Alpha-halocarboxylic acids and derivatives

Cayman Chemical W140 trifluoroacetate salt

An inactive enantiomer of W146; binds weakly to S1P1 (Ki = 4.6 µM for the human receptor); has been used as a negative control in the study of S1P1 receptor signaling

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Cayman Chemical AcDEVDCHO trifluoroacetate s

A potent, reversible inhibitor of caspase-3 and caspase-7 (Kis = 0.23 and 1.6 nM, respectively); also inhibits other caspases (Kis = 18, 1710, 132, 205, 31, 0.92, 60, and 12 nM for caspases-1, -2, -4, -5, -6, -8, -9, and -10, respectively)

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Cayman Chemical AcDEVDCHO trifluoroacetate s

A potent, reversible inhibitor of caspase-3 and caspase-7 (Kis = 0.23 and 1.6 nM, respectively); also inhibits other caspases (Kis = 18, 1710, 132, 205, 31, 0.92, 60, and 12 nM for caspases-1, -2, -4, -5, -6, -8, -9, and -10, respectively)

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Sigma Aldrich Fine Chemicals Biosciences Sodium iodoacetate BioUltra, >=98% | 305-53-3 | MFCD00002686 | 5G

Sodium iodoacetate BioUltra, >=98% | Purity: >=98% | Mol Wt: 207.93 | 305-53-3 | MFCD00002686 | 5G

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Chem-Impex International, Inc. Bromoacetic acid | MFCD00002678 | 100G

Bromoacetic acid, MFCD00002678, 100G

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Sigma Aldrich Fine Chemicals Biosciences Ethyl bromoacetate-2-13C 99 atom % 13C | 85539-84-0 | MFCD00000193 | 1G

Ethyl bromoacetate-2-13C 99 atom % 13C | Purity: 99% (CP) | Mol Wt: 167.99 | 85539-84-0 | MFCD00000193 | 1G

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Sigma Aldrich Fine Chemicals Biosciences Sodium chloroacetate | 3926-62-3 | MFCD00002684 | 25g

Sodium chloroacetate | Purity: 98% | MW:116.48 | 3926-62-3 | MFCD00002684 | 25g

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Chem-Impex International, Inc. 2-Bromopropionic acid | 598-72-1 | MFCD00004211 | 250G

2-Bromopropionic acid, 598-72-1, MFCD00004211, 250G

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Cayman Chemical FAmidine trifluoroacetate sa

A PAD inhibitor (IC50s = 29.5 and 350 µM for PAD1 and PAD3, respectively, in vitro; irreversibly inactivates four PAD subtypes (kinact/KI = 2,800, 380, 170, and 3,000 M-1min-1); cytotoxic to HL-60, MCF-7, and HT-29 cancer cell lines (IC50s = 0.5, 0.5 and 1 μM, respectively)

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Cayman Chemical AcDEVDCHO trifluoroacetate s

A potent, reversible inhibitor of caspase-3 and caspase-7 (Kis = 0.23 and 1.6 nM, respectively); also inhibits other caspases (Kis = 18, 1710, 132, 205, 31, 0.92, 60, and 12 nM for caspases-1, -2, -4, -5, -6, -8, -9, and -10, respectively)

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Medchemexpress LLC Pitavastatin-d5 sodium | 574705-92-3 | 99.5% | 1 MG

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Pitavastatin-d5 sodium is the deuterium-labeled Pitavastatin sodium. Pitavastatin (NK-104) is a potent hydroxymethylglutaryl-CoA (HMG-CoA) reductase inhibitor, inhibiting cholesterol synthesis with an IC50 of 5.8 nM in HepG2 cells. It also acts as an efficient hepatocyte low-density lipoprotein-cholesterol (LDL-C) receptor inducer and exhibits anti-cancer activity.

• Can be used as a tracer
• Internal standard for quantitative analysis by NMR, GC-MS, or LC-MS
• Potent HMG-CoA reductase inhibitor
• Inhibits cholesterol synthesis from acetic acid
• Efficient hepatocyte low-density lipoprotein-cholesterol (LDL-C) receptor inducer
• Exhibits anti-cancer activity

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Ambeed AMBEED

5000893216 SODIUM PROPANE-2-SULFINA 250MG

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CAMBRIDGE ISOTOPE LABORATORIES SODIUM TRIFLUOROACETATE 50UG

NC3072552 SODIUM TRIFLUOROACETATE 50UG

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Ambeed AMBEED

5000882237 BROMOACETIC ACID N-HYDRO 5G

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Sigma Aldrich Fine Chemicals Biosciences Bromoacetic acid-d3 98 atom % D | 14341-48-1 | MFCD00190384 | 5G

Bromoacetic acid-d3 98 atom % D | Purity: 99% (CP) | Mol Wt: 141.97 | 14341-48-1 | MFCD00190384 | 5G

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