Carboxylic acid salts
TARGETMOL CHEMICALS INC BAY-299 5MG
Also available in 10 mg 25 mg 50 mg 100 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. BAY-299 is an effecitve inhibitor of the bromodomain and PHD finger family member BRPF2 and the TATA box binding protein-associated factors TAF1 and TAF1L with IC50s of 67 nM 8 nM and 106 nM respectively. purity: 97%
eMolecules Embonic acid disodium salt monohydrate | 6640-22-8 | MFCD00150357 | 5g
Combi-Blocks, Inc. | Embonic acid disodium salt monohydrate | 5g | 569289880 | QN-0217 | 95.000 | 6640-22-8 | MFCD00150357 | 450.354 | C23H16Na2O7
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Medchemexpress LLC NADH (disodium salt) | 606-68-8 | 98.8% | 709.40 | 100 MG
NADH disodium salt is an orally active reduced coenzyme. It acts as a donor of ADP-ribose units in ADP-ribosylation reactions and a precursor of cyclic ADP-ribose. This compound functions as a regenerative electron donor in cellular energy metabolism, participating in processes such as glycolysis, β-oxidation, and the tricarboxylic acid (TCA) cycle.
- Orally active reduced coenzyme
- Donor of ADP-ribose units
- Precursor of cyclic ADP-ribose
- Plays a role as a regenerative electron donor in cellular energy metabolism, including glycolysis, β-oxidation and the tricarboxylic acid (TCA) cycle
Medchemexpress LLC Suramin sodium salt | 129-46-4 | 100.0% | 25 MG
Suramin sodium salt is a reversible and competitive protein-tyrosine phosphatases (PTPases) inhibitor. It also acts as a potent inhibitor of sirtuins (SirT1, SirT2, and SirT5) and a competitive inhibitor of reverse transcriptase (DNA topoisomerase II). Additionally, this agent is a potent SARS-CoV-2 RNA-dependent RNA polymerase (RdRp) inhibitor, efficiently inhibits IP5K, and functions as an antiparasitic, anti-neoplastic, and anti-angiogenic agent, intended for research use only.
- Reversible and competitive protein-tyrosine phosphatases (PTPases) inhibitor.
- Potent inhibitor of sirtuins (SirT1, SirT2, and SirT5).
- Competitive inhibitor of reverse transcriptase (DNA topoisomerase II).
- Potent SARS-CoV-2 RNA-dependent RNA polymerase (RdRp) inhibitor.
- Efficiently inhibits IP5K.
- Acts as an antiparasitic, anti-neoplastic, and anti-angiogenic agent.
- Intended for research use only.
Medchemexpress LLC 1-palmitoyl-2-oleoyl-sn-glycero-3-phospho-(1'-rac-glycerol) | 268550-95-4 | 99.2% | 25 MG
POPG sodium salt is a negatively charged phospholipid that influences the interactions of membrane proteins with other molecules by altering the charge characteristics of the lipid environment. It increases the apparent affinity of Gαq and Gβ1γ1 for activated NTS1, interacts with the positive charge of peptides, and is useful in Parkinson's disease research.
- Used in the preparation of nanoparticles for co-encapsulating and releasing hydrophilic peptide compounds.
- Increases the apparent affinity of Gαq and Gβ1γ1 for activated NTS1.
- Forms bilayers that can be penetrated by the antimicrobial peptide LL-37.
- Enhances the binding of the PAP248-286 peptide in membranes.
- Useful in Parkinson's disease research.
Medchemexpress LLC NADP disodium salt | 24292-60-2 | 98.8% | 789.39 | 1 ML
NADP disodium salt is a coenzyme involved in cellular electron transfer reactions in biological metabolism. It maintains cellular redox homeostasis, regulates many biological events, and provides reducing ability for synthetic metabolic reactions and redox balance. NADPH, derived from NADP, plays a multifunctional role in regulating inflammation, redox homeostasis, and synthetic metabolism processes.
- Disodium salt form of NADP.
- Coenzyme involved in cellular electron transfer reactions.
- Alternately oxidized (NADP+) and reduced (NADPH).
- Maintains cellular redox homeostasis.
- Regulates many biological events, including cellular metabolism.
- NADPH is a universal electron donor.
- Provides reducing ability for synthetic metabolic reactions and redox balance.
- Regulates inflammation, redox homeostasis, and synthetic metabolism processes.
Apexbio Technology LLC Cefotaxime (sodium salt)(Synonyms: Claforan, Cefotaxime Sodium, Cefotaxim sodium salt, Cefotaxime Na, Sodium cefotaxime), 10mM (in 1mL DMSO), 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
eMolecules p-Nitrophenyl formate | 1865-01-6 | MFCD00014713 | 5g
Oakwood Chemical | p-Nitrophenyl formate | 5g | 537721172 | 341922 | | 1865-01-6 | MFCD00014713 | 167.120 | C7H5NO4
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eMolecules DL-Malic acid disodium salt | 676-46-0 | MFCD00012466 | 25g
Combi-Blocks | DL-Malic acid disodium salt | 25g | 485192103 | QF-0093 | 95.000 | 676-46-0 | MFCD00012466 | 178.051 | C4H4Na2O5
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