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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Leu-Val
CAS:<p>Leu-Val (L-leucyl-L-valine) is a novel potent dipeptide with antibacterial and antimalarial activity.</p>Fórmula:C11H22N2O3Pureza:97.72%Cor e Forma:SolidPeso molecular:230.3Tipranavir
CAS:<p>Tipranavir is a protease inhibitor that inhibits HIV-1 resistant to more than 1 protease inhibitor .Tipranavir effectively inhibits HIV-1 protease enzyme</p>Fórmula:C31H33F3N2O5SPureza:99.85%Cor e Forma:White SolidPeso molecular:602.66Isoprothiolane
CAS:<p>Isoprothiolane is a foliar spray fungicide with eradicant and protectant activities against fungal diseases of rice plant caused by Pyvioutavia oryzae Cav.</p>Fórmula:C12H18O4S2Pureza:99.50%Cor e Forma:SolidPeso molecular:290.40R-1479
CAS:<p>R-1479 (4'-Azidocytidine) is an RdRp inhibitor with an IC50 value of 1.28 μM for HCV RNA replication in the HCV subgenomic replicon system.</p>Fórmula:C9H12N6O5Pureza:98.11% - 99.95%Cor e Forma:SolidPeso molecular:284.23Trifluoromethyl-tubercidin
CAS:<p>TFMT blocks MTr1 at SAM-binding site, curbing influenza virus replication with low toxicity in mice.</p>Fórmula:C12H13F3N4O4Pureza:99.85% - 99.9%Cor e Forma:SoildPeso molecular:334.25MM41
CAS:<p>MM41 is a human telomeric and gene promoter DNA quadruplex stabilizer with an IC50 of <10 nM against the MIA PaCa-2 pancreatic cancer cell line.</p>Fórmula:C44H66N10O6Pureza:99.25%Cor e Forma:SolidPeso molecular:831.06Cyproconazole
CAS:<p>Cyproconazole is a triazole fungicide. It is used agriculturally for protection of crops against a wide variety of fungal pathogens.</p>Fórmula:C15H18ClN3OPureza:98.04%Cor e Forma:Yellow To Brown SolidPeso molecular:291.78Antiviral agent
CAS:<p>Antiviral agent is thiazolidin-4-one with anti-hepatitis B activity</p>Fórmula:C20H21N3O2S2Pureza:99.87%Cor e Forma:SoildPeso molecular:399.53L2P4
<p>L2P4 is a peptide-based fluorescent probe targeting EBNA1 that inhibits the homodimerization of EBNA1 and selectively suppresses the growth of EBV+ tumors. Exhibiting cytotoxicity in EBV-positive C666-1 cells, L2P4 has an LC50 of 46.4 μM.</p>Fórmula:C93H139N25O16S2Cor e Forma:SolidPeso molecular:1927.39C16G2
CAS:<p>C16G2 is a Specific Targeted Antimicrobial Peptide (STAMP) that selectively targets the cariogenic oral pathogen Streptococcus mutans. This compound operates by recognizing and disrupting the bacterial cell membrane, leading to small molecule leakage and the loss of membrane potential, which results in bacterial death. Unlike broad-spectrum antimicrobial peptides, C16G2 exhibits higher selectivity and efficacy against Streptococcus mutans.</p>Fórmula:C190H310N58O42Cor e Forma:SolidPeso molecular:4078.93SCR7
CAS:<p>SCR7, a specific DNA Ligase IV inhibitor, blocks nonhomologous end-joining (NHEJ).</p>Fórmula:C18H14N4OSPureza:98%Cor e Forma:SolidPeso molecular:334.4Chitotriose
