Enamines

1-Morpholino-1-cyclohexene 97.0+%, TCI America™

CAS: 670-80-4 Molecular Formula: C10H17NO Molecular Weight (g/mol): 167.252 MDL Number: MFCD00006163 InChI Key: IIQFBBQJYPGOHJ-UHFFFAOYSA-N Synonym: 4-cyclohex-1-enyl-morpholine,1-morpholino-1-cyclohexene,1-morpholinocyclohexene,n-morpholino-1-cyclohexene,4-1-cyclohexen-1-yl morpholine,morpholine, 4-1-cyclohexen-1-yl,4-cyclohex-1-en-1-yl morpholine,4-1-cyclohexenyl morpholine,1-morpholin-1-ylcyclohexene,1-n-morpholino cyclohexene PubChem CID: 69589 IUPAC Name: 4-(cyclohexen-1-yl)morpholine SMILES: C1CCC(=CC1)N2CCOCC2

Felodipine 98.0+%, TCI America™

CAS: 72509-76-3 Molecular Formula: C18H19Cl2NO4 Molecular Weight (g/mol): 384.253 MDL Number: MFCD00868316 InChI Key: RZTAMFZIAATZDJ-UHFFFAOYSA-N Synonym: felodipine,plendil,flodil,munobal,renedil,dl-felodipine,perfudal,splendil,feloday,prevex PubChem CID: 3333 ChEBI: CHEBI:585948 IUPAC Name: 5-O-ethyl 3-O-methyl 4-(2,3-dichlorophenyl)-2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylate SMILES: CCOC(=O)C1=C(NC(=C(C1C2=C(C(=CC=C2)Cl)Cl)C(=O)OC)C)C

Medchemexpress LLC PF-562271 besylate | 939791-38-5 | 99.2% | 665.66 g·mol⁻¹ | C27H26F3N7O6S2 | 100 MG

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PF-562271 besylate is an ATP-competitive, reversible inhibitor of focal adhesion kinase (FAK) and Pyk2 that exhibits low-nanomolar potency and is used in biochemical and cellular research to probe FAK/Pyk2 signaling pathways.

• Potent inhibition of FAK and Pyk2 with IC50s of 1.5 nM and 13 nM.
• High purity suitable for research applications.
• Chemical formula C27H26F3N7O6S2; molecular weight 665.66 g·mol⁻¹.
• Available in multiple package sizes, including 100 mg.
• Storage: sealed at 4°C; in solvent: -80°C (6 months), -20°C (1 month).

Medchemexpress LLC (S)-Nimodipine | 77940-93-3 | 418.44 | 5 MG

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(S)-Nimodipine ((S)-BAY-e 9736) is an enantiomer of Nimodipine. 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.

• Target: Calcium channel
• Pathway: Membrane transporter/ion channel; neuronal signaling
• Storage (powder): -20°C for 3 years, 4°C for 2 years
• Storage (in solvent): -80°C for 6 months, -20°C for 1 month
• Solubility in vitro: DMSO: 100 mg/mL (238.98 mM; requires ultrasonic)

Medchemexpress LLC Mirogabalin besylate | 1138245-21-2 | MFCD31631215 | 99.6% | 367.46 | C18H25NO5S | 50 MG

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Mirogabalin besylate is a research-grade small molecule that acts as a selective, orally available ligand for the α2δ subunit of voltage-gated calcium channels. It is supplied as a high-purity solid with manufacturer documentation supporting identity, purity, and safe handling for laboratory research.

• High purity (99.6%) suitable for research applications.
• Molecular formula C18H25NO5S; molecular weight 367.46.
• Solid powder formulation supplied in a 50 MG unit.
• Store solid sealed at 4°C, away from moisture; in solution store at -80°C (6 months) or -20°C (1 month).
• Documentation available: datasheet, certificate of analysis, and safety data sheet.

Medchemexpress LLC Mirogabalin besylate | 1138245-21-2 | MFCD31631215 | 99.6% | 367.46 g·mol⁻¹ | C18H25NO5S | 1 ML

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Mirogabalin besylate is the besylate salt of mirogabalin, a selective ligand for the α2δ subunit of voltage-gated calcium channels used in preclinical research. Supplied as a ready-to-use solution in DMSO, it is intended for in vitro and related laboratory applications. Refer to the safety data sheet for handling and storage instructions.

• 10 mM solution in DMSO, 1 mL vial.
• High purity (99.6%) as supplied.
• Molecular weight 367.46 g·mol⁻¹.
• Molecular formula C18H25NO5S.
• Recommended storage: in solvent -80°C (up to 6 months) or -20°C (up to 1 month); solid 4°C (sealed).
• Intended for research use only.

Medchemexpress LLC Mirogabalin besylate | 1138245-21-2 | 99.6% | 367.46 g·mol⁻¹ | C18H25NO5S | 100 MG

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Mirogabalin besylate is a research-grade small molecule ligand for the α2δ subunit of voltage-gated calcium channels, provided as a solid and in solution formats for in vitro and preclinical studies. It is supplied with supporting documents (COA, SDS) and is intended for laboratory research use.

• Selective α2δ subunit ligand for calcium channels.
• High reported purity suitable for biochemical assays.
• White to off-white solid, supplied in multiple package sizes.
• Available as 10 mM solution in DMSO for ready-to-use assays.
• Certificate of analysis and safety data sheet available.
• Store sealed at 4°C; in solvent store at -80°C or -20°C as specified.

Medchemexpress LLC Nimodipine | 66085-59-4 | MFCD00153848 | 99.9% | 500 MG

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Nimodipine is an orally active, well-tolerated, and light-sensitive dihydropyridine calcium antagonist used for the research of cerebrovascular disorders.

• Orally active and well-tolerated dihydropyridine calcium antagonist.
• Light-sensitive compound.
• Molecular formula: C₂₁H₂₆N₂O₇.
• Molecular weight: 418.44.
• Appearance: Solid, light yellow to yellow.
• Shipping at room temperature.
• Storage at 4°C, protected from light.
• In solvent, store at -80°C for 6 months or -20°C for 1 month, protected from light.
• Soluble in DMSO: 100 mg/mL.

Medchemexpress LLC TO-1187 (TFA) | 98.4% | 795.72 | C36H36F3N9O9 | 10 MG

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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 Mirogabalin besylate | 1138245-21-2 | MFCD31631215 | 99.6% | 367.46 | C18H25NO5S | 10 MG

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Mirogabalin besylate is the besylate salt of a selective, orally available ligand for the α2δ subunit of voltage-gated calcium channels, provided for research use with manufacturer-specified purity, solubility, and storage recommendations.

• Selective α2δ ligand with low-nanomolar binding affinity to human α2δ-1 and α2δ-2.
• High purity: 99.57% (manufacturer stated).
• White to off-white solid suitable for analytical and preparative workflows.
• Available as small research packs and as DMSO solutions ready for use.
• Soluble in DMSO at 100 mg/mL; may require sonication and use of fresh DMSO.
• Storage: solid at 4°C sealed, solutions at -20°C to -80°C per stability guidance.
• For research use only; not for human or veterinary use and subject to territorial restrictions.