Microbiology/Virology
Microbiology and virology inhibitors are compounds that target microorganisms, including bacteria, viruses, and fungi, disrupting their growth, replication, or survival. These inhibitors are essential for studying microbial pathogenesis, understanding resistance mechanisms, and developing new antimicrobial and antiviral therapies. Inhibitors in this category are used to combat infectious diseases, explore microbial ecology, and investigate host-pathogen interactions. At CymitQuimica, we provide a broad selection of high-quality microbiology and virology inhibitors to support your research in infectious diseases, microbiology, and virology.
Subcategories of "Microbiology/Virology"
- Antibacterial(2,957 products)
- Antibiotic(920 products)
- Antifection(23 products)
- DHFR(33 products)
- DNA/RNA Synthesis(708 products)
- HBV(176 products)
- HIV Protease(449 products)
- HSV(91 products)
- Integrase(2 products)
- Ribosome(13 products)
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Found 5842 products of "Microbiology/Virology"
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CRAMP (mouse)
CAS:<p>CRAMP (mouse), an antimicrobial peptide, is utilized in the study of biofilm-associated infections [1].</p>Formula:C178H302N50O46Color and Shape:SolidMolecular weight:3878.61AT-9010 tetrasodium
CAS:<p>AT-9010 tetrasodium, from AT-527, inhibits NiRAN essential for viral replication and stops SARS-CoV-2 spread.</p>Formula:C11H13FN5Na4O13P3Color and Shape:SolidMolecular weight:627.13Tioxaprofen
CAS:<p>Tioxaprofen is a novel anti-mycotic drug effective against Trichophyton mentagrophytes and T. rubrum, and it acts as a potent uncoupling agent of mitochondrial respiration [1].</p>Formula:C18H13Cl2NO3SColor and Shape:SolidMolecular weight:394.27Altertoxin III
CAS:<p>Altertoxin III is a mutagenic agent that induces mutations in Salmonella typhimurium strains TA98, TA100, and TA1537. It is isolated from extracts of A. alternata strains that demonstrate mutagenic responses in the Ames Salmonella typhimurium test.</p>Formula:C20H12O6Color and Shape:SolidMolecular weight:348.306Magnesium silicate
CAS:<p>Mg silicate (MgO & SiO2) used in antacids, deodorizing, decolorizing & as antifungal.</p>Formula:MgO3SiColor and Shape:SolidMolecular weight:100.39SPR206 acetate
CAS:<p>SPR206 acetate, a polymyxin analog, fights Gram-negative and MDR bacteria, with MICs of 0.125 mg/L against P. aeruginosa and A. baumannii.</p>Formula:C52H82ClN15O12·xC2H4O2Color and Shape:SolidTuvirumab
CAS:<p>Tuvirumab, a human IgG1 monoclonal antibody, targets HBsAg with high affinity (K=3.6 nM) for chronic hepatitis B research.</p>Color and Shape:LiquidCefotiam dihydrochloride hydrate
<p>Cefotiam dihydrochloride hydrate: parenteral cephalosporin antibiotic with broad-spectrum Gram-positive and Gram-negative activity.</p>Formula:C18H25Cl2N9O4S3·xH2OColor and Shape:SolidMolecular weight:C18H25Cl2N9O4S3.xH2Oc-Fos-IN-1
<p>c-Fos-IN-1 (Compound P16) acts as a c-Jun inhibitor, effectively reducing the mRNA and protein levels of c-Fos. It also inhibits the phosphorylation activity of ERK and the transcriptional activity of AP-1. This compound demonstrates anticancer properties through the inhibition of the ERK/c-Fos/Jun pathway. c-Fos-IN-1 curbs the proliferation and migration of gastric cancer cells, with an IC50 of 2.31 μM for MGC-803 cells, causing cell cycle arrest at the G2/M phase and inducing apoptosis in cancer cells. Additionally, c-Fos-IN-1 hampers the growth of gastric cancer tumors.</p>Formula:C28H35NO3Color and Shape:SolidMolecular weight:433.582Antimonyl potassium tartrate trihydrate
