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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:
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。
signalword
Danger
hcodes
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
新产品
此项目有
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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