Acrylic acids and derivatives
Enzo Life Sciences Amlodipine (1g). CAS: 88150-42-9
Amlodipine is a third generation L-type calcium channel blocker with a unique spectrum of actions, over and above its antihypertensive activity which include stimulation of NO synthase, inhibition of monocyte-endothelial adhesion, inhibition of oxidative stress and sustained duration of action. Purity: ≥98% (Assay). Solubility: Soluble in methanol, DMSO (25mg/ml), 100% ethanol (25mg/ml), dimethyl formamide (25mg/ml) or chloroform. Long Term Storage: Ambient.
eMolecules 68547-97-7 | Medchem Express | Isoguvacine (hydrochloride) | 25mg | 446256124 | HY-100810 | MFCD00055192 | 163.6 | C6H10ClNO2
Medchem Express | Isoguvacine (hydrochloride) | 25mg | 446256124 | HY-100810 | 68547-97-7 | MFCD00055192 | 163.600 | C6H10ClNO2
Medchemexpress LLC 3-Bromopyridin-2-ol | 13466-43-8 | 174.00 | 1 ML
3-Bromopyridin-2-ol is a biochemical reagent suitable for life science research. It functions as a biological material or organic compound, intended strictly for research purposes.
- High purity (99.62%)
- White to light brown solid appearance
- Soluble in DMSO (100 mg/mL)
- Can be formulated for in vivo studies using various co-solvents
- Stable for extended periods under recommended storage conditions
- Used in biochemical assay applications
Medchemexpress LLC (R)-(+)-Bay-K-8644 | 98791-67-4 | C16H15F3N2O4 | 100 MG
(R)-(+)-Bay-K-8644 is a calcium channel inhibitor that inhibits Ba2+ currents (IBa) with an IC50 of 975 nM. While the conventional racemic mixture of Bay K 8644 is widely used as an L-type Ca2+ channel agonist, the (R)-(+)-isomer acts as an antagonist.
- Calcium channel inhibitor
- Inhibits Ba2+ currents (IBa) with an IC50 of 975 nM
- Acts as an antagonist
- (R)-(+)-isomer, distinguishing it from the L-type Ca2+ channel agonist racemic mixture
Medchemexpress LLC Quetiapine-d4 hemifumarate | 1217310-65-0 | 99.8% | C21H21D4N3O2S.1/2C4H4O4 | 5 MG
Quetiapine-d4 hemifumarate is the deuterium labeled Quetiapine hemifumarate. It acts as a 5-HT receptors agonist and a dopamine receptor antagonist, exhibiting antidepressant and anxiolytic effects.
- Can be used as a tracer.
- Can be used as an internal standard for quantitative analysis by NMR, GC-MS, or LC-MS.
Medchemexpress LLC 3-Bromopyridin-2-ol | 13466-43-8 | 174.00 | 50 G
3-Bromopyridin-2-ol is a biochemical reagent and organic compound suitable for life science-related research. It is intended for research use only and should be handled by suitably qualified scientists in equipped facilities.
- High purity: 99.62%
- Molecular weight: 174.00
- Appears as a white to light brown solid
- Can be used as a biological material or organic compound
- Suitable for laboratory research applications
Medchemexpress LLC Elaiophylin | 37318-06-2 | C54H88O18 | 5 MG
Elaiophylin is an autophagy inhibitor that exhibits antitumor activity in ovarian cancer cells. With a molecular weight of 1025.27, it appears as a white to off-white solid and is intended for research use only.
- Autophagy inhibitor
- Exhibits antitumor activity in ovarian cancer cells
- Molecular weight of 1025.27
- White to off-white solid appearance
- Soluble in DMSO for in vitro experiments
- Affects ovarian cancer cell survival during hypoxia
- Leads to activation of cleaved CASP9/caspase-9 and PARP1
- Downregulates BIRC5/survivin
- Suppresses ovarian cancer SKOV3 cell growth in athymic mice
- Achieves significant antitumor effects without toxicity at lower doses
Medchemexpress LLC HY-N0876 5mg Medchemexpress, Arenobufagin CAS:464-74-4 Purity:>98%
Medchemexpress, HY-N0876 5mg Arenobufagin CAS:464-74-4 Purity:>98% Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
Medchemexpress LLC J-2156 | 848647-56-3 | 99.9% | 468.57 | 50 MG
J-2156 is a highly potent and selective somatostatin receptor type 4 (SST4 receptor) agonist, with IC50s of 0.05 nM and 0.07 nM for human and rat SST4 receptors respectively. It is used for the relief of mechanical allodynia and mechanical hyperalgesia in rat models, demonstrating nanomolar affinity for human SST4 receptors and over 400-fold subtype-selectivity against other somatostatin receptors.
- Highly potent and selective somatostatin receptor type 4 (SST4) agonist.
- Exhibits IC50s of 0.05 nM for human SST4 and 0.07 nM for rat SST4 receptors.
- Provides relief for mechanical allodynia and hyperalgesia in rats.
- Binds to human somatostatin receptor subtype 4 with a Ki of 1.2 nM.
- Offers over 400-fold subtype-selectivity against other somatostatin receptors.
- For research use only.