CAS:<p>Antimony potassium tartrate trihydrate, known for its potent emetic properties, is utilized in treating schistosomiasis and leishmaniasis.</p>Formula:C8H4K2O12Sb2·3H2OColor and Shape:SolidMolecular weight:667.87Murepavadin TFA
<p>Murepavadin (POL7080) is a specific, potent antibiotic against P. aeruginosa with MICs of 0.12mg/L, targeting lipopolysaccharide transport.</p>Formula:C73H112N22O16·C2HF3O2Color and Shape:SolidMolecular weight:1667.83Bactenecin 7
CAS:<p>Bactenecin 7, an antibacterial peptide, demonstrates activity in inhibiting Enterobacter cloacae growth, with minimum inhibitory concentrations (MICs) ranging</p>Formula:C323H526N110O60Color and Shape:SolidMolecular weight:6910.33Indolicidin acetate
<p>Indolicidin acetate, a powerful antimicrobial peptide isolated from bovine neutrophil cytoplasmic granules, demonstrates significant effectiveness [1].</p>Formula:C102H136N26O15Color and Shape:SolidMolecular weight:1966.342'-Deoxy-2'-fluoro-l-uridine
CAS:<p>2'-Deoxy-2'-fluoro-1-uridine: an L-nucleoside, inhibits RNA viruses by blocking viral RNA polymerase.</p>Formula:C9H11FN2O5Color and Shape:SolidMolecular weight:246.19Hp1404
CAS:<p>Hp1404 is a novel cationic antimicrobial peptide with specific inhibitory activity against Gram-positive bacteria, including Laburnetin-resistant Staphylococcus aureus (MRSA). Its antibacterial properties, low toxicity, and low likelihood of inducing resistance make it a useful candidate for antimicrobial agent research.</p>Formula:C75H119N17O18Color and Shape:SolidMolecular weight:1546.85Bombolitin III
CAS:<p>Bombolitin III, an antimicrobial peptide sourced from bumblebee venom, possesses lytic activity against erythrocytes and liposomes [1].</p>Formula:C87H157N23O19SColor and Shape:SolidMolecular weight:1861.39Gageotetrin B
CAS:<p>Gageotetrin B exhibits antimicrobial properties, demonstrating higher potency against fungi than bacteria, as evidenced by its MIC (Minimum Inhibitory</p>Formula:C38H70N4O9Color and Shape:SolidMolecular weight:726.98Antifungal agent 58
CAS:<p>Compound A21 is a potent anti-Candida drug effective against Fluconazole-resistant strains, surpassing Miconazole, with MIC 0.06-8 μg/mL.</p>Formula:C18H15F3N2SeColor and Shape:SolidMolecular weight:395.28Galbinic Acid
CAS:<p>Galbinic acid, a lichen-derived depsidone from U. undulata, inhibits B. cereus, B. subtilis, S. aureus, and E. coli, with varying MICs.</p>Formula:C20H14O11Color and Shape:SolidMolecular weight:430.32Cecropin A TFA
<p>Cecropin A TFA: a 37-residue peptide from Hyalaphora cecropia, with antibacterial, anti-inflammatory, and anticancer properties.</p>Formula:C186H314N53O48F3Color and Shape:SolidMolecular weight:4117.8HIV-1 inhibitor-80
<p>HIV-1inhibitor-80 (compound M44) is an HIV-1 inhibitor with an EC50 of 5-148 nM. It demonstrates excellent metabolic stability and low cytotoxicity in human plasma and liver microsomes.</p>Formula:C26H19N7OColor and Shape:SolidMolecular weight:445.475E.coli Gyrase B-IN-1
<p>E.coli Gyrase B-IN-1 (Compound 10g) is an inhibitor of E.coli Gyrase B, demonstrating antibacterial properties. It exhibits potent inhibitory activity against Escherichia coli (E. coli) with a minimum inhibitory concentration (MIC) of 0.12 mM. E.coli Gyrase B-IN-1 shows promise for research in antibacterial agents.</p>Formula:C19H16ClN5O4Color and Shape:SolidMolecular weight:413.81PR-39 TFA
<p>PR-39 TFA, a peptide, noncompetitively inhibits proteasomes, spurring angiogenesis and reducing inflammation and mouse myocardial infarct size.</p>Formula:C231H347F3N70O42Color and Shape:SolidMolecular weight:4833.76Sitafloxacin monohydrate
