H22N4OPureza:99.71% - 99.83%Cor e Forma:SolidPeso molecular:394.47Sotirimod
CAS:<p>Sotirimod（R850） is a novel immunomodulator with antitumor and antiviral activity for the study of actinic keratoses.</p>Fórmula:C14H17N5Pureza:95.87%Cor e Forma:SolidPeso molecular:255.32Rufloxacin hydrochloride
CAS:<p>Rufloxacin HCl (MF-934 HCl): a fluoroquinolone that inhibits topoisomerase and B-cell differentiation.</p>Fórmula:C17H19ClFN3O3SPureza:99.80%Cor e Forma:SolidPeso molecular:399.867β-Lactamase-IN-1
CAS:β-Lactamase-IN-1 (4-(1,3-dihydroxypropan-2-yl)-6-methoxypyrido[2,3-b]pyrazin-3-one) is a β-Lactamase inhibitor and targets the infection of NeisseriaFórmula:C11H13N3O4Pureza:99.89%Cor e Forma:SolidPeso molecular:251.24Tuberculosis inhibitor 3
CAS:<p>Tuberculosis inhibitor 3 is a highly potent and oral anti-tuberculosis drug against both drug-sensitive and drug-resistant Mycobacterium , H37RV & MDR-TB.</p>Fórmula:C21H22F6N4O3SPureza:98.8%Cor e Forma:SolidPeso molecular:524.48Tromantadine hydrochloride
CAS:Tromantadine hydrochloride is an amantadine derivative with antiherpetic activity (inhibits HSV-1 and HSV-2 replication).Fórmula:C16H29ClN2O2Pureza:98%Cor e Forma:SolidPeso molecular:316.87CP-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:443.9L 738372
CAS:<p>L 738372 is a non-nucleoside inhibitor of HIV-1 reverse transcriptase.</p>Fórmula:C18H15N3OCor e Forma:SolidPeso molecular:289.33CGI-17341
CAS:<p>CGI-17341, an oral 5-nitroimidazole antimicrobial, blocks drug-sensitive and resistant tuberculosis at 0.1-0.3 µg/ml.</p>Fórmula:C7H9N3O3Cor e Forma:SolidPeso molecular:183.16Meturedepa
CAS:<p>Meturedepa is an antineoplastic agent.</p>Fórmula:C11H22N3O3PPureza:98%Cor e Forma:SolidPeso molecular:275.28ML366
CAS:<p>ML366 is a Vibrio cholerae Quorum Sensing inhibitor Acting via the LuxO response regulator.</p>Fórmula:C17H19N3O4Pureza:98%Cor e Forma:SolidPeso molecular:329.35Anti-Influenza agent 4
CAS:<p>Anti-Influenza agent 4 selectively inhibits A/Parma (EC50: 62 nM) and A/Roma (EC50: 150 nM) influenza strains.</p>Fórmula:C19H18N2O5SPureza:98.94% - 98.95%Cor e Forma:SolidPeso molecular:386.42Lipoxamycin hemisulfate
CAS:<p>Lipoxamycin hemisulfate (Lipoxamycin) is an inhibitor of serine palmitoyltransferase (IC50 = 21 nM) with antifungal activity.</p>Fórmula:C38H74N4O14SPureza:99.14% - 99.93%Cor e Forma:SolidPeso molecular:843.08NIC
CAS:<p>NIC is an inhibitor of host invasion. It is also an inhibitor of VEGF binding to immobilized heparin.</p>Fórmula:C15H16ClN3O3Pureza:98%Cor e Forma:SolidPeso molecular:321.76Nopol
CAS:Nopol is an inhibitor of alpha-glucosidase.Fórmula:C11H18OPureza:98%Cor e Forma:SolidPeso molecular:166.26MS0017509
CAS:<p>MS0017509 is a DNA damage repair inhibitor.</p>Fórmula:C11H10N4Pureza:98%Cor e Forma:SolidPeso molecular:198.22BPH-652
CAS:<p>BPH-652 is an S. aureus dehydrosqualene synthase (CrtM) inhibitor (Ki: 1.5 nM; IC50: 100-300 nM for S. aureus pigment formation).</p>Fórmula:C16H19K3O7PSPureza:98%Cor e Forma:SolidPeso molecular:503.65Ceforanide lysine
CAS:<p>Ceforanide lysine is an Anti-Infective.</p>Fórmula:C26H35N9O8S2Pureza:98%Cor e Forma:SolidPeso molecular:665.74BMS-663749 lysine
CAS:<p>BMS-663749 lysine is used as a phosphonooxymethyl prodrug 4 for HIV-1 attachment inhibitor.</p>Fórmula:C29H39N6O11PPureza:98%Cor e Forma:SolidPeso molecular:678.63Mollugogenol A
