SMILES string
O=C(O)COC=1C=CC=CC1C(OC(=O)C2N(C(=O)C(C3=CC(OC)=C(OC)C(OC)=C3)CC)CCCC2)CCC4=CC=C(OC)C(OC)=C4
InChI key
UYXSZUBFOQLRNQ-BTIIJPOSSA-N
InChI
1S/C38H47NO11/c1-7-26(25-21-33(46-4)36(48-6)34(22-25)47-5)37(42)39-19-11-10-13-28(39)38(43)50-30(27-12-8-9-14-29(27)49-23-35(40)41)17-15-24-16-18-31(44-2)32(20-24)45-3/h8-9,12,14,16,18,20-22,26,28,30H,7,10-11,13,15,17,19,23H2,1-6H3,(H,40,41)/t26-,28-,30+/m0/s1
assay
≥95%
form
crystalline powder
reaction suitability
reaction type: Amidations, reaction type: Esterifications
storage condition
protect from light
color
white to beige
storage temp.
−20°C
Quality Level
General description
Application
- dTAG system / targeted protein degradation: Used as the binding ligand component in bifunctional degraders (PROTAC-type molecules) that recruit FKBP12 F36V-tagged proteins for proteasomal degradation.
- Chemical biology tool: As a modular building block for constructing degrader molecules, chemical probes, and studying protein knockdown dynamics.
- Drug discovery & functional genomics: Useful for validation of disease targets via induced degradation of tagged proteins.
Features and Benefits
- High affinity ligand for FKBP12 F36V: Enables selective binding to the engineered FKBP12 mutant, which is central to the dTAG system for induced degradation.
- Functionalised with a carboxylic acid ‘exit vector’: The ortho position acid allows further chemical derivatisation (e.g., coupling to warheads/linkers) without interfering with the ligand binding region.
Legal Information
Regulatory Information
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service