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24533-72-0

  • Product Name:pyropheophorbide a
  • Molecular Formula:C33H34 N4 O3
  • Molecular Weight:534.658
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Product Details

Purity:99%

Factory Sells Best Quality pyropheophorbide a 24533-72-0 with GMP standards

  • Molecular Formula:C33H34 N4 O3
  • Molecular Weight:534.658
  • Vapor Pressure:0mmHg at 25°C 
  • Boiling Point:1006.359°C at 760 mmHg 
  • Flash Point:562.426°C 
  • PSA：110.67000 
  • Density:1.259g/cm3 
  • LogP:4.13980 

pyropheophorbide a(Cas 24533-72-0) Usage

General Description

Pyropheophorbide a is a chlorophyll derivative that has been identified as a potential photosensitizer in photodynamic therapy, a treatment for various types of cancer. pyropheophorbide a is known for its ability to generate reactive oxygen species when exposed to light, which can induce cell death in cancerous cells. Pyropheophorbide a has been studied for its potential use in targeting and destroying cancer cells while sparing healthy tissues. Its unique chemical properties make it a promising candidate for further research and development in the field of cancer treatment. Additionally, pyropheophorbide a has also been investigated for its antimicrobial and antioxidant properties, suggesting potential applications in other medical and industrial fields.

InChI:InChI=1/C33H34N4O3/c1-7-19-15(3)23-12-25-17(5)21(9-10-30(39)40)32(36-25)22-11-29(38)31-18(6)26(37-33(22)31)14-28-20(8-2)16(4)24(35-28)13-27(19)34-23/h7,12-14,17,21,34,37H,1,8-11H2,2-6H3,(H,39,40)/b23-12-,24-13-,25-12-,26-14-,27-13-,28-14-,32-22-/t17-,21-/m0/s1

24533-72-0 Relevant articles

In depth analysis of photovoltaic performance of chlorophyll derivative-based "all solid-state" dye-sensitized solar cells

Beljonne, David,Bouclé, Johann,Cangiotti, Michela,Chevrier, Michèle,Clément, Sébastien,Dubois, Philippe,Fattori, Alberto,Kotras, Clément,Lasser, Laurent,Lazzaroni, Roberto,Mehdi, Ahmad,Ottaviani, Maria Francesca,Richeter, Sébastien,Rose, Clémence,Surin, Mathieu

, (2020)

Chlorophyll a derivatives were integrate...

Structure-property relationships for self-assembled zinc chlorin light-harvesting dye aggregates

Huber, Valerie,Sengupta, Sanchita,Wuerthner, Frank

, p. 7791 - 7807 (2008)

A series of zinc 31-hydroxymethyl chlori...

Intramolecular interaction of synthetic chlorophyll heterodyads with different π-skeletons

Fukai, Kazuhiro,Nakamura, Soichi,Tamiaki, Hitoshi

, p. 332 - 340 (2020)

Two heterodyads were prepared from the c...

Controlled stacking and unstacking of peripheral chlorophyll units drives the spring-like contraction and expansion of a semi-artificial helical polymer

Numata, Munenori,Kinoshita, Daiki,Hirose, Naoya,Kozawa, Tomohiro,Tamiaki, Hitoshi,Kikkawa, Yoshihiro,Kanesato, Masatoshi

, p. 1592 - 1598 (2013)

Developing new strategies for controllin...

Self-assembly of amphiphilic molecules in droplet compartments: An approach toward discrete submicrometer-sized one-dimensional structures

Numata, Munenori,Kinoshita, Daiki,Taniguchi, Nobuko,Tamiaki, Hitoshi,Ohta, Akio

, p. 1844 - 1848 (2012)

Self-assembly in a droplet: A supramolec...

Stereoselective reduction, methylation, and phenylation of the 13-carbonyl group in chlorophyll derivatives

Tamiaki, Hitoshi,Monobe, Rie,Koizumi, Shun,Miyatake, Tomohiro,Kinoshita, Yusuke

, p. 677 - 682 (2013)

Regioselective reduction of the 13-carbo...

Triterpenoid chlorin esters: Water column transformation products of chlorophyll a

Harradine, Paul J.,Peakman, Torren M.,Maxwell, James R.

, p. 13427 - 13440 (1996)

The (22R)-30a,30b-dihomohopan-30b-yl and...

Stereoselective reduction, methylation, and phenylation of the 13-carbonyl group in chlorophyll derivatives

Tamiaki, Hitoshi,Monobe, Rie,Koizumi, Shun,Miyatake, Tomohiro,Kinoshita, Yusuke

, p. 967 - 972 (2013)

Regioselective reduction of the 13-carbo...

