Isocycloheterophyllin

Common Name

Isocycloheterophyllin Description

Isocycloheterophyllin is found in fruits. Isocycloheterophyllin is a constituent of wood of Artocarpus heterophyllus (jackfruit).Isocycloheterophyllin belongs to the family of Flavonols. These are compounds that has the 3-hydroxyflavone backbone. Structure

MOLSDFPDBSMILESInChI

Structure for HMDB29471 (Isocycloheterophyllin)

Synonyms

Not Available Chemical Formlia

C30H30O7 Average Molecliar Weight

502.555 Monoisotopic Molecliar Weight

502.199153314 IUPAC Name

11,20,21-trihydroxy-7,7-dimethyl-10-(3-methylbut-2-en-1-yl)-16-(propan-2-ylidene)-2,8,17-trioxapentacyclo[12.9.0.0³,¹².0⁴,⁹.0¹⁸,²³]tricosa-1(14),3(12),4(9),5,10,18(23),19,21-octaen-13-one Traditional Name

11,20,21-trihydroxy-7,7-dimethyl-10-(3-methylbut-2-en-1-yl)-16-(propan-2-ylidene)-2,8,17-trioxapentacyclo[12.9.0.0³,¹².0⁴,⁹.0¹⁸,²³]tricosa-1(14),3(12),4(9),5,10,18(23),19,21-octaen-13-one CAS Registry Number

49794-94-7 SMILES

CC(C)=CCC1=C(O)C2=C(OC3=C(CC(OC4=C3C=C(O)C(O)=C4)=C(C)C)C2=O)C2=C1OC(C)(C)C=C2

InChI Identifier

InChI=1S/C30H30O7/c1-14(2)7-8-16-25(33)24-26(34)19-12-22(15(3)4)35-23-13-21(32)20(31)11-18(23)27(19)36-29(24)17-9-10-30(5,6)37-28(16)17/h7,9-11,13,31-33H,8,12H2,1-6H3

InChI Key

PNKNNRLOQYRSCW-UHFFFAOYSA-N Chemical Taxonomy Description

This compound belongs to the class of organic compounds known as pyranochromenes. These are organic heterocyclic compounds containing a pyran ring fused to a chromene (1-benzopyran) moiety. Kingdom

Organic compounds Super Class

Organoheterocyclic compounds Class

Benzopyrans Sub Class

1-benzopyrans Direct Parent

Pyranochromenes Alternative Parents

  • 2,2-dimethyl-1-benzopyrans
  • Chromones
  • Benzoxepines
  • Catechols
  • Pyranones and derivatives
  • Alkyl aryl ethers
  • Vinylogous acids
  • Heteroaromatic compounds
  • Polyols
  • Oxacyclic compounds
  • Hydrocarbon derivatives
  • Substituents

  • Pyranochromene
  • 2,2-dimethyl-1-benzopyran
  • Chromone
  • Benzoxepine
  • 1,2-diphenol
  • Pyranone
  • Alkyl aryl ether
  • Benzenoid
  • Pyran
  • Heteroaromatic compound
  • Vinylogous acid
  • Polyol
  • Oxacycle
  • Ether
  • Hydrocarbon derivative
  • Organooxygen compound
  • Aromatic heteropolycyclic compound
  • Molecliar Framework

    Aromatic heteropolycyclic compounds External Descriptors

    Not Available Ontology Status

    Expected but not Quantified Origin

  • Endogenous
  • Food
  • Biofunction

    Not Available Application

  • Nutrient
  • Cellliar locations

  • Membrane
  • Physical Properties State

    Not Available Experimental Properties

    Property Value Reference Melting Point231 °CNot Available Boiling PointNot AvailableNot Available Water SolubilityNot AvailableNot Available LogPNot AvailableNot Available

    Predicted Properties

    Property Value Source Water Solubility0.0041 mg/mLALOGPS logP5.6ALOGPS logP5.95ChemAxon logS-5.1ALOGPS pKa (Strongest Acidic)8.34ChemAxon pKa (Strongest Basic)-4.7ChemAxon Physiological Charge0ChemAxon Hydrogen Acceptor Count7ChemAxon Hydrogen Donor Count3ChemAxon Polar Surface Area105.45 Å2ChemAxon Rotatable Bond Count2ChemAxon Refractivity145.36 m3·mol-1ChemAxon Polarizability55.65 Å3ChemAxon Number of Rings5ChemAxon Bioavailability0ChemAxon Rlie of FiveYesChemAxon Ghose FilterYesChemAxon Vebers RlieYesChemAxon MDDR-like RlieYesChemAxon

