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"
Ordenar por
Pureza (%)
0
100
|
0
|
50
|
90
|
95
|
100
BMS-929075
CAS:BMS-929075 is an orally active HCV NS5B replicase (HCV NS5B replicase) palm site variant inhibitor with potency, high oral bioavailability and pharmacokineticFórmula:C31H24F2N4O3Pureza:99.81% - 99.94%Cor e Forma:SolidPeso molecular:538.546-Hydroxy-DOPA
CAS:<p>6-Hydroxy-DOPA is an allosteric inhibitor of RAD52, it inhibits proliferation of BRCA-deficient cancer cells in vitro and also inhibits APE1.</p>Fórmula:C9H11NO5Pureza:97.78% - 97.95%Cor e Forma:SolidPeso molecular:213.19MP265
CAS:<p>MP265 disrupts the MreB cytoskeleton and has antiproliferative effects.</p>Fórmula:C8H10Cl2N2SPureza:99.55%Cor e Forma:SolidPeso molecular:237.15SARS-CoV-2-IN-38
CAS:SARS-CoV-2-IN-38, also known as compound 24, is an inhibitor of SARS-CoV-2 that demonstrates favorable oral bioavailability in mice, with an absorption fractionFórmula:C18H14ClF4NO4Pureza:99.37%Cor e Forma:SolidPeso molecular:419.76Setrobuvir
CAS:<p>Setrobuvir (ANA-598) is an orally active non-nucleoside HCV NS5B polymerase inhibitor with inhibitory effects on de novo RNA synthesis and primer extension with</p>Fórmula:C25H25FN4O6S2Pureza:98.92% - >99.99%Cor e Forma:SolidPeso molecular:560.62ABMA
CAS:<p>ABMA is a broad-spectrum inhibitor shielding cells from viruses, bacteria, and parasites, acting in late endosomes.</p>Fórmula:C18H24BrNOPureza:99.866%Cor e Forma:SolidPeso molecular:350.29116-9e
CAS:<p>116-9e (MAL2-11B) is an Hsp70 chaperone DNAJA1 inhibitor with antiviral properties, inhibits SV40 replication, and can be used to study cancer drug resistance.</p>Fórmula:C31H32N2O5Pureza:99.55%Cor e Forma:SolidPeso molecular:512.6TBT1
CAS:<p>TBT1 is a first-gen MsbA ATPase activator and LPS transport blocker in Acinetobacter, EC50 at 13 μM.</p>Fórmula:C16H14ClNO3SPureza:99.27%Cor e Forma:SolidPeso molecular:335.81SARS-CoV-2-IN-13
CAS:<p>SARS-CoV-2-IN-13, a stable niclosamide analogue, enhances oral bioavailability and inhibits SARS-CoV-2 (IC50: 0.057 μM).</p>Fórmula:C13H8Cl2N2O4Pureza:98.54%Cor e Forma:SolidPeso molecular:327.12BAY-43-9695
CAS:<p>BAY-43-9695 is a non-nucleoside compound with anti-human cytomegalovirus (HCMV) activity. It is the major metabolite of BAY-38-4766.</p>Fórmula:C22H25N3O4SPureza:99.50% - 99.65%Cor e Forma:SolidPeso molecular:427.52QPX7728-OH disodium
CAS:<p>QPX7728 disodium (Xeruborbactam disodium) is a cyclic boronate inhibitor of many serine and metal-β-lactamases, exhibiting antibacterial activity.</p>Fórmula:C10H8BFNa2O5Pureza:>99.99%Cor e Forma:SolidPeso molecular:283.96Bithionol sulfoxide
CAS:<p>Bithionol sulfoxide (Bithionoloxide) is a compound with inhibitory effects against parasites, inhibiting Fasciola hepatica and Schistosoma mansoni.</p>Fórmula:C12H6Cl4O3SPureza:98.76%Cor e Forma:Off White To Tinch Pink Crystalline PowderPeso molecular:372.05ME1111
CAS:<p>ME1111, a succinate dehydrogenase inhibitor of Trichophyton species, serves as an antifungal agent effective against dermatophytes.</p>Fórmula:C12H14N2OPureza:99.45%Cor e Forma:SolidPeso molecular:202.25Azidamfenicol