CAS:<p>Chitotriose, a low molecular weight chitosan oligosaccharide, is extractable from crab shell chitosan. It exhibits antibacterial properties against salmonella.</p>Fórmula:C18H35N3O13Cor e Forma:SolidPeso molecular:501.48Schizophyllan
CAS:<p>Schizophyllan, a member of the β-glucan family, is an extracellular polysaccharide known for its antitumor, antibacterial, and antiparasitic activities.</p>Cor e Forma:SolidMepartricin
CAS:<p>Mepartricin, a polyene macrolide, exhibits both antifungal and antiprotozoal activities and is extensively utilized in studies related to benign prostatic hyperplasia.</p>Cor e Forma:SolidApidaecin IB
CAS:<p>Apidaecin IB is an insect antimicrobial peptide, with MIC values of 8 μM for E. coli (O18K1H7, ML35 and ATCC 25922).</p>Fórmula:C95H150N32O23Pureza:98%Cor e Forma:SolidPeso molecular:2108.446GS-443902
CAS:<p>Remdesivir triphosphate (GS-443902) inhibits RSV/HCV RdRp with IC50s: 1.1/5 µM.</p>Fórmula:C12H16N5O13P3Pureza:98%Cor e Forma:SolidPeso molecular:531.2T2AA
CAS:<p>T2AA (4-[4-[(2S)-2-amino-3-hydroxypropyl]-2,6-diiodophenoxy]phenol) is an inhibitor of proliferating cell nuclear antigen (PCNA) with IC50 of 1 μM for PCNA/PIP-</p>Fórmula:C15H15I2NO3Pureza:99.53%Cor e Forma:SolidPeso molecular:511.09NCGC00029283
CAS:<p>NCGC00029283 is a potent inhibitor of Werner syndrome helicase-nuclease (WRN), displaying inhibitory activity against WRN helicase with an IC 50 value of 2.3 μM</p>Fórmula:C18H12FN3O3Pureza:99.84%Cor e Forma:SolidPeso molecular:337.3RG7800 tetrahydrochloride
<p>RG7800 hydrochloride is an orally active modulator of SMN2 splicing, exhibiting EC50 values of 23 nM for SMN2 splicing and 87 nM for SMN protein production.</p>Fórmula:C24H32Cl4N6OPureza:98%Cor e Forma:SolidPeso molecular:562.36Cefoxitin sodium
CAS:<p>Cefoxitin sodium (Betacef) is a semisynthetic cephamycin antibiotic resistant to beta-lactamase.</p>Fórmula:C16H16N3NaO7S2Pureza:99.19%Cor e Forma:White To Almost White PowderPeso molecular:449.43N2-Acetylaciclovir
CAS:<p>N2-Acetylaciclovir (Aciclovir EP Impurity F) is a derivative of the antiviral compound Aciclovir, which has selective T-cell immunotoxicity.</p>Fórmula:C10H13N5O4Pureza:98.2%Cor e Forma:SolidPeso molecular:267.24Propargylcholine
CAS:<p>Propargylcholine, an alkyne-modified choline, blocks Dgc-catalyzed demethylation in P. aeruginosa.</p>Fórmula:C7H14BrNOPureza:99.70%Cor e Forma:SolidPeso molecular:208.1Cefonicid sodium
CAS:<p>Cefonicid sodium is a broad-spectrum cephalosporin antibiotic that inhibits bacterial cell wall formation.Cost-effective and quality-assured.</p>Fórmula:C18H16N6Na2O8S3Pureza:98.61%Cor e Forma:White Or Off-White Crystalline PowderPeso molecular:586.53Odesivimab
CAS:<p>Odesivimab (REGN-3471) is a human monoclonal antibody against Zaire Ebola virus, with potential antiviral activity.</p>Pureza:95%Cor e Forma:LiquidRomlusevimab
CAS:<p>Romlusevimab (BRII-198) is a recombinant antibody targeting the spike protein of SARS-CoV-2, with antiviral activity.</p>Pureza:95%Cor e Forma:LiquidNeamine tetrahydrochloride
