Difference between revisions of "CPD-173"

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(Created page with "Category:Reaction == Reaction [http://metacyc.org/META/NEW-IMAGE?object=RIBONUCLEOSIDE-DIP-REDUCTI-RXN RIBONUCLEOSIDE-DIP-REDUCTI-RXN] == * direction: ** LEFT-TO-RIGHT * c...")
(Created page with "Category:Metabolite == Metabolite [http://metacyc.org/META/NEW-IMAGE?object=CPD-173 CPD-173] == * smiles: ** C(C1(C=CC=CC=1O))O * inchi key: ** InChIKey=CQRYARSYNCAZFO-UHF...")
 
(One intermediate revision by the same user not shown)
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[[Category:Reaction]]
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[[Category:Metabolite]]
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== Reaction [http://metacyc.org/META/NEW-IMAGE?object=RIBONUCLEOSIDE-DIP-REDUCTI-RXN RIBONUCLEOSIDE-DIP-REDUCTI-RXN] ==
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== Metabolite [http://metacyc.org/META/NEW-IMAGE?object=CPD-173 CPD-173] ==
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* direction:
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* smiles:
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** LEFT-TO-RIGHT
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** C(C1(C=CC=CC=1O))O
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* inchi key:
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** InChIKey=CQRYARSYNCAZFO-UHFFFAOYSA-N
 
* common name:
 
* common name:
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** ribonucleoside-diphosphate reductase activity, thioredoxin disulfide as acceptor
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** salicyl alcohol
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** EsV-1-128
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* molecular weight:
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** EsV-1-180
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** 124.139   
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** Ribonucleoside-diphosphate reductase small chain
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* ec number:
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** [http://enzyme.expasy.org/EC/1.17.4.1 EC-1.17.4.1]
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* Synonym(s):
 
* Synonym(s):
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** saligenin
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** 2-hydroxybenzyl alcohol
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** o-hydroxybenzyl alcohol
  
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== Reaction Formula ==
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== Reaction(s) known to consume the compound ==
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* With identifiers:
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== Reaction(s) known to produce the compound ==
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** 1 [[Red-Thioredoxin]][c] '''+''' 1 [[Ribonucleoside-Diphosphates]][c] '''=>''' 1 [[Ox-Thioredoxin]][c] '''+''' 1 [[WATER]][c] '''+''' 1 [[Deoxy-Ribonucleoside-Diphosphates]][c]
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* [[RXN-12252]]
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* With common name(s):
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== Reaction(s) of unknown directionality ==
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** 1 a reduced thioredoxin[c] '''+''' 1 a ribonucleoside diphosphate[c] '''=>''' 1 an oxidized thioredoxin[c] '''+''' 1 H2O[c] '''+''' 1 a 2'-deoxyribonucleoside 5'-diphosphate[c]
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== Genes associated with this reaction  ==
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Genes have been associated with this reaction based on different elements listed below.
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* [[Ec-06_005120]]
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** ESILICULOSUS_GENOME
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***EC-NUMBER
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* [[Ec-21_002920]]
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** ESILICULOSUS_GENOME
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***GO-TERM
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* [[Ec-11_002170]]
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** ESILICULOSUS_GENOME
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***GO-TERM
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* [[Ec-19_000440]]
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** ESILICULOSUS_GENOME
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***EC-NUMBER
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* [[Ec-06_005570]]
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** ESILICULOSUS_GENOME
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***EC-NUMBER
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== Pathways  ==
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== Reconstruction information  ==
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* Category: [[annotation]]
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** Source: [[annotation-esiliculosus_genome]]
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*** Tool: [[pathwaytools]]
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== External links  ==
 
