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"
Ordenar por
Pureza (%)
0
100
|
0
|
50
|
90
|
95
|
100
NS5A-IN-1
<p>NS5A-IN-1 is a proagent of the HCV NS5A inhibitor Pibrentasvir (ABT-530).</p>Fórmula:C72H86F5N10O14PCor e Forma:SolidPeso molecular:1441.48Dalbavancin hydrochloride
CAS:<p>Dalbavancin HCl (MDL-63397 HCl), a semi-synthetic antibiotic, targets Gram-positive bacteria with low MICs for S. aureus and B. anthracis.</p>Fórmula:C88H101Cl3N10O28Cor e Forma:SolidPeso molecular:1853.15Monascorubrin
CAS:<p>Monascorubrin, from Monascus purpureus mycelium, is an antibiotic against Bacillus subtilis and Candida pseudotropicalis.</p>Fórmula:C23H26O5Cor e Forma:SolidPeso molecular:382.45Antibacterial agent 128
<p>Antibacterial 128, a siderophore-Ciprofloxacin blend with cleavable linker, targets P. aeruginosa and B. pseudomallei.</p>Fórmula:C26H25FN4O9Cor e Forma:SolidPeso molecular:556.5Bio-AMS TFA
<p>Bio-AMS (TFA) inhibits bacterial biotin protein ligase, targets M. tuberculosis, and stops fatty acid/lipid synthesis.</p>Fórmula:C22H30F3N9O9S2Cor e Forma:SolidPeso molecular:685.65Glycoprotein (276-286)
CAS:<p>Known Db-restricted peptide of lymphocytic choriomeningitis virus (LCMV).</p>Fórmula:C46H70N12O17SPureza:98%Cor e Forma:SolidPeso molecular:1095.18VIR-7229
<p>VIR-7229 is a human IgG1 monoclonal antibody that targets the Receptor-Binding Domain (RBD) of the Spike glycoprotein. It exhibits antiviral activity by competing with ACE2 for binding and inducing the shedding of the S1 protein. VIR-7229 is applicable for research on SARS-CoV-2 infections. Recommended isotype control: Human IgG1 kappa, Isotype Control.</p>Cor e Forma:Odour LiquidAntitubercular agent-35
<p>Antitubercular agent-35 (42l) inhibits Mtb H37Rv (MIC 90=1.25 μg/mL) and M. Marinum (MIC 90=2 μg/mL), resists liver degradation, for TB research.</p>Fórmula:C19H13ClN4O2SCor e Forma:SolidPeso molecular:396.85Ledaborbactam
CAS:<p>Iedaborbactam, as a beta-lactamase inhibitor (WO2015191907, Example 62), can be used for the research of bacterial infections.</p>Fórmula:C12H14BNO5Cor e Forma:SolidPeso molecular:263.06Antibacterial agent 162 trifluoromethanesulfonate
<p>Antibacterial agent 162 trifluoromethanesulfonate (compound 7), a dual-function molecule, demonstrates potent inhibitory effects on Staphylococcus aureus,</p>Cor e Forma:Odour SolidMDP1 acetate
<p>MDP1 acetate, a Melittin peptide, damages bacterial membranes and kills MDR S. aureus, E. coli, and P. aeruginosa.</p>Fórmula:C113H206N34O30Cor e Forma:SolidPeso molecular:2521.05Saccharocarcin B
CAS:<p>Saccharocarcin B was isolated from the fermentation broth of the actinomycete Saccharothrix aerocolongenes subsp.antibiotica SCC1886.</p>Fórmula:C68H103NO20Cor e Forma:SolidPeso molecular:1254.559Tomopenem
CAS:<p>Tomopenem is a penem antibiotic.</p>Fórmula:C23H35N7O6SPureza:98%Cor e Forma:SolidPeso molecular:537.635'-O-DMT-N2-DMF-dG
CAS:<p>5'-O-DMT-2'-O-TBDMS-rI, a modified nucleoside, finds application in deoxyribonucleic acid (DNA) or nucleic acid synthesis.</p>Fórmula:C34H36N6O6Cor e Forma:SolidPeso molecular:624.698Cefoselis hydrochloride
CAS:<p>Cefoselis hydrochloride is a widely used beta-lactam antibiotic.</p>Fórmula:C19H23ClN8O6S2Pureza:98%Cor e Forma:SolidPeso molecular:559.02T3SS-IN-2
