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首页-抗体药物偶连体和PROTACs-PROTAC-KG-FP-003
KG-FP-003

Chemical Structure : KG-FP-003

CAS No.: 3066008-42-9

KG-FP-003

货号: PC-25828Not For Human Use, Lab Use Only.

KG-FP-003 is a potent, selective, and durable TEAD PROTAC degrader with biochemicals binding IC50 of 591 nM for CRBN, degrades all TEAD isoforms in NCI-H1299 cells (TEAD1, DC50= 6 nM, TEAD2 DC50= 68 nM, TEAD3 DC50 =12, TEAD4 DC50= 7 nM).

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纯度 & COA & 质检文件 纯度: >98% (HPLC)

生物&药学活性

KG-FP-003 is a potent, selective, and durable TEAD PROTAC degrader with biochemicals binding IC50 of 591 nM for CRBN, degrades all TEAD isoforms in NCI-H1299 cells (TEAD1, DC50= 6 nM, TEAD2 DC50= 68 nM, TEAD3 DC50 =12, TEAD4 DC50= 7 nM).
KG-FP-003 robustly induces formation of the TEAD1–CRBN ternary complex with EC50 of 8 nM.
KG-FP-003 markedly increases TEAD1 ubiquitination, promotes UPS-dependent degradation of TEAD1.
KG-FP-003 exhibits potent antiproliferative activity with IC50 values of 27 nM in NCI-H226 cells and 47 nM in MSTO-211H cells.
KG-FP-003 (3 mg/kg, i.p.) induces pronounced degradation of TEAD1 protein and significant tumor growth inhibition in MSTO-211H pleural mesothelioma xenograft model.

物理化学性质&存储条件

分子量 1049.65
分子式 C58H67ClF2N6O8
外观性状 Solid
CAS No.
储存条件
固体粉末
-20°C 12 个月; 4°C 6 个月
配置液
-80°C 6 个月; -20°C 6 个月
Shipping
Solubility

10 mM in DMSO

Chemical Name/SMILES

(1S,2S)-6-((2S)-5-chloro-2-((((1r,4S)-4-(4-((1-(2-(4-(2,4-dioxotetrahydropyrimidin-1(2H)-yl)-3-methylphenoxy)acetyl)piperidin-4-yl)methyl)piperidine-1-carbonyl)cyclohexyl)amino)methyl)-6-fluoro-2-phenyl-2,3-dihydrobenzofuran-4-yl)-7-fluoro-1-hydroxy-N,2-dimethyl-2,3-dihydro-1H-indene-5-carboxamide

参考文献

1. Cao L, et al. Adv Sci (Weinh). 2025 Oct 5:e03277.

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