697235-39-5,MFCD25541744
Catalog No.:AA00FF6H

697235-39-5 | Episilvestrol

Pack Size
Purity
Availability
Price(USD)
Quantity
  
1mg
99%
1 week  
$685.00   $480.00
- +
  • Technical Information
  • Properties
  • Literature
  • Request for Quotation
  • Download SDS
Technical Information
Catalog Number:
AA00FF6H
Chemical Name:
Episilvestrol
CAS Number:
697235-39-5
Molecular Formula:
C34H38O13
Molecular Weight:
654.6577
MDL Number:
MFCD25541744
SMILES:
OCC(C1COC(C(O1)Oc1cc2OC3(C(c2c(c1)OC)(O)C(C(C3c1ccccc1)C(=O)OC)O)c1ccc(cc1)OC)OC)O
Properties
Computed Properties
 
Complexity:
1050  
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
9  
Defined Bond Stereocenter Count:
0  
Formal Charge:
0  
Heavy Atom Count:
47  
Hydrogen Bond Acceptor Count:
13  
Hydrogen Bond Donor Count:
4  
Isotope Atom Count:
0  
Rotatable Bond Count:
11  
Undefined Atom Stereocenter Count:
0  
Undefined Bond Stereocenter Count:
0  
XLogP3:
1.6  

Literature

Title: Total synthesis of 2''',5'''-diepisilvestrol and its C1''' epimer: key structure activity relationships at C1''' and C2'''.

Journal: Journal of natural products 20120824

Title: Isolation and characterization of minor analogues of silvestrol and other constituents from a large-scale re-collection of Aglaia foveolata.

Journal: Journal of natural products 20101129

Title: Total synthesis of the potent anticancer Aglaia metabolites (-)-silvestrol and (-)-episilvestrol and the active analogue (-)-4'-desmethoxyepisilvestrol.

Journal: Journal of the American Chemical Society 20090204

Title: Total synthesis of (-)-episilvestrol and (-)-silvestrol.

Journal: Angewandte Chemie (International ed. in English) 20070101

Title: Silvestrol and episilvestrol, potential anticancer rocaglate derivatives from Aglaia silvestris.

Journal: The Journal of organic chemistry 20040514

Title: Chambers JM, et al. Synthesis of biotinylated episilvestrol: highly selective targeting of the translation factors eIF4AI/II. Org Lett. 2013 Mar 15;15(6):1406-9.

Title: Hwang BY, et al. Silvestrol and episilvestrol, potential anticancer rocaglate derivatives from Aglaia silvestris. J Org Chem. 2004 May 14;69(10):3350-8.

Title: Daker M, et al. Inhibition of nasopharyngeal carcinoma cell proliferation and synergism of cisplatin with silvestrol and episilvestrol isolated from Aglaia stellatopilosa. Exp Ther Med. 2016 Jun;11(6):2117-2126. Epub 2016 Mar 29.

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Tags:697235-39-5 Molecular Formula|697235-39-5 MDL|697235-39-5 SMILES|697235-39-5 Episilvestrol
Catalog No.: AA00FF6H
697235-39-5,MFCD25541744
697235-39-5 | Episilvestrol
Pack Size: 1mg
Purity: 99%
1 week
$685.00 $480.00
Quantity
- +
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Technical Information
Catalog Number: AA00FF6H
Chemical Name: Episilvestrol
CAS Number: 697235-39-5
Molecular Formula: C34H38O13
Molecular Weight: 654.6577
MDL Number: MFCD25541744
SMILES: OCC(C1COC(C(O1)Oc1cc2OC3(C(c2c(c1)OC)(O)C(C(C3c1ccccc1)C(=O)OC)O)c1ccc(cc1)OC)OC)O
Properties
Complexity: 1050  
Covalently-Bonded Unit Count: 1  
Defined Atom Stereocenter Count: 9  
Defined Bond Stereocenter Count: 0  
Formal Charge: 0  
Heavy Atom Count: 47  
Hydrogen Bond Acceptor Count: 13  
Hydrogen Bond Donor Count: 4  
Isotope Atom Count: 0  
Rotatable Bond Count: 11  
Undefined Atom Stereocenter Count: 0  
Undefined Bond Stereocenter Count: 0  
XLogP3: 1.6  
Literature fold

Title: Total synthesis of 2''',5'''-diepisilvestrol and its C1''' epimer: key structure activity relationships at C1''' and C2'''.

Journal: Journal of natural products20120824

Title: Isolation and characterization of minor analogues of silvestrol and other constituents from a large-scale re-collection of Aglaia foveolata.

Journal: Journal of natural products20101129

Title: Total synthesis of the potent anticancer Aglaia metabolites (-)-silvestrol and (-)-episilvestrol and the active analogue (-)-4'-desmethoxyepisilvestrol.

Journal: Journal of the American Chemical Society20090204

Title: Total synthesis of (-)-episilvestrol and (-)-silvestrol.

Journal: Angewandte Chemie (International ed. in English)20070101

Title: Silvestrol and episilvestrol, potential anticancer rocaglate derivatives from Aglaia silvestris.

Journal: The Journal of organic chemistry20040514

Title: Chambers JM, et al. Synthesis of biotinylated episilvestrol: highly selective targeting of the translation factors eIF4AI/II. Org Lett. 2013 Mar 15;15(6):1406-9.

Title: Hwang BY, et al. Silvestrol and episilvestrol, potential anticancer rocaglate derivatives from Aglaia silvestris. J Org Chem. 2004 May 14;69(10):3350-8.

Title: Daker M, et al. Inhibition of nasopharyngeal carcinoma cell proliferation and synergism of cisplatin with silvestrol and episilvestrol isolated from Aglaia stellatopilosa. Exp Ther Med. 2016 Jun;11(6):2117-2126. Epub 2016 Mar 29.

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