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porphyrin
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porphyrin
porphyrin Chem. (ˈpɔːfɪrɪn) [a. G. porphyrin (Willstätter & Fritzsche 1909, in Ann. d. Chem. CCCLXXI. 33), f. haemato-porphyrin hæmatoporphyrin (s.v. hæmato-), f. Gr. πόρϕυρ-ος purple + -in -in1.] Any of a large class of deeply-coloured red or purple fluorescent crystalline pigments that are substit...
Oxford English Dictionary
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Porphyrin
The third porphyrin that is [18]porphyrin-(2.1.1.0), was reported by Callot and Vogel-Sessler. See also
A porphyrin-related disease: porphyria
Porphyrin coordinated to iron: heme
A heme-containing group of enzymes: Cytochrome P450
Porphyrin
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Phosphorus porphyrin
The chlorines on a P-centered porphyrin are first substituted by an external hydroxyphenyl group on another porphyrin. porphyrin coordinated to phosphorus.
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protoporphyrin
protoˈporphyrin Chem. [a. G. protoporphyrin (Fischer & Lindner 1925, in Zeitschr. f. physiol. Chem. CXLII. 147): see proto- and porphyrin.] Any of a group of fifteen isomeric porphyrins, C34H34N4O4, in which the porphin nucleus has four methyl, two vinyl, and two propionic acid substituents; one iso...
Oxford English Dictionary
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Porphobilinogen
Biosynthesis
In the first step of the porphyrin biosynthesis pathway, porphobilinogen is generated from aminolevulinate (ALA) by the enzyme ALA dehydratase Metabolism
In the typical porphyrin biosynthesis pathway, four molecules of porphobilinogen are concatenated by carbons 2 and 5 of the pyrrole ring (adjacent
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Handbook of Porphyrin Science
Published by World Scientific, the Handbook of Porphyrin Science: With Applications to Chemistry, Physics, Materials Science, Engineering, Biology and
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Boron porphyrins
The Boron porphyrin compounds can be synthesized either from the free base porphyrin or from a lithium porphyrin complex as starting material. and when the substrates are within the porphyrin pocket.
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Transition metal porphyrin complexes
Formation
Metal porphyrin complexes are almost always prepared by direct reaction of a metal halide with the free porphyrin, abbreviated here as H2P:
MClx The porphyrin dianion is an L2X2 ligand.
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Asymmetric porphyrin solar cell dye and preparation ... - Semantic Scholar
The invention relates to an asymmetric D-PI-A type dye and an intermediate material used for a dye-sensitized solar cell and taking porphyrin as a core, and a synthetic preparation method and an application of the dye. In a molecular structure of the dye, donators of alkane and alkoxy in different carbon chain lengths, triple-bond receptors are asymmetrically substituted at the periphery of a ...
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胆色素原
胆色素原(,亦称为卟胆原,简称为PBG)是一种作为卟啉(Porphyrin)生物合成中间体的吡咯(Pyrrole)衍生物,而卟啉(Porphyrin)为合成血基质的原料之一。
由两分子(下图dALA) 在(又称下图之,图上ALA dehydrogenase为误植)催化下缩合、环化而成。
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Cobalt(II)–porphyrin catalysis
Cobalt(II)–porphyrin catalysis is a process in which a Co(II) porphyrin complex acts as a catalyst, inducing and accelerating a chemical reaction. Co(II)–porphyrin catalysts lack vacant cis-coordination sites available (all occupied).
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Abelsonite
Abelsonite is a nickel porphyrin mineral with chemical formula C31H32N4Ni. It was discovered in 1969 in the U.S. The mineral is a deoxophylloerythroetioporphyrin (DPEP), with nickel occupying the center of the porphyrin ring.
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Hexaminolevulinate
Hexaminolevulinate is a structural analogue to 5-aminolevulinic acid (a precursor to the porphyrin ring of heme), and is internalized and processed into After exposure to 360-450 nm light, the porphyrin will fluoresce red.
References
Oncology
Optical imaging
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Timothy D. Lash
Lash is known for his contributions to synthetic porphyrin chemistry.
Career
Timothy D. Lash was born on 13 October 1953, in Salisbury, England. Lash, “Synthesis of Novel Porphyrin Chromophores” in The Porphyrin Handbook, Ed. K. M. Kadish, K. M. Smith and R.
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