<?xml version="1.0" encoding="UTF-8"?>
<compound>
  <version>1.0</version>
  <creation_date>2016-05-19 01:59:31 UTC</creation_date>
  <update_date>2026-04-05 11:42:28 UTC</update_date>
  <accession/>
  <common_name>CURDLAN</common_name>
  <class>SmallMolecule</class>
  <description>CURDLAN is an organic compound with the chemical formula C6H12O6 and an average molecular weight of 180.16 g/mol. CURDLAN belongs to the carbohydrates and carbohydrate conjugates, a subclass of organooxygen compounds within the organic compounds.

In industrial applications, this compound serves as a thickening agent and is used as a processing aid not otherwise specified. CURDLAN is found in or released from 25 recorded sources across various sectors. Within food, food processing and cookware, it is associated with the preparation of malt, fermentation processes for beer, molasses and treatment of molasses, agglomerated sugar products, and cellar tools, among six other sources. In the category of electrical and electronic equipment, it is found in magnets, antennas, communication cables or conductors, line transmission systems, and electric switches, along with two additional sources. Furthermore, it is released from household cleaning and consumer products, including soap dispensers, cigar cigarettes, non electric simulated smoking devices, pipe accessories, other smoking requisites, and two other sources.</description>
  <categories/>
  <types/>
  <synonyms>
    <synonym>beta-D-(1-&gt;3)-Glucan</synonym>
    <synonym>beta-D-Glucopyranose</synonym>
    <synonym>Beta-D-Glucose</synonym>
    <synonym>Glucose oxidase</synonym>
  </synonyms>
  <chemical_formula>C6H12O6</chemical_formula>
  <average_molecular_weight>180.1559</average_molecular_weight>
  <monisotopic_moleculate_weight>180.063388116</monisotopic_moleculate_weight>
  <iupac_name>(2R,3R,4S,5S,6R)-6-(hydroxymethyl)oxane-2,3,4,5-tetrol</iupac_name>
  <traditional_iupac>glucoside</traditional_iupac>
  <cas_registry_number>54724-00-4</cas_registry_number>
  <smiles>OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1O</smiles>
  <inchi>InChI=1S/C6H12O6/c7-1-2-3(8)4(9)5(10)6(11)12-2/h2-11H,1H2/t2-,3-,4+,5-,6-/m1/s1</inchi>
  <inchikey>WQZGKKKJIJFFOK-VFUOTHLCSA-N</inchikey>
  <taxonomy>
    <kingdom>Organic compounds</kingdom>
    <super_class>Organic oxygen compounds</super_class>
    <class>Organooxygen compounds</class>
    <sub_class>Carbohydrates and carbohydrate conjugates</sub_class>
    <direct_parent>Hexoses</direct_parent>
    <alternate_parents>
      <alternative_parent>Hemiacetals</alternative_parent>
      <alternative_parent>Hydrocarbon derivatives</alternative_parent>
      <alternative_parent>Oxacyclic compounds</alternative_parent>
      <alternative_parent>Oxanes</alternative_parent>
      <alternative_parent>Polyols</alternative_parent>
      <alternative_parent>Primary alcohols</alternative_parent>
      <alternative_parent>Secondary alcohols</alternative_parent>
    </alternate_parents>
    <substituents>
      <substituent>Alcohol</substituent>
      <substituent>Aliphatic heteromonocyclic compound</substituent>
      <substituent>Hemiacetal</substituent>
      <substituent>Hexose monosaccharide</substituent>
      <substituent>Hydrocarbon derivative</substituent>
      <substituent>Organoheterocyclic compound</substituent>
      <substituent>Oxacycle</substituent>
      <substituent>Oxane</substituent>
      <substituent>Polyol</substituent>
      <substituent>Primary alcohol</substituent>
      <substituent>Secondary alcohol</substituent>
    </substituents>
    <molecular_framework>Aliphatic heteromonocyclic compounds</molecular_framework>
    <descriptors>
      <descriptor>D-glucopyranose</descriptor>
    </descriptors>
  </taxonomy>
  <status>Detected and Not Quantified</status>
  <origin/>
  <cellular_locations/>
  <biofluid_locations/>
  <tissue_locations/>
  <pathways>
    <pathway>
      <name>Glycolysis</name>
      <smpdb_id>SMP0000040</smpdb_id>
      <kegg_map_id/>
    </pathway>
    <pathway>
      <name>Gluconeogenesis</name>
      <smpdb_id>SMP0000128</smpdb_id>
      <kegg_map_id/>
    </pathway>
    <pathway>
      <name>Trehalose Degradation</name>
      <smpdb_id>SMP0000467</smpdb_id>
      <kegg_map_id/>
    </pathway>
    <pathway>
      <name>Glycogen Storage Disease Type 1A (GSD1A) or Von Gierke Disease</name>
      <smpdb_id>SMP0000374</smpdb_id>
      <kegg_map_id/>
    </pathway>
    <pathway>
      <name>Glycogenosis, Type VII. Tarui Disease</name>
      <smpdb_id>SMP0000531</smpdb_id>
      <kegg_map_id/>
    </pathway>
    <pathway>
      <name>Phosphoenolpyruvate Carboxykinase Deficiency 1 (PEPCK1)</name>
      <smpdb_id>SMP0000560</smpdb_id>
      <kegg_map_id/>
    </pathway>
    <pathway>
      <name>Fructose-1,6-diphosphatase Deficiency</name>
      <smpdb_id>SMP0000562</smpdb_id>
      <kegg_map_id/>
    </pathway>
    <pathway>
      <name>Triosephosphate Isomerase Deficiency</name>
