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Filtered Search Results
eMolecules AstaTech / TERT-BUTYL 4-(4-METHYLTHIAZOL-5-YL)BENZYLCARBAMATE / 0.25g / 696744636 / E71371 / 95.000 / 2308507-34-6 / [null] / 304.410 / C16H20N2O2S
AstaTech / TERT-BUTYL 4-(4-METHYLTHIAZOL-5-YL)BENZYLCARBAMATE / 0.25g / 696744636 / E71371 / 95.000 / 2308507-34-6 / [null] / 304.410 / C16H20N2O2S
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Medchemexpress LLC [Sar9,Met(O2)11]-Substance P | 110880-55-2 | 99.6% | 1393.66 | 25 MG
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[Sar9,Met(O2)11]-Substance P is a tachykinin NK1 receptor selective agonist.
- Target: NK1 receptor
- Cell line: U-373MG ATCC
- IC50 value: 1.1 x 10-10 M
- Increases mean arterial blood pressure and heart rate
- Increases face washing and sniffing
- Produces grooming
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Medchemexpress LLC (2-Butyl-5-nitrobenzofuran-3-yl)(4-hydroxyphenyl)methanone | 141645-16-1 | 99.6% | C19H17NO5 | 10 G
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(2-Butyl-5-nitrobenzofuran-3-yl)(4-hydroxyphenyl)methanone is a drug intermediate for the synthesis of various active compounds.
- Used for synthesis of various active compounds.
- For research use only.
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eMolecules Methyl 2-(2,5-dimethyl-1,3-thiazol-4-yl)acetate | 306937-37-1 | 5G | Purity: 95%
Combi-Blocks | Methyl 2-(2,5-dimethyl-1,3-thiazol-4-yl)acetate | 5G | 306937-37-1 | MFCD02677686
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Medchemexpress LLC Phospho-JNK1/2/3 (Thr183) Antibody | 10 UL
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Phospho-JNK1/2/3 (Thr183) Antibody is a rabbit-derived and non-conjugated IgG polyclonal antibody, targeting Phospho-JNK1/2/3 (Thr183).
- Host: Rabbit
- Clonality: Polyclonal
- Species reactivity: Human, mouse, rat
- Immunogen: Synthetic phosphopeptide corresponding to residues surrounding Thr183 of human Phospho-JNK1/2/3
- Purity: Affinity purified
- Conjugation: Non-conjugated
- Modification: Phosphorylated
- Isotype: IgG
- Appearance: Liquid
- Formulation: Supplied in rabbit IgG in 10 mM phosphate buffered saline, pH 7.4, 150 mM sodium chloride, 0.05% BSA, 0.02% sodium azide and 50% glycerol
- Storage: Stored at -20°C for 1 year. Avoid repeated freeze/thaw cycles
- Shipping: Shipping with blue ice
- Applications: WB, IHC-P, ICC/IF, IP, FC
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eMolecules 4,5-Dimethylthiazol-2-amine | 2289-75-0 | MFCD00462425 | 1g
Ambeed | 4,5-Dimethylthiazol-2-amine | 1g | 490507823 | A137005 | | 2289-75-0 | MFCD00462425 | 128.190 | C5H8N2S
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Medchemexpress LLC Thymidine 3 5 -diph 5mg | 118675-87-9 | 490.12 g/mol | C10H12N2Na4O11P2 | 5 MG
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Thymidine 3',5'-diphosphate tetrasodium is a nucleotide-based biochemical reagent used in research applications where nucleotide analogs and diphosphate compounds are required. It is supplied as a high-purity tetrasodium salt suitable for in vitro studies and enzymatic assays.
- High purity: 98.75%.
- Molecular weight: 490.12 g/mol.
- Chemical formula: C10H12N2Na4O11P2.
- Salt form: tetrasodium for improved solubility.
- Supplied in small laboratory pack sizes, such as a 5 mg vial.
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eMolecules 5-Bromo-2-phenylthiazole-4-carboxylic acid ethyl ester | 914347-21-0 | MFCD08275710 | 1g
Combi-Blocks | 5-Bromo-2-phenylthiazole-4-carboxylic acid ethyl ester | 1g | 388719293 | OR-7701 | 95.000 | 914347-21-0 | MFCD08275710 | 312.180 | C12H10BrNO2S
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Medchemexpress LLC N-(2-fluoro-4-((2-(6-methoxy-1,6-dihydropyridin-3-yl)pyrimidin-4-yl)oxy)phenyl)-1,5-dimethyl-3-oxo-2 | 888719-03-7 | 99.5% | 458.42 g·mol⁻¹ | C25H16F2N4O3 | 10 MG
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MET kinase-IN-4 is a potent, orally active inhibitor of the MET receptor tyrosine kinase intended for research use. It exhibits low-nanomolar MET inhibition and activity against FLT3 and VEGFR-2, supplied as a solid for in vitro and in vivo studies.