<p>T3SS-IN-2 (Compound 2h) serves as an inhibitor of the type three secretion system (T3SS), with applications in bacterial infection research [1].</p>Fórmula:C16H25N3O3Cor e Forma:SolidPeso molecular:307.39Urease-IN-18
<p>Urease-IN-18 (compound 13a) is a non-competitive urease inhibitor with an IC50 value of 1.6 μM. Urease plays a role in maintaining an alkaline environment that supports the survival and proliferation of certain pathogens within the host.</p>Fórmula:C30H27N5O5Cor e Forma:SolidPeso molecular:537.566Antileishmanial agent-30
<p>Compound 17k, also known as Antileishmanial agent-30, effectively inhibits Leishmania with an IC50 of 0.2 μM for L. donovani. It exhibits a CC50 of >100 μM and an SI of >500, indicating significant selectivity and potency.</p>Fórmula:C23H21N5O2Cor e Forma:SolidPeso molecular:399.45PhoPS
<p>PhoPS is a photoactivatable β-lactamase inhibitor. Upon exposure to light, PhoPS releases the active β-lactamase inhibitor Sulbactam. This compound is capable of inhibiting the synthesis of bacterial cell walls and the formation of biofilms in Escherichia coli, thereby exhibiting antibacterial activity.</p>Fórmula:C42H57N5O17SCor e Forma:SolidPeso molecular:935.99BRD1401
<p>BRD1401 is a small molecule that targets the outer membrane protein OprH. It disrupts the interaction between OprH and LPS and can increase membrane fluidity.</p>Fórmula:C17H17N5O3Peso molecular:339.13314TQL-1055
CAS:<p>TQL-1055 is a semi-synthetic analog of the saponin adjuvant QS-21, utilized as an adjuvant in preventive vaccines. It demonstrates potent adjuvant activity with influenza antigens and shows good tolerability when combined with an acellular pertussis vaccine (aP), enhancing anti-pertussis toxin (PT) antibody responses in mice and rabbits. TQL-1055 holds promise for research into chronic Hepatitis B.</p>Fórmula:C59H95NO20Cor e Forma:SolidPeso molecular:1138.38Cox B-IN-1
<p>CoxB-IN-1 (7a) exhibits antiviral activity against Coxsackie B virus (CoxB). This compound demonstrates dual functionality by inhibiting both virus adsorption and replication. Additionally, CoxB-IN-1 (7a) shows significant potential as an inhibitor of the Coxsackie virus 3C protease.</p>Fórmula:C38H32N10O2S2Cor e Forma:SolidPeso molecular:724.856(R)-10,11-Dehydrocurvularin
CAS:<p>10,11-Dehydrocurvularin: antibiotic, activates heat shock response, blocks TGF-β, anti-cancer.</p>Fórmula:C16H18O5Pureza:98%Cor e Forma:SolidPeso molecular:290.31Parvodicin C2
CAS:<p>Parvodicin C2, a glycopeptide antibiotic derived from A. parvosata and part of the parvodicin complex, serves as a component of the A40926 antibiotic complex utilized as a precursor for synthesizing dalbavancin. It exhibits activity against methicillin-sensitive and methicillin-resistant strains of S. aureus, S. epidermidis, S. saprophyticus, S. hemolyticus, and E. faecalis.</p>Fórmula:C83H88Cl2N8O29Cor e Forma:SolidPeso molecular:1732.53(rac)-Xeruborbactam ammonium
<p>(rac)-Xeruborbactam ammonium is a beta-lactamase inhibitor and can be used in the study of bacterial infections.</p>Fórmula:C10H11BFNO4Pureza:99.71%Cor e Forma:SolidPeso molecular:239.01SEQ-9
