GLPBio

GW806742X

Catalog No.: GC36203Purity:>99.50%
ATP 모방체이자 강력한 MLKL(Mixed Lineage Kinase Domain-Like protein) 억제제인 GW806742X는 9.3μM의 Kd로 MLKL 슈도키나제 도메인에 결합합니다.

제품은 연구용으로만 사용됩니다. 인체에 사용할 수 없으며 환자에게 판매하지 않습니다.


GW806742X
Cas No.: 579515-63-2
10mM (in 1mL DMSO)In Stock
$44.00
1
1mgIn Stock
$16.00
1
5mgIn Stock
$35.00
1
10mgIn Stock
$56.00
1
25mgIn Stock
$105.00
1
50mgIn Stock
$168.00
1
100mgIn Stock
$263.00
1

인용 문헌 (Citations)

현재 이 제품에 대한 인용 문헌이 없습니다. 아래는 GlpBio 제품을 인용한 주요 논문입니다.
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    Nature
    641, 529–536 (2025)
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    628, 630–638 (2024)
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    632, 686–694 (2024)
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    618, 1017–1023 (2023)
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    Nature
    610, 366–372 (2022)
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    Cell
    187(9):2288-2304 (2024)
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    Cell
    183(7):1867-1883 (2020)
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    388(6745) (2025)
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    387(6734) (2025)
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    33, 904–922 (2023)
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    31, 1291–1307 (2021)

제품 설명 (Description)

GW806742X, an ATP mimetic and a potent MLKL (Mixed Lineage Kinase Domain-Like protein) inhibitor, binds the MLKL pseudokinase domain with a KD of 9.3μM[1]. GW806742X binds to the ATP pocket of MLKL at the pseudokinase domain by forming two hydrogen bonds, thereby inhibiting necroptosis without impacting apoptosis[2]. GW806742X has been widely used in preclinical models to alleviate acute lung injury in mice and reduce airway inflammation[3].

In vitro, GW806742X treatment for 48 hours inhibited the viability of MDA-MB-231, MDA-MB-468, and MCF 10A cells, with IC50 values of 4.024µM, 3.67µM, and 18.7µM, respectively[4]. 1µM of GW806742X pretreatment for 30 minutes suppressed the phosphorylation of MLKL in L929 cells and reduced autophagy of the cells[5]. Pretreatment with 5µM GW806742X for 1 hour reduced monosodium urate (MSU) crystal-induced necrosis of mouse macrophages and prevented inflammasome activation[6]. Treatment with 0.1µM GW806742X for 24 hours inhibited the maturation and CXCL10 secretion in mouse bone marrow-derived dendritic cells (BMDCs)[7].

In vivo, a single intraperitoneal injection of 100µl of 100µM GW806742X reduced lung bacterial burden and alleviated pathological features associated with Serratia marcescens hemorrhagic pneumonia in mice after 24 hours[8]. A single intraperitoneal injection of GW806742X at a dose of 2mg/kg alleviated cecal ligation and puncture (CLP)-induced multiple organ dysfunction and systemic inflammation and improved survival in mice after 24 hours[9].

References:
[1] Hildebrand J M, Tanzer M C, Lucet I S, et al. Activation of the pseudokinase MLKL unleashes the four-helix bundle domain to induce membrane localization and necroptotic cell death[J]. Proceedings of the National Academy of Sciences, 2014, 111(42): 15072-15077.
[2] Zhou Y, Cai Z, Zhai Y, et al. Necroptosis inhibitors: mechanisms of action and therapeutic potential[J]. Apoptosis, 2024, 29(1): 22-44.
[3] Kang Z, Xuan N, Zhou Q, et al. Targeting alveolar epithelial cells with lipid micelle-encapsulated necroptosis inhibitors to alleviate acute lung injury[J]. Communications Biology, 2025, 8(1): 573.
[4] Liu W, Xu J, Chen L, et al. Discovery of a novel BCL-2 inhibitor GW806742X for the treatment of TNBC[J]. Biochemical Pharmacology, 2025, 237: 116925.
[5] Zhan Q, Jeon J, Li Y, et al. CAMK2/CaMKII activates MLKL in short-term starvation to facilitate autophagic flux[J]. Autophagy, 2022, 18(4): 726-744.
[6] Zhong C, Zeng B, Qiu J, et al. Gout-associated monosodium urate crystal-induced necrosis is independent of NLRP3 activity but can be suppressed by combined inhibitors for multiple signaling pathways[J]. Acta Pharmacologica Sinica, 2022, 43(5): 1324-1336.
[7] Jensen T S, Laursen M F, Schort L, et al. STING and Nonnecroptotic MLKL‐Mediated Mechanisms Improve Dendritic Cell Maturation and Killing of Cancer Cells[J]. European Journal of Immunology, 2025, 55(9): e70044.
[8] González-Juarbe N, Gilley R P, Hinojosa C A, et al. Pore-forming toxins induce macrophage necroptosis during acute bacterial pneumonia[J]. PLoS pathogens, 2015, 11(12): e1005337.
[9] Zhang X, Wu J, Liu Q, et al. RIPK3–MLKL necroptotic signalling amplifies STING pathway and exacerbates lethal sepsis[J]. Clinical and translational medicine, 2023, 13(7): e1334.

