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1801863-88-6

1801863-88-6 Structure

1801863-88-6 Structure
IdentificationBack Directory
[Name]

(4E)-TCO-PEG4-DBCO
[CAS]

1801863-88-6
[Synonyms]

TCO-PEG4-DBCO
(4E)-TCO-PEG4-DBCO
[Molecular Formula]

C38H49N3O8
[MDL Number]

MFCD31811633
[MOL File]

1801863-88-6.mol
[Molecular Weight]

675.82
Chemical PropertiesBack Directory
[Boiling point ]

891.1±65.0 °C(Predicted)
[density ]

1.22±0.1 g/cm3(Predicted)
[solubility ]

Soluble in Partially Water Soluble, DMSO, DCM, DMF
[form ]

Oil
[pka]

11.95±0.46(Predicted)
[color ]

Colorless to light yellow
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P264-P270-P271-P280-P301+P312-P302+P352-P304+P340-P305+P351+P338-P330-P332+P313-P337+P313-P362-P403+P233-P405-P501
Hazard InformationBack Directory
[Description]

TCO-PEG4-DBCO is a heterobifunctional click chemistry reagent containing a TCO and a DBCO moiety. TCO group specifically and efficiently reacts with terrahydrazine at fast speed. DBCO is very reactive toward Azide through copper free click chemistry, the PEG spacer increases the aqueous solubility of the reagent.
[Uses]

TCO-PEG4-DBCO is a PEG-based PROTAC linker can be used in the synthesis of PROTACs. TCO-PEG4-DBCO is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs)[1]. TCO-PEG4-DBCO is a click chemistry reagent, it contains a DBCO group that can undergo strain-promoted alkyne-azide cycloaddition (SPAAC) with molecules containing Azide groups. TCO-PEG4-DBCO also contains a TCO group that can undergo an inverse electron demand Diels-Alder reaction (iEDDA) with molecules containing Tetrazine groups.
[IC 50]

Cleavable Linker; PEGs
[References]

[1] Rahim MK, et al. Enhancing reactivity for bioorthogonal pretargeting by unmasking antibody-conjugated trans-cyclooctenes. Bioconjug Chem. 2015 Feb 18;26(2):352-60. DOI:10.1021/bc500605g
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