Organosulfur Compounds
Medchemexpress LLC ZTA-261 | 3049368-51-3 | 99.9% | 428.32 | 5 MG
ZTA-261 is a highly selective and low toxic thyroid hormone receptor β subtype (THR-β) agonist (IC50=6.3 nM) that reduces body weight and visceral fat through a liothyronine (HY-A0070A) mediated pathway. ZTA-261 can be used in the study of lipid metabolism and obesity prevalence.
- Highly selective and low toxic THR-β agonist.
- Reduces body weight and visceral fat.
- Useful in the study of lipid metabolism and obesity prevalence.
eMolecules Dichloro(p-cymene)tricyclohexylphosphineruthenium(II), min. 97% | 145381-23-3 | | 1g
Strem Chemicals | Dichloro(p-cymene)tricyclohexylphosphineruthenium(II), min. 97% | 1g | 321338666 | 44-0430 | 97.000 | 145381-23-3 | | 586.630 | C28H47Cl2PRu
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eMolecules 6-((2-((4-(2,4-Dichlorophenyl)-5-(5-methyl-1H-imidazol-2-yl)pyrimidin-2-yl)amino)ethyl)amino)nicotinonitrile monohydrochloride | 1797989-42-4 | MFCD30489757 | 50mg
Ambeed | 6-((2-((4-(2,4-Dichlorophenyl)-5-(5-methyl-1H-imidazol-2-yl)pyrimidin-2-yl)amino)ethyl)amino)nicotinonitrile monohydrochloride | 50mg | 525132922 | A219562 | | 1797989-42-4 | MFCD30489757 | 501.800 | C22H19Cl3N8
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eMolecules 2-(2-(DIFLUOROMETHOXY)-6-FLUOROPHENYL)ACETIC ACID | 1261645-53-7 | MFCD18395034 | 1g
AstaTech | 2-(2-(DIFLUOROMETHOXY)-6-FLUOROPHENYL)ACETIC ACID | 1g | 268504206 | CL9375 | 95.000 | 1261645-53-7 | MFCD18395034 | 220.147 | C9H7F3O3
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eMolecules 2-(Difluoromethoxy)-5-methylaniline hydrochloride | 1431962-90-1 | MFCD25371272 | 1g
Apollo Scientific | 2-(Difluoromethoxy)-5-methylaniline hydrochloride | 1g | 562442002 | PC410123 | | 1431962-90-1 | MFCD25371272 | 209.620 | C8H10ClF2NO
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eMolecules 4-(DIFLUOROMETHOXY)-3-FLUOROPHENOL | 184162-48-9 | MFCD18395029 | 1g
AstaTech | 4-(DIFLUOROMETHOXY)-3-FLUOROPHENOL | 1g | 600860065 | 89603 | 95.000 | 184162-48-9 | MFCD18395029 | 178.110 | C7H5F3O2
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eMolecules 2-Isopropylthio-5-trifluoromethylpyridine-3-boronic acid | 1256345-52-4 | MFCD16660272 | 1g
Combi-Blocks | 2-Isopropylthio-5-trifluoromethylpyridine-3-boronic acid | 1g | 117521399 | BB-2557 | 97.000 | 1256345-52-4 | MFCD16660272 | 265.060 | C9H11BF3NO2S
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Chem-Impex International, Inc. Thiomorpholine | MFCD00005974 | 100G
Thiomorpholine, MFCD00005974, 100G
eMolecules 2-(Benzylthio)-5-bromopyrimidine | 79686-18-3 | 1G | Purity: 98%
Combi-Blocks | 2-(Benzylthio)-5-bromopyrimidine | 1G | 79686-18-3 | MFCD16660315
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Sigma Aldrich Fine Chemicals Biosciences Dimethyl sulfide redistill25KG
Dimethyl sulfide is a volatile flavor compound found in butter32) green tea and sweet corn.
eMolecules (R)-Thiomorpholine-3-carboxylic acid hydrochloride | 67362-31-6 | MFCD12913751 | 5g
J & W PharmLab, LLC | (R)-Thiomorpholine-3-carboxylic acid hydrochloride | 5g | 250009695 | 53R0036S | 97.000 | 67362-31-6 | MFCD12913751 | 183.650 | C5H10ClNO2S
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eMolecules 4-Cbz-thiomorpholine-3-carboxylic acid | 90471-66-2 | MFCD04114910 | 1g
J & W PharmLab LLC | 4-Cbz-thiomorpholine-3-carboxylic acid | 1g | 532639000 | 53R0035 | 97.000 | 90471-66-2 | MFCD04114910 | 281.330 | C13H15NO4S
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eMolecules (Isopropylthio)acetic acid | 22818-59-3 | MFCD07801373 | 25g
Oakwood Chemical | (Isopropylthio)acetic acid | 25g | 537720083 | 311009 | | 22818-59-3 | MFCD07801373 | 134.190 | C5H10O2S
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Medchemexpress LLC 2-Amino-5-methylpyrazine | 5521-58-4 | 99.7% | C5H7N3 | 1 G
2-Amino-5-methylpyrazine is an intermediate chemical compound primarily used in the synthesis of LPAR1 antagonists. This product is intended for research purposes only and not for patient use.
- Utilized as an intermediate for LPAR1 antagonist synthesis.
- Purity of 99.7%.
- Appears as a light brown to yellow solid.
- Highly soluble in DMSO.
- Store at 4°C, protected from light.
Medchemexpress LLC 2-Amino-5-methylpyrazine | 5521-58-4 | 99.7% | C5H7N3 | 5 G
2-Amino-5-methylpyrazine is a chemical intermediate designed for research applications. It is utilized in the synthesis of LPAR1 antagonists. This product presents as a solid, ranging in color from light brown to yellow, and boasts a high purity of 99.72%.
- Functions as an intermediate for chemical synthesis.
- Enables the synthesis of LPAR1 antagonists.
- Exhibits a high purity.
- Available as a solid form.
- Displays a light brown to yellow coloration.
- Highly soluble in dimethyl sulfoxide.
- Features multiple dissolution protocols for in vivo studies.
- Intended exclusively for research purposes.