Vinyl halides
Medchemexpress LLC Alizarin Red S sodium | 130-22-3 | 25 MG
Alizarin Red S sodium is an anthraquinone-derived dye that binds calcium ions and is used to stain mineralized deposits in biological samples. It is commonly used in histology and cell biology to assess osteoblast differentiation and bone formation.
- Stains calcium deposits for histology and cell-based assays.
- Forms complexes with calcium for visualization of mineralized matrix.
- Water-soluble sodium salt suitable for aqueous staining procedures.
- Supplied in small laboratory quantities for research use.
Cayman Chemical DmyoInositol1phosphate sodiu
A synthetic, pure phosphoinositol for signal transduction research; can be formed by PLC hydrolysis of phosphatidylinositol or by dephosphorylation of polyphosphate inositols such as Ins(1,3)P2 by inositol polyphosphate 3-phosphatase
Medchemexpress LLC Croscarmellose sodium | 74811-65-7 | 50 MG
Croscarmellose sodium is a pharmaceutical additive approved by the FDA, functioning as an excipient. It acts as a suspending agent, binder, glidant, antiadherent, and disintegrant, improving the stability, solubility, and processability of pharmaceutical preparations and affecting co-administered drug ADME processes.
- Approved by the US Food and Drug Administration (FDA).
- Functions as a suspending agent, binder, glidant, antiadherent, and disintegrant.
- Improves stability, solubility, and processability of pharmaceutical preparations.
- Affects ADME processes of co-administered drugs.
- Promotes dissolution of poorly soluble compounds in water.
- Improves fluidity of drugs as a lubricant in tablets.
- Prevents drug particles from adhering to molds.
- Accelerates drug release and absorption in the gastrointestinal tract.
- Used for thickening or stabilization in the food industry.
Medchemexpress LLC Croscarmellose sodium | 74811-65-7 | 500 MG
Croscarmellose sodium is a pharmaceutical additive approved by the FDA, serving as an excipient to enhance the stability, solubility, and processability of pharmaceutical preparations. It plays a role in the dissolution of poorly soluble compounds, acts as a suspending agent, and improves drug fluidity in tablets. Additionally, it is utilized in the food industry for thickening or stabilization.
- Functions as a suspending agent, binder, glidant, antiadherent, and disintegrant.
- Improves stability, solubility, and processability of pharmaceutical preparations.
- Promotes dissolution of poorly soluble compounds in water.
- Acts as a lubricant in tablets to improve drug fluidity.
- Prevents drug particles from adhering to molds.
- Accelerates drug release and absorption in the gastrointestinal tract.
- Used for thickening or stabilization in the food industry.
Medchemexpress LLC Flucloxacillin sodium | 1847-24-1 | 98.0% | C19H16ClFN3NaO5S | 1 ML
Flucloxacillin sodium is an active antibiotic effective against gram-positive and gram-negative bacteria. It is for research use only and not sold to patients. In a study with male Wistar rats, Flucloxacillin sodium (200 mg/kg; i.p.; three times/day, for 21 days) was effective against common bacterial strains in periprosthetic infection, leading to reduced germs in the biofilm and bone tissue.
- Active against gram-positive and gram-negative bacteria.
- Effective in reducing germs in biofilm and bone tissue in a rat study.
- For research use only.
Medchemexpress LLC Flucloxacillin sodium | 1847-24-1 | 98.0% | C19H16ClFN3NaO5S | 1 G
Flucloxacillin sodium is an active antibiotic that effectively targets both gram-positive and gram-negative bacteria. With a purity of 98.02%, it is commonly used in research and has shown efficacy in reducing germs in biofilm and bone tissue in periprosthetic infections. This compound is also being investigated in various clinical trials for conditions such as cellulitis, wound infection, and osteomyelitis.
