PF-9366 是一种有效的甲硫氨酸腺苷转移酶 (Mat2A) 抑制剂，IC₅₀ 值和 K_d 值分别为 420 nM 和 170 nM。

PF-9366 is a human methionine adenosyltransferase 2A (Mat2A) inhibitor, with an IC 50 of 420 nM and a K d of 170 nM.

Solid

IC50: 420 nM (Mat2A)
Kd: 170 nM (Mat2A)

PF-9366 is a Mat2A inhibitor, with an IC50 of 420 nM and a Kd of 170 nM. PF-9366 displays no substantial off-target activity in GPCRs, neurotransporters, phosphodiesterases, and ion channels. PF-9366 has inhibitory activity against Mat2A in cancer cells. PF-9366 inhibits cellular S-Adenosyl-L-methionine (SAM) production with an IC50 of 1.2 μM in H520 lung carcinoma cells. PF-9366 is more potent in Huh-7 cells against SAM synthesis, with an IC50 of 255 nM, and also suppresses the proliferation of cells with an IC50 of 10 μM. has not independently confirmed the accuracy of these methods. They are for reference only.

Room temperature in continental US; may vary elsewhere.

Powder -20°C 3 years；4°C 2 years

[1]. Quinlan CL, et al. Targeting S-adenosylmethionine biosynthesis with a novel allosteric inhibitor of Mat2A. Nat Chem Biol. 2017 Jul;13(7):785-792.

In Vitro: DMSO : 10 mg/mL (28.50 mM; Need ultrasonic)配制储备液