Organo-Metalloid Compounds
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- (1)
- (1)
- (1)
- (1)
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- (5)
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- (1)
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Filtered Search Results
eMolecules 2857-97-8 | Bromotrimethylsilane | Oakwood Chemicals | MFCD00000048 | 153.094 | C3H9BrSi | 90.000 | C[Si](C)(C)Br | 1g | 480170680
Bromotrimethylsilane | Oakwood Chemicals | 2857-97-8 | MFCD00000048 | 153.094 | C3H9BrSi | 90.000 | C[Si](C)(C)Br | 1g | 480170680
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eMolecules 2857-97-8 | Bromotrimethylsilane | Oakwood Chemicals | MFCD00000048 | 153.094 | C3H9BrSi | 90.000 | C[Si](C)(C)Br | 5g | 480170681
Bromotrimethylsilane | Oakwood Chemicals | 2857-97-8 | MFCD00000048 | 153.094 | C3H9BrSi | 90.000 | C[Si](C)(C)Br | 5g | 480170681
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Aobchem 1-Phenyl-3-(trimethylsilyl)prop-2-yn-1-one | 95% | CAS 13829-77-1 | C12H14OSi | 500mg
1-Phenyl-3-(trimethylsilyl)prop-2-yn-1-one | 95% | CAS 13829-77-1 | C12H14OSi | 500mg
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Aobchem 4-Bromo-1-(triisopropylsilyl)-1H-pyrazole | 97% | CAS 2408382-51-2 | C12H23BrN2Si | 10g
4-Bromo-1-(triisopropylsilyl)-1H-pyrazole | 97% | CAS 2408382-51-2 | C12H23BrN2Si | 10g
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Aobchem 2 4 6-Trimethoxy- -(trifluoromethyl)benzenemethanol | ≥95% | CAS 1273861-99-6 | C11H13F3O4 | 5g
2 4 6-Trimethoxy- -(trifluoromethyl)benzenemethanol | ≥95% | CAS 1273861-99-6 | C11H13F3O4 | 5g
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Aobchem Trimethyl(3-phenoxyphenyl)silane | 95% | CAS 22515-27-1 | C15H18OSi | 250mg
Trimethyl(3-phenoxyphenyl)silane | 95% | CAS 22515-27-1 | C15H18OSi | 250mg
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Aobchem 2 6-Difluoro-3-(trimethylsilyl)benzaldehyde | 97% | CAS 2901103-47-5 | C10H12F2OSi | 500mg
2 6-Difluoro-3-(trimethylsilyl)benzaldehyde | 97% | CAS 2901103-47-5 | C10H12F2OSi | 500mg
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Aobchem 4-(Cyclopent-1-en-1-yl)-1 1 -biphenyl | 97% | CAS 415898-27-0 | C17H16 | 250mg
4-(Cyclopent-1-en-1-yl)-1 1 -biphenyl | 97% | CAS 415898-27-0 | C17H16 | 250mg
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Aobchem 2-Bromo-2 2-difluoro-1-morpholinoethanone | ≥95% | CAS 149229-27-6 | C6H8BrF2NO2 | 25g
2-Bromo-2 2-difluoro-1-morpholinoethanone | ≥95% | CAS 149229-27-6 | C6H8BrF2NO2 | 25g
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Medchemexpress LLC Ms-PEG5-t-butyl ester | 870487-48-2 | C16H32O9S | 25 MG
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Ms-PEG5-t-butyl ester is a PEG-based PROTAC linker designed for use in the synthesis of PROTACs. PROTACs are molecules that contain two different ligands connected by a linker, one for an E3 ubiquitin ligase and the other for a target protein. They leverage the intracellular ubiquitin-proteasome system to selectively degrade target proteins.
- PROTAC linker
- PEG-based structure
- Target PROTACs
- Pathway PROTAC
- Used in the synthesis of PROTACs
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Medchemexpress LLC Aminooxy-PEG3-acid | 1807540-79-9 | 95.0% | 237.25 | 100 MG
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Aminooxy-PEG3-acid is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs. PROTACs contain two different ligands connected by a linker; one is a ligand for an E3 ubiquitin ligase and the other is for the target protein. PROTACs exploit the intracellular ubiquitin-proteasome system to selectively degrade target proteins.
- PEG-based PROTAC linker
- Used in the synthesis of PROTACs
- Exploits the intracellular ubiquitin-proteasome system
- Selectively degrades target proteins
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eMolecules 252881-74-6 | H2N-PEG3-CH2CH2COOtBu | Acrotein ChemBio Inc. | MFCD06201017 | 277.361 | C13H27NO5 | 97.000 | CC(C)(C)OC(=O)CCOCCOCCOCCN | 5g | 487536523
H2N-PEG3-CH2CH2COOtBu | Acrotein ChemBio Inc. | 252881-74-6 | MFCD06201017 | 277.361 | C13H27NO5 | 97.000 | CC(C)(C)OC(=O)CCOCCOCCOCCN | 5g | 487536523
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Medchemexpress LLC DPC-681 | 284661-68-3 | 99.72% | 669.85 | 50 MG
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DPC-681 is a potent and selective inhibitor of HIV protease, effective against wild-type HIV-1. It is intended for research use only.
- Potent and selective inhibitor of HIV protease.
- Effective against wild-type HIV-1.
- Shows no loss in potency toward recombinant mutant HIVs with the D30N mutation.
- Fivefold or smaller loss in potency toward mutant variants with three to five amino acid substitutions.
- Suitable for laboratory research applications.
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Medchemexpress LLC Dbco-PEG3-VC-Exatecan | 2754384-70-6 | 96.7% | 1331.44 g/mol | C71H79FN10O15 | 10 MG
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DBCO-PEG3-VC-Exatecan is a drug-linker conjugate used in antibody-drug conjugate (ADC) research that couples a DBCO-functionalized PEG3 valine-citrulline cleavable linker to the topoisomerase I inhibitor exatecan.
- Provides a cleavable valine-citrulline (VC) linker for intracellular release.
- Includes a DBCO handle for strain-promoted azide-alkyne cycloaddition (click chemistry).
- Incorporates a PEG3 spacer to improve solubility and linker flexibility.
- Delivers exatecan, a DNA topoisomerase I inhibitor payload.
- High purity (~96.7%) and large molecular weight (~1331.44 g/mol).
- Soluble in DMSO at 50 mg/mL with ultrasonic assistance.
- Stored sealed at -20 °C; in solution, stable at -80 °C for 6 months and -20 °C for 1 month.
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Medchemexpress LLC NH2-PEG3-C6-Cl | 1261350-60-0 | 95.0% | 267.79 | 100 MG
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NH2-PEG3-C6-Cl is a PEG-based PROTAC linker used in the synthesis of PROTACs. PROTACs (Proteolysis Targeting Chimeras) contain two different ligands connected by a linker; one for an E3 ubiquitin ligase and the other for the target protein. These molecules exploit the intracellular ubiquitin-proteasome system to selectively degrade target proteins.
- PEG-based PROTAC linker
- Used in the synthesis of PROTACs
- Facilitates selective protein degradation
- For research use only
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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