CAS:<p>Neamine tetrahydrochloride has antimicrobial and neuroprotective activities and inhibits the growth of pancreatic cancer cells.</p>Fórmula:C12H30Cl4N4O6Pureza:98.98% - 99.09%Cor e Forma:SolidPeso molecular:468.2(±)15-HEPE
CAS:<p>(±)15-HEPE is a racemic mixture of monohydroxy fatty acids 15 (R) -HEPE and 15 (S) -HEPE, with antibacterial activity.</p>Fórmula:C20H30O3Cor e Forma:SolidPeso molecular:318.45Quilseconazole Formic acid(1340593-70-5 Free base)
<p>Quilseconazole Formic acid is a selective inhibitor of fungal Cyp51 with potent activities against Cryptococcus neoformans and Cryptococcus gattii.</p>Fórmula:C23H16F7N5O4Pureza:99.56% - 99.84%Cor e Forma:SoildPeso molecular:559.39Tetrazolast
CAS:<p>Tetrazolast has anticancer activity and may have antifungal activity.</p>Fórmula:C10H6N8Pureza:99.06%Cor e Forma:SolidPeso molecular:238.21Tetramycin
CAS:<p>Tetramycin (Tetramycin A) is a macrolide antibiotic isolated from Streptomyces hygrospinosus var. Beijingensis, a new and highly effective polyene antibiotic.</p>Fórmula:C35H53NO13Pureza:95.28%Cor e Forma:SolidPeso molecular:695.79Saframycin S
CAS:<p>Saframycin S, an antibiotic featuring a Racemomycin group, demonstrates inhibitory effects against Ehrlich ascites tumor. The LD50 value of Saframycin S in ddY mice is 3.2 mg/kg (i.p.).</p>Fórmula:C28H31N3O9Cor e Forma:SolidPeso molecular:553.56S1b3inL1
CAS:<p>S1b3inL1 is a macrocylcic peptide inhibitor of the SARS-CoV-2 spike protein. It binds with high affinity to a conserved site on the spike protein, effectively suppressing the infection of various SARS-CoV-2 variants. S1b3inL1 exhibits antiviral activity.</p>Fórmula:C103H158N30O24SCor e Forma:SolidPeso molecular:2232.61WRN inhibitor 18
CAS:<p>WRN inhibitor 18 (compound 306) is an orally active inhibitor of WRN with demonstrated anticancer activity in vivo.</p>Fórmula:C35H35F6N5O5SCor e Forma:SolidPeso molecular:751.74WRN inhibitor 16
<p>WRN inhibitor 16 (Example 83) is an orally active WRN inhibitor. In a SW48 xenograft mouse tumor model, WRN inhibitor 16 did not cause tumor regression.</p>Fórmula:C31H30F4N4O5SCor e Forma:SolidPeso molecular:646.65Antiviral agent 65
CAS:<p>Antiviralagent 65 (compound 9) is an antiviral agent targeting the H1N1 influenza virus, with an EC50 of 7 μg/mL.</p>Fórmula:C20H24O3Cor e Forma:SolidPeso molecular:312.4Fosetyl-aluminum
CAS:<p>Fosetyl-aluminum is a systemic fungicide that controls downy mildews and Phytophthora diseases, used on a variety of crops including fruits and vegetables。</p>Fórmula:C6H18AlO9P3Pureza:99.52%Cor e Forma:SolidPeso molecular:354.1Extracellular Death Factor TFA
<p>Extracellular death factor TFA (EDF TFA) is a linear pentapeptide that communicating cells produce and release, which activates the cell death pathway.</p>Pureza:98.77%Cor e Forma:Odour SolidDestomycin A
