Alcohols and polyols
- (1)
- (55)
- (347)
- (39)
- (4)
- (8)
- (7)
- (55)
- (3)
- (7)
- (18)
- (1)
- (4)
- (153)
- (1)
- (65)
- (27)
- (14)
- (3)
- (1)
- (1)
- (10)
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- (1)
- (1)
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- (1)
- (1)
- (1)
- (6)
- (2)
- (30)
- (4)
- (20)
- (10)
- (2)
- (10)
- (4)
- (5)
- (395)
- (6)
- (102)
- (21)
- (50)
- (31)
- (61)
- (13)
- (14)
- (1)
- (2)
- (1)
- (26)
- (6)
- (4)
- (1)
- (6)
- (1)
- (462)
- (9)
- (46)
- (11)
- (45)
- (6)
- (1)
- (7)
- (10)
- (145)
- (114)
- (6)
- (5)
- (1)
- (1)
- (1)
- (1)
- (2)
- (1)
- (4)
- (7)
- (14)
- (2)
- (1)
- (6)
- (5)
- (1)
- (12)
- (21)
- (5)
- (2)
- (2)
- (2)
- (16)
- (2)
- (30)
- (2)
- (4)
- (1)
- (2)
- (20)
- (10)
- (4)
- (15)
- (1)
- (4)
- (6)
- (2)
- (2)
- (2)
- (2)
- (4)
- (3)
- (1)
- (28)
- (29)
- (7)
- (3)
- (5)
- (1)
- (36)
- (5)
- (4)
- (2)
- (5)
- (4)
- (17)
- (15)
- (4)
- (5)
- (2)
- (5)
- (4)
- (33)
- (4)
- (2)
- (6)
- (8)
- (2)
- (2)
- (8)
- (7)
- (7)
- (2)
- (1)
- (26)
- (1)
- (1)
- (1)
- (2)
- (1)
- (3)
- (4)
- (3)
- (1)
- (15)
- (12)
- (1)
- (2)
- (2)
- (7)
- (12)
- (1)
- (14)
- (24)
- (1)
- (8)
- (4)
- (1)
- (2)
- (1)
- (17)
- (2)
- (6)
- (5)
- (2)
- (1)
- (5)
- (3)
- (4)
- (24)
- (5)
- (3)
- (5)
- (14)
- (1)
- (1)
- (1)
- (11)
- (3)
- (2)
- (4)
- (11)
- (2)
- (7)
- (4)
- (1)
- (1)
- (3)
- (6)
- (11)
- (5)
- (3)
- (1)
- (2)
- (11)
- (14)
- (7)
- (2)
- (2)
- (1)
- (3)
- (2)
- (10)
- (1)
- (2)
- (4)
- (4)
- (3)
- (1)
- (3)
- (5)
- (1)
- (1)
- (2)
- (10)
- (2)
- (2)
- (3)
- (7)
- (1)
- (5)
- (4)
- (1)
- (2)
- (9)
- (4)
- (2)
- (12)
- (4)
- (1)
- (1)
- (5)
- (3)
- (10)
- (2)
- (5)
- (1)
- (1)
- (1)
- (10)
- (5)
- (1)
- (2)
- (2)
- (6)
- (14)
- (2)
- (4)
- (1)
- (2)
- (1)
- (1)
- (1)
- (1)
- (4)
- (2)
- (1)
- (1)
- (4)
- (2)
- (3)
- (2)
- (4)
- (3)
- (1)
- (4)
- (5)
- (1)
- (4)
- (5)
- (9)
- (1)
- (5)
- (5)
- (2)
- (1)
- (1)
- (2)
- (5)
- (3)
- (5)
- (2)
- (1)
- (2)
- (2)
- (2)
- (1)
- (4)
- (2)
- (1)
- (2)
- (2)
- (11)
- (9)
- (1)
- (1)
- (2)
- (1)
- (1)
- (3)
- (1)
- (1)
- (10)
- (1)
- (1)
- (1)
- (2)
- (4)
- (11)
- (1)
- (2)
- (4)
- (20)
- (21)
- (1)
- (2)
- (8)
- (2)
- (3)
- (3)
- (8)
- (4)
- (2)
- (1)
- (1)
- (3)
- (1)
- (2)
- (3)
- (2)
- (1)
- (2)
- (1)
- (1)
- (2)
- (1)
- (5)
- (12)
- (9)
- (1)
- (2)
- (1)
- (1)
- (1)
- (1)
- (3)
- (4)
- (1)
- (1)
- (1)
- (7)
- (2)
- (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)
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- (1)
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- (2)
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- (2)
- (1)
- (1)
- (1)
- (1)
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- (14)
- (1)
- (1)
- (2)
- (1)
- (2)
- (2)
- (4)
- (1)
- (1)
- (4)
- (5)
- (1)
- (2)
- (2)
- (1)
- (10)
- (4)
- (1)
- (9)
- (1)
- (8)
- (1)
- (2)
- (2)
- (2)
- (5)
- (1)
- (1)
- (1)
- (1)
- (1)
- (2)
- (1)
- (1)
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- (1)
- (1)
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- (2)
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- (1)
- (1)
- (1)
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- (1)
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- (1)
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- (1)
- (2)
- (1)
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- (1)
- (2)
- (1)
- (1)
- (6)
- (1)
- (1)
- (15)
- (2)
- (1)
- (2)
- (1)
- (1)
- (2)
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- (1)