- Potent MET inhibition (IC50 1.9 nM).
- Additional activity against FLT3 (IC50 4 nM) and VEGFR-2 (IC50 27 nM).
- High purity: 99.5%.
- Solid, off-white to light yellow appearance.
- Soluble in DMSO at 100 mg/mL; ultrasonic recommended.
- Storage: 4°C sealed; in solution -80°C for 6 months, -20°C for 1 month.
- Molecular formula C25H16F2N4O3; molecular weight 458.42 g·mol⁻¹.
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Medchemexpress LLC S-methyl-KE-298 | 143584-75-2 | ≥98.0% | 252.33 g/mol | C13H16O3S | 25 MG
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S-methyl-KE-298 is the S-methylated active metabolite of KE-298, reported to inhibit matrix metalloproteinase-1 (MMP-1) production in rheumatoid arthritis synovial cells. It is supplied as a purified research chemical (solid) for laboratory assays and analytical work.
- Reported inhibitor of matrix metalloproteinase-1 (MMP-1) production in RA synovial cells.
- High purity (≥98.0%) suitable for analytical and biological research.
- Molecular weight 252.33 g/mol and chemical formula C13H16O3S.
- Available in small research pack sizes such as 25 mg and recommended refrigerated storage.
- Product page includes a downloadable datasheet with characterization data.
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Medchemexpress LLC 2-Hydroxy-4-methylth 10mM 1mL | 583-91-5 | 150.20 | C5H10O3S | 1 ML
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2-Hydroxy-4-(methylthio)butyric acid is an organic acid used as an orally active source of methionine for research applications. Supplied as a ready-to-use 10 mM solution in DMSO (1 mL) and in larger liquid quantities, it is used in studies of methylation, nutrient supplementation, and lactation.
- Ready-to-use 10 mM solution in DMSO (1 mL) for convenient dosing.
- Available in bulk liquid quantities for formulation and scale-up.
- Modulates expression of methylation-related mRNAs such as BHMT, MTR, MAT1A, SAHH, and PCK1.
- Serves as an orally active methionine precursor for nutritional and physiological studies.
- Identified by CAS 583-91-5; molecular weight 150.20; formula C5H10O3S.
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Medchemexpress LLC tert-Butyl 4-(6-aminopyridin-3-yl)piperazine-1-carboxylate | 571188-59-5 | MFCD11594962 | 100.0% | 278.36 | 100 G
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tert-Butyl 4-(6-aminopyridin-3-yl)piperazine-1-carboxylate is a drug intermediate used for the synthesis of various active compounds. This product is for research use only and is not intended for sale to patients.
- Drug intermediate for the synthesis of various active compounds.
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Sigma Aldrich Fine Chemicals Biosciences 245-Trimethylthiazole 98 f100G
2 4 5-Trimethylthiazole is a sulfur-containing heterocyclic compound mainly found in meat products such as chicken broth cooked beef and roasted lamb fat.
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Medchemexpress LLC AGI-5198 | 1355326-35-0 | 99.9% | 462.56 | 50 MG
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AGI-5198 (IDH-C35) is a potent and selective mutant IDH1R132H inhibitor with an IC50 of 0.07 μM. It is designed for research use only.
- Potent and selective mutant IDH1R132H inhibitor.
- Inhibits mutant IDH1 enzyme in TS603 glioma cells.
- Does not impair colony formation of wild-type IDH1 glioma lines.
- Reverses increased reactive oxygen species, DNA double-strand breaks, and cell death after ionizing radiation in IDH1(R132H) mutated cancer cells.
- Causes significant growth inhibition of human glioma xenografts in vivo.
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eMolecules 2-Bromo-5-methylthiazole-4-carboxylic acid | 1194374-25-8 | MFCD12404925 | 1g
Ambeed | 2-Bromo-5-methylthiazole-4-carboxylic acid | 1g | 525006648 | A113490 | | 1194374-25-8 | MFCD12404925 | 222.060 | C5H4BrNO2S
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