    Spectra Spectra

    Spectrum Type Description Splash Key Predicted LC-MS/MS

    Predicted LC-MS/MS Spectrum – 10V, PositiveNot Available Predicted LC-MS/MS

    Predicted LC-MS/MS Spectrum – 20V, PositiveNot Available Predicted LC-MS/MS

    Predicted LC-MS/MS Spectrum – 40V, PositiveNot Available Predicted LC-MS/MS

    Predicted LC-MS/MS Spectrum – 10V, NegativeNot Available Predicted LC-MS/MS

    Predicted LC-MS/MS Spectrum – 20V, NegativeNot Available Predicted LC-MS/MS

    Predicted LC-MS/MS Spectrum – 40V, NegativeNot Available

    Biological Properties Cellliar Locations

  • Membrane
  • Biofluid Locations

    Not Available Tissue Location

    Not Available Pathways

    Not Available Normal Concentrations Not Available Abnormal Concentrations

    Not Available Associated Disorders and Diseases Disease References

    None Associated OMIM IDs

    None External Links DrugBank ID

    Not Available DrugBank Metabolite ID

    Not Available Phenol Explorer Compound ID

    Not Available Phenol Explorer Metabolite ID

    Not Available FoodDB ID

    FDB000593 KNApSAcK ID

    Not Available Chemspider ID

    Not Available KEGG Compound ID

    Not Available BioCyc ID

    Not Available BiGG ID

    Not Available Wikipedia Link

    Not Available NuGOwiki Link

    HMDB29471 Metagene Link

    HMDB29471 METLIN ID

    Not Available PubChem Compound

    Not Available PDB ID

    Not Available ChEBI ID

    Not Available

    Product: Triptorelin

    References Synthesis Reference Not Available Material Safety Data Sheet (MSDS) Not Available General References
    1. (). Yannai, Shmuel. (2004) Dictionary of food compounds with CD-ROM: Additives, flavors, and ingredients. Boca Raton: Chapman & Hall/CRC.. .

    PMID: 17209801

    Isocycloheterophyllin

    Common Name

    Isocycloheterophyllin Description

    Isocycloheterophyllin is found in fruits. Isocycloheterophyllin is a constituent of wood of Artocarpus heterophyllus (jackfruit).Isocycloheterophyllin belongs to the family of Flavonols. These are compounds that has the 3-hydroxyflavone backbone. Structure

    MOLSDFPDBSMILESInChI

    Structure for HMDB29471 (Isocycloheterophyllin)

    Synonyms

    Not Available Chemical Formlia

    C30H30O7 Average Molecliar Weight

    502.555 Monoisotopic Molecliar Weight

    502.199153314 IUPAC Name

    11,20,21-trihydroxy-7,7-dimethyl-10-(3-methylbut-2-en-1-yl)-16-(propan-2-ylidene)-2,8,17-trioxapentacyclo[12.9.0.0³,¹².0⁴,⁹.0¹⁸,²³]tricosa-1(14),3(12),4(9),5,10,18(23),19,21-octaen-13-one Traditional Name

    11,20,21-trihydroxy-7,7-dimethyl-10-(3-methylbut-2-en-1-yl)-16-(propan-2-ylidene)-2,8,17-trioxapentacyclo[12.9.0.0³,¹².0⁴,⁹.0¹⁸,²³]tricosa-1(14),3(12),4(9),5,10,18(23),19,21-octaen-13-one CAS Registry Number

    49794-94-7 SMILES

    CC(C)=CCC1=C(O)C2=C(OC3=C(CC(OC4=C3C=C(O)C(O)=C4)=C(C)C)C2=O)C2=C1OC(C)(C)C=C2

    InChI Identifier

    InChI=1S/C30H30O7/c1-14(2)7-8-16-25(33)24-26(34)19-12-22(15(3)4)35-23-13-21(32)20(31)11-18(23)27(19)36-29(24)17-9-10-30(5,6)37-28(16)17/h7,9-11,13,31-33H,8,12H2,1-6H3

    InChI Key

    PNKNNRLOQYRSCW-UHFFFAOYSA-N Chemical Taxonomy Description

    This compound belongs to the class of organic compounds known as pyranochromenes. These are organic heterocyclic compounds containing a pyran ring fused to a chromene (1-benzopyran) moiety. Kingdom

