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Filtered Search Results
Medchemexpress LLC Cyclooctyne-o-amido-peg4-vc-pab-gly-gly-nh-o-co-exatecan | 2699066-62-9 | 97.3% | 1396.51 | C69H90FN11O19 | 1 MG
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Cyclooctyne-O-amido-PEG4-VC-PAB-Gly-Gly-NH-O-CO-Exatecan is a cleavable drug-linker conjugate intended for antibody-drug conjugate (ADC) research, where Exatecan serves as the cytotoxic payload. Supplied as a solid for research use only, it is used in conjugation chemistry and ADC synthesis.
- Molecular formula: C69H90FN11O19.
- Molecular weight: 1396.51.
- Purity: 97.3%.
- Physical state: solid.
- Cas number: 2699066-62-9.
- Available sizes: 1 mg and 5 mg vials; larger quantities available by quotation.
- Storage: 4°C under nitrogen; in solvent: -80°C (up to 6 months) or -20°C (up to 1 month), stored under nitrogen.
- For research use only; not for human or veterinary use.
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Apexbio Technology LLC SKA 31 40172-65-4 50mg
SKA 31 (CAS 40172-65-4) is a small-molecule activator of calcium-activated potassium channels selectively targeting KCa3 1 KCa2 2 KCa2 1 and KCa2 3 subtypes It exhibits EC50 values of 260 nM for KCa3 1 1 9 M for KCa2 2 and 2 9 M for both KCa2 1 and KCa2 3 By facilitating the activation of these channels SKA 31 enhances endothelium-derived hyperpolarizing factor (EDHF) responses This compound is employed to investigate endothelial function and signal transduction with notable utility in studies exploring blood pressure regulation and related vascular mechanisms
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Medchemexpress LLC VII-31 25 mg
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VII-31 25MG
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Chemscene CHEMSCENE
5000579946 EEDQ 1KG
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Chemscene CHEMSCENE
5000579947 EEDQ 250G
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Medchemexpress LLC PYRROLOQUINOLINE QUI 50 mg
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PYRROLOQUINOLINE QUI 50MG
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Medchemexpress LLC SKA-31 25 mg
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SKA-31 25MG
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Medchemexpress LLC 2 5 -DIMETHOXY-1 1 100 mg
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2 5 -DIMETHOXY-1 1 100MG
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Ambeed AMBEED
5000884057 33-DIMETHOXY-27101316-PE 5G
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Aobchem 2 6-Dimethoxy-4-formylphenylboronic acid | ≥95% | CAS 1256355-34-6 | C9H11BO5 | 500mg
2 6-Dimethoxy-4-formylphenylboronic acid | ≥95% | CAS 1256355-34-6 | C9H11BO5 | 500mg
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eMolecules 4965-36-0 | 7-Bromoquinoline | Oakwood Chemical | MFCD03695823 | 208.058 | C9H6BrN | 97.000 | Brc1ccc2cccnc2c1 | 5g | 537699226
7-Bromoquinoline | Oakwood Chemical | 4965-36-0 | MFCD03695823 | 208.058 | C9H6BrN | 97.000 | Brc1ccc2cccnc2c1 | 5g | 537699226
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eMolecules 4965-36-0 | 7-Bromoquinoline | Oakwood Chemical | MFCD03695823 | 208.058 | C9H6BrN | 97.000 | Brc1ccc2cccnc2c1 | 100g | 537699228
7-Bromoquinoline | Oakwood Chemical | 4965-36-0 | MFCD03695823 | 208.058 | C9H6BrN | 97.000 | Brc1ccc2cccnc2c1 | 100g | 537699228
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eMolecules 5622-36-6 | Methyl 2-(quinolin-6-yl)acetate | ChemScene | MFCD04038669 | 201.225 | C12H11NO2 | 98.000 | COC(=O)Cc1ccc2ncccc2c1 | 1g | 569143723
Methyl 2-(quinolin-6-yl)acetate | ChemScene | 5622-36-6 | MFCD04038669 | 201.225 | C12H11NO2 | 98.000 | COC(=O)Cc1ccc2ncccc2c1 | 1g | 569143723
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Medchemexpress LLC Amine-PEG3-lys(PEG3-N3)-PEG3-N3 | 2244602-35-3 | 98.0% | 750.84 g/mol | C30H58N10O12 | 50 MG
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Amine-PEG3-Lys(PEG3-N3)-PEG3-N3 is a branched polyethylene glycol (PEG)-based linker with an amine terminus and azide functional groups. It is designed for use in antibody-drug conjugate (ADC) synthesis and general bioconjugation workflows where orthogonal azide chemistry and an amine handle are required.
- Branched PEG linker with amine and azide handles.
- Suitable for azide-alkyne click chemistry and amine coupling.
- High purity (98.0%).
- Available in multiple pack sizes, including 50 MG.
- Appearance: yellow to brown oil; stored at -20°C (pure) or -80°C in solvent for extended stability.
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Medchemexpress LLC Azide-PEG-amine | 95.0% | 100 MG
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Azide-PEG-amine (MW 5000) is a PEG-based PROTAC linker designed for the synthesis of PROTACs. This molecule functions as a versatile click chemistry reagent, enabling crucial reactions in chemical biology and drug discovery.
- PEG-based PROTAC linker
- Used in the synthesis of PROTACs
- Functions as a click chemistry reagent
- Contains an azide group
- Participates in copper-catalyzed azide-alkyne cycloaddition reactions (CuAAc) with alkyne groups
- Participates in strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with DBCO or BCN groups
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