Informazioni sul prodotto
- 3-Phorbinepropanoic acid, 9-ethenyl-14-ethyl-21-(methoxycarbonyl)-4,8,13,18-tetramethyl-20-oxo-, magnesium complex, [3S-(3α,4β,21β)]-
- Magnesate(1-), (9-ethenyl-14-ethyl-21-(methoxycarbonyl)-4,8,13,18-tetramethyl-20-oxo-3-phorbinepropanoato(3-)-N23,N24,N25,N26)-, hydrogen, (SP-4-2-(3S-(3alpha,4beta,21beta)))-
- Magnesate(1-), [(3S,4S,21R)-9-ethenyl-14-ethyl-21-(methoxycarbonyl)-4,8,13,18-tetramethyl-20-oxo-3-phorbinepropanoato(3-)-κN<sup>23</sup>,κN<sup>24</sup>,κN<sup>25</sup>,κN<sup>26</sup>]-, hydrogen (1:1), (SP-4-2)-
- Magnesate(1-), [(3S,4S,21R)-9-ethenyl-14-ethyl-21-(methoxycarbonyl)-4,8,13,18-tetramethyl-20-oxo-3-phorbinepropanoato(3-)-κN<sup>23</sup>,κN<sup>24</sup>,κN<sup>25</sup>,κN<sup>26</sup>]-, hydrogen, (SP-4-2)-
- Magnesate(1-), [9-ethenyl-14-ethyl-21-(methoxycarbonyl)-4,8,13,18-tetramethyl-20-oxo-3-phorbinepropanoato(3-)-N<sup>23</sup>,N<sup>24</sup>,N<sup>25</sup>,N<sup>26</sup>]-, hydrogen, [SP-4-2-[3S-(3α,4β,21β)]]-
- Magnesate(1-), [9-ethenyl-14-ethyl-21-(methoxycarbonyl)-4,8,13,18-tetramethyl-20-oxo-3-phorbinepropanoato(3-)-κN<sup>23</sup>,κN<sup>24</sup>,κN<sup>25</sup>,κN<sup>26</sup>]-, hydrogen, [SP-4-2-[3S-(3α,4β,21β)]]-
- Magnesium, [dihydrogen 21-carboxy-14-ethyl-4,8,13,18-tetramethyl-20-oxo-9-vinyl-3-phorbinepropionato(2-)]-, 21-methyl ester
- Magnesium-pheophorbide A
- Phorbine, magnesate(1-) deriv.
- magnesium (3S,4S,21R)-3-(2-carboxyethyl)-9-ethenyl-14-ethyl-21-(methoxycarbonyl)-4,8,13,18-tetramethyl-20-oxo-23,25-didehydrophorbine-23,25-diide
- Vedi altri sinonimi
- magnesium hydrogen 3-[9-ethenyl-14-ethyl-21-(methoxycarbonyl)-4,8,13,18-tetramethyl-20-oxido-23,25-didehydro-4,21-dihydro-3H-phorbin-23-id-3-yl]propanoate (1:1:1)
Chlorophyllide A is a chlorophyll molecule that has been synthesized by the enzymatic conversion of an existing chlorophyll molecule. It can be used as a model system for studying the physiological function of chlorophyll and its role in photosynthesis. The synthesis of Chlorophyllide A has been shown to be biocompatible with cells and tissues, making it an excellent candidate for drug delivery systems. The synthesis of this molecule is achieved through a reaction mechanism involving glutamate dehydrogenase, which adds a hydroxyl group to the cysteine residue on the chlorophyll molecule. This reaction takes place in low light conditions, which prevents photodegradation of this molecule. Chlorophyllide A also has a pH optimum at around pH 7-8 and does not react with proteins or nucleic acids.
Proprietà chimiche
Richiesta tecnica su: 3D-FC165287 Chlorophyllide A
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