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ω-Laurinlactam (Highly Pure)

$395.00

Catalog Number: B2012391 (100 mg)
ω-Laurinlactam (Highly Pure) is a high quality ω-Laurinlactam. This product has been used as molecular tool for various biochemical applications. It has also been used in a wide array of other chemical and immunological applications. Custom bulk amounts of this product are available upon request.

Live enquiry about this product via Text/SMS: 1-858-900-3210.

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SKU: B2012391 Categories: , Tag:

Description

ω-Laurinlactam (Highly Pure)
Catalog number: B2012391
Lot number: Batch Dependent
Expiration Date: Batch dependent
Amount: 100 mg
Molecular Weight or Concentration: 197.3. g/mol
Supplied as: Powder
Applications: molecular tool for various biochemical applications
Storage: -20°C
Keywords: Cyclododecanone Isooxime
Grade: Biotechnology grade. All products are highly pure. All solutions are made with Type I ultrapure water (resistivity >18 MΩ-cm) and are filtered through 0.22 um.

References:
1: Matusik E, Lambiotte F, Tone A, Lemtir J. [Pharmacokinetic modifications and pharmacokinetic/pharmacodynamic optimization of beta-lactams in ICU] Ann Pharm Fr. 2021 Jul;79(4):346-360.
2: Jiang J, Sigua LH, Chan A, Kalra P, Pomerantz WCK, Schönbrunn E, Qi J, Georg GI. Dihydropyridine Lactam Analogs Targeting BET Bromodomains ChemMedChem. 2022 Jan 5;17(1):e202100407.
3: Deshmukh AR, Bhawal BM, Krishnaswamy D, Govande VV, Shinkre BA, Jayanthi A. Azetidin-2-ones, synthon for biologically important compounds Curr Med Chem. 2004 Jul;11(14):1889-920.
4: Piccichè M, Pinto A, Griera R, Bosch J, Amat M. Total Synthesis of (-)-Cylindricine H Org Lett. 2022 Jul 29;24(29):5356-5360.
5: Dien Bard J, Hindler JA, Gold HS, Limbago B. Rationale for eliminating Staphylococcus breakpoints for β-lactam agents other than penicillin, oxacillin or cefoxitin, and ceftaroline Clin Infect Dis. 2014 May;58(9):1287-96.
6: Vickers S, Polsky SL. The biotransformation of nitrogen containing xenobiotics to lactams Curr Drug Metab. 2000 Dec;1(4):357-89.
7: Long DH, Townsend CA. Acyl Donor Stringency and Dehydroaminoacyl Intermediates in β-Lactam Formation by a Non-ribosomal Peptide Synthetase ACS Chem Biol. 2021 May 21;16(5):806-812.
8: Alves AJS, Alves NG, Caratão CC, Esteves MIM, Fontinha D, Bártolo I, Soares MIL, Lopes SMM, Prudêncio M, Taveira N, Pinho E Melo TMVD. Spiro-Lactams as Novel Antimicrobial Agents Curr Top Med Chem. 2020;20(2):140-152.
9: Martín JF, García-Estrada C, Ullán RV. Transport of substrates into peroxisomes: the paradigm of β-lactam biosynthetic intermediates Biomol Concepts. 2013 Apr;4(2):197-211.
10: Giamarellou H. beta-Lactams without a suicide inhibitor Clin Microbiol Infect. 2008 Jan;14 Suppl 1:194-7.

Products Related to ω-Laurinlactam (Highly Pure) can be found at Chemicals

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