(S, R, S) -AHPC-Me-C6-NH2
(S, R, S) -AHPC-Me-C6-NH2 can be used for the synthesis of PROTAC[1]. (S, R, S) -AHPC-Me-C6-NH2 (Compound SI-9) contains VHL ligand 2 (HY-112078) [2].
Product Specifications
CAS Number
[2411422-49-4]
UNSPSC
12352005
Target
E3 Ligase Ligand-Linker Conjugates
Type
Reference compound
Related Pathways
PROTAC
Applications
Cancer-programmed cell death
Field of Research
Others
Assay Protocol
https://www.medchemexpress.com/s-r-s-ahpc-me-c6-nh2.html
Purity
99.81
Solubility
DMSO : ≥ 100 mg/mL
Smiles
NCCCCCCC(N[C@@H](C(C)(C)C)C(N1[C@@H](C[C@H](C1)O)C(N[C@H](C2=CC=C(C3=C(N=CS3)C)C=C2)C)=O)=O)=O
Molecular Formula
C30H45N5O4S
Molecular Weight
571.77
References & Citations
[1]Haibing Zhou, et al. Oseltamivir PROTAC compound, preparation method thereof and application thereof in anti-influenza virus drugs. Patent CN112592331A.|[2]Bondeson DP, et al. Systematic profiling of conditional degron tag technologies for target validation studies. Nat Commun. 2022 Sep 20;13 (1) :5495.
Shipping Conditions
Blue Ice
Storage Conditions
-20°C (Powder, sealed storage, away from moisture)
Scientific Category
Reference compound1
Clinical Information
No Development Reported
Available Sizes
Curated Selection
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