CAS:<p>Sitafloxacin monohydrate (DU6859a) is a potent fluoroquinolone antibiotic with broad-spectrum anti-bacterial and anti-chlamydial effects.</p>Formula:C19H20ClF2N3O4Color and Shape:SolidMolecular weight:427.83Uvaretin
CAS:<p>Uvaretin demonstrates potent antibacterial activity against B. subtilis (EC50: 8.7 μM) and S. epidermidis (IC50: 7.9 μM).</p>Formula:C23H22O5Color and Shape:SolidMolecular weight:378.424Elastase-IN-3
CAS:<p>Compound 15015-57-3, with CAS No. 15015-57-3, is a fragment molecule that serves as an important scaffold for molecular linking, expansion, and modification. Compound 15015-57-3 provides a structural basis and research tool for the design and screening of novel drug candidates, and is commonly used in drug discovery, drug synthesis, and related research.</p>Formula:C12H10O2S2Purity:98.58%Color and Shape:SolidMolecular weight:250.33Antifungal agent 108
<p>Antifungalagent 108 (compound 14d) is an original imidazo[1,2-b]pyridazine derivative that exhibits potent antifungal activity against Madurella mycetomatis (MM55 strain) with an IC50 of 0.9 μM. The compound shows an IC50 of 14.3 μM for cell viability in NIH-3T3 mouse fibroblasts.</p>Color and Shape:Odour SolidMDP1
<p>MDP1, a Melittin-based peptide, disrupts and kills various bacteria, including MDR strains of S. aureus, E. coli, and P. aeruginosa, by damaging membranes.</p>Formula:C111H202N34O28Color and Shape:SolidMolecular weight:2461Z-Antiepilepsirine
CAS:<p>Z-Antiepilepsirine, an amide alkaloid from Piper capense L.f, has antiplasmodial properties with an IC50 of 27 µM against Plasmodium falciparum W2.</p>Formula:C15H17NO3Color and Shape:SolidMolecular weight:259.3Leucanicidin
CAS:<p>Leucanicidin: a macrolide from S. halstedii, toxic to L. separata larvae at 20 ppm; LD50: 0.23-0.42 µg/ml for some worms.</p>Formula:C42H70O13Color and Shape:SolidMolecular weight:783.009Etimicin sulfate
CAS:<p>Etimicin sulfate, a fourth-generation aminoglycoside antibiotic, is now widely used in clinical settings because of its high efficacy and low toxicity.</p>Formula:C21H43N5O7·xH2O4SColor and Shape:SolidOligomycin C
CAS:<p>Oligomycin C is an antifungal agent isolated from Streptomyces strain.</p>Formula:C45H74O10Purity:98%Color and Shape:SolidMolecular weight:775.06Astodrimer
CAS:<p>Astodrimer: large (~3-4 nm, ~16.5 kDa), negative dendrimer with broad-spectrum antiviral, virucidal, and antibacterial properties.</p>Color and Shape:SolidHBV Seq1 aa:93-100
<p>HBV Seq1 aa:93-100 is a hepatitis B virus (HBV) core antigen 93-100 peptide fragment [1] .</p>Formula:C42H79N13O10SColor and Shape:SolidMolecular weight:958.22Kalimantacin A
CAS:<p>Kalimantacin A: a potent antibiotic effective against MRSA and other staphylococci.</p>Formula:C30H48N2O7Color and Shape:SolidMolecular weight:548.715'-O-DMT-N4-Ac-2'-F-dC
CAS:<p>5’-O-DMT-N4-Ac-2’-F-dC is a modified nucleoside and can be used to synthesize DNA or RNA.</p>Formula:C32H32FN3O7Color and Shape:SolidMolecular weight:589.61Maximin 49
<p>Maximin 49, an antimicrobial peptide, exhibits antibacterial activity against S.</p>Formula:C120H209N33O33Color and Shape:SolidMolecular weight:2642.14Api137
<p>Api137 is an antimicrobial peptide that disrupts bacterial growth by blocking translation processes.</p>Formula:C104H171N37O22Color and Shape:SolidMolecular weight:2291.71Protein kinase G inhibitor-1
CAS:<p>Protein kinase G inhibitor-1 is a potent Protein kinase G inhibitor, IC50= 0.9 uM.</p>Formula:C14H18N2O2SPurity:98.11%Color and Shape:SoildMolecular weight:278.37HIV Protease Substrate 1 TFA
