60524-14-3 Usage
General Description
5-Amino-3-pyridinecarboxamide, also known as nicotinamide, is a water-soluble vitamin and a member of the B-complex family. It is an essential nutrient that plays a crucial role in energy production within the cells and is important for maintaining healthy skin, nerves, and digestive system. Nicotinamide is also a precursor to the coenzyme nicotinamide adenine dinucleotide (NAD+), which is involved in various metabolic processes, including DNA repair and aging. Additionally, nicotinamide has been found to have anti-inflammatory and antioxidant properties, making it beneficial for managing certain skin conditions and supporting overall health and well-being.
Check Digit Verification of cas no
The CAS Registry Mumber 60524-14-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,5,2 and 4 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 60524-14:
(7*6)+(6*0)+(5*5)+(4*2)+(3*4)+(2*1)+(1*4)=93
93 % 10 = 3
So 60524-14-3 is a valid CAS Registry Number.
InChI:InChI=1/C6H7N3O/c7-5-1-4(6(8)10)2-9-3-5/h1-3H,7H2,(H2,8,10)
60524-14-3Relevant articles and documents
PIPERIDIN-1- YL-N-PYRYDI NE-3-YL-2-OXOACET AM IDE DERIVATIVES USEFUL FOR THE TREATMENT OF MTAP-DEFICIENT AND/OR MT A-ACCUMULATING CANCERS
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Paragraph 0544, (2022/02/09)
Compounds are provided according to Formula (I) and pharmaceutically acceptable salts thereof, and pharmaceutical compositions thereof; wherein R1, R2, R3, R4, R6, R7, R8 and n are as defined herein. Compounds of the present invention are contemplated useful for the prevention and treatment of a variety of conditions.
Synthesis of (aryloxyacetylamino)-isonicotinic/nicotinic acid analogues as potent hypoxia-inducible factor (HIF)-1α inhibitors
Boovanahalli, Shanthaveerappa K.,Jin, Xuejun,Jin, Yinglan,Kim, Jin Hwan,Dat, Nguyen Tien,Hong, Young-Soo,Lee, Jeong Hyung,Jung, Sang-Hun,Lee, Kyeong,Lee, Jung Joon
, p. 6305 - 6310 (2008/09/17)
We report a new series of HIF-1α inhibitors which were obtained through structural modifications of previously reported lead 1. The in vitro inhibitory potencies of newly synthesized compounds were evaluated against hypoxia-induced HIF-1 activation using