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Structure−Activity Relationships in the Oxidation of Para-Substituted Benzylamine Analogues by Recombinant Human Liver Monoamine Oxidase A<sup>,</sup>

https://doi.org/10.1021/bi990920y
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44/44 checkable references clean · checked 2026-07-23

Every reference with a DOI in the deposited reference list resolved to a known work in Crossref or DataCite at the dated check, and none carried a retraction, withdrawal, or removal notice.

13 without a DOI — not checked. A reference deposited without a DOI is never matched by title or guessed at; it stays outside the checked set, and this line discloses that.

The 44 checked references that resolve
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Biochemistry and genetics of monoamine oxidase
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Spectral and kinetic studies of imine product formation in the oxidation of p-(N,N-dimethylamino)benzylamine analogs by monoamine oxidase B
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Monoamine oxidase B catalysis in low aqueous medium. Direct evidence for an imine product
resolves10.1016/0301-0082(94)90081-7
The functional role of monoamine oxidases A and B in the mammalian central nervous system
resolves10.1073/pnas.85.13.4934
cDNA cloning of human liver monoamine oxidase A and B: molecular basis of differences in enzymatic properties.
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The Covalently‐Bound Flavin of Hepatic Monoamine Oxidase
resolves10.1021/bi00189a011
Structure-Activity Relationships in the Oxidation of Benzylamine Analogs by Bovine Liver Mitochondrial Monoamine Oxidase B
resolves10.1021/bi00232a038
Kinetic mechanism of monoamine oxidase A
resolves10.1021/bi00532a028
Kinetic studies on the catalytic mechanism of liver monoamine oxidase
resolves10.1016/S0021-9258(19)41384-7
Determination of dissociation constants and specific rate constants of enzyme-substrate (or protein-ligand) interactions from rapid reaction kinetic data
resolves10.1016/S0021-9258(17)38856-7
Purification and properties of mitochondrial monoamine oxidase type A from human placenta.
resolves10.1021/bi00060a003
Substrate-specific enhancement of the oxidative half-reaction of monoamine oxidase
resolves10.1021/bi00086a007
Oxidation of tetrahydrostilbazole by monoamine oxidase A demonstrates the effect of alternate pathways in the kinetic mechanism
resolves10.1021/ja00543a052
A mechanism for mitochondrial monoamine oxidase catalyzed amine oxidation
resolves10.1021/ja00727a049
Model reactions and a general mechanism for flavoenzyme-catalyzed dehydrogenations
resolves10.1021/ja00076a017
Mechanistic analysis of the 3-methyllumiflavin-promoted oxidative deamination of benzylamine. A potential model for monoamine oxidase catalysis
resolves10.3109/00498259509061889
Aminium cation radical mechanism proposed for monoamine oxidase B catalysis: are there alternatives?
resolves10.1021/bi960749f
Observation of a Flavin Semiquinone in the Resting State of Monoamine Oxidase B by Electron Paramagnetic Resonance and Electron Nuclear Double Resonance Spectroscopy<sup>,</sup>
resolves10.1021/j100785a001
van der Waals Volumes and Radii
resolves10.1021/bi00232a035
Structure-function studies of substrate oxidation by bovine serum amine oxidase: relationship to cofactor structure and mechanism
resolves10.1021/bi00128a012
Reactions of benzylamines with methylamine dehydrogenase. Evidence for a carbanionic reaction intermediate and reaction mechanism similar to eukaryotic quinoproteins
resolves10.1021/bi00003a015
Mechanistic Studies of Aromatic Amine Dehydrogenase, a Tryptophan Tryptophylquinone Enzyme
resolves10.1074/jbc.272.8.4924
On The Mechanism of D-Amino Acid Oxidase
resolves10.1073/pnas.94.18.9590
On the reaction mechanism of <scp>l</scp> -lactate oxidase: Quantitative structure-activity analysis of the reaction with <i>para</i> -substituted  <scp>l</scp> -mandelates
resolves10.1074/jbc.273.23.14074
Monoamine Oxidase Contains a Redox-active Disulfide
resolves10.1016/S0006-291X(05)80914-3
Catalytically active monoamine oxidase type A from human liver expressed in Saccharomyces cerevisiae contains covalent FAD
resolves10.1016/0006-291X(91)92048-O
Differences in substrate specificities of monoamine oxidase A from human liver and placenta
resolves10.1021/ja01614a053
Reduction of Organic Compounds by Mixed Hydrides. I. Nitriles
resolves10.1016/0097-8485(90)80007-O
A critical comparison of least absolute deviation fitting (robust) and least squares fitting: The importance of error distributions
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The presence of a reducible disulfide bond in milk xanthine oxidase.
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Calculation of substrate dissociation constants from steady-state isotope effects in enzyme-catalyzed reactions
resolves10.1021/bi00683a013
Steady-state analysis of kinetic isotope effects in enzymic reactions
resolves10.1021/ja00134a038
Mechanistic probes of monoamine oxidase B catalysis: Rapid-scan stopped flow and magnetic field independence of the reductive half-reaction
resolves10.1016/S0021-9258(18)91940-X
Human Liver Mitochondrial Monoamine Oxidase
resolves10.1021/bi00838a011
Human liver mitochondrial monoamine oxidase. II. Determinants of substrate and inhibitor specificities
resolves10.1021/ja01018a024
Field and resonance components of substituent effects
resolves10.1021/ja00981a022
Oxidations of Amines. II. Substituent Effects in Chlorine Dioxide Oxidations
resolves10.1021/ja00981a023
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resolves10.1021/j100727a007
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Facile proton-transfer reactions of N,N-dimethylaniline cation radicals
resolves10.1007/978-1-4757-1592-7
The Proton in Chemistry
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Importance of C<sup>4a</sup>-and N<sup>5</sup>-covalent adducts in the flavin oxidation of carbanions
resolves10.1021/jo00050a032
Acidities and homolytic bond dissociation energies (BDEs) of benzyl-type carbon-hydrogen bonds in sterically congested substrates
resolves10.1081/DMR-100101916
BENZYLAMINE ANALOG BINDING STUDIES AS PROBES OF THE SUBSTRATE SITES OF MONOAMINE OXIDASES A AND B*
The 13 references without a DOI — listed, not checked
no DOI — not checkedbi990920yb00007/bi990920yb00007_1
no DOI — not checkedin Advances in Electron Transfer Chemistry
no DOI — not checkedTetrahedron 53, 5027−5046
no DOI — not checkedK. J.
no DOI — not checkedExploring QSAR. Fundamentals and Applications in Chemistry and Biology
no DOI — not checkedbi990920yb00024/bi990920yb00024_1
no DOI — not checkedExploring QSAR. Hydrophobic, Electronic, and Steric Constants
no DOI — not checkedbi990920yb00036/bi990920yb00036_1
no DOI — not checkedbi990920yb00044/bi990920yb00044_1
no DOI — not checkedbi990920yb00046/bi990920yb00046_1
no DOI — not checkedin Progress in Bioorganic Chemistry
no DOI — not checkedin Comprehensive Carbanion Chemistry
no DOI — not checkedmonoamine oxidase
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