CAS:<p>Destomycin A, an aminoglycoside antibiotic, exhibits activity against bacterial (Gram-positive and Gram-negative), antifungal, and anthelmintic agents. It inhibits peptide synthesis in Escherichia coli cells and stimulates adenylate cyclase in animal tissues.</p>Fórmula:C20H37N3O13Cor e Forma:SolidPeso molecular:527.52AB-161
CAS:<p>AB-161 is an orally active destabilizer of HBV RNA and an inhibitor of PAPD5/7, primarily targeting the liver. It treats hepatitis B virus (HBV) infection by reducing hepatitis B surface antigen (HBsAg) levels, exhibiting an EC50 value of 2.2 nM for HBsAg. AB-161 is applicable in HBV infection research.</p>Fórmula:C21H21F2N3O5Cor e Forma:SolidPeso molecular:433.41MCG-02
<p>MCG-02 is an inhibitor of cruzain (CRZ) and cathepsin L-like protease (CATL), capable of inhibiting CRZ in Trypanosoma cruzi and CATL in Trypanosoma brucei, with IC50 values of 0.2 μM and 0.02 μM, respectively.</p>Fórmula:C13H13N3O2SCor e Forma:SolidPeso molecular:275.33IAV replication-IN-1
CAS:<p>IAV replication-IN-1 (compound 3h) can reduce the upregulation of inflammatory factors and apoptosis caused by IAV infection and alleviate lung damage resulting from IAV infection.</p>Fórmula:C23H22N2O5S2Cor e Forma:SolidPeso molecular:470.56Ap4dT
CAS:<p>Ap4dT serves as an inhibitor of human adenylate kinase isozyme 1 (hAK1), effectively suppressing the synthesis of ATP and ADP, with IC50 values of 42 μM and 38 μM, respectively.</p>Fórmula:C20H41N11O20P4Cor e Forma:SolidPeso molecular:879.5Se2h
<p>Se2h is a cruzain inhibitor exhibiting potent activity against intracellular amastigotes of Trypanosoma cruzi (EC50< 1 μM, SI> 10), with an inhibitory effect on cruzain of IC50< 100 nM (SI> 5.55). Compared to Benznidazole and cruzain inhibitor K777, Se2h shows superior selectivity and inhibition while its selenazole structure reduces selenium-related toxicity. Se2h demonstrates antiparasitic activity and holds promise for Chagas disease research.</p>Fórmula:C12H13ClN4O2SeCor e Forma:SolidPeso molecular:359.67Antileishmanial agent-31
CAS:<p>Antileishmanial agent-31 (Compound p1) is a pyrazole derivative exhibiting antileishmanial activity with an IC50 of 35.53 μg/mL. Furthermore, Antileishmanial agent-31 demonstrates high stability and is applicable in studies focused on leishmaniasis treatment.</p>Fórmula:C11H11ClN2Cor e Forma:SolidPeso molecular:206.67CpCDPK1/TgCDPK1-IN-2
CAS:<p>CpCDPK1/TgCDPK1-IN-2 is a dual inhibitor of CpCDPK1 and TgCDPK1 with IC50 values of 12 and 5 nM for CpCDPK1 and TgCDPK1, respectively.CpCDPK1/TgCDPK1-IN-2 can</p>Fórmula:C20H21N5OPureza:99.12%Cor e Forma:SoildPeso molecular:347.41FLDKFNHEAEDLFYQSSL
<p>FLDKFNHEAEDLFYQSSL is an 18-residue peptide that binds to the SARS-CoV-2 receptor-binding domain (RBD). It inhibits the entry of SARS-CoV-2 and also interacts with binding residues (Leu455, Phe456, Ala475, and Gln493).</p>Fórmula:C102H143N23O32Cor e Forma:SolidPeso molecular:2203.36Myristoyl glutamic acid
CAS:<p>Myristoyl glutamic acid （N-Myristoyl-L-glutamic acid） is a myristoyl glutamic acid, a surfactant that can be added to evolved make-up with foaming and partial</p>Fórmula:C19H35NO5Pureza:99%Cor e Forma:SolidPeso molecular:357.48Antiviral agent 36