CAS:<p>Azidamfenicol inhibits ribosomal peptidyltransferase with a Ki of 22 µM. Azidamfenicol is a broad-spectrum chloramphenicol-like antibiotic.</p>Fórmula:C11H13N5O5Pureza:99.61%Cor e Forma:SolidPeso molecular:295.25JPD447
CAS:JPD447, a derivative of MAC-0547630, represents a new class of UppS inhibitors designed to enhance the efficacy of β-lactam antibiotics.Fórmula:C20H23FN4Pureza:99.69%Cor e Forma:SolidPeso molecular:338.42Methyl 2-amino-5-bromobenzoate
CAS:<p>Methyl 2-amino-5-bromobenzoate (Methyl 5-Bromoanthranilate) is an HCV NS5b RNA polymerase inhibitor with antimicrobial activity.</p>Fórmula:C8H8BrNO2Pureza:98.05%Cor e Forma:SolidPeso molecular:230.06CDD-1845
CAS:<p>CDD-1845, a non-covalent, non-peptide inhibitor, exhibits potent inhibition of SARS-CoV-2 M^pro with a K_i value of 3 nM.</p>Fórmula:C34H31N5O2Pureza:98%Cor e Forma:SolidPeso molecular:541.64Emzadirib
CAS:<p>Emzadirib (RAD51-IN-2) is a potent RAD51 inhibitor with potential anticancer activity for the study of DNA damage repair.</p>Fórmula:C27H40N4O6S2Pureza:99.79% - 99.9%Cor e Forma:SolidPeso molecular:580.76BRL44385
CAS:<p>BRL44385 is an effective and selective inhibitor of the replication of HSV-1 and HSV2, Epstein-Barr virus (EBV), and varicella-zoster virus (VZV).</p>Fórmula:C8H11N5O3Pureza:98%Cor e Forma:SolidPeso molecular:225.2Acorafloxacin HCl
CAS:<p>Acorafloxacin: broad-spectrum fluoroquinolone antibacterial for acute skin infections and pneumonia.</p>Fórmula:C21H24ClF2N3O4Pureza:98%Cor e Forma:SolidPeso molecular:455.88ThrRS-IN-3
<p>ThrRS-IN-3: Potent inhibitor of Salmonella enterica ThrRS, IC50 = 19 nM, Kd = 34 nM, with antibacterial effects.</p>Fórmula:C31H30Cl2N6O5Cor e Forma:SolidPeso molecular:637.51SARS-CoV-2-IN-44
CAS:<p>SARS-CoV-2-IN-44, an inhibitor of SARS-CoV-2, effectively suppresses viral replication with an EC50 value of 0.6μM and exhibits negligible cytotoxicity in Calu-</p>Fórmula:C18H16O5Pureza:98%Cor e Forma:SolidPeso molecular:312.32AB131
CAS:<p>AB131, an inhibitor of MSMEG 6649 and Rv2172c (KD values of 0.16 and 0.02 μM, respectively), enhances the antimycobacterial efficacy of the antitubercular agent</p>Fórmula:C21H19NO6SCor e Forma:SolidPeso molecular:413.445,6,7,8-Tetrahydro-8-deazahomofolic acid
CAS:<p>5,6,7,8-Tetrahydro-8-deazahomofolic acid is a potential thymidylate synthase (TS) inhibitor and other folate related enzymes inhibitor.</p>Fórmula:C21H26N6O6Cor e Forma:SolidPeso molecular:458.47Ibuzatrelvir
CAS:<p>Ibuzatrelvir (PF-07817883) is an antiviral compound designed to inhibit the SARS-CoV-2 3CL protease, and is utilized in the treatment of COVID-19 [1].</p>Fórmula:C21H30F3N5O5Pureza:98%Cor e Forma:SolidPeso molecular:489.49Cap-dependent endonuclease-IN-13
CAS:<p>Cap-dependent endonuclease-IN-13 is a potent inhibitor of cap-dependent endonuclease (CEN) and shows research potential against influenza virus infection (</p>Fórmula:C25H20F2N4O4SCor e Forma:SolidPeso molecular:510.51CDD-1733
