Alcohols and polyols
- (1)
- (55)
- (350)
- (41)
- (4)
- (8)
- (7)
- (55)
- (3)
- (7)
- (18)
- (1)
- (4)
- (155)
- (1)
- (63)
- (29)
- (14)
- (3)
- (1)
- (1)
- (10)
- (3)
- (2)
- (2)
- (1)
- (1)
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- (1)
- (1)
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- (6)
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- (30)
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- (20)
- (10)
- (2)
- (10)
- (4)
- (5)
- (399)
- (6)
- (102)
- (22)
- (50)
- (31)
- (62)
- (13)
- (14)
- (1)
- (2)
- (1)
- (25)
- (6)
- (4)
- (1)
- (6)
- (1)
- (463)
- (9)
- (46)
- (10)
- (46)
- (6)
- (1)
- (6)
- (13)
- (148)
- (114)
- (9)
- (5)
- (1)
- (1)
- (1)
- (1)
- (2)
- (1)
- (1)
- (4)
- (7)
- (14)
- (2)
- (1)
- (6)
- (5)
- (1)
- (1)
- (12)
- (21)
- (5)
- (2)
- (2)
- (1)
- (2)
- (16)
- (2)
- (30)
- (1)
- (4)
- (1)
- (2)
- (1)
- (20)
- (10)
- (4)
- (15)
- (1)
- (4)
- (6)
- (2)
- (1)
- (2)
- (2)
- (2)
- (1)
- (4)
- (3)
- (1)
- (28)
- (29)
- (7)
- (3)
- (5)
- (1)
- (36)
- (5)
- (4)
- (2)
- (5)
- (4)
- (17)
- (14)
- (4)
- (5)
- (1)
- (2)
- (5)
- (1)
- (4)
- (37)
- (4)
- (2)
- (6)
- (8)
- (2)
- (2)
- (9)
- (7)
- (7)
- (2)
- (1)
- (1)
- (26)
- (1)
- (1)
- (1)
- (2)
- (1)
- (3)
- (4)
- (2)
- (1)
- (14)
- (12)
- (1)
- (3)
- (2)
- (7)
- (12)
- (1)
- (1)
- (14)
- (24)
- (1)
- (8)
- (4)
- (1)
- (2)
- (1)
- (22)
- (2)
- (6)
- (5)
- (2)
- (1)
- (5)
- (3)
- (4)
- (24)
- (5)
- (3)
- (5)
- (14)
- (1)
- (1)
- (1)
- (11)
- (3)
- (2)
- (4)
- (11)
- (2)
- (6)
- (4)
- (1)
- (3)
- (6)
- (11)
- (5)
- (4)
- (1)
- (2)
- (11)
- (14)
- (7)
- (2)
- (3)
- (1)
- (3)
- (1)
- (2)
- (1)
- (10)
- (1)
- (2)
- (4)
- (4)
- (1)
- (3)
- (1)
- (3)
- (5)
- (1)
- (1)
- (2)
- (1)
- (1)
- (10)
- (2)
- (2)
- (3)
- (7)
- (1)
- (1)
- (5)
- (4)
- (1)
- (2)
- (9)
- (4)
- (2)
- (12)
- (4)
- (1)
- (5)
- (4)
- (10)
- (2)
- (5)
- (1)
- (1)
- (1)
- (10)
- (6)
- (1)
- (2)
- (2)
- (6)
- (14)
- (2)
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- (1)
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- (1)
- (1)
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- (1)
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- (2)
- (1)
- (1)
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- (3)
- (2)
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- (1)
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- (1)
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- (9)
- (1)
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- (5)
- (2)
- (1)
- (1)
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- (1)
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- (1)
- (1)
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- (21)
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- (1)
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- (1)
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- (1)
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- (1)
- (1)
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- (1)
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- (1)
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- (1)
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- (1)
- (2)
- (1)
- (1)
- (5)
- (4)
- (3)
- (1)
- (1)
- (4)
- (6)
- (1)
- (1)
- (1)
- (5)
- (1)
- (1)
- (4)
- (1)
- (1)
- (1)
- (2)
- (1)
- (1)
- (2)
- (1)
- (1)
- (1)
- (1)
- (1)
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- (1)
- (2)
- (1)
- (2)
- (2)
- (5)
- (2)
- (1)
- (1)
- (1)
- (1)
- (3)
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- (1)
- (1)
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- (1)
- (2)
- (2)
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- (1)
- (1)
- (4)
- (5)
- (2)
- (2)
- (1)
- (10)
- (4)
- (1)
- (9)
- (1)
- (8)
- (1)
- (1)
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- (2)
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- (1)
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- (3)
- (4)
- (1)
- (1)
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- (1)
- (1)
- (1)
- (1)
- (4)
- (1)
- (5)
- (1)
- (7)
- (1)
- (2)
- (1)
- (7)
- (1)
- (2)
- (1)
- (1)
- (6)
- (1)
- (1)
- (15)
- (2)
- (1)
- (2)
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- (2)
- (1)
