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rottlerin

Structure via PubChem · Public domain (PubChem)

EntityQ7370686· pop 5· linked from 324 articles

Also known as mallotoxin, Kamalin, 3'-((8-cinnamoyl-5,7-dihydroxy-2,2-dimethyl-2H-1-benzopyran-6-yl)methyl)-2',4',6'-trihydroxy-5'-methyl-acetophenone

Rottlerin (mallotoxin) is a polyphenol natural product isolated from the Asian tree Mallotus philippensis. Rottlerin displays a complex spectrum of pharmacology.

Chemical data

Formula
C30H28O8
Molecular weight
516.5 g/mol
IUPAC name
(E)-1-[6-[(3-acetyl-2,4,6-trihydroxy-5-methylphenyl)methyl]-5,7-dihydroxy-2,2-dimethylchromen-8-yl]-3-phenylprop-2-en-1-one
SMILES
CC1=C(C(=C(C(=C1O)C(=O)C)O)CC2=C(C(=C3C(=C2O)C=CC(O3)(C)C)C(=O)/C=C/C4=CC=CC=C4)O)O
InChIKey
DEZFNHCVIZBHBI-ZHACJKMWSA-N
XLogP
5.9
Polar surface area
145 Ų
H-bond donors
5
H-bond acceptors
8
Formal charge
0

via PubChem

Drug data · ChEMBL

Molecule type
Small molecule

via ChEMBL · EBI

Wikidata facts

Mass
516.178418
Show 6 more facts
chemical formula
C₃₀H₂₈O₈
found in taxon
Mallotus philippensis
isomeric SMILES
CC1=C(C(=C(C(=C1O)C(=O)C)O)CC2=C(C3=C(C(=C2O)C(=O)/C=C/C4=CC=CC=C4)OC(C=C3)(C)C)O)O
canonical SMILES
CC1=C(C(=C(C(=C1O)C(=O)C)O)CC2=C(C3=C(C(=C2O)C(=O)C=CC4=CC=CC=C4)OC(C=C3)(C)C)O)O
subject has role
enzyme inhibitor
Sources (3)

via Wikidata · CC0

~5 min read

Encyclopedic overview

10 sections
Contents
  • Effects
  • Uncoupler of oxidative phosphorylation
  • Potassium channel opener
  • Role in cardioplegia reperfusion
  • Contractility and vascular effects
  • Akt activation
  • Antioxidant properties
  • Ineffective PKCδ selective inhibitor
  • Sources
  • References

Rottlerin (mallotoxin) is a polyphenol natural product isolated from the Asian tree Mallotus philippensis. Rottlerin displays a complex spectrum of pharmacology.

== Effects ==

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

Available in 5 languages

via Wikidata sitelinks · CC0