Enamines
Sigma Aldrich Fine Chemicals Biosciences 1-Pyrrolidino-1-cyclopentene 98% | 7148-07-4 | MFCD00003162 | 10G
1-Pyrrolidino-1-cyclopentene 98% | Purity: 98% | Mol Wt: 137.22 | 7148-07-4 | MFCD00003162 | 10G
TARGETMOL CHEMICALS INC Cisatracurium besylate 50MG
Also available in 1 mL, 10 mg, 25 mg, 100 mg, 200 mg, 500 mg and bulk. Please contact Fisher for quotes. Cisatracurium besylate (51W89) is a nondepolarizing skeletal muscle relaxant intended for intravenous administration. Purity 98%
Medchemexpress LLC (S)-Nimodipine | 77940-93-3 | 99.9% | 418.44 | 1 MG
(S)-Nimodipine is an enantiomer of Nimodipine, a light-sensitive dihydropyridine calcium antagonist. This orally active and well-tolerated compound is utilized in the research of cerebrovascular disorders.
- Enantiomer of Nimodipine
- Orally active
- Dihydropyridine calcium antagonist
- Target: Calcium channel
- Pathway: Membrane transporter/ion channel; neuronal signaling
- Appearance: White to off-white solid
- Purity: 99.9%
- Molecular formula: C21H26N2O7
Apexbio Technology LLC Amlodipine Besylate 111470-99-6 10mM (in 1mL DMSO)
Amlodipine Besylate (CAS 111470-99-6) is a long-acting calcium channel blocker that reduces blood pressure primarily through inhibition of calcium ion influx via voltage-gated calcium channels Calcium channel modulation influences critical cellular signaling pathways In cortical neurons exposed to oxidative stress Amlodipine Besylate ( 5 M) preserves cellular viability by reducing oxidative damage enhancing pro-survival signals and suppressing apoptotic pathways It has also demonstrated proliferative effects on human epidermoid carcinoma (A431) cells Furthermore clinical studies indicate that Amlodipine Besylate decreases peripheral vascular resistance and myocardial oxygen demand in angina patients and effectively lowers arterial pressure in hypertensive feline models
Medchemexpress LLC (R)-Nimodipine | 77940-92-2 | 99.87% | 100 MG
(R)-Nimodipine is an orally active, blood-brain barrier-permeable L-type calcium channel blocker with an IC50 of 5 nM. It inhibits corticosterone release by blocking calcium channels on the hypothalamic-pituitary-adrenal axis, which can reverse immobilization stress-induced memory impairment and behavioral abnormalities. It is for research use only.
- Inhibits corticosterone release
- Reverses immobilization stress-induced memory impairment
- Used in studies related to aneurysmal subarachnoid hemorrhage
- Used in studies related to cerebral ischemia
- Used in studies related to epilepsy
- Used in studies related to age-related degenerative neurological diseases
- Used in studies related to alcohol intoxication
Medchemexpress LLC (R)-Nimodipine | 77940-92-2 | 99.9% | 50 MG
(R)-Nimodipine is an orally active, blood-brain barrier-permeable L-type calcium channel blocker with an IC50 of 5 nM. It inhibits corticosterone release by blocking calcium channels on the hypothalamic-pituitary-adrenal axis, which can reverse immobilization stress-induced memory impairment and behavioral abnormalities.
- Used in studies related to aneurysmal subarachnoid hemorrhage
- Used in studies related to cerebral ischemia
- Used in studies related to epilepsy
- Used in studies related to age-related degenerative neurological diseases
- Used in studies related to alcohol intoxication
Accela Chembio Inc Isopropyl 3-aminocrotonate | 100g | 14205-46-0 | MFCD00134272 | 97+% | Shelf Life: 1260 Days | Light Sensitive/+4
Isopropyl 3-aminocrotonate | 100g | 14205-46-0 | MFCD00134272 | 97+% | Shelf Life: 1260 Days | Light Sensitive/+4
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 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
Medchemexpress LLC Amlodipine Besylate, USP | 111470-99-6 | MFCD00887594 | >=98% | 1 G
Amlodipine besylate is an antianginal agent and an orally active dihydropyridine calcium channel blocker. It functions by blocking voltage-dependent L-type calcium channels, which inhibits the initial influx of calcium. This compound is suitable for research related to high blood pressure and cancer.
- Antianginal agent: Used in research for angina.
- Orally active: Convenient for oral administration in research settings.
- Dihydropyridine calcium channel blocker: A specific type of calcium channel blocker with a well-defined mechanism of action.
- Mechanism of action: Blocks voltage-dependent L-type calcium channels, inhibiting calcium influx.
- Versatile research applications: Applicable for research concerning high blood pressure and cancer.
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).
Medchemexpress LLC Amlodipine maleate | 88150-47-4 | 99.9% | 5 G
Amlodipine maleate is a dihydropyridine calcium channel blocker that acts as an orally active antianginal agent. It blocks voltage-dependent L-type calcium channels, inhibiting the initial influx of calcium. This compound is used in research for high blood pressure and cancer studies.
- Blocks voltage-dependent L-type calcium channels
- Inhibits initial influx of calcium
- Attenuates uridine 5′-triphosphate (UTP)-induced increases of intracellular calcium
- Inhibits store-operated calcium influx
Sigma Aldrich Fine Chemicals Biosciences Adrenochrome | 54-06-8 | MFCD00069732 | 250mg
AdrenochromePurity: | MW: 179.17 | 54-06-8 | MFCD00069732 | 250mg
Med Vet International AmLodipine Besylate Tablets (Norvsac), 10mg, 1000ct
VET LICENSE NEEDS TO BE PROVIDED IN 3-4 BUSINESS DAYS OR ORDER WILL BE CANCELLED
Amlodipine Besylate Tablets (norvsac), 10mg, 1000ct
Medchemexpress LLC PF-562271 besylate | 939791-38-5 | MFCD16038299 | 99.2% | 665.66 g·mol⁻¹ | C27H26F3N7O6S2 | 5 MG
PF-562271 besylate is a small-molecule, ATP-competitive, reversible inhibitor of focal adhesion kinase (FAK) and Pyk2 used in research to study FAK pathway modulation. It is supplied as the besylate salt for laboratory use and has been evaluated in preclinical and clinical studies.
- Potent ATP-competitive inhibitor of FAK and Pyk2 (IC50 1.5 nM and 13 nM).
- Reversible mechanism suitable for biochemical and cellular assays.
- Supplied as besylate salt for improved stability and handling.
- High chemical purity (99.17%) for reproducible results.
- Molecular weight 665.66 g·mol⁻¹, molecular formula C27H26F3N7O6S2.
- Intended for research use only; not for human or veterinary use.