PTD10

PTD10 is a selective and potent BTK PROTAC degrader (DC50 = 0.5 nM, KD = 2.28 nM). PTD10 can recruit cereblon (CRBN) E3 ligase and form a ternary complex with BTK, thereby mediating the ubiquitination and proteasome-dependent degradation of BTK. PTD10 inhibits cancer cells proliferation, and induces cell apoptosis via activation of the caspase-dependent pathway and mitochondrial pathway. PTD10 potently inhibits the BCR, AKT and NF-κB signaling pathway. PTD10 can be used for researches of B-cell malignancies and autoimmune disease .


Cat. No.: EX-A9649	Purity: >98%

	Chemical structure of PTD10

For research only, Do not use for Human!

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CAS No.	2642231-19-2
Purity	>98%
Formula	C49H51N11O8
Mol Weight	921.9981
Color	Light yellow to yellow
State	Solid
Solubility	Soluble in DMSO
Shelf Life	>3 years if stored properly
Storage	Powder -20℃ 3 years, 4℃ 2 years; In solvent -20℃ 1 month;
Shipping	Shipped under ambient temperature as non-hazardous chemical. This product is stable enough for a few weeks during ordinary shipping and time spent in Customs.

Reference:	[1]. Li YQ, et al. Discovery of Novel Bruton's Tyrosine Kinase PROTACs with Enhanced Selectivity and Cellular Efficacy. J Med Chem. 2023;66(11):7454-7474.
CoA	CoA of PTD10

Smiles:	O=C1C=2N(C3=C(C2)CC(C)(C)C3)CCN1C4=C(CO)C(=CC=N4)C=5C=C(NC6=CC=C(C=N6)N7[C@@H](C)CN(C(CNC8=C9C(C(=O)N(C9=O)C%10C(=O)NC(=O)CC%10)=CC=C8)=O)CC7)C(=O)N(C)C5


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