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MedKoo Cat#: 597874 | Name: Hydroxyproline palmitamide
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Description:

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

Hydroxyproline palmitamide is a bioactive chemical.

Chemical Structure

Hydroxyproline palmitamide
Hydroxyproline palmitamide
CAS#41736-92-9

Theoretical Analysis

MedKoo Cat#: 597874

Name: Hydroxyproline palmitamide

CAS#: 41736-92-9

Chemical Formula: C21H39NO4

Exact Mass: 369.2879

Molecular Weight: 369.54

Elemental Analysis: C, 68.25; H, 10.64; N, 3.79; O, 17.32

Price and Availability

Size Price Availability Quantity
25mg USD 350.00 2 Weeks
100mg USD 850.00 2 Weeks
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Related CAS #
No Data
Synonym
Hydroxyproline palmitamide; N-Palmitoylhydroxyproline;
IUPAC/Chemical Name
(2S,4R)-4-hydroxy-1-palmitoylpyrrolidine-2-carboxylic acid
InChi Key
SRHSPJGTSWHUTH-MOPGFXCFSA-N
InChi Code
InChI=1S/C21H39NO4/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-20(24)22-17-18(23)16-19(22)21(25)26/h18-19,23H,2-17H2,1H3,(H,25,26)/t18-,19+/m1/s1
SMILES Code
O=C(O)[C@H]1N(C(CCCCCCCCCCCCCCC)=O)C[C@H](O)C1
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
2934.99.03.00
More Info

Preparing Stock Solutions

The following data is based on the product molecular weight 369.54 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
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Bioimpacts. 2013;3(2):97-100. doi: 10.5681/bi.2013.020. Epub 2013 Jun 8. PubMed PMID: 23878793; PubMed Central PMCID: PMC3713876. 8: Yamauchi R, Watanabe S, Martín AS, Iwamoto S. Effect of α-tocopherol on the hemin-catalyzed decomposition of 1-palmitoyl-2-linoleoyl-3-sn-phosphatidylcholine 13-hydroperoxide in micelles and liposomes. Chem Phys Lipids. 2014 Dec;184:61-8. doi: 10.1016/j.chemphyslip.2014.10.001. Epub 2014 Oct 13. PubMed PMID: 25454362. 9: Shaghaghi M, Chen MT, Hsueh YW, Zuckermann MJ, Thewalt JL. Effect of Sterol Structure on the Physical Properties of 1-Palmitoyl-2-oleoyl-sn-glycero-3-phosphocholine Membranes Determined Using (2)H Nuclear Magnetic Resonance. Langmuir. 2016 Aug 2;32(30):7654-63. doi: 10.1021/acs.langmuir.6b01401. Epub 2016 Jul 19. PubMed PMID: 27341069. 10: Bhagavat R, Saqib A, Karigar C. Molecular docking studies of novel palmitoyl-ligands for cyclooxygenase-2. Chem Biol Drug Des. 2012 Jun;79(6):1043-8. doi: 10.1111/j.1747-0285.2012.01359.x. Epub 2012 Mar 16. PubMed PMID: 22339889. 11: Bayés-García L, Calvet T, Cuevas-Diarte MA, Ueno S. In situ crystallization and transformation kinetics of polymorphic forms of saturated-unsaturated-unsaturated triacylglycerols: 1-palmitoyl-2,3-dioleoyl glycerol, 1-stearoyl-2,3-dioleoyl glycerol, and 1-palmitoyl-2-oleoyl-3-linoleoyl glycerol. Food Res Int. 2016 Jul;85:244-258. doi: 10.1016/j.foodres.2016.05.011. Epub 2016 May 11. PubMed PMID: 29544841. 12: Grasso EJ, Oliveira RG, Maggio B. Surface interactions, thermodynamics and topography of binary monolayers of Insulin with dipalmitoylphosphatidylcholine and 1-palmitoyl-2-oleoylphosphatidylcholine at the air/water interface. J Colloid Interface Sci. 2016 Feb 15;464:264-76. doi: 10.1016/j.jcis.2015.11.034. Epub 2015 Nov 19. PubMed PMID: 26624532. 13: Mitchell DA, Hamel LD, Ishizuka K, Mitchell G, Schaefer LM, Deschenes RJ. The Erf4 subunit of the yeast Ras palmitoyl acyltransferase is required for stability of the Acyl-Erf2 intermediate and palmitoyl transfer to a Ras2 substrate. J Biol Chem. 2012 Oct 5;287(41):34337-48. doi: 10.1074/jbc.M112.379297. Epub 2012 Aug 16. PubMed PMID: 22904317; PubMed Central PMCID: PMC3464540. 14: Son HJ, Ha SC, Hwang EY, Kim EA, Ahn JY, Choi SY, Cho SW. Roles of cysteine residues in the inhibition of human glutamate dehydrogenase by palmitoyl-CoA. BMB Rep. 2012 Dec;45(12):707-12. PubMed PMID: 23261056; PubMed Central PMCID: PMC4133811. 15: Aby E, Gumps K, Roth A, Sigmon S, Jenkins SE, Kim JJ, Kramer NJ, Parfitt KD, Korey CA. Mutations in palmitoyl-protein thioesterase 1 alter exocytosis and endocytosis at synapses in Drosophila larvae. Fly (Austin). 2013 Oct-Dec;7(4):267-79. doi: 10.4161/fly.26630. Epub 2013 Oct 3. PubMed PMID: 24091420; PubMed Central PMCID: PMC3896500. 16: Pelletier G, Rigden M, Poon R. 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