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Filtered Search Results
eMolecules EMOLECULES INC
5000471858 TERT-BUTYL PIPERIDINE-4-CAR 1G
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eMolecules EMOLECULES INC
5000471043 4-AMINO-1-BOC-PIPERIDINE-4- 1G
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Medchemexpress LLC 3-Amino-2,6-piperidinedione | 2353-44-8 | 100.0% | 128.13 | 10 G
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3-Amino-2,6-piperidinedione is a synthetic intermediate used in the design of antitumor compounds. This product is intended for research use only and has not been fully validated for medical applications.
- Synthetic intermediate for antitumor compound design
- Stable under recommended storage conditions
- Should be stored at 4°C, protected from light
- For research use only
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Medchemexpress LLC Pomalidomide-amido-C | 50MG
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Pomalidomide-amido-C | 50MG
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Medchemexpress LLC Lenalidomide-acetylene-C5-COOH | 2429878-72-6 | 99.3% | 100 MG
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Lenalidomide-acetylene-C5-COOH is a Lenalidomide-based Cereblon ligand used in the recruitment of CRBN protein. It can be connected to a ligand for protein by a linker to form PROTAC. This compound is a click chemistry reagent, containing an Alkyne group that can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.
- Lenalidomide-based Cereblon ligand
- Used in the recruitment of CRBN protein
- Can be connected to a ligand for protein by a linker to form PROTAC
- Functions as a click chemistry reagent
- Contains an alkyne group that undergoes copper-catalyzed azide-alkyne cycloaddition (CuAAc) with azide groups
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Medchemexpress LLC (S,R)-GSK321 | 1816272-18-0 | 98.6% | 50 MG
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(S,R)-GSK321 is the (S,R)-enantiomer of GSK321, a potent and selective mutant IDH1 inhibitor with strong activity against various mutant IDH1 forms and high selectivity over IDH2. It induces a decrease in intracellular 2-HG, helps abrogate myeloid differentiation block, and promotes granulocytic differentiation in leukemic blasts and more immature stem-like cells. This compound is intended for research use in studies related to acute myeloid leukemia (AML) and other cancers, and is not sold to patients.
- Potent and selective mutant IDH1 inhibitor
- High selectivity over IDH2
- Induces a decrease in intracellular 2-HG
- Abrogates myeloid differentiation block
- Induces granulocytic differentiation
- Suitable for research on acute myeloid leukemia (AML) and other cancers
- Molecular weight: 501.55
- Chemical formula: C28H28FN5O3
- Appearance: white to off-white solid
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eMolecules EMOLECULES INC
5000483441 TERT-BUTYL PIPERIDINE-4-CA 10G
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Matrix Scientific 4-PHENYLPIPERIDINE MF C11H15N MW 161.25 CAS 771-99-3 MDL MFCD00006002 QTY 5 UOM G
4-PHENYLPIPERIDINE MF C11H15N MW 161.25 CAS 771-99-3 MDL MFCD00006002 QTY 5 UOM G
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Medchemexpress LLC Lenalidomide-propargyl-C2-NH2 hydrochloride | 2489242-23-9 | 98.0% | C18H20ClN3O3 | 10MG
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Small and/or specialty supplier based on Federal laws and SBA requirements.
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Lenalidomide-propargyl-C2-NH2 hydrochloride is a lenalidomide-derived cereblon (CRBN) ligand provided as the hydrochloride salt and intended as a building block for targeted protein degradation research and click-chemistry conjugation in PROTAC development.
- Lenalidomide-derived CRBN ligand for E3 ligase recruitment.
- Contains a propargyl (alkyne) handle for click chemistry conjugation.
- Supplied as the hydrochloride salt for improved handling and stability.
- High purity (98.0%).
- Chemical formula C18H20ClN3O3; molecular weight 361.82.
- Suitable for chemical biology and PROTAC design applications.
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AdipoGen Ropivacaine HCl H2O
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Chemical. CAS 132112-35-7. Formula C17H26N2O . HCl . H2O. MW 274.4 . 36.5 . 18.0. Synthetic. Ropivacaine is a long-acting amide local anaesthetic agent. Ropivacaine is a potent and reversible blocker of sodium channels in nerve fibers. It is a pure S-enantiomer and less lipophilic than racemic sodium channel blockers, such as bupivacaine and is less likely to penetrate large myelinated motor fibres, resulting in a relatively reduced motor blockade. Thus, ropivacaine has a greater degree of motor sensory differentiation, which could be useful when motor blockade is undesirable. The reduced lipophilicity is also associated with decreased potential for central nervous system toxicity and cardiotoxicity.
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eMolecules EMOLECULES INC
5000491582 4-METHYLPIPERIDINE 1G
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eMolecules 2S 3S-2-9H-FLUOREN-9-Y 25MG
5000190794 2S 3S-2-9H-FLUOREN-9-Y 25MG
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eMolecules 2S 3S-2-9H-FLUOREN-9-Y 50MG
5000190795 2S 3S-2-9H-FLUOREN-9-Y 50MG
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eMolecules 2S 3S-2-9H-FLUOREN-9- 100MG
5000190796 2S 3S-2-9H-FLUOREN-9- 100MG
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eMolecules 2S 3S-2-9H-FLUOREN-9- 500MG
5000190798 2S 3S-2-9H-FLUOREN-9- 500MG
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