Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C43H58N2O13 |
| Molecular Weight | 810.9262 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 9 / 9 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CCN(CC)C(=O)COC1=CC2=C(O)C3=C(O)C(C)=C4O[C@](C)(O\C=C\[C@H](OC)[C@@H](C)[C@@H](OC(C)=O)[C@H](C)[C@H](O)[C@H](C)[C@@H](O)[C@@H](C)\C=C\C=C(C)C(=O)N2)C(=O)C4=C13
InChI
InChIKey=VFYNXKZVOUXHDX-VDPUEHCXSA-N
InChI=1S/C43H58N2O13/c1-12-45(13-2)31(47)20-55-30-19-28-38(51)33-32(30)34-40(26(8)37(33)50)58-43(10,41(34)52)56-18-17-29(54-11)23(5)39(57-27(9)46)25(7)36(49)24(6)35(48)21(3)15-14-16-22(4)42(53)44-28/h14-19,21,23-25,29,35-36,39,48-51H,12-13,20H2,1-11H3,(H,44,53)/b15-14+,18-17+,22-16-/t21-,23+,24+,25+,29-,35-,36+,39+,43-/m0/s1
Rifamides (NSC-143418) are drugs used in the treatment of tuberculosis. They also have immunosuppressive activity, the exact mechanism of which is still unknown, although the ability of rifamides to inhibit tumor necrosis factor (TNF)-induced NF-kB activation may be associated with it. A variety of rifamide analogues exist, such as rifamycin B, rifapentine, rifamycin SV, rifabutin and rifampicin.
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Potentiation of rifampicin, rifampicin analogs, and tetracycline against animal cells by amphotericin B and polymyxin B. | 1973-06 |
|
| Desacetyl-rifamycins: preparation and antibacterial properties. | 1968-03-15 |
|
| In vitro bacteriological studies on rifamycin B diethylamide (rifamide). | 1965-07 |
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NCI_THESAURUS |
C258
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C152215
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SUB10308MIG
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m9610
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2750-76-7
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C009186
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CHEMBL2103908
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1952
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100000080580
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143418
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DTXSID901023450
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133099
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220-390-8
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TS121H7U7E
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6433345
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ACTIVE MOIETY