Microbiologie/Virologie
Les inhibiteurs en microbiologie et virologie sont des composés qui ciblent les microorganismes, y compris les bactéries, les virus et les champignons, perturbant leur croissance, leur réplication ou leur survie. Ces inhibiteurs sont essentiels pour étudier la pathogénie microbienne, comprendre les mécanismes de résistance et développer de nouvelles thérapies antimicrobiennes et antivirales. Les inhibiteurs de cette catégorie sont utilisés pour combattre les maladies infectieuses, explorer l'écologie microbienne et étudier les interactions hôte-pathogène. Chez CymitQuimica, nous offrons une large sélection d'inhibiteurs de haute qualité en microbiologie et virologie pour soutenir vos recherches en maladies infectieuses, microbiologie et virologie.
Sous-catégories appartenant à la catégorie "Microbiologie/Virologie"
- Antibactérien(3.153 produits)
- Antibiotique(932 produits)
- Antifection(24 produits)
- DHFR(34 produits)
- Synthèse ADN/ARN(774 produits)
- VHB(182 produits)
- Protéase du VIH(477 produits)
- HSV(94 produits)
- Intégrase(2 produits)
- Ribosome(13 produits)
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6158 produits trouvés pour "Microbiologie/Virologie"
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4-Chloropyridine
CAS :4-Chloropyridine acts as an inhibitor of Nicotinamide N-methyltransferase (NNMT). Serving as a substrate for NNMT, this compound enhances the electrophilicity at the C4 position through methylation of the pyridine nitrogen. This modification facilitates an aromatic nucleophilic substitution reaction with the non-catalytic cysteine (C159) in NNMT, ultimately leading to suicidal activity inhibition of the enzyme. 4-Chloropyridine is a promising candidate for the development of activity-based probes targeting NNMT functions.Formule :C5H4ClNCouleur et forme :SolidMasse moléculaire :113.55Antimalarial agent 2
Antimalarial agent 2 is an orally active, novel antimalarial agent that exhibits rapid in vitro killing effects.Formule :C27H25N3O5Couleur et forme :SolidMasse moléculaire :471.5Fenbenicillin potassium
CAS :<p>Fenbenicillin (Phenbenicillin) potassium is a semi-synthetic penicillin with antibacterial spectrum activity.</p>Formule :C22H22KN2O5SCouleur et forme :SolidMasse moléculaire :465.584Chitinase-IN-5
Chitinase-IN-5 (8i) blocks OfChi-h (IC50: 0.051 μM), has insecticidal qualities, useful for eco-friendly pest control.Formule :C20H21ClFN7Couleur et forme :SolidMasse moléculaire :413.88MurA-IN-6
CAS :MurA-IN-6 (Compound L16) is a selective MurA inhibitor with an IC50 of 26.63 μM. It exhibits antibacterial activity by inhibiting the function of MurA, a key protein essential for bacterial cell wall synthesis.Formule :C22H17N3O3SCouleur et forme :SolidMasse moléculaire :403.454SPR7
SPR7 is a potent and selective rhodesain inhibitor (Ki: 0.51 nM). SPR7 exhibited antiparasitic effects against T. b. brucei (EC50: 1.65 μM).Formule :C30H32ClN3O3Couleur et forme :SolidMasse moléculaire :518.05Imidocarb dihydrochloride monohydrate
Imidocarb dihydrochloride monohydrate is an effective antiprotozoal agent against the parasite B. bovis (IC50: 87 μg/ml).Formule :C19H24Cl2N6O2Couleur et forme :SolidMasse moléculaire :439.34TLR8 agonist 4
<p>TLR8 agonist 4 inhibits wild-type and lamivudine/entecavir-resistant HBV; IC50: 0.15 μM and 0.10 μM.</p>Formule :C28H27N5O5SCouleur et forme :SolidMasse moléculaire :545.61Alpibectir
CAS :<p>Alpibectir has antibacterial activity [1].</p>Formule :C12H14F6N2O2Couleur et forme :SolidMasse moléculaire :332.24Antibacterial agent 68
Antibacterial agent 68 targets drug-resistant E. coli at 0.007 mM with low cytotoxicity.Formule :C26H25BrN4O7Couleur et forme :SolidMasse moléculaire :585.4Antibacterial agent 281
CAS :Antibacterialagent 281 (Compound 95,186) effectively inhibits the growth of GAS by binding to the ligand-binding pocket of SPs0871, competing with the ligand. It exhibits concentration-dependent growth inhibition against Streptococcus pyogenes (S. pyogenes).Formule :C23H24N6OCouleur et forme :SolidMasse moléculaire :400.48BRD-4592
CAS :BRD-4592 is an allosteric inhibitor targeting tryptophan synthase (TrpAB) of Mycobacterium tuberculosis. It binds at the α-β subunit interface of TrpAB, with an IC50 of 70.9 nM for the α subunit and 22.6 nM for the β subunit.Formule :C17H15FN2OCouleur et forme :SolidMasse moléculaire :282.312RCB18350
CAS :<p>RCB18350 is an antituberculosis agent and an isoxazole derivative. It demonstrates bacteriostatic properties by inhibiting the growth of Mycobacterium tuberculosis, with a minimum inhibitory concentration (MIC) of 1.25 μg/mL. RCB18350 is effective against multi-drug resistant Mycobacterium tuberculosis (MDR-TB) clinical isolates, Mycobacterium bovis BCG, and Mycobacterium avium, all of which are slow-growing mycobacteria.</p>Formule :C19H18F3N3O4SCouleur et forme :SolidMasse moléculaire :441.424Antibacterial agent 262
CAS :<p>Antibacterialagent 262 (compound A23) is a potent antibacterial agent that inhibits the activity of Xanthomonas oryzae pv oryzae. It also disrupts the integrity of bacterial cell membranes by preventing the formation of biofilms of Xanthomonas oryzae pv oryzae.</p>Formule :C17H18F2N6O4S3Couleur et forme :SolidMasse moléculaire :504.554FPI-1465