<p>HIV Protease Substrate 1 TFA, a fluorogenic substrate for HIV protease, facilitates the investigation of the enzyme's activity [1].</p>Formula:C94H134F3N27O25SColor and Shape:SolidMolecular weight:2131.29Thiocoraline
CAS:<p>Thiocoraline: depsipeptide, DNA intercalator, antibacterial, anticancer, targets Gram-positive, inhibits polymerases, cytotoxic to cancer cells.</p>Formula:C48H56N10O12S6Color and Shape:SolidMolecular weight:1157.39Tenofovir-C3-O-C12-trimethylsilylacetylene ammonium
CAS:<p>Tenofovir-C3-O-C12 has a longer half-life, potent anti-HIV effects, and better pharmacokinetics than tenofovir.</p>Formula:C29H55N6O5PSiColor and Shape:SolidMolecular weight:626.855Antituberculosis agent-9
<p>Antituberculosis agent-9 (Compound 5a), an orally administered compound, demonstrates potent antitubercular activity, exhibiting a minimum inhibitory</p>Formula:C25H29ClN4OColor and Shape:SolidMolecular weight:436.98Anti-MRSA agent 15
<p>Anti-MRSA agent 15 (Compound 9o10) exhibits antimicrobial activity, inhibiting methicillin-resistant Staphylococcus aureus (MRSA) with a minimum inhibitory concentration (MIC) of 0.0625 μg/mL. It demonstrates low hemolytic activity and minimal cytotoxicity. Additionally, Anti-MRSA agent 15 shows anti-infection activity in mice.</p>Color and Shape:Odour SolidHAP-1
CAS:<p>HAP-1, a synovial-targeted transduction peptide, selectively mediates the internalization of protein complexes into synovial cells of human and rabbit origin.</p>Formula:C60H90N18O17Color and Shape:SolidMolecular weight:1335.47Lauryl-LF 11 TFA
<p>Lauryl-LF 11 TFA, a N-terminally acylated analogue of LF11, exhibits antibacterial activity [1].</p>Formula:C83H135F3N26O17Color and Shape:SolidMolecular weight:1826.12Hepcidin-20 (human)
CAS:<p>Hepcidin-20: human peptide, antifungal, hinders biofilm & bacterial metabolism in PIA+/- strains.</p>Formula:C85H135N27O23S9Color and Shape:SolidMolecular weight:2191.73LL-BM123γ2
CAS:<p>LL-BM123γ2 is an antimicrobial agent that exhibits activity against various microorganisms. It is utilized in research related to antimicrobial properties.</p>Formula:C37H59N13O13Color and Shape:SolidMolecular weight:893.94Antituberculosis agent-13
<p>Antituberculosis agent-13 (Compound 11) demonstrates antituberculosis activity, effectively inhibiting both wild-type and mutant strains of Mycobacterium tuberculosis, with an IC50 range of 4-62.5 nM. Additionally, Antituberculosis agent-13 exhibits anti-leukemia properties, inhibiting MOLM-13 with an IC50 of 3.8 μM.</p>Formula:C15H14N2O5Color and Shape:SolidMolecular weight:302.282Elvucitabine
CAS:<p>Elvucitabine, a reverse transcriptase inhibitor, is used potentially for the treatment of HBV infection and HIV infection.</p>Formula:C9H10FN3O3Color and Shape:SolidMolecular weight:227.19JNJ-7184
CAS:<p>JNJ-7184 is a non-nucleoside inhibitor of the RSV-Large (L) polymerase, with pEC50 and pCC50 values of 7.86 and 4.29, respectively, in Hela cells. It inhibits the initiation or early elongation phases, thereby preventing RSV replication and transcription.</p>Formula:C30H27FN4O3Color and Shape:SolidMolecular weight:510.56MurA-IN-5
<p>MurA-IN-5 (compound 4c) demonstrates a minimum inhibitory concentration (MIC) of 1.95 μg/mL against Escherichia coli and exhibits significant potency as a MurA inhibitor with an IC50 of 3.77 μg/mL. It also shows antibiofilm activity against various microorganisms, indicating its potential in combating biofilm-related infections.</p>Formula:C33H28N6O2Color and Shape:SolidMolecular weight:540.614Manumycin B