- Active against gram-positive and gram-negative bacteria
- Effective in periprosthetic infection models
- Reduces germs in biofilm and bone tissue
- Purity of 98.02%
- Soluble in water and DMSO
- Involved in clinical trials for various bacterial infections
Accela Chembio Inc Ethyl 3-chloro-5-(trifluoromethyl)-2-pyridinecarboxylate | 5g | 128073-16-5 | MFCD06656414 | 97+% | Shelf Life: 1080 Days | Light Sensitive/n2/+4
Ethyl 3-chloro-5-(trifluoromethyl)-2-pyridinecarboxylate | 5g | 128073-16-5 | MFCD06656414 | 97+% | Shelf Life: 1080 Days | Light Sensitive/n2/+4
eMolecules 3-Chlorophthalic anhydride, tech grade | Combi-Blocks | 117-21-5 | MFCD00023107 | 182.560 | C8H3ClO3 | 80.000 | Clc1cccc2C(=O)OC(=O)c12 | 100g | 257648523
3-Chlorophthalic anhydride, tech grade | Combi-Blocks | 117-21-5 | MFCD00023107 | 182.560 | C8H3ClO3 | 80.000 | Clc1cccc2C(=O)OC(=O)c12 | 100g | 257648523
Medchemexpress LLC Rp-8-Br-cAMPS sodium | 925456-59-3 | 446.15 | 1 MG
Rp-8-Br-cAMPS sodium is an analog of cAMP and an inhibitor of PKA. It occupies cAMP binding sites on PKA type I regulatory subunits, preventing PKA dissociation and activation. It can be used in the study of tumors and retrovirus-induced immune deficiency. Rp-8-Br-cAMPS sodium also inhibits insulin secretion.
- Completely blocks the ability of 2-chloroadenosine to inhibit LAK cytotoxicity.
- Significantly reduces the inhibitory effect of 2-chloroadenosine on cytokine production.
- Inhibits insulin secretion in 832/13 cells.
- Improves immune function in a mouse retrovirus infection model.
Cayman Chemical DmyoInositol1phosphate sodiu
A synthetic, pure phosphoinositol for signal transduction research; can be formed by PLC hydrolysis of phosphatidylinositol or by dephosphorylation of polyphosphate inositols such as Ins(1,3)P2 by inositol polyphosphate 3-phosphatase
Matrix Scientific 2-BROMO-2-BUTENE-25G
2-Bromo-2-butene, 98%; 25g,C4H7Br, MFCD00000141, mw 135.01, [13294-71-8]
Medchemexpress LLC Silmitasertib sodium salt | 1309357-15-0 | 99.9% | C19H11ClN3NaO2 | 5 MG
Silmitasertib sodium salt is an orally bioavailable, highly selective, and potent CK2 inhibitor (IC50 values of 1 nM against CK2α and CK2α'). It induces cell-cycle arrest and selectively causes apoptosis in cancer cells, attenuates PI3K/Akt signaling, and demonstrates antiproliferative activity correlating with CK2α catalytic subunit expression. It also prevents leukemic cells from engaging a functional UPR to buffer proteotoxic stress and decreases pro-survival ER chaperon BIP/Grp78 expression.
- Causes cell-cycle arrest
- Induces apoptosis in cancer cells
- Attenuates PI3K/Akt signaling
- Exhibits antiproliferative activity
- Prevents leukemic cells from engaging a functional UPR
- Decreases pro-survival ER chaperon BIP/Grp78 expression
- Induces cytotoxicity
- Suppresses CK2-mediated PI3K/Akt/mTOR signaling pathways
- Demonstrates robust antitumor activity in murine xenograft models
Cayman Chemical DmyoInositol3phosphate sodiu
Synthetic, pure phosphoinositol for signal transduction research; can be formed by the dephosphorylation of polyphosphate inositols such as Ins(3,4)P2 by inositol polyphosphate 4-phosphatase
Cayman Chemical DmyoInositol1phosphate sodiu
A synthetic, pure phosphoinositol for signal transduction research; can be formed by PLC hydrolysis of phosphatidylinositol or by dephosphorylation of polyphosphate inositols such as Ins(1,3)P2 by inositol polyphosphate 3-phosphatase