Category:FL7A

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=={{Bilingual|アントシアニンの概要|Overview}}==
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'''{{Bilingual|アントシアニジン|Anthocyanidins}}'''
 
{{Twocolumn|
 
{{Twocolumn|
The Greek word origin of anthocyanin is "flower" ἀνθός (anthos) and "blue" κυανός (kyanos).  Water-soluble pigments from flowers and fruits in red, blue, and purple are originally called anthocyan.  The flavonoid backbone without sugar (shown below) is called anthocyanidin (it is called aglycon because it is devoid of glyco), and structure with sugars is called anthocyanin.
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Anthocyanidins are the flavonoid backbone of anthocyanins without glycosylation (called aglycon). The 6 most common anthocyanidins are:
 
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[[FL7AAANS0001|pelargonidin]], [[FL7AACNS0001|cyanidin]], [[FL7AAGNS0001|delphinidin]], [[FL7AADNS0001|peonidin]], [[FL7AAHNS0001|petunidin]], and [[FL7AAINS0001|malvidin]].
Except for carotenoid (yellow) or indigo (deep blue), most pigments of plant origin are anthocyanins.
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They are conjugated with sugars, hydroxycinnamates, and organic acids such as acetate.
* [[Wikipedia:Anthocyanin]]
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アントシアニンの語源はギリシャ語で「花」意味するἀνθός (anthos)と, 「青」を意味するκυανός (kyanos)です。果実や花の赤、紫、青に対応する水溶性色素はアントシアンと呼ばれます。そのうち、糖を持たず右上に示されたフラボノイド骨格だけの場合をアントシアニディンanthocyanidin (糖が無い形なのでa + glycoでアグリコンと呼ばれます), 配糖体のものをアントシアニンanthocyaninと呼びます。
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アントシアニンの糖がついていない状態(アグリコンと呼びます)をアントシアニジンと呼びます。
 
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基本となる骨格は[[FL7AAANS0001|ペラルゴニジン]]、[[FL7AACNS0001|シアニジン]]、[[FL7AAGNS0001|デルフィニジン]]、[[FL7AADNS0001|ペオニジン]]、[[FL7AAHNS0001|ペチュニジン]]、[[FL7AAINS0001|マルビジン]]の7種で、これらに糖や桂皮酸、酢酸などの有機酸が付加されてアントシアニンとなります。
黄色のカロテノイドや藍色のインディゴを除くと、ほとんどの植物由来の色素はアントシアニンです。
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* [[Wikipedia:jp:アントシアニン]]
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{{FL_digit56|FL7A}}
 
{{FL_digit56|FL7A}}

Latest revision as of 10:27, 19 August 2010

Anthocyanin


Flavonoid Top Molecule Index Author Index Journals Structure Search Food New Input

Upper classes : FL Flavonoid : FL7 Anthocyani(di)n

Contents

[edit] Overview

Anthocyanidins

Anthocyanidins are the flavonoid backbone of anthocyanins without glycosylation (called aglycon). The 6 most common anthocyanidins are: pelargonidin, cyanidin, delphinidin, peonidin, petunidin, and malvidin. They are conjugated with sugars, hydroxycinnamates, and organic acids such as acetate.

Fl7a.png


[edit] Major Plant Families

The number in each family is counted as the number of genera (not species) listed in our registered references. Each reference record is accessible by clicking the link in compound pages. The taxonomy follows the APG-II classification. For details (or if the figure is broken), visit this page.

各科のカウントは種名でなく文献に記載された属名の数です。文献は代謝物ページのリンクからたどれ、分類はAPG-IIです。左の図が表示されない場合はここをクリックしてください。

[edit] Patterns of Hydroxylation

The 5th and 6th digits of our flavonoid ID indicates the hydroxylation patterns of A-ring and B-ring (See the upper-right figure. The leftmost ring is A, rightmost is B), respectively. The following chart is spanned by these 2 digits. R indicates H or CH3, and R' indicates H or R. Numbers are IUPAC positions. The value in each cell (such as GS: glycosilation only) corresponds to the 7th and 8th digits, which is explained at the bottom of this page.