CAS:<p>CDD-1733 is a potent, non-covalent, and non-peptide inhibitor of the SARS-CoV-2 main protease (Mpro) with an inhibition constant (K i) of 12 nM.</p>Fórmula:C34H32F3N5O2Pureza:98%Cor e Forma:SolidPeso molecular:599.65WRN inhibitor 2
CAS:<p>WRN Inhibitor 2 (example 118), a potent inhibitor of the WRN (Werner Syndrome ATP-dependent helicase enzyme), exhibits a pIC50 value of 7.0 or greater [1].</p>Fórmula:C15H11F3N2O5S2Pureza:98%Cor e Forma:SolidPeso molecular:420.388-Azahypoxanthine
CAS:<p>8-Azahypoxanthine (NSC-22709) inhibits hypoxanthine-guanine-xanthine phosphoribosyltransferase and has antimalarial properties.</p>Fórmula:C4H3N5OPureza:99.66%Cor e Forma:Light Yellow To Light Beige Fine CrystallinePeso molecular:137.1Antibacterial agent 159
CAS:<p>Compound 6d (Antibacterial agent 159) is an antibiotic effective against impetigo and Clostridium difficile infection (CDI), with no observed recurrence for CDI</p>Fórmula:C51H50N16O10S6Pureza:98%Cor e Forma:SolidPeso molecular:1239.43ddUTP
CAS:<p>ddUTP (2′,3′-Dideoxyuridine-5′-triphosphate) serves as a selective inhibitor of HIV and AMV reverse transcriptases with Ki values of 0.05 µM for HIV and 1 µM</p>Fórmula:C9H15N2O13P3Pureza:98%Cor e Forma:SolidPeso molecular:448.111A 74704
CAS:A 74704 is a pseudo C2-symmetric inhibitor of HIV-1 protease and its diester analog.Fórmula:C43H52N4O7Pureza:98%Cor e Forma:SolidPeso molecular:736.9SARS-CoV-2 Mpro-IN-12
CAS:<p>SARS-CoV-2 Mpro-IN-12 (compound D026) serves as an inhibitor of the main protease (Mpro) of SARS-CoV-2, exhibiting antiviral properties [1].</p>Fórmula:C20H17NO3Pureza:98%Cor e Forma:SolidPeso molecular:319.35D1N52
CAS:<p>D1N52 is a potent inhibitor of the SARS-CoV-2 3CL protease, demonstrating an inhibitory concentration half-maximal (IC50) value of 0.53 μM [1].</p>Fórmula:C20H13F4N5O3Pureza:98%Cor e Forma:SolidPeso molecular:447.34Mirincamycin HCl
CAS:<p>Mirincamycin HCl is a close analog of the drug clindamycin used for the treatment of Plasmodium falciparum blood stages.</p>Fórmula:C19H36Cl2N2O5SPureza:98%Cor e Forma:SolidPeso molecular:475.47DDD85646
CAS:<p>DDD85646 is an inhibitor of T. brucei N-myristoyltransferase with a Ki of 1.44 nM, an IC50 of 2 nM and an EC50 of 2 nM. The IC50 of hNMT is 4 nM.</p>Fórmula:C21H24Cl2N6O2SPureza:97.8% - 99.76%Cor e Forma:SolidPeso molecular:495.43NSC 288387
CAS:<p>NSC 288387, a pan-flavivirus MTase inhibitor, binds to the SAM-binding pocket and effectively inhibits Zika virus (ZIKV) with an IC50 of 0.2 μM, also preventing</p>Fórmula:C19H16N4O3Pureza:98%Cor e Forma:SolidPeso molecular:348.36Pexiganan acetate
CAS:<p>Pexiganan acetate (MSI 78), a 22-residue peptide analogue of magainin 2, disrupts bacterial membranes or walls, leading to antibacterial activity.</p>Fórmula:C122H210N32O22·xC2H4O2Pureza:99.88%Cor e Forma:SolidPeso molecular:2477.22 (free base)U 104489
CAS:<p>U 104489 (PNU-104489) is a novel specific inhibitor of human immunodeficiency virus 1 (HIV-1), showing effective activity against BHA-P-resistant HIV-1MF.</p>Fórmula:C26H36N6O3SCor e Forma:SolidPeso molecular:512.67Lagociclovir valactate
