Basic information Safety Supplier Related

Atibeprone

Basic information Safety Supplier Related

Atibeprone Basic information

Product Name:
Atibeprone
Synonyms:
  • Atibeprone
  • 2H-1-Benzopyran-2-one, 3,4-dimethyl-7-[[5-(1-methylethyl)-1,3,4-thiadiazol-2-yl]methoxy]-
CAS:
153420-96-3
MF:
C17H18N2O3S
MW:
330.4
Mol File:
153420-96-3.mol
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Atibeprone Usage And Synthesis

Originator

Atibeprone,BASF

Uses

Atibeprone (Lu 53439) is a selective MAO-B inhibitor. Atibeprone has antidepressant activity[1][2].

Manufacturing Process

10 mmol of 7-methoxy-3,4-dimethylcoumarin were stirred with 10 mmol (4.04 g) of Lawesson's reagent (2,4-bis(4-methoxyphenyl)-1,3-dithia-2,4- diphosphetane 2,4-disulfide) in 20 ml of toluene at 90°C for 1-2.5 h. After cooling, the solvent was distilled off, the residue was taken up in DMF, and water was added. The precipitate was filtered off with suction and the crude 3,4-dimethyl-7-(2-isopropyl-1,3,4-thiadiazol-5-ylmethoxy)-2-thiocoumarin was purified by recrystallization from methanol or by column chromatography (silica gel, methylene chloride). Yield: 98%, melting point: 134-135°C.

Therapeutic Function

Antidepressant

References

[1] L?scher W,et al. Inhibition of monoamine oxidase type A, but not type B, is an effective means of inducing anticonvulsant activity in the kindling model of epilepsy. J Pharmacol Exp Ther. 1999 Mar;288(3):984-92. PMID:10027835
[2] Chhajed M, et al. Synthesis of 5-arylidine amino-1,3,4-thiadiazol-2-[(N-substituted benzyol)]sulphonamides endowed with potent antioxidants and anticancer activity induces growth inhibition in HEK293, BT474 and NCI-H226 cells. Med Chem Res. 2014;23(6):3049-3064. DOI:10.1007/s00044-013-0890-z

AtibeproneSupplier

TargetMol Chemicals Inc.
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+1-781-999-5354; +17819995354
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Suzhou Meishi Biotechnology Co., Ltd.
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1173954148q
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meishipharma@126.com
Shanghai Yifei Biotechnology Co. , Ltd.
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021-65675885 18964387627
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TargetMol Chemicals Inc.
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15002134094
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marketing@targetmol.cn
Sangon Biotech (Shanghai) Co.,Ltd.
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400-821-026
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Sales@sangon.com
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