CAS :<p>FPI-1465: Dual serine-β-lactamase & PBP inhibitor; IC50 PBP2=1.0 μg/mL; Kd CTX-M-15=0.011μM, OXA-48=5.3μM.</p>Formule :C11H18N4O7SCouleur et forme :SolidMasse moléculaire :350.35HIV-1 inhibitor-17
HIV-1 inhibitor-18 blocks HIV-1 capsid, acts on NL4-3 strain (EC50: 2.57 μM), has low cytotoxicity (MT-4 CC50: >8.55).Formule :C32H32N4O5SCouleur et forme :SolidMasse moléculaire :584.69HT1171
CAS :<p>HT1171 is a potent and selective inhibitor of the Mycobacterium tuberculosis proteasome. It exhibits strong antitubercular activity against Mycobacterium tuberculosis H37Rv, with a MIC90 of 2 μg/mL and MIC of 4 μg/mL. At a concentration of 100 μM, HT1171 shows an inhibition rate of 53.8% against normal human liver cells (L02). HT1171 is applicable in antituberculosis drug research.</p>Formule :C7H4N2O4S2Couleur et forme :SolidMasse moléculaire :244.248Antibacterial agent 261
CAS :Antibacterialagent 261 (compound 43) is a potent inhibitor of the peptide deformylase (PDF) enzyme, demonstrating IC50 values of 2.5 nM against Staphylococcus aureus (S. aureus) and 10.6 nM against Escherichia coli (E. coli).Formule :C18H24N4O3S2Couleur et forme :SolidMasse moléculaire :408.538Methyl piperazine-2-carboxylate
CAS :Methyl piperazine-2-carboxylate (compound 4) is a potent activator of METTL3/METTL14/WTAP. It enhances the production of HIV-1p24 viral particles and increases the level of N6-methyladenosine in the viral RNA genome.Formule :C6H12N2O2Couleur et forme :SolidMasse moléculaire :144.172HBV-IN-11
CAS :HBV-IN-11 is a potent inhibitor of HBsAg secretion (EC50: 0.46 μM).Formule :C21H24ClNO6Couleur et forme :SolidMasse moléculaire :421.87Antifungal agent 12
Antifungal agent 12 is a new fluconazole-like compound that exhibits good antifungal effects.Formule :C20H16F3N7O2S2Couleur et forme :SolidMasse moléculaire :507.51Antibacterial agent 87
Antibacterial agent 87 is an effective antibacterial agent that acts on MRSA (MIC: 0.125 μg/ml), MRSE (MIC: 0.0625 μg/ml) and S. aureus (MIC: 0.0625 μg/ml).Formule :C31H46N2O6SCouleur et forme :SolidMasse moléculaire :574.77FG-2101
CAS :FG-2101 is a selective, orally active non-hydroxamate LpxC inhibitor with an IC50 of approximately 1 nM. It demonstrates exceptional selectivity over other bacterial and human metalloproteases. FG-2101 is useful for studying infections caused by Gram-negative bacteria, including resistant strains.Formule :C30H32N5O6PCouleur et forme :SolidMasse moléculaire :589.579Antibacterial agent 77
<p>Antibacterial agent 77 (compound 12) is an antibacterial agent [1].</p>Formule :C22H27N3OSCouleur et forme :SolidMasse moléculaire :381.53GSK-3036656 free base
CAS :GSK656 (GSK3036656) inhibits Mtb LeuRS with IC50 of 0.20 μM, promising for tuberculosis treatment.Formule :C10H13BClNO4Couleur et forme :SolidMasse moléculaire :257.48PptT-IN-3
PptT-IN-3 (5p), an inhibitor of PptT in Mycobacterium tuberculosis, IC50=3.5μM, is key for TB research.Formule :C16H27N5O3SCouleur et forme :SolidMasse moléculaire :369.48RhlR antagonist 1
RhlR antagonist 1: IC50 of 26 μM, selective for RhlR, inhibits P. aeruginosa biofilm and virulence factors.Formule :C12H10F2OCouleur et forme :SolidMasse moléculaire :208.2Gougerotin
CAS :Gougerotin is an inhibitor of protein synthesis.Formule :C16H25N7O8Couleur et forme :SolidMasse moléculaire :443.41Chitin synthase inhibitor 8
Chitin synthase inhibitor 8 is a chitin synthase (CHS) inhibitor with broad-spectrum antifungal effects that can be used in studies related to fungal infectionsFormule :C23H23N3O5Couleur et forme :SolidMasse moléculaire :421.45BM635 hydrochloride
<p>BM635 hydrochloride, an MmpL3 inhibitor, strongly blocks Divergent bacteriophage H37Rv (MIC50: 0.08 μM), with doubled in vivo potency.</p>Formule :C25H30ClFN2OCouleur et forme :SolidMasse moléculaire :428.97HCV-IN-40
CAS :<p>HCV-IN-39 is a potent oral drug inhibiting HCV, effective on GT1a (EC50: 0.259μM), GT1b (EC50: 0.434μM), GT1b CES1 (EC50: 0.069μM) replicons.</p>Formule :C21H26BrFN3O9PCouleur et forme :SolidMasse moléculaire :594.32Trypanothione synthetase-IN-4
Trypanothione synthetase-IN-4, an L. infantum inhibitor, has potent anti-leishmanicidal properties (EC50: 0.6 μM).Formule :C29H52INO2Couleur et forme :SolidMasse moléculaire :573.63BAY-364
CAS :BAY-364 (BAY-299N) functions as an inhibitor targeting the second bromine domain in TAF1, demonstrating inhibitory effects on TAF1 in Kasumi-1 cells, CD34+Formule :C23H19N3O4Couleur et forme :SolidMasse moléculaire :401.41Fabimycin
CAS :Fabimycin, a FabI inhibitor, combats drug-resistant gram-negative bacterial infections effectively.Formule :C23H25ClN4O3Couleur et forme :SolidMasse moléculaire :440.92NBD-14189
CAS :NBD-14189: Potent HIV-1 entry blocker, binds gp120, IC50: 89 nM, strong antiviral (EC50 <200 nM).Formule :C18H16F4N4O2SCouleur et forme :SolidMasse moléculaire :428.40NFC nitro probe 1
CAS :<p>NFC nitro probe 1 (compound 18) is a chemical probe designed for the detection of Mtb, exhibiting high potency against both R-Mtb and NR-Mtb.</p>Formule :C19H19NO6Couleur et forme :SolidMasse moléculaire :357.357Chitin synthase inhibitor 9
CHS inhibitor 9: a broad-spectrum antifungal for studying fungal infections.Formule :C24H25N3O6Couleur et forme :SolidMasse moléculaire :451.47WM382
