1012054-59-9,MFCD15528940
Catalog No.:AA0003VH

1012054-59-9 | CUDC-101

Pack Size
Purity
Availability
Price(USD)
Quantity
  
5mg
98%(HPLC)
in stock  
$59.00   $42.00
- +
10mg
98%(HPLC)
in stock  
$110.00   $77.00
- +
25mg
98%(HPLC)
in stock  
$216.00   $152.00
- +
100mg
98%(HPLC)
in stock  
$647.00   $453.00
- +
1000mg
99% (HPLC)
in stock  
$6,295.00   $4,407.00
- +
  • Technical Information
  • Properties
  • Upstream Synthesis Route
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
Technical Information
Catalog Number:
AA0003VH
Chemical Name:
CUDC-101
CAS Number:
1012054-59-9
Molecular Formula:
C24H26N4O4
Molecular Weight:
434.4876
MDL Number:
MFCD15528940
SMILES:
ONC(=O)CCCCCCOc1cc2c(ncnc2cc1OC)Nc1cccc(c1)C#C
Properties
Computed Properties
 
Complexity:
624  
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0  
Defined Bond Stereocenter Count:
0  
Formal Charge:
0  
Heavy Atom Count:
32  
Hydrogen Bond Acceptor Count:
7  
Hydrogen Bond Donor Count:
3  
Isotope Atom Count:
0  
Rotatable Bond Count:
12  
Undefined Atom Stereocenter Count:
0  
Undefined Bond Stereocenter Count:
0  
XLogP3:
4  

Upstream Synthesis Route

[1]Patent:US2009/76022,2009,A1,.Locationinpatent:Page/Pagecolumn68

[1]Patent:US2009/111772,2009,A1,

[2]Patent:US2009/111772,2009,A1,

[1]Patent:US2009/111772,2009,A1,

[1]Patent:US2009/111772,2009,A1,

[1]Patent:US2009/111772,2009,A1,

Downstream Synthesis Route

[1]JournalofMedicinalChemistry,2010,vol.53,p.2000-2009

[2]Patent:WO2008/33747,2008,A2.Locationinpatent:Page/Pagecolumn117

[3]Patent:US2009/76022,2009,A1.Locationinpatent:Page/Pagecolumn69-70

[4]Patent:US2009/111772,2009,A1.Locationinpatent:Page/Pagecolumn68

1012054-59-9    74-88-4   
7-(4-(3-ethynylphenylamino)-7-methoxyquinazolin-6-yloxy)-N-methoxyheptanamide 

[1]Patent:WO2008/33747,2008,A2.Locationinpatent:Page/Pagecolumn151

[2]Patent:US2009/76022,2009,A1.Locationinpatent:Page/Pagecolumn83

[3]Patent:US2009/111772,2009,A1.Locationinpatent:Page/Pagecolumn81

[1]Patent:WO2008/33747,2008,A2.Locationinpatent:Page/Pagecolumn152

[2]Patent:US2009/76022,2009,A1.Locationinpatent:Page/Pagecolumn83

[3]Patent:US2009/111772,2009,A1.Locationinpatent:Page/Pagecolumn82

1012054-59-9    87-69-4   
CUDC-101tartrate 

[1]Patent:US2009/76022,2009,A1.Locationinpatent:Page/Pagecolumn88

Literature

Title: A Phase I Study of CUDC-101, a Multitarget Inhibitor of HDACs, EGFR, and HER2, in Combination with Chemoradiation in Patients with Head and Neck Squamous Cell Carcinoma.

Journal: Clinical cancer research : an official journal of the American Association for Cancer Research 20150401

Title: Phase I first-in-human study of CUDC-101, a multitargeted inhibitor of HDACs, EGFR, and HER2 in patients with advanced solid tumors.

Journal: Clinical cancer research : an official journal of the American Association for Cancer Research 20141001

Title: Identification of potent Yes1 kinase inhibitors using a library screening approach.

Journal: Bioorganic & medicinal chemistry letters 20130801

Title: Cancer network disruption by a single molecule inhibitor targeting both histone deacetylase activity and phosphatidylinositol 3-kinase signaling.

Journal: Clinical cancer research : an official journal of the American Association for Cancer Research 20120801

Title: Multi-targeted hybrids based on HDAC inhibitors for anti-cancer drug discovery.

Journal: Archives of pharmacal research 20120201

Title: Anti-tumour activity of afatinib, an irreversible ErbB family blocker, in human pancreatic tumour cells.