== External links  ==
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* RHEA:
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* CAS : 90-01-7
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** [http://www.ebi.ac.uk/rhea/reaction.xhtml?id=23252 23252]
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* PUBCHEM:
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* LIGAND-RXN:
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** [http://pubchem.ncbi.nlm.nih.gov/summary/summary.cgi?cid=5146 5146]
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** [http://www.genome.jp/dbget-bin/www_bget?R04294 R04294]
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* HMDB : HMDB59709
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* UNIPROT:
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* LIGAND-CPD:
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** [http://www.uniprot.org/uniprot/P89462 P89462]
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** [http://www.genome.jp/dbget-bin/www_bget?C02323 C02323]
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** [http://www.uniprot.org/uniprot/Q7M0K8 Q7M0K8]
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* CHEMSPIDER:
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** [http://www.uniprot.org/uniprot/Q91YM8 Q91YM8]
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** [http://www.chemspider.com/Chemical-Structure.4962.html 4962]
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** [http://www.uniprot.org/uniprot/P09938 P09938]
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* CHEBI:
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** [http://www.uniprot.org/uniprot/Q8IL94 Q8IL94]
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** [http://www.ebi.ac.uk/chebi/searchId.do?chebiId=16464 16464]
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** [http://www.uniprot.org/uniprot/P32984 P32984]
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* METABOLIGHTS : MTBLC16464
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** [http://www.uniprot.org/uniprot/P50647 P50647]
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{{#set: smiles=C(C1(C=CC=CC=1O))O}}
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** [http://www.uniprot.org/uniprot/P50650 P50650]
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{{#set: inchi key=InChIKey=CQRYARSYNCAZFO-UHFFFAOYSA-N}}
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** [http://www.uniprot.org/uniprot/P50620 P50620]
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{{#set: common name=salicyl alcohol}}
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** [http://www.uniprot.org/uniprot/O83972 O83972]
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{{#set: molecular weight=124.139    }}
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** [http://www.uniprot.org/uniprot/P43755 P43755]
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{{#set: common name=saligenin|2-hydroxybenzyl alcohol|o-hydroxybenzyl alcohol}}
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** [http://www.uniprot.org/uniprot/Q9PJ87 Q9PJ87]
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{{#set: produced by=RXN-12252}}
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** [http://www.uniprot.org/uniprot/P39452 P39452]
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** [http://www.uniprot.org/uniprot/O66503 O66503]
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** [http://www.uniprot.org/uniprot/Q9JU45 Q9JU45]
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** [http://www.uniprot.org/uniprot/P47473 P47473]
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** [http://www.uniprot.org/uniprot/P37146 P37146]
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** [http://www.uniprot.org/uniprot/O26748 O26748]
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** [http://www.uniprot.org/uniprot/O28609 O28609]
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** [http://www.uniprot.org/uniprot/Q9PIR3 Q9PIR3]
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** [http://www.uniprot.org/uniprot/Q9JU43 Q9JU43]
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** [http://www.uniprot.org/uniprot/P55982 P55982]
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** [http://www.uniprot.org/uniprot/P03190 P03190]
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** [http://www.uniprot.org/uniprot/P00452 P00452]
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** [http://www.uniprot.org/uniprot/P69924 P69924]
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** [http://www.uniprot.org/uniprot/P07201 P07201]
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** [http://www.uniprot.org/uniprot/P26713 P26713]
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** [http://www.uniprot.org/uniprot/P11158 P11158]
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** [http://www.uniprot.org/uniprot/P11157 P11157]
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** [http://www.uniprot.org/uniprot/P23921 P23921]
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** [http://www.uniprot.org/uniprot/P31350 P31350]
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** [http://www.uniprot.org/uniprot/Q60561 Q60561]
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** [http://www.uniprot.org/uniprot/Q03604 Q03604]
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** [http://www.uniprot.org/uniprot/P37426 P37426]
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** [http://www.uniprot.org/uniprot/P17424 P17424]
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** [http://www.uniprot.org/uniprot/P36602 P36602]
