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Filtered Search Results
eMolecules 13577-19-0 | ChemScene | 8-Iodo-1-naphthoic acid | 100mg | 596090966 | CS-0159360 | MFCD00075758 | 298.079 | C11H7IO2
Medchem Express | GNE-6468 | 5mg | 495800665 | HY-19775 | 1677668-27-7 | 433.850 | C23H16ClN3O4
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eMolecules 223418-74-4 | 2-Methoxy-3-(tributylstannyl)pyridine | Synthonix - Stock | MFCD01319029 | 398.178 | C18H33NOSn | 97.000 | CCCC[Sn](CCCC)(CCCC)c1cccnc1OC | 1g | 525920394
2-Methoxy-3-(tributylstannyl)pyridine | Synthonix - Stock | 223418-74-4 | MFCD01319029 | 398.178 | C18H33NOSn | 97.000 | CCCC[Sn](CCCC)(CCCC)c1cccnc1OC | 1g | 525920394
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Medchemexpress LLC (R)-N-(1-(Naphthalen-1-yl)ethyl)-3-(3-(trifluoromethyl)phenyl)propanamide | 1005450-55-4 | 99.1% | C22H20F3NO | 1 G
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This product is a drug intermediate used for the synthesis of various active compounds. It is supplied as a white to off-white solid with high purity, ensuring reliability for laboratory applications. This substance is intended for research use only and is not for medical applications or sale to patients.
- Used as a drug intermediate for synthesizing active compounds
- Solid, white to off-white appearance
- Purity of 99.1%
- Stable under recommended storage conditions
- For research use only
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Medchemexpress LLC Rilmazafone hydrochloride | 85815-37-8 | 511.79 | 100 MG
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Rilmazafone hydrochloride is a benzodiazepine (omega) ligand, intended for research use only.
- Solid storage at 4°C
- Sealed storage, away from moisture
- In solvent storage at -80°C for 6 months
- In solvent storage at -20°C for 1 month
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Aobchem AOBCHEM
5000876044 3-BROMO-2-FLUOROPHENYL THIOP
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eMolecules 107484-69-5 | Ambeed | 5-Chloro-8-iodo-16-naphthyridine | 250mg | 490558900 | A383352 | MFCD16250553 | 290.49 | C8H4ClIN2
ChemScene | 2-Bromo-67-dihydro-5H-cyclopenta[b]pyridine | 100mg | 654747259 | CS-0199277 | 1140240-18-1 | MFCD11870046 | 198.063 | C8H8BrN
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Medchemexpress LLC Fenspiride hydrochloride | 5053-08-7 | 99.1% | C15H21ClN2O2 | 1 ML
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Fenspiride hydrochloride is an orally active, non-steroidal anti-inflammatory agent that acts as an antagonist of the H1-histamine receptor. It inhibits phosphodiesterase 3 (PDE3), phosphodiesterase 4 (PDE4), and phosphodiesterase 5 (PDE5) activities. This compound can be used for research related to respiratory diseases.
- Antagonist of the H1-histamine receptor
- Inhibits phosphodiesterase 3, phosphodiesterase 4, and phosphodiesterase 5 activities
- Useful for research on respiratory diseases
- Inhibits histamine-induced contraction of isolated guinea pig trachea (in vitro)
- Reduces lipopolysaccharide-induced tumor necrosis factor concentrations (in vivo)
- Reduces primed stimulation of alveolar macrophages (in vivo)
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eMolecules 13826-27-2 | 2,2'-Bi-1,3,2-benzodioxaborole | Accela ChemBio (ASD) | MFCD09842343 | 237.810 | C12H8B2O4 | 95.000 | O1B(Oc2ccccc12)B1Oc2ccccc2O1 | 100g | 517258234
2,2'-Bi-1,3,2-benzodioxaborole | Accela ChemBio (ASD) | 13826-27-2 | MFCD09842343 | 237.810 | C12H8B2O4 | 95.000 | O1B(Oc2ccccc12)B1Oc2ccccc2O1 | 100g | 517258234
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Medchemexpress LLC Benzenesulfonamide, 4-[(6-amino-4-pyrimidinyl)amino]-, hydrochloride (1:1) | 21886-12-4 | 99.6% | 301.75 | 25 MG
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PNU112455A hydrochloride is an ATP-competitive inhibitor of CDK2 and CDK5. It binds to the ATP site of CDK2 and CDK5 with Kms of 3.6 and 3.2 μM, respectively. This product is for research use only and is not sold to patients.
- ATP-competitive CDK2 and CDK5 inhibitor.
- Binds to the ATP site of CDK2 and CDK5.
- Purity: 99.56%.
- Available in various sizes and concentrations, including solid and solution forms.
- Soluble in DMSO and H2O.
- Provided with detailed solubility and storage information for both in vitro and in vivo applications.
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Aobchem AOBCHEM
5000875436 4-ISOPROPOXY-1-NAPHTHOIC ACID
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Medchemexpress LLC Mebeverine hydrochloride | 2753-45-9 | 99.85% | C25H36ClNO5 | 100 MG
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Mebeverine hydrochloride is a β-phenylethylamine derivative and a musculotropic agent. It potently blocks intestinal peristalsis by directly blocking voltage-operated sodium channels and inhibiting intracellular calcium accumulation.
- Molecular weight: 466.01
- Appearance: Solid
- Color: White to off-white
- Soluble in DMSO at ≥ 155 mg/mL (332.61 mM)
- Inhibits alpha1 action by limiting calcium mobilization on receptor stimulation in guinea-pig taenia caeci smooth muscle cells
- Exhibits atropine-like properties at 6x10^-6 M
- Causes a small hyperpolarization of muscle cells (2.1 + 0.5 mV) and suppresses spike activity at 6x10^-5 M
- Related to metabolic or endocrine disease, endocrinology
- Acts on sodium channel
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Medchemexpress LLC Lurasidone hydrochloride | 367514-88-3 | 99.86% | C28H37ClN4O2S | 100 MG
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Lurasidone hydrochloride is a chemical reagent from MedChemExpress that functions as an antagonist for both dopamine D2 and 5-HT7 receptors. It also acts as a partial agonist of the 5-HT1A receptor.
- Antagonist of dopamine D2 and 5-HT7 receptors
- Partial agonist of 5-HT1A receptor
- Suitable for neurological disease research
- Stable under recommended storage conditions
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Selleck Chemical LLC TA-02
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TA-02 is a p38 MAPK inhibitor with IC50 of 20 nM TA-02 especially inhibits TGFBR-2
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Aobchem AOBCHEM
5000864442 2- 4-BROMOPHENYL METHOXY -1 3
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eMolecules 28493-54-1 | Benzyltributylstannane | Synthonix - Stock | MFCD30741350 | 381.191 | C19H34Sn | 95.000 | CCCC[Sn](CCCC)(CCCC)Cc1ccccc1 | 250mg | 525911853
Benzyltributylstannane | Synthonix - Stock | 28493-54-1 | MFCD30741350 | 381.191 | C19H34Sn | 95.000 | CCCC[Sn](CCCC)(CCCC)Cc1ccccc1 | 250mg | 525911853
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