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233691-67-3,MFCD02683946
Catalog No.:AA002MWL

233691-67-3 | Boc-lys(ac)-amc

Pack Size
Purity
Availability
Price(USD)
Quantity
  
5mg
≥98%
in stock  
$80.00   $56.00
- +
10mg
≥98%
in stock  
$142.00   $99.00
- +
25mg
≥ 99% (HPLC)
in stock  
$212.00   $148.00
- +
50mg
in stock  
$236.00   $165.00
- +
100mg
95%
in stock  
$273.00   $192.00
- +
250mg
95%
in stock  
$511.00   $358.00
- +
1g
≥ 99% (HPLC)
in stock  
$1,927.00   $1,349.00
- +
  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
Technical Information
Catalog Number:
AA002MWL
Chemical Name:
Boc-lys(ac)-amc
CAS Number:
233691-67-3
Molecular Formula:
C23H31N3O6
Molecular Weight:
445.5087
MDL Number:
MFCD02683946
SMILES:
CC(=O)NCCCC[C@@H](C(=O)Nc1ccc2c(c1)oc(=O)cc2C)NC(=O)OC(C)(C)C
Properties
Computed Properties
 
Complexity:
743  
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
1  
Heavy Atom Count:
32  
Hydrogen Bond Acceptor Count:
6  
Hydrogen Bond Donor Count:
3  
Rotatable Bond Count:
10  
XLogP3:
2.2  

Downstream Synthesis Route

[1]JournalofMedicinalChemistry,2016,vol.59,p.1613-1633

[2]Patent:WO2016/179398,2016,A1.Locationinpatent:Paragraph0092;0121;0130;0131

[3]AngewandteChemie-InternationalEdition,2019,vol.58,p.15904-15909    Angew.Chem.,2019,vol.131,p.16051-16056,6

[4]Pharmazie,2000,vol.55,p.601-606

[5]Patent:WO2014/18979,2014,A1.Locationinpatent:Page/Pagecolumn98-99

[6]Patent:US9365498,2016,B2.Locationinpatent:Page/Pagecolumn245;246;248;249

[7]Patent:US2019/216754,2019,A1.Locationinpatent:Paragraph0807;0821;0826

233691-67-3   
N-(4-methyl-7-coumarinyl)-N-α-(tert-butyloxycarbonyl)-lysinamide 

[1]Hoffmann;Brosch;Loidl;Jung[Pharmazie,2000,vol.55,#8,p.601-606]

[2]Madsen,AndreasS.;Olsen,ChristianA.[AngewandteChemie-InternationalEdition,2012,vol.51,#36,p.9083-9087][AngewandteChemie,2012,vol.124,#36,p.9217-9221,5]

[3]CurrentPatentAssignee:TEXASA&MUNIVERSITYSYSTEM-WO2020/236146,2020,A1Locationinpatent:Paragraph0094;00111;00172-00173

[1]CurrentPatentAssignee:QUESTDIAGNOSTICSINC-WO2006/69096,2006,A1Locationinpatent:Page/Pagecolumn97

[2]CurrentPatentAssignee:ABBVIEINC-WO2007/109178,2007,A2Locationinpatent:Page/Pagecolumn101

[1]Locationinpatent:bodytextHenkes,LeonhardM.;Haus,Patricia;Jäger,Felix;Ludwig,Joachim;Meyer-Almes,Franz-Josef[BioorganicandMedicinalChemistry,2012,vol.20,#2,p.985-995]

[1]CurrentPatentAssignee:MASSGENERALBRIGHAMINC;BROADINSTITUTE-WO2014/18979,2014,A1Locationinpatent:Page/Pagecolumn98-99

[2]CurrentPatentAssignee:MASSACHUSETTSINSTITUTEOFTECHNOLOGY;MASSGENERALBRIGHAMINC;BROADINSTITUTE-US9365498,2016,B2Locationinpatent:Page/Pagecolumn245;246;249

[3]CurrentPatentAssignee:KDACTHERAPEUTICS-US2019/216754,2019,A1Locationinpatent:Paragraph0807;0821;0827

Literature

Title: Chemical phylogenetics of histone deacetylases.

Journal: Nature chemical biology 20100301

Title: Subtype selective substrates for histone deacetylases.

Journal: Journal of medicinal chemistry 20041007

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SDS
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