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Filtered Search Results
eMolecules 252881-74-6 | NH2-PEG3-C2-Boc | Ambeed | MFCD06201017 | 277.361 | C13H27NO5 | 97.000 | CC(C)(C)OC(=O)CCOCCOCCOCCN | 250mg | 506388579
NH2-PEG3-C2-Boc | Ambeed | 252881-74-6 | MFCD06201017 | 277.361 | C13H27NO5 | 97.000 | CC(C)(C)OC(=O)CCOCCOCCOCCN | 250mg | 506388579
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Medchemexpress LLC N-Boc-dolaproine | 120205-50-7 | 99.96% | 287.36 | 500 MG
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N-Boc-dolaproine ((2R,3R)-BOC-dolaproine) is the amino acid residue of the pentapeptide Dolastatin 10. Dolastatin 10 inhibits tubulin polymerization and mitosis and has anticancer activity. N-Boc-dolaproine is a key intermediate used in the synthesis of Dolastatin 10.
- Amino acid residue of Dolastatin 10
- Inhibits tubulin polymerization
- Inhibits mitosis
- Has anticancer activity
- Key intermediate for Dolastatin 10 synthesis
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eMolecules 142253-54-1 | 1-(N-BOC)-3-cyanoazetidine | Synthonix - Stock | MFCD06796640 | 182.223 | C9H14N2O2 | 97.000 | CC(C)(C)OC(=O)N1CC(C1)C#N | 5g | 525909494
1-(N-BOC)-3-cyanoazetidine | Synthonix - Stock | 142253-54-1 | MFCD06796640 | 182.223 | C9H14N2O2 | 97.000 | CC(C)(C)OC(=O)N1CC(C1)C#N | 5g | 525909494
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eMolecules 21075-83-2 | 1-Boc-1-methylhydrazine | AA Blocks LLC | MFCD05669700 | 146.190 | C6H14N2O2 | 0.000 | CN(N)C(=O)OC(C)(C)C | 25g | 410160127
1-Boc-1-methylhydrazine | AA Blocks LLC | 21075-83-2 | MFCD05669700 | 146.190 | C6H14N2O2 | 0.000 | CN(N)C(=O)OC(C)(C)C | 25g | 410160127
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Medchemexpress LLC Boc-Aminooxy-PEG2-C2-amine | 252378-69-1 | 98.0% | C11H24N2O5 | 250 MG
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Boc-Aminooxy-PEG2-C2-amine is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs. It is for research use only.
- PEG-based PROTAC linker
- Can be used in the synthesis of PROTACs
- For research use only
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Medchemexpress LLC Carbonic Anhydrase 1 10ug
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Carbonic Anhydrase 10 Protein a member of the carbonic anhydrase family plays a role in the regulation of pH and ion transport It is expressed in various tissues including the brain liver and kidney The potential involvement of Carbonic Anhydrase 10 Protein in diseases and its physiological functions make it a subject of interest in biomedical research Carbonic Anhydrase 10 Protein Mouse (HEK293 His) is the recombinant mouse-derived Carbonic Anhydrase 10 protein expressed by HEK293 with C-His labeled tag
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Medchemexpress LLC (Z)-Zolucatetide ((Z)-FOG-001; I-67) | 98.2% | 2076.39 | 5 MG
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(Z)-Zolucatetide is a structural isomer of Zolucatetide and acts as a potent β-catenin inhibitor with an IC50 of <50 nM. It inhibits β-catenin and T-cell factor (TCF) transcription factor interaction, suppresses cell proliferation, and induces cell cycle arrest in target cells. It has shown anti-tumor efficacy in mice bearing COLO320DM colon cancer cell xenografts and can be used for the study of colon cancer.
- Potent β-catenin inhibitor with an IC50 of less than 50 nM.
- Inhibits β-catenin and T-cell factor (TCF) transcription factor interaction.
- Suppresses cell proliferation.
- Induces cell cycle arrest in target cells.
- Exhibits anti-tumor efficacy in mice bearing COLO320DM colon cancer cell xenografts.
- Useful for the study of colon cancer.