<p>SEQ-9 is an orally active inhibitor targeting the Mycobacterium tuberculosis (Mtb) 23S bacterial ribosome, demonstrating an inhibitory concentration (IC50)</p>Fórmula:C60H100N4O20SCor e Forma:SolidPeso molecular:1229.5223-O-Demycinosyltylosin
CAS:<p>23-O-Demycinosyltylosin (23-DMT), an acyl derivative of tylosin, exhibits antibacterial activity [1].</p>Fórmula:C38H63NO13Cor e Forma:SolidPeso molecular:741.91LL D05139(β)
CAS:<p>LL D05139(beta) is an novel antitumor antibiotic agent.</p>Fórmula:C8H12N4O5Pureza:98%Cor e Forma:SolidPeso molecular:244.2Antibacterial agent 182
<p>Antibacterialagent 182 (compound 8c) is an antibacterial agent that exhibits activity against various Gram-positive bacteria, particularly displaying efficacy against vancomycin-resistant Enterococcus faecium (MIC ≤0.125 μg/mL). At sub-MIC levels, Antibacterialagent 182 can inhibit biofilm formation by Staphylococcus aureus and Pseudomonas aeruginosa.</p>Fórmula:C14H5Br4F3N2OSPeso molecular:621.68082WAY-329764
CAS:<p>WAY-329764 is an antibacterial agent.</p>Fórmula:C25H25N3OSPureza:98.86%Cor e Forma:SolidPeso molecular:415.555'-O-TBDMS-N2-ibu-dG
CAS:<p>5'-O-TBDMS-N2-ibu-dG: a nucleoside derivative with strong anti-BVDV activity, useful in lead compound synthesis.</p>Fórmula:C20H33N5O5SiCor e Forma:SolidPeso molecular:451.59NagZ-IN-1
<p>NagZ-IN-1 (Compound 11h) is a β-N-acetylglucosaminidase inhibitor with a Ki of 3.3 μM. It is applicable in antibacterial research, especially for studies related to Pseudomonas aeruginosa infections.</p>Cor e Forma:Odour SolidProteasome-IN-6
<p>Proteasome-IN-6 (Compound J-80) inhibits the β5 catalytic subunit of the Trypanosoma brucei 20S proteasome, effectively blocking T. b. brucei, T. b. gambiense, and T. b. rhodesiense with EC50 values of 157 nM, 220 nM, and 156 nM, respectively. Additionally, Proteasome-IN-6 has demonstrated antitrypanosomal activity in a mouse model.</p>Fórmula:C35H45F3N4O6Cor e Forma:SolidPeso molecular:674.75Antimicrobial agent-39
<p>Antimicrobial agent-39 (Compound 8i) is an antibiotic that targets the 50S ribosomal subunit, inhibiting bacterial protein synthesis. It disrupts bacterial cell membranes, causing leakage of cellular contents and demonstrating broad-spectrum antibacterial activity. Additionally, Antimicrobial agent-39 targets organic cation transporters (OCT) and accumulates in infected kidneys, improving pyelonephritis in mouse models.</p>Fórmula:C36H46BrN3O4SCor e Forma:SolidPeso molecular:696.74Lysozyme chloride
CAS:<p>Lysozyme chloride: enzyme that kills gram-positive bacteria; used in HIV, emphysema research.</p>Cor e Forma:SolidTSO-13
<p>TSO-13 is an inhibitor of the major cysteine protease Cruzipain found in Trypanosoma cruzi, with an IC50 of 2.2 μM. In Vero cells, TSO-13 also suppresses T. cruzi, exhibiting an IC50 of 1.9 μM.</p>Fórmula:C32H36N4O4S2Cor e Forma:SolidPeso molecular:604.78Laidlomycin
CAS:<p>Laidlomycin, a polyether, polycyclic, monocarboxylic acid, possesses inhibitory activity against various Mycoplasma species, especially Acholeplasma laidlawii.</p>Fórmula:C37H62O12Pureza:98%Cor e Forma:SolidPeso molecular:698.88HIV p17 Gag (77-85)