Details of the 3rd Class: Hydroxylation pattern of A and B rings (5th and 6th digits)

Position of -OH (-OCH3) groups
      6th digit →
5th digit ↓

FL A.png FL B.png FL C.png FL D.png FL E.png FL F.png FL G.png FL H.png FL I.png FL J.png FL K.png FL L.png FL 8.png FL 9.png
 A (104 pages)  B (0 pages)  C (177 pages)  D (41 pages)  E (0 pages)  F (0 pages)  G (116 pages)  H (35 pages)  I (62 pages)  J (0 pages)  K (0 pages)  L (0 pages)  8 (0 pages)  9 (0 pages)
FL A .png  A (500 pages)  GA (8 pages) GL (76 pages) GO (6 pages) GS (6 pages) NS (1 pages)  CL (1 pages) DL (1 pages) GA (21 pages) GL (133 pages) GO (7 pages) GS (7 pages) NS (1 pages)  GA (3 pages) GL (29 pages) GO (3 pages) GS (3 pages) NS (1 pages)  GA (17 pages) GL (76 pages) GO (7 pages) GS (7 pages) NS (1 pages)  GA (1 pages) GL (24 pages) GO (3 pages) GS (3 pages) NS (1 pages)  GA (1 pages) GL (41 pages) GO (5 pages) GS (5 pages) NS (1 pages)
FL B .png  B (12 pages)  GL (1 pages) NS (1 pages)  GL (1 pages) GO (1 pages) GS (1 pages) NS (1 pages)  GA (1 pages) GL (1 pages) NS (1 pages)  GO (1 pages) GS (1 pages) NS (1 pages)
FL C .png  C (6 pages)  GL (1 pages) NS (1 pages)  GL (3 pages) NS (1 pages)
FL D .png  D (2 pages)  NS (2 pages)
FL E .png  E (11 pages)  GL (2 pages) NS (1 pages)  GL (3 pages) NS (1 pages)  GL (3 pages) NS (1 pages)
FL F .png  F (4 pages)  GL (4 pages)
FL G .png  G (0 pages)
FL 1 .png  1 (0 pages)
FL 2 .png  2 (0 pages)
FL 3 .png  3 (0 pages)
FL 4 .png  4 (0 pages)
FL 9 .png  9 (0 pages)

Abbreviations used in the above chart

First Characters 

N not glycosylated; G O-glycoside; C C-glycoside; D both glycosides;

Second Characters 

S not modified; M alkylated; I prenylated; R cyclic-prenylated; F furanoFL; P pyranoFL; D furano and pyranoFL; N phenylpropanoid; C others;

Special Second Character only for Anthycyanin (FL7) 

A Galactosylated; L Glucosylated; O modified with other sugars;

[edit] Other Unusual Patterns

These types are not classified in the above chart.

Quinone  QU (0 pages) alpha-Hydroxy  HX (0 pages) beta-Hydroxy  HY (0 pages) Peltogynoid  PT (0 pages)
Retrocalchone  RT (0 pages) Dehydro-backbone  WX (0 pages) Additional rings  RN (0 pages) Others  UN (0 pages)
Pyranoanthocyanin (FL7 only)  RX (8 pages)

[edit] Patterns of Glycosylation

The 7th and 8th digits of the flavonoid ID indicates the glycosylation, and other modification patterns, respectively. The following chart is spanned by these 2 digits. The value in each cell (such as AA for the standard form) corresponds to the 5th and 6th digits.


Details of the 4th Class: Glycosylation patterns (7th and 8th digits)
      7th digit →
8th digit ↓
No glycosylation  N (18 pages) O-glycoside  G (523 pages) C-glycoside  C (1 pages) O- & C-glycoside  D (1 pages)
no modification  S (51 pages)  AA (1 pages) AC (1 pages) AD (1 pages) AG (1 pages) AH (1 pages) AI (1 pages) BC (1 pages) BG (1 pages) BH (1 pages) BI (1 pages) CD (1 pages) CI (1 pages) DI (2 pages) EA (1 pages) EC (1 pages) EG (1 pages) RX (1 pages)  AA (6 pages) AC (7 pages) AD (3 pages) AG (7 pages) AH (3 pages) AI (5 pages) BG (1 pages) BI (1 pages)
alkylated  M (0 pages)
prenylated  I (0 pages)
cyclic prenylated  R (0 pages)
furano FL  F (0 pages)
pyrano FL  P (0 pages)
furano & pyrano FL  D (0 pages)
prenylpropanoid  N (0 pages)
others  C (0 pages)
3-Gal related A N.A.  AA (8 pages) AC (21 pages) AD (3 pages) AG (17 pages) AH (1 pages) AI (1 pages) BH (1 pages) N.A. N.A.
3-Glc related L N.A.  AA (76 pages) AC (133 pages) AD (29 pages) AG (76 pages) AH (24 pages) AI (41 pages) BC (1 pages) BG (1 pages) BH (1 pages) CD (1 pages) CI (3 pages) EA (2 pages) EC (3 pages) EG (3 pages) FA (4 pages) RX (7 pages) N.A. N.A.
other sugar at 3 O N.A.  AA (6 pages) AC (7 pages) AD (3 pages) AG (7 pages) AH (3 pages) AI (5 pages) BG (1 pages) BI (1 pages) N.A. N.A.

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