CAS:<p>Lagociclovir valactate is a prodrug of Lagociclovir . Lagociclovir valactate is an orally active anti- HBV agent [1] .</p>Fórmula:C18H25FN6O6Cor e Forma:SolidPeso molecular:440.43RSV L-protein-IN-2
CAS:<p>RSV L-protein-IN-2 (Compound A), a noncompetitive inhibitor of the RSV polymerase (IC50: 4.5 μM), exhibits antiviral activity against long RSV strains (EC50: 1.</p>Fórmula:C32H36N4O5Pureza:98%Cor e Forma:SolidPeso molecular:556.65Micronomicin
CAS:<p>Micronomicin (Gentamicin C2b) is an antibiotic exhibiting antibacterial and bactericidal capacity.</p>Fórmula:C20H41N5O7Pureza:97.05% - 99.79%Cor e Forma:SolidPeso molecular:463.57XZ426
CAS:<p>XZ426 is a potent integrase strand transfer inhibitor with anti- HIV activity .</p>Fórmula:C22H24F2N4O4Cor e Forma:SolidPeso molecular:446.45Votoplam
CAS:<p>Votoplam functions as a gene splicing modulator, employed in the inhibition of Huntington's disease [1].</p>Fórmula:C21H25N9OPureza:98%Cor e Forma:SolidPeso molecular:419.48ALS-8112
CAS:ALS-8112 is a inhibitor of respiratory syncytial virus (RSV) polymerase. The 5'-triphosphate form of ALS-8112 inhibits RSV polymerase (IC50: 0.02 μM).Fórmula:C10H13ClFN3O4Pureza:98.90%Cor e Forma:SolidPeso molecular:293.68Loflucarban
CAS:<p>Loflucarban (Fluonilid) is an antimycotic compoud.</p>Fórmula:C13H9Cl2FN2SPureza:98.08% - 98.15%Cor e Forma:SolidPeso molecular:315.19RO-7
CAS:<p>RO-7 is a next-generation polymerase (PA) endonuclease influenza A and B viruses inhibitor.</p>Fórmula:C24H20F3N3O3SPureza:98%Cor e Forma:SolidPeso molecular:487.49DHX9-IN-6
CAS:DHX9-IN-6 is a highly effective ATP-dependent RNA helicase A (DHX9) inhibitor, used in cancer research.Fórmula:C23H18ClFN4O4S2Pureza:99.71%Cor e Forma:SolidPeso molecular:533Laxifloran
CAS:<p>Laxifloran possesses antibacterial and antifungal properties.</p>Fórmula:C17H18O5Cor e Forma:SolidPeso molecular:302.32Antimalarial agent 10
CAS:<p>Compound 17b, an amino alcohol-quinoline, targets Pf3D7 (IC50: 14.9 nM) and PfW2 (IC50: 11 nM) with selectivity index >770.</p>Fórmula:C23H22F6N2O2Cor e Forma:SolidPeso molecular:472.42TAS-114
CAS:<p>TAS-114 is a dUTPase and DPD inhibitor that modulates catabolic pathways to improve systemic availability of 5-FU.</p>Fórmula:C21H29N3O6SPureza:99.76%Cor e Forma:SolidPeso molecular:451.54Azaconazole
CAS:<p>Azaconazole, an agricultural fungicide, is used for controlling powdery mildew on crops and bean rust.</p>Fórmula:C12H11Cl2N3O2Cor e Forma:SolidPeso molecular:300.14Prochloraz manganese
CAS:<p>Prochloraz manganese, an antifungal agent utilized in the agricultural sectors [1], serves to protect crops by inhibiting fungal growth.</p>Fórmula:C60H64Cl14MnN12O8Cor e Forma:SolidPeso molecular:1632.51NSC309401 dihydrochloride
CAS:<p>NSC309401 is an E. coli dihydrofolate reductase inhibitor with an IC50 value of 189 nM and a dissociation constant (Kd) of 14.57 nM [1].</p>Fórmula:C17H18Cl2N6Cor e Forma:SolidPeso molecular:377.27N-Acetylpurinomycin
CAS:<p>N-Acetylpurinomycin is a selective agonist of CB2 receptor.</p>Fórmula:C24H31N7O6Cor e Forma:SolidPeso molecular:513.55Caerulomycin A
