Startseite>>Signaling Pathways>> PROTAC>> E3 Ligase Ligand-Linker Conjugate>>Thalidomide 4'-ether-alkylC6-amine

Thalidomide 4'-ether-alkylC6-amine

Katalog-Nr.GC50528

Thalidomide 4'-ether-alkylC6-amine ist ein synthetisiertes E3-Ligase-Ligand-Linker-Konjugat, das in PROTAC dTAG-13, einem Abbauer von FKBP12F36V und BET, verwendet wird.

Products are for research use only. Not for human use. We do not sell to patients.

Thalidomide 4'-ether-alkylC6-amine Chemische Struktur

Cas No.: 2245697-88-3

Größe Preis Lagerbestand Menge
25 mg
216,00 $
Auf Lager

Tel:(909) 407-4943 Email: sales@glpbio.com

Kundenbewertungen

Basiert auf Kundenrezensionen.

  • GlpBio Citations

    GlpBio Citations
  • Bioactive Compounds Premium Provider

    Bioactive Compounds Premium Provider

Sample solution is provided at 25 µL, 10mM.

Description Chemical Properties Product Documents Related Products

Functionalized cereblon ligand for PROTAC® research and development; incorporates an E3 ligase ligand plus a C6 alkyl linker ready for conjugation to a target protein ligand. Part of a range of functionalized tool molecules for PROTACs R&D. This product has been recently renamed. The previous name for this product was Thalidomide - linker 4 PROTAC® is a registered trademark of Arvinas Operations, Inc., and is used under license.

Nabet et al (2018) The dTAG system for immediate and target-specific protein degradation. Nat.Chem.Biol. 14 431 PMID:29581585 |Erb et al (2017) Transcription control by the ENL YEATS domain in acute leukaemia. Nature. 543 270 PMID:28241139

Bewertungen

Review for Thalidomide 4'-ether-alkylC6-amine

Average Rating: 5 ★★★★★ (Based on Reviews and 28 reference(s) in Google Scholar.)

5 Star
100%
4 Star
0%
3 Star
0%
2 Star
0%
1 Star
0%
Review for Thalidomide 4'-ether-alkylC6-amine

GLPBIO products are for RESEARCH USE ONLY. Please make sure your review or question is research based.

Required fields are marked with *

You may receive emails regarding this submission. Any emails will include the ability to opt-out of future communications.