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(2.968 produtos)
- Antibiótico(922 produtos)
- Antifecção(23 produtos)
- DHFR(33 produtos)
- Síntese de DNA/RNA(711 produtos)
- HBV(177 produtos)
- HIV Protease(451 produtos)
- HSV(91 produtos)
- Integrase(2 produtos)
- Ribossomo(13 produtos)
Exibir 2 mais subcategorias
Foram encontrados 5863 produtos de "Microbiologia/Virologia"
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Metallo-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:326.76SSAA09E1
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:199.3Crisnatol
CAS:<p>Crisnatol (BWA770U) is an oral anticancer DNA intercalator, toxic to breast cancer cells, not skin fibroblasts.</p>Fórmula:C23H23NO2Cor e Forma:SolidPeso molecular:345.43GAK inhibitor 2
CAS:<p>GAK inhibitor 2, IC50: 0.024μM, strongly blocks GAK; potent against dengue virus, EC50: 1.049μM.</p>Fórmula:C20H23N3O3SCor e Forma:SolidPeso molecular:385.48Antimicrobial agent-4
CAS:<p>Antimicrobial agent-4 (6a) has potent activity against pathogens; binds target enzyme with 10.0 kcal/mol affinity.</p>Fórmula:C22H16ClN5O2SCor e Forma:SolidPeso molecular:449.91Mtb-cyt-bd oxidase-IN-7
<p>Mtb-cyt-bd oxidase-IN-7 inhibits Cyt-bd with 4.17 μM affinity and has anti-tuberculosis properties.</p>Fórmula:C18H14F3NO2Cor e Forma:SolidPeso molecular:333.3HSV-1/HSV-2-IN-2
CAS:<p>HSV-1/HSV-2-IN-2 is a compound that acts as an inhibitor of HSV-1, HSV-2, and VV, demonstrating antiviral activity with EC50 values of 6.8, 8.9, and 8.9 μM,</p>Fórmula:C17H14ClFN4OSCor e Forma:SolidPeso molecular:376.84β-Lactamase-IN-7
CAS:<p>β-Lactamase-IN-7 (compound 14) effectively inhibit Klebsiella pneumoniae that is a potent inhibitor of VIM-Type metallo-β-lactamase with Ki values of 1.26 μM</p>Fórmula:C16H15N3S2Cor e Forma:SolidPeso molecular:313.44L 870810
CAS:<p>L 870810 is a small-molecule inhibitor of HIV-1 integrase with potent antiviral activity in cell culture and good pharmacokinetic properties.</p>Fórmula:C20H19FN4O4SCor e Forma:SolidPeso molecular:430.45(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:377.4HPV18-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(+)-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:372.45Antifungal agent 69
CAS:<p>Antifungal agent 69 (compound 13), a eugenol-imidazole derivative, demonstrates targeted activity against Candida albicans with a minimum inhibitory</p>Fórmula:C23H23ClN2O4Cor e Forma:SolidPeso molecular:426.89Buclosamide
CAS:<p>Buclosamide is a topical antimycotic agent that can be used in dermatomycoses [1].</p>Fórmula:C11H14ClNO2Cor e Forma:SolidPeso molecular:227.693'-Deoxyuridine-5'-triphosphate
CAS:<p>3'-dUTP, a nucleotide analogue, competitively inhibits RNA polymerases I & II, with a Ki of 2.0 µM.</p>Fórmula:C9H15N2O14P3Cor e Forma:SolidPeso molecular:468.145,10-Dideazaaminopterin
CAS:<p>5,10-Dideazaaminopterin is an antileukemic drug.</p>Fórmula:C21H22N6O5Pureza:98%Cor e Forma:SolidPeso molecular:438.44Influenza virus-IN-5
CAS:<p>Influenza virus-IN-5 (Compound 5f) is an influenza virus hemagglutinin (HA) inhibitor that acts on the A/H3N2 virus (EC50: 1 nM).</p>Fórmula:C21H26ClN3O2SCor e Forma:SolidPeso molecular:419.97Urease-IN-7
CAS:<p>Urease-IN-7 (Compound 5k) acts as a competitive inhibitor of the enzyme urease, exhibiting an IC50 value of 3.33 μM and a K_i of 3.62 μM.</p>Fórmula:C16H10BrFN4SCor e Forma:SolidPeso molecular:389.24Sudoterb HCl
CAS:<p>Sudoterb has anti-tubercular activity.</p>Fórmula:C29H30Cl2F3N5OPureza:98%Cor e Forma:SolidPeso molecular:592.48Aranotin
