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Merck
CN
所有图片(1)

主要文件

SML0656

Sigma-Aldrich

洛克米兰酰胺

≥96% (HPLC)

别名:

(1R,2R,3S,3aR,8bS)-2,3,3a,8b-四氢-1,8b-二羟基-6,8-二甲氧基-3a-(4-甲氧基苯基)-N,N-二甲基-3-苯基-1H-环戊[b]苯并呋喃-2-羧酰胺, NSC 326408, Roc-A, 洛克米兰酰胺A

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About This Item

经验公式(希尔记法):
C29H31NO7
CAS号:
分子量:
505.56
UNSPSC代码:
12352200
NACRES:
NA.77

质量水平

方案

≥96% (HPLC)

表单

film

颜色

colorless

运输

wet ice

储存温度

−20°C

SMILES字符串

N(C)(C)C(=O)[C@H]1[C@H]([C@@]2([C@@](Oc5c2c(cc(c5)OC)OC)([C@@H]1c4ccccc4)c3ccc(cc3)OC)O)O

InChI

1S/C29H31NO7/c1-30(2)27(32)23-24(17-9-7-6-8-10-17)29(18-11-13-19(34-3)14-12-18)28(33,26(23)31)25-21(36-5)15-20(35-4)16-22(25)37-29/h6-16,23-24,26,31,33H,1-5H3/t23-,24-,26-,28+,29+/m1/s1

InChI key

DAPAQENNNINUPW-IDAMAFBJSA-N

一般描述

已知楝酰胺来自于四氢苯并呋喃,并且也是树兰属植物的一种活性化合物。

应用

楝酰胺已被用作抗癌药用于治疗肠病毒71型神经发病机制并对抑制素的作用进行了研究。

生化/生理作用

楝酰胺与成骨细胞分化相关。在类风湿关节炎中,楝酰胺可能通过阻止参与其中的细胞因子的表达而抑制炎症。
楝酰胺是一种从树兰属中分离的有效抗癌剂。楝酰胺可抑制蛋白的合成而不影响DNA或RNA合成。最近的研究表明,楝酰胺可与禁止素(PHB)1和2结合,阻止PHB与CRaf之间的相互作用并抑制CRaf的活化,进而抑制CRaf-MEK-ERK信号转导。此外,楝酰胺也是一种抑制NF-κB和NF-AT活化的免疫抑制剂。
楝酰胺是一种有效的抗癌剂。

特点和优势

《受体分类和信号转导》手册的 MAPKKK 页面有该化合物的介绍。想要浏览手册的其他页面, 请单击此处

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable


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Baudouin Gerard et al.
Journal of the American Chemical Society, 126(42), 13620-13621 (2004-10-21)
A unified biomimetic approach to the aglain-forbaglin-rocaglamide classes of natural products is reported. The approach involves photogeneration of oxidopyryliums via excited-state intramolecular proton transfer (ESIPT) of 3-hydroxyflavones followed by [3+2] dipolar cycloaddition to the aglain core. An alpha-ketol (acyloin) rearrangement
Soyoung Kim et al.
Anti-cancer agents in medicinal chemistry, 6(4), 319-345 (2006-07-18)
During the past few years, a group of cyclopenta[b]benzofurans from the plant genus Aglaia has received broad scientific attention as interesting natural product lead compounds with potential anticancer and insecticidal activities. Since the first cyclopenta[b]benzofuran derivative, rocaglamide, from Aglaia elliptifolia
C Schneider et al.
Phytochemistry, 54(8), 731-736 (2000-10-03)
Bark of Aglaia spectabilis collected on the island of Phu Quoc (Vietnam) yielded insecticidal cyclopentatetrahydrobenzofurans of the rocaglamide type including four new natural products. Structure elucidation of the new compounds is described. All rocaglamide derivatives isolated exhibited strong insecticidal activity
Rocaglamide-A Potentiates Osteoblast Differentiation by Inhibiting NF-?B Signaling.
Li A, et al.
Molecular Cell, 38(11), 941-941 (2015)
F I Bohnenstengel et al.
Zeitschrift fur Naturforschung. C, Journal of biosciences, 54(12), 1075-1083 (2000-02-24)
Thirteen naturally occurring 1H-cyclopenta[b]benzofuran lignans of the rocaglamide type as well as one naturally occurring aglain congener all of them isolated from three Aglaia species (Aglaia duperreana, A. oligophylla and A. spectabilis) collected in Vietnam were studied for their antiproliferative

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