<?xml version="1.0" encoding="UTF-8"?>
<compound>
  <version>1.0</version>
  <creation_date>2026-03-31 20:50:17 UTC</creation_date>
  <update_date>2026-05-20 19:28:18 UTC</update_date>
  <accession/>
  <common_name>Chrysomycin B</common_name>
  <class>SmallMolecule</class>
  <description>Chrysomycin B is an organic compound with the chemical formula C27H28O9. Chrysomycin B belongs to the carbohydrates and carbohydrate conjugates, a subclass of organooxygen compounds within the organic compounds. It is found in or released from one recorded source: healthcare, pharmaceuticals &amp; veterinary products (antibiotics). Recorded exposure routes for this compound include oral and inhalation.</description>
  <categories/>
  <types/>
  <synonyms>
    <synonym>1,5-Anhydro-6-deoxy-1-(1-hydroxy-10,12-dimethoxy-8-methyl-6-oxo-6H-dibenzo[c,h]chromen-4-yl)-3-C-methylhexitol</synonym>
    <synonym>1-hydroxy-10,12-dimethoxy-8-methyl-4-(3,4,5-trihydroxy-4,6-dimethyloxan-2-yl)naphtho[1,2-c]isochromen-6-one</synonym>
    <synonym>4-(6-deoxy-3-C-methyl-?-gulopyranosyl)-1-hydroxy-10,12-dimethoxy-8-methyl-6H-benzo[d]naphtho[1,2-b]pyran-6-one</synonym>
    <synonym>4-?(6-?DEOXY-?3-?C-?METHYL-?BETA-?GULOPYRANOSYL)-?1-?HYDROXY-?10,?12-?DIMETHOXY-?8-?METHYL-?6H-?BENZO[D]PHTHO[1,?2-?B]PYRAN-?6-?ONE</synonym>
    <synonym>6H-Benzo(d)naphtho(1,2-b)pyran-6-one, 4-(6-deoxy-3-C-methyl-beta-gulopyranosyl)-1-hydroxy-10,12-dimethoxy-8-methyl-</synonym>
    <synonym>6H-Benzo[d]naphtho[1,2-b]pyran-6-one, 4-(6-deoxy-3-C-methyl-.beta.-D-gulopyranosyl)-1-hydroxy-10,12-dimethoxy-8-methyl-</synonym>
    <synonym>Albacarcin M</synonym>
    <synonym>Chrysomycin B</synonym>
    <synonym>Hexitol, 1,5-anhydro-6-deoxy-1-C-(1-hydroxy-10,12-dimethoxy-8-methyl-6-oxo-6H-benzo[d]naphtho[1,2-b]pyran-4-yl)-3-C-methyl-</synonym>
    <synonym>VIRENOMYCIN</synonym>
    <synonym>VIRENOMYCIN M</synonym>
  </synonyms>
  <chemical_formula>C27H28O9</chemical_formula>
  <average_molecular_weight/>
  <monisotopic_moleculate_weight>496.173332</monisotopic_moleculate_weight>
  <iupac_name/>
  <traditional_iupac/>
  <cas_registry_number>83852-56-6;92934-54-8</cas_registry_number>
  <smiles/>
  <inchi>InChI=1S/C27H28O9/c1-11-8-15-19(17(9-11)33-4)14-10-18(34-5)21-16(28)7-6-13(20(21)22(14)36-26(15)31)23-25(30)27(3,32)24(29)12(2)35-23/h6-10,12,23-25,28-30,32H,1-5H3</inchi>
  <inchikey>BJPYMDSMDBCKEP-UHFFFAOYSA-N</inchikey>
  <taxonomy>
    <kingdom/>
    <super_class/>
    <class/>
    <sub_class/>
    <direct_parent/>
    <alternate_parents/>
    <substituents/>
    <molecular_framework/>
    <descriptors/>
  </taxonomy>
  <status>Detected and Not Quantified</status>
  <origin/>
  <cellular_locations/>
  <biofluid_locations/>
  <tissue_locations/>
  <pathways/>
  <state/>
  <appearance/>
  <experimental_properties/>
  <predicted_properties>
    <property>
      <kind>mono_mass</kind>
      <value>496.173332</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>formula</kind>
      <value>C27H28O9</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>inchi</kind>
      <value>InChI=1S/C27H28O9/c1-11-8-15-19(17(9-11)33-4)14-10-18(34-5)21-16(28)7-6-13(20(21)22(14)36-26(15)31)23-25(30)27(3,32)24(29)12(2)35-23/h6-10,12,23-25,28-30,32H,1-5H3</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>inchikey</kind>
      <value>BJPYMDSMDBCKEP-UHFFFAOYSA-N</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:0x00007f7282b16b00&gt;</health_effects>
  <symptoms/>
  <treatment/>
  <drugbank_id/>
  <hmdb_id/>
  <pubchem_compound_id>174343</pubchem_compound_id>
  <chembl_id/>
  <chemspider_id>152079</chemspider_id>
  <kegg_id/>
  <uniprot_id/>
  <omim_id/>
  <chebi_id/>
  <biocyc_id/>
  <ctd_id/>
  <stitch_id/>
  <actor_id/>
  <pdb_id/>
  <wikipidia/>
  <general_references/>
  <targets>
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</compound>
