Enamines
eMolecules 391624-46-7 | (9H-Fluoren-9-yl)Methyl (2-Aminoethyl)Carbamate Hydrochloride | AA Blocks LLC | MFCD00830741 | 318.800 | C17H19ClN2O2 | 0.000 | Cl.NCCNC(=O)OCC1c2ccccc2-c2ccccc12 | 100g | 816441728
(9H-Fluoren-9-yl)Methyl (2-Aminoethyl)Carbamate Hydrochloride | AA Blocks LLC | 391624-46-7 | MFCD00830741 | 318.800 | C17H19ClN2O2 | 0.000 | Cl.NCCNC(=O)OCC1c2ccccc2-c2ccccc12 | 100g | 816441728
Selleck Chemical LLC PF-562271 Besylate S2672-1g
PF-562271 Besylate is the benzenesulfonate salt of PF-562271 which is a potent ATP-competitive reversible inhibitor of FAK with IC50 of 1 5 nM 10-fold less potent for Pyk2 than FAK and 100-fold selectivity against other protein kinases except for some CDKs Phase 1
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 Benzamide, n-hydroxy-3-[1-[(phenylthio)methyl]-1h-1,2,3-triazol-4-yl]- | 1316652-41-1 | MFCD21363002 | 99.3% | 326.37 g/mol | C16H14N4O2S | 10 MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000227030.png-250.jpg)
Medchemexpress LLC Benzamide, n-hydroxy-3-[1-[(phenylthio)methyl]-1h-1,2,3-triazol-4-yl]- | 1316652-41-1 | MFCD21363002 | 99.3% | 326.37 g/mol | C16H14N4O2S | 10 MG
NCC-149 is a selective histone deacetylase 8 (HDAC8) inhibitor used in neural differentiation research. It is a small-molecule benzamide derivative (C16H14N4O2S; MW 326.37 g/mol; CAS 1316652-41-1) supplied as a solid with documented purity and batch COA.
- Selective HDAC8 inhibitor useful for neural differentiation studies.
- Batch-specific purity reported at 99.3% (COA).
- Available as a small 10 MG solid suitable for research-scale experiments.
- Solid stable at -20°C for up to 3 years; solvent solutions require colder storage.
- Comes with COA, SDS, and product datasheet for quality and safety information.
eMolecules 354824-17-2 | 5-(Aminomethyl)-N,N-dimethylpyridin-2-amine | Combi-Blocks | MFCD08272104 | 151.213 | C8H13N3 | 98.000 | CN(C)c1ccc(CN)cn1 | 1g | 117575175
5-(Aminomethyl)-N,N-dimethylpyridin-2-amine | Combi-Blocks | 354824-17-2 | MFCD08272104 | 151.213 | C8H13N3 | 98.000 | CN(C)c1ccc(CN)cn1 | 1g | 117575175
eMolecules 14205-39-1 | METHYL 3-AMINOCROTONATE | AstaTech | MFCD00071534 | 115.132 | C5H9NO2 | 97.000 | COC(=O)\C=C(\C)N | 25g | 482916541
METHYL 3-AMINOCROTONATE | AstaTech | 14205-39-1 | MFCD00071534 | 115.132 | C5H9NO2 | 97.000 | COC(=O)\C=C(\C)N | 25g | 482916541
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
Sigma Aldrich Fine Chemicals Biosciences Nimodipine | 66085-59-4 | MFCD00153848 | 500MG
Nimodipine | Purity: >=98% (HPLC) | Mol Wt: 418.44 | 66085-59-4 | MFCD00153848 | 500MG
Apexbio Technology LLC Amlodipine 88150-42-9 1g
Amlodipine (CAS 88150-42-9) is a dihydropyridine-based small molecule that functions as a long-acting calcium channel blocker It selectively inhibits L-type calcium channels on vascular smooth muscle and cardiac myocytes thereby reducing intracellular calcium influx This action leads to vasodilation and decreased vascular resistance Amlodipine is widely utilized in biomedical research to investigate calcium signaling pathways vascular tone modulation and cardiovascular pharmacology Its mechanistic profile also makes it a reference compound in studies evaluating novel antihypertensive or vasodilatory agents
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 (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
Medchemexpress LLC (S)-Nimodipine | 77940-93-3 | 418.44 | 5 MG
(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)