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Merck
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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:
84573-16-0
分子量:
505.56
分類程式碼代碼:
12352200
NACRES:
NA.77

化驗

≥96% (HPLC)

形狀

film

顏色

colorless

運輸包裝

wet ice

儲存溫度

−20°C

SMILES 字串

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 密鑰

DAPAQENNNINUPW-IDAMAFBJSA-N

相关类别

一般說明

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。

應用

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。

特點和優勢

《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。

儲存類別代碼

11 - Combustible Solids

水污染物質分類（WGK）

WGK 3

閃點（°F）

Not applicable

閃點（°C）

Not applicable

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number
017M4708V
043M4761V

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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
Bernd Baumann et al.
The Journal of biological chemistry, 277(47), 44791-44800 (2002-09-19)
Crude extracts from different Aglaia species are used as anti-inflammatory remedies in the traditional medicine of several countries from Southeast Asia. Because NF-kappaB transcription factors represent key regulators of genes involved in immune and inflammatory responses, we supposed that the
John A Malona et al.
Journal of the American Chemical Society, 131(22), 7560-7561 (2009-05-19)
The total syntheses of aglafolin, rocagloic acid, and rocaglamide using Nazarov cyclization are described. Generation of the necessary oxyallyl cation intermediate was accomplished via peracid oxidation of an allenol ether to generate an unusual oxycarbenium ion species that undergoes cyclization.
Baudouin Gerard et al.
Journal of the American Chemical Society, 128(24), 7754-7755 (2006-06-15)
Enantioselective syntheses of methyl rocaglate and the related natural products rocaglamide and rocaglaol are outlined. The approach involves enantioselective [3 + 2] photocycloaddition promoted by chiral Brønsted acids (TADDOLs) to afford an aglain precursor followed by a ketol shift/reduction sequence
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
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The extracellular signal regulated kinase (ERK1 and ERK2) pathways are activated by mitogens and play an important role in controlling cell growth and differentiation.

MAPKKKs

The extracellular signal regulated kinase (ERK1 and ERK2) pathways are activated by mitogens and play an important role in controlling cell growth and differentiation.

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