CAS:<p>Manumycin B is an antibiotic with antitumor properties. It acts as an inhibitor of acetylcholinesterase (AChE) with an IC50 value of 15 mM.</p>Formula:C28H34N2O7Color and Shape:SolidMolecular weight:510.58Amp1EP9
<p>Amp1EP9: antimicrobial peptide, non-toxic, combats multidrug-resistant bacteria.</p>Formula:C90H173N21O16Color and Shape:SolidMolecular weight:1805.47Lactoferricin B (4-14), bovine TFA
Lactoferricin B (4-14), bovine (TFA), a 4-14 residue peptide from lactoferrin, has broad-spectrum antimicrobial properties.Color and Shape:LiquidST166 free acid
CAS:<p>ST166 free acid is an inhibitor of the PhoP-DNA complex formation, with IC50 values of 18 μM and 24 μM, effectively hindering the binding of PhoP and MtrAC to DNA. Additionally, ST166 free acid exhibits antibacterial activity against Mycobacterium marinum.</p>Formula:C6H12O6S6Color and Shape:SolidMolecular weight:372.55TWH106
<p>TWH106 is an inhibitor of the cyclophilin (Cyp) enzyme, exhibiting strong affinity for CypA and CypB with dissociation constants (KD) of 53 nM and 139 nM, respectively. It effectively inhibits the replication of HIV and HCV, demonstrating antiviral activity.</p>Color and Shape:Odour SolidErythromycin A enol ether
CAS:<p>Erythromycin A enol ether is a degradation product of Erythromycin A which is a macrolide antibiotic.</p>Formula:C37H65NO12Purity:99.94%Color and Shape:SolidMolecular weight:715.91Cefquinome
CAS:<p>Cefquinome is a cephem antibiotic that inhibits Enterobacteriaceae (family [1]).</p>Formula:C23H24N6O5S2Purity:98%Color and Shape:SolidMolecular weight:528.6MDP1 acetate
<p>MDP1 acetate, a Melittin peptide, damages bacterial membranes and kills MDR S. aureus, E. coli, and P. aeruginosa.</p>Formula:C113H206N34O30Color and Shape:SolidMolecular weight:2521.05Pol (476-484), HIV-1 RT Epitope
CAS:<p>Pol (476-484), HIV-1 RT Epitope is a biologically active peptide and represents the dominant HLA A*0201-restricted epitope within HIV-1 reverse transcriptase (</p>Formula:C46H78N12O12Color and Shape:SolidMolecular weight:991.18Laccase-IN-5
<p>Laccase-IN-5 (Compound 2b) is an inhibitor of laccase with an IC50 of 0.82 μM. It enhances cell membrane permeability, restricts mycelial growth, disrupts cell walls, and induces oxidative stress responses. Laccase-IN-5 exhibits antifungal activity against various plant pathogenic fungi and oomycetes, effectively inhibiting B. dothidea with an EC50 of 0.96 mg/L.</p>Formula:C16H17FN2OColor and Shape:SolidMolecular weight:272.317m-Chloramphenicol
CAS:<p>m-Chloramphenicol, an impurity, hinders bacterial protein synthesis as a potent broad-spectrum antibiotic.</p>Formula:C11H12Cl2N2O5Color and Shape:SolidMolecular weight:323.13α-Cembrenediol
<p>α-Cembrenediol is a useful organic compound for research related to life sciences and the catalog number is T124625.</p>Formula:C20H34O2Color and Shape:SolidMolecular weight:306.49Anisocoumarin H
CAS:<p>Anisocoumarin H is a useful organic compound for research related to life sciences. The catalog number is T126178 and the CAS number is 123237-86-5.</p>Formula:C19H22O4Color and Shape:SolidMolecular weight:314.381Antibacterial agent 267
<p>Antibacterialagent 267 (Compound h19) is a derivative of pleuromutilin with potent antibacterial activity against Gram-positive bacteria. It demonstrates efficacy in a mouse model infected with methicillin-resistant Staphylococcus aureus (MRSA).</p>Formula:C30H43NO6S2Color and Shape:SolidMolecular weight:577.8Wulfenioidin H