CAS:<p>Mollugogenol A: a Gammacerane saponin from Mollugo pentaphylla with antifungal and spermatocidal properties; damages sperm membrane.</p>Fórmula:C30H52O4Cor e Forma:SolidPeso molecular:476.73Azosulfamide
CAS:<p>Azosulfamide is an azo compound with similar antibacterial effect as sulfanilamide.</p>Fórmula:C18H16N4Na2O10S3Cor e Forma:SolidPeso molecular:590.5GSK729
CAS:<p>GSK729 is a novel potent EchA6 inhibitor.</p>Fórmula:C16H16F3N3O2Pureza:98%Cor e Forma:SolidPeso molecular:339.31Phenethicillin potassium
CAS:<p>Phenethicillin potassium is a potassium salt form of phenethicillin with antibacterial activity.</p>Fórmula:C17H20KN2O5SPureza:98%Cor e Forma:SolidPeso molecular:403.51BAS00127538
CAS:<p>BAS00127538 is an Lipid II inhibitor.</p>Fórmula:C31H28BF4NOCor e Forma:SolidPeso molecular:517.37HHL-6
CAS:<p>HHL-6 is a c-Fos and BDNF protein expression modulator.</p>Fórmula:C19H26N2O3Cor e Forma:SolidPeso molecular:330.42GSK1829820A
CAS:<p>GSK1829820A is a Mycobacterium tuberculosis H37Rv non-cytotoxic inhibitor.</p>Fórmula:C15H15N3OSPureza:98%Cor e Forma:SolidPeso molecular:285.36GSK951A
CAS:<p>GSK951A blocks EchA6 and FAS-II, halts mycolic acid formation and MAMES in M. bovis BCG; FAMEs stay mostly unchanged.</p>Fórmula:C24H23F3N4O3Pureza:98%Cor e Forma:SolidPeso molecular:472.46Grepafloxacin, (S)-
CAS:<p>Grepafloxacin, (S)- is an oral broad-spectrum fluoroquinolone antibacterial used for the treatment of bacterial infections.</p>Fórmula:C19H22FN3O3Cor e Forma:SolidPeso molecular:359.39DprE1-IN-377790
CAS:<p>DprE1-IN-377790 is a novel DprE1 inhibitor, killing M. tuberculosis.</p>Fórmula:C13H16N4O2Cor e Forma:SolidPeso molecular:260.29Lufotrelvir
CAS:Lufotrelvir (PF-07304814), a prodrug of PF-00835231, is a potent SARS-CoV-2 3CL protease inhibitor with antiviral properties, Ki 174nM.Fórmula:C24H33N4O9PPureza:99.43% - >99.99%Cor e Forma:SolidPeso molecular:552.51REV7/REV3L-IN-1
CAS:<p>REV7/REV3L-IN-1 is a inhibitor of REV7/REV3L interaction(IC50 of 78 μM),</p>Fórmula:C19H21N3O3SPureza:98%Cor e Forma:SolidPeso molecular:371.45Antibacterial agent 96
CAS:<p>Compound 4k is potent against drug-susceptible and resistant M. tuberculosis but toxic to HepG2 and Vero cells.</p>Fórmula:C18H15Cl2NO2Cor e Forma:SolidPeso molecular:348.22DprE1-IN-1
CAS:<p>DprE1-IN-1: Potent, oral DprE1 inhibitor; stable in hepatocytes, low toxicity, anti-bacilli in macrophages, -1.29 log10 CFU.</p>Fórmula:C19H21N3O6S2Cor e Forma:SolidPeso molecular:451.52AIC-292
CAS:<p>AIC-292 is a potent, tolerable reverse transcriptase inhibitor active against various HIV-1 strains, including NNRTI-resistant K103N, G190A, Y181C.</p>Fórmula:C19H12Cl2F2N4O2Cor e Forma:SolidPeso molecular:437.23TH-Z93
CAS:<p>TH-Z93 is a potent FPPS inhibitor (IC50:90 nM) and a lipophilic bisphosphonate.</p>Fórmula:C12H22N2O7P2Pureza:98.37%Cor e Forma:SolidPeso molecular:368.26CK-2-68
CAS:<p>CK-2-68 is a potent inhibitor of PfNDH2.</p>Fórmula:C24H17ClF3NO2Pureza:98%Cor e Forma:SolidPeso molecular:443.85BMS-585248
CAS:<p>BMS-585248 is a highly effective HIV-1 adhesion inhibitor that targets the viral envelope protein gp120.</p>Fórmula:C22H18FN7O3Cor e Forma:SolidPeso molecular:447.42GNF179 (Metabolite)
CAS:<p>GNF179 metabolite is a potent (4.8 nM vs. W2 strain) derivative of 8,8-dimethyl IP with strong in vitro stability and oral bioavailability.</p>Fórmula:C14H16FN3Pureza:98%Cor e Forma:SolidPeso molecular:245.3Cap-dependent endonuclease-IN-8
