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3-Pyridinecarboxamide, N-[2-(3,4-dihydroxyphenyl)ethyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

84454-97-7

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84454-97-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 84454-97-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,4,5 and 4 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 84454-97:
(7*8)+(6*4)+(5*4)+(4*5)+(3*4)+(2*9)+(1*7)=157
157 % 10 = 7
So 84454-97-7 is a valid CAS Registry Number.

84454-97-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name N-[2-(3,4-dihydroxyphenyl)ethyl]pyridine-3-carboxamide

1.2 Other means of identification

Product number -
Other names N-Nicotinoyldopamine

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:84454-97-7 SDS

84454-97-7Relevant academic research and scientific papers

N-Nicotinoyl dopamine inhibits skin pigmentation by suppressing of melanosome transfer

Kim, Bora,Hwang, Jae Sung,Kim, Hyun-Soo

, p. 250 - 256 (2015)

We investigated the inhibitory effects of a niacinamide derivative, N-Nicotinoyl dopamine (NND) on melanogenesis. NND inhibits melanosome transfer in a normal human melanocyte-keratinocyte co-culture system and through phagocytic ability without affecting viability of cells while it did not show inhibitory effects of tyrosinase and melanin synthesis in B16F10 mouse melanoma cells. In addition, safety of NND was verified through performing neural stem cell morphology assay. Our findings indicate that NND may potentially be used for cosmetic industry for improvement of skin whitening and therapies related with several skin disorders, and the effect of NND may be acquired via reduction of melanosome transfer.

Synthesis of nicotinamide derivatives having a hydroxy-substituted benzene ring and the influence of their structures on the apoptosis-inducing activity against leukemia cells

Yamaguchi, Tomoko,Matsumura, Yuriko,Ishii, Takuya,Tokuoka, Yoshikazu,Kurita, Keisuke

experimental part, p. 289 - 297 (2012/03/27)

With the view of developing novel apoptosis-inducing agents against malignant cells, nicotinamide derivatives containing substituted O-benzoyl-tyrosine, dopamine, and norepinephrine residues were synthesized. Antiproliferative activity measurements using leukemia U937 cells revealed that the benzoyl-tyrosine derivative having two hydroxys at C-2 and C-3 on the benzoyl group, and the one having a hydroxy at C-2 and a methoxy at C-4 proved the most potent among the 9 nicotinamide derivatives. The IC50 values of these compounds were 0.87 and 3.15 μM, which indicates their noteworthy activity compared with epigallocatechin gallate, a catechin component in green tea known for its noticeable activity. The cell death process was confirmed to be the result of apoptosis by agarose gel electrophoresis and dye staining, suggesting the high potential of these compounds as apoptosis-inducing anticancer agents. Drug Dev Res 72: 289-297, 2011.

Improved Delivery through Biological Membranes. 13. Brain-Specific Delivery of Dopamine with a Dihydropyridine Pyridinium Salt Type Redox Delivery System

Bodor, Nicholas,Farag, Hassan H.

, p. 528 - 534 (2007/10/02)

The dihydropyridine pyridinium salt type redox delivery system was used for the brain-specific delivery of dopamine.In vivo administration of the catechol-protected dopamine coupled with 1,4-dihydrotrigonelline as the carrier resulted in brain-specifi

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