      <smpdb_id>SMP0000563</smpdb_id>
      <kegg_map_id/>
    </pathway>
    <pathway>
      <name>Fanconi-Bickel Syndrome</name>
      <smpdb_id>SMP0000572</smpdb_id>
      <kegg_map_id/>
    </pathway>
    <pathway>
      <name>Glycogenosis, Type IB</name>
      <smpdb_id>SMP0000573</smpdb_id>
      <kegg_map_id/>
    </pathway>
    <pathway>
      <name>Glycogenosis, Type IC</name>
      <smpdb_id>SMP0000574</smpdb_id>
      <kegg_map_id/>
    </pathway>
    <pathway>
      <name>Glycogenosis, Type IA. Von Gierke Disease</name>
      <smpdb_id>SMP0000581</smpdb_id>
      <kegg_map_id/>
    </pathway>
    <pathway>
      <name>Glycogenosis, Type VII. Tarui Disease</name>
      <smpdb_id>SMP0125707</smpdb_id>
      <kegg_map_id/>
    </pathway>
    <pathway>
      <name>Fanconi-Bickel Syndrome</name>
      <smpdb_id>SMP0125708</smpdb_id>
      <kegg_map_id/>
    </pathway>
    <pathway>
      <name>Glycogen Storage Disease Type 1A (GSD1A) or Von Gierke Disease</name>
      <smpdb_id>SMP0125790</smpdb_id>
      <kegg_map_id/>
    </pathway>
    <pathway>
      <name>Phosphoenolpyruvate Carboxykinase Deficiency 1 (PEPCK1)</name>
      <smpdb_id>SMP0125791</smpdb_id>
      <kegg_map_id/>
    </pathway>
    <pathway>
      <name>Fructose-1,6-diphosphatase Deficiency</name>
      <smpdb_id>SMP0125792</smpdb_id>
      <kegg_map_id/>
    </pathway>
    <pathway>
      <name>Triosephosphate Isomerase Deficiency</name>
      <smpdb_id>SMP0125793</smpdb_id>
      <kegg_map_id/>
    </pathway>
    <pathway>
      <name>Glycogenosis, Type IB</name>
      <smpdb_id>SMP0125794</smpdb_id>
      <kegg_map_id/>
    </pathway>
    <pathway>
      <name>Glycogenosis, Type IC</name>
      <smpdb_id>SMP0125795</smpdb_id>
      <kegg_map_id/>
    </pathway>
    <pathway>
      <name>Glycogenosis, Type IA. Von Gierke Disease</name>
      <smpdb_id>SMP0125796</smpdb_id>
      <kegg_map_id/>
    </pathway>
  </pathways>
  <state/>
  <appearance/>
  <experimental_properties/>
  <predicted_properties>
    <property>
      <kind>logp</kind>
      <value>-2.57</value>
      <source>ALOGPS</source>
    </property>
    <property>
      <kind>logs</kind>
      <value>0.64</value>
      <source>ALOGPS</source>
    </property>
    <property>
      <kind>solubility</kind>
      <value>7.82e+02 g/l</value>
      <source>ALOGPS</source>
    </property>
    <property>
      <kind>logp</kind>
      <value>-2.9</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>pka_strongest_acidic</kind>
      <value>11.3</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>pka_strongest_basic</kind>
      <value>-3</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>iupac</kind>
      <value>(2R,3R,4S,5S,6R)-6-(hydroxymethyl)oxane-2,3,4,5-tetrol</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>average_mass</kind>
      <value>180.1559</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>mono_mass</kind>
      <value>180.063388116</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>smiles</kind>
      <value>OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1O</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>formula</kind>
      <value>C6H12O6</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>inchi</kind>
      <value>InChI=1S/C6H12O6/c7-1-2-3(8)4(9)5(10)6(11)12-2/h2-11H,1H2/t2-,3-,4+,5-,6-/m1/s1</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>inchikey</kind>
      <value>WQZGKKKJIJFFOK-VFUOTHLCSA-N</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>polar_surface_area</kind>
      <value>110.38</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>refractivity</kind>
      <value>35.92</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>polarizability</kind>
      <value>16.35</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>rotatable_bond_count</kind>
      <value>1</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>acceptor_count</kind>
      <value>6</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>donor_count</kind>
      <value>5</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>physiological_charge</kind>
      <value>0</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>formal_charge</kind>
      <value>0</value>
      <source>ChemAxon</source>
    </property>
  </predicted_properties>
  <route_of_exposure/>
  <mechanism_of_toxicity/>
  <metabolism/>
  <toxicity/>
  <lethaldose/>
  <carcinogenicity/>
  <use_source/>
  <min_risk_level/>
  <health_effects>#&lt;HealthEffect::ActiveRecord_Associations_CollectionProxy:0x00007f722447eb20&gt;</health_effects>
  <symptoms/>
  <treatment/>
  <drugbank_id/>
  <hmdb_id/>
  <pubchem_compound_id>64689</pubchem_compound_id>
  <chembl_id/>
  <chemspider_id/>
  <kegg_id/>
  <uniprot_id/>
  <omim_id/>
  <chebi_id/>
  <biocyc_id/>
  <ctd_id/>
  <stitch_id/>
  <actor_id/>
  <pdb_id/>
  <wikipidia/>
  <general_references/>
  <targets>
    <target>
      <target_id/>
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  </targets>
</compound>
