latamoxef   Click here for help

GtoPdb Ligand ID: 12031

Synonyms: 6059-S | LY127935 | moxalactam | Moxam®
Approved drug
latamoxef is an approved drug (FDA (1981))
Compound class: Synthetic organic
Comment: Latamoxef is an oxacephem molecule developed by the Shionogi Research Laboratories (Osaka, Japan) [3]. It belongs to the β-lactam class of antibacterial compounds.
2D Structure
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Physico-chemical Properties
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Hydrogen bond acceptors 13
Hydrogen bond donors 4
Rotatable bonds 10
Topological polar surface area 231.6
Molecular weight 520.1
XLogP 0.3
No. Lipinski's rules broken 1
SMILES / InChI / InChIKey
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Canonical SMILES CO[C@@]1(NC(=O)C(c2ccc(cc2)O)C(=O)O)C(=O)N2[C@@H]1OCC(=C2C(=O)O)CSc1nnnn1C
Isomeric SMILES Cn1c(nnn1)SCC1=C(N2[C@@H]([C@@](C2=O)(NC(=O)C(c2ccc(cc2)O)C(=O)O)OC)OC1)C(=O)O
InChI InChI=1S/C20H20N6O9S/c1-25-19(22-23-24-25)36-8-10-7-35-18-20(34-2,17(33)26(18)13(10)16(31)32)21-14(28)12(15(29)30)9-3-5-11(27)6-4-9/h3-6,12,18,27H,7-8H2,1-2H3,(H,21,28)(H,29,30)(H,31,32)/t12?,18-,20+/m1/s1
InChI Key JWCSIUVGFCSJCK-CAVRMKNVSA-N
References
1. Brown RB, Klar J, Lemeshow S, Teres D, Pastides H, Sands M. (1986)
Enhanced bleeding with cefoxitin or moxalactam. Statistical analysis within a defined population of 1493 patients.
Arch Intern Med, 146 (11): 2159-64. [PMID:3778044]
2. Carmine AA, Brogden RN, Heel RC, Romankiewicz JA, Speight TM, Avery GS. (1983)
Moxalactam (latamoxef). A review of its antibacterial activity, pharmacokinetic properties and therapeutic use.
Drugs, 26 (4): 279-333. [PMID:6354685]
3. Otsuka H, Nagata W, Yoshioka M, Narisada M, Yoshida T, Harada Y, Yamada H. (1981)
Discovery and development of Moxalactam (6059-S): the chemistry and biology of 1-oxacephems.
Med Res Rev, 1 (3): 217-48. [PMID:6213825]
4. Weitekamp MR, Aber RC. (1983)
Prolonged bleeding times and bleeding diathesis associated with moxalactam administration.
JAMA, 249 (1): 69-71. [PMID:6217353]