Antiviral agent 36 (compound 27), a potent inhibitor of both dengue (DENV) and Zika (ZIKV) viruses, demonstrates replication inhibition with EC50 values of 100Fórmula:C30H32N4O3Pureza:98%Cor e Forma:SolidPeso molecular:496.6Antiparasitic agent-20
<p>Antiparasitic Agent-20 (Compound 1p) exhibits broad-spectrum activity as a parasitic inhibitor, demonstrating efficacy against T.</p>Pureza:98%Cor e Forma:Odour SolidMelimine
<p>Melimine, a hybrid antimicrobial peptide derived from Melittin and Protamine, exhibits broad-spectrum activity against various microorganisms, including</p>Fórmula:C158H290N74O35Pureza:98%Cor e Forma:SolidPeso molecular:3786.47Taq DNA polymerase
CAS:<p>Taq DNA polymerase is a thermostable enzyme utilized in polymerase chain reactions (PCR) to amplify DNA sequences [1].</p>Pureza:98%Cor e Forma:SolidDihydrodehydrodiconiferyl alcohol 9-O-β-D-xylopyranoside
CAS:<p>Dihydrodehydrodiconiferyl alcohol 9-O-β-D-xylopyranoside serves as an anti-hepatitis B virus (anti-HBV) agent, effectively inhibiting the secretion of HBV</p>Fórmula:C25H32O10Pureza:98%Cor e Forma:SolidPeso molecular:492.52DNA polymerase-IN-2
DNA polymerase-IN-2 (Compd 3c), a coumarin derivative, demonstrates inhibitory activity towards Taq DNA polymerase, with an IC50 value of 48.25 μM, and holdsFórmula:C14H12O5SPureza:98%Cor e Forma:SolidPeso molecular:292.31Gramicidin B
CAS:<p>Gramicidin B is a nonribosomal peptide with antibiotic properties [1].</p>Fórmula:C97H139N19O17Pureza:98%Cor e Forma:SolidPeso molecular:1843.26HA-IN-1
<p>HA-IN-1 (compound 5g), a high-affinity Hemagglutinin (HA) ligand, targets the trypsin cleavage site of HA to inhibit HA-mediated membrane fusion and decrease</p>Fórmula:C42H35NO6Pureza:98%Cor e Forma:SolidPeso molecular:649.73Citrullinated LL-37 3cit
<p>Citrullinated LL-37 3cit is a host defense peptide with potent immunomodulatory and antimicrobial properties, demonstrating direct antiviral activity against</p>Fórmula:C205H337N57O56Pureza:98%Cor e Forma:SolidPeso molecular:4496.22Z-L(D-Val)G-CHN2
<p>Z-L(D-Val)G-CHN2, an isoform of Z-LVG-CHN2, serves as a cell-permeable and irreversible inhibitor of cysteine proteinase.</p>Fórmula:C22H31N5O5Pureza:98%Cor e Forma:SolidPeso molecular:445.51Antimalarial agent 31
<p>Compound 31 (compound 7k) is an orally active inhibitor of Plasmodium falciparum aspartic protease, plasmepsin X (PMX), with antimalarial properties [1].</p>Fórmula:C36H47N3O4Pureza:98%Cor e Forma:SolidPeso molecular:585.78Antitrypanosomal agent 17
<p>Compound 17 (Compd 7a) exhibits potent antiamastigote activity, demonstrated by its IC50 value of 0.03 μM against the T. congolense strain IL3000 [1].</p>Pureza:98%Cor e Forma:Odour SolidSARS-CoV-2-IN-42
<p>SARS-CoV-2-IN-42 (Compound 8q) effectively inhibits SARS-CoV-2 replication with an EC50 value of 0.4 μM and demonstrates no significant toxicity to the host</p>Fórmula:C20H20O7Pureza:98%Cor e Forma:SolidPeso molecular:372.37SARS-CoV-2-IN-67