- (2)
- (2)
- (1)
- (2)
- (1)
- (1)
- (1)
- (3)
- (1)
- (4)
- (2)
- (2)
- (2)
- (1)
- (2)
- (2)
- (2)
- (1)
- (1)
- (2)
- (12)
- (4)
- (2)
- (1)
- (5)
- (1)
- (1)
- (1)
- (3)
- (2)
- (1)
- (2)
- (1)
- (1)
- (1)
- (3)
- (1)
- (2)
- (1)
- (4)
- (1)
- (2)
- (1)
- (1)
- (1)
- (1)
- (1)
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- (3)
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- (2)
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- (1)
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- (1)
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- (2)
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- (1)
- (1)
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- (9)
- (2)
- (1)
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- (6)
- (9)
- (3)
- (2)
- (1)
- (1)
- (1)
- (2)
- (1)
- (1)
- (2)
- (27)
- (2)
- (1)
- (2)
- (1)
- (4)
- (3)
- (2)
- (4)
- (3)
- (2)
- (7)
- (2)
- (18)
- (16)
- (1)
- (4)
- (2)
- (4)
- (60)
- (5)
- (2)
- (1)
- (1)
- (30)
- (2)
- (2)
- (11)
- (82)
- (12)
- (4)
- (1)
- (3)
- (7)
- (5)
- (1)
- (81)
- (3)
- (378)
- (4)
- (40)
- (21)
- (1)
- (19)
- (1)
- (21)
- (16)
- (1)
- (2)
- (20)
- (2)
- (2)
- (3)
- (67)
- (1)
- (1)
- (1)
- (4)
- (8)
- (1)
- (2)
- (2)
- (1)
- (1)
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- (2)
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- (3)
- (3)
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- (2)
- (2)
- (2)
- (7)
- (4)
- (85)
- (1)
- (5)
- (72)
- (3)
- (5)
- (237)
- (4)
- (2)
- (2)
- (21)
- (279)
- (17)
- (1)
- (6)
- (273)
- (28)
- (2)
- (25)
- (2)
- (3)
- (2)
- (2)
- (2)
- (6)
- (3)
- (2)
- (3)
- (48)
- (3)
- (418)
- (6)
- (3)
- (6)
- (5)
- (6)
- (3)
- (1)
- (4)
- (21)
- (2)
- (4)
- (11)
- (1)
- (8)
- (2)
- (704)
- (11)
- (3)
- (4)
- (2)
- (9)
- (1)
- (2)
- (2)
- (66)
- (2)
- (2)
- (3)
- (4)
- (33)
- (2)
- (31)
- (2)
- (3)
- (3)
- (3)
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- (3)
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- (2)
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- (1)
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Filtered Search Results
Medchemexpress LLC VU0453379 hydrochloride | 99.0% | 471.03 | 1 ML
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VU0453379 hydrochloride is a highly selective and central nervous system (CNS) penetrant positive allosteric modulator (PAM) of glucagon-like peptide-1R (GLP-1R). It exhibits an EC50 of 1.3 μM.
- Highly selective positive allosteric modulator.
- Central nervous system (CNS) penetrant.
- Modulates glucagon-like peptide-1R (GLP-1R).
- Demonstrates an EC50 of 1.3 μM.
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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Medchemexpress LLC Alosetron hydrochloride | 122852-69-1 | MFCD03453647 | 99.6% | 10 MG
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Small and/or specialty supplier based on Federal laws and SBA requirements.
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Alosetron hydrochloride is a potent, selective 5-HT3 receptor antagonist provided for research use in studies of irritable bowel syndrome and visceral nociception. It is supplied as a high-purity solid and is also available as ready-to-use 10 mM solutions for laboratory assays.
- Potent and selective 5-HT3 receptor antagonist.
- Used in research on diarrhea-predominant irritable bowel syndrome and visceral nociception.