CAS :<p>WM382, a potent dual PMIX/X inhibitor, has IC50s of 1.4 nM/0.03 nM and effective against various malaria stages.</p>Formule :C29H36N4O4Couleur et forme :SolidMasse moléculaire :504.62Enzyme-IN-3 disodium
CAS :<p>Enzyme-IN-3 disodium (compound 7) is a selective inhibitor of Mycobacterium tuberculosis shikimate kinase with an IC50 of 1.6 μM. Additionally, Enzyme-IN-3 disodium exhibits antibacterial properties.</p>Formule :C20H13N3Na2O8S2Couleur et forme :SolidMasse moléculaire :533.442HBV-IN-19 TFA
CAS :<p>HBV-IN19 TFA suppresses HBsAg, hampers HBV infection, and aids in HBV research.</p>Formule :C26H31F3N2O8Couleur et forme :SolidMasse moléculaire :556.53Anti-Influenza agent 3
Compound 11h: Potent, low-toxicity anti-influenza, inhibits M2 ion channels. EC50: 3.29μM (H3N2), 2.45μM (H1N1).Formule :C16H22ClNOSCouleur et forme :SolidMasse moléculaire :311.87Antitumor agent-74
Antitumor agent-74, a quinazoline derivative, inhibits DNA, arrests cell cycle, and induces apoptosis with agent-75.Formule :C26H23FN6Couleur et forme :SolidMasse moléculaire :438.5ZINC000104379474
ZINC000104379474 is a compound that targets SARS-CoV-2 endoribonuclease.Formule :C27H33N3O10Couleur et forme :SolidMasse moléculaire :559.57BRD-K98645985
CAS :BRD-K98645985: BAF inhibitor, binds ARID1A, reverses HIV-1 latency, EC50 ~2.37μM, alters nucleosome placement.Formule :C33H43N5O4Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :573.73Cefclidin
CAS :Cefclidin (Cefclidine) is a cephalosporin compound.Formule :C21H26N8O6S2Couleur et forme :SolidMasse moléculaire :550.611Cephalosporin C
CAS :<p>Cephalosporin C exhibits relatively weak resistance to Gram-positive and Gram-negative bacteria. It is stable against penicillinase, but can be decomposed by cephalosporinase. When hydrolyzed to remove its side chain, it yields 7-amino-cefenoic acid (7-ACA), which is an essential raw material for the production of semisynthetic cephalosporins.</p>Formule :C16H21N3O8SCouleur et forme :SolidMasse moléculaire :415.418Colistin adjuvant-2
Colistin adjuvant-2 is a compound that acts as a potentiation agent for colistin, effectively enhancing its activity against Gram-negative bacteria [1].Formule :C14H7Cl2F3N2OCouleur et forme :SolidMasse moléculaire :347.12ZK-316
CAS :ZK-316 is a potent and broad-spectrum NNRTI inhibitor with an EC50 range of 0.99 to 75.1 nM. It is applicable for HIV research.Formule :C27H22D6N6O3S2Couleur et forme :SolidMasse moléculaire :554.72NBTIs-IN-5
CAS :NBTIs-IN-5 inhibits Mycobacterium abscessus DNA with IC50 1.5μM, halts growth at MIC90 0.4μM.Formule :C24H25F3N4O2Couleur et forme :SolidMasse moléculaire :458.48NITD-688
CAS :NITD-688 is a pan-serotype inhibitor targeting the dengue virus NS4B protein, effective through oral administration.Formule :C25H32N4O3S2Couleur et forme :SolidMasse moléculaire :500.68Purine phosphoribosyltransferase-IN-2
Purine PRTase-IN-2 inhibits Pf, Pv, Tbr PRT; Ki: 30, 20, 2 nM.Formule :C11H15N5Na4O10P2Couleur et forme :SolidMasse moléculaire :531.17(±)-Tuaimenal A
CAS :(±)-Tuaimenal A ((+)-1) is a secondary metabolite and a derivative of Sesamol. It exhibits potent inhibitory activity against SARS-CoV-2 3CLpro, with an IC50 of 33.3 μM. (±)-Tuaimenal A is applicable in research related to SARS-CoV-2 infection.Formule :C23H30O4Couleur et forme :SolidMasse moléculaire :370.48FWM-1
<p>FWM-1 blocks SARS-CoV-2 NSP13, hinders ATP binding, with -328.6 kcal/mol binding energy.</p>Formule :C15H11ClN4O4S2Couleur et forme :SolidMasse moléculaire :410.86Antifungal agent 127
CAS :<p>Antifungalagent 127 (Compound 6c) is an antifungal agent with potent inhibitory activity against Botrytis cinerea and Rhizoctonia solani.</p>Formule :C13H12ClN3OCouleur et forme :SolidMasse moléculaire :261.707XR8-89
CAS :XR8-89, a potent PLpro inhibitor (IC50=0.1μM), blocks SARS-CoV-2 replication; useful for research.Formule :C29H36N4O2SCouleur et forme :SolidMasse moléculaire :504.69HBV-IN-48
CAS :<p>HBV-IN-48, an HBV inhibitor, exhibits potent antiviral activity against HBV in HepDE19 cells, demonstrated by its EC 50 value of 0.005 μM. Additionally, it effectively reduces serum HBV DNA levels in mouse models of HBV infection.</p>Formule :C22H15F4N3O3Couleur et forme :SolidMasse moléculaire :445.37TCMDC-125431
TCMDC-125431 is a novel inhibitor of Plasmodium calcium kinetics with minimal inhibition of haemoglobin crystals.Formule :C25H27N3O2SCouleur et forme :SolidMasse moléculaire :433.57Quorum sensing-IN-9
CAS :<p>Quorum sensing-IN-9 (Compound 7d) inhibits quorum sensing in Pseudomonas aeruginosa by binding to the PqsR protein. It suppresses the expression of quorum sensing system-related genes lasB, rhlA, and pqsA, thereby preventing the production of virulence factors elastase, pyocyanin, and rhamnolipid. Quorum sensing-IN-9 disrupts the motility of P. aeruginosa, inhibits biofilm formation, and reduces the bacterium's virulence and pathogenicity. Additionally, it exhibits anti-infective activity in the Galleria mellonella larval model.</p>Formule :C9H10OS2Couleur et forme :SolidMasse moléculaire :198.305Pibrozelesin
CAS :Pibrozelesin, a water-soluble duocarmycin B2 derivative, binds AT-rich DNA, blocking replication and inducing cell death.Formule :C32H36BrN5O8Couleur et forme :SolidMasse moléculaire :698.56Deprodone