<p>SARS-CoV-2-IN-67 (Compound 16), a derivative of vitamin K, exhibits anti-SARS-CoV-2 properties, with an effective concentration (EC50) of 64.8 μM in VeroE6/</p>Pureza:98%Cor e Forma:Odour SolidSARS-CoV-2-IN-54
<p>SARS-CoV-2-IN-54 (Compound 2), a SARS-CoV-2 inhibitor, exhibits antiviral activity by impeding the virus in Vero E6 cells with an inhibitory concentration (IC50</p>Fórmula:C63H59N11O16S3Pureza:98%Cor e Forma:SolidPeso molecular:1322.4β-Herpesvirus protease-IN-1
<p>β-Herpesvirus protease-IN-1 (compound 19) serves as an inhibitor of β-herpesvirus protease, exhibiting IC50 values of 2.5 μM for HCMVPro and 0.33 μM for HHV6Pro</p>Pureza:98%Cor e Forma:Odour SolidSARS-CoV-2 3CLpro-IN-17
<p>Compound 3h, also known as SARS-CoV-2 3CLpro-IN-17, is a selective inhibitor of the SARS-CoV-2 3CL protease, demonstrating an IC50 of 0.322 μM [1].</p>Fórmula:C16H9N3OS2Pureza:98%Cor e Forma:SolidPeso molecular:323.39RdRP-IN-6
<p>RdRP-IN-6 (compound 27) is an inhibitor of RNA-dependent RNA polymerase (RdRp), exhibiting an IC90 value of 14.1 μM.</p>Fórmula:C41H67N8O7PSi2Pureza:98%Cor e Forma:SolidPeso molecular:871.16Lugdunin
CAS:<p>Lugdunin is an antibiotic peptide that disrupts membrane potential in bacteria, demonstrating activity against Gram-positive species including S.</p>Fórmula:C40H62N8O6SPureza:98%Cor e Forma:SolidPeso molecular:783.04Antitrypanosomal agent 16
<p>Antitrypanosomal agent 16 functions as a potent trypanocide, exhibiting an inhibitory concentration 50 (IC50) of 0.04μM against the T.</p>Pureza:98%Cor e Forma:Odour SolidSARS-CoV-2-IN-50
<p>SARS-CoV-2-IN-50 (Compound X77C) is a potent inhibitor of the SARS-CoV-2 main protease (M^pro), exhibiting high affinity for the enzyme's catalytic site [1].</p>Fórmula:C26H28FN5O4Pureza:98%Cor e Forma:SolidPeso molecular:493.53Antileishmanial agent-21
<p>Antileishmanial agent-21 (compound 4e) functions as an inhibitor of Leishmania pteridine reductase 1 (Lm-PTR1), employing an anti-folate mechanism.</p>Fórmula:C21H16N2O3Pureza:98%Cor e Forma:SolidPeso molecular:344.36SARS-CoV-2-IN-53
<p>ARS-CoV-2-IN-53 (Compd 5d) exhibits an inhibitory effect on SARS-CoV-2 replication, with an effective concentration (EC50) value of 14.3 μM, and demonstrates</p>Fórmula:C23H18F2N2O4SPureza:98%Cor e Forma:SolidPeso molecular:456.46Anticancer agent 140
<p>Compound 140 (Compd 3) exhibits potential anticancer and antiparasitic activities [1].</p>Fórmula:C20H26N2OPureza:98%Cor e Forma:SolidPeso molecular:310.43Simaravibart
<p>Simaravibart (MAD-0004J08), an IgG1κ monoclonal antibody, specifically targets the receptor-binding domain of the SARS-CoV-2 spike (S) glycoprotein [1].</p>Pureza:98%Cor e Forma:Odour LiquidNSC89641
<p>NSC89641 demonstrates potent inhibition of MERS-CoV M^pro, achieving an IC_50 value of less than 3.5 µM.</p>Fórmula:C19H18N6O12Pureza:98%Cor e Forma:SolidPeso molecular:522.3810-Hydroxyaloin A