CAS:<p>Aranotin, from Arachniotus aureus, inhibits RNA viruses by blocking RNA polymerase.</p>Fórmula:C20H18N2O7S2Cor e Forma:SolidPeso molecular:462.5Mtb-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:393.56(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:433.48SARS-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:405.36AB-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:461.85Phosphoglycolohydroxamic acid
CAS:<p>Phosphoglycolohydroxamic acid inhibits aldolase/triose-phosphate isomerase; used in antibacterial/antifungal research.</p>Fórmula:C2H6NO6PCor e Forma:SolidPeso molecular:171.05Edelfosine
CAS:<p>inhibits phosphatidylinositol phospholipase C</p>Fórmula:C27H58NO6PPureza:98%Cor e Forma:SolidPeso molecular:523.73Antiparasitic agent-2
CAS:<p>Compound 8a: potent against L. infantum (IC50=7.28μM) & T. cruzi (IC50=2.30μM); mildly toxic to HepG2 (CC50=26.79μM).</p>Fórmula:C20H17N3O3Cor e Forma:SolidPeso molecular:347.37HBV-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:397.85MMV676584
CAS:<p>MMV676584 has anti-tuberculosis avtivity. MMV676584 is a novel drug candidate for eumycetoma .</p>Fórmula:C12H8ClFN2OS2Cor e Forma:SolidPeso molecular:314.79HBV-IN-21
CAS:<p>HBV-IN-21 inhibits HBV DNA replication (IC50: 2.2 μM) and binds HBV capsid protein well (KD: 60.0 μM).</p>Fórmula:C17H17FN4OS2Cor e Forma:SolidPeso molecular:376.47Tenofovir maleate
CAS:<p>Tenofovir Disoproxil Fumarate is a nucleotide reverse transcriptase inhibitor used in the treatment of HIV and chronic Hepatitis B.</p>Fórmula:C13H18N5O8PCor e Forma:SolidPeso molecular:403.28PXYC12
CAS:<p>PXYC12 inhibits Mtb RpsA, key in trans-translation; binds RpsA-CTD (Kd 2.67μM) and RpsA-CTD Δ438A (Kd 4.67μM).</p>Fórmula:C15H15N5O2SCor e Forma:SolidPeso molecular:329.38Metallo-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:250.14Bay 41-4109 (less active enantiomer)
CAS:Bay 41-4109 less active enantiomer shows less activity than Bay 41-4109. BAY 41-4109 is a potent HBV inhibitor (IC50: 53 nM).Fórmula:C18H13ClF3N3O2Pureza:98%Cor e Forma:SolidPeso molecular:395.762',5-Difluoro-2'-deoxycytidine
CAS:<p>2',5-Difluoro-2'-deoxycytidine has potent anti-HCV activity and toxicity to rRNA.</p>Fórmula:C9H11F2N3O4Pureza:98%Cor e Forma:SolidPeso molecular:263.2Metallo-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:302.37BK 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:494.88HIV-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:357.62SDH-IN-5
CAS:<p>SDH-IN-5 (compound 7d), a potent inhibitor of succinate dehydrogenase (SDH) with an IC50 of 3.293 μM, additionally demonstrates antifungal efficacy, exhibiting</p>Fórmula:C16H19F2N3O2Cor e Forma:SolidPeso molecular:323.34DHDPS-IN-1
CAS:<p>DHDPS-IN-1 (compound 8), a DHDPS inhibitor with 39 μM IC50, has potential in antibacterial and herbicidal applications.</p>Fórmula:C13H11NO5SCor e Forma:SolidPeso molecular:293.3Furalaxyl
CAS:<p>Furalaxyl is an fungicide of acyl amino chiral.</p>Fórmula:C17H19NO4Cor e Forma:SolidPeso molecular:301.34BAY-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:288.34Antiparasitic 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:333.34BMH-23
CAS:<p>BMH-23 is an RNA polymerase I inhibitor that acts by causing nucleolar stress and showing potent anticancer activity across many tumor types.</p>Fórmula:C15H15N3Pureza:98%Cor e Forma:SolidPeso molecular:237.3Datelliptium chloride
CAS:<p>Datelliptium chloride is a DNA-intercalating agent derived from ellipticine. Datelliptium chloride shows anti-tumor activities.</p>Fórmula:C23H28ClN3OPureza:98%Cor e Forma:SolidPeso molecular:397.94JMI-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:336.39Tuberculosis 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:524.48Bentysrepinine
CAS:Bentysrepinine, a novel anti-HBV agent, inhibits DNA-HBV and cccDNA activities for the treatment of hepatitis B virus (HBV)-infected hepatitis.Fórmula:C29H35N3O4Pureza:98%Cor e Forma:SolidPeso molecular:489.61REV7/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:371.45DprE1-IN-377790
