161822-04-4 Usage
General Description
The chemical compound "(2S)-4-amino-N-[(1R,2S,3S,4R,5S)-3,5-diamino-4-[(2R,3R,6S)-3-amino-6-( aminomethyl)oxan-2-yl]oxy-2-[(2S,3R,4R,5S,6R)-3,4-diamino-5-hydroxy-6- (hydroxymethyl)oxan-2-yl]oxy-cyclohexyl]-2-hydroxy-butanamide" is a complex organic molecule that contains amino groups and hydroxyl groups. It is composed of cyclohexyl, butanamide, and various amino sugar moieties. (2S)-4-amino-N-[(1R,2S,3S,4R,5S)-3,5-diamino-4-[(2R,3R,6S)-3-amino-6-( aminomethyl)oxan-2-yl]oxy-2-[(2S,3R,4R,5S,6R)-3,4-diamino-5-hydroxy-6- (hydroxymethyl)oxan-2-yl]oxy-cyclohexyl]-2-hydroxy-butanamide is likely to have biological activity and may be involved in biological processes such as protein synthesis or cell signaling. Its detailed structure suggests that it may have a role in the formation or modification of glycoproteins or glycolipids. Further research is needed to understand its specific biological function and potential applications.
Check Digit Verification of cas no
The CAS Registry Mumber 161822-04-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,1,8,2 and 2 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 161822-04:
(8*1)+(7*6)+(6*1)+(5*8)+(4*2)+(3*2)+(2*0)+(1*4)=114
114 % 10 = 4
So 161822-04-4 is a valid CAS Registry Number.
InChI:InChI=1/C22H46N8O8/c23-4-3-12(32)20(34)30-11-5-10(26)18(37-21-9(25)2-1-8(6-24)35-21)16(29)19(11)38-22-15(28)14(27)17(33)13(7-31)36-22/h8-19,21-22,31-33H,1-7,23-29H2,(H,30,34)/t8-,9+,10-,11+,12-,13+,14+,15+,16+,17+,18+,19-,21+,22+/m0/s1
161822-04-4Relevant articles and documents
Synthesis of 2'-amino-2'-deoxyarbekacin and its analogs having potent activity against methicillin-resistant Staphylococcus aureus
Kondo,Ikeda,Ikeda,Takeuchi,Usui,Ishii,Kudo,Gomi,Shibahara
, p. 821 - 832 (2007/10/02)
Based on our studies on the enzymatic modifications of arbekacin by methicillin-resistant Staphylococcus aureus (MRSA), replacement of the 2'-hydroxyl group by an amino group in arbekacin was designed to synthesize derivatives that would be active against