<p>Wulfenioidin H (Compound 5), a diterpenoid, demonstrates anti-Zika virus (ZIKV) activity by inhibiting the expression of the ZIKV envelope (E) protein,</p>Formula:C21H28O3Color and Shape:SolidMolecular weight:328.45Antitubercular agent-38
<p>Antitubercular Agent-38, a derivative of Benzothiazinones (BTZs), demonstrates potent antituberculosis activity while maintaining low cardiac toxicity and</p>Formula:C22H28F3N5O3SColor and Shape:SolidMolecular weight:499.55Dihydroobionin B
<p>Dihydroobionin B exhibits potent (please insert the rest of the sentence for revision).</p>Formula:C21H26O5Color and Shape:SolidMolecular weight:358.43β-Cedrene
CAS:<p>β-Cedrene ((+)-β-Cedrene), a sesquiterpene isolated from both Centaurea kotschyi var. kotschyi and Centaurea kotschyi var. decumbens, exhibits a broad range of biological activities, including antibacterial, anti-inflammatory, antispasmodic, tonic, diuretic, sedative, insecticidal, and antifungal properties. Additionally, β-Cedrene acts as a potent competitive inhibitor of the CYP2B6-mediated bupropion hydroxylase activity, demonstrating a K i value of 1.6 μM [1] [2].</p>Formula:C15H24Color and Shape:SolidMolecular weight:204.35Iboxamycin
CAS:<p>Iboxamycin: potent, orally active antibiotic effective against Gram-positive and Gram-negative bacteria in mice.</p>Formula:C22H39ClN2O6SColor and Shape:SolidMolecular weight:495.07Antibacterial agent 165
<p>Antibacterial agent 165 (compound 3), a hydroxyquinoline derivative, effectively inhibits methicillin-resistant Staphylococcus aureus (MRSA) [1], demonstrating</p>Color and Shape:Odour SolidBurnettramic Acid A
CAS:<p>Burnettramic acid A: Fungus-derived, fights B. subtilis, S. aureus, C. albicans, S. cerevisiae. Toxic to NS-1 cells, not to fibroblasts.</p>Formula:C41H71NO12Color and Shape:SolidMolecular weight:770.00Furaltadone L-tartrate
CAS:<p>Furaltadone L-tartrate, a nitrofuran, may help study Salmonella enteritidis in chickens; it's an antibacterial agent against staphylococci.</p>Formula:C17H22N4O12Color and Shape:SolidMolecular weight:474.38AB-343
<p>AB-343 is a selective covalent inhibitor of SARS-CoV-2 Mpro with an IC50 of 8 nM and a Ki of 2.8 nM. It effectively inhibits the main protease of SARS-CoV-2 and several other coronaviruses and is active against some resistant variants. AB-343 can be utilized in research related to diseases associated with coronavirus infections.</p>Formula:C26H34F5N5O4Color and Shape:SolidMolecular weight:575.57YJ182
<p>YJ182 is an NDM-1 inhibitor with an IC50 of 0.23 μM, and additionally inhibits IMP-1, VIM-2, GIM-1, and MMP-2 with respective IC50 values of 0.25, 0.61, 0.49,</p>Formula:C21H15N3O4SColor and Shape:SolidMolecular weight:405.43Lankacyclinone C
<p>Lankacyclinone C, a congener of lankacidin C devoid of the δ-lactone moiety, exhibits antitumor activity.</p>Formula:C24H33NO5Color and Shape:SolidMolecular weight:415.52Antifungal agent 60
<p>Antifungal agent 60 (compound 16), a broad-spectrum ergosterol biosynthesis inhibitor, demonstrates potent activity against seven human pathogenic fungal</p>Formula:C22H18F2N4O2Color and Shape:SolidMolecular weight:408.4Kadsuralignan A
CAS:<p>Kadsuralignan A (compound 1), a dibenzocyclooctadiene lignan extracted from the leaves and stems of Schisandra lancifolia, exhibits anti-HIV activity, with an</p>Formula:C22H26O7Color and Shape:SolidMolecular weight:402.44Antibacterial agent 56
CAS:<p>Antibacterial agent 56 (example 22) is a antibacterial agent.</p>Formula:C11H13N4NaO8SColor and Shape:SolidMolecular weight:384.30Nikkomycin N
CAS:<p>Nikkomycin N is a bioactive chemical.</p>Formula:C15H20N4O10Color and Shape:SolidMolecular weight:416.343Enzyme-IN-2
