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CHEBI ONTOLOGY - ANNOTATIONS

The Chemical Entities of Biological Interest (ChEBI) ontology is downloaded weekly from EMBL-EBI at http://www.ebi.ac.uk/chebi/. The data is made available under the Creative Commons License (CC BY 3.0, http://creativecommons.org/licenses/by/3.0/). For more information see: Degtyarenko et al. (2008) ChEBI: a database and ontology for chemical entities of biological interest. Nucleic Acids Res. 36, D344–D350.
Term:benserazide
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Accession:CHEBI:64187 term browser browse the term
Definition:A carbohydrazide that results from the formal condensation of the carboxy group of DL-serine with the primary amino group of 4-(hydrazinylmethyl)benzene-1,2,3-triol. An aromatic-L-amino-acid decarboxylase inhibitor (DOPA decarboxylase inhibitor) that does not enter the central nervous system, it is used as its hydrochloride salt as an adjunct to levodopa in the treatment of parkinsonism. By preventing the conversion of levodopa to dopamine in the periphery, it causes an increase in the amount of levodopa reaching the central nervous system and so reduces the required dose. Benserazide has no antiparkinson actions when given alone.
Synonyms:exact_synonym: 2-amino-3-hydroxy-N'-(2,3,4-trihydroxybenzyl)propanehydrazide
 related_synonym: DL-serine 2-(2,3,4-trihydroxybenzyl)hydrazide;   DL-serine 2-[(2,3,4-trihydroxyphenyl)methyl]hydrazide;   Formula=C10H15N3O5;   InChI=1S/C10H15N3O5/c11-6(4-14)10(18)13-12-3-5-1-2-7(15)9(17)8(5)16/h1-2,6,12,14-17H,3-4,11H2,(H,13,18);   InChIKey=BNQDCRGUHNALGH-UHFFFAOYSA-N;   Ro 4-4602;   Ro 44602;   SMILES=NC(CO)C(=O)NNCc1ccc(O)c(O)c1O;   benserazida;   benserazidum
 xref: CAS:322-35-0;   Drug_Central:314;   KEGG:D03082;   LINCS:LSM-5097
 xref_mesh: MESH:D001545
 xref: PMID:12703659;   PMID:22236652;   Patent:BE619015;   Patent:US3178476;   Reaxys:3984490;   Wikipedia:Benserazide
 cyclic_relationship: is_conjugate_base_of CHEBI:64190

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              benserazide 0
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                        hydrogen molecular entity 0
                          hydrides 0
                            inorganic hydride 0
                              pnictogen hydride 0
                                nitrogen hydride 0
                                  azane 0
                                    ammonia 0
                                      organic amino compound 0
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                                          benserazide 0
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