CAS:<p>Caerulomycin A (Caerulomycin) (Cerulomycin; Caerulomycin) is an antifungal compound.</p>Fórmula:C12H11N3O2Pureza:99.28%Cor e Forma:SolidPeso molecular:229.23Antiproliferative agent-18
CAS:<p>Compound 5k (Antiproliferative Agent-18) is an antiproliferative agent that exhibits moderate antibacterial and antifungal activities [1].</p>Fórmula:C26H27FN2OSCor e Forma:SolidPeso molecular:434.57Streptovitacin A
CAS:<p>Streptovitacin A boosts growth inhibition against fungi.</p>Fórmula:C15H23NO5Pureza:98%Cor e Forma:SolidPeso molecular:297.35NS5A-IN-2
CAS:<p>NS5A-IN-2, a potent inhibitor, is highly effective against HCV 1b and shows increased activity for GT 3a with good metabolic stability.</p>Fórmula:C46H45N7O7Pureza:98%Cor e Forma:SolidPeso molecular:807.89Propamidine
CAS:<p>Propamidine acts as a covalent inhibitor of TMPRSS2 and exhibits antibacterial properties. [1]</p>Fórmula:C17H20N4O2Pureza:98%Cor e Forma:SolidPeso molecular:312.37MoTPS1-IN-1
CAS:MoTPS1-IN-1 is a potent MoTPS1 inhibitor with antifungal anti-inflammatory activity that acts through interaction with Glu396 study ulcerative colitis.Fórmula:C23H27F3N2O4Pureza:99.76%Cor e Forma:SoildPeso molecular:452.47Influenza virus-IN-6
CAS:<p>Influenza virus-IN-6 (Compound 35) serves as a potent inhibitor targeting the N-terminal domain of the polymerase acidic protein (PA N ) endonuclease subunit of</p>Fórmula:C27H26ClNO7Pureza:98%Cor e Forma:SolidPeso molecular:511.95DU-34569 Maleate
CAS:<p>DU-34569 Maleate, an antiviral agent, acts against influenza A, parainfluenza Sendai, coxsackie A21, and rhinovirus.</p>Fórmula:C18H27NO4Pureza:98%Cor e Forma:SolidPeso molecular:321.41L-742001 Hydrochloride
CAS:<p>L-742001 Hydrochloride is an RNA polymerase inhibitor.</p>Fórmula:C23H25Cl2NO4Cor e Forma:SolidPeso molecular:450.36NK007
CAS:<p>NK007 is a novel anti-SARS-CoV-2 agent with an EC 50 value of 30 nM.</p>Fórmula:C28H33NO9Cor e Forma:SolidPeso molecular:527.56Mansonone F
CAS:<p>Mansonone F is a topoisomerase II inhibitor with cytotoxic and topo inhibitory potencies.</p>Fórmula:C15H12O3Cor e Forma:SolidPeso molecular:240.25hDHODH-IN-1
CAS:<p>hDHODH-IN-1 is an inhibitor of human dihydroorotate dehydrogenase (hDHODH) with an anti-inflammatory effect.</p>Fórmula:C17H14N2O2Pureza:99.97%Cor e Forma:SolidPeso molecular:278.31BVDU 5′-Triphosphate
CAS:<p>BVDU 5′-Triphosphate is an antiviral agent labeled with 5′-Triphosphate that specifically targets viral DNA polymerase.</p>Fórmula:C11H16BrN2O14P3Pureza:98%Cor e Forma:SolidPeso molecular:573.08Arbemnifosbuvir
CAS:<p>Arbemnifosbuvir, a drug interfering with the nidovirus DdRp-associated nucleotidyltransferase (NiRAN) domain of non-structural protein 12 (nsp12), is utilized</p>Fórmula:C24H33FN7O7PPureza:98%Cor e Forma:SolidPeso molecular:581.53Zevotrelvir
CAS:<p>Zevotrelvir (Compound 52) serves as an inhibitor of coronavirus, demonstrating IC50 values below 0.1 μM for 229E hCoV protease and below 0.1 mM for SARS-CoV-3C-</p>Fórmula:C28H26F3N5O3Pureza:98%Cor e Forma:SolidPeso molecular:537.53RNA polymerase II-IN-1
