Oxazinanes
![eMolecules Pharmablock / tert-butyl (3R5R)-3-amino-5-fluoropiperidine-1-carboxylate / 25mg / 551145590 / PBS63419 / 0.000 / 1932247-39-6 / [null] / 218.272 / C10H19FN2O2](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502462618.JPG-250.jpg)
eMolecules Pharmablock / tert-butyl (3R5R)-3-amino-5-fluoropiperidine-1-carboxylate / 25mg / 551145590 / PBS63419 / 0.000 / 1932247-39-6 / [null] / 218.272 / C10H19FN2O2
Pharmablock / tert-butyl (3R5R)-3-amino-5-fluoropiperidine-1-carboxylate / 25mg / 551145590 / PBS63419 / 0.000 / 1932247-39-6 / [null] / 218.272 / C10H19FN2O2
TARGETMOL CHEMICALS INC AT-121 hydrochloride 1MG
Also available in 5 mg, 10 mg, 25 mg, 50 mg and bulk. Please contact Fisher for quotes. AT-121 hydrochloride is a dual agonist of nociception and mu opioid receptor with Ki values of 3.67 and 16.49 nM, respectively.AT-121 hydrochloride is a safe, non-addictive, pain relieving compound with anti-injury and analgesic activity. AT-121 hydrochloride is a safe, non-addictive, pain relieving compound with anti-injury and analgesic activity. Purity 97.28%
Cayman Chemical SH1152 hydrochloride
A potent, specific, ATP-competitive, and cell permeable inhibitor of ROCK (Ki = 1.6 nM); more potent inhibitor of ROCK than either Y-27632 (Ki = 140 nM) or HA-1077 (Ki = 330 nM); poorly inhibits PKA, PKC, and MLCK
TARGETMOL CHEMICALS INC FILAMINAST 5MG
Also available in 1 mg 10 mg 25 mg 50 mg 100 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. Filaminast (UNII-CDD69JC61J) is an analog of a phosphodiesterase 4 inhibitor (PDE4 inhibitor) and roliplam which is used as an anti-asthma drug. purity: 99%
Medchemexpress LLC Tebanicline dihydrochloride | 209326-19-2 | 99.5% | C9H13Cl3N2O | 10MG
Tebanicline dihydrochloride is the dihydrochloride salt of tebanicline (ebanicline/ABT-594), a neuronal nicotinic acetylcholine receptor agonist reported to have potent analgesic activity. Supplied as a research-grade solid with supplier characterization and safety documentation, it is intended for in vitro and in vivo research where well-defined pharmacological activity is required.
- High purity suitable for research applications.
- Solid, white to off-white appearance for easy handling.
- Molecular formula C9H13Cl3N2O and molecular weight 271.57 g/mol.
- Available in multiple small pack sizes for dose-ranging studies.
- Provided with supplier datasheet and safety documentation.
Selleck Chemical LLC Kevetrin hydrochloride
Kevetrin hydrochloride (Thioureidobutyronitrile) is a water-soluble small molecule and activator of the tumor suppressor protein p53 with potential antineoplastic activity
Medchemexpress LLC 5-Methyl-2-(2H-1,2,3-triazol-2-yl)benzoic acid | 956317-36-5 | MFCD18382679 | C10H9N3O2 | 100 G
5-Methyl-2-(2H-1,2,3-triazol-2-yl)benzoic acid is a chemical compound primarily used as an intermediate in organic synthesis and medicinal chemistry, particularly in the synthesis of Suvorexant. It is intended for laboratory research purposes.
- Used as an intermediate in organic synthesis.
- Utilized in medicinal chemistry.
- Key component in the synthesis of Suvorexant.
- Stable under recommended storage conditions.
- Available as a solid.
- Melting point: 174-176 °C.
- Boiling point: 413 °C.
eMolecules Pharmablock (USA) Inc (2R)-2-(methoxymethyl)azetidine 1g 254809222 PBN20120953 935668-82-9 MFCD11977227 101.149 C5H11NO
Pharmablock (USA) Inc (2R)-2-(methoxymethyl)azetidine 1g 254809222 PBN20120953 935668-82-9 MFCD11977227 101.149 C5H11NO
Selleck Chemical LLC K-115 hydrochloride dihydrate
Ripasudil hydrochloride dihydrate is a potent ROCK inhibitor with IC50 of 51 nM and 19 nM for ROCK1 and ROCK2 respectively used for the treatment of glaucoma and ocular hypertension
Medchemexpress LLC Mirodenafil dihydrochloride | 862189-96-6 | 99.1% | 604.59 | 1 ML
Mirodenafil dihydrochloride is an orally active, potent, reversible, and selective phosphodiesterase 5 (PDE5) inhibitor. It also functions as a glucocorticoid receptor (GR) modulator and activates the Wnt/β-catenin signaling pathway. It is used in research for conditions such as erectile dysfunction (ED), Alzheimer's disease (AD), and systemic sclerosis (SSc).
- Exerts neuroprotective functions by activating the cGMP/PKG/CREB signaling pathway.
- Enhances neuronal survival by protecting mitochondrial membrane potential and inhibiting apoptosis.
- Inhibits GSK-3β signaling, reducing tau phosphorylation and decreasing Aβ production.
- Inhibits transcriptional activity and homodimerization of glucocorticoid receptor.
- Ameliorates dermal fibrosis in SSc mouse models by inhibiting TGF-β signaling pathway.
Selleck Chemical LLC Cefmenoxime hydrochloride S4647-100mg
Cefmenoxime (SCE-1365) a potent inhibitor of Enterobacteriaceae is a cephalosporin antibiotic that is administered intravenously or intramuscularly
Medchemexpress LLC W-13 hydrochloride | 88519-57-7 | MFCD00058030 | 99.9% | 349.28 g/mol | C14H18Cl2N2O2S | 1 ML
W-13 hydrochloride is a calmodulin antagonist used in research to probe calmodulin-dependent signaling and has been reported to inhibit growth of tamoxifen-resistant human breast cancer cells. The product is offered as solid powder in multiple sizes and as a ready-to-use 10 mM solution in DMSO for cell-based assays.
- Calmodulin antagonist activity suitable for signaling studies.
- Reported inhibition of tamoxifen-resistant breast cancer cell growth.
- Available as solid powder and 10 mM solution in DMSO for convenience.
- High purity for reproducible experimental results.
- Molecular weight 349.28 g/mol; CAS 88519-57-7.
TARGETMOL CHEMICALS INC LY 456236 HYDROCHLORIDE 5MG
Also available in 1 mg 10 mg 25 mg 50 mg 100 mg 500 mg and bulk. Please contact Fisher for quotes. LY 456236 hydrochloride (MPMQ hydrochloride) is an mGlu1 receptor antagonist with an ic50 value of 143 nM. LY456236 has selective non-competitive and oral activity and can inhibit the hydrolysis of inositol phosphate with IC50 of 0.145 uM. LY 456236 hydrochloride inhibited EGFR with IC50 of 0.91 uM. purity: 99%
Selleck Chemical LLC RS-102895 Hydrochloride
RS-102895 hydrochloride (HCl) is a potent antagonist of Chemokine (C-C motif) receptor 2 (CCR2) with IC50 of 360 nM and shows no effect on CCR1 RS-102895 hydrochloride also inhibits human 1a and 1d receptors rat brain cortex 5-HT1a receptor in cells with IC50s of 130 nM 320 nM 470 nM respectively