CAS :Deprodone is an active compound that inhibits key processes such as bacterial cell wall synthesis by interacting with hydrolase and transferase proteins of methicillin-resistant Staphylococcus aureus (MRSA). It is applied in the research of MRSA infections, inflammatory skin diseases, intestinal disorders, and fatty acid metabolism disorders.Formule :C21H28O4Couleur et forme :SolidMasse moléculaire :344.44HC2210
CAS :HC2210 exhibits antibacterial effects against Mycobacterium abscessus (Mab) with an EC50 of 0.72 µM. It modulates the expression of Mab genes associated with oxidative stress and lipid metabolism. HC2210 is applicable for studies on Mab infections.Formule :C17H18N4O9Couleur et forme :SolidMasse moléculaire :422.354,5'-Dimethylangelicin-NHS
NHS-modified coumarin, 4,5'-Dimethylangelicin-NHS, shows photochemical activity & photosensitivity.Formule :C21H19NO7SCouleur et forme :SolidMasse moléculaire :429.44BMIM-TFSI
CAS :<p>BMIM-TFSI (compound8) is an HIV-1 integrase inhibitor that effectively suppresses both the 3'-processing (3'-P) and strand transfer (ST) steps of the integration process. It is applicable in HIV-1 research.</p>Formule :C10H15F6N3O4S2Couleur et forme :SolidMasse moléculaire :419.364MsbA-IN-4
<p>MsbA-IN-4 (Compound 32) is a highly selective and potent inhibitor of MsbA (IC50: 3 nM).MsbA-IN-4 inhibits Escherichia coli (MIC: 12 μM).</p>Formule :C23H18Cl2FN5OCouleur et forme :SolidMasse moléculaire :470.33Antibacterial agent 81
CAS :Antibacterial agent 81 blocks DNA transcription, targets S. aureus (MIC 12.5μM) & M. smegmatis (MIC 7.8μM). Used in infection research.Formule :C33H28N2O8Couleur et forme :SolidMasse moléculaire :580.58NS2B/NS3-IN-2
<p>Potent dengue inhibitor NS2B/NS3-IN-2 (IC50: 6 nM, Ki: 0.66 μM) boosts cell viability, non-toxic.</p>Formule :C24H21N3O5SCouleur et forme :SolidMasse moléculaire :463.51CDA-IN-1
CAS :<p>CDA-IN-1 (Compound vs#2-1) is an inhibitor of chitin deacetylase (CDA) that exhibits antifungal activity. By inhibiting fungal CDA activity, it activates plant immune responses and leads to the accumulation of reactive oxygen species (ROS), hindering fungal growth. At a concentration of 100 μM, CDA-IN-1 achieves inhibition rates of 86.9% on P. xanthii's PxCDA1 and 74.5% on PxCDA2. CDA-IN-1 is applicable in research on fungal plant diseases, such as cucumber powdery mildew and tomato gray mold.</p>Formule :C15H14N2O6Couleur et forme :SolidMasse moléculaire :318.281Antimicrobial agent-38
CAS :<p>Antimicrobial agent-38 (compound 10) effectively inhibits methicillin-resistant Staphylococcus aureus (S. aureus) strain ATCC 700699 and non-resistant strain ATCC 29213, with minimum inhibitory concentrations (MIC) of 32 mg/L and 64 mg/L, respectively.</p>Formule :C14H11N3O4SCouleur et forme :SolidMasse moléculaire :317.32BMS-818251
CAS :BMS-818251 is a potent small-molecule inhibitor that targets HIV-1 entry, with an EC50 value of 0.019 nM. It exhibits over 10 times greater efficacy on the cross-subtype panels of the 208-HIV-1 strain compared to BMS-626529. BMS-818251 enhances potency through interactions with gp120 residues in the conserved β20-β21 hairpin.Formule :C29H26N6O5SCouleur et forme :SolidMasse moléculaire :570.619Antitubercular agent-11
Antitubercular agent-11 (Compound 1e) is an antitubercular agent with a bulkier electron-donating group (Bu-t) that shows the best MIC value of 0.060 μg/mL [1].Formule :C16H15N3O4Couleur et forme :SolidMasse moléculaire :313.31PLpro-IN-6
CAS :<p>PLpro-IN-6 (compound 6) serves as an inhibitor for the papain-like protease (PLpro), demonstrating potent activity with an IC 50 of 0.019 μM against the SARS-CoV-2 PLpro enzyme.</p>Formule :C29H30N6OCouleur et forme :SolidMasse moléculaire :478.59MPro N3
CAS :Mpro inhibitor blocks MHV-A29, HCoV-229E, FOPV (IC50: 2.7–8.8 μM), and SARS-CoV-2 (IC50: 16.8 μM) in plaque assays.Formule :C35H48N6O8Couleur et forme :SolidMasse moléculaire :680.79GSK_WRN4
CAS :<p>GSK_WRN4 is a WRN helicase inhibitor with anti-cancer activity, inhibiting MSI tumor cell growth by inducing DNA double-strand breaks, useful in cancer research</p>Formule :C16H20N2O4SDegré de pureté :99.95%Couleur et forme :SolidMasse moléculaire :336.41Antibacterial agent 76
Antibacterial agent 76 (compound 9) is a potent antibacterial agent.Formule :C23H27N3O2SCouleur et forme :SolidMasse moléculaire :409.54DPC 684
CAS :DPC 684 is a potent and selective HIV-1 protease inhibitor with an IC90 of 5.7-40 nM and a Ki of 0.021 nM. It competitively inhibits HIV-1 protease, preventing viral polyprotein cleavage. Compared to cellular proteases, DPC 684 shows high selectivity for retroviral proteases. The compound exhibits low protein binding and offers broad-spectrum inhibition against various wild-type and mutant HIV-1 proteases, with an IC90 of 1.9-6.3 nM. DPC 684 is significant for HIV research.Formule :C35H48FN5O5SCouleur et forme :SolidMasse moléculaire :669.85ZLM-66
<p>ZLM-66: Doravirine analog, HIV-1 NNRTI inhibitor, IC50: 41nM, EC50: HIV-1 13nM, cIAP1 0.32nM; useful in AIDS research.</p>Couleur et forme :SolidHIV-1 inhibitor-41
<p>HIV-1 inhibitor-41 (B23): Oral non-nucleoside reverse transcriptase blocker, EC50 of 50 nM (E138K), 20.8 nM (WT), low hERG/CYP impact, non-toxic.</p>Formule :C16H15F2N3OSCouleur et forme :SolidMasse moléculaire :335.37Pyriofenone
