Reactive Nonmetal Salts
LiChropur™ Methanesulfonic Acid, For HPLC, 99.5% (T), MilliporeSigma™ Supelco™
CAS: 75-75-2 Molecular Formula: CH4O3S Molecular Weight (g/mol): 96.10 MDL Number: MFCD00007518 InChI Key: AFVFQIVMOAPDHO-UHFFFAOYSA-N IUPAC Name: methanesulfonic acid SMILES: CS(O)(=O)=O
LiChropur™ Potassium phosphate dibasic, For HPLC, 99.0-101.0% (T), MilliporeSigma™ Supelco™
CAS: 11-4-7758 Molecular Formula: HK2O4P Molecular Weight (g/mol): 174.17 MDL Number: MFCD00011383 InChI Key: ZPWVASYFFYYZEW-UHFFFAOYSA-L Synonym: Dipotassium hydrogenphosphate; Dipotassium phosphate; sec.-Potassium phosphate IUPAC Name: dipotassium hydrogen phosphate SMILES: [K+].[K+].OP([O-])([O-])=O
Sulfanilic Acid 99.0+%, TCI America™
CAS: 121-57-3 Molecular Formula: C6H7NO3S Molecular Weight (g/mol): 173.186 MDL Number: MFCD00007886 InChI Key: HVBSAKJJOYLTQU-UHFFFAOYSA-N Synonym: sulfanilic acid,sulphanilic acid,p-aminobenzenesulfonic acid,sulfanilsaeure,aniline-4-sulfonic acid,benzenesulfonic acid, 4-amino,aniline-p-sulfonic acid,aniline-p-sulphonic acid,p-aminophenylsulfonic acid,sulfanilicacid PubChem CID: 8479 ChEBI: CHEBI:27500 IUPAC Name: 4-aminobenzenesulfonic acid SMILES: C1=CC(=CC=C1N)S(=O)(=O)O
Medchemexpress LLC Gypsogenin | 639-14-5 | 99.5% | 25 MG
Gypsogenin is a pentacyclic triterpenoid sapogenin (CAS 639-14-5) used for research. It has molecular formula C30H46O4 and a molecular weight of 470.68 g/mol, and is reported to show antiangiogenic activity and cytotoxicity against H460 cells. Typically supplied as a 25 mg research sample.
- High purity (≈99.5%).
- Soluble in DMSO (25 mg/mL); may require sonication and freshly opened DMSO.
- Recommended storage: 4°C; in solvent, -80°C (6 months) or -20°C (1 month); protect from light.
- Intended for research use; not for human or clinical use.
Medchemexpress LLC Gypsogenin | 639-14-5 | 99.5% | 5 MG
Gypsogenin is an oleanane-type triterpenoid shown to have antiangiogenic activity and significant cytotoxicity against H460 cells. It is supplied as a solid research reagent, typically dissolved in DMSO for biological assays and stored protected from light.
- Natural triterpenoid with antiangiogenic activity.
- Shows significant cytotoxicity against H460 cell line.
- Empirical formula C30H46O4 and molecular weight 470.7 g/mol.
- Purity typically 99.5% as supplied.
- Soluble in DMSO at 25 mg/mL; ultrasonic assistance recommended.
- Storage: 4°C protected from light; in solvent store at -80°C up to 6 months.
- Supplied as a 5 mg solid suitable for laboratory research use.
Medchemexpress LLC Bigelovin 10mg | 3668-14-2 | 304.34 | C17H20O5 | 10 MG
Bigelovin is a sesquiterpene lactone (CAS 3668-14-2; C17H20O5; MW 304.34) that acts as a selective retinoid X receptor α (RXRα) agonist. It suppresses tumor growth by inducing apoptosis and autophagy via inhibition of the mTOR pathway and modulation of reactive oxygen species (ROS). Supplied for research use with documented solubility and storage guidance.
- Selective retinoid X receptor α (RXRα) agonist activity.
- Induces apoptosis and autophagy in cancer model studies.
- Available in small research quantities suitable for in vitro and in vivo formulation.
- Includes detailed solubility and stock preparation guidance.
- Storage guidance provided: protect from light at 4°C; solvent storage conditions included.
Medchemexpress LLC IR415 25mg | 452967-14-5 | 296.34 | C13H14F2N4S | 25 MG
IR415 is a research compound that inhibits hepatitis B virus (HBV) replication by blocking HBx activity. It selectively binds HBx (reported Kd = 2 nM) and reverses HBx-mediated suppression of RNA interference; characterized for dose-dependent inhibition of HBx in vitro.
- Selective HBx inhibitor (Kd = 2 nM).
- Demonstrated dose-dependent inhibition of HBx activity in cell assays.
- Chemical formula C13H14F2N4S; molecular weight 296.34.
- High purity (reported ≥98% by HPLC).
- Available as a powdered research reagent; store powder at -20°C for long-term stability.
Medchemexpress LLC (R)-pirtobrutinib | 2101700-14-3 | 99.8% | C22H21F4N5O3 | 10MG
(R)-Pirtobrutinib is the R-enantiomer of pirtobrutinib (LOXO-305), a selective, non-covalent Bruton's tyrosine kinase (BTK) inhibitor used for biochemical and cellular research into BTK signaling and resistance mutations, including C481 substitutions. The compound is supplied as a high-purity solid with established solubility and storage profiles for laboratory use.
- High purity (99.8%).
- Selective, non-covalent BTK inhibitor active against C481 substitution mutations.
- Soluble in DMSO (≈200 mg/mL); ultrasonic assistance recommended.
- Light yellow to yellow solid appearance.
- Stable under defined storage: powder -20°C (3 years) or 4°C (2 years); in solvent -80°C (6 months) or -20°C (1 month).
- Intended for research use only.
Medchemexpress LLC Hh-Ag1.5 (SAg1.5) | 612542-14-0 | ≥98.0% | 526.04 | C28H26ClF2N3OS | 10MG
Hh-Ag1.5 is a small-molecule agonist of the Hedgehog signaling pathway that activates Smoothened (Smo) and induces Gli-dependent transcription. It is used in vitro to stimulate Hh signaling, with reported activity at subnanomolar concentrations and documented application in reprogramming and expansion of quiescent liver stem cells.
- Potent Hedgehog pathway agonist with EC50 ≈ 1 nM.
- Selective Smoothened (Smo) receptor agonist with Ki ≈ 0.52 nM.
- Facilitates expansion of quiescent liver stem cells in vitro at 5 μM.
- High purity suitable for cellular assays (≥98% by HPLC).
- Molecular weight 526.04; formula C28H26ClF2N3OS; soluble in DMSO.