Peroxide decoloration of CI acid orange 7 catalyzed by manganese chlorophyll derivatives at the surfaces of micelles and lipid bilayers

Ishigure, Shuichi,Mitsui, Tatsuro,Ito, Shingo,Kondo, Yuji,Kawabe, Shigeki,Kondo, Masaharu,Dewa, Takehisa,Mino, Hiroyuki,Itoh, Shigeru,Nango, Mamoru

, p. 7774 - 7782 (2010)

Manganese-substituted chlorophyll a deri...

Conjugates of natural chlorins and isobornylphenols with a different length of the spacer between the chlorin and terpenephenolic fragments: synthesis and antioxidant activity

Khudyaeva,Belykh,Shevchenko,Maximova,Zainullina,Vakhitova, Yu. V.,Shchukina,Buravlev,Chukicheva, I. Yu.,Kutchina

, p. 2157 - 2164 (2017)

Conjugates containing chlorine and isobo...

Novel carotenoid pyropheophorbide A esters from abalone

Maoka, Takashi,Etoh, Tetsuji,Akimoto, Naoshige,Yasui, Hiroyuki

, p. 3012 - 3015 (2011)

A series of carotenoid pyropheophorbide ...

Nanoparticles of water-soluble dyads based on amino acid fullerene C60 derivatives and pyropheophorbide: Synthesis, photophysical properties, and photodynamic activity

Belik, A. Yu.,Buyanovskaya, A. G.,Filatova, N. V.,Goryachev, N. S.,Klemenkova, Z. S.,Koifman, M. O.,Kotelnikov, A. I.,Romanova, V. S.,Rybkin, A. Yu.,Sadkov, A. P.,Talanova, V. N.,Terentiev, A. A.

, (2021)

Synthesis, spectral properties, and phot...

Efficient synthesis of pyropheophorbide-a and its derivatives

Pallenberg, Alexander J.,Dobhal, Mahabeer P.,Pandey, Ravindra K.

, p. 287 - 290 (2004)

A new and simplified method of preparing...

Phototoxic effects of pyropheophorbide-a from chlorophyll-a on cervical cancer cells

Chaturvedi, Pankaj Kumar,Kim, Yong-Wan,Kim, Sang Soo,Ahn, Woong Shick

, p. 182 - 187 (2014)

Photodynamic therapy (PDT) is a promisin...

Efficient two-electron reduction of dioxygen to hydrogen peroxide with one-electron reductants with a small overpotential catalyzed by a cobalt chlorin complex

Mase, Kentaro,Ohkubo, Kei,Fukuzumi, Shunichi

, p. 2800 - 2808 (2013)

A cobalt chlorin complex (CoII(Ch)) effi...

Push-pull pyropheophorbides for nonlinear optical imaging

Khadria, Anjul,De Coene, Yovan,Gawel, Przemyslaw,Roche, Cécile,Clays, Koen,Anderson, Harry L.

, p. 947 - 956 (2017)

Pyropheophorbide-a methyl ester (PPa-OMe...

Synthesis of zinc chlorophyll homo/hetero-dyads and their folded conformers with porphyrin, chlorin, and bacteriochlorin π-systems

Tamiaki, Hitoshi,Fukai, Kazuhiro,Shimazu, Hideki,Shoji, Sunao

, p. 121 - 128 (2014)

Zinc complex of pyropheophorbide-b, a de...

Novel chlorophyll a derivatives with ester-linked galactose fragments for photodynamic therapy and fluorescence diagnostics of cancer

Mal'Shakova, Marina V.,Velegzhaninov, Ilya O.,Rasova, Elena E.,Belykh, Dmitry V.

, p. 135 - 144 (2021/01/11)

In the present work, a number of chlorop...

24533-72-0 Process route

fucoxanthin pyropheophorbide A ester

fucoxanthin pyropheophorbide A ester

fucoxanthin

fucoxanthin

pyropheophorbide A
24533-72-0

pyropheophorbide A

Conditions
Conditions Yield
With 4-oxo-2,2,6,6-tetramethylpiperidin-oxyl; In ethanol; pH=7.5; aq. phosphate buffer;
pyrochlorophyll a

pyrochlorophyll a

pyropheophytin a
14409-87-1

pyropheophytin a

2-hydroxyethyl disulfide pyropheophorbide

2-hydroxyethyl disulfide pyropheophorbide

pyropheophorbide a
24533-72-0

pyropheophorbide a

Conditions
Conditions Yield
With bis(2-hydroxyethyl) disulfide; water; chlorophyll chlorophyllido-hydrolase; EC 3.1.1.14; In acetone; for 24h;
41 % Chromat.
6 % Chromat.
10 % Chromat.

24533-72-0 Upstream products

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    methyl pyropheophorbide a

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