- (1)
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- (1)
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- (2)
- (2)
- (2)
- (1)
- (2)
- (2)
- (2)
- (1)
- (1)
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- (2)
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- (1)
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- (3)
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- (7)
- (1)
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- (16)
- (1)
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- (2)
- (4)
- (60)
- (5)
- (2)
- (1)
- (1)
- (30)
- (2)
- (2)
- (11)
- (81)
- (12)
- (4)
- (1)
- (3)
- (7)
- (5)
- (1)
- (81)
- (3)
- (378)
- (4)
- (40)
- (21)
- (1)
- (19)
- (1)
- (22)
- (16)
- (1)
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- (21)
- (2)
- (2)
- (2)
- (1)
- (67)
- (1)
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- (1)
- (1)
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- (2)
- (2)
- (2)
- (7)
- (4)
- (86)
- (1)
- (5)
- (72)
- (3)
- (5)
- (238)
- (4)
- (2)
- (2)
- (21)
- (281)
- (17)
- (1)
- (6)
- (279)
- (28)
- (2)
- (25)
- (2)
- (3)
- (2)
- (2)
- (2)
- (6)
- (3)
- (2)
- (3)
- (48)
- (3)
- (418)
- (6)
- (3)
- (6)
- (5)
- (47)
- (6)
- (3)
- (1)
- (4)
- (21)
- (16)
- (2)
- (4)
- (11)
- (1)
- (8)
- (2)
- (731)
- (11)
- (3)
- (4)
- (2)
- (9)
- (1)
- (2)
- (2)
- (66)
- (2)
- (2)
- (18)
- (3)
- (4)
- (33)
- (2)
- (31)
- (39)
- (2)
- (3)
- (3)
- (3)
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- (3)
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- (7)
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- (6)
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- (6)
- (7)
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- (6)
- (2)
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- (3)
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- (9)
- (2)
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- (1)
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- (7)
- (2)
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- (4)
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- (2)
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- (6)
- (2)
- (4)
- (1)
- (1)
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- (8)
- (2)
- (3)
- (2)
- (12)
- (6)
- (2)
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- (2)
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- (2)
- (5)
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- (11)
- (1)
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- (1)
- (7)
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- (1)
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- (1)
- (12)
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- (10)
- (2)
- (1)
- (12)
- (3)
- (3)
- (1)
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Filtered Search Results
Medchemexpress LLC Sevelamer hydrochloride | 152751-57-0 | 98.0% | 186.08 (monomer) | 5 G
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Small and/or specialty supplier based on Federal laws and SBA requirements.
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Sevelamer hydrochloride is an orally active phosphate binding agent primarily used for research related to hyperphosphatemia in chronic kidney disease. This compound consists of polyallylamine crosslinked with epichlorohydrin, and is intended for research use only, not for patient treatment.
- Orally active phosphate binding agent
- Used for research of hyperphosphatemia with chronic kidney disease
- Composed of polyallylamine crosslinked with epichlorohydrin
- Decreases serum levels of gut-derived uremic toxins (such as IAA) in vitro
- Reduces serum phosphate levels in Npt2b-deficient mice in vivo
- Leads to a significant decrease in osteoclast number in uremic WT mice
- Store at 4°C sealed, away from moisture for solid form
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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Medchemexpress LLC Yonkenafil hydrochloride | 804519-64-0 | 99.4% | 524.08 g/mol | C24H34ClN5O4S | 25MG
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Small and/or specialty supplier based on Federal laws and SBA requirements.
