Details
| Stereochemistry | UNKNOWN |
| Molecular Formula | C23H32N4O7S |
| Molecular Weight | 508.588 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 1 / 4 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CC1(C)SC(NC1C(O)=O)C(NC(=O)CC2=CC=CC=C2)C(=O)NCCCC[C@H](NC=O)C(O)=O
InChI
InChIKey=TXKNSNYUJUCKMI-YUCHZMFVSA-N
InChI=1S/C23H32N4O7S/c1-23(2)18(22(33)34)27-20(35-23)17(26-16(29)12-14-8-4-3-5-9-14)19(30)24-11-7-6-10-15(21(31)32)25-13-28/h3-5,8-9,13,15,17-18,20,27H,6-7,10-12H2,1-2H3,(H,24,30)(H,25,28)(H,26,29)(H,31,32)(H,33,34)/t15-,17?,18?,20?/m0/s1
Libecillide is a specific monovalent penicilloyl hapten inhibitor of allergic reactions to penicillin. A depression of skin hypersensitivity to PPL and/or penicillin and penicillin derivatives sometimes persisting for weeks and months was obvious in numerous allergic patients submitted to combined libecillide-penicillin treatment. A depressing effect on antipenicillin antibody titers detected by passive hemaglutination was also manifest in some patients. The overall tolerance of libecillide in allergic patients has been very good. Nevertheless, the major obstacle to a wider general use of libecillide at the present time appears to be the occurrence of positive skin reactions to that compound in approximately 5 percent of patients allergic to penicillin.
Approval Year
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Systematic Name | English |
| Classification Tree | Code System | Code | ||
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NCI_THESAURUS |
C29578
Created by
admin on Wed Apr 02 09:30:13 GMT 2025 , Edited by admin on Wed Apr 02 09:30:13 GMT 2025
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C81133
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76968192
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100000082288
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3421
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CHEMBL2104809
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27826-45-5
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DTXSID101043410
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19ONH7KRJ3
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SUB08501MIG
Created by
admin on Wed Apr 02 09:30:13 GMT 2025 , Edited by admin on Wed Apr 02 09:30:13 GMT 2025
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PRIMARY |
ACTIVE MOIETY