accessibility menu, dialog, popup

UserName
Viewing profile as user:

Reactive Nonmetal Salts

Reactive nonmetal salts are ionic compounds formed with elements classified as reactive nonmetals. These salts are available in a variety of chemical compositions and quantities, and most are formed from the five gaseous reactive nonmetals.

Filtered Search Results

Products from some of our suppliers do not display in filtered search results. Please clear all filters to see these products.

Narrow Results

Narrow Results

category

brands

  • (1)
  • (2)
  • (11)

special interests

  • (14)

Search Within Results
Keyword Search:
1 – 14 of 14 results
1

Medchemexpress LLC ((1R,2S,4R)-4-((5-(1-(3-bromobenzyl)-1H-pyrazole-3-carbonyl)pyrimidin-4-yl)amino)-2-hydroxycyclopentyl)methyl sulfamate | 1644342-14-2 | 99.8% | 551.41 | 1 ML
SDP

ML-792 is a potent and selective inhibitor of SAE/SUMO1 and SAE/SUMO2 in enzymatic assays with IC50 values of 3 and 11 nM, respectively. It shows significantly less activity against NAE/NEDD8 and UAE/ubiquitin. This compound inhibits SAE and SUMO-pathway activities in HCT116 cells, and decreases cancer cell viability in various cancer cell lines. This compound is for research use only.

  • Potent and selective inhibitor of SAE/SUMO1 and SAE/SUMO2.
  • Inhibits SAE and SUMO-pathway activities in HCT116 cells.
  • Inhibits cell proliferation and decreases cancer cell viability in various cancer cell lines (MDA-MB-468, MDA-MB-231, HCT116, Colo-205, and A375).

ENCOMPASS_PREFERRED
2

Enzo Life Sciences MnTMPyP. pentachloride (10mg)
SDP

Cell permeable superoxide dismutase (SOD) mimetic and peroxynitrite scavenger. Catalyzes the dismutation of O2- even in the presence of excess EDTA. Displays a protective effect against H2O2 mediated injury in astroglial cells. Purity: ≥95% (TLC). Solubility: Soluble in water or aqueous buffers (e.g. 0.1M TRIS-HCl, pH 9.0 containing 1mM EDTA (>50mg/ml) or PBS, pH 7.2 (4mg/ml)). Long Term Storage: -20°C.

ENCOMPASS_PREFERRED
3

Enzo Life Sciences MnTMPyP. pentachloride (50mg)
SDP

Cell permeable superoxide dismutase (SOD) mimetic and peroxynitrite scavenger. Catalyzes the dismutation of O2- even in the presence of excess EDTA. Displays a protective effect against H2O2 mediated injury in astroglial cells. Purity: ≥95% (TLC). Appearance: Black crystalline powder. Solubility: Soluble in water or aqueous buffers (e.g. 0.1M TRIS-HCl, pH 9.0 containing 1mM EDTA (>50mg/ml) or PBS, pH 7.2 (4mg/ml)). Long Term Storage: -20°C.

ENCOMPASS_PREFERRED
4

AdipoGen MnTMPyP pentachloride
SDP

Chemical. CAS 100012-18-8. Formula C44H36MnN8Cl5. MW 909. Cell permeable superoxide dismutase SOD mimetic. Peroxynitrite scavenger. Displays a protective effect against H2O2 mediated injury. Neuroprotective. Oxidative stress inhibitor. Apoptosis inhibitor. Reduces inflammation.

ENCOMPASS_PREFERRED
5

Medchemexpress LLC Hh-Ag1.5 (SAg1.5) | 612542-14-0 | ≥98.0% | 526.04 | C28H26ClF2N3OS | 10MG
SDP

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.

ENCOMPASS_PREFERRED
6

Medchemexpress LLC ML-792 | 1644342-14-2 | 99.8% | 551.41 | 50 MG
SDP

ML-792 is a potent and selective inhibitor of SAE/SUMO1 and SAE/SUMO2 in enzymatic assays, with IC50 values of 3 nM and 11 nM, respectively. It demonstrates significantly less activity against NAE/NEDD8 and UAE/ubiquitin. This product is for research use only.

  • Potent and selective inhibitor of SAE/SUMO1 and SAE/SUMO2.
  • IC50 values of 3 nM for SAE/SUMO1 and 11 nM for SAE/SUMO2.
  • Significantly less activity against NAE/NEDD8 and UAE/ubiquitin.
  • Purity: 99.76%.
  • CAS number: 1644342-14-2.
  • Molecular weight: 551.41.
  • Appearance: solid, white to off-white.
  • Inhibits SAE and SUMO-pathway activities in HCT116 cells.
  • Inhibits cell proliferation and decreases cancer cell viability.
  • Demonstrates dose-dependent viability effect.
  • Revealed dose-dependent decrease in SAE and UBC9 thioester levels.
  • Soluble in DMSO: 100 mg/mL (181.35 mM).

ENCOMPASS_PREFERRED
7

Medchemexpress LLC Gypsogenin | 639-14-5 | 99.5% | 5 MG
SDP

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.

ENCOMPASS_PREFERRED
8

Medchemexpress LLC Yangambin | 13060-14-5 | MFCD04307767 | 5 MG
SDP

Yangambin is a furofuran lignan isolated from various plants. It functions as a selective PAF receptor antagonist and inhibits Ca2+ influx through voltage-gated Ca2+ channels, reducing intracellular Ca2+ in vascular smooth muscle cells, which leads to peripheral vasodilation. This compound also exhibits antiallergic and anti-inflammatory activities.

