Indalpine
- CAS No.
- 63758-79-2
- Chemical Name:
- Indalpine
- Synonyms
- Upstene;LM-5008;lipstene;Indalpino;indalpine;3-(2-(4-piperidyl)ethyl)-indol;3-(2-(4-piperidinyl)ethyl)-1h-indol;3-[2-(4-Piperidinyl)ethyl]-1H-indole;3-(2-(PIPERIDIN-4-YL)ETHYL)-1H-INDOLE;1H-Indole, 3-[2-(4-piperidinyl)ethyl]-
- CBNumber:
- CB7483055
- Molecular Formula:
- C15H20N2
- Molecular Weight:
- 228.33
- MDL Number:
- MFCD00115893
- MOL File:
- 63758-79-2.mol
FDA UNII | V35562QSVT |
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Indalpine Chemical Properties,Uses,Production
Description
Indalpine is a non-tricyclic antidepressant with a serotonin selective profile. It is 6-7 times more potent than fluoxetine and clomipramine in inhibiting serotonin reuptake in vitro in rat brain synaptosomes. Statistically significant clinical effects within one week of onset of treatment have been reported. An anxiolytic effect may accompany the antidepressant effect. Indalpine appears devoid of anticholinergic and cardiovascular side effects and does not promote weight gain or affect appetite.
Originator
Pharmuka (France)
Definition
ChEBI: Indalpine is a member of indoles.
Manufacturing Process
0.5 g of bis(methoxy-2ethoxy)sodium aluminum hydride in a 70% solution in toluene is added to a solution of 0.29 g of (indolyl-3)(piperidyl-4-methyl) ketone in 10 ml of toluene. The mixture is heated under refluxing conditions for 15 hours, then cooled to 0°C. 10 ml of an aqueous solution of 5N sodium hydroxide is added dropwise thereto, followed by stirring for 1 hour. The organic phase is decanted, washed with water, dried using potassium carbonate and evaporated under partial vacuum. 0.26 g of oil is obtained, which is purified by chromatography and hydrochloride formation. The productobtained is 0.1 g of (indolyl-3)-2-ethyl-4-piperidine hydrochloride which has a melting point of 167°C.
brand name
Lm 5008;UPSTENE.
Therapeutic Function
Antidepressant
World Health Organization (WHO)
Indalpine, an antidepressant with serotoninergic action, was introduced in 1983 and marketed exclusively in France. In 1984 its use was associated with cases of leucopenia and agranulocytosis which led to the voluntary suspension of clinical trials in the USA. In 1985 the major manufacturer voluntarily withdrew the drug from the market.
Indalpine Preparation Products And Raw materials
Raw materials
Preparation Products
Supplier | Tel | Country | ProdList | Advantage | |
---|---|---|---|---|---|
TargetMol Chemicals Inc. | +1-781-999-5354 +1-00000000000 | marketing@targetmol.com | United States | 32161 | 58 |
Finetech Industry Limited | +86-27-87465837 +8618971612321 | info@finetechnology-ind.com | China | 9639 | 58 |
TargetMol Chemicals Inc. | +8613564774135 | zijue.cai@tsbiochem.com | United States | 19885 | 58 |
Finetech Industry Limited | 027-87465837 19945049750 | sales@finetechnology-ind.com | China | 9648 | 58 |
Nanjing Shizhou Biology Technology Co.,Ltd | 025-85560043 15850508050 | info@synzest.com | China | 9286 | 58 |
TargetMol Chemicals Inc. | 4008200310 | marketing@tsbiochem.com | China | 24644 | 58 |
Shaanxi Cuikang Pharmaceutical Technology Co., Ltd | 18049165724 13186333400 | cuichengbio@163.com | China | 2775 | 58 |
Anhui Henuo Biotechnology Co., Ltd | 0555-2761852 | China | 19410 | 58 | |
Anhui Henuo Biotechnology Co., Ltd | 18455579438 | China | 16684 | 58 | |
Shanghai Zhiyun Biotechnology Co., Ltd | 13119135307 | 3809801531@qq.com | China | 2767 | 58 |
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