CAS:<p>Targeting HIV Gag p17 (77-85) with intracellular Ab cDNA disrupts viral replication pre/post-integration.</p>Fórmula:C44H72N10O15Pureza:98%Cor e Forma:SolidPeso molecular:981.1OP-145
CAS:<p>OP-145 is a derivative of the antimicrobial peptide LL-37, known for its antibacterial properties against multiple MRSA strains. This compound is applicable in studies on chronic suppurative otitis media.</p>Fórmula:C142H246N46O31Peso molecular:3093.76Alisporivir
CAS:<p>Alisporivir (Debio-025) is a cyclophilin A inhibitor that disrupts the interaction between CypA and NS5A. HCV activity in vivo and in vitro.</p>Fórmula:C63H113N11O12Pureza:99.95%Cor e Forma:SolidPeso molecular:1216.64Telithromycin
CAS:<p>Telithromycin is a macrolide antibiotic and erythromycin derivative,70S bacterial ribosome, antimicrobial, respiratory infections,inhibits protein synthesis.</p>Fórmula:C43H65N5O10Pureza:98%Cor e Forma:SolidPeso molecular:812Epithienamycin E
CAS:<p>Epithienamycin E is a member of the class of carbapenems. Epithienamycin E has a role as a bacterial metabolite.</p>Fórmula:C13H16N2O8S2Cor e Forma:SolidPeso molecular:392.4Antifungal agent 82
<p>Antifungal agent 82 (compound G34) demonstrates outstanding in vitro antifungal efficacy against Valsa mali, exhibiting an EC50 value of 0.57 μg/mL, and has</p>Cor e Forma:Odour SolidAcrB-IN-1
CAS:<p>AcrB-IN-1 (Compound H6) is a highly effective inhibitor of AcrB, utilized for the reversal of bacterial multidrug resistance [1].</p>Fórmula:C32H39N3O4Cor e Forma:SolidPeso molecular:529.67Lychnopholide
CAS:<p>Lychnopholide is isolated from Vanillosmopsis erythropappa.</p>Fórmula:C20H22O6Cor e Forma:SolidPeso molecular:358.39Mycalolide B
CAS:<p>Mycalolide-B, from marine sponges, blocks actomyosin ATPase, stopping ATP-triggered contraction without Ca2+.</p>Fórmula:C52H74N4O17Cor e Forma:SolidPeso molecular:1027.175Influenza NP (147-155) (TFA)
<p>This peptide is a H2-Db-restricted epitope from Influenza nucleoprotein (147-155).</p>Fórmula:C50H83F3N16O16Pureza:98%Cor e Forma:SolidPeso molecular:1221.29γ-Glutamyl Transferase-IN-1
<p>Gamma-Glutamyl Transferase-IN-1 (compound 4de), a β-carboline 1-hydrazide inhibitor, exhibits antifungal and antibacterial properties by targeting</p>Cor e Forma:Odour Solid5'-O-TBDMS-Bz-dA
CAS:<p>5’-O-TBDMS-Bz-dA is a nucleoside with protective and modification effects.</p>Fórmula:C23H31N5O4SiCor e Forma:SolidPeso molecular:469.617Ditiocarb
CAS:<p>Ditiocarb speeds up copper cementation, cuts HIV risk, and boosts high-risk breast cancer immunoresearch.</p>Fórmula:C5H11NS2Cor e Forma:SolidPeso molecular:149.28Benzylpenicillin
CAS:<p>Benzylpenicillin, a penicillin derivative, treats infections using sodium or potassium salts. Effective against gram-positive bacteria and gram-negative cocci.</p>Fórmula:C16H18N2O4SPureza:98%Cor e Forma:Amorphous White Powder SolidPeso molecular:334.39HRSV/hCoV-229E-IN-1
<p>HRSV/hCoV-229E-IN-1 (compound 8X) is an effective inhibitor of HRSV and hCoV-229E, with an IC50 value of 2.1 µM for hCoV-229E. Additionally, HRSV/hCoV-229E-IN-1 can inhibit cell viability.</p>Fórmula:C20H20N2O3Cor e Forma:SolidPeso molecular:336.384Beludavimab
