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210344-97-1

中文名稱 MVPQJUFFTWWKBT-LBDWYMBGSA-N
英文名稱 MVPQJUFFTWWKBT-LBDWYMBGSA-N
CAS 210344-97-1
分子式 C31H39FN4O9
分子量 630.66
MOL 文件 210344-97-1.mol
更新日期 2024/03/07 12:03:44
210344-97-1 結(jié)構(gòu)式 210344-97-1 結(jié)構(gòu)式

基本信息

中文別名
606210
化合物Z-YVAD-FMK
英文別名
MVPQJUFFTWWKBT-LBDWYMBGSA-N
L-Alaninamide, N-[(phenylmethoxy)carbonyl]-L-tyrosyl-L-valyl-N-[(1S)-3-fluoro-1-(2-methoxy-2-oxoethyl)-2-oxopropyl]- (9CI)

物理化學(xué)性質(zhì)

沸點(diǎn)945.2±65.0 °C(Predicted)
密度1.261±0.06 g/cm3(Predicted)
酸度系數(shù)(pKa)9.81±0.15(Predicted)
形態(tài)Solid
顏色White to off-white
序列Z-Tyr-Val-Ala-Asp-FMK
MVPQJUFFTWWKBT-LBDWYMBGSA-N價(jià)格(試劑級(jí))
報(bào)價(jià)日期產(chǎn)品編號(hào)產(chǎn)品名稱CAS號(hào)包裝價(jià)格
2026/07/06S8507MVPQJUFFTWWKBT-LBDWYMBGSA-N
Z-YVAD-FMK
210344-97-15mg4370元
2026/07/06S8507Z-YVAD-FMK210344-97-110mM (1mL in DMSO)5135.13元
2026/07/06S8507Z-YVAD-FMK210344-97-125mg13423.9元

常見問題列表

生物活性
Z-YVAD-FMK 是一種具有抗炎和抗腫瘤活性的細(xì)胞滲透性的、不可逆的 caspase-1 特異性抑制劑。
靶點(diǎn)
TargetValue
caspase-1
()
體外研究

Z-YVAD-FMK (100 μM; 24 hours) significantly downregulated the growth inhibition induced by butyrate in Caco-2 cells. Z-YVAD-FMK (20 μM; pre 1 hour; 24 hours) attenuates the apoptotic induction of III-10 on both HepG2 and BEL-7402 cells, the apoptotic rate of -10 on HepG2 cells is reduced by Z-VAD-FMK from 19.88% to 8.34%, while that on BEL-7402 cells is reduced from 17.56% to 11.98%. Z-YVAD-FMK (1-10 μM; 24 hours) shows inhibitory effect in various cells against TNFr- or anti-CD95-induced cell death, exhibits IC 50 values of 0.0015 μM (Murine hepatocytes), 0.027 μM (Murine hepatocytes), 4.8 μM (HepG2), 5.8 μM (HepG2), 1.6 μM (Hela) and 1.1 μM (Jurkat), respectively.

Cell Viability Assay

Cell Line: Caco-2 cells
Concentration: 0-100 μM
Incubation Time: 24 hours
Result: Inhibited Caco-2 cells growth.

Apoptosis Analysis

Cell Line: BEL-7402 and HepG2 cells
Concentration: 20 μM
Incubation Time: Pre 1 hour; 24 hours
Result: Induced a caspase-dependent apoptosis in cells.
體內(nèi)研究

Z-VAD-FMK (intraperitoneal?injection; 10mg/kg; pre- 30 minutes) significantly delayed preterm delivery at 18 hours, but after 36 hours treatment, non different exists between Z-VAD-FMK-pretreated and control groups.

Animal Model: Day 14.5 pregnant CD1 mice
Dosage: 10?mg/kg
Administration: Intraperitoneal?injection; 10mg/kg; pre-30 minutes
Result: Prevented HK-GBS-induced preterm delivery.
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