29840-65-1 Usage
Description
7-Amino-heptanoic acid ethyl ester hydrochloride, also known as 7-Aminoheptanoic Acid Ethyl Ester, is an omega-amino acid ester derived from the 7-aminoheptanoic acid. It is characterized by its unique chemical structure, which includes an ethyl ester group attached to the omega position of the heptanoic acid chain. 7-Amino-heptanoic acid ethyl ester hydrochloride exhibits potential biological activities and is considered a promising candidate for pharmaceutical applications.
Uses
Used in Pharmaceutical Industry:
7-Amino-heptanoic acid ethyl ester hydrochloride is used as a building block for the synthesis of potential anticancer agents. Its unique chemical structure allows for the development of novel compounds with enhanced anti-cancer properties, targeting various cancer types and potentially improving treatment outcomes.
Used in Anticancer Applications:
7-Amino-heptanoic acid ethyl ester hydrochloride is used as a precursor in the development of new anticancer drugs. Its omega-amino acid ester structure provides a versatile platform for the design and synthesis of innovative therapeutic agents that can target specific cancer-related pathways, potentially leading to more effective and targeted cancer treatments.
Check Digit Verification of cas no
The CAS Registry Mumber 29840-65-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,8,4 and 0 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 29840-65:
(7*2)+(6*9)+(5*8)+(4*4)+(3*0)+(2*6)+(1*5)=141
141 % 10 = 1
So 29840-65-1 is a valid CAS Registry Number.
InChI:InChI=1/C9H19NO2.ClH/c1-2-12-9(11)7-5-3-4-6-8-10;/h2-8,10H2,1H3;1H
29840-65-1Relevant articles and documents
Novel heterobivalent tacrine derivatives as cholinesterase inhibitors with notable selectivity toward butyrylcholinesterase
Elsinghorst, Paul W.,González Tanarro, Camino M.,Gütschow, Michael
, p. 7540 - 7544 (2007/10/03)
Two series of novel heterobivalent tacrine derivatives were synthesized. A trimethoxy substituted benzene was linked to the tacrine moiety by a hydrazide-based linker. The compounds were evaluated as cholinesterase inhibitors, and trimethoxybenzoic acid derivatives with 11- or 12-atom spacers were the most potent inhibitors of human acetylcholinesterase. The inhibitors showed a surprising selectivity toward human butyrylcholinesterase, where several trimethoxyphenylpropionic acid derivatives had IC50 values less than 250 pM.