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Filtered Search Results
Cayman Chemical 8 12isoiPF2aVId11
An internal standard for the quantification of 8,12-iso-iPF2α-VI by GC- or LC-MS.
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eMolecules 3-AMINOISOQUINOLINE-8-CARBOXYLIC ACID HCL | 1337882-40-2 | MFCD28291832 | 1g
AstaTech | 3-AMINOISOQUINOLINE-8-CARBOXYLIC ACID HCL | 1g | 200614905 | 68507 | 95.000 | 1337882-40-2 | MFCD28291832 | 224.640 | C10H9ClN2O2
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Medchemexpress LLC Benzyl-PEG7-amine 5mg
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Benzyl-PEG7-amine is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs[1]
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Ambeed 4 6 2 3Methylbenzylidene hydra
4-(6-(2-(3-Methylbenzylidene)hydrazinyl)-2-(2-(pyridin-2-yl)ethoxy)pyrimidin-4-yl)morpholine dimethanesulfonate, 870087-36-8, 98%
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Ambeed 6Cyclopropylpyridin3amine
6-Cyclopropylpyridin-3-amine, 1159821-66-5, 95%
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Ambeed Dicyclohexyl 2 6 diisopropoxy
Dicyclohexyl(2',6'-diisopropoxy-[1,1'-biphenyl]-2-yl)phosphine, 787618-22-8, 97%
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Ambeed tertButyl 5bromopyridin3yl ca
tert-Butyl (5-bromopyridin-3-yl)carbamate, 361550-43-8, 95%
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Medchemexpress LLC 2-(2-methoxyethoxy)ethanamine | 31576-51-9 | MFCD09032941 | 99.9% | 119.16 g/mol | C5H13NO2 | 1 G
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m-PEG2-Amine is a methoxy-terminated polyethylene glycol (PEG2) linker bearing a terminal primary amine used for bioconjugation and medicinal chemistry. It is commonly employed as a PEG-based PROTAC linker and as a cleavable linker in antibody-drug conjugate (ADC) synthesis.
- Methoxy-terminated PEG2 spacer with a terminal primary amine.
- Suitable for PROTAC synthesis and as a cleavable ADC linker.
- Hydrophilic spacer improves solubility and flexibility of conjugates.
- High purity for reliable conjugation reactions.
- Store at 4°C and protect from light; in solution, store long-term at -80°C.
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Ambeed 1 1 Thiocarbonylbis pyridin2 1
1,1'-Thiocarbonylbis(pyridin-2(1H)-one), 102368-13-8, 95%
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Medchemexpress LLC Trifluoperazine dihydrochloride | 440-17-5 | 99.9% | 50 MG
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Trifluoperazine dihydrochloride is an antipsychotic agent that functions by blocking central dopamine receptors. It also acts as a potent α1-adrenergic receptor antagonist and a NUPR1 inhibitor, demonstrating anticancer activity. Furthermore, it is a calmodulin inhibitor and inhibits P-glycoprotein. This compound is utilized in research for schizophrenia and acts as a reversible inhibitor of influenza virus morphogenesis by interfering with cellular CaM and/or CaM-dependent functions.
- Blocks central dopamine receptors
- Potent α1-adrenergic receptor antagonist
- Potent NUPR1 inhibitor with anticancer activity
- Calmodulin inhibitor
- Inhibits P-glycoprotein
- Utilized in research for schizophrenia
- Acts as a reversible inhibitor of influenza virus morphogenesis
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Medchemexpress LLC 3,6,9,12,15,18-Hexaoxanonadecan-1-amine | 184357-46-8 | ≥97.0% | 5 G
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m-PEG6-Amine is a PEG-based PROTAC linker that can be utilized in the synthesis of PROTACs. It also functions as a cleavable ADC linker employed in the synthesis of antibody-drug conjugates (ADCs).
- PEG-based PROTAC linker
- Utilized in the synthesis of PROTACs
- Cleavable ADC linker
- Employed in the synthesis of antibody-drug conjugates (ADCs)
- PROTACs exploit the intracellular ubiquitin-proteasome system for selective protein degradation
- ADCs comprise an antibody attached to a cytotoxin via an ADC linker
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TARGETMOL CHEMICALS INC 8-Prenylnaringenin 1MG
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Also available in 1 mL, 5 mg, 10 mg, 25 mg, 50 mg, 100 mg and bulk. Please contact Fisher for quotes. 8-Prenylnaringenin is a phytoestrogen with high estrogenic activity, Purity 99.67%
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eMolecules METHYL 1-AMINOISOQUINOLINE-6-CARBOXYLATE TFA SALT | 1956385-65-1 | MFCD29074428 | 1g
AstaTech | METHYL 1-AMINOISOQUINOLINE-6-CARBOXYLATE TFA SALT | 1g | 164730521 | VT1109 | 95.000 | 1956385-65-1 | MFCD29074428 | 316.236 | C13H11F3N2O4
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Medchemexpress LLC 3,6,9,12,15,18-Hexaoxanonadecan-1-amine | 184357-46-8 | ≥97.0% | 10 G
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Small and/or specialty supplier based on Federal laws and SBA requirements.
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m-PEG6-Amine is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs. It is also a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs). PROTACs exploit the intracellular ubiquitin-proteasome system to selectively degrade target proteins, while ADCs are comprised of an antibody to which is attached an ADC cytotoxin through an ADC linker.
- PEG-based PROTAC linker
- Cleavable ADC linker
- Used in the synthesis of PROTACs
- Used in the synthesis of antibody-drug conjugates (ADCs)
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Medchemexpress LLC m-PEG9-Amine | 211859-73-3 | >97.0% | 5 G
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m-PEG9-Amine is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs, and also functions as a cleavable ADC linker utilized in the synthesis of antibody-drug conjugates (ADCs). It facilitates the construction of compounds that either selectively degrade target proteins via the ubiquitin-proteasome system or enable targeted delivery of cytotoxic drugs.
- Functions as a PEG-based PROTAC linker
- Suitable for the synthesis of PROTACs
- Acts as a cleavable ADC linker
- Used in the synthesis of antibody-drug conjugates (ADCs)
- Supports targeted protein degradation via the ubiquitin-proteasome system
- Enables targeted delivery of cytotoxic drugs
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