    Organic compounds Super Class

    Organoheterocyclic compounds Class

    Benzopyrans Sub Class

    1-benzopyrans Direct Parent

    Pyranochromenes Alternative Parents

  • 2,2-dimethyl-1-benzopyrans
  • Chromones
  • Benzoxepines
  • Catechols
  • Pyranones and derivatives
  • Alkyl aryl ethers
  • Vinylogous acids
  • Heteroaromatic compounds
  • Polyols
  • Oxacyclic compounds
  • Hydrocarbon derivatives
  • Substituents

  • Pyranochromene
  • 2,2-dimethyl-1-benzopyran
  • Chromone
  • Benzoxepine
  • 1,2-diphenol
  • Pyranone
  • Alkyl aryl ether
  • Benzenoid
  • Pyran
  • Heteroaromatic compound
  • Vinylogous acid
  • Polyol
  • Oxacycle
  • Ether
  • Hydrocarbon derivative
  • Organooxygen compound
  • Aromatic heteropolycyclic compound
  • Molecliar Framework

    Aromatic heteropolycyclic compounds External Descriptors

    Not Available Ontology Status

    Expected but not Quantified Origin

  • Endogenous
  • Food
  • Biofunction

    Not Available Application

  • Nutrient
  • Cellliar locations

  • Membrane
  • Physical Properties State

    Not Available Experimental Properties

    Property Value Reference Melting Point231 °CNot Available Boiling PointNot AvailableNot Available Water SolubilityNot AvailableNot Available LogPNot AvailableNot Available

    Predicted Properties

    Property Value Source Water Solubility0.0041 mg/mLALOGPS logP5.6ALOGPS logP5.95ChemAxon logS-5.1ALOGPS pKa (Strongest Acidic)8.34ChemAxon pKa (Strongest Basic)-4.7ChemAxon Physiological Charge0ChemAxon Hydrogen Acceptor Count7ChemAxon Hydrogen Donor Count3ChemAxon Polar Surface Area105.45 Å2ChemAxon Rotatable Bond Count2ChemAxon Refractivity145.36 m3·mol-1ChemAxon Polarizability55.65 Å3ChemAxon Number of Rings5ChemAxon Bioavailability0ChemAxon Rlie of FiveYesChemAxon Ghose FilterYesChemAxon Vebers RlieYesChemAxon MDDR-like RlieYesChemAxon

    Spectra Spectra

    Spectrum Type Description Splash Key Predicted LC-MS/MS

    Predicted LC-MS/MS Spectrum – 10V, PositiveNot Available Predicted LC-MS/MS

    Predicted LC-MS/MS Spectrum – 20V, PositiveNot Available Predicted LC-MS/MS

    Predicted LC-MS/MS Spectrum – 40V, PositiveNot Available Predicted LC-MS/MS

    Predicted LC-MS/MS Spectrum – 10V, NegativeNot Available Predicted LC-MS/MS

    Predicted LC-MS/MS Spectrum – 20V, NegativeNot Available Predicted LC-MS/MS

    Predicted LC-MS/MS Spectrum – 40V, NegativeNot Available

    Biological Properties Cellliar Locations

  • Membrane
  • Biofluid Locations

    Not Available Tissue Location

    Not Available Pathways

    Not Available Normal Concentrations Not Available Abnormal Concentrations

    Not Available Associated Disorders and Diseases Disease References

    None Associated OMIM IDs

    None External Links DrugBank ID

    Not Available DrugBank Metabolite ID

    Not Available Phenol Explorer Compound ID

    Not Available Phenol Explorer Metabolite ID

    Not Available FoodDB ID

    FDB000593 KNApSAcK ID

    Not Available Chemspider ID

    Not Available KEGG Compound ID

    Not Available BioCyc ID

    Not Available BiGG ID

    Not Available Wikipedia Link

    Not Available NuGOwiki Link

    HMDB29471 Metagene Link

    HMDB29471 METLIN ID

    Not Available PubChem Compound

    Not Available PDB ID

    Not Available ChEBI ID

    Not Available

    Product: Triptorelin

    References Synthesis Reference Not Available Material Safety Data Sheet (MSDS) Not Available General References
    1. (). Yannai, Shmuel. (2004) Dictionary of food compounds with CD-ROM: Additives, flavors, and ingredients. Boca Raton: Chapman & Hall/CRC.. .

    PMID: 17209801