Enamines
Sigma Aldrich Fine Chemicals Biosciences Potassium indigotrisulfonate ozone-scavenging reagent | 67627-18-3 | MFCD00013160 | 5G
Potassium indigotrisulfonate ozone-scavenging reagent | Purity: >60% (HPLC) | Mol Wt: 616.72 | 67627-18-3 | MFCD00013160 | 5G
Medchemexpress LLC Nimodipine | 66085-59-4 | 99.9% | 1 ML
Nimodipine is an orally active, well-tolerated, and light-sensitive dihydropyridine calcium antagonist. It is primarily used for the research of cerebrovascular disorders and is intended for research use only.
- Orally active and well-tolerated
- Light-sensitive dihydropyridine calcium antagonist
- Used in research for cerebrovascular disorders
- Available as a light yellow to yellow solid
- For research use only
Sigma Aldrich Fine Chemicals Biosciences Amlodipine impurity G European Pharmacopoeia (EP) Reference Standard | 43067-01-2 | MFCD00194047 |
Amlodipine impurity G European Pharmacopoeia (EP) Reference Standard | Mol Wt: 335.78 | 43067-01-2 | MFCD00194047 |
Medchemexpress LLC (R)-Nimodipine | 77940-92-2 | 99.9% | 1 MG
(R)-Nimodipine | 77940-92-2 | 99.9% | 1 MG
Medchemexpress LLC (R)-Nimodipine ((R)-BAY-e 9736) | 77940-92-2 | 99.9% | 5 MG
(R)-Nimodipine ((R)-BAY-e 9736) | 77940-92-2 | 99.9% | 5 MG
Medchemexpress LLC Nimodipine (BAY-e 9736) | 66085-59-4 | 99.9% | 1 G
Nimodipine (BAY-e 9736) is an orally active, well-tolerated, and light-sensitive dihydropyridine calcium antagonist. It can be used for the research of cerebrovascular disorders.
- Orally active
- Well-tolerated
- Light-sensitive
- Dihydropyridine calcium antagonist
- Used for the research of cerebrovascular disorders
Sigma Aldrich Fine Chemicals Biosciences Nimodipine | 66085-59-4 | MFCD00153848 | 500MG
Nimodipine | Purity: >=98% (HPLC) | Mol Wt: 418.44 | 66085-59-4 | MFCD00153848 | 500MG
Medchemexpress LLC (R)-Amlodipine | 103129-81-3 | MFCD06809924 | 99.5% | 408.88 g/mol | C20H25ClN2O5 | 10 MG
(R)-Amlodipine is the R-enantiomer of amlodipine, a dihydropyridine L-type calcium channel inhibitor supplied as an off-white to light yellow solid for research use. It is commonly used in pharmacological and formulation studies that require the isolated enantiomer.
- High purity (99.45%).
- Molecular weight 408.88 g/mol.
- Chemical formula C20H25ClN2O5.
- Soluble in DMSO at 100 mg/mL; ultrasonic recommended.
- In vivo formulation protocols yield ≥2.5 mg/mL solubility in listed vehicles.
- Available in small research sizes (e.g., 10 mg).
- Storage: powder -20°C for up to 3 years; in solvent -80°C for 6 months or -20°C for 1 month.
Medchemexpress LLC TO-1187 (TFA) | 98.4% | 795.72 | C36H36F3N9O9 | 10 MG
TO-1187 TFA is a selective PROTAC degrader that targets HDAC6 and recruits cereblon to promote ubiquitination and proteasomal degradation of HDAC6. Supplied as a trifluoroacetic acid salt in solid form, it is intended as a research tool for cellular and preclinical studies investigating HDAC6 biology and PROTAC-mediated target removal.
- Selective HDAC6 degrader with DC50 of 5.81 nM.
- Engages cereblon to induce ubiquitination and proteasomal degradation.
- High chemical purity (98.4%) suitable for biochemical and cellular assays.
- Provided as a solid TFA salt for stable handling and storage.
- Includes analytical documentation such as COA, H NMR, LCMS, and RP-HPLC.
- Storage recommended at 4°C under nitrogen; in solvent store at -80°C (6 months) or -20°C (1 month).
Sigma Aldrich Fine Chemicals Biosciences Adrenochrome | 54-06-8 | MFCD00069732 | 250mg
AdrenochromePurity: | MW: 179.17 | 54-06-8 | MFCD00069732 | 250mg
Medchemexpress LLC Methyl but-3-enoate 25g
Methyl but-3-enoate is a drug intermediate for synthesis of various active compounds