Alcohols and polyols
- (1)
- (55)
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- (4)
- (8)
- (7)
- (55)
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- (18)
- (1)
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- (156)
- (1)
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- (1)
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- (1)
- (1)
- (1)
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- (30)
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- (20)
- (10)
- (2)
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- (395)
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- (102)
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- (50)
- (31)
- (62)
- (13)
- (14)
- (1)
- (2)
- (1)
- (25)
- (6)
- (4)
- (1)
- (6)
- (1)
- (464)
- (9)
- (46)
- (11)
- (46)
- (6)
- (1)
- (7)
- (12)
- (145)
- (116)
- (7)
- (5)
- (1)
- (1)
- (1)
- (1)
- (2)
- (1)
- (1)
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- (7)
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- (1)
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- (1)
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- (2)
- (2)
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- (30)
- (1)
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- (1)
- (2)
- (1)
- (20)
- (10)
- (4)
- (15)
- (1)
- (4)
- (6)
- (2)
- (1)
- (2)
- (2)
- (2)
- (4)
- (3)
- (1)
- (28)
- (29)
- (7)
- (3)
- (5)
- (1)
- (36)
- (5)
- (4)
- (2)
- (5)
- (4)
- (17)
- (15)
- (4)
- (5)
- (1)
- (2)
- (5)
- (1)
- (4)
- (37)
- (4)
- (2)
- (6)
- (8)
- (2)
- (2)
- (8)
- (7)
- (7)
- (2)
- (1)
- (1)
- (26)
- (1)
- (1)
- (1)
- (2)
- (1)
- (3)
- (4)
- (2)
- (1)
- (15)
- (12)
- (1)
- (2)
- (2)
- (7)
- (12)
- (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)
- (7)
- (4)
- (1)
- (1)
- (3)
- (6)
- (11)
- (5)
- (3)
- (1)
- (2)
- (11)
- (14)
- (7)
- (2)
- (2)
- (1)
- (3)
- (1)
- (2)
- (1)
- (10)
- (1)
- (2)
- (4)
- (4)
- (1)
- (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)
- (4)
- (10)
- (2)
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- (1)
- (1)
- (1)
- (10)
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- (1)
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- (1)
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- (60)
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- (30)
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- (11)
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- (1)
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Filtered Search Results
Medchemexpress LLC SB-277011 hydrochloride | 215804-67-4 | 99.59% | 475.02 | 50 MG
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SB-277011 hydrochloride is a potent and selective dopamine D3 receptor (D3R) antagonist, demonstrating high oral bioavailability and brain penetrance. It exhibits significant selectivity over other dopamine receptors and possesses an excellent pharmacokinetic profile in rats. This compound has been shown to effectively reverse the effects of quinelorane and reduce cocaine self-administration in preclinical studies.
- Potent and selective D3 receptor antagonist
- High oral bioavailability and brain penetrance
- 80- to 100-fold selectivity over other dopamine receptors
- Excellent pharmacokinetic profile
- Reverses quinelorane effects in nucleus accumbens
- Reduces intravenous cocaine self-administration
- Inhibits basal and cocaine-enhanced locomotion
- Appearance: solid, off-white to light yellow
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% | 1 ML
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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 functions by increasing the uptake of dopamine and noradrenaline. It has been observed to increase pain threshold, cardiac rate, and myocardial contractility.
- Increases dopamine and noradrenaline uptake
- Increases pain threshold
- Positive chronotropic effect on cardiac rate
- Positive inotropic effect on myocardial contractility
- For research use only
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
Small and Specialty Supplier Partner
Small and/or specialty supplier based on Federal laws and SBA requirements.
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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 Amprolium (hydrochloride) | 137-88-2 | 98.8% | 1 ML
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Amprolium hydrochloride is provided as a 10 mM solution in 1 mL, with a purity of 98.8%. This product is intended for research use only and should be handled by qualified personnel in appropriately equipped facilities.
- 10 mM solution in 1 mL
- Purity: 98.8% (HPLC)
- Recommended storage: 4°C for sealed solutions, away from moisture
- For longer-term storage in solvent: -80°C for 6 months or -20°C for 1 month
- Can be shipped at room temperature if shipment duration is less than 2 weeks
- Intended for research applications
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Medchemexpress LLC Fendiline (hydrochloride) | 13636-18-5 | 99.8% | 1 ML
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Fendiline hydrochloride is a diphenylalkylamine type of antianginal agent that acts as an L-type calcium channel blocker with an IC50 of 17 μM. It is also identified as a selective K-Ras inhibitor, showing no effect on H-Ras and N-Ras. It inhibits K-Ras plasma membrane localization (IC50 of 9.64 μM) and K-Ras signal output. Additionally, Fendiline hydrochloride is a STING agonist and has demonstrated the ability to inhibit the growth of multiple refractory cold tumors. This product is provided as a 10 mM solution in 1 mL of DMSO with a purity of 99.78%.
- Acts as an L-type calcium channel blocker
- Functions as a selective K-Ras inhibitor
- Inhibits K-Ras plasma membrane localization
- Suppresses K-Ras signal output
- Prevents proliferation of various cancer cell lines
- Serves as a STING agonist
- Inhibits growth of refractory cold tumors
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Medchemexpress LLC Pumosetrag Hydrochloride | 194093-42-0 | 99.8% | 339.84 | 25 MG
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Pumosetrag Hydrochloride is an orally available 5-HT3 partial agonist developed for the treatment of irritable bowel syndrome and gastroesophageal reflux disease. It is intended for research use only.
