Chemical structure
Cat.No.
Product Name
CAS no.
Target
YN250002 Bay 41-4109 racemate 298708-79-9
BAY 41-4109 racemate is a mixture of R-isomer of BAY 41-4109 and S-isomer of BAY 41-4109. BAY 41-4109 an antiviral compound that inhibits human hepatitis B virus (HBV) with IC50 of 53 nM.
YN250001 Bay 41-4109 298708-81-3
BAY 41-4109 is a potent inhibitor of human hepatitis B virus (HBV) with an IC50 of 53nM.
YN250090 Reutericyclin 303957-69-9
Reutericyclin (Reutericycline), a unique tetramic acid, is an antibiotic produced by some strains ofLactobacillus reuteri. Reutericyclin (Reutericycline) exhibits a broad inhibitory spectrum includingLactobacillus spp.,Bacillus subti...
YN251830 Flagelin 22 304642-91-9
Flagelin 22 (Flagellin 22), a fragment of bacterial flagellin, is an effective elicitor in both plants and algae.
YN250680 Ridinilazole 308362-25-6
Ridinilazole is a novelantibacterialwith MICs range of 0.06-0.25 µg/mL (MIC90=8 µg/mL) againstC. difficile.
YN250124 Gatifloxacin mesylate 316819-28-0
Gatifloxacin mesylate (AM-1155; BMS-206584; PD135432) is a potent fluoroquinoloneantibioticwith broad-spectrum antibacterial activity. Gatifloxacin mesylate inhibits bacterialtype II topoisomerases(IC50=13.8 μg/ml forS. aureu...
YN480813 GAK inhibitor 49 319492-82-5
GAK inhibitor 49 is a potent, ATP-competitive and highly selectivecyclin G associated kinase (GAK)inhibitor with a Ki of 0.54nM and a cellIC50 of 56nM. GAK inhibitor 49 also shows binding to RIPK2.
YN250664 Squalamine lactate 320725-47-1
Squalamine lactate is an aminosterol compound discovered in the tissues of the dogfish shark, with antimicrobial activity, and used for the treatment of neovascular age-related macular degeneration.
YN251849 OV-1, sheep 326855-45-2
OV-1, sheep is an alpha-helical antimicrobial ovispirin peptide derived from SMAP29 peptide (sheep), which inhibits several antibiotic-resistant bacterial strains including mucoid and nonmucoid Pseudomonas aeruginosa.
YN250859 Tildipirosin 328898-40-4
Tildipirosin, a long-acting macrolide, has antibiotic activity.
AX20017 is a small-molecule protein kinase G (PknG) inhibitor with an IC50 of 0.39μM.
YN250693 Peramivir 330600-85-6
Peramivir (RWJ-270201;BCX-1812) is a highly potent, selective and orally active influenza virusneuraminidase (NA)inhibitor, with IC50 values ranging form 0.9 to 4.3nM for nine NA subtypes.
YN250833 S.pombe lumazine synthase-IN... 331726-35-3
S.pombe lumazine synthase-IN-1 is an inhibitor oflumazine synthaseswith Ki values of 243μM and 9.6μM forSchizosaccharomyces pombe and Mycobacterium tuberculosislumazine synthases, respectively.
I2906 showed antimycobacterial and cytotoxic activity against mycobacterium tuberculosis.
ABMA is a broad-spectrum inhibitor of intracellular toxins and pathogens. ABMA efficiently protects cells against various toxins and pathogens includingviruses,intracellular bacteria and parasite. ABMA selectively acts at ho...
NBD-557 is a potentially HIV-1 inhibitor.
NBD-556, a CD4 mimetic, is a potentHIV-1entry inhibitor that blocks the gp120-CD4 interaction. NBD-556 shows potent cell fusion and virus-cell fusion inhibitory activity at low micromolar levels.
TAK-220 is a selective and orally bioavailableCCR5antagonist, with IC50s of 3.5nM and 1.4nM for inhibition on the binding of RANTES and MIP-1α to CCR5, respectively, but shows no effect on the binding to CCR1...
YN250834 Nucleozin 341001-38-5
Nucleozin is an antivirus agent that targets influenza A nucleoprotein (NP). Nucleozin triggers the aggregation of NP and inhibits its nuclear accumulation.
YN250629 Pritelivir 348086-71-5
Pritelivir (BAY 57-1293) is a potent helicase primase inhibitor, exhibiting antiviral effect on herpes simplex virus (HSV) with IC50 of 20 nM for both HSV-1 and HSV-2.
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