C16-PHYTOCERAMIDE
C16-PHYTOCERAMIDE Basic information
- Product Name:
- C16-PHYTOCERAMIDE
- Synonyms:
-
- C16 Phytoceramide (t18:0/16:0)
- C16-PHYTOCERAMIDE
- N-HEXADECANOYL-PHYTOSPHINGOSINE
- N-16:0 Phytosphingosine
- Hexadecanamide, N-[(1S,2S,3R)-2,3-dihydroxy-1-(hydroxymethyl)heptadecyl]-
- N-[(1S,2S,3R)-2,3-dihydroxy-1-(hydroxymethyl)heptadecyl]-hexadecanamide
- armillaramide.
- CAS:
- 111149-09-8
- MF:
- C34H69NO4
- MW:
- 555.92
- Mol File:
- 111149-09-8.mol
C16-PHYTOCERAMIDE Chemical Properties
- storage temp.
- Store at -20°C, protect from light
- solubility
- Chloroform:Methanol (5:1): soluble
- form
- A solid
C16-PHYTOCERAMIDE Usage And Synthesis
Description
C16 Phytoceramide (t18:0/16:0) is a phytoceramide, which is a family of sphingolipids found in the intestine, kidney, and extracellular spaces of the stratum corneum of the mammalian epidermis. C16 Phytoceramide (t18:0/16:0) is composed of a phytosphingosine backbone amine-linked to a C16 fatty acid chain. The levels of C16 phytoceramide (t18:0/16:0) increase following heat stress in S. cerevisiae. It has been used with other ceramides to create stratum corneum substitutes to study percutaneous penetration and psoriasis in vitro. [Matreya, LLC. Catalog No. 2035]
Uses
Armillaramide (Desulfated ircisulfamide) is an ester product.
Definition
ChEBI: N-hexadecanoylphytosphingosine is a phytoceramide compound having a hexadecanoyl group attached to the nitrogen atom. It is a N-acylphytosphingosine and a N-palmitoyl-sphingoid base.
References
[1] M. W. CROSSMAN C H. Biosynthesis of phytosphingosine by the rat.[J]. The Journal of Biological Chemistry, 1977, 22 1: 5815-5819. DOI: 10.1016/s0021-9258(17)40095-0
[2] YUKIKO MIZUTANI Yasuyuki I Akio Kihara. Identification of the human sphingolipid C4-hydroxylase, hDES2, and its up-regulation during keratinocyte differentiation[J]. FEBS Letters, 2004, 563 1: Pages 93-97. DOI: 10.1016/s0014-5793(04)00274-1
[3] DAVID J. MONTEFUSCO. Distinct Signaling Roles of Ceramide Species in Yeast Revealed Through Systematic Perturbation and Systems Biology Analyses[J]. Science Signaling, 2013, 6 299. DOI: 10.1126/scisignal.2004515
[4] MIRANDA DE JAGER . Preparation and characterization of a stratum corneum substitute for in vitro percutaneous penetration studies[J]. Biochimica et biophysica acta. Biomembranes, 2006, 1758 5: Pages 636-644. DOI: 10.1016/j.bbamem.2006.04.001
[5] LINE HOLLESEN BASSE Joke A B Dani?l Groen. Permeability and lipid organization of a novel psoriasis stratum corneum substitute[J]. International Journal of Pharmaceutics, 2013, 457 1: Pages 275-282. DOI: 10.1016/j.ijpharm.2013.08.086
C16-PHYTOCERAMIDESupplier
- Tel
- 1-516-6625404
- support@alfa-chemistry.com
- Tel
- 0512-69561983 13914027025
- zhang_q@medinoah.com
- Tel
- 400-9205774
- sales@glpbio.cn
- Tel
- 027-59626688 18771149750
- sales@amyjet.com
- Tel
- 021-65675885 18964387627
- customer_service@efebio.com