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Yonkenafil hydrochloride is a research-grade phosphodiesterase 5 (PDE5) inhibitor intended for preclinical and biochemical studies. The compound is supplied as a hydrochloride salt, with molecular formula C24H34ClN5O4S and molecular weight 524.08 g/mol. It is typically used as a reference or test compound in pharmacology and neurobiology research where PDE5 modulation is of interest.
- PDE5 inhibitor suitable for biochemical and cellular assays.
- Reported high purity (99.4%) for consistent experimental results.
- Available in small milligram pack sizes for assay development.
- Hydrochloride salt form for improved handling and stability.
- Molecular properties provided for formulation and dosing calculations.
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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Medchemexpress LLC Octodrine hydrochloride | 5984-59-8 | 98.0% | 500 MG
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Small and/or specialty supplier based on Federal laws and SBA requirements.
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Octodrine hydrochloride is a central nervous activator that increases the uptake of dopamine and noradrenaline. It increases the pain threshold, cardiac rate, and myocardial contractility. This product is for research use only.
- Increases uptake of dopamine and noradrenaline
- Increases pain threshold
- Increases cardiac rate
- Increases myocardial contractility
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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Medchemexpress LLC Yonkenafil hydrochloride | 804519-64-0 | 99.4% | 524.08 | C24H34ClN5O4S | 100MG
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Yonkenafil hydrochloride is a phosphodiesterase 5 (PDE5) inhibitor provided as the hydrochloride salt for preclinical research. It has been reported to reduce cerebral infarction and neuronal damage and to modulate neurogenesis, with formulation guidance for both in vitro and in vivo use.
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Medchemexpress LLC Topotecan hydrochloride | 119413-54-6 | MFCD00866235 | 99.9% | 457.91 | 100 MG
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Topotecan hydrochloride is a potent Topoisomerase I inhibitor with significant antineoplastic activities. It is intended for research and analytical applications, playing a role in studies related to cancer, autophagy, and apoptosis.
- Potent Topoisomerase I inhibitor
- Demonstrates antineoplastic activities
- Inhibits the proliferation of human glioma cells
- Induces cell cycle arrest in G0/G1 and S phases
- Promotes apoptosis in various cell lines
- Store at 4°C, sealed, away from moisture and light
- Store in solvent at -80°C for 2 years or -20°C for 1 year
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Medchemexpress LLC Alfuzosin hydrochloride | 81403-68-1 | 99.7% | 50 MG
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Alfuzosin hydrochloride is an orally active, selective and competitive α1-adrenoceptor antagonist. It relaxes the muscles of the prostate and bladder neck, aiding in urination. This compound can be used in the study of benign prostatic hyperplasia (BPH).
- Orally active
- Selective and competitive α1-adrenoceptor antagonist
- Relaxes the muscles of the prostate and bladder neck
- Aids in urination
- Can be used in the study of benign prostatic hyperplasia (BPH)
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Medchemexpress LLC Epz020411 (hydrochloride) | 2070015-25-5 | 98.15% | 10MM 1ML
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EPZ020411 hydrochloride is a selective inhibitor of PRMT6 with an IC50 of 10 nM. It demonstrates more than 10-fold selectivity for PRMT6 over PRMT1 and PRMT8 and can be used for cancer research.
- Selective inhibitor of PRMT6 (IC50 of 0.01 μM).
- Exhibits over 10-fold selectivity for PRMT6 compared to PRMT1 and PRMT8.
- Decreases H3R2 methylation in A375 cells.
- Reduces neomycin- and cisplatin-induced cell apoptosis and increases hair cell survival.
- Attenuates neomycin- and cisplatin-induced hearing loss in mice.
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Medchemexpress LLC SAR407899 hydrochloride | 923262-96-8 | MFCD20485429 | 99.1% | 280.75 g/mol | C14H17ClN2O2 | 10 MG
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SAR407899 hydrochloride is a selective, potent, ATP-competitive inhibitor of Rho-associated kinases (ROCK), supplied as a high-purity solid for preclinical biochemical and cellular research. It is used to probe ROCK-mediated signaling, vascular tone, and smooth muscle responses in vitro and in vivo.
- Selective ATP-competitive ROCK inhibitor with ROCK-2 IC50 ≈135 nM.
- Demonstrates Ki values of 36 nM (human) and 41 nM (rat).
- High purity (99.1%) suitable for research applications.
- Solid, light yellow to khaki appearance; stable when stored sealed at 4°C.
