Page last updated: 2024-11-06

boc-glycine

Description Research Excerpts Clinical Trials Roles Classes Pathways Study Profile Bioassays Related Drugs Related Conditions Protein Interactions Research Growth Market Indicators

Description

Boc-glycine, also known as tert-butoxycarbonylglycine, is a protected amino acid commonly used in peptide synthesis. It is synthesized by reacting glycine with di-tert-butyl dicarbonate in the presence of a base. The tert-butoxycarbonyl (Boc) group acts as a protecting group for the amino group of glycine, preventing unwanted side reactions during peptide chain elongation. Boc-glycine is a crucial building block in solid-phase peptide synthesis (SPPS), a widely employed method for synthesizing peptides. It is used to introduce glycine residues into the growing peptide chain. The Boc protecting group is stable under mild acidic conditions but can be easily removed using trifluoroacetic acid (TFA) at the end of the synthesis. Boc-glycine's importance stems from its role in enabling the efficient and controlled assembly of peptides, which have diverse biological functions and therapeutic applications. It is studied to understand its synthesis, reactivity, and its application in peptide synthesis.'

BOC-glycine: RN given refers to parent cpd [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID78288
CHEMBL ID508605
SCHEMBL ID17906
MeSH IDM0092948

Synonyms (146)

Synonym
AC-138
EN300-35227
n-((1,1-dimethylethoxy)carbonyl)glycine
einecs 224-864-5
nsc 127669
nalpha-tert-butyloxycarbonylglycine
glycine, n-carboxy-, n-tert-butyl ester
glycine, n-((1,1-dimethylethoxy)carbonyl)-
n.alpha.-tert-butyloxycarbonylglycine
n-tert-butyloxycarbonylglycine
tert-butoxycarbonylglycine
boc-gly-oh
glycine,1-dimethylethoxy)carbonyl]-
nsc-127669
tert-butyloxycarbonylglycine
4530-20-5
boc-glycine
n-(carbo-tert-butoxy)glycine
n-t-butyloxycarbonyl glycine
nsc127669
n-(tert-butoxycarbonyl)glycine
n(a)-tert-butyloxycarbonylglycine
n-[(1,1-dimethylethoxy)carbonyl]glycine
t-butoxycarbonylglycine
glycine, n-tert-butyl ester
glycine, n-[(1,1-dimethylethoxy)carbonyl]-
glycine,n-tert.butyloxycarbonyl
inchi=1/c7h13no4/c1-7(2,3)12-6(11)8-4-5(9)10/h4h2,1-3h3,(h,8,11)(h,9,10
boc-gly-oh, 98%
boc-gly-oh, >=99.0% (t)
B1185
n-boc-glycine
AKOS000163644
STL068907
n-alpha-t-boc-glycine
CHEMBL508605
2-[(2-methylpropan-2-yl)oxycarbonylamino]acetic acid
[(tert-butoxycarbonyl)amino]acetic acid
2-{[(tert-butoxy)carbonyl]amino}acetic acid
tert-butoxycarbonylamino-acetic acid
n-boc-l-glycine
A826767
M03287
2-[(tert-butoxy)carbonylamino]acetic acid
FT-0602334
AM20100157
AB00256
[(t-butoxycarbonyl)amino]acetic acid
BP-30202
AB01314432-03
2-((tert-butoxycarbonyl)amino)acetic acid
t-butoxycarbonyl- glycine
tert.butoxycarbonylglycine
n-tert.butyloxycarbonylglycine
(tert-butoxycarbonyl)-glycine
((tert-butoxycarbonyl)amino)acetic acid
n-tert.butyloxycarbonyl glycine
n-boc-gly
n-tert-butoxycarbonyl-glycine
n-bocglycine
(tert-butoxycarbonylamino)acetic acid
tert-butoxycarbonyl-glycine
n-(tert.butoxycarbonyl)glycine
n-tert-butoxycarbonyl glycine
t-butyloxycarbonyl glycine
tert-butoxycarbonylaminoacetic acid
t-butyloxycarbonylglycine
boc-gly
2-[(tert-butoxycarbonyl)amino]acetic acid
n-(1,1-dimethylethoxycarbonyl)glycine
tert.-butoxycarbonylglycine
n-tert-butyloxycarbonyl glycine
n-tert-butyloxycarbonyl-2-aminoacetic acid
n-(tert-butoxy-carbonyl)glycine
t-butoxycarbonylaminoacetic acid
t-butoxycarbonyl-glycine
tert-butyloxycarbonyl glycine
tert-butoxycarbonyl glycine
2-tert-butoxycarbonylaminoacetic acid
n-(t-butoxycarbonyl)glycine
boc glycine
tert. butoxycarbonyl glycine
n-t-butoxycarbonyl glycine
bocglyoh
n-tert-butoxycarbonylglycine
n-t-boc-glycine
n-t-butyloxycarbonylglycine
n-{[(1,1-dimethylethyl)oxy]carbonyl}glycine
n-tertbutoxycarbonylglycine
boc-glycine-oh
n-boc glycine
n-(tertiary butoxycarbonyl)glycine
nalpha-boc-glycine
n-(tert-butoxycarbonyl)-glycine
t-butoxycarbonyl glycine
carbotertbutoxyglycine
(tert-butoxycarbonyl)glycine
n-tert.-butoxycarbonylglycine
n-(tert.-butyloxycarbonyl)-glycine
n-tert-butyloxycarbonyl-glycine
n-(boc)-glycine
n-((tert-butyloxy)carbonyl)glycine
n-(tert-butoxycarbonyl) glycine
n-(tertbutoxycarbonyl)glycine
tert-butoxycarbonylamino acetic acid
2-(tert-butoxy-carbonyl-amino)acetic acid
n-t-butoxycarbonylglycine
2-{(tert-butoxycarbonyl)amino}acetic acid
2-(tert-butoxycarbonylamino) acetic acid
boc-glyoh
n-tert.butoxycarbonyl-glycine
t-boc-gly
boc-l-glycine
2-((tert-butoxycarbonyl)amino) acetic acid
boc-glycine oh
t-butoxycarbonylamino acetic acid
t-butoxy carbonylamino-acetic acid
n-(t-butoxycarbonyl)-glycine
n-boc-gly-oh
2-(tert-butoxycarbonylamino)acetic acid
n-t-butoxycarbonyl-glycine
boc gly-oh
n-carbo-tert-butoxyglycine
tert.-butyloxycarbonylglycine
n-tert-butoxy carbonyl-glycine
n-tertiarybutoxycarbonylglycine
n-[(1,1-dimethylethoxy)carbonyl]-glycine
t-boc-glycine
SCHEMBL17906
n-.alpha.-tert-butyloxycarbonylglycine
[(tert-butoxycarbonyl)amino]acetic acid #
DTXSID2063509
Q-200739
J-300132
Z56974835
F9995-1166
boc-gly-oh-15n;n-(tert-butoxycarbonyl)glycine-15n;glycine-15n,n-t-bocderivative;106665-75-2;boc-[15n]gly-oh;486701_aldrich
mfcd00002690
n-alpha-t-butyloxycarbonyl-glycine
CS-W008705
NCGC00334944-01
2-(boc-amino)acetic acid
AS-11190
BCP23287
n-tert-boc-glycine-oh
HY-Y0978
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Protein Targets (1)

