74213-96-0 Usage
Uses
Used in Pharmaceutical Research:
4-(2-nitroethyl)phenyl hexopyranoside is used as a potential substrate or inhibitor for its ability to interact with enzymes and receptors. This interaction is crucial for understanding enzyme mechanisms and receptor functions, which can lead to the development of new drugs and therapies.
Used in Drug Development:
Due to its unique structure and potential biological activity, 4-(2-nitroethyl)phenyl hexopyranoside is used in drug development as a starting point for designing new pharmaceutical compounds. Its properties may contribute to the creation of innovative treatments for various diseases and conditions.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 4-(2-nitroethyl)phenyl hexopyranoside is utilized for its potential to contribute to the discovery and optimization of new drug candidates. Its reactivity and specific properties can be harnessed to create molecules with desired therapeutic effects.
Used in Biological Studies:
4-(2-nitroethyl)phenyl hexopyranoside is employed in biological studies to explore its interactions with biological systems. Understanding these interactions can provide insights into the compound's potential applications and help in the development of targeted therapies.
Overall, 4-(2-nitroethyl)phenyl hexopyranoside's diverse applications in research, pharmaceuticals, and medicinal chemistry highlight its potential as a versatile and valuable compound in the scientific community.
Check Digit Verification of cas no
The CAS Registry Mumber 74213-96-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,2,1 and 3 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 74213-96:
(7*7)+(6*4)+(5*2)+(4*1)+(3*3)+(2*9)+(1*6)=120
120 % 10 = 0
So 74213-96-0 is a valid CAS Registry Number.
74213-96-0Relevant articles and documents
Medicinal foodstuffs. II. On the bioactive constituents of the tuber of Sagittaria trifolia L. (Kuwai, Alismataceae): Absolute stereostructures of trifoliones A, B, C, and D, sagittariosides a and b, and arabinothalictoside
Yoshikawa,Yoshizumi,Murakami,Matsuda,Yamahara,Murakami
, p. 492 - 499 (2007/10/03)
From the medicinal foodstuff 'kuwai', the tuber of Sagittaria trifolia L., four bioactive diterpene ketones, trifoliones A, B, C, and D, two diterpene glucosides, sagittariosides a and b, and a nitroethylphenol glycoside, arabinothalictoside, were isolated, together with six known diterpenes. Their absolute stereostructures were determined on the basis of chemical and physicochemical evidence which included the application of a modified Mosher's method and an exciton chirality method. Among the diterpene constituents, trifoliones A, B, C, and D exhibited inhibitory effects on the histamine release from rat mast cells induced by compound 48/80 and calcium ionophore A-23187.
Isolation and Structure of Thalictoside
Ina, Hiroji,Iida, Hideo
, p. 726 - 729 (2007/10/02)
Thalictoside (1), a novel glycoside containing a nitro group, was isolated from Thalictrum aquilegifolium and the structure was shown to be 4-hydroxy-1-(2-nitroethyl)benzene 4-O-β-D-glucopyranoside on the basis of chemical transformations, spectral analys
UN NOUVEL HETEROSIDE NITRE EXTRAIT D'ANNONA SQUAMOSA
Forgacs, P.,Desconclois, J. F.,Provost, J.,Tiberghien, R.,Touche, A.
, p. 1251 - 1252 (2007/10/02)
A new glycoside was isolated from a 60percent methanol extract of dried leaves and stems of Annona squamosa.Its chemical structure was determined as 4-(-2-nitroethyl)-1-benzene.Key Word Index -- Annona squamosa; Annonaceae; primeveroside; 4-(-2-nitroethyl)phenol; 4-(-2-aminoethyl)phenol; tyramine.
