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rhododendrin

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rhododendrin

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Rhododendrin (betuloside) is an arylbutanoid glycoside and a phenylpropanoid, a type of natural phenol. It can be found in the leaves of Rhododendron aureum or in Cistus salviifolius.

In the Vinony graph

Within Vinony's link graph, rhododendrin is referenced by 19 other articles, and connects out to digital object identifier, chemical formula and phenol.

It sits within the topics 4-Hydroxyphenyl compounds, Chembox image size set and Phenylpropanoids.

Its subject is documented across 6 Wikipedia language editions.

Chemical data

Formula
C16H24O7
Molecular weight
328.36 g/mol
IUPAC name
(2R,3S,4S,5R,6R)-2-(hydroxymethyl)-6-[(2R)-4-(4-hydroxyphenyl)butan-2-yl]oxyoxane-3,4,5-triol
SMILES
C[C@H](CCC1=CC=C(C=C1)O)O[C@H]2[C@@H]([C@H]([C@@H]([C@H](O2)CO)O)O)O
InChIKey
KLLYDTMVSVIJEH-YYMOATHLSA-N
XLogP
0.3
Polar surface area
120 Ų
H-bond donors
5
H-bond acceptors
7
Formal charge
0

via PubChem

Drug data · ChEMBL

Molecule type
Small molecule

via ChEMBL · EBI

Wikidata facts

Mass
328.152203
Show 5 more facts
canonical SMILES
CC(CCC1=CC=C(C=C1)O)OC2C(C(C(C(O2)CO)O)O)O
chemical formula
C₁₆H₂₄O₇
isomeric SMILES
C[C@H](CCC1=CC=C(C=C1)O)O[C@H]2[C@@H]([C@H]([C@@H]([C@H](O2)CO)O)O)O
Commons category
Rhododendrin
has characteristic
bitterness
Sources (2)

via Wikidata · CC0

~1 min read

Encyclopedic overview

1 sections
Contents
  • References

{{chembox | Name = Rhododendrin | ImageFile = Rhododendrin.svg | ImageSize = 200px | ImageName = Chemical structure of Rhododendrin | ImageAlt = Chemical structure of Rhododendrin | IUPACName = (2R)-4-(4-Hydroxyphenyl)butan-2-yl β-D-glucopyranoside | SystematicName = (2R,3S,4S,5R,6R)-2-(Hydroxymethyl)-6-{[(2R)-4-(4-hydroxyphenyl)butan-2-yl]oxy}oxane-3,4,5-triol | OtherNames = Betuloside(-)-Rhododendrin |Section1= |Section2= |Section3= }}

Rhododendrin (betuloside) is an arylbutanoid glycoside and a phenylpropanoid, a type of natural phenol. It can be found in the leaves of Rhododendron aureum or in Cistus salviifolius.

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

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