Details
Stereochemistry | ABSOLUTE |
Molecular Formula | C31H51NO8 |
Molecular Weight | 565.7385 |
Optical Activity | UNSPECIFIED |
Defined Stereocenters | 11 / 11 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
[H][C@@]2(O[C@H]1[C@@H](CC=O)C[C@@H](C)C(=O)\C=C\C(C)=C\[C@H](C)[C@@H](CC)OC(=O)C[C@@H](O)[C@@H]1C)O[C@H](C)C[C@@H]([C@H]2O)N(C)C
InChI
InChIKey=OBUIQEYZGMZXPJ-NPQHDNJNSA-N
InChI=1S/C31H51NO8/c1-9-27-20(4)14-18(2)10-11-25(34)19(3)15-23(12-13-33)30(22(6)26(35)17-28(36)39-27)40-31-29(37)24(32(7)8)16-21(5)38-31/h10-11,13-14,19-24,26-27,29-31,35,37H,9,12,15-17H2,1-8H3/b11-10+,18-14+/t19-,20+,21-,22+,23+,24+,26-,27-,29-,30-,31+/m1/s1
Repromicin is a compound that was reported in the literature in the 1990’s. Repromicin derivatives were found to have potent antibacterial activity against the Gram-negative pathogen Pasteurella multocida and Pasteurella heamolytica (in vitro and in vivo). Subcutaneous administration (single dose) in animals was found to control induced pasteurellosis (in swine) and induced respiratory disease (in cattle).
Approval Year
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NCI_THESAURUS |
C52588
Created by
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100000080530
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SUB10282MIG
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G5WU4SAO6B
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4247
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C152193
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9937853
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56689-42-0
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CHEMBL2105624
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DTXSID501024032
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ACTIVE MOIETY