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Merck
CN

E31804

5-羟基-2-甲基吲哚-3-羧酸乙酯

97%

别名:

NSC 405600

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关于此项目

经验公式(希尔记法):
C12H13NO3
化学文摘社编号:
分子量:
219.24
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
231-507-7
MDL number:
Assay:
97%
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InChI key

BSNHKSUAAMJXBB-UHFFFAOYSA-N

InChI

1S/C12H13NO3/c1-3-16-12(15)11-7(2)13-10-5-4-8(14)6-9(10)11/h4-6,13-14H,3H2,1-2H3

SMILES string

CCOC(=O)c1c(C)[nH]c2ccc(O)cc12

assay

97%

mp

205-208 °C (lit.)

Application

Reactant for preparation of:
  • Potential anti-inflammatory and analgesic agents
  • Histamine-3 receptor inverse agonists for the treatment of obesity
  • Tubulin Polymerization Inhibitors
  • 4,7-dioxoindole-3-methyl prodrugs
  • Antagonists at M4 muscarinic receptors

存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Pascale David Pierson et al.
Journal of medicinal chemistry, 52(13), 3855-3868 (2009-05-22)
Obesity is a major risk factor in the development of conditions such as hypertension, hyperglycemia, dyslipidemia, coronary artery disease, and cancer. Several pieces of evidence across different species, including primates, underscore the implication of the histamine 3 receptor (H(3)R) in
Thomas M Böhme et al.
Journal of medicinal chemistry, 45(14), 3094-3102 (2002-06-28)
Previously, we reported on PD 102807 (41) as being the most selective synthetic M(4) muscarinic antagonist identified to date. Synthesized analogues of 41 showed no improvement in affinity and selectivity at that time. However, several newly synthesized compounds exhibit a
Ferrer, S.; et al.
Tetrahedron, 59, 3445-3445 (2003)
Badiger, J.; et al.
ARKIVOC (Gainesville, FL, United States), 217-217 (2009)
Jing-Ping Liou et al.
Journal of medicinal chemistry, 51(14), 4351-4355 (2008-07-01)
1-Aroylindoline, 1-aroyl-1,2,3,4-tetrahydroquinoline, and 1-aroylindole derivatives were synthesized and evaluated for anticancer activity. The 4-amino and 4-hydroxy-1-aroylindoles 26 and 27 with IC 50 of 0.9 and 0.6 microM, respectively, exhibited antitubulin activity superior or comparable to that of colchicine and combretastatin

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