CAS:<p>Beludavimab, a monoclonal antibody, targets SARS-CoV-2 spike protein with an EC50 of 14.9 ng/mL and Kd 0.21 nM.</p>Cor e Forma:LiquidHIV-1 inhibitor-59
<p>HIV-1 Inhibitor-59 (Compound I-5b) effectively inhibits both wild-type and mutant strains of HIV-1, with EC50 values ranging from 5.62 to 171 nM.</p>Fórmula:C28H28FN5O3SCor e Forma:SolidPeso molecular:533.621-O-Methylemodin
CAS:<p>1-O-Methylemodin, a natural product isolated from Zopfiella longicaudata, exhibits antifungal activity [1].</p>Fórmula:C16H12O5Cor e Forma:SolidPeso molecular:284.26Lienomycin
CAS:<p>Lienomycin is a pentaene macrolide antitumor antibiotic generated by Actinomyces vendargensis Struyk et Stheeman. It has inonphore-like action.</p>Fórmula:C67H107NO18Pureza:98%Cor e Forma:SolidPeso molecular:1214.582HPV16 E7 (86-93)
CAS:<p>HPV16 E7 oncoprotein fragment (amino acids 86-93) binds strongly to HLA-A*0201; may aid in cervical cancer vaccine development.</p>Fórmula:C37H66N8O10SPureza:98%Cor e Forma:SolidPeso molecular:815.03Diphyllin O-glucoside
<p>Diphyllin O-glucoside is a useful organic compound for research related to life sciences and the catalog number is T125096.</p>Fórmula:C27H26O12Cor e Forma:SolidPeso molecular:542.493Lycomarasmine
CAS:<p>Lycomarasmine is a bioactive chemical.</p>Fórmula:C9H15N3O7Cor e Forma:SolidPeso molecular:277.233Enduracidin B
CAS:<p>Enduracidin B, a polypeptide antibiotic, is a prominent constituent of Enduracidin. This antibiotic is synthesized by Streptomyces fungicides.</p>Fórmula:C108H140Cl2N26O31Cor e Forma:SolidPeso molecular:2369.36Antifungal agent 128
<p>Antifungalagent 128 (Compound 3ja) is an antifungal agent that, in combination with Fluconazole, has a MIC range of 0.5-4 μg/mL against C. albicans strains. It is applicable in the study of anti-infective therapies.</p>Cor e Forma:Odour SolidSDH-IN-8
<p>SDH-IN-8 (compound G40) is a potent inhibitor of succinate dehydrogenase (SDH), demonstrating an IC50 value of 27 nM against porcine SDH and exhibits fungicidal</p>Fórmula:C18H14Cl3F4N3OCor e Forma:SolidPeso molecular:470.68Gepotidacin S enantiomer
<p>Gepotidacin S enantiomer is an S enantionmer of gepotidacin.</p>Fórmula:C24H28N6O3Pureza:98%Cor e Forma:SolidPeso molecular:448.52Protoneogracillin
CAS:<p>Protoneogracillin: anti-fungal vs. P.oryzae (MMDC=94.0μM), cytotoxic on K562 cells (IC50=6.6μM).</p>Fórmula:C51H84O23Cor e Forma:SolidPeso molecular:1065.2BU-2313 A
CAS:<p>BU-2313 A is a new antibiotic complex. It also active against anaerobes.</p>Fórmula:C27H35NO9Pureza:98%Cor e Forma:SolidPeso molecular:517.57Ophiobolin B
CAS:<p>Ophiobolin B is a sesterterpene Helminthosporium oryzae metabolite, inhibits proton extrusion from maize coleoptiles.</p>Fórmula:C25H38O4Pureza:98%Cor e Forma:SolidPeso molecular:402.57CysHHC10
CAS:<p>CysHHC10 is a synthetic antimicrobial peptide (AMP), and exhibits strong anti-microbial properties against both Gram-positive and Gram-negative bacteria.</p>Fórmula:C77H107N23O10SPureza:98%Cor e Forma:SolidPeso molecular:1546.89Ecubectedin
CAS:<p>Ecubectedin (PM14), a derivative of ecteinascidins family, has antitumor and antimicrobial properties.</p>Fórmula:C41H44N4O10SCor e Forma:SolidPeso molecular:784.87FtsZ-IN-8
