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205309-81-5

中文名稱 DL-TBOA
英文名稱 DL-TBOA
CAS 205309-81-5
分子式 C11H13NO5
分子量 239.22
MOL 文件 205309-81-5.mol
205309-81-5 結(jié)構(gòu)式 205309-81-5 結(jié)構(gòu)式

基本信息

中文別名
化合物 T11055
英文別名
DL-TBOA
BYOBCYXURWDEDS-IUCAKERBSA-N
D,L-THREO-B-BENZYLOXYASPARTATE
DL-threo-β-Benzyloxyasparticacid
DL-THREO-BETA-BENZYLOXYASPARTIC ACID
D-Aspartic acid, 3-(phenylmethoxy)-, (3R)-rel-

物理化學(xué)性質(zhì)

儲(chǔ)存條件Desiccate at -20°C
溶解度<23.92mg/ml in DMSO;insoluble in H2O
形態(tài)固體
顏色白色
DL-TBOA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
2024/11/08HY-107522DL-TBOA
DL-TBOA
205309-81-55mg2900元
2024/11/08HY-107522DL-TBOA
DL-TBOA
205309-81-510mM * 1mLin DMSO3190元
2024/11/08HY-107522DL-TBOA
DL-TBOA
205309-81-510mg4500元

常見問(wèn)題列表

生物活性
DL-TBOA 是一種有效的不可運(yùn)輸?shù)呐d奮性氨基酸轉(zhuǎn)運(yùn)蛋白抑制劑,對(duì)興奮性氨基酸轉(zhuǎn)運(yùn)蛋白 1 (EAAT1),EAAT2 和 EAAT3 的 IC50 值分別為 70 μM,6 μM 和 6 μM。DL-TBOA 抑制表達(dá)人 EAAT1 和 EAAT2 的 COS-1 細(xì)胞攝取 [14C]谷氨酸,Ki 值分別為 42 μM 和 5.7 μM。DL-TBOA 以競(jìng)爭(zhēng)性方式阻斷 EAAT4 和 EAAT5,Ki 值分別為 4.4 μM 和 3.2 μM。
靶點(diǎn)

IC50: 70 μM (EAAT1), 6 μM (EAAT2) and 6 μM (EAAT3); Ki: 42 μM (human EAAT1), 5.7 μM (human EAAT2), 4.4 μM (EAAT4) and 3.2 μM (EAAT5)

體外研究

DL-TBOA (70-350 μM; 48 hours; HCT116 and LoVo cell lines) treatment concentration-dependently enhances SN38-induced loss of viability. DL-TBOA reversed Oxaliplatin-induced loss of viability.
DL-TBOA (350 μM; 24 hours; HCT116 and LoVo cell lines) treatment decreases p53 induction by SN38 and oxaliplatin.

Cell Viability Assay

Cell Line: HCT116 and LoVo cell lines
Concentration: 70 μM, 350 μM
Incubation Time: 48 hours
Result: Enhanced SN38-induced, and counteracted Oxaliplatin-induced, cell death.

Cell Viability Assay

Cell Line: HCT116 and LoVo cell lines
Concentration: 350 μM
Incubation Time: 24 hours
Result: p53 induction by SN38 and oxaliplatin was decreased.
體內(nèi)研究

DL-TBOA (10 nmol; i.c.v.) to morphine-dependent rats significantly facilitates the expression of naloxone-precipitated somatic signs and conditioned place aversion.

Animal Model: Male Sprague-Dawley rats (180-250 g)
Dosage: 1 nmol, 3 nmol, 10 nmol
Administration: Intracerebroventricularly injection (i.c.v.)
Result: Dose dependently facilitated various somatic signs induced by Naloxone (0.1 mg/kg)-precipitated morphine withdrawal.
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