Thalidomide-O-C5-NH2|CAS 2307477-23-0|DC Chemicals

Cas No.:	2307477-23-0
Chemical Name:	Thalidomide-O-C5-NH2
SMILES:	O=C1N(C(CC2)C(NC2=O)=O)C(C3=C1C=CC=C3OCCCCCN)=O
Formula:	C₁₈H₂₁N₃O₅
M.Wt:	359.38
Sotrage:	2 years -20°C Powder, 2 weeks 4°C in DMSO, 6 months -80°C in DMSO

Cat. No.	Product name	Field of application
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DC47675	Thalidomide-Piperazine-Piperidine hydrochloride	Thalidomide-Piperazine-Piperidine hydrochloride is a synthesized E3 ligase ligand-linker conjugate. Thalidomide-Piperazine-Piperidine hydrochloride incorporates the Thalidomide based cereblon ligand and a linker used in PROTAC technology.
DC47674	2-(2,6-Dioxopiperidin-3-yl)phthalimidine-C5-Br	2-(2,6-Dioxopiperidin-3-yl)phthalimidine-C5-Br is a E3 ligase ligand-linker conjugate for PROTAC.
DC47673	(S,R,S)-AHPC-Me-decanedioic acid	(S,R,S)-AHPC-Me-decanedioic acid is an E3 ligase ligand-linker conjugate that can be used in the synthesis of PROTACs.
DC47672	Thalidomide-4-O-C10-COOH	Thalidomide-4-O-C10-COOH is a E3 ligase ligand-linker conjugate that can be used in the synthesis of PROTACs.
DC47671	(S,R,S)-AHPC-CO-C9-acid	(S,R,S)-AHPC-CO-C9-acid is an E3 ligase ligand-linker conjugate that can be connected to the ligand for protein to form PROTACs.
DC47670	cIAP1 Ligand-Linker Conjugates 16	cIAP1 Ligand-Linker Conjugates 16 is an E3 ligase ligand-linker conjugate that can be used in the synthesis of PROTACs.
DC47204	Thalidomide-Piperazine-PEG1-NH2 diTFA	Thalidomide-Piperazine-PEG1-NH2 diTFA is a synthesized E3 ligase ligand-linker conjugate that incorporates the Thalidomide based cereblon ligand and a linker used in PROTAC technology.
DC47167	Thalidomide-Piperazine-PEG2-NH2 diTFA	Thalidomide-Piperazine-PEG2-NH2 diTFA is a synthesized E3 ligase ligand-linker conjugate that incorporates the Thalidomide based cereblon ligand and a linker used in PROTAC technology.
DC47128	Pom-8PEG	Pom-8PEG, an E3 ligase ligand-linker conjugate, incorporates a cereblon (CRBN) ligand for the E3 ubiquitin ligase and an 8-unit PEG linker. Pom-8PEG can be used in the synthesis of PROTAC, such as IDO1 PROTAC degrader.