<p>Enzyme-IN-2 (compound 15) serves as a potent urease inhibitor, exhibiting anti-ureolytic activity with a K i of 2.36 µM and an IC 50 of 0.75 µM [1].</p>Formula:C9H11O7PColor and Shape:SolidMolecular weight:262.15Diphyllin O-glucoside
<p>Diphyllin O-glucoside is a useful organic compound for research related to life sciences and the catalog number is T125096.</p>Formula:C27H26O12Color and Shape:SolidMolecular weight:542.493T3SS-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>Formula:C16H25N3O3Color and Shape:SolidMolecular weight:307.39Antipain
CAS:<p>Antipain, from Actinomycetes, blocks proteases and combats MNNG-induced genetic changes.</p>Formula:C27H44N10O6Purity:98%Color and Shape:SolidMolecular weight:604.713Antibacterial agent 162 trifluoromethanesulfonate
<p>Antibacterial agent 162 trifluoromethanesulfonate (compound 7), a dual-function molecule, demonstrates potent inhibitory effects on Staphylococcus aureus,</p>Color and Shape:Odour SolidEFdA-TP tetraammonium
<p>EFdA-TP tetraammonium is a potent HIV-1 RT inhibitor and DNA synthesis blocker, acting as an ICT or DCT.</p>Formula:C12H27N9O12P3Color and Shape:SolidMolecular weight:601.31Luminamicin
CAS:<p>Luminamicin is active against anaerobic bacteria, especially Clostridium sp.; isolated from actinomycete strain OMR-59.</p>Formula:C32H38O12Color and Shape:SolidMolecular weight:614.644Averufin
CAS:<p>Averufin is a natural product that can be used as a reference standard. The CAS number of Averufin is 14016-29-6.</p>Formula:C20H16O7Color and Shape:SolidMolecular weight:368.341Phosphomannose isomerase
CAS:<p>Phosphomannose isomerase, the initial enzyme in GDP-Man biosynthesis, catalytically facilitates the interconversion of fructose-6-phosphate (Fru6P) and mannose-</p>Color and Shape:SolidAntifungal 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>Color and Shape:Odour SolidParvodicin 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>Formula:C83H88Cl2N8O29Color and Shape:SolidMolecular weight:1732.53Dihydromaniwamycin E
<p>Dihydromaniwamycin E is a heat-shock metabolite exhibiting antiviral activity against influenza and SARS-CoV-2 viruses [1].</p>Formula:C10H22N2O2Color and Shape:SolidMolecular weight:202.29Drimentine C
CAS:<p>Drimentine C: a terpene diketopiperazine antibiotic; inhibits NS-1 cell growth by 63% (12.5 μg/ml) and 98% (100 μg/ml).</p>Formula:C31H41N3O2Color and Shape:SolidMolecular weight:487.68HA Peptide TFA
<p>HA Peptide (TFA): 9-amino acid sequence from influenza HA, used in protein isolation and detection.</p>Formula:C55H68F3N9O19Color and Shape:SolidMolecular weight:1216.19Antitrypanosomal agent 18
<p>Compound 18 (compound 8b), a nitrofuran derivative, exhibits potent in vitro trypanocidal activity, with an IC50 value of 0.03 μM [1].</p>Color and Shape:Odour SolidGrepafloxacin
CAS:<p>Grepafloxacin, an oral fluoroquinolone antibiotic, effectively treats respiratory infections, especially Streptococcus pneumoniae.</p>Formula:C19H22FN3O3Color and Shape:SolidMolecular weight:359.39Amphotericin A
CAS:<p>Amphotericin A is a potent antifungal antibiotic [1] .</p>Formula:C47H75NO17Color and Shape:SolidMolecular weight:926.09Antifungal agent 72
<p>Antifungal agent 72 (Compound B8) demonstrates potent activity by inhibiting the efflux pump function and downregulating resistance-associated genes via</p>Formula:C13H14N4OSColor and Shape:SolidMolecular weight:274.34Obtusalin
CAS:<p>Obtusalin, a triterpenoid initially identified in R. dauricum, exhibits UV absorption at 210 nm and possesses antibacterial properties.</p>Formula:C30H50O2Color and Shape:SolidMolecular weight:442.72