<p>FtsZ-IN-8: Strong FtsZ inhibitor, blocks bacterial cell division, low resistance risk, minimal toxicity to mammalian cells.</p>Fórmula:C27H28BrN3O2Cor e Forma:SolidPeso molecular:506.43HIV-1 inhibitor-81
<p>HIV-1inhibitor-81 (Compound 14g) is an HIV-1 protease inhibitor with a Ki of 1.6 nM. This compound exhibits antiviral activity against HIV-1, with an EC50 value of 250 nM.</p>Fórmula:C32H44N2O8SCor e Forma:SolidPeso molecular:616.77SARS-CoV-2 Mpro-IN-30
<p>SARS-CoV-2 Mpro-IN-30 (compound L2) is a SARS-CoV-2 Mpro inhibitor with an IC50 value of 9.1 nM.</p>Cor e Forma:Odour SolidAntifungal agent 124
<p>Antifungalagent 257 (Compound 7e) is a broad-spectrum antifungal agent with an EC50 value of 4.15 μM against F. graminearum.</p>Fórmula:C26H21Cl2F2N5O4SCor e Forma:SolidPeso molecular:608.444Surgumycin
CAS:<p>Surgumycin is a carbonyl-conjugated pentaenic antibiotic.</p>Fórmula:C36H60O11Cor e Forma:SolidPeso molecular:668.865Tilatamig samrotecan
<p>Tilatamig samrotecan (AZD9592) is an antibody-drug conjugate (ADC) designed to deliver a topoisomerase I inhibitor (TOP1i). It targets epidermal growth factor receptor (EGFR) and c-MET and demonstrates antitumor activity. The compound induces DNA double-strand breaks, elevates pRAD50 and γH2AX expression, and inhibits the growth of non-small cell lung cancer.</p>Cor e Forma:Odour SolidTrypanothione synthetase-IN-2
<p>Trypanothione synthetase-IN-2: competitive inhibitor for Leishmania TryS, IC50 5.4 μM with spermidine.</p>Fórmula:C41H69N7O11Cor e Forma:SolidPeso molecular:836.03Antiparasitic agent-24
<p>Antiparasitic agent-24 (Compound 14a) is an antiparasitic compound with EC50 values of 0.005 μM for L. maj, 0.069 μM for L. don, 0.82 μM for T. brucei, and 4.1 μM for T. cruzi.</p>Fórmula:C23H22ClN7O2SCor e Forma:SolidPeso molecular:495.98Midecamycin acetate
CAS:<p>Midecamycin acetate is a broad-spectrum antibiotic active against Gram-positive and some Gram-negative strains.</p>Fórmula:C45H71NO17Pureza:98%Cor e Forma:White Or Offt-White Crystalline PowderPeso molecular:898.04Ertapenem
CAS:<p>Ertapenem: injectable carbapenem with broad antimicrobial spectrum, resistant to many beta-lactamases.</p>Fórmula:C22H25N3O7SCor e Forma:SolidPeso molecular:475.51Urechistachykinin I
CAS:<p>Urechistachykinin I (Uru-TK I) is an invertebrate kalinin-related peptide (TRPs) isolated from thylakoid nematodes.</p>Fórmula:C50H85N19O14Pureza:98%Cor e Forma:SolidPeso molecular:1176.33PF 5081090
CAS:<p>PF 5081090 has a wide range of applications in life science related research.</p>Fórmula:C18H21FN2O6SCor e Forma:SolidPeso molecular:412.43Julifloricine
CAS:<p>Julifloricine is an alkaloid isolated from Prosopis juliflora that has antimicrobial activity.</p>Fórmula:C40H75N3O2Cor e Forma:SolidPeso molecular:630.04AAA-10
CAS:<p>AAA-10 is an orally active inhibitor of bile salt hydrolase (BSH) in B. intestinalis that acts on B. thetarBSH (IC50: 10 nM) and B. longumrBSH (IC50: 80 nM).</p>Fórmula:C25H41FO5SCor e Forma:SolidPeso molecular:472.655'-O-DMT-rU
CAS:<p>5’-O-DMT-rU is a modified nucleoside and can be used to synthesize RNA.</p>Fórmula:C30H30N2O8Cor e Forma:SolidPeso molecular:546.57Antifungal agent 52