  • Selective PAF receptor antagonist
  • Inhibits Ca2+ influx through voltage-gated Ca2+ channels
  • Reduces intracellular Ca2+ in vascular smooth muscle cells
  • Demonstrates antiallergic activity (IC50 of 33.8 μM)
  • Demonstrates anti-inflammatory activity (IC50 of 37.4 μM)
  • Purity: 98.27%
  • Molecular weight: 446.49
  • Formula: C24H30O8
  • Appearance: Solid, white to off-white
  • For research use only

ENCOMPASS_PREFERRED
9

Medchemexpress LLC Gypsogenin | 639-14-5 | 99.5% | 25 MG
SDP

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.

ENCOMPASS_PREFERRED
10

Medchemexpress LLC IR415 25mg | 452967-14-5 | 296.34 | C13H14F2N4S | 25 MG
SDP

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.

ENCOMPASS_PREFERRED
11

Medchemexpress LLC Bigelovin 5mg | 3668-14-2 | 304.34 g/mol | C17H20O5 | 5 MG
SDP

Bigelovin is a sesquiterpene lactone research compound used to induce apoptosis and autophagy through reactive oxygen species-mediated inhibition of mTOR signaling. It is supplied for in vitro research use and is provided in small, high-purity quantities with specified storage conditions to preserve stability.

  • Induces apoptosis and autophagy via ROS-mediated mTOR pathway inhibition.
  • High purity suitable for in vitro research (product page lists 99.92%).
  • Molecular formula C17H20O5; molecular weight 304.34 g/mol.
  • Provided in small-quantity vials appropriate for cell-based assays and biochemical studies.
  • Store protected from light; refrigerated storage recommended; in solution store at low temperatures per datasheet.

ENCOMPASS_PREFERRED
12

Medchemexpress LLC Yangambin | 13060-14-5 | MFCD04307767 | 98.3% | 446.49 | C24H30O8 | 10 MG
SDP

Yangambin is a furofuran lignan supplied for laboratory research that functions as a calcium-channel inhibitor and platelet-activating factor (PAF) receptor antagonist. It reduces intracellular Ca2+ in vascular smooth muscle cells and has reported antiallergic and anti-inflammatory activity in vitro.

  • Acts as a calcium-channel inhibitor and PAF receptor antagonist.
  • Shows antiallergic and anti-inflammatory activity in vitro.
  • High purity (≈98.3%), suitable for biochemical and pharmacological assays.
  • Soluble in DMSO (50 mg/mL) and compatible with several in vivo formulations (≥1.25 mg/mL reported).
  • Furofuran lignan chemical class, C24H30O8, MW 446.49 Da.
  • Store at 4°C protected from light; in solution store at -80°C (6 months) or -20°C (1 month).

ENCOMPASS_PREFERRED
13

Medchemexpress LLC 3-chloro-4,7-difluoro-N-[trans-4-(methylamino)cyclohexyl]-N-[[3-(4-pyridinyl)phenyl]methyl]-benzo[b]thi | 612542-14-0 | MFCD12032128 | 99.9% | 526.04 | C28H26ClF2N3OS | 25MG
SDP

Hh-Ag1.5 (SAg1.5) is a potent small-molecule agonist of the Hedgehog signaling pathway that activates the Smoothened (Smo) receptor. It is supplied as a white to off-white solid with high reported purity and is used as a research tool to activate Hh signaling in cellular and in vivo studies. The compound is highly soluble in DMSO and has documented storage recommendations for powder and solutions.

  • Potent Hedgehog pathway agonist with EC50 ≈ 1 nM.
  • Activates Smoothened to induce downstream GLI transcription activity.
  • High purity suitable for research (99.9%).
  • Soluble in DMSO at 50 mg/mL; in vivo formulations achievable at ≥2.5 mg/mL.
  • Stable as powder when stored cold; aliquot solutions to avoid freeze-thaw.
  • Demonstrated biological activity in liver stem cell expansion at 5 μM in vitro.

ENCOMPASS_PREFERRED
14

Medchemexpress LLC 3-chloro-4,7-difluoro-N-[4-(methylamino)cyclohexyl]-N-[(3-pyridin-4-ylphenyl)methyl]-1-benzothiophen | 612542-14-0 | 99.9% | 526.04 | C28H26ClF2N3OS | 50MG
SDP

Hh-Ag1.5 is a potent small-molecule agonist of the Hedgehog signaling pathway (EC50 ≈ 1 nM) for use in in vitro and in vivo pathway activation and stem-cell reprogramming studies. Supplied as a white to off-white solid at high purity, it is formulated for research and preclinical applications.

  • Potency: EC50 1 nM (Hedgehog)
  • CAS number: 612542-14-0
  • Molecular formula: C28H26ClF2N3OS
  • Molecular weight: 526.04
  • Purity: 99.9%
  • Appearance: white to off-white solid
  • Solubility: DMSO 50 mg/mL (use fresh DMSO; ultrasonic may be required)
  • Storage: powder -20°C (3 years), 4°C (2 years)
  • Typical pack sizes: 1 mg, 5 mg, 10 mg, 25 mg, 50 mg, 100 mg

ENCOMPASS_PREFERRED