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Home Other Building Blocks (10S)-1,8-dihydroxy-3-(hydroxymethyl)-10-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-9,10-dihydroanthracen-9-one

(10S)-1,8-dihydroxy-3-(hydroxymethyl)-10-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-9,10-dihydroanthracen-9-one

CAS No.:
1415-73-2
Catalog Number:
AG001GID
Molecular Formula:
C21H22O9
Molecular Weight:
418.3940
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
1g
98%
In Stock USA
United States
$19
- +
5g
98%
In Stock USA
United States
$44
- +
25g
98%
In Stock USA
United States
$100
- +
100g
98%
In Stock USA
United States
$350
- +
Product Description
Catalog Number:
AG001GID
Chemical Name:
(10S)-1,8-dihydroxy-3-(hydroxymethyl)-10-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-9,10-dihydroanthracen-9-one
CAS Number:
1415-73-2
Molecular Formula:
C21H22O9
Molecular Weight:
418.3940
MDL Number:
MFCD00151160
IUPAC Name:
(10S)-1,8-dihydroxy-3-(hydroxymethyl)-10-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-10H-anthracen-9-one
InChI:
InChI=1S/C21H22O9/c22-6-8-4-10-14(21-20(29)19(28)17(26)13(7-23)30-21)9-2-1-3-11(24)15(9)18(27)16(10)12(25)5-8/h1-5,13-14,17,19-26,28-29H,6-7H2/t13-,14+,17-,19+,20-,21+/m1/s1
InChI Key:
AFHJQYHRLPMKHU-OSYMLPPYSA-N
SMILES:
OCc1cc(O)c2c(c1)[C@@H]([C@@H]1O[C@H](CO)[C@H]([C@@H]([C@H]1O)O)O)c1c(C2=O)c(O)ccc1
EC Number:
215-808-0
UNII:
648RW354S9
Properties
Complexity:
630  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
6  
Defined Bond Stereocenter Count:
0
Exact Mass:
418.126g/mol
Formal Charge:
0
Heavy Atom Count:
30  
Hydrogen Bond Acceptor Count:
9  
Hydrogen Bond Donor Count:
7  
Isotope Atom Count:
0
Molecular Weight:
418.398g/mol
Monoisotopic Mass:
418.126g/mol
Rotatable Bond Count:
3  
Topological Polar Surface Area:
168A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
-0.1  
Literature
Title Journal
In vitro antimicrobial and antioxidant activities of anthrone and chromone from the latex of Aloe harlana Reynolds. Phytotherapy research : PTR 20111201
[Effects of enhanced UV-B radiation on leaf anthraquinones content and cell ultrastructure of Aloe vera L]. Ying yong sheng tai xue bao = The journal of applied ecology 20100101
The content of secondary phenol metabolites in pruned leaves of Aloe arborescens, a comparison between two methods: leaf exudates and leaf water extract. Journal of natural medicines 20081001
On the interaction of the anthraquinone barbaloin with negatively charged DMPG bilayers. Langmuir : the ACS journal of surfaces and colloids 20080415
Antioxidant actions of phenolic compounds found in dietary plants on low-density lipoprotein and erythrocytes in vitro. Journal of the American College of Nutrition 20070601
Antidiabetic effects of dietary administration of Aloe arborescens Miller components on multiple low-dose streptozotocin-induced diabetes in mice: investigation on hypoglycemic action and systemic absorption dynamics of aloe components. Journal of ethnopharmacology 20060220
Membrane-related effects underlying the biological activity of the anthraquinones emodin and barbaloin. Biochemical pharmacology 20040801
[Contents of barbaloin-related compounds in aloe drinks and their change during storage]. Shokuhin eiseigaku zasshi. Journal of the Food Hygienic Society of Japan 20020601
Determination of aloenin, barbaloin and isobarbaloin in aloe species by micellar electrokinetic chromatography. Journal of chromatography. B, Biomedical sciences and applications 20010305
Properties