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
[H][C@]4(O[C@H]1CC[C@@H](O[C@@H]1C)N2C=CC(NC(=O)C3=CC=C(NC(=O)[C@@](C)(N)CO)C=C3)=NC2=O)O[C@H](C)[C@H]([C@H](O)[C@H]4O)N(C)C
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 |
---|---|---|
Protein synthesis in Mycobacterium tuberculosis H37Rv and the effect of streptomycin in streptomycin-susceptible and -resistant strains. | 1973 Sep |
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Screening for new compounds with antiherpes activity. | 1984 Oct |
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Examination of protecting groups in the synthesis of nucleosides by intramolecular glycosylation. | 2004 |
|
NMR structure of the peptidyl transferase RNA inhibitor antibiotic amicetin. | 2007 Feb |
Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 08:58:26 GMT 2023
by
admin
on
Sat Dec 16 08:58:26 GMT 2023
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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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17650-86-1
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m1661
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