Aminophenols
Medchemexpress LLC AT7519 Hydrochloride | 902135-91-5 | 98.6% | C16H18Cl3N5O2 | 25 MG
AT7519 Hydrochloride is a potent inhibitor of CDKs, with IC50s of 210, 47, 100, 13, 170, and <10 nM for CDK1, CDK2, CDK4 to CDK6, and CDK9, respectively. It is for research use only.
- Potent inhibitor of CDKs.
- Induces dose-dependent cytotoxicity and apoptosis in multiple myeloma cells.
- Inhibits cell cycle progression and induces apoptosis in human tumor cell lines.
- Inhibits transcription and RNA polymerase II in leukemia cell lines.
- Inhibits tumor growth in human xenograft mouse models.
- Investigated in clinical trials for various cancers.
Cayman Chemical Methylhexanamine hydrochlori
A simple aliphatic amine that was once marketed as a nasal decongestant but is now sold as a bodybuilding supplement; sold as a mild stimulant in the form of party pills; intended for forensic or research purposes
Medchemexpress LLC R 59-022 hydrochlori 10mg | 93076-98-3 | 10MG
R 59-022 (DKGI-I) hydrochloride is a DGK inhibitor (IC50 2 8 M) R 59-022 hydrochloride inhibits the phosphorylation of OAG to OAPA R 59-022 hydrochloride is a 5-HT Receptor antagonist and activates protein kinase C (PKC) R 59-022 hydrochloride potentiates thrombin-induced diacylglycerol production in platelets and inhibits phosphatidic acid production in neutrophils[1 [2 [3 [4
eMolecules 6291-01-6 | Cyclobutanamine hydrochloride | ChemScene | MFCD00034953 | 107.580 | C4H10ClN | 97.000 | Cl.NC1CCC1 | 1g | 582633316
Cyclobutanamine hydrochloride | ChemScene | 6291-01-6 | MFCD00034953 | 107.580 | C4H10ClN | 97.000 | Cl.NC1CCC1 | 1g | 582633316
Medchemexpress LLC CGP71683 hydrochloride | 192322-50-2 | MFCD07783999 | 99.4% | 512.07 | C26H30ClN5O2S | 10 MG
CGP71683 hydrochloride is the hydrochloride salt of a selective neuropeptide Y Y5 receptor antagonist used as a research tool in neuroscience and endocrinology. It is supplied as a high-purity solid for non-clinical laboratory use, with supporting datasheet and certificate of analysis available.
- Selective antagonist for the neuropeptide Y Y5 receptor (Ki ~1.3 nM).
- High reported purity, 99.4%.
- Molecular weight 512.07 g/mol; chemical formula C26H30ClN5O2S.
- CAS number 192322-50-2 for unambiguous identification.
- Solid powder suitable for dissolution in appropriate solvents for assays.
- Supplied with datasheet and certificate of analysis for quality assurance.
- Available in small milligram pack sizes for screening and mechanistic studies.
Medchemexpress LLC Delapril hydrochloride | 83435-67-0 | 98.0% | 489.00 g·mol⁻¹ | C26H33ClN2O5 | 1 ML
Delapril hydrochloride is the hydrochloride salt of delapril, an angiotensin-converting enzyme (ACE) inhibitor used in cardiovascular research and preclinical studies. The compound is provided both as a ready-to-use 10 mM solution in DMSO (1 mL) and in solid quantities. Typical reported purity is 98.0% and the molecular weight is 489.00 g·mol⁻¹. Store and handle according to supplier safety data.
- ACE inhibitor used in cardiovascular research.
- Available as 10 mM solution in DMSO (1 mL) and as solid quantities.
- High reported purity, 98.0%.
- Molecular weight 489.00 g·mol⁻¹.
- CAS number 83435-67-0 for unambiguous identification.
- Store solid at 4°C; store solution frozen for long-term stability.