Journal: British journal of cancer 20111108

Title: Manipulating protein acetylation in breast cancer: a promising approach in combination with hormonal therapies?

Journal: Journal of biomedicine & biotechnology 20110101

Title: CUDC-101, a multitargeted inhibitor of histone deacetylase, epidermal growth factor receptor, and human epidermal growth factor receptor 2, exerts potent anticancer activity.

Journal: Cancer research 20100501

Title: Discovery of 7-(4-(3-ethynylphenylamino)-7-methoxyquinazolin-6-yloxy)-N-hydroxyheptanamide (CUDc-101) as a potent multi-acting HDAC, EGFR, and HER2 inhibitor for the treatment of cancer.

Journal: Journal of medicinal chemistry 20100311

Title: Xiong Cai et al Discovery of 7-(4-(3-Ethynylphenylamino)-7-methoxyquinazolin-6-yloxy)-N-hydroxyheptanamide (CUDC-101) as a Potent Multi-Acting HDAC, EGFR, and HER2 Inhibitor for the Treatment of Cancer J. Med. Chem., 2010, 53 (5), pp 2000–2009

Title: Lai CJ, et al. CUDC-101, a multitargeted inhibitor of histone deacetylase, epidermal growth factor receptor, and human epidermal growth factor receptor 2, exerts potent anticancer activity.Cancer Res. 2010 May 1;70(9):3647-56. Epub 2010 Apr 13.

Title: Sun H, et al. CUDC-101, a Novel Inhibitor of Full-Length Androgen Receptor (flAR) and Androgen Receptor Variant 7 (AR-V7) Activity: Mechanism of Action and In Vivo Efficacy. Horm Cancer. 2016 Jun;7(3):196-210.

Title: Zhang L, et al. Dual inhibition of HDAC and EGFR signaling with CUDC-101 induces potent suppression of tumor growth and metastasis in anaplastic thyroid cancer. Oncotarget. 2015 Apr 20;6(11):9073-85.

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Additional Info:
SDS
Related Products of 1012054-59-9
Tags:1012054-59-9 Molecular Formula|1012054-59-9 MDL|1012054-59-9 SMILES|1012054-59-9 CUDC-101
Catalog No.: AA0003VH
1012054-59-9,MFCD15528940
1012054-59-9 | CUDC-101
Pack Size: 5mg
Purity: 98%(HPLC)
in stock
$59.00 $42.00
Pack Size: 10mg
Purity: 98%(HPLC)
in stock
$110.00 $77.00
Pack Size: 25mg
Purity: 98%(HPLC)
in stock
$216.00 $152.00
Pack Size: 100mg
Purity: 98%(HPLC)
in stock
$647.00 $453.00
Pack Size: 1000mg
Purity: 99% (HPLC)
in stock
$6,295.00 $4,407.00
Quantity
- +
Add to Card
Order Now
bulk Quotation Request
Technical Information
Catalog Number: AA0003VH
Chemical Name: CUDC-101
CAS Number: 1012054-59-9
Molecular Formula: C24H26N4O4
Molecular Weight: 434.4876
MDL Number: MFCD15528940
SMILES: ONC(=O)CCCCCCOc1cc2c(ncnc2cc1OC)Nc1cccc(c1)C#C
Properties
Complexity: 624  
Covalently-Bonded Unit Count: 1  
Defined Atom Stereocenter Count: 0  
Defined Bond Stereocenter Count: 0  
Formal Charge: 0  
Heavy Atom Count: 32  
Hydrogen Bond Acceptor Count: 7  
Hydrogen Bond Donor Count: 3  
Isotope Atom Count: 0  
Rotatable Bond Count: 12  
Undefined Atom Stereocenter Count: 0  
Undefined Bond Stereocenter Count: 0  
XLogP3: 4  
Upstream Synthesis Route
1012920-21-6    1012054-59-9 

[1]Patent:US2009/76022,2009,A1,.Locationinpatent:Page/Pagecolumn68

29823-18-5    1012054-59-9 

[1]Patent:US2009/111772,2009,A1,

[2]Patent:US2009/111772,2009,A1,

905306-05-0    1012054-59-9 

[1]Patent:US2009/111772,2009,A1,

1012057-22-5    1012054-59-9 

[1]Patent:US2009/111772,2009,A1,

1012057-25-8    1012054-59-9 

[1]Patent:US2009/111772,2009,A1,

Downstream Synthesis Route
1012057-21-4    1012054-59-9 

[1]JournalofMedicinalChemistry,2010,vol.53,p.2000-2009

[2]Patent:WO2008/33747,2008,A2.Locationinpatent:Page/Pagecolumn117

[3]Patent:US2009/76022,2009,A1.Locationinpatent:Page/Pagecolumn69-70

[4]Patent:US2009/111772,2009,A1.Locationinpatent:Page/Pagecolumn68

1012054-59-9    74-88-4   
7-(4-(3-ethynylphenylamino)-7-methoxyquinazolin-6-yloxy)-N-methoxyheptanamide 

