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3-Chloro-D-alanine dehydrochlorinase
Known as:
3-chloro-D-alanine chloride-lyase (deaminating)
, 3-chloro-D-alanine hydrogen chloride-lyase
, CAHC-lyase
National Institutes of Health
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2 relations
3-chloro-D-alanine dehydrochlorinase activity
Broader (1)
Lyase
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2016
2016
Discovery of 3-Chloro-N-{(S)-[3-(1-ethyl-1H-pyrazol-4-yl)phenyl][(2S)-piperidine-2-yl]methyl}-4-(trifluoromethyl)pyridine-2-carboxamide as a Potent Glycine Transporter 1 Inhibitor.
Shuji Yamamoto
,
Tsuyoshi Shibata
,
+4 authors
H. Kawamoto
Chemical and pharmaceutical bulletin
2016
Corpus ID: 46057617
A novel glycine transporter 1 (GlyT1) inhibitor was designed by the superposition of different chemotypes to enhance its…
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2016
2016
Identification of 1-Methyl-N-(propan-2-yl)-N-({2-[4-(trifluoromethoxy)phenyl]pyridin-4-yl}methyl)-1H-imidazole-4-carboxamide as a Potent and Orally Available Glycine Transporter 1 Inhibitor.
Shuji Yamamoto
,
H. Ohta
,
+5 authors
A. Yasuhara
Chemical and pharmaceutical bulletin
2016
Corpus ID: 21358279
We previously identified 3-chloro-N-{(S)-[3-(1-ethyl-1H-pyrazol-4-yl)phenyl][(2S)-piperidine-2-yl]methyl}-4-(trifluoromethyl…
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2016
2016
Solution thermodynamics and preferential solvation of 3-chloro-N-phenyl-phthalimide in acetone + methanol mixtures
Grecia Angeline del Mar Areiza Aldana
,
Diego Iván Caviedes Rubio
,
+4 authors
N. Carmona
2016
Corpus ID: 54536453
The thermodynamic properties of the 3-chloro-N-phenyl-phthalimide in acetone + methanol cosolvent mixtures were obtained from…
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2014
2014
Isolation of three chemical constituents of Mangifera indica wood extract and their characterization by some spectroscopic techniques
K. Madan
,
R. Tripathi
,
Akanksha Tripathi
,
Ruchi Singh
,
H. Dwivedi
2014
Corpus ID: 944826
Mangifera indica, commonly called Mango or Amra belongs to a family of Anacardiaceae. The plant is used as antiasthamatic…
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2003
2003
Discovery and characterization of a potent and selective non-amidine inhibitor of human factor Xa.
A. Liang
,
D. Light
,
+6 authors
M. Snider
Biochemical Pharmacology
2003
Corpus ID: 24540546
2003
2003
Novel High Energy Intermediate Analogues with Triazasterol-Related Structures as Potential Inhibitors of the Ergosterol Biosynthesis II [1]. Optimization of the Synthesis of 1,6,7,11b-Tetrahydro…
E. Gössnitzer
,
Asbjoern Punkenhofer
2003
Corpus ID: 97970941
Summary. Various routes for an effective synthesis of 1,6,7,11b-tetrahydro-2H-pyrimido[4,3-a]isoquinolin-4-amine and its 9…
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2000
2000
Biologically stable [(18)F]-labeled benzylfluoride derivatives.
Yasuhiro Magata
,
Lixin Lang
,
D. Kiesewetter
,
E. Jagoda
,
M. Channing
,
W. C. Eckelman
Nuclear Medicine and Biology
2000
Corpus ID: 19885375
1997
1997
Aminobenzoic acid compounds as HOCl traps for activated neutrophils.
Z. She
,
D. Mays
,
A. Sagone
,
W. B. Davis
Free Radical Biology & Medicine
1997
Corpus ID: 28831742
1996
1996
Interaction of S 21007 with 5-HT3 receptors. In vitro and in vivo characterization.
P. Delagrange
,
M. Emerit
,
+7 authors
M. Hamon
European Journal of Pharmacology
1996
Corpus ID: 4520443
1988
1988
Deprivation of the mutagenic property of quinoline: inhibition of mutagenic metabolism by fluorine substitution.
Kazuhiko Takahashi
,
Masatsugu Kamiya
,
Yoko Sengoku
,
Kohfuku Kohda
,
Yutaka Kawazoe
Chemical and pharmaceutical bulletin
1988
Corpus ID: 45425978
3-Fluoro-, 2-and 3-chloro-quinolines were deficient in mutagenicity in S. typhimurium TA100, whereas all the other fluoro and…
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