CAS:<p>Compound 6c, a tetrazole derivative, inhibits ergosterol synthesis and disrupts C. albicans cell membranes with potent antifungal effects.</p>Fórmula:C25H19BrClFN6OCor e Forma:SolidPeso molecular:553.81Altromycin C
CAS:<p>Altromycin C is a new pluramycin-like antibiotic.</p>Fórmula:C46H57NO17Pureza:98%Cor e Forma:SolidPeso molecular:895.94trans-β-Terpineol
CAS:<p>Trans-β-terpineol, a monoterpenoid compound extracted from Schinus terebinthifolius leaves, exhibits antioxidant and antibacterial properties.</p>Fórmula:C10H18OCor e Forma:SolidPeso molecular:154.25HPV16-E711-20 epitope
CAS:<p>HPV16-E711-20: HLA-A*0201-restricted CTL epitope, binds strongly to HLA-A2.</p>Fórmula:C53H83N11O19SPureza:98%Cor e Forma:SolidPeso molecular:1210.35Voxvoganan trihydrochloride
<p>Voxvoganan (LTX-109) trihydrochloride, a topical antimicrobial, demonstrates a high efficacy against S.</p>Fórmula:C43H72Cl3N11O3Cor e Forma:SolidPeso molecular:897.46Antibacterial agent 163
<p>Antibacterial agent 163 (compound 1), a hydroxyquinoline derivative, potently inhibits methicillin-resistant Staphylococcus aureus (MRSA) [1].</p>Cor e Forma:Odour SolidCC 1014
CAS:<p>CC 1014 is a polypeptide antibiotic isolated from Penicillium lilacinum that inhibits phosphorylation of ADP, Mg ATPase.</p>Fórmula:C62H111N11O13Pureza:98%Cor e Forma:SolidPeso molecular:1218.63412R-LOX-IN-2
CAS:<p>12R-LOX-IN-2 is a 12R-LOX inhibitor that inhibits the hyperproliferation of psoriatic cells and can be used in the study of psoriasis and other skin diseases.</p>Fórmula:C19H13NOPureza:99.84%Cor e Forma:SolidPeso molecular:271.31XT-4
CAS:<p>XT-4, an antimicrobial peptide originating from the skin secretions of Xenopus tropicalis, exhibits potent activity against E.</p>Fórmula:C107H176N28O27SCor e Forma:SolidPeso molecular:2318.78Bromochloroacetonitrile
CAS:<p>Bromochloroacetonitrile, a water disinfection by-product, is mutagenic and can break DNA strands.</p>Fórmula:C2HBrClNCor e Forma:SolidPeso molecular:154.393-Phenyl-1H-indole
CAS:<p>3-Phenyl-1H-indole has antibacterial activity and can inhibit Klebsiella pneumoniae, Escherichia coli, Candida albicans, Staphylococcus aureus, etc.</p>Fórmula:C14H11NPureza:99.74%Cor e Forma:SolidPeso molecular:193.24Betonicine
CAS:<p>Betonicine, an l-alpha-amino acid, is in herbs, spices, pulses, and mainly urine.</p>Fórmula:C7H13NO3Cor e Forma:SolidPeso molecular:159.19Tetrahydrorhombifoline
CAS:<p>Tetrahydrorhombifoline, a quinolizidine alkaloid found in the aerial parts of Genista vuralii A.</p>Fórmula:C15H24N2OCor e Forma:SolidPeso molecular:248.367-O-Demethyl rapamycin
CAS:<p>Novolimus is a macrocyclic lactone with anti-proliferative properties. It has similar efficacy to currently available agents but requires a lower dose.</p>Fórmula:C50H77NO13Cor e Forma:SolidPeso molecular:900.16Teixobactin
CAS:<p>Teixobactin is a recently described antibiotic .</p>Fórmula:C58H95N15O15Pureza:98%Cor e Forma:SolidPeso molecular:1242.488Ro 19-9638
CAS:<p>Ro 19-9638 is the N-oxide of Ro 15-0216.</p>Fórmula:C15H19N5O5Cor e Forma:SolidPeso molecular:349.34Nitidanin
<p>Nitidanin is a useful organic compound for research related to life sciences and the catalog number is T125599.</p>Fórmula:C21H24O8Cor e Forma:SolidPeso molecular:404.415
