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AZD 5582

AZD 5582

中文名稱AZD 5582
中文同義詞二聚化SMAC MIMETICS,IAPS抑制劑;(2S,2'S)-1,1'-((S,2S,2'S)-2,2'-(((1S,1'S,2R,2'R)-(己-2,4-二炔-1,6-二基雙(氧))雙(2,3-二氫-1H-茚-2,1-二基))雙(環(huán)己烷-3,1-二基))雙(2-((S)-2-(甲胺基)丙胺基)乙?;?雙(吡咯烷-2-甲酰胺);化合物 AZD5582;AZD5582試劑;AZD5582 ,S7362;AZD5582試劑
英文名稱AZD-5582
英文同義詞AZD-5582;3,3'-[2,4-Hexadiyne-1,6-diylbis[oxy[(1S,2R)-2,3-dihydro-1H-indene-2,1-diyl]]]bis[N-methyl-L-alanyl-(2S)-2-cyclohexylglycyl-L-prolinamide];AZD5582;AZD-5582;AZD 5582;CS-2673;(S,S,2S,2'S)-N,N'-((1S,1'S,2R,2'R)-(hexa-2,4-diyne-1,6-diylbis(oxy))bis(2,3-dihydro-1H-indene-2,1-diyl))bis(1-((S)-2-cyclohexyl-2-((S)-2-(methylamino)propanamido)acetyl)pyrrolidine-2-carboxamide);L-Prolinamide, 3,3'-[2,4-hexadiyne-1,6-diylbis[oxy[(1S,2R)-2,3-dihydro-1H-indene-2,1-diyl]]]bis[N-methyl-L-alanyl-(2S)-2-cyclohexylglycyl-;ZD5582;(2S,2'S)-1,1'-((S,2S,2'S)-2,2'-(((1S,1'S,2R,2'R)-(Hexa-2,4-diyne-1,6-diylbis(oxy))bis(2,3-dihydro-1H-indene-2,1-diyl))bis(cyclohexane-3,1-diyl))bis(2-((S)-2-(methylamino)propanamido)acetyl))bis(pyrrolidine-2-carboxamide)
CAS號(hào)1258392-53-8
分子式C58H78N8O8
分子量1015.29
EINECS號(hào)
相關(guān)類別細(xì)胞生物學(xué)試劑;抑制劑
Mol文件1258392-53-8.mol
結(jié)構(gòu)式AZD 5582 結(jié)構(gòu)式

AZD 5582 性質(zhì)

沸點(diǎn)1207.3±65.0 °C(Predicted)
密度1.26±0.1 g/cm3(Predicted)
儲(chǔ)存條件4°C, protect from light, stored under nitrogen
溶解度DMF:30mg/mL; DMSO:15mg/mL;乙醇:30mg/mL
形態(tài)結(jié)晶固體
酸度系數(shù)(pKa)12.99±0.40(Predicted)
顏色白色至黃色
InChIKeyBRCXWBBDZROUEZ-WCMFYDHYSA-N

AZD 5582 用途與合成方法

AZD5582 是 IAP 拮抗劑,可以有效與 cIAP1,cIAP2 和 XIAP 的 BIR3 結(jié)構(gòu)域結(jié)合, IC50 值分別為 15,21,15 nM。AZD5582 誘導(dǎo)凋亡 (apoptosis)。

cIAP1

15 nM (IC 50 )

cIAP2

21 nM (IC 50 )

XIAP

15 nM (IC 50 )

AZD5582 (20 nM; 48 hours) inhibits cell viability by cooperation with IFNγ or viral double-stranded RNA (dsRNA) in H1975 NSCLC cells. AZD5582 (20 nM; 17 or 25 hours) downregulates cIAP-1, activates RIPK1 (upstream regulator of caspase-8), and triggers the activation of extrinsic (caspase-8) and intrinsic (caspase-9) apoptosis pathways, causing the cleavage of caspase-3 and caspase-7. AZD5582 (20 nM; 48 hours) involves in apoptosis due to induction of cell death and active caspase-3/8 activities by AZD5582 and IFNγ co-treatment in HCC827 NSCLC cells.

Cell Viability Assay

Cell Line: H1975 NSCLC cell line
Concentration: 20 nM
Incubation Time: 48 hours
Result: Cooperated with IFNγ or viral double-stranded RNA (dsRNA) to inhibit cell viability even cell death.

Apoptosis Analysis

Cell Line: HCC827 NSCLC cell line
Concentration: 20 nM
Incubation Time: 48 hours
Result: Had an inhibitory effect on cell viability by cooperating with IFNγ.

Western Blot Analysis

Cell Line: H1975 NSCLC cell line
Concentration: 20 nM
Incubation Time: 17 or 25 hours
Result: Down-regulated cIAP-1, activated RIPK1 (upstream regulator of caspase-8), triggered the cleavage (activation) of caspase-3,7,8 and 9.

AZD5582 (intravenous injection; 0.1-3.0 mg/kg; once a week; 2 weeks) causes degradation of cIAP1 and caspase 3 cleavage in tumor cells, and after a two-week treatment, the tumors largely resolved; when the mice are given a medium dose (0.5 mg/kg) of AZD5582, cIAP1 degrades after administration, but it takes a while time to reach apoptosis-inducing effect.

Animal Model: MDA-MB-231 xenograft-bearing mice
Dosage: 0.1 mg/kg, 0.5 mg/kg, 3.0 mg/kg
Administration: Intravenous injection; once a week; 2 weeks
Result: Resulted in cIAP1 degradation and caspase-3 cleavage within tumor cells and causes substantial tumor regressions following two weekly doses of 3.0 mg/kg

安全信息

WGK GermanyWGK 3
存儲(chǔ)類別11 - 可燃固體

MSDS信息

更新日期產(chǎn)品編號(hào)產(chǎn)品名稱CAS號(hào)包裝價(jià)格
2026/06/05HY-12600AZD 5582
AZD5582
1258392-53-82mg660元
2026/06/05HY-12600AZD 5582
AZD5582
1258392-53-85mg990元

AZD 5582 上下游產(chǎn)品信息

"AZD 5582"相關(guān)產(chǎn)品信息
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