CAS:<p>Hydroxyaloin A (10-10-Hydroxyaloin A) is a potent inhibitor of SARS-CoV-2, demonstrating significant efficacy in binding to the active site of the SARS-CoV-2</p>Fórmula:C21H22O10Pureza:98%Cor e Forma:SolidPeso molecular:434.39SARS-CoV-2-IN-65
<p>SARS-CoV-2-IN-65 (compound 2f (81)) is a potent, orally active reversible inhibitor of SARS-CoV-2 entry, primarily obstructing the RBD:ACE2 interaction and</p>Pureza:98%Cor e Forma:Odour SolidMptpB-IN-2
<p>MptpB-IN-2 (compound 20), a selective inhibitor for mycobacterium tuberculosis protein tyrosine phosphatase B (MptpB), exhibits half maximal inhibitory</p>Fórmula:C23H20F3NO3S2Pureza:98%Cor e Forma:SolidPeso molecular:479.54HBV-IN-36
<p>HBV-IN-36 (also known as compound 42) is a hepatitis B virus (HBV) inhibitor with an IC50 of 2 μM, exhibiting anti-HBV activity characterized by an EC50 of 0.58</p>Fórmula:C21H18ClFN4O2Pureza:98%Cor e Forma:SolidPeso molecular:412.84Wulfenioidin F
<p>Wulfenioidin F, a diterpenoid isolated from the whole plant of Orthosiphon wulfenioides, exhibits anti-Zika virus (ZIKV) activity with an EC50 of 8.07 μM and</p>Fórmula:C21H28O3Pureza:98%Cor e Forma:SolidPeso molecular:328.45H-Arg-OtBu dihydrochloride
CAS:<p>H-Arg-OtBu (dihydrochloride) is a membrane-targeting antimicrobial that engages the negatively charged bacterial membrane through electrostatic and hydrophobic</p>Fórmula:C10H24Cl2N4O2Pureza:98%Cor e Forma:SolidPeso molecular:303.23HBV-IN-40
<p>HBV-IN-40 (Compound 11826096), with an IC50 of 0.7 µM, serves as a potent HBV inhibitor and exhibits antiviral activity [1].</p>Fórmula:C29H55Cl4N11Pureza:98%Cor e Forma:SolidPeso molecular:699.63Crexavibart
CAS:<p>Crexavibart (BMS-986413; C-144-LS), an IgG1 λ2 antibody, specifically targets the receptor-binding domain of the SARS-CoV-2 spike (S) glycoprotein [1].</p>Pureza:98%Cor e Forma:LiquidMPI60
<p>MPI60 is a potent inhibitor of SARS-CoV-2 main protease (M^pro) exhibiting high antiviral efficacy, low cellular cytotoxicity, and considerable in vitro</p>Fórmula:C24H31N3O5Pureza:98%Cor e Forma:SolidPeso molecular:441.52Antileishmanial agent-19
<p>Compound F27 (Antileishmanial agent-19) is an antileishmanial compound effective against L.</p>Fórmula:C22H18N4O3Pureza:98%Cor e Forma:SolidPeso molecular:386.4Antitrypanosomal agent 13
<p>Compound 4b (antitrypanosomal agent 13) is a potent antitrypanosomal with notable trypanocidal and cytotoxic activities, exhibiting GI50 values of 0.18 μM</p>Fórmula:C47H81N2NaO10SPureza:98%Cor e Forma:SolidPeso molecular:889.21SARS-CoV-2 nsp14-IN-4
<p>SARS-CoV-2 nsp14-IN-4 (Compound 12q), a non-cytotoxic and cell-permeable inhibitor of SARS-CoV-2 nsp14 methyltransferase (IC50 = 19 nM), is employed in COVID-19</p>Fórmula:C31H27N7O6SPureza:98%Cor e Forma:SolidPeso molecular:625.65Pezadeftide
CAS:<p>Pezadeftide, a potent antifungal peptide, readily penetrates fungal cells, eliciting an immediate mitochondrial response that leads to hyperpolarization of the</p>Pureza:98%Cor e Forma:SolidNPD-2975
