Clomocycline |
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| Other names | (2Z,4S,4aS,5aS,6S,12aS)-7-chloro-4-dimethylamino-6,10,11,12a-tetrahydroxy-2-[hydroxy-(hydroxymethylamino)methylidene]-6-methyl-4,4a,5,5a-tetrahydrotetracene-1,3,12-trione |
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(4S,4aS,5aS,6S,12aR)-7-Chloro-4-(dimethylamino)-1,6,10,11,12a-pentahydroxy-N-(hydroxymethyl)-6-methyl-3,12-dioxo-4,4a,5,5a-tetrahydrotetracene-2-carboxamide
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| Formula | C23H25ClN2O9 |
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| Molar mass | 508.91 g·mol−1 |
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| 3D model (JSmol) | |
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Clc1c4c(c(O)cc1)C(\O)=C3\C(=O)[C@]2(O)C(=O)/C(C(=O)[C@@H](N(C)C)[C@@H]2C[C@@H]3[C@@]4(O)C)=C(\O)NCO
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InChI=1S/C23H25ClN2O9/c1-22(34)8-6-9-16(26(2)3)18(30)14(21(33)25-7-27)20(32)23(9,35)19(31)12(8)17(29)13-11(28)5-4-10(24)15(13)22/h4-5,8-9,16,27-28,30-31,34-35H,6-7H2,1-3H3,(H,25,33)/t8?,9-,16-,22-,23-/m0/s1 YKey:GJGDLRSSCNAKGL-BJNNJSPUSA-N Y
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Clomocycline is a tetracycline antibiotic. It is used to treat Pustulosis palmaris et plantaris.[1]
References
- ^ Ward JM, Corbett MF, Hanna MJ (September 1976). "A double-blind trial of clomocycline in the treatment of persistent palmoplantar pustulosis". The British Journal of Dermatology. 95 (3): 317–322. doi:10.1111/j.1365-2133.1976.tb07020.x. PMID 788767. S2CID 38040660.
Antibacterials that inhibit protein synthesis (J01A, J01B, J01F, J01G, QJ01XQ) |
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| 30S | Aminoglycosides (initiation inhibitors) | | -mycin (Streptomyces) | |
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| -micin (Micromonospora) | |
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| other | |
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Tetracycline antibiotics (tRNA binding) | | Tetracyclines | |
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| Glycylcyclines | |
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| 50S | Oxazolidinone (initiation inhibitors) |
- Eperezolid
- Linezolid#
- Posizolid
- Radezolid
- Ranbezolid
- Sutezolid
- Tedizolid
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| Peptidyl transferase | |
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| MLS (transpeptidation/translocation) | | Macrolides | |
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| Azalides | |
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| Ketolides | |
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| Lincosamides | |
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| Oxepanoprolinamides | |
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| Streptogramins |
- Pristinamycin (IA, IIA, IIB)
- NXL103 (Flopristin, Linopristin)
- Quinupristin/dalfopristin (Dalfopristin, Quinupristin)
- Streptogramin A
- Streptogramin B
- Virginiamycin (S1)
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- #WHO-EM
- ‡Withdrawn from market
- Clinical trials:
- †Phase III
- §Never to phase III
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