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amylopectin

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amylopectin

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Amylopectin is a water-insoluble polysaccharide and highly branched polymer of α-glucose units found in plants. It is one of the two components of starch, the other being amylose. thumb|Relation of amylopectin to starch granule|center Plants store starch within specialized organelles called amyloplasts. To generate energy, the plant hydrolyzes the starch, releasing the glucose subunits. Humans and other animals that eat plant foods also use amylase, an enzyme that assists in breaking down amylopectin, to initiate the hydrolysis of starch.

OverviewAI-generated

Amylopectin is a chemical compound with the formula C₃₀H₅₂O₂₆. Its molecular mass is listed as 828.274682, while another source records a weight of 828.7. The substance has a charge of 0 and an xlogp value of -10.6.

Structural data indicates that amylopectin contains 17 hydrogen bond donors and 26 hydrogen bond acceptors. The topological polar surface area (TPSA) is 427. A canonical SMILES representation for the molecule is provided in chemical databases.

The subject is associated with a Commons category titled "Amylopectin." It has been referenced by 176 other encyclopedia articles. Additionally, a search query for amylopectin on PubMed yields a count of 3647 results.

Synthesized by Vinony from 15 facts across 4 sources: Wikidata, PubMed, PubChem, Vinony graph. Generated from structured data (not the Wikipedia text) and checked against those facts — may still contain errors.

Chemical data

Formula
C30H52O26
Molecular weight
828.7 g/mol
IUPAC name
(2R,3R,4S,5S,6R)-2-[(2R,3S,4R,5R,6S)-6-[[(2R,3S,4R,5R,6R)-4,5-dihydroxy-3-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-6-[(2R,3S,4R,5R,6S)-4,5,6-trihydroxy-2-(hydroxymethyl)oxan-3-yl]oxyoxan-2-yl]methoxy]-4,5-dihydroxy-2-(hydroxymethyl)oxan-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol
SMILES
C([C@@H]1[C@H]([C@@H]([C@H]([C@H](O1)O[C@@H]2[C@H](O[C@@H]([C@@H]([C@H]2O)O)OC[C@@H]3[C@H]([C@@H]([C@H]([C@H](O3)O[C@@H]4[C@H](O[C@@H]([C@@H]([C@H]4O)O)O)CO)O)O)O[C@@H]5[C@@H]([C@H]([C@@H]([C@H](O5)CO)O)O)O)CO)O)O)O)O
InChIKey
WMGFVAGNIYUEEP-WUYNJSITSA-N
XLogP
-10.6
Polar surface area
427 Ų
H-bond donors
17
H-bond acceptors
26
Formal charge
0

via PubChem

Wikidata facts

Has part
hydrogen
Mass
828.274682
Show 4 more facts
canonical SMILES
C(C1C(C(C(C(O1)OC2C(OC(C(C2O)O)OCC3C(C(C(C(O3)OC4C(OC(C(C4O)O)O)CO)O)O)OC5C(C(C(C(O5)CO)O)O)O)CO)O)O)O)O
Commons category
Amylopectin
chemical formula
C₃₀H₅₂O₂₆
isomeric SMILES
C([C@@H]1[C@H]([C@@H]([C@H]([C@H](O1)O[C@@H]2[C@H](O[C@@H]([C@@H]([C@H]2O)O)OC[C@@H]3[C@H]([C@@H]([C@H]([C@H](O3)O[C@@H]4[C@H](O[C@@H]([C@@H]([C@H]4O)O)O)CO)O)O)O[C@@H]5[C@@H]([C@H]([C@@H]([C@H](O5)CO)O)O)O)CO)O)O)O)O
Sources (3)

via Wikidata · CC0

~16 min read

Encyclopedic overview

15 sections
Contents
  • Structure
  • History
  • Metabolism
  • Applications
  • Food
  • Textiles
  • Engineering
  • Clinical applications
  • Drug delivery
  • Tissue engineering
  • Fibers
  • Bionanocomposites
  • See also
  • References
  • External links

Amylopectin is a water-insoluble polysaccharide and highly branched polymer of α-glucose units found in plants. It is one of the two components of starch, the other being amylose. thumb|Relation of amylopectin to starch granule|center Plants store starch within specialized organelles called amyloplasts. To generate energy, the plant hydrolyzes the starch, releasing the glucose subunits. Humans and other animals that eat plant foods also use amylase, an enzyme that assists in breaking down amylopectin, to initiate the hydrolysis of starch.

Starch is made of about 70–80% amylopectin by weight, though it varies depending on the source. For example, it ranges from lower percent content in long-grain rice, amylomaize, and russet potatoes to 100% in glutinous rice, waxy potato starch, and waxy corn. Amylopectin is highly branched, being formed of 2,000 to 200,000 glucose units. Its inner chains are formed of 20–24 glucose subunits.thumb|100px|Structure of the amylopectin molecule|center

Excerpted from Wikipedia’s “amylopectin” article, available under the CC BY-SA 4.0 licence.

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