CAS:<p>RNA polymerase II-IN-1 (19iv), an amatoxin, inhibits Pol II at 36.66 nM IC50, is more toxic to cancer cells, less to normal cells than α-Amanitin.</p>Fórmula:C38H53N11O12SPureza:98%Cor e Forma:SolidPeso molecular:887.96Daldinone A
CAS:<p>Daldinone A (Compound 4), isolated from Nigrospora oryzae, exhibits antibacterial properties, specifically demonstrating antimicrobial potential against P. aeruginosa [1].</p>Fórmula:C20H16O5Cor e Forma:SolidPeso molecular:336.34ZINC03129319
CAS:<p>ZINC03129319 is an inhibitor of dengue virus (DENV) NS2B-NS3 protease.</p>Fórmula:C24H14N2O6S2Pureza:90%Cor e Forma:SolidPeso molecular:490.51COH1
CAS:<p>COH1 is a ribonucleotide reductase (RR) inhibitor utilized in research pertaining to cancer, mitochondrial diseases, and neurodegenerative disorders [1].</p>Fórmula:C11H10N2O3SPureza:98%Cor e Forma:SolidPeso molecular:250.27SARS-CoV-2 3CLpro-IN-2
CAS:<p>SARS-CoV-2 3CLpro-IN-2 is a potent inhibitor of the 3CL protease pair and has shown research potential for SARS-CoV-2 disease.</p>Fórmula:C21H18F5N5O4Cor e Forma:SolidPeso molecular:499.39Cochliodone A
CAS:<p>Cochliodone A, a bioactive compound isolated from the deep-sea fungus Chaetomium sp., exhibits both antibacterial and anticancer properties.</p>Fórmula:C34H38O12Cor e Forma:SolidPeso molecular:638.66H3B-968
CAS:<p>H3B-968 is a potent inhibitor of Werner syndrome protein (WRN) with an IC50 of approximately 10 nM, effectively targeting its helicase, ATPase, and exonuclease</p>Fórmula:C22H18F6N4O4SPureza:98%Cor e Forma:SolidPeso molecular:548.46Antibacterial agent 154
CAS:<p>Antibacterial Agent 154 (Compound 7), a Fluoroquinolone derivative, exhibits broad-spectrum efficacy against both Gram-positive and Gram-negative bacteria when</p>Fórmula:C25H28ClFN4O5Cor e Forma:SolidPeso molecular:518.97Japonilure
CAS:<p>Japonilure is an agent of insecticide and pheromone.</p>Fórmula:C14H24O2Pureza:98%Cor e Forma:SolidPeso molecular:224.34Antibacterial agent 92
<p>Antibacterial agent 92 inhibits Salmonella's aaRS; IC50 of 0.58 μM for Se ThrRS. Exhibits antibacterial effects.</p>Fórmula:C30H28Cl2F3N5O4Cor e Forma:SolidPeso molecular:650.48Oxamniquine
CAS:<p>Oxamniquine is an effective compound for the treatment of schistosomiasis.</p>Fórmula:C14H21N3O3Pureza:98%Cor e Forma:Pale Yellow Crystals From Isopropanol SolidPeso molecular:279.33HCV-IN-43
CAS:<p>HCV-IN-43 (compound 2), an HCV NS5B protein inhibitor, efficiently inhibits HCV virus replication and is utilized in the study of HCV infection [1].</p>Fórmula:C26H26FN3O5SCor e Forma:SolidPeso molecular:511.57JNJ4796
CAS:<p>JNJ4796 is an oral fusion inhibitor that neutralizes influenza A group 1 by blocking HA-mediated fusion, mimicking bnAbs.</p>Fórmula:C28H27N9O3Pureza:98%Cor e Forma:SolidPeso molecular:537.57Avarofloxacin
CAS:Avarofloxacin (JNJ-Q2) is a fluoroquinolone for treating bacterial skin infections and pneumonia.Fórmula:C21H23F2N3O4Cor e Forma:SolidPeso molecular:419.42Cefteram
CAS:<p>Cefteram (T-2525), an orally active ester of the cephalosporin class, is the free acid form of Cefteram pivoxil.</p>Fórmula:C16H17N9O5S2Cor e Forma:SolidPeso molecular:479.49GSK-625433
