>>Signaling Pathways>> Apoptosis>> KEAP1-Nrf2>>MIND4-17

MIND4-17

Catalog No.GC70520

MIND4-17 Keap1의 C151 잔기를 공가로 수식하는 강력한 NRF2 활성제입니다.

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MIND4-17 Chemical Structure

Cas No.: 345989-24-4

Size 가격 재고 수량
5 mg
US$108.00
재고 있음
10 mg
US$162.00
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25 mg
US$341.00
재고 있음
50 mg
US$511.00
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100 mg
US$766.00
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Sample solution is provided at 25 µL, 10mM.

Description Chemical Properties Product Documents
MIND4-17 is a potent NRF2 activator that covalently modifies a C151 residue of Keap1. MIND4-17 disrupts Keap1-Nrf2 association, leading to Nrf2 protein stabilization and nuclear translocation. MIND4‐17 exerts potent antioxidant activity.

MIND4-17 (0.1-2 μM; 24 hr) significantly and concentration-dependently increases the expression of the canonical ARE genes Nqo1, Hmox1, Srx1, and to a lesser degree Gclc[1].
MIND4-17 (0.1-2 μM; 24 hr) shows a concentration-dependent induction of NQO1 and GCLM proteins in both WT and HD mutant ST14A cells[1].
MIN4-17 (0.1-10 μM) reduces ROS levels and nitrogen intermediates production in microglia[1].

MIND4‐17 (2 mg/kg; intravitreal injection; once) activates Nrf2 signaling and attenuates retinal dysfunction by light damage in mice[2].

References:
[1]. Luisa Quinti, et al. SIRT2- and NRF2-Targeting Thiazole-Containing Compound with Therapeutic Activity in Huntington's Disease Models. Cell Chem Biol. 2016 Jul 21;23(7):849-861.
[2]. Nan Chen, et al. The Nrf2 activator MIND4-17 protects retinal ganglion cells from high glucose-induced oxidative injury. J Cell Physiol. 2020 Oct;235(10):7204-7213.

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