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2-[(1-benzylpiperidin-4-yl)amino]-N-(3-chlorophenyl)nicotinamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1346265-80-2

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1346265-80-2 Usage

Chemical Structure

Not provided in the material

Molecular Weight

Not provided in the material

Mechanism of Action

Selective dopamine D3 receptor antagonist

Therapeutic Potential

Being evaluated in clinical trials for the treatment of neurological and psychiatric disorders, including drug addiction, schizophrenia, and Parkinson's disease

Preclinical Studies

Exhibited promising results

Selective Targeting

Dopamine D3 receptors

Unique Properties

Selective targeting of dopamine D3 receptors makes it a promising candidate for the development of novel treatments for neurological and psychiatric disorders.

Check Digit Verification of cas no

The CAS Registry Mumber 1346265-80-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,4,6,2,6 and 5 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1346265-80:
(9*1)+(8*3)+(7*4)+(6*6)+(5*2)+(4*6)+(3*5)+(2*8)+(1*0)=162
162 % 10 = 2
So 1346265-80-2 is a valid CAS Registry Number.

1346265-80-2Downstream Products

1346265-80-2Relevant academic research and scientific papers

BRN-103, a novel nicotinamide derivative, inhibits VEGF-induced angiogenesis and proliferation in human umbilical vein endothelial cells

Choi, Hye-Eun,Yoo, Min-Sang,Choi, Jung-Hye,Lee, Jae Yeol,Kim, Je Hak,Kim, Ji Han,Lee, Joon Kwang,Kim, Gyu Il,Park, Yong,Chi, Yong Ha,Paik, Soo Heui,Lee, Joo Han,Lee, Kyung-Tae

, p. 6236 - 6241 (2011)

Anti-angiogenesis is regarded as an effective strategy for cancer treatment, and vascular endothelial growth factor (VEGF) plays a key role in the regulations of angiogenesis and vasculogenesis. In the present study, the authors synthesized five novel nicotinamide derivatives which structurally mimic the receptor tyrosine kinase inhibitor sunitinib and evaluated their anti-angiogenic effects. Transwell migration assays revealed that 2-(1-benzylpiperidin-4-yl) amino-N-(3-chlorophenyl) nicotinamide (BRN-103), among the five derivatives most potently inhibited VEGF-induced human umbilical vein endothelial cells (HUVECs). In addition, BRN-103 dose-dependently inhibited VEGF-induced migration, proliferation, and capillary-like tube formation of HUVECs and vessel sprouting from mouse aortic rings. To understand the molecular mechanisms responsible for these activities, the authors examined the effect of BRN-103 on VEGF signaling pathways in HUVECs. BRN-103 was found to suppress the VEGF-induced phosphorylation of VEGF receptor 2 (VEGR2) and the activations of AKT and eNOS. Taken together, these results suggest that BRN-103 inhibits VEGF-mediated angiogenesis signaling in human endothelial cells.

NOVEL COMPOUND HAVING ANGIOGENESIS INHIBITORY ACTIVITY, METHOD FOR PREPARING SAME, AND PHARMACEUTICAL COMPOSITION COMPRISING SAME

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Paragraph 0096; 0097, (2014/07/23)

Disclosed are an anti-angiogenic compound, represented by Chemical Formula I, or a pharmaceutically acceptable salt thereof, a preparation method thereof, and a pharmaceutically acceptable composition including the same. Because the compound of Chemical Formular I potently suppresses the angiogenesis, the compound of Chemical Formula I is applicable to the prevention and treatment of diseases caused by aberrant activity of vascular endothelial growth factor, and available as an anti-angiogenic agent.

Novel Compound Having Angiogenesis Inhibitory Activity, Method for Preparing Same, and Pharmaceutical Composition Comprising Same

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Paragraph 0211; 0212, (2014/09/29)

Disclosed are an anti-angiogenic compound, represented by Chemical Formula I, or a pharmaceutically acceptable salt thereof, a preparation method thereof, and a pharmaceutically acceptable composition including the same. Because the compound of Chemical Formula I potently suppresses the angiogenesis, the compound of Chemical Formula I is applicable to the prevention and treatment of diseases caused by aberrant activity of vascular endothelial growth factor, and available as an anti-angiogenic agent.

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