CAS:<p>Cap-dependent endonuclease-IN-8, from CN111410661A (I-196), inhibits CENs, halting orthomyxovirus replication, like influenza A/B/C.</p>Fórmula:C29H23F2N3O6SCor e Forma:SolidPeso molecular:579.57SARS-CoV-IN-1
CAS:SARS-CoV-IN-1 is an effective SARS-CoV replication inhibitor(EC50 of 4.9 μM in Vero cells).Fórmula:C23H24ClFeN3OPureza:98%Cor e Forma:SolidPeso molecular:449.76MmpL3-IN-3
CAS:<p>MmpL3-IN-3 (Compound 12), an MmpL3 inhibitor, exhibits potent anti-tuberculosis activity with a minimum inhibitory concentration (MIC) of 0.1 μM against H37Rv</p>Fórmula:C26H33ClN2SiCor e Forma:SolidPeso molecular:437.09Vps34-IN-2
CAS:<p>Vps34-IN-2 is a potent and selective Vps34 inhibitor (IC50s: 2 and 82 nM on the Vps34 enzymatic assay and the GFP-FYVE cellular assay, respectively).</p>Fórmula:C18H25F3N4O3Pureza:98%Cor e Forma:SolidPeso molecular:402.41Synthalin 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:210.28CWHM-1008
CAS:CWHM-1008: Oral antimalarial, EC50 - 46 nM (3D7 strain), 21 nM (Dd2 resistant).Fórmula:C22H26F3N3OCor e Forma:SolidPeso molecular:405.46VU0420373
CAS:<p>VU0420373 activates HssRS at EC50 10.7 μM, induces heme synthesis, toxic to S. aureus.</p>Fórmula:C15H11FN2OCor e Forma:SolidPeso molecular:254.26Furalazine
CAS:<p>Furalazine: antimicrobial, treats cholera, more effective than chloramphenicol in shortening stool culture positivity.</p>Fórmula:C9H7N5O3Pureza:98%Cor e Forma:SolidPeso molecular:233.18Oxaquin
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:Nucleoside-Analog-1 is a 4′-Azidocytidine analogue, used to against Hepatitis C virus replication.Fórmula:C9H9N5O5Pureza:98%Cor e Forma:SolidPeso molecular:267.2Acoziborole
CAS: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.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:465.13G0507
CAS:G0507, a potent pyrrolopyrimidinedione, blocks E. coli growth by activating σE stress and targeting LolCDE ABC Transporter.Fórmula:C18H15N3O3SCor e Forma:SolidPeso molecular:353.39L 739594
CAS:<p>L 739594 is an inhibitor of HIV-1 protease.</p>Fórmula:C31H47N3O6Pureza:98%Cor e Forma:SolidPeso molecular:557.72Zidebactam sodium salt
CAS:Zidebactam sodium salt is a potent inhibitor of β-lactamase, and also is an inhibitor of penicillin-binding protein2 (PBP2)(IC50 of 0.26 μg/mL).Fórmula:C13H21N5NaO7SPureza:98%Cor e Forma:SolidPeso molecular:414.39HIV-1 inhibitor-28
CAS:<p>HIV-1 inhibitor-28: potent, selective, EC50=58 nM, low MT-4 cell toxicity (CC50=38.6 μM), valuable in AIDS research.</p>Fórmula:C26H32N6O3SCor e Forma:SolidPeso molecular:508.64GSK983
CAS:<p>GSK983 inhibits DHODH to halt cell growth and dengue virus replication, acting as a broad-spectrum antiviral.</p>Fórmula:C18H16ClN3OPureza:98%Cor e Forma:SolidPeso molecular:325.79SARS-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:407.269-OxoOTrE
CAS:<p>9-OxoOTrE, made by oxidizing 9-HpOTrE, has antimicrobial effects on plant pathogens like bacteria and fungi.</p>Fórmula:C18H28O3Cor e Forma:SolidPeso molecular:292.41APOBEC3G-IN-1
CAS:<p>APOBEC3G-IN-1 (MN136.0185) is a targeted APOBEC3G inhibitor with anti-HIV activity for the study of infectious diseases and cancer.</p>Fórmula:C15H11NO3Pureza:96.54%Cor e Forma:SolidPeso molecular:253.25Antibacterial agent 106
CAS:<p>Compound 106 is an orally active antibacterial with biofilm-fighting properties, kills 99.7% of MRSA in macrophages.</p>Fórmula:C20H24N6SCor e Forma:SolidPeso molecular:380.51Grepafloxacin Hydrochloride