- Applicable to studies of vascular tone, smooth muscle relaxation, and ROCK signaling pathways.
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Medchemexpress LLC Zenidolol hydrochloride | 72795-01-8 | 99.7% | 313.86 | 1 ML
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Zenidolol hydrochloride (ICI-118551 hydrochloride) is a highly selective β2 adrenergic receptor antagonist. It exhibits Kis of 0.7, 49.5, and 611 nM for β2, β1, and β3 receptors, respectively, making it a potent research tool for studying adrenergic receptor activity.
- Inhibits cAMP accumulation with an IC50 of 1.7 μM in IMCD cells.
- Induces prominent vasorelaxation of norepinephrine pre-contracted PA.
- Significantly affects beat duration in failing human heart.
- Reduces systolic pressure in the pulmonary circuit in mice.
- Negative inotropic effect not cAMP-related.
- Available in solid, solution, or solid + solvent formats.
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Medchemexpress LLC VU0357017 hydrochloride | 1135242-13-5 | 98.63% | 369.89 | 1 ML
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VU0357017 hydrochloride is a potent, selective, and brain-penetrant allosteric agonist of the M1 muscarinic acetylcholine receptor, with an EC50 of 477 nM. It is highly selective for M1, showing no activity at M2-M5 receptors up to 30 μM. This compound is used in research for conditions such as Alzheimer's disease and schizophrenia.
- Potent and selective M1 muscarinic acetylcholine receptor agonist.
- Exhibits brain penetrant properties.
- Highly selective for M1 over M2-M5 receptors.
- Used for the research of Alzheimer's disease and schizophrenia.
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Medchemexpress LLC Sri-37330 hydrochloride | 2322245-49-6 | 99.7% | C16H20ClF3N4O2S | 250 MG
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SRI-37330 hydrochloride is an orally bioavailable thioredoxin-interacting protein (TXNIP) inhibitor. It inhibits glucagon secretion and function, reduces hepatic glucose production, and reverses hepatic steatosis. It can be used for type 2 diabetes research.
- Inhibits activity of human TXNIP promoter in INS-1 cells.
- Inhibits mRNA and protein levels of TXNIP.
- Inhibits polymerase II (Pol II) binding to the E-box motif region of the TXNIP promoter.
- Lowers glucagon secretion in TC1-6 cells.
- Inhibits glucagon-induced glucose output from primary hepatocytes.
- Decreases glucagon secretion and blocks hepatic glucose output in mice.
- Reverses obesity- and STZ-induced diabetes and hepatic steatosis in mice.
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Medchemexpress LLC Sematilide hydrochloride | 101526-62-9 | MFCD01667315 | 99.3% | 349.88 g·mol⁻1 | C14H24ClN3O3S | 100 MG
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Sematilide hydrochloride is a class III antiarrhythmic research compound that selectively blocks the cardiac IKr (hERG) potassium channel. It inhibits the delayed rectifier K+ current in a concentration-dependent manner (reported IC50 ≈ 25 μM) and is supplied as the hydrochloride salt for in vitro electrophysiology and pharmacology studies. Typical purity is 99.33%.
- Selective IKr (hERG) channel blocker
- Inhibits delayed rectifier K+ current (IC50 ≈ 25 μM)
- Intended for in vitro electrophysiology and pharmacology studies
- High purity suitable for analytical applications
- Available in milligram pack sizes for research use
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Medchemexpress LLC Leelamine hydrochloride | 16496-99-4 | 98.1% | 321.93 | 100 MG
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Leelamine hydrochloride is a tricyclic diterpene molecule extracted from the bark of pine trees. It acts as a cannabinoid receptor type 1 (CB1) agonist and inhibits SREBP1-regulated fatty acid/lipid synthesis in prostate cancer cells, independent of androgen receptor status. It also suppresses the transcriptional activity of the androgen receptor, which regulates fatty acid synthesis.
- Acts as a cannabinoid receptor type 1 (CB1) agonist.
- Inhibits SREBP1-regulated fatty acid/lipid synthesis in prostate cancer cells.
- Suppresses transcriptional activity of the androgen receptor.
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Medchemexpress LLC SAR407899 HYDROCHLO 50 mg
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SAR407899 HYDROCHLO 50MG
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Medchemexpress LLC TENAPANOR HYDROCHLO 100 mg
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TENAPANOR HYDROCHLO 100MG
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