94359-66-7 Usage
Uses
Used in Pharmaceutical Development:
[(25R)-26-(Acetyloxy)-3α-hydroxy-5α-cholestan-15α-yl]2-(acetylamino)-2-deoxy-β-D-glucopyranoside is used as a potential therapeutic agent for various medical conditions due to its unique steroid glucoside structure and potential biological activities.
Used in Medical Research:
[(25R)-26-(Acetyloxy)-3α-hydroxy-5α-cholestan-15α-yl]2-(acetylamino)-2-deoxy-β-D-glucopyranoside is used as a subject of study in medical research to explore its biological activities, interactions with biological systems, and possible applications in the treatment or management of specific diseases.
Used in Drug Delivery Systems:
In the field of drug delivery, [(25R)-26-(Acetyloxy)-3α-hydroxy-5α-cholestan-15α-yl]2-(acetylamino)-2-deoxy-β-D-glucopyranoside may be utilized as a component in the design of novel drug carriers, aiming to improve the delivery, bioavailability, and therapeutic outcomes of associated pharmaceuticals.
Used in Chemical Synthesis:
As a derivative of cholesterol, [(25R)-26-(Acetyloxy)-3α-hydroxy-5α-cholestan-15α-yl]2-(acetylamino)-2-deoxy-β-D-glucopyranoside can be used as a starting material or intermediate in the synthesis of other complex steroidal compounds with potential applications in various industries, including pharmaceuticals, agrochemicals, and materials science.
Check Digit Verification of cas no
The CAS Registry Mumber 94359-66-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,4,3,5 and 9 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 94359-66:
(7*9)+(6*4)+(5*3)+(4*5)+(3*9)+(2*6)+(1*6)=167
167 % 10 = 7
So 94359-66-7 is a valid CAS Registry Number.
InChI:InChI=1/C37H63NO9/c1-20(19-45-23(4)41)8-7-9-21(2)28-17-29(46-35-32(38-22(3)40)34(44)33(43)30(18-39)47-35)31-26-11-10-24-16-25(42)12-14-36(24,5)27(26)13-15-37(28,31)6/h20-21,24-35,39,42-44H,7-19H2,1-6H3,(H,38,40)/t20-,21-,24?,25?,26?,27?,28-,29-,30+,31?,32-,33-,34+,35-,36+,37-/m1/s1
94359-66-7Relevant academic research and scientific papers
Synthesis of the shark repellent pavoninin-4
Williams, John R.,Gong, Hua,Hoff, Nathan,Olubodun, Olaoluwa I.
, p. 10732 - 10736 (2007/10/03)
The first synthesis of the shark repellent pavoninin-4, 3, was achieved in 12 steps with 21% overall yield from diosgenin, 8. Key reactions involve an efficient synthesis of the C-15α hydroxyl steroid from a C-16β hydroxyl steroid by an unexpected 1,2-tra
PAVONININS, SHARK-REPELLING AND ICHTHYOTOXIC STEROID N-ACETYLGLUCOSAMINIDES FROM THE DEFENSE SECRETION OF THE SOLE PARDACHIRUS PAVONINUS (SOLEIDAE)
Tachibana, Kazuo,Sakaitani, Masahiro,Nakanishi, Koji
, p. 1027 - 1038 (2007/10/02)
Six steroid N-acetylglucosaminides, pavoninins-1 to -6, have been isolated from the defense secretion of the sole P.pavoninus guided by ichthyotoxicity and hemolytic activity, and their structures determined to be 1-6 by spectroscopic studies and chemical correlations.The pavoninins are considered to be the factors responsible for the repellent property of the sole against predatory fishes.