CAS:<p>DprE1-IN-377790 is a novel DprE1 inhibitor, killing M. tuberculosis.</p>Fórmula:C13H16N4O2Cor e Forma:SolidPeso molecular:260.29Grepafloxacin, (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:359.39BMVC2
CAS:<p>BMVC2 (o-BMVC), a carbazole derivative of BMVC, is a G-quadruplex (G4) stabilizer.</p>Fórmula:C28H25I2N3Cor e Forma:SolidPeso molecular:657.33DNAC-1
CAS:<p>DNAC-1 is against Gram-positive and Gram-negative pathogens potentiator of β-lactam activity.</p>Fórmula:C11H9BrN2S2Pureza:98%Cor e Forma:SolidPeso molecular:313.24PSI-7409 tetrasodium
CAS:<p>PSI-7409 tetrasodium, a sofosbuvir metabolite, inhibits GT 1b, 2a, 3a, 4a NS5B polymerases with IC50s of 1.6, 2.8, 0.7, 2.6 μM.</p>Fórmula:C10H16FN2Na4O14P3Pureza:98%Cor e Forma:SolidPeso molecular:592.117Suberosol
CAS:<p>Suberosol possesses anti-HIV replication activity.</p>Fórmula:C31H50O2Pureza:98%Cor e Forma:SolidPeso molecular:454.73Tedizolid phosphate disodium salt
CAS:<p>Tedizolid phosphate: novel prodrug antibiotic targeting MRSA, VRE, and other Gram-positive bacteria.</p>Fórmula:C17H16FN6Na2O6PPureza:98%Cor e Forma:SolidPeso molecular:496.3032-Mc-1,4-NHQ
CAS:<p>2-Mc-1,4-NHQ, an inhibitor of the Cdc42-PBD interaction, blocks the association of Cdc42 with the PBD.</p>Fórmula:C12H10O3Pureza:98%Cor e Forma:SolidPeso molecular:202.21TDR32570
CAS:<p>TDR32570 is an antimalarial agent.</p>Fórmula:C22H21F3N2O3Pureza:98%Cor e Forma:SolidPeso molecular:418.41Ianthelliformisamine A TFA
CAS:Ianthelliformisamine A TFA, an antibiotic enhancer, is used to against resistant Gram-negative bacteria.Fórmula:C24H34Br2F6N4O6Pureza:98%Cor e Forma:SolidPeso molecular:748.356Nucleoside-Analog-2
CAS:<p>Nucleoside-Analog-2 is a 4'-Azidocytidine analogue, used to against Hepatitis C virus (HCV) replication.</p>Fórmula:C9H11N5O6Pureza:98%Cor e Forma:SolidPeso molecular:285.21SARS-CoV-IN-2
CAS:<p>SARS-CoV-IN-2 is an effective SARS-CoV replication inhibitor</p>Fórmula:C24H26ClFeN3OPureza:98%Cor e Forma:SolidPeso molecular:463.78LP10
CAS:<p>LP10 is a reverse type I inhibitor of Mycobacterium tuberculosis CYP125A1 and a Potent type II inhibitor of Trypanosoma cruzi CYP51.</p>Fórmula:C24H28N4O2Cor e Forma:SolidPeso molecular:404.5Reverse 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:343.45Azosulfamide
CAS:<p>Azosulfamide is an azo compound with similar antibacterial effect as sulfanilamide.</p>Fórmula:C18H16N4Na2O10S3Cor e Forma:SolidPeso molecular:590.5Mollugogenol 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:476.73BMS-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:678.63TachypleginA
CAS:<p>TachypleginA is a parasite motility and invasion inhibitor.</p>Fórmula:C22H21F2NOPureza:98%Cor e Forma:SolidPeso molecular:353.4NPD9948
CAS:<p>NPD9948 is a competitive inhibitor of MTH1.</p>Fórmula:C13H14N6Cor e Forma:SolidPeso molecular:254.29S-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:545.42Xenalamine
CAS:<p>Xenalamine is a synthetic compound of antiviral.</p>Fórmula:C23H21NO4Pureza:98%Cor e Forma:SolidPeso molecular:375.42HI-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:396.3Penciclovir Sodium
CAS:antiviral drugFórmula:C10H14N5NaO3Pureza:98%Cor e Forma:SolidPeso molecular:275.2396PC170942 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:425.97SARS-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:638.73Besifloxacin
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:393.84Influenza 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:456.6Grepafloxacin 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:395.86Bivittoside A
