Procyanidin C1 structure
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Common Name | Procyanidin C1 | ||
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CAS Number | 37064-30-5 | Molecular Weight | 866.77200 | |
Density | 1.747g/cm3 | Boiling Point | N/A | |
Molecular Formula | C45H38O18 | Melting Point | N/A | |
MSDS | Chinese USA | Flash Point | N/A |
Use of Procyanidin C1Procyanidin C1 is a natural polyphenol, causes DNA damage, cell cycle arrest, and induces apoptosis. Procyanidin C1 decreases the level of Bcl-2, but enhances BAX, caspase 3 and 9 expression in cancer cells[1]. |
Name | procyanidin C1 |
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Synonym | More Synonyms |
Description | Procyanidin C1 is a natural polyphenol, causes DNA damage, cell cycle arrest, and induces apoptosis. Procyanidin C1 decreases the level of Bcl-2, but enhances BAX, caspase 3 and 9 expression in cancer cells[1]. |
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Related Catalog | |
Target |
Apoptosis[1] |
References |
Density | 1.747g/cm3 |
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Molecular Formula | C45H38O18 |
Molecular Weight | 866.77200 |
Exact Mass | 866.20600 |
PSA | 331.14000 |
LogP | 4.44390 |
Index of Refraction | 1.826 |
Storage condition | ?20°C |
CHEMICAL IDENTIFICATION
HEALTH HAZARD DATAACUTE TOXICITY DATAMUTATION DATA
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RIDADR | NONH for all modes of transport |
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~98% Procyanidin C1 CAS#:37064-30-5 |
Literature: Kozikowski, Alan P.; Tuckmantel, Werner; Romanczyk JR., Leo J. Patent: US2004/116718 A1, 2004 ; Location in patent: Page 10 ; |
~% Procyanidin C1 CAS#:37064-30-5 |
Literature: Morimoto; Nonaka; Nishioka Chemical and Pharmaceutical Bulletin, 1986 , vol. 34, # 2 p. 633 - 642 |
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Detail
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Literature: Morimoto; Nonaka; Nishioka Chemical and Pharmaceutical Bulletin, 1986 , vol. 34, # 2 p. 633 - 642 |
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Detail
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Literature: Morimoto; Nonaka; Nishioka Chemical and Pharmaceutical Bulletin, 1986 , vol. 34, # 2 p. 633 - 642 |
~%
Detail
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Literature: Morimoto; Nonaka; Nishioka Chemical and Pharmaceutical Bulletin, 1986 , vol. 34, # 2 p. 633 - 642 |
UHPLC-PDA-ESI/HRMSn profiling method to identify and quantify oligomeric proanthocyanidins in plant products.
J. Agric. Food Chem. 62(39) , 9387-400, (2014) Oligomeric proanthocyanidins were successfully identified by UHPLC-PDA-HRMS(n) in a selection of plant-derived materials (jujube fruit, Fuji apple, fruit pericarps of litchi and mangosteen, dark choco... |
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A galloylated dimeric proanthocyanidin from grape seed exhibits dentin biomodification potential.
Fitoterapia 101 , 169-78, (2015) Grape seeds are a rich source of polyphenols, especially proanthocyanidins (PACs), and are also known for the presence of galloylated oligomeric PACs (OPACs). The present study focuses on the phytoche... |
Procyanidol C1 |
(2R,3R,4S)-2-(3,4-dihydroxyphenyl)-4-[(2R,3R)-2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-8-yl]-8-[(2R,3R,4R)-2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-4-yl]-3,4-dihydro-2H-chromene-3,5,7-triol |
Procyanidin C1 |