실험 프로토콜 (Protocol)

Cell experiment [1]:

Cell lines

MDA-MB-231 cells

Preparation Method

MDA-MB-231 cells were cultured in Leibovitz's L15 medium, supplemented with 10% fetal bovine serum and 1% penicillin-streptomycin, at 37°C in an incubator with 5% CO2. SCC131 viable cells were seeded and counted using a hemocytometer in a complete nutrient medium at a concentration of 8×103 cells/ml per well in 96‐well plates, then incubated for 24 hours. Cells were treated with different concentrations of GW806742X (0, 5, 10, 15, and 20µM). After 48h, cell viability was measured.

Reaction Conditions

0, 5, 10, 15, and 20µM; 48h

Applications

GW806742X treatment markedly decreased the cell viability of MDA-MB-231 cells in a dose-dependent manner.
Animal experiment [2]:

Animal models

C57BL/6 mice

Preparation Method

C57BL/6 mice (8 weeks old) were housed under controlled conditions with a relative humidity of 55%±5%, room temperature maintained at 23°C-24°C, and a 12h light/dark cycle. Mice were anesthetized with a mixture of intraperitoneal xylazine (50mg/kg) and ketamine (50mg/kg). A longitudinal incision was made to the middle of the abdomen, and the cecum was exposed. The cecum was ligated with a 5.0 monofilament suture just distal to the ileocecal junction (with more than 90% of the cecum ligated) and punctured with an 18-gauge needle. A small amount of feces was gently squeezed out of the perforation to ensure patency of the puncture. The cecum was then placed back into the peritoneal cavity, and the incision was closed. In sham surgical controls, the cecum was exposed but not ligated or punctured and then returned to the abdominal cavity. All mice received 0.5ml of PBS immediately after surgery for fluid resuscitation. Mice received an intraperitoneal injection of 3mg/kg GSK-872 or 2mg/kg GW806742X dissolved in SBE-β-CD solution at 24h after cecal ligation and puncture. Intestine, lung, and kidney tissues were collected for analysis.

Dosage form

2mg/kg; once; i.p.

Applications

GW806742X treatment attenuated CLP-induced tissue injury in mice.

References:
[1] Liu W, Xu J, Chen L, et al. Discovery of a novel BCL-2 inhibitor GW806742X for the treatment of TNBC[J]. Biochemical Pharmacology, 2025, 237: 116925.
[2] Zhang X, Wu J, Liu Q, et al. RIPK3–MLKL necroptotic signalling amplifies STING pathway and exacerbates lethal sepsis[J]. Clinical and translational medicine, 2023, 13(7): e1334.

제품 문서 (Product Documents)

Purity:>99.50%Appearance:A solid

화학적 특성 (Chemical Properties)

CAS 번호
579515-63-2
SMILES
O=S(C1=CC=CC(NC2=NC=CC(N(C)C3=CC=C(NC(NC4=CC=C(OC(F)(F)F)C=C4)=O)C=C3)=N2)=C1)(N)=O
분자식
C25H22F3N7O4S
분자량
573.55
용해도
DMSO: ≥ 125 mg/mL (217.94 mM)
보관
Store at -20°C
배송 조건
평가용 샘플은 아이스팩과 함께 배송됩니다. 그 외 용량은 실온 배송되며, 요청 시 아이스팩과 함께 배송할 수 있습니다.

계산 도구 (Calculators)몰 농도 / 희석 / 분자량 / 단위 변환 / 생체 내 제형 / 용해도

g/mol

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