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Merck
CN

S1250

(-)-α-散道宁

≥99%

别名:

(3 S ,5a S ,9b S )-3a,5,5a,9b-四氢-3,5a,9-三甲基萘 [1,2- b 呋喃-2,8 (3H,4 H ) 二酮, Semenen

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关于此项目

经验公式(希尔记法):
C15H18O3
化学文摘社编号:
分子量:
246.30
UNSPSC Code:
12352204
NACRES:
NA.83
PubChem Substance ID:
EC Number:
207-560-7
Beilstein/REAXYS Number:
89489
MDL number:
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产品名称

(-)-α-散道宁, ≥99%

InChI

1S/C15H18O3/c1-8-10-4-6-15(3)7-5-11(16)9(2)12(15)13(10)18-14(8)17/h5,7-8,10,13H,4,6H2,1-3H3/t8-,10-,13-,15-/m0/s1

InChI key

XJHDMGJURBVLLE-BOCCBSBMSA-N

SMILES string

C[C@H]1[C@@H]2CC[C@@]3(C)C=CC(=O)C(C)=C3[C@H]2OC1=O

assay

≥99%

mp

172-173 °C (lit.)

storage temp.

2-8°C

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Application

(−)-α-山道年已被用作一种桉叶烷型倍半萜烯,用于研究其对231MFP乳腺癌细胞存活率下降的影响。

Biochem/physiol Actions

(−)-α-山道年具有抗蠕虫特性。它对肠道蛔虫有治疗作用。

General description

(−)-α-山道年是(Santonin)一种倍半萜烯内酯。它存在于青蒿属植物中。

pictograms

Skull and crossbones

signalword

Danger

Hazard Classifications

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral

存储类别

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges

法规信息

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历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Fungal hydroxylation of (-)-alpha-santonin
Bustos D A
Report Intl Narcotics Control Brd 03, 2, 1-6 (2012)
Chapter 3 - Natural Products
Sharma S and Anand N
Pharmacognosy Journal , 25(7), 71-123 (1997)
Parthenolide Covalently targets and inhibits focal adhesion kinase in breast cancer cells
Berdan C A, et al.
Cell Chemical Biology, 26(7), 1027-1035 (2019)
Xing Chen et al.
The journal of physical chemistry. A, 115(26), 7815-7822 (2011-06-02)
The CASSCF and CASPT2 methodologies have been used to explore the potential energy surfaces of lumisantonin in the ground and low-lying triplet states along the photoisomerization pathways. Calculations indicate that the (1)(nπ*) state is the accessible low-lying singlet state with
Lin Yang et al.
Yao xue xue bao = Acta pharmaceutica Sinica, 40(9), 834-837 (2005-12-14)
To obtain more valuable derivatives for the further structural modification of 6beta-santonin (1) via biotransformation by using cell suspension cultures of Phytolacca acinosa. The substrate 1 was incubated with cell suspension cultures of P. acinosa, the products were obtained by

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