MedKoo Cat#: 145138 | Name: LB 11058

Description:

WARNING: This product is for research use only, not for human or veterinary use.

LB 11058 is a novel parenteral cephalosporin with a C-3 pyrimidinyl-substituted vinyl sulfide group and a C-7 2-amino-5-chloro-1,3-thiazole group. LB 11058 is very active against Streptococcus pneumoniae. LB 11058 was also very active against both beta-hemolytic streptococci. LB 11058 has a susceptibility pattern similar to that of S. aureus, with all isolates being inhibited at </=1 micro g/ml. LB 11058 also showed reasonable in vitro activity against Enterococcus faecalis, including vancomycin-resistant strains (MIC(50), 1 micro g/ml), and Bacillus spp. (MIC(50), 0.25 micro g/ml).

Chemical Structure

LB 11058
LB 11058
CAS#591207-81-7

Theoretical Analysis

MedKoo Cat#: 145138

Name: LB 11058

CAS#: 591207-81-7

Chemical Formula: C18H15ClN8O6S3

Exact Mass: 569.9965

Molecular Weight: 571.00

Elemental Analysis: C, 37.86; H, 2.65; Cl, 6.21; N, 19.62; O, 16.81; S, 16.84

Price and Availability

This product is currently not in stock but may be available through custom synthesis. To ensure cost efficiency, the minimum order quantity is 1 gram. The estimated lead time is 2 to 4 months, with pricing dependent on the complexity of the synthesis (typically high for intricate chemistries). Quotes for quantities below 1 gram will not be provided. To request a quote, please click the button below. Note: If this product becomes available in stock in the future, pricing will be listed accordingly.
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Related CAS #
No Data
Synonym
LB-11058; LB11058; LB 11058;
IUPAC/Chemical Name
(6R,7R)-7-((Z)-2-(2-amino-5-chlorothiazol-4-yl)-2-(hydroxyimino)acetamido)-3-((E)-2-((2-amino-6-oxo-3,6-dihydropyrimidin-4-yl)thio)vinyl)-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid
InChi Key
POXQRKGEFBKVOI-OKDNWOHVSA-N
InChi Code
1S/C18H15ClN8O6S3/c19-12-8(25-18(21)36-12)9(26-33)13(29)24-10-14(30)27-11(16(31)32)5(4-35-15(10)27)1-2-34-7-3-6(28)22-17(20)23-7/h1-3,10,15,33H,4H2,(H2,21,25)(H,24,29)(H,31,32)(H3,20,22,23,28)/b2-1+,26-9-/t10-,15-/m1/s1
SMILES Code
[H][C@]12SCC(\C=C\SC3=CC(=O)N=C(N)N3)=C(N1C(=O)[C@H]2NC(=O)C(=N/O)\C4=C(Cl)SC(N)=N4)C(O)=O
Appearance
To be determined
Purity
>98% (or refer to the Certificate of Analysis)
Shipping Condition
Shipped under ambient temperature as non-hazardous chemical. This product is stable enough for a few weeks during ordinary shipping and time spent in Customs.
Storage Condition
Dry, dark and at 0 -4 C for short term (days to weeks) or -20 C for long term(months to years).
Solubility
To be determined
Shelf Life
>2 years if stored properly
Drug Formulation
To be determined
Stock Solution Storage
0 - 4 C for short term (days to weeks), or -20 C for long term (months).
HS Tariff Code
2934.99.9001
More Info

Preparing Stock Solutions

The following data is based on the product molecular weight 571.00 Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which will affect the solvent volumes required to prepare stock solutions.

Recalculate based on batch purity %
Concentration / Solvent Volume / Mass 1 mg 5 mg 10 mg
1 mM 1.15 mL 5.76 mL 11.51 mL
5 mM 0.23 mL 1.15 mL 2.3 mL
10 mM 0.12 mL 0.58 mL 1.15 mL
50 mM 0.02 mL 0.12 mL 0.23 mL
1: Sader HS, Johnson DM, Jones RN. In vitro activities of the novel cephalosporin LB 11058 against multidrug-resistant Staphylococci and Streptococci. Antimicrob Agents Chemother. 2004 Jan;48(1):53-62. doi: 10.1128/AAC.48.1.53-62.2004. PMID: 14693518; PMCID: PMC310188. 2: Bert F. Facteurs de risque et traitement des infections à Staphylococcus aureus méticilline-résistant [Risk factors and treatment of methicillin- resistant Staphylococcus aureus infections]. Presse Med. 2002 Nov 30;31(38):1792-6. French. PMID: 12497719. 3: Vouillamoz J, Entenza JM, Hohl P, Moreillon P. LB11058, a new cephalosporin with high penicillin-binding protein 2a affinity and activity in experimental endocarditis due to homogeneously methicillin-resistant Staphylococcus aureus. Antimicrob Agents Chemother. 2004 Nov;48(11):4322-7. doi: 10.1128/AAC.48.11.4322-4327.2004. PMID: 15504859; PMCID: PMC525417.