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Merck
CN

SML0932

Sigma-Aldrich

补骨脂定

≥98% (HPLC)

别名:

3,9-二羟基-2-异戊二烯, 3,9-二羟基-2-(3-甲基-2-丁烯基)-6H-苯并呋喃[3,2-c] [1]苯并吡喃-6-酮

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About This Item

经验公式(希尔记法):
C20H16O5
CAS号:
分子量:
336.34
MDL编号:
UNSPSC代码:
12352200
NACRES:
NA.77

质量水平

方案

≥98% (HPLC)

表单

powder

颜色

white to beige

溶解性

DMSO: 5 mg/mL, clear (warmed)

储存温度

−20°C

SMILES字符串

CC(C)=CCC1=C(C=C(OC2=O)C(C(OC3=C4)=C2C3=CC=C4O)=C1)O

InChI

1S/C20H16O5/c1-10(2)3-4-11-7-14-17(9-15(11)22)25-20(23)18-13-6-5-12(21)8-16(13)24-19(14)18/h3,5-9,21-22H,4H2,1-2H3

InChI key

YABIJLLNNFURIJ-UHFFFAOYSA-N

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生化/生理作用

补骨脂定是一种从补骨脂中提取的 Coumestan 衍生物。它能通过抑制环氧酶-2(COX-2)和5-脂氧合酶(5-LOX)表达表现出抗炎特性。除了抗癌和抗炎效果之外,补骨脂定还具有抗氧化、抗菌和抗抑郁作用。补骨脂定参与胰岛素信号的调控。它是用于治疗出血、遗尿、尿频、白癜风和牛皮癣等传统药物的主要成分。
补骨脂素是一种呋喃香豆素的天然产物,其已用于中药。 补骨脂素是一种PTP1B抑制剂,已被证明具有多种抗癌活性。补骨脂素在不依赖雄激素的前列腺癌细胞中可诱导ROS生成,从而导致细胞增殖受到抑制。研究已经发现补骨脂素可下调NOTCH1信号转导,并导致乳腺癌干细胞和乳腺癌细胞中的生长停滞。
补骨脂素是一种呋喃香豆素的天然产物,具有抗癌活性; PTP1B抑制剂。

特点和优势

该化合物是细胞凋亡研究的推荐产品。点击此处,了解更多精选的细胞凋亡产品。了解更多有关用于其他研究领域的生物活性小分子的信息,请访问sigma.com/discover-bsm

象形图

Exclamation mark

警示用语:

Warning

危险声明

预防措施声明

危险分类

Acute Tox. 4 Oral

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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访问文档库

Hee Jung Yang et al.
Biochemical pharmacology, 82(5), 524-534 (2011-06-15)
Radiotherapy is the most significant non-surgical cure for the elimination of tumor, however it is restricted by two major problems: radioresistance and normal tissue damage. Efficiency improvement on radiotherapy is demanded to achieve cancer treatment. We focused on radiation-induced normal
Li-Tao Yi et al.
Progress in neuro-psychopharmacology & biological psychiatry, 32(2), 510-519 (2007-11-17)
The antidepressant-like effects of psoralidin isolated from the seeds of Psoralea corylifolia were investigated in the forced swimming test (FST) in ICR strain of male mice. Psoralidin significantly decreased immobility time and increased swimming behavior without altering climbing behavior in
Pallab Pahari et al.
The Journal of organic chemistry, 74(7), 2750-2754 (2009-03-04)
A base-catalyzed condensation of phenyl acetate with acid chloride, followed by intramolecular cyclization and microwave-assisted cross-metathesis reaction, leads to the first total synthesis of psoralidin, a natural product with a broad range of biological activities, in a highly convergent and
Sung-Jin Lee et al.
Archives of pharmacal research, 32(7), 1061-1065 (2009-07-31)
Quinone reductase (QR) is a protective phase II enzyme against mutagens and carcinogens which is inducible by a number of chemical compounds in plants. This study was carried out to investigate effects of the fractions from the seeds of Psoralea
Y M Yang et al.
Planta medica, 62(4), 353-354 (1996-08-01)
A cytotoxic coumestan derivative, psoralidin (1), was isolated from the seed of Psoralea corylifolia. The IC50 values of 1 against SNU-1 and SNU-16 carcinoma cell lines were 53 and 203 micrograms/ml, respectively, indicating cytotoxic activity against stomach carcinoma cell lines.

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