CAS :Pyriofenone (IKF-309) is an aryl phenyl ketone fungicide predominantly used to control powdery mildew on crops such as cereals, rice, fruit trees, and vegetables. It exhibits moderate efficacy against rice blast disease. Pyriofenone functions through prevention, residue activity, treatment, rainfastness, translaminar action, and fumigation.Formule :C18H20ClNO5Couleur et forme :SolidMasse moléculaire :365.81Emtricitabine triphosphate
CAS :Emtricitabine triphosphate is an active metabolite of Emtricitabine, a drug for HIV/HBV that inhibits reverse transcriptase.Formule :C8H13FN3O12P3SCouleur et forme :SolidMasse moléculaire :487.19FtsZ-IN-13
CAS :<p>FtsZ-IN-13 (Compound C11) functions as an inhibitor of the temperature-sensitive mutant Z (FtsZ), exhibiting IC50 values of 47.97 μM for FtsZSa and 34 μM for FtsZPa. It demonstrates notable antibacterial activity against Staphylococcus aureus (with a minimum inhibitory concentration of 2 μg/mL), cystic fibrosis Staphylococcus aureus clinical isolates, and methicillin-resistant Staphylococcus aureus (MRSA). FtsZ-IN-13 is applicable in research on antibiotic resistance.</p>Formule :C18H14N2O4S2Couleur et forme :SolidMasse moléculaire :386.445MetRS-IN-1
CAS :MetRS-IN-1 (Compound 27) is an inhibitor of E. coli methionyl-tRNA synthetase (MetRS) with an IC50 value of 237 nM [1].Formule :C15H13N3O4SCouleur et forme :SolidMasse moléculaire :331.35N6-Benzoyl-2'-deoxyadenosine monohydrate
CAS :<p>N6-Benzoyl-2'-deoxyadenosine monohydrate is a nucleoside analogue that helps diagnose bacterial infections by binding to double-stranded DNA and altering its structure, which can subsequently be detected using electrophoresis.</p>Formule :C17H19N5O5Couleur et forme :SolidMasse moléculaire :373.363Antileishmanial agent-4
Antileishmanial agent-4, a ribonucleoside analogue, functions as an antileishmanial agent [1].Formule :C17H18N4O4Couleur et forme :SolidMasse moléculaire :342.35Cap-dependent endonuclease-IN-14
CAS :Cap-dependent endonuclease-IN-14 hinders CEN and could treat influenza virus infections. (Patent CN113620948A, compound 1-c).Formule :C30H23FN2O6SCouleur et forme :SolidMasse moléculaire :558.58Antileishmanial agent-5
Antileishmanial agent-4, a ribonucleoside analogue, targets L.infantum and T.cruzi with EC50s of 0.68 μM and 0.83 μM.Formule :C17H17ClN4O4Couleur et forme :SolidMasse moléculaire :376.79RdRP-IN-4
RdRP-IN-4, an oral arylbenzohydrazide, inhibits influenza A/B by targeting PB1 of RdRP, with EC50s of 53 nM (H1N1) and 20 nM (Flu B), and aids infected mice.Formule :C17H17Br2N3O2Couleur et forme :SolidMasse moléculaire :455.14ACHN-975
CAS :ACHN-975: potent LpxC inhibitor with subnanomolar activity; targets many gram-negative bacteria; MIC ≤1 μg/mL.Formule :C20H23N3O4Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :369.41HRO761
CAS :HRO761 is a potent Werne r syndrome RecQ DNA deconjugase (WRN) inhibitor that can be used to study cancers such as colon and stomach cancer.Formule :C31H31ClF3N9O5Degré de pureté :98.74% - 99.62%Couleur et forme :SolidMasse moléculaire :702.08LeuRS-IN-1 hydrochloride
CAS :<p>LeuRS-IN-1 hydrochloride is a Mycobacterium tuberculosis leucyl-tRNA synthetase inhibitor with antileukemic activity and antimalarial activity.</p>Formule :C10H14BCl2NO3Degré de pureté :97.34% - 99.61%Couleur et forme :SolidMasse moléculaire :277.94Cap-dependent endonuclease-IN-1
CAS :Cap-dependent endonuclease-IN-1: potent, oral inhibitor with antiviral properties against influenza.Formule :C27H22F2N2O6SDegré de pureté :99.53% - 99.61%Couleur et forme :SolidMasse moléculaire :540.54Vaniprevir
CAS :Vaniprevir is a competitive HCV NS3/4A protease inhibitor, an antiviral(hepatitis C virus) drug that acts directly and blocks the viral replication process.Formule :C38H55N5O9SDegré de pureté :97.41%Couleur et forme :SolidMasse moléculaire :757.94Tigemonam
CAS :<p>Tigemonam is a monobactam, a novel orally administered monobactam that protects against gram-negative aerobic bacterial pathogens. Cost-effective and quality-assured.</p>Formule :C12H15N5O9S2Degré de pureté :99.03% - >99.99%Couleur et forme :SolidMasse moléculaire :437.41CCF0058981
CAS :<p>CCF0058981: noncovalent inhibitor for SARS-CoV-2 & -1 proteases; IC50s: 68 nM (SC2) & 19 nM (SC1). Potential COVID-19 research use.</p>Formule :C24H19ClN6ODegré de pureté :98.94%Couleur et forme :SoildMasse moléculaire :442.9Rupintrivir
CAS :Rupintrivirvr (AG7088) is a mimetic peptide inhibitor of rhinovirus (HRV) 3C cysteine protease with antiviral activity for the study of viral infections.Formule :C31H39FN4O7Degré de pureté :97.72% - 99.35%Couleur et forme :SolidMasse moléculaire :598.66Eravacycline dihydrochloride
CAS :<p>Eravacycline dihydrochloride (TP-434-046) is a potent and broad-spectrum antibacterial agent against six E. coli (MICs: 0.125-0.25 mg/L).</p>Formule :C27H33Cl2FN4O8Degré de pureté :94.59% - 95%Couleur et forme :SolidMasse moléculaire :631.48D75-4590
CAS :<p>D75-4590, a β-1,6-Glucan synthetase inhibitor, combats fungal infections by targeting cell walls.</p>Formule :C21H27N5Degré de pureté :98.56% - 98.85%Couleur et forme :SolidMasse moléculaire :349.47CTPS1-IN-1