- Orally available 5-HT3 partial agonist
- Developed for treatment of irritable bowel syndrome and gastroesophageal reflux disease
- Exhibits regional and species specificities
- Delays liquid gastric emptying
- Relaxes the proximal stomach
- Stimulates fasting antroduodenal migrating motor complex activity
- Accelerates small intestinal transit
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Medchemexpress LLC Ponatinib hydrochloride | 1114544-31-8 | 99.8% | 569.02 | 25 MG
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Ponatinib hydrochloride, also known as AP24534 hydrochloride, is an orally active multi-targeted kinase inhibitor. It inhibits various kinases with IC50s including 0.37 nM for Abl, 1.1 nM for PDGFRα, 1.5 nM for VEGFR2, 2.2 nM for FGFR1, and 5.4 nM for Src.
- Purity of 99.76%
- CAS number: 1114544-31-8
- Molecular weight: 569.02
- Appears as an off-white to light yellow solid
- Soluble in DMSO at 25 mg/mL
- Targets Bcr-Abl, FGFR, PDGFR, VEGFR, Src, and Autophagy pathways
- Store at 4°C, sealed, away from moisture; in solvent, store at -80°C for 6 months or -20°C for 1 month
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Medchemexpress LLC Tiaramide hydrochloride | 35941-71-0 | MFCD01702832 | 98.7% | 392.30 | C15H19Cl2N3O3S | 5 MG
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Tiaramide hydrochloride is the hydrochloride salt of tiaramide, an analgesic research compound provided in milligram quantities for laboratory use. It is a light yellow solid with molecular formula C15H19Cl2N3O3S and molecular weight 392.30 g·mol-1. Typical purity is 98.7%, and the compound is commonly handled in DMSO for in vitro and pharmacological studies.
- Hydrochloride salt form for improved stability
- High purity (approximately 98.7%)
- Available in milligram-scale sizes for research use
- Light yellow solid suitable for analytical testing
- Soluble in DMSO for biological assays
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Medchemexpress LLC SRI-011381 hydrochloride | 2070014-88-7 | 99.6% | 365.94 | C20H32ClN3O | 200 MG
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SRI-011381 hydrochloride is an orally active TGF-β signaling agonist reported to exhibit neuroprotective effects in vitro and in vivo. It is supplied as a solid or as a DMSO solution for research use and is provided at high chemical purity.
- Orally active TGF-β signaling agonist.
- Promotes proliferation of mouse lung fibroblasts in vitro.
- Increases TGF-β1, NALP3, collagen-1, and α-SMA expression.
- Demonstrates neuroprotective effects in animal models, reducing inflammation and neuron loss.
- Available as a solid and as 10 mM solution in DMSO in multiple package sizes.
- High purity suitable for research applications.
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eMolecules 51285-26-8 | Picolinimidamide hydrochloride | ChemScene | MFCD00052271 | 157.600 | C6H8ClN3 | 95.000 | Cl.NC(=N)c1ccccn1 | 25g | 572163656
Picolinimidamide hydrochloride | ChemScene | 51285-26-8 | MFCD00052271 | 157.600 | C6H8ClN3 | 95.000 | Cl.NC(=N)c1ccccn1 | 25g | 572163656
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Accela Chembio Inc Trans-(1r | 2r)-2-aminocyclopentanol Hydrochloride | 25g | 68327-11-7 | MFCD09834692 | 95+% | Shelf Life: 1260 Days | Light Sensitive/moisture Sensitive/+4
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Trans-(1r | 2r)-2-aminocyclopentanol Hydrochloride | 25g | 68327-11-7 | MFCD09834692 | 95+% | Shelf Life: 1260 Days | Light Sensitive/moisture Sensitive/+4
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Aobchem AOBCHEM
5000905607 1- M-TOLYL CYCLOPENTANOL 250MG
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eMolecules 51285-26-8 | 2-Amidinopyridine Hydrochloride | Accela ChemBio (ASD) | MFCD00052271 | 157.600 | C6H8ClN3 | 95.000 | Cl.NC(=N)c1ccccn1 | 1g | 510407894
2-Amidinopyridine Hydrochloride | Accela ChemBio (ASD) | 51285-26-8 | MFCD00052271 | 157.600 | C6H8ClN3 | 95.000 | Cl.NC(=N)c1ccccn1 | 1g | 510407894
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Medchemexpress LLC Lecozotan hydrochloride | 433282-68-9 | 98.7% | 520.02 | 5 MG
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Lecozotan hydrochloride (SRA-333) hydrochloride is an orally active and selective antagonist of 5-HT1A with a Ki of 4.5 nM for cloned human 5-HT1A receptor. It enhances the stimulated release of glutamate and acetylcholine in the hippocampus and possesses cognitive-enhancing properties. This product has the potential for mild-to-moderate Alzheimer's disease (AD) research.
- Orally active and selective 5-HT1A antagonist.
- Enhances the release of glutamate and acetylcholine in the hippocampus.
- Possesses cognitive-enhancing properties.
- Potential for mild-to-moderate Alzheimer's disease research.
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