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Search Results for " a 128 "

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Compounds

Cat No. Product Name Synonyms Targets
T28943 Telomycin A-128,A 128,A128,NSC 235069,Antibiotic 128
elomycin is a cyclic depsipeptide antibiotic with activity against Gram-positive bacteria.
TN2281 Sinapaldehyde trans-3,5-Dimethoxy-4-hydroxy cinnamaldehyde Antibacterial
Sinapaldehyde (trans-3,5-Dimethoxy-4-hydroxy cinnamaldehyde) is a natural product. Sinapaldehyde exhibits moderate antibacterial against Methicillin resistant S. aureus (MRSA) and E. coli with MIC values of 128 and 128 μ...
T25651 Lecimibide DuP128,DuP-128,DuP 128 Acyltransferase
Lecimibide (DuP 128) is a potent and selective inhibitor of acyl coenzyme A: cholesterol acyltransferase (ACAT), which can be used to study diseases due to high lipids.
T6726 VU0361737 ML-128,VU 0361737 GluR
VU0361737 (ML-128) is a specific positive allosteric modulator (PAM) of mGlu4 receptor.The EC50 of VU 0361737 is 240 nM for the human receptors. The EC50 of VU 0361737 is110 nM for rat receptors.It exhibits weak activity...
T29630 AD 128 AD128,AD-128
AD 128 is a bioactive chemical and therapeutic agent.
T28477 PZ-128 PZ 128
PZ-128, a PAR1 antagonist, is used potentially for the treatment of thrombosis.
T70359 GK-128 hydrochloride
GK-128 hydrochloride is a 5-hydroxytryptamine(3) receptor antagonist and an anti-emetic.
T38917 Antibacterial agent 50
Antibacterial agent 50 (example 47) is a compound that exhibits antibacterial activity. It shows minimum inhibitory concentration (MIC) values of 32, 64, and 128 mcg/mL against three strains of E. coli, namely NCTC 13351...
T79004 ATP synthase inhibitor 2 TFA
ATP Synthase Inhibitor 2 (Compound 22) TFA is a potent inhibitor of Pseudomonas aeruginosa ATP synthase with an IC50 value of 10 μg/mL. It effectively halts ATP synthesis in Pseudomonas aeruginosa at a concentration of 1...
T29175 YKAs3003 YKAs-3003
YKAs3003, a potent inhibitor of pathogenic KAS III, displays minimal inhibitory concentration (MIC) values in the range 128-256 microg/mL against various bacteria.
T80276 Lynronne-3
Lynronne-3, an antimicrobial peptide, demonstrates activity against Gram-positive bacteria, including multi-drug resistant (MDR) strains, with a minimum inhibitory concentration (MIC) ranging from 32-128 μg/mL for methic...
T76948 Zenocutuzumab
Zenocutuzumab (MCLA-128) is a humanized bispecific IgG1 antibody with Fab arms that specifically target the extracellular domains of HER2 and HER3 [1].
T72907 Ac-SVVVRT-NH2
Ac-SVVVRT-NH2, a PGC-1α modulator, enhances the activity of the human PGC-1α promoter (114%), elevates PGC-1α mRNA levels (125%), and promotes intracellular lipid accumulation (128%) in subcutaneous human adipocytes. Thi...
T61649 ATP synthase inhibitor 2
ATP Synthase Inhibitor 2, a compound targeting Pseudomonas aeruginosa (PA) ATP synthase with an IC50 of 10 μg/mL, fully inhibits the ATP synthesis activity of PA at a concentration of 128 μg/mL [1].
T75001 Antibacterial agent 128
Antibacterial Agent 128, a siderophore analog-Ciprofloxacin (Ciprofloxacin) conjugate connected via a cleavable linker, demonstrates effective antibiotic properties. Specifically, it exhibits activity against P. aerugino...
T83698 Cathelicidin-2 (128-153) (chicken) TFA Fowlicidin-2 (128-153),CATH-2 (128-153),Myeloid Antimicrobial Peptide 27 (128-153)
Cathelicidin-2 (CATH-2) (128-153) is a synthetic antimicrobial peptide derived from amino acids 128-153 of chicken CATH-2, demonstrating activity against pathogens such as E. coli, S. aureus, S. enteritidis, and B. globi...
T13146 Thienopyridone Others
Thienopyridone is a potent and selective inhibitor of phosphatase of regenerating liver (PRL) phosphatase(IC50s of 173 nM, 277 nM and 128 nM for PRL-1, PRL-2, and PRL-3, respectively), and induces p130Cas cleavage and ap...
T61387 Bromodomain inhibitor-10
Bromodomain inhibitor-10 (compound 128) is a highly potent inhibitor of bromodomain activity. It exhibits strong binding affinity with K d values of 15.0 nM and 2500 nM for BRD4-1 and BRD4-2, respectively. Furthermore, B...
T36318 28-Acetylbetulin
28-Acetylbetulin is a lupane triterpenoid and derivative of the cholesterol biosynthesis inhibitor betulin that has been found inM. chiapensisand has anti-inflammatory and anticancer activities.1,2It inhibits LPS-induced...
T38321 A-39183A
A-39183A is an active component of the A-39183 antibiotic complex produced by aerobic fermentation of Streptomyces NRRL 12049. It has activity against penicillin-resistant S. aureus 3055 and S. faecalis X66 (MICs = 32 an...
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