CAS :CTPS1-IN-1 is a cytidine-5′ triphosphate synthase 1 (CTPS1) inhibitor with potential antitumor activity and can be used to study autoimmune diseases.Formule :C21H22N6O4S2Degré de pureté :99.46%Couleur et forme :SolidMasse moléculaire :486.57JTK-109
CAS :JTK-109 is an inhibitor of hepatitis C virus NS5B RNA-dependent RNA polymerase inhibitor and inhibits G1b and G3a subgenomic replicons and recombinant enzymes.Formule :C37H33ClFN3O4Degré de pureté :98.48% - 99.68%Couleur et forme :SolidMasse moléculaire :638.13IDX184
CAS :IDX184 is a potent, orally active, targeted HCV polymerase inhibitor and nucleoside polymerase.IDX184 effectively inhibits HCV polymerase (IC50=0.31 μM, Ki=52.3Formule :C25H35N6O9PSDegré de pureté :97.15%Couleur et forme :SolidMasse moléculaire :626.62FGI-106 tetrahydrochloride
CAS :FGI-106 tetrahydrochloride demonstrates potent inhibitory activity across a broad spectrum of viruses, including those causing hemorrhagic fevers such as EbolaFormule :C28H42Cl4N6Degré de pureté :99.68%Couleur et forme :SolidMasse moléculaire :604.48SR 11302
CAS :SR 11302 is an inhibitor of activator protein-1 (AP-1).Formule :C26H32O2Degré de pureté :98.65%Couleur et forme :SolidMasse moléculaire :376.53Durlobactam sodium salt
CAS :Durlobactam sodium salt (ETX2514) have an IC50 values of 4, 14 and 190 nM against class A KPC-2, class C AmpC and class D OXA-24.Cost-effective and quality-assured.Formule :C8H10N3NaO6SDegré de pureté :97.01% - 99.03%Couleur et forme :SolidMasse moléculaire :299.23Haloxon
CAS :Haloxon is an organophosphorus anthelmintic. Haloxon is used against nematodes of the abomasum and small intestine in ruminants.Formule :C14H14Cl3O6PCouleur et forme :SolidMasse moléculaire :415.59Reutericyclin
CAS :Reutericyclin is a unique tetramic acid, is an antibiotic produced by some strains of Lactobacillus reuteri.Formule :C20H31NO4Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :349.46L-Eflornithine monohydrochloride
CAS :L-Eflornithine is an irreversible ornithine decarboxylase (ODC) inhibitor with a KD of 1.3±0.3 µM, and a Kinact of 0.15±0.03 min-1. L-Eflornithine monohydrochloride (L-DFMO monohydrochloride) is an enantiomer of Eflornithine.Formule :C6H13ClF2N2O2Couleur et forme :SolidMasse moléculaire :218.632'-Hydroxy-4'-methylacetophenone
CAS :<p>2'-Hydroxy-4'-methylacetophenone, a phenolic compound isolated from Angelicae koreana roots possesses acaricidal property. 2'-Hydroxy-4'-methylacetophenone has acaricidal activity, it could be used in the preparation of 4'-methyl-2'-[(p-tolylsulfonyl) oxy] acetophenone.</p>Formule :C9H10O2Degré de pureté :99.88%Couleur et forme :Black LiquidMasse moléculaire :150.17α-Terpineol
CAS :<p>Terpineol possesses antifungal activity against Trichophyton mentagrophytes, it also exhibits strong antimicrobial activity against periodontopathic and cariogenic bacteria. α-Terpineol (Terpineol) shows anticonvulsant, and anti-inflammatory activities, it inhibits the gene expression of the IL-6 receptor.</p>Formule :C10H18ODegré de pureté :97.55%Couleur et forme :Colorless LiquidMasse moléculaire :154.25Ethyl 4-hydroxy-2-methyl-2H-benzo[e][1,2]thiazine-3-carboxylate 1,1-dioxide
CAS :Ethyl 4-hydroxy-2-methyl-2H-benzo[e][1,2]thiazine-3-carboxylate 1,1-dioxide is a useful organic compound for research related to life sciences. The catalog number is T65688 and the CAS number is 24683-26-9.Formule :C12H13NO5SCouleur et forme :SolidMasse moléculaire :283.3Pulcherriminic acid
CAS :<p>Pulcherriminic acid, a cyclic dipeptide, chelates Fe3+, forms pulcherrimin, and has antimicrobial properties used in food, agriculture, and medicine.</p>Formule :C12H20N2O4Couleur et forme :SolidMasse moléculaire :256.30Bacampicillin hydrochloride
CAS :Bacampicillin hydrochloride is an improved oral bioavailability penicillin antibiotic which is a prodrug of ampicillin.Formule :C21H28ClN3O7SDegré de pureté :98%Couleur et forme :SolidMasse moléculaire :501.985'-O-DMT-N6-ibu-dA
CAS :5'-O-DMT-N6-ibu-dA can be utilized in the synthesis of oligodeoxyribonucleotides.Formule :C35H37N5O6Couleur et forme :SolidMasse moléculaire :623.71Lenampicillin hydrochloride
CAS :<p>Lenampicillin hydrochloride is an orally active prodrug of Ampicillin. Lenampicillin hydrochloride is an effective beta-lactam antibacterial agent that inhibits bacterial penicillin-binding proteins. It is applied in the investigation of suppurative skin </p>Formule :C21H24ClN3O7SDegré de pureté :98%Couleur et forme :SolidMasse moléculaire :497.952-Mercaptopyridine N-oxide sodium
CAS :<p>2-Mercaptopyridine N-oxide sodium is a useful organic compound for research related to life sciences. The catalog number is T66776 and the CAS number is 3811-73-2.</p>Formule :C5H4NNaOSCouleur et forme :SolidMasse moléculaire :149.14N-Butylthiophosphoric triamide
CAS :<p>N-Butylthiophosphoric triamide is a useful organic compound for research related to life sciences. The catalog number is T65336 and the CAS number is 94317-64-3.</p>Formule :C4H14N3PSCouleur et forme :SolidMasse moléculaire :167.21MuRF1-IN-2
CAS :MuRF1-IN-2 (Example 3) is a MuRF1 inhibitor used to study conditions linked to muscle wasting, encompassing both skeletal and cardiac muscle atrophy [1].Formule :C23H22N2O7Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :438.43Stearyl gallate