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** [http://www.uniprot.org/uniprot/P36603 P36603]
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** [http://www.uniprot.org/uniprot/P50643 P50643]
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** [http://www.uniprot.org/uniprot/P50645 P50645]
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** [http://www.uniprot.org/uniprot/Q66662 Q66662]
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** [http://www.uniprot.org/uniprot/Q66663 Q66663]
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** [http://www.uniprot.org/uniprot/P49723 P49723]
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** [http://www.uniprot.org/uniprot/P50651 P50651]
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** [http://www.uniprot.org/uniprot/P78027 P78027]
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** [http://www.uniprot.org/uniprot/P74240 P74240]
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** [http://www.uniprot.org/uniprot/O36410 O36410]
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** [http://www.uniprot.org/uniprot/O36411 O36411]
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** [http://www.uniprot.org/uniprot/P49730 P49730]
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** [http://www.uniprot.org/uniprot/Q89941 Q89941]
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** [http://www.uniprot.org/uniprot/Q98526 Q98526]
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** [http://www.uniprot.org/uniprot/O41111 O41111]
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** [http://www.uniprot.org/uniprot/Q9YMK7 Q9YMK7]
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** [http://www.uniprot.org/uniprot/Q9YMI1 Q9YMI1]
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** [http://www.uniprot.org/uniprot/Q9YMI0 Q9YMI0]
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** [http://www.uniprot.org/uniprot/O57175 O57175]
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** [http://www.uniprot.org/uniprot/O39262 O39262]
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** [http://www.uniprot.org/uniprot/O39263 O39263]
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** [http://www.uniprot.org/uniprot/Q9YTK7 Q9YTK7]
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** [http://www.uniprot.org/uniprot/Q9YTK6 Q9YTK6]
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** [http://www.uniprot.org/uniprot/Q9UW15 Q9UW15]
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** [http://www.uniprot.org/uniprot/Q9SJ20 Q9SJ20]
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** [http://www.uniprot.org/uniprot/P03175 P03175]
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** [http://www.uniprot.org/uniprot/P09247 P09247]
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** [http://www.uniprot.org/uniprot/P09248 P09248]
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** [http://www.uniprot.org/uniprot/P28847 P28847]
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** [http://www.uniprot.org/uniprot/P28846 P28846]
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** [http://www.uniprot.org/uniprot/P69520 P69520]
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** [http://www.uniprot.org/uniprot/Q01319 Q01319]
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** [http://www.uniprot.org/uniprot/P10224 P10224]
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** [http://www.uniprot.org/uniprot/P16782 P16782]
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** [http://www.uniprot.org/uniprot/P20503 P20503]
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** [http://www.uniprot.org/uniprot/P26685 P26685]
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** [http://www.uniprot.org/uniprot/P12848 P12848]
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{{#set: direction=LEFT-TO-RIGHT}}
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{{#set: common name=ribonucleoside-diphosphate reductase activity, thioredoxin disulfide as acceptor}}
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{{#set: common name=EsV-1-128}}
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{{#set: common name=EsV-1-180}}
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{{#set: common name=Ribonucleoside-diphosphate reductase small chain}}
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{{#set: ec number=EC-1.17.4.1}}
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{{#set: gene associated=Ec-06_005120|Ec-21_002920|Ec-11_002170|Ec-19_000440|Ec-06_005570}}
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{{#set: in pathway=}}
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{{#set: reconstruction category=annotation}}
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{{#set: reconstruction source=annotation-esiliculosus_genome}}
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{{#set: reconstruction tool=pathwaytools}}
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Latest revision as of 20:53, 21 March 2018

Metabolite CPD-173

  • smiles:
    • C(C1(C=CC=CC=1O))O
  • inchi key:
    • InChIKey=CQRYARSYNCAZFO-UHFFFAOYSA-N
  • common name:
    • salicyl alcohol
  • molecular weight:
    • 124.139
  • Synonym(s):
    • saligenin
    • 2-hydroxybenzyl alcohol
    • o-hydroxybenzyl alcohol

Reaction(s) known to consume the compound

Reaction(s) known to produce the compound

Reaction(s) of unknown directionality

External links

  • CAS : 90-01-7
  • PUBCHEM:
  • HMDB : HMDB59709
  • LIGAND-CPD:
  • CHEMSPIDER:
  • CHEBI:
  • METABOLIGHTS : MTBLC16464




Retrieved from "http://gem-aureme.irisa.fr/ectogem/index.php?title=CPD-173&oldid=30059"