MedKoo Cat#: 530756 | Name: L-Lysinamide

Description:

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

L-Lysinamide is a bioactive chemical.

Chemical Structure

L-Lysinamide
L-Lysinamide
CAS#32388-19-5

Theoretical Analysis

MedKoo Cat#: 530756

Name: L-Lysinamide

CAS#: 32388-19-5

Chemical Formula: C6H15N3O

Exact Mass: 145.1215

Molecular Weight: 145.21

Elemental Analysis: C, 49.63; H, 10.41; N, 28.94; O, 11.02

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 #
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Synonym
L-Lysinamide
IUPAC/Chemical Name
Hexanamide, 2,6-diamino-, (2S)-
InChi Key
HKXLAGBDJVHRQG-YFKPBYRVSA-N
InChi Code
InChI=1S/C6H15N3O/c7-4-2-1-3-5(8)6(9)10/h5H,1-4,7-8H2,(H2,9,10)/t5-/m0/s1
SMILES Code
O=C(N)[C@@H](N)CCCCN
Appearance
Solid powder
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
Soluble in DMSO
Shelf Life
>3 years if stored properly
Drug Formulation
This drug may be formulated in DMSO
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 145.21 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: Drugs and Lactation Database (LactMed) [Internet]. Bethesda (MD): National Library of Medicine (US); 2006-. Available from http://www.ncbi.nlm.nih.gov/books/NBK501918/ PubMed PMID: 30000978. 2: Drugs and Lactation Database (LactMed) [Internet]. Bethesda (MD): National Library of Medicine (US); 2006-. Available from http://www.ncbi.nlm.nih.gov/books/NBK500975/ PubMed PMID: 30000034. 3: Chopra A. [(99m)Tc]Cyclo(L-homocysteinyl-N-methyl-L-phenylalanyl-L-tyrosyl-D-tryptophyl-L-l ysyl-L-valyl), (1‡1´)-sulfide with 3-[(mercaptoacetyl)amino]-L-alanyl-L-lysyl-L-cysteinyl-L-lysinamide. 2008 Mar 27 [updated 2008 May 27]. Molecular Imaging and Contrast Agent Database (MICAD) [Internet]. Bethesda (MD): National Center for Biotechnology Information (US); 2004-2013. Available from http://www.ncbi.nlm.nih.gov/books/NBK23269/ PubMed PMID: 20641471. 4: Zahmatkesh S, Vakili MR. Synthesis and Characterization of New Optically Active Poly (ethyl L-lysinamide)s and Poly (ethyl L-lysinimide)s. J Amino Acids. 2010;2010:910906. doi: 10.4061/2010/910906. Epub 2010 Jul 13. PubMed PMID: 22331998; PubMed Central PMCID: PMC3276056. 5: Furuta S, Shimada O, Doi N, Ukai K, Nakagawa T, Watanabe J, Imaizumi M. General pharmacology of KP-102 (GHRP-2), a potent growth hormone-releasing peptide. Arzneimittelforschung. 2004;54(12):868-80. PubMed PMID: 15646371. 6: Doi N, Hirotani C, Ukai K, Shimada O, Okuno T, Kurasaki S, Kiyofuji T, Ikegami R, Futamata M, Nakagawa T, Ase K, Chihara K. Pharmacological characteristics of KP-102 (GHRP-2), a potent growth hormone-releasing peptide. Arzneimittelforschung. 2004;54(12):857-67. PubMed PMID: 15646370. 7: Levengood J, Ataide SF, Roy H, Ibba M. Divergence in noncognate amino acid recognition between class I and class II lysyl-tRNA synthetases. J Biol Chem. 2004 Apr 23;279(17):17707-14. Epub 2004 Jan 27. PubMed PMID: 14747465. 8: Choi JS, Lee EJ, Jang HS, Park JS. New cationic liposomes for gene transfer into mammalian cells with high efficiency and low toxicity. Bioconjug Chem. 2001 Jan-Feb;12(1):108-13. PubMed PMID: 11170373. 9: Kliment'eva TA, Galaev IuV, Brel' AK. [Activity and properties of L-lysine amidase in Salmonella strains]. Ukr Biokhim Zh (1978). 1990 Jul-Aug;62(4):84-7. Russian. PubMed PMID: 2238158. 10: Wang SS, Carpenter FH. Kinetic studies at high pH of the trypsin-catalyzed hydrolysis of N-alpha-benzoyl derivatives of L-arginamide, L-lysinamide, and S-2-aminoethyl-L-cysteinamide and related compounds. J Biol Chem. 1968 Jul 10;243(13):3702-10. PubMed PMID: 5658546.