Other Measurements

ProteinTaxonomyMeasurementAverageMin (ref.)Avg (ref.)Max (ref.)Bioassay(s)
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023]

Bioassays (3)

Assay IDTitleYearJournalArticle
AID388273Ratio of Vm(app) to Km(app) for rat recombinant peptidylglycine alpha-amidating monooxygenase2008Bioorganic & medicinal chemistry, Dec-01, Volume: 16, Issue:23
Substituted hippurates and hippurate analogs as substrates and inhibitors of peptidylglycine alpha-hydroxylating monooxygenase (PHM).
AID388272Activity of rat recombinant peptidylglycine alpha-amidating monooxygenase assessed as stimulation of oxygen consumption2008Bioorganic & medicinal chemistry, Dec-01, Volume: 16, Issue:23
Substituted hippurates and hippurate analogs as substrates and inhibitors of peptidylglycine alpha-hydroxylating monooxygenase (PHM).
AID388274Ratio of Vm(app) to Km(app) for rat recombinant peptidylglycine alpha-amidating monooxygenase relative to hippuric acid2008Bioorganic & medicinal chemistry, Dec-01, Volume: 16, Issue:23
Substituted hippurates and hippurate analogs as substrates and inhibitors of peptidylglycine alpha-hydroxylating monooxygenase (PHM).
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (8)

TimeframeStudies, This Drug (%)All Drugs %
pre-19901 (12.50)18.7374
1990's1 (12.50)18.2507
2000's5 (62.50)29.6817
2010's1 (12.50)24.3611
2020's0 (0.00)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 42.07

According to the monthly volume, diversity, and competition of internet searches for this compound, as well the volume and growth of publications, there is estimated to be strong demand-to-supply ratio for research on this compound.

MetricThis Compound (vs All)
Research Demand Index42.07 (24.57)
Research Supply Index2.20 (2.92)
Research Growth Index4.90 (4.65)
Search Engine Demand Index55.31 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (42.07)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews0 (0.00%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other8 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]