CAS:<p>Grepafloxacin Hydrochloride is an antimicrobial agent, oral broad-spectrum fluoroquinolone. It is used to treat bacterial infections.</p>Fórmula:C19H23ClFN3O3Cor e Forma:SolidPeso molecular:395.86HIV-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:417.37RHI002-Me
CAS:<p>RHI002-Me is a methylated derivative of RHI002, a selective inhibitor of human RNaseH2.</p>Fórmula:C18H19N3O2S2Pureza:98%Cor e Forma:SolidPeso molecular:373.49Influenza 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:456.6MPO
CAS:<p>MPO (5-(4'-Methoxyphenyl)-oxazole) is a hatch and growth of Caenorhabditis Elegans inhibitor.</p>Fórmula:C10H9NO2Pureza:99.86%Cor e Forma:SolidPeso molecular:175.18CBR-3465
CAS:<p>CBR-3465 is an inhibitor of mycobacterium tuberculosis (Mtb) type II NADH dehydrogenase. The MIC of CBR-3465 against Mtb is 0.16 μM [1].</p>Fórmula:C16H18FN3O2SCor e Forma:SolidPeso molecular:335.4Antiviral 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:399.45Laburnetin
CAS:<p>Laburnetin: an isoflavone antibacterial, combats fungi/S. vesicarium, boosts MRSA methicillin susceptibility, used in pest control.</p>Fórmula:C20H18O6Cor e Forma:SolidPeso molecular:354.35GlyRS-IN-1
CAS:GlyRS-IN-1 is an inhibitor of glycyl-tRNA synthase (GlyRS). It can inhibit the growth of bacteria.Fórmula:C12H17N7O7SCor e Forma:SolidPeso molecular:403.37HIV-1 inhibitor-21
CAS:<p>HIV-1 inhibitor-21 (compound 9b) blocks HIV-1 RT effectively (IC50: 0.55 μM), targeting wild-type and K103N strains, with low toxicity (CC50: 10.2 μM).</p>Fórmula:C28H24N6O2Cor e Forma:SolidPeso molecular:476.53Dihydropteroate synthase-IN-1
CAS:<p>"Dihydropteroate synthase-IN-1 (5g) inhibits DHPS and cytochrome P450, useful as radiographic diagnostic material."</p>Fórmula:C19H23N5O4S2Cor e Forma:SolidPeso molecular:449.55Besifloxacin
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:393.84SARS-CoV-2-IN-18
CAS:<p>SARS-CoV-2-IN-18 (Compound 26) is a potent inhibitor of SARS-CoV-2 3C-like protease (IC50 = 45 nM) [1].</p>Fórmula:C20H14N2O3Cor e Forma:SolidPeso molecular:330.34FadD32 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:401.89RSV-IN-4
CAS:<p>RSV-IN-4 is a dual inhibitor for RSV and IAV with an EC50 of 11.76 μM.</p>Fórmula:C18H18N2O2SCor e Forma:SolidPeso molecular:326.41SARS-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:657.333CPLro-IN-2
CAS:<p>3CPLro-IN-2: Potent oral SARS-CoV-2 3CLpro inhibitor, IC50: 1.55 μM, Ki: 6.09 μM, targets vital COVID-19 protein.</p>Fórmula:C32H24BrNO2Cor e Forma:SolidPeso molecular:534.44Lupulon
CAS:<p>Lupulon has a role as an apoptosis inducer, antimicrobial agent, angiogenesis inhibitor, and antineoplastic agent.</p>Fórmula:C26H38O4Cor e Forma:SolidPeso molecular:414.58Penciclovir Sodium
CAS:antiviral drugFórmula:C10H14N5NaO3Pureza:98%Cor e Forma:SolidPeso molecular:275.2396Bofumustine
CAS:<p>Bofumustine is a chloroethyl nitrosourea with anti tumor properties.</p>Fórmula:C18H21ClN4O9Cor e Forma:SolidPeso molecular:472.83SARS-CoV MPro-IN-1
CAS:<p>MProinhibitor 11b blocks SARS-CoV-2 main protease (IC50=0.04 μM), cuts viral yield and RNA in Vero E6 cells (EC50=0.72 μM).</p>Fórmula:C25H25FN4O4Cor e Forma:SolidPeso molecular:464.49YM-53601
CAS:<p>YM-53601 is an SQS inhibitor that inhibits adipogenic biosynthesis and lipid secretion in rodents.YM-53601 is a cholesterol-lowering agent that inhibits FDFT1.</p>Fórmula:C21H22ClFN2OPureza:99.65%Cor e Forma:SolidPeso molecular:372.86