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eMolecules 194413-58-6 | (Z)-Semaxinib | TargetMol | MFCD09763655 | 238.290 | C15H14N2O | 0.000 | Cc1cc(C)c(\C=C2/C(=O)Nc3ccccc23)[nH]1 | 100mg | 761049727
(Z)-Semaxinib | TargetMol | 194413-58-6 | MFCD09763655 | 238.290 | C15H14N2O | 0.000 | Cc1cc(C)c(\C=C2/C(=O)Nc3ccccc23)[nH]1 | 100mg | 761049727
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Selleck Chemical LLC Guggulsterone E&Z S3792-10mM/1mL
Guggulsterone is one of the active constituent of Commiphora mukul It occurs in two isomeric forms namely Z-GS and E-GS Guggulsterone act as antagonist ligands for the bile acid receptor farnesoid X receptor and as active ingredients responsible for the hypolipidemic activity
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Medchemexpress LLC (E/Z)-J147 | 1146963-51-0 | 99.5% | 350.34 | 1 ML
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(E/Z)-J147 is a potent, orally active, neuroprotective agent designed for cognitive enhancement. It readily crosses the blood-brain barrier and is being studied for its potential in treating Alzheimer's disease. The compound can inhibit monoamine oxidase B and the dopamine transporter, promoting cell survival.
- Exceptionally potent and orally active
- Neuroprotective agent for cognitive enhancement
- Readily crosses the blood-brain barrier
- Inhibits monoamine oxidase B (MAO B) and the dopamine transporter
- Promotes HT22 and primary cell survival
- Enhances memory and dendritic spine number in old mice
- Potential for Alzheimer's disease treatment
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Medchemexpress LLC 4,7,10,13,16,19,22,25-Octaoxaheptacosanoic acid, 27-azido-, 1,1-dimethylethyl ester | 1623791-99-0 | 95.0% | 25 MG
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Azido-PEG8-Boc is a PEG- and alkyl/ether-based PROTAC linker integral to the synthesis of Proteolysis-Targeting Chimeras (PROTACs). This versatile compound also functions as a click chemistry reagent, featuring an azide group that facilitates specific bioconjugation reactions. It readily engages in copper-catalyzed azide-alkyne cycloaddition (CuAAc) with alkyne-containing molecules and strain-promoted alkyne-azide cycloaddition (SPAAC) with compounds possessing DBCO or BCN groups, offering broad utility in chemical biology applications.
- PEG- and alkyl/ether-based linker
- Facilitates PROTAC synthesis
- Functions as a click chemistry reagent
- Contains an azide group for bioconjugation
- Supports copper-catalyzed azide-alkyne cycloaddition (CuAAc)
- Enables strain-promoted alkyne-azide cycloaddition (SPAAC) with DBCO or BCN groups
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Medchemexpress LLC N-Boc-dolaproine dicyclohexylamine | 1369427-40-6 | 99.9% | 468.67 | 500 MG
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N-Boc-dolaproine dicyclohexylamine is an amino acid residue of the pentapeptide Dolastatin 10. Dolastatin 10 inhibits tubulin polymerization and mitosis and has anticancer activity. This product also contains dicyclohexylamine and is intended for research use only.
- Inhibits tubulin polymerization
- Inhibits mitosis
- Possesses anticancer activity
- Suitable for laboratory research applications
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Medchemexpress LLC S - - -3-Boc-2 2-di 1g | 1G
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S - - -3-Boc-2 2-di 1g | 1G
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Medchemexpress LLC 1-Boc-3-(hydroxymethyl)pyrrolidine | 114214-69-6 | 98.5% | C10H19NO3 | 1 ML
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1-Boc-3-(hydroxymethyl)pyrrolidine is an intermediate used to synthesize a FGFR1/2/3/4 inhibitor (Compound 2). It is also utilized in cancer research.
- Used to synthesize a FGFR1/2/3/4 inhibitor
- Utilized in cancer research
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Medchemexpress LLC Br-Boc-C2-azido | 1120364-53-5 | >98% | 236.07 | 1 G
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Br-Boc-C2-azido is an alkyl/ether-based PROTAC linker used in the synthesis of PROTACs. It acts as a click chemistry reagent due to its Azide group, enabling participation in copper-catalyzed azide-alkyne cycloaddition reactions (CuAAc) with alkyne-containing molecules, and strain-promoted alkyne-azide cycloaddition (SPAAC) with DBCO or BCN groups.
- Alkyl/ether-based linker for PROTAC synthesis
- Functions as a click chemistry reagent
- Enables copper-catalyzed azide-alkyne cycloaddition (CuAAc)
- Facilitates strain-promoted alkyne-azide cycloaddition (SPAAC)
- Supports PROTACs in degrading target proteins via the ubiquitin-proteasome system
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