- High purity suitable for analytical and in vitro applications.
- Available as a solid and as pre-made 10 mM solutions for convenience.
- Characterization includes CAS 122852-69-1 and molecular weight 330.81 g/mol.
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![Medchemexpress LLC Benzoic acid, 2-[4-[2-(1-piperidinyl)ethoxy]benzoyl]-, methyl ester, hydrochloride (1:1) | 1248-42-6 | 99.9% | 403.90 | 25 MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/default.jpg-250.jpg)
Medchemexpress LLC Benzoic acid, 2-[4-[2-(1-piperidinyl)ethoxy]benzoyl]-, methyl ester, hydrochloride (1:1) | 1248-42-6 | 99.9% | 403.90 | 25 MG
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Pitofenone hydrochloride is a spasmolytic compound that inhibits the acetylcholinesterase (AChE) activity from bovine erythrocytes and electric eel with Kis of 36 and 45 μM, respectively. It also exhibits anticonvulsant activity when combined with diclofenac and fenpivirine.
- Spasmolytic compound
- Inhibits acetylcholinesterase (AChE) activity
- Anticonvulsant activity in combination with diclofenac and fenpivirine
- Appearance: Solid
- Color: White to off-white
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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Medchemexpress LLC Drofenine hydrochloride | 548-66-3 | 98.1% | 1 ML
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Drofenine hydrochloride is a potent competitive cholinesterase inhibitor. It acts as a BChE inhibitor with a Ki value of 3 μM and is intended for research use only.
- Potent competitive cholinesterase inhibitor
- BChE inhibitor
- Ki value of 3 μM
- Suitable for research use
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Medchemexpress LLC Yonkenafil hydrochloride | 804519-64-0 | 99.4% | 524.08 | C24H34ClN5O4S | 5MG
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Yonkenafil hydrochloride is the hydrochloride salt of a selective phosphodiesterase 5 (PDE5) inhibitor supplied for research use. It is provided as a high-purity solid suitable for in vitro and preclinical studies involving PDE5-related pathways, neuroscience, and pharmacology. Typical solvent compatibility includes DMSO; follow the SDS and laboratory safety procedures.
- High purity suitable for research.
- Solid form for accurate weighing and formulation.
- Soluble in DMSO for assay preparation.
- Appropriate for in vitro and preclinical pharmacology studies.
- Available in small-scale vials for dose-ranging experiments.
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Medchemexpress LLC Nimustine hydrochloride (ACNU) | 55661-38-6 | 98.2% | 309.15 | 1 ML
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Nimustine hydrochloride (ACNU) is the hydrochloride salt form of Nimustine. It functions as an alkylating agent by inducing DNA double-strand breaks (DSBs) and inter-strand crosslinks (ICLs), which activates the DNA damage response (DDR) signaling pathway. It also activates the p38 MAPK/JNK signaling pathway and demonstrates antitumor activity.
- Induces DNA double-strand breaks and inter-strand crosslinks.
- Activates DNA damage response signaling.
- Activates p38 MAPK/JNK signaling.
- Demonstrates antitumor activity.
- Exhibits cytotoxicity against human U87MG cells.
- Induces apoptosis in LN-229 cells.
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Medchemexpress LLC SRI-37330 hydrochloride | 2322245-49-6 | 99.7% | C16H20ClF3N4O2S | 25 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. This compound can be used for type 2 diabetes research.
- Inhibits activity of human TXNIP promoter in INS-1 cells.
- Decreases mRNA and protein levels of TXNIP in INS-1 cells.
- 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 action in mice.
- Blocks hepatic glucose output in mice.
- Reverses obesity- and streptozotocin-induced diabetes and hepatic steatosis in mice.
- Well tolerated in male C57BL/6J mice.
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Medchemexpress LLC Claramine hydrochloride | 1430194-56-1 | 99.1% | 625.45 g/mol | C37H73ClN4O | 10 MG
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Claramine hydrochloride is a steroidal polyamine research compound reported to cross the blood-brain barrier and to modulate lipid membrane properties. It is supplied as a powder for laboratory research use only.
- Molecular formula: C37H73ClN4O.
- Molecular weight: 625.45 g/mol.
- Cas number: 1430194-56-1.
- Form: powder, white to off-white solid.
- Purity: 99.1% (HPLC, batch certificate of analysis).
- Solubility: DMSO 2.2 mg/mL (3.52 mM; ultrasonic warming to 60°C recommended).
- Storage: powder -20°C (up to 3 years) or 4°C (up to 2 years); in solvent -80°C (up to 6 months).
- Intended use: for research use only, not for human or clinical applications.