<p>NPD-2975 (compound 30) is an orally active antitrypanosomal agent effective against Human African Trypanosomiasis (HAT), demonstrating acceptable metabolic</p>Fórmula:C14H13FN4OPureza:98%Cor e Forma:SolidPeso molecular:272.28E07 aptamer
<p>SARS-CoV-2 nsp14-IN-4 (Compound 12q) is a selective inhibitor of the SARS-CoV-2 nsp14 methyltransferase with an IC50 of 19 ± 2.5 nM.</p>Pureza:98%Cor e Forma:Odour SolidSARS-CoV-2 3CLpro-IN-19
<p>SARS-CoV-2 3CLpro-IN-19 (Compound C5a), a non-covalent, non-peptide inhibitor of the SARS-CoV-2 3CLpro enzyme, exhibits potent in vitro activity with an IC50 of</p>Fórmula:C24H22ClN3O2SPureza:98%Cor e Forma:SolidPeso molecular:451.97Aurein 2.3
CAS:<p>Aurein 2.3, an antibiotic antimicrobial peptide, partially inhibits E. coli ATPase activity and suppresses cell growth [1] [2].</p>Fórmula:C76H131N19O19Pureza:98%Cor e Forma:SolidPeso molecular:1614.976-C-Methylquercetin-3,4'-dimethyl ether
<p>6-C-Methylquercetin-3,4'-dimethyl ether is a flavonol derivative extracted from Bauhinia thonningii Schum leaves, displaying antibacterial effects on Gram-</p>Fórmula:C18H16O7Pureza:98%Cor e Forma:SolidPeso molecular:344.32Antileishmanial agent-22
<p>Antileishmanial agent-22 (compound 15b) serves as an antiparasitic and antibacterial, exhibiting activities against Leishmania (IC50 = 0.408 μM), malaria, and</p>Fórmula:C29H26Cl2N4O3Pureza:98%Cor e Forma:SolidPeso molecular:549.45RdRP-IN-7
<p>RdRP-IN-7, a RNA-dependent RNA polymerase (RdRp) inhibitor, demonstrates efficacy against SARS-CoV-2 infection with an inhibitory concentration (IC50) of 8.2 μM</p>Fórmula:C26H45N7O3Si2Pureza:98%Cor e Forma:SolidPeso molecular:559.85ZINC61142882
<p>ZINC61142882 is a SARS-CoV-2 Nsp14 N7-Methyltransferase inhibitor with an IC50 value of 6 μM [1].</p>Fórmula:C16H11BrN4O3Pureza:98%Cor e Forma:SolidPeso molecular:387.19SARS-CoV-2 Mpro-IN-8
<p>SARS-CoV-2 Mpro-IN-8 (compound 6b) is an antiviral agent effective against SARS-CoV-2 [1].</p>Fórmula:C33H35ClN3O5PPureza:98%Cor e Forma:SolidPeso molecular:620.07T4 RNA ligase
<p>T4 RNA ligase is an enzyme that facilitates the ligation of single-stranded DNA.</p>Pureza:98%Cor e Forma:Odour SolidSARS-CoV-2-IN-48
<p>SARS-CoV-2-IN-48 (compound 19) is an inhibitor of SARS-CoV-2, exhibiting an IC50 of 2.7 μM against the Omicron BA.1 variant and demonstrating antiviral</p>Fórmula:C26H25NO7Pureza:98%Cor e Forma:SolidPeso molecular:463.48Antimalarial agent 27
<p>Antimalarial agent 27 (compound 11a) potently inhibits P.</p>Fórmula:C10H11NNaO5PPureza:98%Cor e Forma:SolidPeso molecular:279.16JNJ-8003
<p>JNJ-8003 is a potent inhibitor of RSV Polymerase, effectively impeding the early stages of RNA transcription and replication by inhibiting nucleotide</p>Pureza:98%Cor e Forma:Odour Solid8304-vs
<p>8304-vs is a macrocyclic anti-Plasmodial compound that irreversibly binds to and inhibits the Plasmodium proteasome, effectively halting the growth of</p>Fórmula:C35H53N5O8SPureza:98%Cor e Forma:SolidPeso molecular:703.89