CAS:<p>GSK-625433: Homochiral inhibitor blocks HCV genotypes 1a/1b polymerase.</p>Fórmula:C26H32N4O5SCor e Forma:SolidPeso molecular:512.62Phylloflavan
CAS:<p>Phylloflavan, an antileishmanial compound, exhibits an intracellular half maximal effective concentration (EC50) of 3.2 nM in RAW 264.7 cells and inhibits the</p>Fórmula:C26H26O10Pureza:98%Cor e Forma:SolidPeso molecular:498.48ZIKV-IN-1
CAS:<p>ZIKV-IN-1 blocks Zika virus effectively (EC50: 2.8 μM, EC90: 6.8 μM), targets the RdRp domain, and is low-toxic.</p>Fórmula:C21H18BrF2N3O3Cor e Forma:SolidPeso molecular:478.29Propiolactone
CAS:<p>Propiolactone (β-propiolactone; 2-Oxetanone), a chemosterilant, effectively inactivates viruses, rendering them non-infectious.</p>Fórmula:C3H4O2Pureza:98%Cor e Forma:SolidPeso molecular:72.06KNI-272
CAS:<p>Kynostatin-272 is a HIV protease inhibitor. KNI-272 blocked the maturation of viral particles.</p>Fórmula:C33H41N5O6S2Cor e Forma:SolidPeso molecular:667.84Antibacterial agent 93
<p>Antibacterial agent 93: potent aaRS inhibitor; effective against certain gram-positive and negative bacteria.</p>Fórmula:C29H28Cl3N5O4Cor e Forma:SolidPeso molecular:616.92Antibacterial agent 135
CAS:<p>Antibacterial Agent 135 (example 7) effectively inhibits various bacteria, including P.</p>Fórmula:C11H15N5O6SCor e Forma:SolidPeso molecular:345.33Valnemulin
CAS:<p>Valnemulin, a broad-spectrum pleuromutilin antibiotic, targets peptidyl transferase within the 50S ribosomal subunit, effectively used in veterinary medicine to address swine diseases such as B. hyodysenteriae and M. hyopneumoniae.</p>Fórmula:C31H52N2O5SCor e Forma:SolidPeso molecular:564.83NEU-730
CAS:<p>NEU-730, a novel inhibitor of TbrPDEB1, shows modest inhibition of T. brucei proliferation.</p>Fórmula:C25H29NO5Pureza:98%Cor e Forma:SolidPeso molecular:423.5SARS-CoV-2/MERS Mpro-IN-1
<p>SARS-CoV-2/MERS Mpro-IN-1 is a potent inhibitor of the main proteases in SARS-CoV-2 and MERS, exhibiting IC50 values of 0.10 and 0.06 µM, respectively.</p>Fórmula:C30H36N4O7Cor e Forma:SolidPeso molecular:564.63Icofungipen
CAS:Icofungipen is an oral antifungals with active against Candida species.Fórmula:C7H11NO2Pureza:98%Cor e Forma:SolidPeso molecular:141.17FIKK9.1-IN-1
CAS:<p>FIKK9.1-IN-1 (Compound 1), an antimalarial agent (IC50: 2.68 μg/mL), serves as a FIKK9.1 inhibitor by interacting with the ATP-binding residues within FIKK9.1,</p>Fórmula:C22H22N2SePureza:98%Cor e Forma:SolidPeso molecular:393.38BLI-489 Hydrate
CAS:<p>BLI-489 hydrate is a penicillin β-lactamase inhibitor that acts on classes A and C and some class D β-lactamases.</p>Fórmula:C13H10N3NaO4SCor e Forma:SolidPeso molecular:327.29HBV-IN-8
CAS:<p>HBV-IN-6 is a potent inhibitor of HBV (EC50: 287.9 nM).</p>Fórmula:C21H25ClFN5O5S2Cor e Forma:SolidPeso molecular:546.04G4/HDAC-IN-1
<p>G4/HDAC-IN-1, a G4/HDAC dual inhibitor, IC50 1.1 µM, blocks TNBC growth, useful in cancer research.</p>Fórmula:C36H49ClFN7O4Cor e Forma:SolidPeso molecular:698.27
