CAS 14897-06-4

clorofillide a

Descrizione:

clorofillide a è un derivato della clorofilla che svolge un ruolo cruciale nella fotosintesi, principalmente presente in piante, alghe e cianobatteri. È un pigmento verde che assorbe l'energia luminosa, facilitando la conversione dell'energia solare in energia chimica. Strutturalmente, clorofillide a è caratterizzato da un anello di porfirina con un ion di magnesio centrale, essenziale per le sue proprietà di assorbimento della luce. A differenza della clorofilla a, clorofillide a è privo della coda di fitolo, rendendolo più polare e solubile in acqua. Questo composto mostra una forte assorbimento nelle regioni blu e rossa dello spettro luminoso, vitale per l'efficienza fotosintetica. clorofillide a è anche coinvolto in vari processi biochimici, inclusa la sintesi della clorofilla e la regolazione della crescita delle piante. La sua presenza è significativa negli studi relativi alla fisiologia vegetale, ecologia e biochimica, poiché funge da indicatore della salute e produttività delle piante. Inoltre, clorofillide a ha potenziali applicazioni nelle industrie alimentari e cosmetiche grazie alle sue proprietà antiossidanti.

Formula: C₃₅H₃₄MgN₄O₅

InChI: InChI=1/C35H36N4O5.Mg/c1-8-19-15(3)22-12-24-17(5)21(10-11-28(40)41)32(38-24)30-31(35(43)44-7)34(42)29-18(6)25(39-33(29)30)14-27-20(9-2)16(4)23(37-27)13-26(19)36-22;/h8,12-14,17,21,31H,1,9-11H2,2-7H3,(H3,36,37,38,39,40,41,42);/q;+2/p-2/t17-,21-,31+;/m0./s1

InChI key: InChIKey=ANWUQYTXRXCEMZ-NYABAGMLSA-L

SMILES: CC1=C2[N-]3[Mg+2]45[N]=6C(=C7C3=C1C(=O)[C@@H]7C(OC)=O)[C@@H](CCC([O-])=O)[C@H](C)C6C=C8[N-]4C(=CC9=[N]5C(=C2)C(CC)=C9C)C(C=C)=C8C.[H+]

Sinonimi:

• 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-)-κN²³,κN²⁴,κN²⁵,κN²⁶]-, 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-)-κN²³,κN²⁴,κN²⁵,κN²⁶]-, hydrogen, (SP-4-2)-
• 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-(3α,4β,21β)]]-
• Magnesate(1-), [9-ethenyl-14-ethyl-21-(methoxycarbonyl)-4,8,13,18-tetramethyl-20-oxo-3-phorbinepropanoato(3-)-κN²³,κN²⁴,κN²⁵,κN²⁶]-, 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
• 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)
• Magnesate(1-), [(3S,4S,21R)-9-ethenyl-14-ethyl-21-(methoxycarbonyl)-4,8,13,18-tetramethyl-20-oxo-3-phorbinepropanoato(3-)-κN23,κN24,κN25,κN26]-, 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-)-κN23,κN24,κN25,κN26]-, hydrogen, (SP-4-2)-
• Magnesate(1-), [9-ethenyl-14-ethyl-21-(methoxycarbonyl)-4,8,13,18-tetramethyl-20-oxo-3-phorbinepropanoato(3-)-κN23,κN24,κN25,κN26]-, hydrogen, [SP-4-2-[3S-(3α,4β,21β)]]-
• Chlorophyllide a

Chlorophyllide A

CAS: 14897-06-4

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.

Formula: C₃₅H₃₄MgN₄O₅

Purezza: 90%Min

Colore e forma: Powder

Peso molecolare: 614.97 g/mol

Ref: 3D-FC165287