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Medchemexpress LLC Befiradol hydrochloride | 2436760-81-3 | MFCD31731608 | 99.9% | 430.32 g/mol | C20H23Cl2F2N3O | 10 MG
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Befiradol hydrochloride is a selective 5-HT1A receptor agonist provided for research use. It modulates serotonergic and dopaminergic activity in cortical regions and is used in preclinical pharmacology studies to investigate 5-HT1A-mediated mechanisms and models of neurological disorders. The material is supplied with supporting documentation for analytical and safety purposes.
- Selective 5-HT1A receptor agonist for receptor pharmacology studies.
- Demonstrated activity on dorsal raphe and medial prefrontal cortex neurotransmission.
- High chemical purity suitable for analytical and in vivo research.
- Supplied with certificate of analysis and safety data sheet.
- Available in multiple pack sizes for small-scale and bulk use.
- Not for human or clinical use; for research use only.
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Medchemexpress LLC Slp7111228 hydrochloride | 1449768-48-2 | 98.0% | 5 MG
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SLP7111228 hydrochloride is the hydrochloride salt of SLP7111228 supplied as a solid research reagent for biochemical assay use. It has formula C22H34ClN5O, molecular weight 419.99, and CAS 1449768-48-2. Store sealed at -20°C; in solution store at -80°C for long-term stability.
- Hydrochloride salt form.
- Solid, white/off-white appearance.
- Molecular formula C22H34ClN5O.
- Molecular weight 419.99.
- CAS number 1449768-48-2.
- Storage: -20°C; in solvent -80°C (6 months), -20°C (1 month).
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Medchemexpress LLC Antalarmin hydrochloride | 220953-69-5 | MFCD05664721 | 99.9% | 415.01 g/mol | C24H35ClN4 | 1 ML
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Antalarmin hydrochloride is a non-peptide corticotropin-releasing hormone receptor 1 (CRHR1) antagonist used in research to suppress CRH-induced ACTH secretion and to study stress- and inflammation-related responses in animal models.
- Selective CRHR1 antagonist with reported Ki ≈ 1 nM.
- CAS number 220953-69-5.
- Molecular formula C24H35ClN4, MW 415.01 g/mol.
- Available as a solid or as a 10 mM solution in DMSO (1 mL).
- High purity (~99.9%) suitable for analytical and in vivo preparations.
- Recommended storage: solid at -20°C; in solvent store at -80°C for long term.
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Medchemexpress LLC Alectinib Hydrochloride | 1256589-74-8 | 99.9% | 200 MG
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Alectinib (CH5424802; RO5424802; RG7853) Hydrochloride is a potent, selective, and orally available ALK inhibitor. It has an IC50 of 1.9 nM and a Kd value of 2.4 nM (in an ATP-competitive manner). It also inhibits ALK F1174L and ALK R1275Q with IC50s of 1 nM and 3.5 nM, respectively. Alectinib demonstrates effective central nervous system (CNS) penetration.
- Potent and selective ALK inhibitor
- Orally available
- Effective central nervous system (CNS) penetration
- Inhibits ALK F1174L and ALK R1275Q
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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 Acotiamide hydrochloride | 185104-11-4 | 99.6% | 10 MG
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Acotiamide hydrochloride is a research-grade small molecule and reversible acetylcholinesterase (AChE) inhibitor (IC50 1.79 μM) used to study gastric motility, delayed gastric emptying, and functional dyspepsia. Supplied as the hydrochloride salt with high reported purity for biochemical and pharmacological research.
- Selective, reversible AChE inhibitor with reported IC50 1.79 μM.
- Suitable for studies of gastric motility and functional dyspepsia models.
- Reported high purity (99.62%), appropriate for assay use.
- Storage: sealed at 4°C; in solvent store at -80°C (6 months) or -20°C (1 month).
- Provided in small milligram pack sizes for laboratory research.
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Medchemexpress LLC Trazodone hydrochloride | 25332-39-2 | 99.6% | 100 MG
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Trazodone hydrochloride is a triazolopyridine derivative that belongs to the class of serotonin receptor antagonists and reuptake inhibitors (SARIs). It has antidepressant and anti-insomnious activity, exerting antagonistic properties against α1- and α2-adrenergic receptors and histamine H1 receptors with minimal anticholinergic effects.
- Triazolopyridine derivative
- Serotonin receptor antagonist and reuptake inhibitor
- Exhibits antidepressant activity
- Possesses anti-insomnious activity
- Antagonizes α1- and α2-adrenergic receptors
- Antagonizes histamine H1 receptors
- Shows minimal anticholinergic effects
- Demonstrates neuroprotective effects
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