Carboxylic acid salts
AdipoGen Diazidostilbenedisulfonic acid
Chemical. CAS 2718-90-3. Formula C14H8N6Na2O6S2 . 4H2O. MW 538.42. Synthetic. A reagent for enzyme immobilisation on fibroin by photo-crosslinking. The reagent is water-soluble over a wide pH range.
Apexbio Technology LLC GSK1349572 sodiuM salt 1051375-19-9 50mg
GSK1349572 sodium salt (CAS 1051375-19-9) is a small-molecule inhibitor targeting HIV integrase It is designed to inhibit the integrase-mediated strand transfer process thereby blocking the integration of viral DNA into the host genome GSK1349572 sodium salt exerts its biological activity primarily through interaction with the enzyme s two-metal ion catalytic site inhibiting strand transfer In in vitro studies GSK1349572 sodium salt demonstrates potent antiviral inhibition with a protein-adjusted IC50 of approximately 38 nM in the presence of 100% human serum Based on these pharmacological properties GSK1349572 sodium salt holds research potential in antiviral studies evaluation of resistance profiles and drug development of integrase inhibitors for HIV therapy
eMolecules Ambeed / Copper(II) stearate / 5g / 552706342 / A322268 / / 660-60-6 / MFCD27987126 / 630.498 / C36H70CuO4
Ambeed / Copper(II) stearate / 5g / 552706342 / A322268 / / 660-60-6 / MFCD27987126 / 630.498 / C36H70CuO4
Sigma Aldrich Fine Chemicals Biosciences dUTP PCR Grade sodium salt
dUTP PCR Grade is a 100 mM clear colorless SOLUTIONon of the sodium salt (pH 8.3).
Selleck Chemical LLC Nigericin sodium salt
Nigericin sodium salt is an antibiotic derived from Streptomyces hygroscopicus that works by acting as an H K and Pb2 ionophore Nigericin can activate NLRP3 inflammasome to induce pro-inflammatory and immunostimulatory processes
Apexbio Technology LLC Cefotaxime (sodium salt)(Synonyms: Claforan, Cefotaxime Sodium, Cefotaxim sodium salt, Cefotaxime Na, Sodium cefotaxime), 5g, CAS: 64485-93-4.
Cefotaxime sodium (CAS 64485-93-4) is a third-generation cephalosporin antibiotic belonging to the -lactam group characterized by inhibition of bacterial cell-wall synthesis through binding to penicillin-binding proteins In vitro analyses show strong inhibitory efficacy against various bacterial species notably cefotaxime exhibits an MIC below 0 1 g/ml against Streptococcus pneumoniae It also demonstrates high activity against Haemophilus influenzae including -lactamase-producing strains In vivo mouse model studies revealed that combination therapy of cefotaxime with minocycline enhanced survival following Vibrio vulnificus infection compared to single-agent treatments Clinically cefotaxime has been evaluated in pneumonia therapy demonstrating good tolerance and therapeutic utility in targeting susceptible bacterial pathogens
Strem, An Ascensus Company CAS# 2966-50-9. 25g. Silver trifluoroacetate, min. 98%. MFCD00013199
CAS# 2966-50-9. 25g. Silver trifluoroacetate, min. 98%. MFCD00013199. Molecular Weight: 220.88. Molecular Formula: AgOOCCF3. Color/form: white to off-white pwdr. Strem# 93-4736. http://www.strem.com/catalog/v/93-4736/
Apexbio Technology LLC Cefoxitin (sodium salt) 33564-30-6 1g
Cefoxitin sodium salt (CAS 33564-30-6) is a small-molecule inhibitor targeting penicillin-binding proteins (PBPs) It is designed to inhibit PBPs thereby interfering with bacterial cell wall synthesis and peptidoglycan cross-linking Cefoxitin sodium salt exerts its biological activity primarily through inhibition of cell wall synthesis by binding to PBPs In in vitro enzymatic assays Cefoxitin sodium salt demonstrates inhibitory activity against various gram-positive and gram-negative bacteria with previously reported IC50 values in the low micromolar range due to its resistance to certain beta-lactamases including AmpC -lactamases Based on these pharmacological properties Cefoxitin sodium salt holds research potential in investigations of bacterial resistance mechanisms antimicrobial sensitivity profiling and beta-lactamase enzyme kinetics
Medchemexpress LLC DG013B formate | 99.6% | 650.66 | C30H43N4O10P | 5 MG
DG013B formate is an epimeric phosphinic acid tripeptide-mimetic compound with weak affinity for ERAP1 and ERAP2. It is commonly used as a negative control in biochemical and binding studies involving aminopeptidases and related analogues.
Medchemexpress LLC SMD-3040 (formate) | 3033109-92-8 | 99.8% | 989.2 g/mol | C53H68N10O7S | 10 MG
SMD-3040 formate is a research-grade PROTAC degrader that selectively targets SMARCA2, producing robust degradation (DC50: 12 nM; Dmax: 91%) and inhibiting proliferation of certain tumor cell lines. It has demonstrated in vivo antitumor activity in xenograft models and is supplied as the formate salt for laboratory research (not for human use).
- Potent SMARCA2 degradation (DC50: 12 nM; Dmax: 91%).
- Demonstrated in vivo antitumor activity in xenograft models.
- High chemical purity (~99.8%).
- Supplied as the formate salt for laboratory use.
- Suitable for cell-based and in vivo pharmacology studies (research use only).
- Recommended storage: 4°C sealed; in solvent: -80°C (6 months), -20°C (1 month).
eMolecules 3-(3-Bromo-phenoxy)-propionic acid | 18386-03-3 | MFCD00774355 | 1g
Combi-Blocks | 3-(3-Bromo-phenoxy)-propionic acid | 1g | 117555346 | SS-3244 | 95.000 | 18386-03-3 | MFCD00774355 | 245.072 | C9H9BrO3
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Apexbio Technology LLC CX-4945 sodium salt 1309357-15-0 50mg
CX-4945 sodium salt (Silmitasertib sodium salt CAS 1309357-15-0) is a potent and selective inhibitor of casein kinase 2 (CK2) effectively targeting both the CK2 and CK2 catalytic subunits By inhibiting CK2 activity CX-4945 disrupts signaling pathways involved in cell cycle progression transcriptional regulation and cell survival The compound exhibits oral bioavailability and is widely utilized in research focused on tumor biology mechanistic studies of signaling cascades and the functional characterization of protein kinases