(Q105377594)

English

Heteroclitin G

chemical compound

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Statements

type of chemical entity

0 references

11-Hydroxy-3,17,18-trimethoxy-12,13-dimethyl-5,7-dioxapentacyclo[10.7.0.01,15.02,10.04,8]nonadeca-2,4(8),9,15,17-pentaen-19-one

1 reference

based on heuristic

inferred from SMILES

1 reference

based on heuristic

inferred from SMILES

400.152203108 dalton

1 reference

based on heuristic

inferred from SMILES

stereoisomer of

(1S,11S,12S,13R)-11-hydroxy-3,17,18-trimethoxy-12,13-dimethyl-5,7-dioxapentacyclo[10.7.0.01,15.02,10.04,8]nonadeca-2,4(8),9,15,17-pentaen-19-one

2 references

based on heuristic

inferred from InChIKey

based on heuristic

inferred from InChI

(1R,11S,12S,13R)-11-hydroxy-3,17,18-trimethoxy-12,13-dimethyl-5,7-dioxapentacyclo[10.7.0.01,15.02,10.04,8]nonadeca-2,4(8),9,15,17-pentaen-19-one

1 reference

based on heuristic

inferred from InChI

(1S,11R,12S,13R)-11-hydroxy-3,17,18-trimethoxy-12,13-dimethyl-5,7-dioxapentacyclo[10.7.0.01,15.02,10.04,8]nonadeca-2,4(8),9,15,17-pentaen-19-one

1 reference

based on heuristic

inferred from InChI

chemical formula

C₂₂H₂₄O₇

0 references

canonical SMILES

O=C1C(OC)=C(OC)C=C2CC(C)C3(C)C(O)C4=CC=5OCOC5C(OC)=C4C123

0 references

isomeric SMILES

COC1=C(OC)C(=O)[C@@]23C(=C1)C[C@@H](C)[C@@]2(C)[C@@H](O)c1cc2c(c(OC)c13)OCO2

0 references

Kadsura angustifolia

1 reference

Lignans from Kadsura angustifolia

Kadsura heteroclita

1 reference

Isolation of novel lignans, heteroclitins F and G, from the stems of Kadsura heteroclita, and anti-lipid peroxidative actions of heteroclitins A-G and related compounds in the in vitro rat liver homogenate system

Identifiers

InChI=1S/C22H24O7/c1-10-6-11-7-13(25-3)17(26-4)20(24)22(11)15-12(19(23)21(10,22)2)8-14-16(18(15)27-5)29-9-28-14/h7-8,10,19,23H,6,9H2,1-5H3/t10-,19+,21+,22+/m1/s1

0 references

ZIWBGKHKHFLTJE-FDTHIAJZSA-N

0 references

1 reference

17 September 2022

based on heuristic

inferred from InChIKey

UniChem compound ID

1 reference

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