CAS :Stearyl gallate is a useful organic compound for research related to life sciences. The catalog number is T65655 and the CAS number is 10361-12-3.Formule :C25H42O5Couleur et forme :SolidMasse moléculaire :422.606ABT-072 potassium trihydrate
CAS :ABT-072, also known as potassium trihydrate, is a highly effective non-nucleoside inhibitor of the HCV NS5B polymerase, administered orally. This compound exhibits potent activity against HCV GT1a (with an EC50 of 1 nM) and HCV GT1b (with an EC50 of 0.3 nM).Formule :C24H32KN3O8SCouleur et forme :SolidMasse moléculaire :561.69Nortopixantrone
CAS :<p>Nortopixantrone(BBR 3438) is a novel 9-azacyclophenanthracene pyrazole that shows antitumor activity in a human prostate cancer model.</p>Formule :C20H24N6O2Degré de pureté :>99.99%Couleur et forme :SolidMasse moléculaire :380.44Oleandomycin
CAS :Oleandomycin, a macrolide antibiotic structurally similar to Erythromycin, exhibits antimicrobial activity.Formule :C35H61NO12Degré de pureté :98%Couleur et forme :White Amorphous Powder SolidMasse moléculaire :687.86Hexahydrohippuric acid
CAS :Hexahydrohippuric acid is a useful organic compound for research related to life sciences. The catalog number is T65235 and the CAS number is 32377-88-1.Formule :C9H15NO3Couleur et forme :SolidMasse moléculaire :185.2231-Naphthalenemethanol
CAS :1-Naphthalenemethanol is a natural product for research related to life sciences. The catalog number is T67143 and the CAS number is 4780-79-4.Formule :C11H10OCouleur et forme :SolidMasse moléculaire :158.2trans-Clopenthixol dihydrochloride
CAS :<p>Trans-Clopenthixol dihydrochloride ((E)-Clopenthixol dihydrochloride), an antibiotic without neuroleptic effects, has demonstrated in vitro efficacy against Pseudomonas aeruginosa and Plasmodium falciparum, as referenced in [1] [2].</p>Formule :C22H27Cl3N2OSDegré de pureté :98%Couleur et forme :SolidMasse moléculaire :473.89Tetraconazole
CAS :Tetraconazole is an agent of pesticides.Formule :C13H11Cl2F4N3OCouleur et forme :Liquid ViscousMasse moléculaire :372.14NSC639828
CAS :NSC639828 is an efficient inhibitor of DNA polymerase α, exhibiting a remarkable IC50 value of 70 μM. Additionally, NSC639828 demonstrates substantial antitumor activity, making it a promising candidate for cancer research.Formule :C18H13BrClN5O3Couleur et forme :SolidMasse moléculaire :462.69Ulifloxacin
CAS :Ulifloxacin is a useful organic compound for research related to life sciences. The catalog number is T65577 and the CAS number is 112984-60-8.Formule :C16H16FN3O3SCouleur et forme :SolidMasse moléculaire :349.38l-Atabrine dihydrochloride
CAS :l-Atabrine dihydrochloride displays antiprion activity. l-Atabrine dihydrochloride is a less active enantiomer of quinacrine.Formule :C23H31Cl2N3ODegré de pureté :98%Couleur et forme :SolidMasse moléculaire :436.42Ramifenazone
CAS :Ramifenazone is a drug of nonsteroidal anti-inflammatory.Formule :C14H19N3ODegré de pureté :98%Couleur et forme :SolidMasse moléculaire :245.32A 53868A
CAS :<p>A 53868A is an antibiotic, it is isolated from Streptomyces luridus.</p>Formule :C11H22N3O5PDegré de pureté :98%Couleur et forme :SolidMasse moléculaire :307.287Sulfamonomethoxine sodium
CAS :<p>Sulfamonomethoxine sodium is a long-acting sulfonamide antibacterial agent utilized in blood kinetic studies; it inhibits dihydropteroate synthetase, thereby blocking folic acid synthesis [1].</p>Formule :C11H11N4NaO3SDegré de pureté :98%Couleur et forme :SolidMasse moléculaire :302.29Antiviral agent 5
CAS :Antiviral agent 5 is a crucial intermediate utilized in the development of antiviral agents that specifically target 3C and 3CL proteases, which includes the SARS-CoV-2 M pro enzyme.Formule :C18H30N2O7Couleur et forme :SolidMasse moléculaire :386.445FtsZ-IN-10
CAS :<p>Compound GK02084(SC) may have activity against the GTP site of Bs‐FtsZ.</p>Formule :C15H13ClN2O4SDegré de pureté :98%Couleur et forme :SolidMasse moléculaire :352.79CRS3123 dihydrochloride
CAS :CRS3123 (REP-3123) dihydrochloride is an orally active, fully synthetic antimicrobial agent that effectively inhibits Clostridioides difficile methionyl-tRNA synthetase (MetRS). CRS3123 dihydrochloride can be used in the study of Clostridioides difficile infection (CDI).Formule :C19H21Br2Cl2N3O2SCouleur et forme :SolidMasse moléculaire :586.16Rhizocticin A
CAS :Rhizocticin A is a potential inhibitor of threonine synthase.Formule :C11H22N5O6PDegré de pureté :98%Couleur et forme :SolidMasse moléculaire :351.3Erythromycylamine
CAS :Erythromycylamine is a useful organic compound for research related to life sciences. The catalog number is T64443 and the CAS number is 26116-56-3.Formule :C37H70N2O12Couleur et forme :SolidMasse moléculaire :734.969Cefetamet pivoxyl
CAS :<p>Cefetamet pivoxyl, a cephalosporin antibiotic, effectively inhibits 355 enteropathogens, including Gram-negative bacteria (ausgenommen Pseudomonas aeruginosa) and Legionella pneumophila [1].</p>Formule :C20H25N5O7S2Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :511.57Policresulen
CAS :<p>Policresulen is a useful organic compound for research related to life sciences. The catalog number is T66902 and the CAS number is 101418-00-2.</p>Formule :C8H10O5SCouleur et forme :SolidMasse moléculaire :218.22Phosalacine
