Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C29H42N6O9 |
| Molecular Weight | 618.6786 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 9 / 9 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
C[C@H]1O[C@H](CC[C@@H]1O[C@H]2O[C@H](C)[C@H]([C@H](O)[C@H]2O)N(C)C)N3C=CC(NC(=O)C4=CC=C(NC(=O)[C@@](C)(N)CO)C=C4)=NC3=O
InChI
InChIKey=HDNVYHWHCVTDIV-ZENIWSRCSA-N
InChI=1S/C29H42N6O9/c1-15-19(44-26-24(38)23(37)22(34(4)5)16(2)43-26)10-11-21(42-15)35-13-12-20(33-28(35)41)32-25(39)17-6-8-18(9-7-17)31-27(40)29(3,30)14-36/h6-9,12-13,15-16,19,21-24,26,36-38H,10-11,14,30H2,1-5H3,(H,31,40)(H,32,33,39,41)/t15-,16-,19+,21-,22-,23+,24-,26-,29+/m1/s1
| Molecular Formula | C29H42N6O9 |
| Molecular Weight | 618.6786 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ABSOLUTE |
| Additional Stereochemistry | No |
| Defined Stereocenters | 9 / 9 |
| E/Z Centers | 0 |
| Optical Activity | UNSPECIFIED |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| NMR structure of the peptidyl transferase RNA inhibitor antibiotic amicetin. | 2007-02 |
|
| NMR and molecular modelling studies of the binding of amicetin antibiotic to conserved secondary structural motifs of 23S ribosomal RNAs. | 2006-03 |
|
| Examination of protecting groups in the synthesis of nucleosides by intramolecular glycosylation. | 2004 |
|
| Kinetics of inhibition of ribonuclease P activity by peptidyltransferase inhibitors. Effect of antibiotics on RNase P. | 2003-03 |
|
| Screening for new compounds with antiherpes activity. | 1984-10 |
|
| Protein synthesis in Mycobacterium tuberculosis H37Rv and the effect of streptomycin in streptomycin-susceptible and -resistant strains. | 1973-09 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 22:24:48 GMT 2025
by
admin
on
Mon Mar 31 22:24:48 GMT 2025
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| Record UNII |
0909X15C85
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| Record Status |
Validated (UNII)
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| Record Version |
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