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Details

Stereochemistry ACHIRAL
Molecular Formula C3H5NO3
Molecular Weight 103.0767
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of FORMYLGLYCINE

SMILES

OC(=O)CNC=O

InChI

InChIKey=UGJBHEZMOKVTIM-UHFFFAOYSA-N
InChI=1S/C3H5NO3/c5-2-4-1-3(6)7/h2H,1H2,(H,4,5)(H,6,7)

HIDE SMILES / InChI

Molecular Formula C3H5NO3
Molecular Weight 103.0767
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Recent N-atom containing compounds from indo-pacific invertebrates.
2010-11-10
Computational exploration of the mechanism of alcohol oxidation by dioxygen activated with biquinolyl-containing cu complexes.
2010-04-05
Sulfatase activities towards the regulation of cell metabolism and signaling in mammals.
2010-03
Efficient, chemoselective synthesis of immunomicelles using single-domain antibodies with a C-terminal thioester.
2009-07-20
Molecular basis of multiple sulfatase deficiency, mucolipidosis II/III and Niemann-Pick C1 disease - Lysosomal storage disorders caused by defects of non-lysosomal proteins.
2009-04
Characterization of the arylsulfatase I (ARSI) gene preferentially expressed in the human retinal pigment epithelium cell line ARPE-19.
2009
A new member of the alkaline phosphatase superfamily with a formylglycine nucleophile: structural and kinetic characterisation of a phosphonate monoester hydrolase/phosphodiesterase from Rhizobium leguminosarum.
2008-12-05
Sulfotransferases, sulfatases and formylglycine-generating enzymes: a sulfation fascination.
2008-10
New aldehyde tag sequences identified by screening formylglycine generating enzymes in vitro and in vivo.
2008-09-17
Function and structure of a prokaryotic formylglycine-generating enzyme.
2008-07-18
In vitro characterization of AtsB, a radical SAM formylglycine-generating enzyme that contains three [4Fe-4S] clusters.
2008-07-15
The non-catalytic N-terminal extension of formylglycine-generating enzyme is required for its biological activity and retention in the endoplasmic reticulum.
2008-04-25
ERp44 mediates a thiol-independent retention of formylglycine-generating enzyme in the endoplasmic reticulum.
2008-03-07
Paralog of the formylglycine-generating enzyme--retention in the endoplasmic reticulum by canonical and noncanonical signals.
2008-03
Molecular analysis of SUMF1 mutations: stability and residual activity of mutant formylglycine-generating enzyme determine disease severity in multiple sulfatase deficiency.
2008-01
Generation of quinoneimine intermediates in the bioactivation of 3-(N-phenylamino)alanine (PAA) by human liver microsomes: a potential link between eosinophilia-myalgia syndrome and toxic oil syndrome.
2007-10
Formamide as the main building block in the origin of nucleic acids.
2007-08-16
Human sulfatases: a structural perspective to catalysis.
2007-08
Probing the oxygen-binding site of the human formylglycine-generating enzyme using halide ions.
2007-05
SUMF1 enhances sulfatase activities in vivo in five sulfatase deficiencies.
2007-04-15
Ethanol decreases rat hepatic arylsulfatase A activity levels.
2006-11
Electron transfer in amino acid.nucleic acid base complexes: EPR, ENDOR, and DFT study of X-irradiated N-formylglycine.cytosine complex crystals.
2006-07-20
Alkaline Phosphatases : Structure, substrate specificity and functional relatedness to other members of a large superfamily of enzymes.
2006-06
Diversity in domain architectures of Ser/Thr kinases and their homologues in prokaryotes.
2005-09-19
De novo calcium/sulfur SAD phasing of the human formylglycine-generating enzyme using in-house data.
2005-08
Sulphatase activities are regulated by the interaction of sulphatase-modifying factor 1 with SUMF2.
2005-07
Molecular basis for multiple sulfatase deficiency and mechanism for formylglycine generation of the human formylglycine-generating enzyme.
2005-05-20
Three-dimensional structures of sulfatases.
2005
Overexpression of inactive arylsulphatase mutants and in vitro activation by light-dependent oxidation with vanadate.
2004-09-01
Crystal structure of a covalent intermediate of endogenous human arylsulfatase A.
2003-08-01
Posttranslational modification of serine to formylglycine in bacterial sulfatases. Recognition of the modification motif by the iron-sulfur protein AtsB.
2003-01-24
Identification of formylglycine in sulfatases by matrix-assisted laser desorption/ionization time-of-flight mass spectrometry.
2003-01
Estrone 3-sulfate mimics, inhibitors of estrone sulfatase activity: homology model construction and docking studies.
2002-12-17
Optosensing properties of fac-Re(CO)(3)(dpknph)Cl (dpknph=di-2-pyridyl ketone p-nitrophenyl hydrazone) toward chemotactic N-formylamino acids.
2002-04-08
Characterization of posttranslational formylglycine formation by luminal components of the endoplasmic reticulum.
2001-12-14
Conserved core structure and active site residues in alkaline phosphatase superfamily enzymes.
2001-12-01
Heparan N-sulfatase: cysteine 70 plays a role in the enzyme catalysis and processing.
2001-09-21
1.3 A structure of arylsulfatase from Pseudomonas aeruginosa establishes the catalytic mechanism of sulfate ester cleavage in the sulfatase family.
2001-06
Crystal structure of an enzyme-substrate complex provides insight into the interaction between human arylsulfatase A and its substrates during catalysis.
2001-01-12
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:34:01 GMT 2025
Edited
by admin
on Mon Mar 31 18:34:01 GMT 2025
Record UNII
11F24CG16M
Record Status Validated (UNII)
Record Version
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Name Type Language
NSC-15826
Preferred Name English
FORMYLGLYCINE
Systematic Name English
FORMYLGLYCIN
Systematic Name English
N-FORMYLGLYCINE
Systematic Name English
GLYCINE, N-FORMYL-
Systematic Name English
(FORMYLAMINO)ACETIC ACID
Systematic Name English
Code System Code Type Description
CHEBI
21717
Created by admin on Mon Mar 31 18:34:01 GMT 2025 , Edited by admin on Mon Mar 31 18:34:01 GMT 2025
PRIMARY
ECHA (EC/EINECS)
219-649-8
Created by admin on Mon Mar 31 18:34:01 GMT 2025 , Edited by admin on Mon Mar 31 18:34:01 GMT 2025
PRIMARY
NSC
15826
Created by admin on Mon Mar 31 18:34:01 GMT 2025 , Edited by admin on Mon Mar 31 18:34:01 GMT 2025
PRIMARY
PUBCHEM
75606
Created by admin on Mon Mar 31 18:34:01 GMT 2025 , Edited by admin on Mon Mar 31 18:34:01 GMT 2025
PRIMARY
FDA UNII
11F24CG16M
Created by admin on Mon Mar 31 18:34:01 GMT 2025 , Edited by admin on Mon Mar 31 18:34:01 GMT 2025
PRIMARY
CAS
2491-15-8
Created by admin on Mon Mar 31 18:34:01 GMT 2025 , Edited by admin on Mon Mar 31 18:34:01 GMT 2025
PRIMARY
EPA CompTox
DTXSID10179615
Created by admin on Mon Mar 31 18:34:01 GMT 2025 , Edited by admin on Mon Mar 31 18:34:01 GMT 2025
PRIMARY