CAS :<p>Phosalacine, isolated from Kitasatosporia phosalacinea, is a new herbicidal antibiotic that contains phosphinothricin.</p>Formule :C14H28N3O6PDegré de pureté :98%Couleur et forme :SolidMasse moléculaire :365.367Ethynylcytidine
CAS :<p>Ethynylcytidine is a nucleoside antimetabolite.</p>Formule :C11H13N3O5Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :267.24BMS-378806
<p>BMS-378806 is an HIV inhibitor with EC50: 0.85-26.5nM for various strains.</p>Formule :C22H22N4O4Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :406.43PqsR/LasR-IN-1
CAS :PqsR/LasR-IN-1 (Compound 2a) is a potent inhibitor of LasR and PqsR systems in P. aeruginosa. PqsR/LasR-IN-1 is also a inhibitor of hERG (IC50= 6.77 μM).Formule :C24H20ClNO3Couleur et forme :SolidMasse moléculaire :405.87Pseudomonic acid C
CAS :Pseudomonic acid C is the analogue of Pseudomonic Acid D which is an antibiotic agent from Pseudomonas fluorescens.Formule :C26H44O8Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :484.625'-DMT-3'-TBDMS-ibu-rG
CAS :<p>5'-DMT-3'-TBDMS-ibu-rG is a modified nucleoside employed in deoxyribonucleic acid (DNA) synthesis.</p>Formule :C41H51N5O8SiCouleur et forme :SolidMasse moléculaire :769.96Darobactin
CAS :<p>Darobactin is an antibiotic effective against critical Gram-negative pathogens, demonstrating activity both in vitro and in animal infection models [1].</p>Formule :C47H55N11O12Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :966.01(S)-2-Ethylbutyl 2-(((S)-(4-nitrophenoxy)(phenoxy)phosphoryl)amino)propanoate
CAS :(S)-2-Ethylbutyl 2-(((S)-(4-nitrophenoxy)(phenoxy)phosphoryl)amino)propanoate is a useful organic compound for research related to life sciences. The catalog number is T64602 and the CAS number is 1354823-36-1.Formule :C21H27N2O7PCouleur et forme :SolidMasse moléculaire :450.428TP0586532
CAS :<p>TP0586532 is effective against carbapenem-resistant Klebsiella pneumoniae and does not pose a cardiovascular risk.</p>Formule :C26H28N4O4Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :460.52Oxindole
CAS :<p>Oxindole (Indolin-2-one) is an aromatic heterocyclic building block. 2-indolinone derivatives have become lead compounds in the research of kinase inhibitors.Oxindole structure has been used in receptor tyrosine kinases (RTKs) inhibitors such as SU4984 and intedanib, the RTK family represents an important therapeutic target for anti-cancer drug development.</p>Formule :C8H7NODegré de pureté :99.34%Couleur et forme :Off-White Crystalline PowderMasse moléculaire :133.15Pritelivir mesylate
CAS :Pritelivir mesylate is active against herpes simplex virus types 1 and 2 (IC50: 0.02 μM against HSV1-2). Pritelivir mesylate is an inhibitor of the viral helicase-primase complex. Pritelivir mesylate shows antiviral activity in vitro and in animal modelsFormule :C19H22N4O6S3Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :498.6d-Atabrine dihydrochloride
CAS :d-Atabrine hydrochloride is the active enantiomer of quinacrine and has anti-pr virus activity.Formule :C23H31Cl2N3ODegré de pureté :98%Couleur et forme :SolidMasse moléculaire :436.42PKUMDL-LTQ-301
CAS :PKUMDL-LTQ-301 is a potent inhibitor of HipA toxin. PKUMDL-LTQ-301 also inhibits E. coli persistence.Formule :C30H28N2O4Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :480.55MitoE10
CAS :MitoE10 is an effective mitochondrial targeting antioxidant.Formule :C42H55O5PSCouleur et forme :SolidMasse moléculaire :702.92HBV-IN-34
CAS :<p>HBV-IN-34 (compound 17i) is a potent inhibitor of HBsAg production, demonstrating remarkable in vitro anti-HBV efficacy with EC50 values of 0.018 μM for HBV DNA</p>Formule :C21H19F2N7Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :407.42DprE1-IN-8
CAS :<p>DprE1-IN-8 is a potent inhibitor of DprE1, exhibiting an IC50 of less than 0.75 μM.</p>Formule :C19H12F3N5O4SDegré de pureté :98%Couleur et forme :SolidMasse moléculaire :463.39HIV-1 integrase inhibitor
CAS :Hiv-1 integrase inhibitor is an effective anti-HIV drug.Formule :C11H9N3O4Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :247.21Cap-dependent endonuclease-IN-9
CAS :<p>Cap-dependent endonuclease-IN-9, a strong influenza inhibitor, shows low toxicity, good pharmacokinetics, and dynamic action.</p>Formule :C29H22F2N4O7SDegré de pureté :98%Couleur et forme :SolidMasse moléculaire :608.57Insecticidal agent 6
CAS :<p>Compound Im (Insecticidal agent 6) is a potent inhibitor of insect ryanodine receptors (RyRs), exhibiting an EC50 of 0.6308 µM against S.</p>Formule :C19H14BrCl2N5O4Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :527.16SARS-CoV-2-IN-68
CAS :<p>SARS-CoV-2-IN-68 (compound 6C) is a covalent inhibitor of both SARS-CoV-2 PLpro and Mpro, exhibiting potent antiviral properties by targeting the Zn-finger</p>Formule :C14H12N2OSeDegré de pureté :98%Couleur et forme :SolidMasse moléculaire :303.22Yhhu6669
CAS :<p>Yhhu6669 is an anti-HBV agent that suppresses viral DNA and replication by promoting DNA-free capsid assembly, effectively reducing HBV DNA and HBcAg levels in</p>Formule :C29H28ClFN6O3Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :563.02HBV-IN-38
CAS :<p>HBV-IN-38 (Example 193), an HBV DNA inhibitor with an EC50 value of ≤100 nM, serves as a research tool for investigating viral infections [1].</p>Formule :C18H16F3N5O4S2Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :487.48
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