ChemicalBook--->CAS DataBase List--->112898-42-7

112898-42-7

112898-42-7 Structure

112898-42-7 Structure
IdentificationBack Directory
[Name]

IMIPRAMINE-D3 HYDROCHLORIDE 98 ATOM % D
[CAS]

112898-42-7
[Synonyms]

Imipramine-d3 hydrochloride
[2H3]-Imipramine hydrochloride
2H3]-Imipramine hydrochloride salt
IMIPRAMINE-D3 HYDROCHLORIDE 98 ATOM % D
10,11-Dihydro-N-methyl-N-(methyl-d3)-5H-dibenz[b,f]azepine-5-propanamine
[Molecular Formula]

C19H25ClN2
[MDL Number]

MFCD00070405
[MOL File]

112898-42-7.mol
[Molecular Weight]

316.87
Safety DataBack Directory
[Hazard Codes ]

Xn
[Risk Statements ]

20/21/22-36/37/38
[Safety Statements ]

26-36
[WGK Germany ]

3
Hazard InformationBack Directory
[Uses]

Imipramine-d3 (hydrochloride) is deuterium labeled Imipramine (hydrochloride). Imipramine is an orally active tertiary amine tricyclic antidepressant. Imipramine is a Fascin1 inhibitor with antitumor activities. Imipramine also inhibits serotonin transporter with an IC50 value of 32 nM. Imipramine stimulates U-87MG glioma cells autophagy and induces HL-60 cell apoptosis. Imipramine shows neuroprotective and immunomodulatory effects[1][2][3][4][5][6].
[References]

[1] Russak EM, et al. Impact of Deuterium Substitution on the Pharmacokinetics of Pharmaceuticals. Ann Pharmacother. 2019;53(2):211-216. DOI:10.1177/1060028018797110
[2] Alburquerque-González B, et al. New role of the antidepressant imipramine as a Fascin1 inhibitor in colorectal cancer cells. Exp Mol Med. 2020 Feb;52(2):281-292. DOI:10.1038/s12276-020-0389-x
[3] Jeon SH, et al. The tricyclic antidepressant imipramine induces autophagic cell death in U-87MG glioma cells. Biochem Biophys Res Commun. 2011 Sep 23;413(2):311-7. DOI:10.1016/j.bbrc.2011.08.093
[4] Xia Z, et al. The antidepressants imipramine, clomipramine, and citalopram induce apoptosis in human acute myeloid leukemia HL-60 cells via caspase-3 activation. J Biochem Mol Toxicol. 1999;13(6):338-47. DOI:10.1002/(sici)1099-0461(1999)13:63.0.co;2-7
[5] Ramirez K, et al. Imipramine attenuates neuroinflammatory signaling and reverses stress-induced social avoidance. Brain Behav Immun. 2015 May;46:212-20. DOI:10.1016/j.bbi.2015.01.016
[6] Balkovetz DF, et al. Evidence for an imipramine-sensitive serotonin transporter in human placental brush-border membranes. J Biol Chem. 1989 Feb 5;264(4):2195-8. PMID:2914900
112898-42-7 suppliers list
Company Name: Shanghai Beiwanta Biotechnology Co., Ltd.  
Tel: 021-67187366 19901745723
Website: http://www.bwtlab.com/
Company Name: Nanjing Shizhou Biology Technology Co.,Ltd  
Tel: 17301488900
Website: www.synzest.com
Company Name: SHANGHAI ZZBIO CO., LTD.  
Tel: 13917991872 13816009161
Website: www.zzsrm.cn/
Company Name: RENI Pharmaceutical Technology Co., Ltd  
Tel: 028-87865381 18108190480
Website: www.scjctc.com/
Company Name: ShangHai ZskBio CO., LTD  
Tel: 021-58056897 15399714481
Website: www.zsklab.cn
Company Name: TLC Pharmaceutical Standards Ltd.  
Tel: 18012923235
Website: www.tlcstandards.com/
Company Name: CLEARSYNTH LABS LTD.  
Tel: +91-22-45045900
Website: www.clearsynth.com
Company Name: Shanghai Hao Zhun Biological Technology Co., Ltd.  
Tel: 15800340161
Website: www.zzsrm.com
Company Name: Riedel-de Haen AG  
Tel: 800 558-9160
Website: www.sigmaaldrich.com
Company Name: SIGMA-RBI  
Tel: 800 736 3690 (Orders)
Website: www.sigma-aldrich.com
Tags:112898-42-7 Related Product Information
113-52-0 494-19-9