75629-19-5,MFCD05662262
Catalog No.:AA00G5YD

75629-19-5 | Kuwanon G

Pack Size
Purity
Availability
Price(USD)
Quantity
  
5mg
99%
1 week  
$527.00   $369.00
- +
  • Technical Information
  • Properties
  • Literature
  • Request for Quotation
  • Download SDS
Technical Information
Catalog Number:
AA00G5YD
Chemical Name:
Kuwanon G
CAS Number:
75629-19-5
Molecular Formula:
C40H36O11
Molecular Weight:
692.7072
MDL Number:
MFCD05662262
SMILES:
CC(=CCc1c(oc2c(c1=O)c(O)cc(c2[C@H]1C=C(C)C[C@H]([C@@H]1C(=O)c1ccc(cc1O)O)c1ccc(cc1O)O)O)c1ccc(cc1O)O)C
Properties
Computed Properties
 
Complexity:
1380  
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
3  
Defined Bond Stereocenter Count:
0  
Formal Charge:
0  
Heavy Atom Count:
51  
Hydrogen Bond Acceptor Count:
11  
Hydrogen Bond Donor Count:
8  
Isotope Atom Count:
0  
Rotatable Bond Count:
7  
Undefined Atom Stereocenter Count:
0  
Undefined Bond Stereocenter Count:
0  
XLogP3:
7.3  

Literature

Title: Kuwanon G attenuates atherosclerosis by upregulation of LXRα-ABCA1/ABCG1 and inhibition of NFκB activity in macrophages.

Journal: Toxicology and applied pharmacology 20180215

Title: [Study on Diels-Alder type adducts from stem barks of Morus yunanensis].

Journal: Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica 20090201

Title: Kuwanon G: an antibacterial agent from the root bark of Morus alba against oral pathogens.

Journal: Journal of ethnopharmacology 20030201

Title: [Chemistry and biosynthesis of prenylflavonoids].

Journal: Yakugaku zasshi : Journal of the Pharmaceutical Society of Japan 20010701

Title: Cytotoxic activity of low molecular weight polyphenols against human oral tumor cell lines.

Journal: Anticancer research 20000101

Title: Non-peptide bombesin receptor antagonists, kuwanon G and H, isolated from mulberry.

Journal: Biochemical and biophysical research communications 19950815

Title: Mihara S, et al. Non-peptide bombesin receptor antagonists, kuwanon G and H, isolated from mulberry. Biochem Biophys Res Commun. 1995 Aug 15;213(2):594-9.

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Tags:75629-19-5 Molecular Formula|75629-19-5 MDL|75629-19-5 SMILES|75629-19-5 Kuwanon G
Catalog No.: AA00G5YD
75629-19-5,MFCD05662262
75629-19-5 | Kuwanon G
Pack Size: 5mg
Purity: 99%
1 week
$527.00 $369.00
Quantity
- +
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Technical Information
Catalog Number: AA00G5YD
Chemical Name: Kuwanon G
CAS Number: 75629-19-5
Molecular Formula: C40H36O11
Molecular Weight: 692.7072
MDL Number: MFCD05662262
SMILES: CC(=CCc1c(oc2c(c1=O)c(O)cc(c2[C@H]1C=C(C)C[C@H]([C@@H]1C(=O)c1ccc(cc1O)O)c1ccc(cc1O)O)O)c1ccc(cc1O)O)C
Properties
Complexity: 1380  
Covalently-Bonded Unit Count: 1  
Defined Atom Stereocenter Count: 3  
Defined Bond Stereocenter Count: 0  
Formal Charge: 0  
Heavy Atom Count: 51  
Hydrogen Bond Acceptor Count: 11  
Hydrogen Bond Donor Count: 8  
Isotope Atom Count: 0  
Rotatable Bond Count: 7  
Undefined Atom Stereocenter Count: 0  
Undefined Bond Stereocenter Count: 0  
XLogP3: 7.3  
Literature fold

Title: Kuwanon G attenuates atherosclerosis by upregulation of LXRα-ABCA1/ABCG1 and inhibition of NFκB activity in macrophages.

Journal: Toxicology and applied pharmacology20180215

Title: [Study on Diels-Alder type adducts from stem barks of Morus yunanensis].

Journal: Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica20090201

Title: Kuwanon G: an antibacterial agent from the root bark of Morus alba against oral pathogens.

Journal: Journal of ethnopharmacology20030201

Title: [Chemistry and biosynthesis of prenylflavonoids].

Journal: Yakugaku zasshi : Journal of the Pharmaceutical Society of Japan20010701

Title: Cytotoxic activity of low molecular weight polyphenols against human oral tumor cell lines.

Journal: Anticancer research20000101

Title: Non-peptide bombesin receptor antagonists, kuwanon G and H, isolated from mulberry.

Journal: Biochemical and biophysical research communications19950815

Title: Mihara S, et al. Non-peptide bombesin receptor antagonists, kuwanon G and H, isolated from mulberry. Biochem Biophys Res Commun. 1995 Aug 15;213(2):594-9.

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