TD-106

Modify Date: 2024-01-22 23:08:02

TD-106 structure	Common Name	TD-106
	CAS Number	2250288-69-6	Molecular Weight	273.25
	Density	N/A	Boiling Point	N/A
	Molecular Formula	C₁₂H₁₁N₅O₃	Melting Point	N/A
	MSDS	N/A	Flash Point	N/A

Use of TD-106

TD-106 is a cereblon (CRBN) modulator, which can be used for targeted protein degradation. BRD4 PROTACs with TD-106 induce BRD4 degradation[1].

Name	TD-106

Description	TD-106 is a cereblon (CRBN) modulator, which can be used for targeted protein degradation. BRD4 PROTACs with TD-106 induce BRD4 degradation[1].
Related Catalog	Research Areas >> Cancer Signaling Pathways >> Metabolic Enzyme/Protease >> E1/E2/E3 Enzyme Signaling Pathways >> PROTAC >> PROTAC
Target	CRBN[1]
In Vitro	TD-106 (0.1 nM, 1 nM, 10 nM, 100 nM, 1000 nM, 10 μM, and 100 μM; 72 hours) inhibits the proliferation of NCI-H929 myeloma cell line with an CC50 of 0.039 μM[1]. TD-106 (1, 10, 100, and 1000 nM) induces the degradation of IKZF1/3 in NCI-H929 cells[1]. Cell Cytotoxicity Assay[1] Cell Line: NCI-H929 cells Concentration: 72 hours Incubation Time: 0.1 nM, 1 nM, 10 nM, 100 nM, 1000 nM, 10 μM, and 100 μM Result: Inhibited cell proliferation with an CC50 of 0.039 μM.
In Vivo	TD-106 (50 mg/kg; intraperitoneally; q.d. for 14 days) possesses anti-myeloma activity in SCID mice with TMD-8 xenograft model. Animal Model: Female SCID (CB-17/IcrCri-scid) mice with TMD-8 xenograft model[1] Dosage: 50 mg/kg Administration: Intraperitoneally (i.p.); q.d. for 14 days Result: Treatment inhibited tumor growth during this duration.
References	[1]. Kim SA, et al. A novel cereblon modulator for targeted protein degradation. Eur J Med Chem. 2019 Mar 15;166:65-74.

Molecular Formula	C₁₂H₁₁N₅O₃
Molecular Weight	273.25
Storage condition	2-8℃

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