CAS:Bivittoside A is a non-sulfated hexoside analog obtained from Bovine sea cucumber with antifungal activity and potential antitumor activity.Fórmula:C41H66O12Pureza:98%Cor e Forma:SolidPeso molecular:750.96Acyclovir alaninate
CAS:<p>Acyclovir alanine is a pro-drug of Acyclovir. Acyclovir works by decreasing the production of DNA of the virus and it shows very low cytotoxicity.</p>Fórmula:C11H16N6O4Cor e Forma:SolidPeso molecular:296.28L-708906
CAS:<p>L-708906 is the Human Immunodeficiency Virus Type 1 inhibitor.</p>Fórmula:C24H20O6Pureza:98%Cor e Forma:SolidPeso molecular:404.41APOBEC3G-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:253.25BPH-651
CAS:<p>BPH-651 is a CrtM inhibitor.</p>Fórmula:C19H21NOCor e Forma:SolidPeso molecular:279.38HIV-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:508.64L 739594
CAS:<p>L 739594 is an inhibitor of HIV-1 protease.</p>Fórmula:C31H47N3O6Pureza:98%Cor e Forma:SolidPeso molecular:557.72Furalazine
CAS:<p>Furalazine: antimicrobial, treats cholera, more effective than chloramphenicol in shortening stool culture positivity.</p>Fórmula:C9H7N5O3Pureza:98%Cor e Forma:SolidPeso molecular:233.18A 75925
CAS:<p>A 75925, a nonnucleoside reverse transcriptase inhibitors (NNRTI), works to inhibit HIV-1 replication.</p>Fórmula:C44H54N4O8Pureza:98%Cor e Forma:SolidPeso molecular:766.92Vps34-IN-2
CAS: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).Fórmula:C18H25F3N4O3Pureza:98%Cor e Forma:SolidPeso molecular:402.41GNF179 (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:245.3Vif-A3G Inhibitor N.41
CAS:<p>Vif-A3G Inhibitor N.41 is a HIV-1 inhibitor-targeting drug. It causes Vif-dependent degradation of human APOBEC3G, thereby inhibiting the Vif-A3G interaction.</p>Fórmula:C15H14N2O2Pureza:98%Cor e Forma:SolidPeso molecular:254.28Rosaramicin
CAS:<p>Rosaramicin, a lipid-soluble basic macrolide, is an antibacterial substance similar to erythromycin but with a better activity against Gram-negative bacteria.</p>Fórmula:C31H51NO9Pureza:98%Cor e Forma:SolidPeso molecular:581.74TH-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:368.26Antiparasitic agent-4
CAS:<p>Compound 4q: Antiparasitic; IC50: 8.51 μM (L. infantum), 2.20 μM (T. cruzi); HepG2 cytotoxicity: CC50 18.97 μM.</p>Fórmula:C16H13N3O2Cor e Forma:SolidPeso molecular:279.29MAC173979
CAS:<p>MAC173979 inhibits E. coli de novo PABA biosynthesis and growth.</p>Fórmula:C9H5Cl2NO3Pureza:98%Cor e Forma:SolidPeso molecular:246.05ZTB23(R)
CAS:<p>ZTB23(R) is the first potent and selective inhibitor of Mycobacterium tuberculosis Zmp1.</p>Fórmula:C20H15NO5S2Pureza:98%Cor e Forma:SolidPeso molecular:413.47Fumaramidmycin
CAS:<p>Fumaramidmycin is an antibiotic that is produced by Streptomyces kurssanovii NR-7GG1.</p>Fórmula:C12H12N2O3Pureza:98%Cor e Forma:SolidPeso molecular:232.24Sulfametrole
CAS:<p>Sulfametrole: oral, potent antibacterial for HIV, severe pneumonia, UTIs research.</p>Fórmula:C9H10N4O3S2Cor e Forma:SolidPeso molecular:286.33Ametoctradin
CAS:<p>Ametoctradin is a Qo-site inhibitor of mitochondrial respiratory complex III and is used in the study of oomycete diseases.</p>Fórmula:C15H25N5Pureza:99.65%Cor e Forma:SolidPeso molecular:275.39Sp-TTPαS
CAS:Sp-TTPαS is a competitive inhibitor of the catalytic activity of sterile alpha motif and HD domain containing protein 1 (SAMHD1). It competitively inhibits TTP hydrolysis, with a Ki value of 46 µM.Fórmula:C10H17N2O13P3SPeso molecular:498.23Linogliride fumarate
CAS:<p>Linogliride fumarate, a guanidine derivative, stimulates insulin release by blocking ATP-sensitive K+ channels, enhancing glucose tolerance.</p>Fórmula:C20H26N4O5Pureza:98%Cor e Forma:SolidPeso molecular:402.451ML344
CAS:<p>ML344 is a CqsS/LuxQ agonist probe that acts as an inducer of light production without autoinducers.</p>Fórmula:C13H19N5Pureza:98%Cor e Forma:SolidPeso molecular:245.32