Medchemexpress LLC RS 67333 hydrochloride | 168986-60-5 | 99.7% | 389.36 g/mol | C19H30Cl2N2O2 | 5 MG
RS 67333 hydrochloride is a research-grade small-molecule partial agonist of the 5-HT4 (serotonin) receptor, supplied as a solid for laboratory use. It is intended for neuroscience and receptor-signaling studies and is provided with specification details and storage recommendations for research environments.
- Potent, selective 5-HT4 receptor partial agonist.
- High purity (≈99.7%).
- Molecular weight 389.36 g/mol.
- Solid, light yellow to yellow appearance.
- Recommended for research use only with sealed, moisture-free storage.
Medchemexpress LLC SBI-810 (hydrochloride) | 2772746-58-2 | 99.6% | 483.05 | 1 ML
SBI-810 hydrochloride is a functionally selected β-arrestin-biased neurotensin receptor 1 (NTSR1) allosteric modulator. It modulates NTSR1 G protein signaling in a G protein-specific manner in the presence of the endogenous ligand, neurotensin (NT). This compound fully antagonizes NT-induced activation of Gq, partially antagonizes NT-induced activation of Gi1, and is permissive of NTSR1 activation of GoA and G12.
- Functionally selected β-arrestin-biased neurotensin receptor 1 (NTSR1) allosteric modulator.
- Modulates NTSR1 G protein signaling in a G protein-specific manner with neurotensin (NT).
- Fully antagonizes NT-induced activation of Gq.
- Partially antagonizes NT-induced activation of Gi1.
- Permissive of NTSR1 activation of GoA and G12.
- For research use only.
eMolecules 56621-99-9 | Ambeed | N2N2-Dimethylpyrimidine-25-diamine | 250mg | 552737660 | A497416 | MFCD11656641 | 138.174 | C6H10N4
Ambeed | N2N2-Dimethylpyrimidine-25-diamine | 250mg | 552737660 | A497416 | 56621-99-9 | MFCD11656641 | 138.174 | C6H10N4
eMolecules 1259484-97-3 | Medchem Express | SKI-178 | 5mg | 599150633 | HY-12892 | MFCD01913555 | 394.431 | C21H22N4O4
Ambeed | 7-Chloro-[124]triazolo[15-a]pyridine | 100mg | 601097454 | A515415 | 1427452-48-9 | MFCD23708543 | 153.570 | C6H4ClN3
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![eMolecules 86347-15-1 | Medetomidine Hydrochloride | Key Organics/BIONET236.740 | C13H17ClN2 | 99.000 | Cl.CC(c1cnc[nH]1)c1cccc(C)c1C | 3mg | 564356413](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000128175.jpg-250.jpg)
eMolecules 86347-15-1 | Medetomidine Hydrochloride | Key Organics/BIONET236.740 | C13H17ClN2 | 99.000 | Cl.CC(c1cnc[nH]1)c1cccc(C)c1C | 3mg | 564356413
Medetomidine Hydrochloride | Key Organics/BIONET | 86347-15-1236.740 | C13H17ClN2 | 99.000 | Cl.CC(c1cnc[nH]1)c1cccc(C)c1C | 3mg | 564356413
Medchemexpress LLC DC-Chol hydrochloride | 166023-21-8 | >99.9% | 537.26 | 250 MG
DC-Chol hydrochloride is a cationic lipid that inhibits Aβ40 fibril formation and amyloidogenesis of oxidized hCT. It enhances the body's immune response to antigens by inducing the production of Th1 (IL-2 and IFN-γ) and Th2 (IL-5) cytokines. This compound is also utilized as a gene delivery vector.
- Can inhibit Aβ40 fibril formation
- Strongly inhibits amyloidogenesis of oxidized hCT in a dose-dependent manner
- Induces production of Th1 (IL-2 and IFN-γ) and Th2 (IL-5) cytokines
- Enhances the body's immune response to antigens
- Used as a gene delivery vector
- Can be used in research for hepatitis B vaccines to improve vaccine immunity