[1]Patent:WO2008/33747,2008,A2.Locationinpatent:Page/Pagecolumn151

[2]Patent:US2009/76022,2009,A1.Locationinpatent:Page/Pagecolumn83

[3]Patent:US2009/111772,2009,A1.Locationinpatent:Page/Pagecolumn81

1012054-59-9    2719-27-9    1012054-99-7 

[1]Patent:WO2008/33747,2008,A2.Locationinpatent:Page/Pagecolumn152

[2]Patent:US2009/76022,2009,A1.Locationinpatent:Page/Pagecolumn83

[3]Patent:US2009/111772,2009,A1.Locationinpatent:Page/Pagecolumn82

1012054-59-9    87-69-4   
CUDC-101tartrate 

[1]Patent:US2009/76022,2009,A1.Locationinpatent:Page/Pagecolumn88

Literature fold

Title: A Phase I Study of CUDC-101, a Multitarget Inhibitor of HDACs, EGFR, and HER2, in Combination with Chemoradiation in Patients with Head and Neck Squamous Cell Carcinoma.

Journal: Clinical cancer research : an official journal of the American Association for Cancer Research20150401

Title: Phase I first-in-human study of CUDC-101, a multitargeted inhibitor of HDACs, EGFR, and HER2 in patients with advanced solid tumors.

Journal: Clinical cancer research : an official journal of the American Association for Cancer Research20141001

Title: Identification of potent Yes1 kinase inhibitors using a library screening approach.

Journal: Bioorganic & medicinal chemistry letters20130801

Title: Cancer network disruption by a single molecule inhibitor targeting both histone deacetylase activity and phosphatidylinositol 3-kinase signaling.

Journal: Clinical cancer research : an official journal of the American Association for Cancer Research20120801

Title: Multi-targeted hybrids based on HDAC inhibitors for anti-cancer drug discovery.

Journal: Archives of pharmacal research20120201

Title: Anti-tumour activity of afatinib, an irreversible ErbB family blocker, in human pancreatic tumour cells.

Journal: British journal of cancer20111108

Title: Manipulating protein acetylation in breast cancer: a promising approach in combination with hormonal therapies?

Journal: Journal of biomedicine & biotechnology20110101

Title: CUDC-101, a multitargeted inhibitor of histone deacetylase, epidermal growth factor receptor, and human epidermal growth factor receptor 2, exerts potent anticancer activity.

Journal: Cancer research20100501

Title: Discovery of 7-(4-(3-ethynylphenylamino)-7-methoxyquinazolin-6-yloxy)-N-hydroxyheptanamide (CUDc-101) as a potent multi-acting HDAC, EGFR, and HER2 inhibitor for the treatment of cancer.

Journal: Journal of medicinal chemistry20100311

Title: Xiong Cai et al Discovery of 7-(4-(3-Ethynylphenylamino)-7-methoxyquinazolin-6-yloxy)-N-hydroxyheptanamide (CUDC-101) as a Potent Multi-Acting HDAC, EGFR, and HER2 Inhibitor for the Treatment of Cancer J. Med. Chem., 2010, 53 (5), pp 2000–2009

Title: Lai CJ, et al. CUDC-101, a multitargeted inhibitor of histone deacetylase, epidermal growth factor receptor, and human epidermal growth factor receptor 2, exerts potent anticancer activity.Cancer Res. 2010 May 1;70(9):3647-56. Epub 2010 Apr 13.

Title: Sun H, et al. CUDC-101, a Novel Inhibitor of Full-Length Androgen Receptor (flAR) and Androgen Receptor Variant 7 (AR-V7) Activity: Mechanism of Action and In Vivo Efficacy. Horm Cancer. 2016 Jun;7(3):196-210.

Title: Zhang L, et al. Dual inhibition of HDAC and EGFR signaling with CUDC-101 induces potent suppression of tumor growth and metastasis in anaplastic thyroid cancer. Oncotarget. 2015 Apr 20;6(11):9073-85.

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