![(2S)-2-[[(2S)-6-amino-2-[[(2S)-2-[[(2S)-2-[[(2S)-6-amino-2-(hexadecanoylamino)hexanoyl]amino]-3-hy…](https://static.cymitquimica.com/cas-image/thumb-webp/352725-2s-2-2s-6-amino-2-2s-2-2s-2-2s-6-amino-2-hexadecanoylamino-hexanoyl-amino-3-hydroxy-butanoyl-amino-3-hydroxy-butanoyl-amino-hexanoyl-amino-3-hydroxy-propanoic-acid.webp)
CAS 214047-00-4
:ácido (2S)-2-[[(2S)-6-amino-2-[[(2S)-2-[[(2S)-2-[[(2S)-6-amino-2-(hexadecanoylamino)hexanoil]amino]-3-hidroxi-butanoil]amino]-3-hidroxi-butanoil]amino]hexanoil]amino]-3-hidroxi-propanoico
Descripción:
La sustancia química con el nombre "(2S)-2-[[[2S)-6-amino-2-[[(2S)-2-[[(2S)-2-[[(2S)-6-amino-2-(hexadecanoylamino)hexanoyl]amino]-3-hidroxi-butanoyl]amino]-3-hidroxi-butanoyl]amino]hexanoyl]amino]-3-hidroxi-ácido propanoico" y número CAS "214047-00-4" es un derivado peptídico complejo caracterizado por múltiples residuos de aminoácidos y grupos funcionales. Este compuesto presenta una serie de centros quirales, lo que indica que existe en formas estereoisoméricas específicas, que pueden influir significativamente en su actividad biológica e interacciones. La presencia de grupos amino sugiere potencial para enlaces de hidrógeno y reactividad, mientras que el grupo hexadecanoylamino indica una porción de ácido graso que puede mejorar la permeabilidad de la membrana o la lipofilia. Además, la incorporación de grupos hidroxilo contribuye a su solubilidad y potencial para formar enlaces de hidrógeno. En general, esta sustancia probablemente exhiba una relevancia biológica significativa, posiblemente en aplicaciones terapéuticas, debido a su complejidad estructural y la presencia de grupos funcionales que pueden interactuar con sistemas biológicos.
Fórmula:C39H75N7O10
InChI:InChI=1/C39H75N7O10/c1-4-5-6-7-8-9-10-11-12-13-14-15-16-23-32(50)42-29(21-17-19-24-40)36(52)45-34(28(3)49)38(54)46-33(27(2)48)37(53)43-30(22-18-20-25-41)35(51)44-31(26-47)39(55)56/h27-31,33-34,47-49H,4-26,40-41H2,1-3H3,(H,42,50)(H,43,53)(H,44,51)(H,45,52)(H,46,54)(H,55,56)/t27?,28?,29-,30-,31-,33-,34-/m0/s1
Clave InChI:WSGCRSMLXFHGRM-DEVHWETNSA-N
SMILES:CCCCCCCCCCCCCCCC(=N[C@@H](CCCCN)C(=N[C@@H](C(C)O)C(=N[C@@H](C(C)O)C(=N[C@@H](CCCCN)C(=N[C@@H](CO)C(=O)O)O)O)O)O)O
Sinónimos:- L-serine, N2
- N2
- Matrixyl Acetate
- L-Serine, N2-(1-Oxohexadecyl)-L-Lysyl-L-Threonyl-L-Threonyl-L-Lysyl-
- Palmitoyl Pentapeptide
- Pal-Kttks
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(2S,5S,8S,11S,14S)-5,14-Bis(4-aminobutyl)-8,11-bis((R)-1-hydroxyethyl)-2-(hydroxymethyl)-4,7,10,13,16-pentaoxo-3,6,9,12,15-pentaazahentriacontan-1-oic acid
CAS:Fórmula:C39H75N7O10Pureza:97%Forma y color:SolidPeso molecular:802.0537Matrixyl
CAS:Matrixyl (PAL-Lys-Thr-Thr-Lys-Ser) is a matrikine used in anti-wrinkle cosmetics.Fórmula:C39H75N7O10Forma y color:SolidPeso molecular:802.0537Matrixyl
CAS:Fórmula:C39H75N7O10Pureza:95%~98%Forma y color:White to Off-white PowderPeso molecular:802.054Palmitoyl pentapeptide 4 acetate
CAS:Palmitoyl pentapeptide 4 acetate is a medicinal compound that has been shown to have anticancer properties. It works by inducing apoptosis, or programmed cell death, in cancer cells. This compound has been used in traditional Chinese medicine to treat various types of tumors. Palmitoyl pentapeptide 4 acetate acts as an inhibitor of kinases, which are enzymes that play a crucial role in the regulation of cell growth and division. It has been shown to be effective against multiple types of cancer cells, including those found in the urine. This compound is an analog of a natural protein kinase inhibitor and is often used in combination with other inhibitors for maximum effect.Fórmula:C39H75N7O10•(C2H4O2)xPureza:Min. 95%Forma y color:PowderPalmitoyl pentapeptide trifluoroacetic acid
CAS:Palmitoyl pentapeptide trifluoroacetic acid is a synthetic molecule that has been shown to have antimicrobial and anti-inflammatory properties. It has been shown to reduce the activity of gsh-px, which is an enzyme involved in the metabolism of glutathione. This compound also inhibits the production of ATP in cells, which may be responsible for its cancer-inhibiting effects. Palmitoyl pentapeptide trifluoroacetic acid has been shown to inhibit skin cancer cell growth by interfering with fatty acid synthesis and increasing epidermal growth factor levels.Fórmula:C41H76N7O12Pureza:Min. 95%Forma y color:PowderPeso molecular:802.05 g/mol
