Home Other Building Blocks 7432-21-5
7432-21-5,MFCD00065700
Catalog No.:AA00ICFG

7432-21-5 | Z-Trp-OH

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5g
97%
in stock  
$6.00   $4.00
- +
10g
97%
in stock  
$7.00   $5.00
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25g
97%
in stock  
$16.00   $11.00
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100g
97%
in stock  
$62.00   $43.00
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500g
97%
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$220.00   $154.00
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  • Technical Information
  • Properties
  • Upstream Synthesis Route
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
  • Technical Information
  • Properties
  • Upstream Synthesis Route
  • Downstream Synthesis Route
  • Literature
Technical Information
Catalog Number:
AA00ICFG
Chemical Name:
Z-Trp-OH
CAS Number:
7432-21-5
Molecular Formula:
C19H18N2O4
Molecular Weight:
338.3572
MDL Number:
MFCD00065700
SMILES:
O=C(N[C@H](C(=O)O)Cc1c[nH]c2c1cccc2)OCc1ccccc1 C19H18N2O4
Properties
Computed Properties
 
Complexity:
464  
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
1  
Heavy Atom Count:
25  
Hydrogen Bond Acceptor Count:
4  
Hydrogen Bond Donor Count:
3  
Rotatable Bond Count:
7  
XLogP3:
2.3  

Upstream Synthesis Route

[1]Synthesis,2006,#3,p.411-424

[2]JournaloftheAmericanChemicalSociety,1980,vol.102,#13,p.4537-4538

[3]TetrahedronLetters,1982,vol.23,#19,p.1985-1988

[4]JournalofBiologicalChemistry,1948,vol.175,p.39,46

[1]JournaloftheAmericanChemicalSociety,1958,vol.80,p.1486,1488

[1]TetrahedronLetters,2012,vol.53,#47,p.6430-6432

[2]TetrahedronLetters,2006,vol.47,#36,p.6393-6396

[3]Synthesis,1986,#11,p.958-960

[4]BioorganicandMedicinalChemistry,2016,vol.24,#3,p.462-473

[5]Patent:CN105884674,2016,A,.Locationinpatent:Paragraph0085;0086;0087

[6]JournalofBiologicalChemistry,1948,vol.175,p.39,46

[7]JournalofBiologicalChemistry,1936,vol.114,p.253,254

[8]Patent:US2007/111930,2007,A1,.Locationinpatent:Page/Pagecolumn21-22

[9]OrganicandBiomolecularChemistry,2013,vol.11,#22,p.3742-3755

[10]OrganicandBiomolecularChemistry,2015,vol.13,#26,p.7177-7192

[11]BioorganicandMedicinalChemistryLetters,2016,vol.26,#20,p.5000-5006

[12]MedChemComm,2017,vol.8,#8,p.1640-1654

[1]Tetrahedron,2000,vol.56,#43,p.8433-8441

[1]BulletinoftheChemicalSocietyofJapan,1985,vol.58,#12,p.3570-3575

[2]ChemischeBerichte,1985,vol.118,#2,p.468-482

Downstream Synthesis Route

[1]Kleijn,LaurensH.J.;Müskens,FrederikeM.;Oppedijk,SabineF.;DeBruin,Gerjan;Martin,NathanielI.[TetrahedronLetters,2012,vol.53,#47,p.6430-6432]

[2]PavanKumar;SomiReddy;Narender;Surendra;Nageswar;RamaRao[TetrahedronLetters,2006,vol.47,#36,p.6393-6396]

[3]Wuensch,E.;Graf,W.;Keller,O.;Keller,W.;Wersin,G.[Synthesis,1986,#11,p.958-960]

[4]Huang,Yuanqiong;Liu,Yongxian;Liu,Yuxiu;Song,Hongjian;Wang,Qingmin[BioorganicandMedicinalChemistry,2016,vol.24,#3,p.462-473]

[5]CurrentPatentAssignee:NANKAIUNIVERSITY-CN105884674,2016,ALocationinpatent:Paragraph0085;0086;0087

[6]Smith[JournalofBiologicalChemistry,1948,vol.175,p.39,46]Bauguess;Berg[JournalofBiologicalChemistry,1936,vol.114,p.253,254]

[7]CurrentPatentAssignee:DRREDDY'SLABORATORIESLIMITED-US2007/111930,2007,A1Locationinpatent:Page/Pagecolumn21-22

[8]Hwang,Tsong-Long;Hung,Chih-Hao;Hsu,Ching-Yun;Huang,Yin-Ting;Tsai,Yu-Chi;Hsieh,Pei-Wen[OrganicandBiomolecularChemistry,2013,vol.11,#22,p.3742-3755]

[9]Alqahtani,Norah;Porwal,SuheelK.;James,ElleD.;Bis,DanaM.;Karty,JonathanA.;Lane,AmyL.;Viswanathan,Rajesh[OrganicandBiomolecularChemistry,2015,vol.13,#26,p.7177-7192]

[10]Zur,ArikA.;Chien,Huan-Chieh;Augustyn,Evan;Flint,Andrew;Heeren,Nathan;Finke,Karissa;Hernandez,Christopher;Hansen,Logan;Miller,Sydney;Lin,Lawrence;Giacomini,KathleenM.;Colas,Claire;Schlessinger,Avner;Thomas,AllenA.[BioorganicandMedicinalChemistryLetters,2016,vol.26,#20,p.5000-5006]

[11]Paul,Saurav;Roy,Ashalata;Deka,SumanJyoti;Panda,Subhankar;Srivastava,GopalNarayan;Trivedi,Vishal;Manna,Debasis[MedChemComm,2017,vol.8,#8,p.1640-1654]

[1]JournalofMedicinalChemistry,1988,vol.31,p.295-300

[1]OrganicLetters,2010,vol.12,p.1220-1223

[2]TetrahedronLetters,2008,vol.49,p.7184-7186

[3]MedChemComm,2017,vol.8,p.1640-1654

[4]JournalofOrganicChemistry,1989,vol.54,p.1664-1668

[5]JournaloftheChemicalSociety.Chemicalcommunications,1988,p.970-971

[1]ChemistryLetters,1988,p.1125-1128

10466-56-5    7432-21-5   
N-carbobenzoxy-L-tryptophanyl-L-isoleucineamide 

[1]JournaloftheChemicalSociety.PerkintransactionsI,1998,p.319-325

Literature

Title: Mechanism of the binding of Z-L-tryptophan and Z-L-phenylalanine to thermolysin and stromelysin-1 in aqueous solutions.

Journal: Biochimica et biophysica acta 20120201

Title: Analyte separation by OMNiMIPs imprinted with multiple templates.

Journal: Biosensors & bioelectronics 20091115

Title: Addition of N-carbobenzyloxy-L-tryptophan as a co-template molecule to molecularly imprinted polymer monoliths for (+)-nilvadipine.

Journal: Journal of chromatography. A 20080328

Title: On the orange color of Z-Trp-ONPo.

Journal: The journal of peptide research : official journal of the American Peptide Society 20050101

Title: Thermodynamic parameters monitoring the equilibrium shift of enzyme-catalyzed hydrolysis/synthesis reactions in favor of synthesis in mixtures of water and organic solvent.

Journal: Biotechnology and bioengineering 20030120

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SDS
Tags:7432-21-5 Molecular Formula|7432-21-5 MDL|7432-21-5 SMILES|7432-21-5 Z-Trp-OH