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905232

(S,R,S)-AHPC-C6-PEG3-butyl amine hydrochloride

≥95%

Synonym(e):

(2S,4R)-1-((S)-22-Amino-2-(tert-butyl)-4-oxo-10,13,16-trioxa-3-azadocosanoyl)-4-hydroxy-N-(4-(4-methylthiazol-5-yl)benzyl)pyrrolidine-2-carboxamide, (S,R,S)-AHPC-6-2-2-6-NH2 HCl salt, Crosslinker−E3 ligase ligand conjugate, Protein degrader building block for PROTAC® research, Template for synthesis of targeted protein degrader, VH032 conjugate

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Ihnen/SKUVerfügbarkeitPreis
50 mg
Warenkorb auf Verfügbarkeit prüfen
€ 1.220,00

Über diesen Artikel

Empirische Formel (Hill-System):
C38H61N5O7S · xHCl
Molekulargewicht:
731.99 (free base basis)
MDL number:
UNSPSC Code:
12352101
NACRES:
NA.22

€ 1.220,00


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ligand

VH032

assay

≥95%

form

powder or crystals

reaction suitability

reactivity: carboxyl reactive, reagent type: ligand-linker conjugate

functional group

amine

storage temp.

2-8°C

SMILES string

NCCCCCCOCCOCCOCCCCCC(N[C@H](C(N1[C@H](C(NCC2=CC=C(C3=C(C)N=CS3)C=C2)=O)C[C@@H](O)C1)=O)C(C)(C)C)=O.Cl

InChI

1S/C38H61N5O7S.ClH/c1-28-34(51-27-41-28)30-15-13-29(14-16-30)25-40-36(46)32-24-31(44)26-43(32)37(47)35(38(2,3)4)42-33(45)12-8-7-11-19-49-21-23-50-22-20-48-18-10-6-5-9-17-39;/h13-16,27,31-32,35,44H,5-12,17-26,39H2,1-4H3,(H,40,46)(H,42,45);1H/t31-,32+,35-;/

InChI key

AROZTUBYMZDNDZ-PRVWZYNMSA-N

Application

Protein degrader builiding block (S,R,S)-AHPC-C6-PEG3-butyl amine (HCl salt) enables the synthesis of molecules for targeted protein degradation and PROTAC (proteolysis-targeting chimeras) technology. This conjugate contains a von Hippel-Lindau (VHL)-recruiting ligand, a linker with both hydrophobic and hydrophilic moieties, and a pendant amine for reactivity with a carboxyl group on the target ligand. Because even slight alterations in ligands and crosslinkers can affect ternary complex formation between the target, E3 ligase, and PROTAC, many analogs are prepared to screen for optimal target degradation. When used with other protein degrader building blocks with a pendant amine, parallel synthesis can be used to more quickly generate PROTAC libraries that feature variation in crosslinker length, composition, and E3 ligase ligand.

Automate your VHL-PEG based PROTACs with Synple Automated Synthesis Platform (SYNPLE-SC002)

Legal Information

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

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Dieser Artikel
905275905380905399
description

≥95%

description

≥95%

description

≥95%

description

-

assay

≥95%

assay

≥95%

assay

≥95%

assay

≥95%

functional group

amine

functional group

amine

functional group

alkyl halide

functional group

alkyl halide

reaction suitability

reactivity: carboxyl reactive, reagent type: ligand-linker conjugate

reaction suitability

reactivity: carboxyl reactive, reagent type: ligand-linker conjugate

reaction suitability

reactivity: sulfuryl reactive, reagent type: ligand-linker conjugate

reaction suitability

reactivity: sulfuryl reactive, reagent type: ligand-linker conjugate

storage temp.

2-8°C

storage temp.

2-8°C

storage temp.

2-8°C

storage temp.

2-8°C

form

powder or crystals

form

powder or crystals

form

solid

form

liquid

ligand

VH032

ligand

VH032

ligand

VH032

ligand

VH032


Lagerklasse

11 - Combustible Solids

flash_point_f

Not applicable

flash_point_c

Not applicable



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