Organonitrogen Compounds
Selleck Chemical LLC (1R.2R)-trans-N-Boc-1.2-cyclohexanediamine S3896-25mg
(1R 2R)-trans-N-Boc-1 2-cyclohexanediamine is an intermediate in organic synthesis
amido}(p-cymene)ruthenium(II), min. 95% RuCl[(R,R)-Tsdpen](p-cymene) | 192139-92-7 | | 1g](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502169480.JPG-250.jpg)
eMolecules Chloro{[(1R,2R)-(-)-2-amino-1,2-diphenylethyl](4-toluenesulfonyl)amido}(p-cymene)ruthenium(II), min. 95% RuCl[(R,R)-Tsdpen](p-cymene) | 192139-92-7 | | 1g
Strem Chemicals | Chloro{[(1R,2R)-(-)-2-amino-1,2-diphenylethyl](4-toluenesulfonyl)amido}(p-cymene)ruthenium(II), min. 95% RuCl[(R,R)-Tsdpen](p-cymene) | 1g | 321338507 | 44-0148 | 95.000 | 192139-92-7 | | 636.210 | C31H35ClN2O2RuS
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Medchemexpress LLC Phosphoenolpyruvic acid cyclohexylammonium salt | 10526-80-4 | 98.0% | 267.22 | 1 G
Phosphoenolpyruvic acid cyclohexylammonium salt | 10526-80-4 | 98.0% | 267.22 | 1 G
Medchemexpress LLC Phosphoenolpyruvic acid tricyclohexylammonium salt | 35556-70-8 | 99.7% | 465.56 | 5 MG
Phosphoenolpyruvic acid tricyclohexylammonium salt is a glycolysis metabolite featuring a high-energy phosphate group. It plays a role in both glycolysis and gluconeogenesis, serving as an energy source for ATP production under energy-limited conditions. Additionally, this compound demonstrates cytoprotective and anti-oxidative properties.
- Glycolysis metabolite.
- Contains a high-energy phosphate group.
- Involved in glycolysis and gluconeogenesis.
- Provides energy for ATP synthesis.
- Exhibits cytoprotective properties.
- Offers anti-oxidative benefits.
eMolecules 259214-55-6 | ChemScene | (1S2R)-1-((tert-Butoxycarbonyl)amino)-2-vinylcyclopropanecarboxylic acid | 1g | 536831138 | CS-B0184 | MFCD06795884 | 227.26 | C11H17NO4
Medchem Express | Nelociguat | 5mg | 437899540 | HY-78237 | 625115-52-8 | MFCD22741546 | 408.397 | C19H17FN8O2
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c1ccccc1)N1CCCC1 | 25g | 112528723](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502170171.JPG-250.jpg)
eMolecules 123620-80-4 | (1S,2R)-1-PHENYL-2-(1-PYRROLIDINYL)PROPAN-1-OL | AstaTech | MFCD02093492 | 205.301 | C13H19NO | 97.000 | C[C@H]([C@@H](O)c1ccccc1)N1CCCC1 | 25g | 112528723
(1S,2R)-1-PHENYL-2-(1-PYRROLIDINYL)PROPAN-1-OL | AstaTech | 123620-80-4 | MFCD02093492 | 205.301 | C13H19NO | 97.000 | C[C@H]([C@@H](O)c1ccccc1)N1CCCC1 | 25g | 112528723
eMolecules 102601-34-3 | CAPSO sodium salt | MFCD00070063 | 5g
Medchem Express | ALDH3A1-IN-1 | 5mg | 786489554 | HY-144670 | 1039855-56-5 | 250.298 | C13H18N2O3
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eMolecules 472-66-2 | 2,6,6-Trimethyl-1-cyclohexane-1-acetaldehyde | Oakwood Chemical | MFCD00012057 | 166.264 | C11H18O | 80.000 | CC1=C(CC=O)C(C)(C)CCC1 | 1g | 537710891
2,6,6-Trimethyl-1-cyclohexane-1-acetaldehyde | Oakwood Chemical | 472-66-2 | MFCD00012057 | 166.264 | C11H18O | 80.000 | CC1=C(CC=O)C(C)(C)CCC1 | 1g | 537710891
eMolecules 15827-56-2 | cis-1,4-Cyclohexanediamine | Chem-Impex | MFCD00035862 | 114.192 | C6H14N2 | 98.000 | NC1CCC(N)CC1 | 1g | 112760151
cis-1,4-Cyclohexanediamine | Chem-Impex | 15827-56-2 | MFCD00035862 | 114.192 | C6H14N2 | 98.000 | NC1CCC(N)CC1 | 1g | 112760151
Medchemexpress LLC DB-0646 | 2769753-59-3 | 98.0% | C52H51F3N14O7 | 10MG
DB-0646 is a proteolysis-targeting chimera (PROTAC) developed as a multi-kinase degrader for laboratory research. It induces ubiquitination and proteasomal degradation of target kinases and is supplied as a solid for biochemical and cellular studies. Intended for research use only; not for human or veterinary applications.
- Multi-kinase degrader mechanism suitable for kinase-targeted studies.
- High purity (98.0%) appropriate for in vitro assays.
- Molecular weight 1041.05 with formula C52H51F3N14O7.
- Available in small pack sizes for screening and optimization.
- Stable under recommended storage conditions; follow supplier guidance.
Medchemexpress LLC Phosphoenolpyruvic acid (tricyclohexylammonium salt) | 35556-70-8 | 99.7% | 465.56 | 5G
Phosphoenolpyruvic acid tricyclohexylammonium salt is a glycolysis metabolite with a high-energy phosphate group. It is involved in glycolysis and gluconeogenesis, and used as an energy source to produce ATP under energy-limited conditions. This compound also exhibits cytoprotective and anti-oxidative properties. It is for research use only.
- Glycolysis metabolite with a high-energy phosphate group
- Involved in glycolysis and gluconeogenesis
- Used as an energy source to produce ATP under energy-limited conditions
- Exhibits cytoprotective and anti-oxidative properties
- Appearance: Solid, White to off-white
- Initial source: Endogenous metabolite
- Shipping: Room temperature in continental US; may vary elsewhere
- Storage: -20°C, sealed storage, away from moisture
Medchemexpress LLC Phosphoenolpyruvic acid potassium | 4265-07-0 | 99.86% | 206.13 | 5 G
Phosphoenolpyruvic acid potassium is a glycolysis metabolite featuring a high-energy phosphate group. It plays a crucial role in glycolysis and gluconeogenesis, serving as an energy source to produce ATP under energy-limited conditions.
- Involved in glycolysis and gluconeogenesis.
- Functions as an energy source to produce ATP.
- Exhibits cytoprotective properties.
- Shows anti-oxidative properties.
Medchemexpress LLC Phosphoenolpyruvic acid potassium-13C2 | 201996-39-6 | 97.0% | 208.12 | 1 MG
Phosphoenolpyruvic acid (potassium)-13C2 is the 13C labeled version of Phosphoenolpyruvic acid potassium. This compound is a glycolysis metabolite that contains a high-energy phosphate group. It participates in both glycolysis and gluconeogenesis, serving as an energy source to generate ATP under conditions of limited energy. Additionally, Phosphoenolpyruvic acid potassium has demonstrated cytoprotective and anti-oxidative properties.
- 13C labeled compound, useful as a tracer.
- Can be utilized as an internal standard for quantitative analysis using methods like NMR, GC-MS, or LC-MS.
- Involved in glycolysis and gluconeogenesis.
- Acts as an energy source for ATP production in energy-limited conditions.
- Exhibits cytoprotective properties.
- Shows anti-oxidative properties.