Details
Stereochemistry | ABSOLUTE |
Molecular Formula | C29H38N4O9.C16H18N2O5S |
Molecular Weight | 937.023 |
Optical Activity | UNSPECIFIED |
Defined Stereocenters | 8 / 8 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
[H][C@]12SC(C)(C)[C@@H](N1C(=O)[C@@]2([H])NC(=O)COC3=CC=CC=C3)C(O)=O.[H][C@@]45C[C@@]6([H])C(C(=O)C7=C(O)C=CC=C7[C@@]6(C)O)=C(O)[C@]4(O)C(=O)C(C(=O)NCN8CCN(CCO)CC8)=C(O)[C@H]5N(C)C
InChI
InChIKey=MEGKRPMNPGTIIG-VNYBMUHKSA-N
InChI=1S/C29H38N4O9.C16H18N2O5S/c1-28(41)15-5-4-6-18(35)19(15)23(36)20-16(28)13-17-22(31(2)3)24(37)21(26(39)29(17,42)25(20)38)27(40)30-14-33-9-7-32(8-10-33)11-12-34;1-16(2)12(15(21)22)18-13(20)11(14(18)24-16)17-10(19)8-23-9-6-4-3-5-7-9/h4-6,16-17,22,34-35,37-38,41-42H,7-14H2,1-3H3,(H,30,40);3-7,11-12,14H,8H2,1-2H3,(H,17,19)(H,21,22)/t16-,17-,22-,28+,29-;11-,12+,14-/m01/s1
DescriptionSources: https://www.ncbi.nlm.nih.gov/pubmed/4955820
Sources: https://www.ncbi.nlm.nih.gov/pubmed/4955820
Penimepicycline is a salt of beta-lactam antibiotic penicillin V and tetracycline antibiotic pipacycline. Penimepicycline exerts a bactericidal action on the streptococci, and a bacteriostatic action on various gram-positive and gram-negative bacilli, as well as on the penicillin-resistant staphylococci. In the 1960s it was studied in Japan for the treatment of urological, respiratory, gynecological and other infections.
Approval Year
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Classification Tree | Code System | Code | ||
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WHO-ATC |
J01AA10
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WHO-VATC |
QJ01AA10
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Code System | Code | Type | Description | ||
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225-002-0
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m868
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100000082501
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75258
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Penimepicycline
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4599-60-4
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3RGQ4B6E87
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DB13264
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2084
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C166691
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SUB09668MIG
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DTXSID20905088
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C005470
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1271
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PARENT (SALT/SOLVATE)
PARENT (SALT/SOLVATE)
SUBSTANCE RECORD