917184

BocA1V1PF2-OC₁₀-NH₂ hydrochloride

• Synonym(e): 10-Aminodecyl (S)-2-((S)-1-((S)-2-((S)-2-((tert-butoxycarbonyl)amino)propanamido)-3,3-dimethylbutanoyl)pyrrolidine-2-carboxamido)-3-(4-fluorophenyl)propanoate hydrochloride, AVP conjugate for IAP-mediated protein degrader development, SNIPER building block
• Empirische Formel (Hill-System): C₃₈H₆₂FN₅O₇ · xHCl
• Molekulargewicht: 719.93 (free base basis)
• MDL-Nummer: MFCD34602188
• UNSPSC-Code: 41116105
• NACRES: NA.22

Eigenschaften

• ligand: BocA1V1PF2
• Qualitätsniveau: 100
• Form: powder
• Eignung der Reaktion: reactivity: carboxyl reactive; reagent type: ligand-linker conjugate
• Funktionelle Gruppe: amine
• Lagertemp.: 2-8°C
• SMILES String: C[C@H](NC(OC(C)(C)C)=O)C(N[C@H](C(N1CCC[C@H]1C(N[C@H](C(OCCCCCCCCCCN)=O)CC2=CC=C(C=C2)F)=O)=O)C(C)(C)C)=O.Cl
• InChI: 1S/C38H62FN5O7.ClH/c1-26(41-36(49)51-38(5,6)7)32(45)43-31(37(2,3)4)34(47)44-23-16-17-30(44)33(46)42-29(25-27-18-20-28(39)21-19-27)35(48)50-24-15-13-11-9-8-10-12-14-22-40;/h18-21,26,29-31H,8-17,22-25,40H2,1-7H3,(H,41,49)(H,42,46)(H,43,45);1H/t26-,29-,30-,3
• InChIKey: RUPLAKBBVZSRKK-YOHNHNBXSA-N

Beschreibung

Anwendung

Protein degrader building block BocA1V1PF2-OC₁₀-NH₂ hydrochloride enables the synthesis of molecules for targeted protein degradation and SNIPER (specific and non-genetic inhibitor of apoptosis protein (IAP)-dependent protein erasers) technology.

Developed in partnership with ComInnex, this conjugate contains an in silico-derived IAP-recruiting ligand, an alkyl-chain crosslinker, and a pendant amine for reactivity with an acid on a target warhead. Because even slight alterations in ligands and crosslinkers can affect ternary complex formation between the target, E3 ligase, and protein degrader, many analogs are prepared to screen for optimal target degradation. When used with other When used with other protein degrader building blocks with a terminal amine, including CRBN and VHL targeted, parallel synthesis can be used to more quickly generate SNIPER and PROTAC^® degrader libraries that feature variation in crosslinker length, composition, and E3 ligase ligand. Learn more about the novel IAP ligands generated through virtual screening of AVP mimetics in our Technology Spotlight.

Building blocks in this series:
917478 BocA1V1PF2
916927 BocA1V1PF2-OC₆-NH₂ hydrochloride
917184 BocA1V1PF2-OC₁₀-NH₂ hydrochloride
917435 BocA1V1PF2-OPEG₁-NH₂ hydrochloride
917680 BocA1V1PF2-OPEG₃-NH₂ hydrochloride

Sonstige Hinweise

In Vivo Knockdown of Pathogenic Proteins via Specific and Nongenetic Inhibitor of Apoptosis Protein (IAP)-dependent Protein Erasers (SNIPERs)

SNIPERs−Hijacking IAP activity to induce protein degradation

E3 Ligase Ligands for PROTACs: How They Were Found and How to Discover New Ones

Rechtliche Hinweise

PROTAC is a registered trademark of Arvinas Operations, Inc., and is used under license

Sicherheitshinweise

• Lagerklassenschlüssel: 11 - Combustible Solids
• WGK: WGK 3
• Flammpunkt (°F): Not applicable
• Flammpunkt (°C): Not applicable