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Filtered Search Results
Chem-Impex International, Inc. Cytosine 1-b-D-arabinofuranoside | MFCD00066487 | 1G
Cytosine 1-b-D-arabinofuranoside, MFCD00066487, 1G
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Chem-Impex International, Inc. D(+)-Glucose, anhydrous | 50-99-7 | MFCD00148912 | 5KG
D(+)-Glucose, anhydrous, 50-99-7, MFCD00148912, 5KG
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Medchemexpress LLC GLUCOSE-6-PHOSPHATE 5UG
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5000195531 GLUCOSE-6-PHOSPHATE 5UG
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Medchemexpress LLC SR-1114 1mg | 2769141-82-2 | 830.86 g/mol | C39H42N8O11S | 1 MG
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SR-1114 is a PROTAC degrader that targets the ENL protein and induces cereblon-dependent degradation, making it useful for research into epigenetic regulation and cancer biology.
- PROTAC mechanism: induces targeted degradation of ENL
- Physical form: solid powder for laboratory use
- Molecular weight: 830.86 g/mol
- Chemical formula: C39H42N8O11S
- High purity suitable for research applications
- Recommended storage: powder -20°C (long term) or 4°C (short term)
- Available in milligram-scale pack sizes for research use
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Sigma Aldrich Fine Chemicals Biosciences D- -Glucose BioUltra anhyd1KG
D9 D- -Glucose BioUltra anhyd1KG
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Medchemexpress LLC Guanosine, N-(1-oxobutyl)-, cyclic 3',5'-(hydrogen phosphate) 2'-butanoate, sodium salt (1:1) | 51116-00-8 | 99.7% | 50 MG
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Dibutyryl-cGMP sodium (Bt2cGMP sodium) is a cell-permeable cGMP analogue that preferentially activates cGMP-dependent protein kinase (PKG). It inhibits the release of [3H]-arachidonic acid from γ thrombin-stimulated human platelets and induces peripheral antinociception via activation of ATP-sensitive K+ channels. It is for research use only and not sold to patients.
- Appearance: solid
- Color: white to light yellow
- Molecular weight: 507.37
- Formula: C18H23N5NaO9P
- Solubility in H2O: 100 mg/mL (197.09 mM; requires ultrasonic)
- Solubility in DMSO: 100 mg/mL (197.09 mM; requires ultrasonic; hygroscopic DMSO has a significant impact on solubility)
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GRAINGER INC D--MANNOSE 25G
502781194 D--MANNOSE 25G
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Medchemexpress LLC α-D-Glucose-1-phosphate disodium | 56401-20-8 | 99.9% | 25 MG
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α-D-Glucose-1-phosphate disodium is utilized as a foundational compound in the synthesis of glucuronic acid. This substance also functions as a cytostatic agent, playing a crucial role in cardiopathic therapy, and exhibits characteristics as an antibiotic, an immunosuppressive agent, and an element involved in circulatory system therapy.
- Starting material for glucuronic acid synthesis
- Functions as a cytostatic compound
- Essential for cardiopathic therapy
- Exhibits antibiotic properties
- Acts as an immunosuppressive agent
- Used as a circulatory system therapy element
- Identified as an endogenous metabolite
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eMolecules 129451-75-8 | Adenosine, N-benzoyl-5'-O-[bis(4-methoxyphenyl)phenylmethyl]-3'-O-[(1,1-dimethylethyl)dimethylsilyl]-, 2'-[2-cyanoethyl N,N-bis(1-methylethyl)phosphoramidite] | MFCD00274109 | 1g
Ambeed | tert-Butyl 3-(4-(4455-tetramethyl-132-dioxaborolan-2-yl)phenoxy)azetidine-1-carboxylate | 50mg | 789349231 | A1058447 | 1505515-91-2 | MFCD22683476 | 375.270 | C20H30BNO5
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Chem-Impex International, Inc. Adenosine | 58-61-7 | MFCD00005752 | 25G
Adenosine, 58-61-7, MFCD00005752, 25G
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Chem-Impex International, Inc. Uridine | 58-96-8 | MFCD00006526 | 100G
Uridine, 58-96-8, MFCD00006526, 100G
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Chem-Impex International, Inc. D(+)-Mannose | 3458-28-4 | MFCD00064122 | 250G
D(+)-Mannose, 3458-28-4, MFCD00064122, 250G
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Chem-Impex International, Inc. L-(+)-Arabinose | 87-72-9 | MFCD00135866 | 250G
L-(+)-Arabinose, 87-72-9, MFCD00135866, 250G
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Medchemexpress LLC D-mannose, 6-(dihydrogen phosphate) (sodium) | 70442-25-0 | MFCD00135859 | 98.8% | 282.01166324 Da | C6H12NaO9P | 50mg
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D-Mannose 6-(dihydrogen phosphate) (sodium) is a class of biochemical reagents used in glycobiology research Glycobiology studies the structure synthesis biology and evolution of sugars It involves carbohydrate chemistry enzymology of glycan formation and degradation protein-glycan recognition and the role of glycans in biological systems This field is closely related to basic research biomedicine and biotechnology[1]
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Medchemexpress LLC Palbociclib monohydrochloride | 827022-32-2 | 99.98% | C24H30ClN7O2 | 2 G
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Palbociclib monohydrochloride (PD 0332991) is an orally active, selective inhibitor of CDK4 and CDK6. It demonstrates potent anti-proliferative activity and induces cell cycle arrest in cancer cells. This compound is utilized in research for HR-positive and HER2-negative breast cancer, as well as hepatocellular carcinoma.
- Orally active, selective inhibitor of CDK4 and CDK6.
- Demonstrates potent anti-proliferative activity.
- Induces cell cycle arrest in cancer cells.
- Utilized in research for HR-positive and HER2-negative breast cancer.
- Used in research for hepatocellular carcinoma.
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