142217-77-4 Usage
Description
(1S,2S,3S,5S)-5-(2-Amino-6-(benzyloxy)-9H-purin-9-yl)-3-(benzyloxy)-2-(benzyloxymethyl)cyclopentanol is a cyclopentanol derivative featuring a purine moiety with an amino group and multiple benzyloxy groups. This complex compound is characterized by its chiral centers and the presence of lipophilic benzyl groups, which may contribute to its potential biological activity and pharmacokinetic properties.
Uses
Given the provided materials, there are no explicit uses listed for this specific compound. However, based on the general properties of similar compounds, we can infer potential applications:
Used in Pharmaceutical Industry:
(1S,2S,3S,5S)-5-(2-Amino-6-(benzyloxy)-9H-purin-9-yl)-3-(benzyloxy)-2-(benzyloxymethyl)cyclopentanol could be used as a pharmaceutical agent for its potential interaction with purine receptors or enzymes, which may have implications in the treatment of diseases related to purine metabolism.
Used in Drug Development Research:
In the field of drug development, this compound might serve as a lead molecule for the design of new therapeutics, given its unique structure and potential biological activity. Further research would be required to explore its efficacy and safety.
Used in Chemical Synthesis:
(1S,2S,3S,5S)-5-(2-Amino-6-(benzyloxy)-9H-purin-9-yl)-3-(benzyloxy)-2-(benzyloxymethyl)cyclopentanol could also be utilized as an intermediate in the synthesis of other complex organic molecules, particularly those with potential applications in medicinal chemistry or material science.
Check Digit Verification of cas no
The CAS Registry Mumber 142217-77-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,2,2,1 and 7 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 142217-77:
(8*1)+(7*4)+(6*2)+(5*2)+(4*1)+(3*7)+(2*7)+(1*7)=104
104 % 10 = 4
So 142217-77-4 is a valid CAS Registry Number.
InChI:InChI=1/C32H33N5O4/c33-32-35-30-28(31(36-32)41-19-24-14-8-3-9-15-24)34-21-37(30)26-16-27(40-18-23-12-6-2-7-13-23)25(29(26)38)20-39-17-22-10-4-1-5-11-22/h1-15,21,25-27,29,38H,16-20H2,(H2,33,35,36)/t25-,26+,27+,29+/m1/s1
142217-77-4Relevant articles and documents
Method for synthesizing Entecavir intermediate
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Paragraph 0031-0034, (2020/03/05)
The invention relates to a method for synthesizing an Entecavir intermediate and particularly relates to a method for synthesizing a compound represented by a formula I. According to the method, firstly, amino of 6-benzyloxy guanine is protected, and thus
BMS-200475, a novel carbocyclic 2'-deoxyguanosine analog with potent and selective anti-hepatitis B virus activity in vitro
Bisacchi,Chao,Bachard,Daris,Innaimo,Jacobs,Kocy,Lapointe,Martel,Merchant,Slusarchyk,Sundeen,Young,Colonno,Zahler
, p. 127 - 132 (2007/10/03)
BMS-200475, a never carbocyclic analog of 2'-deoxyguanosine, is a potent inhibitor of hepatitis B virus in vitro (ED50 = 3 nM) with relatively low cytotoxicity (CC50 = 21-120 μM). A practical 10-step asymmetric synthesis was developed affording BMS-200475 in 18% overall chemical yield and > 99% optical purity. The enantiomer of BMS-200475 as well as the adenine, thymine, and iodouracil analogs are much less active.