(Q105228157)

English

[(9R,10S,11S)-3,4,5,19-tetramethoxy-9,10-dimethyl-15,17-dioxatetracyclo[10.7.0.02,7.014,18]nonadeca-1(19),2,4,6,12,14(18)-hexaen-11-yl] acetate

chemical compound

In more languages

Statements

type of chemical entity

0 references

(3,4,5,19-Tetramethoxy-9,10-dimethyl-15,17-dioxatetracyclo[10.7.0.02,7.014,18]nonadeca-1(19),2,4,6,12,14(18)-hexaen-11-yl) acetate

1 reference

based on heuristic

inferred from SMILES

458.19406792 dalton

1 reference

based on heuristic

inferred from SMILES

stereoisomer of

(6R,7R,8S)-8-Acetoxy-5,6,7,8-tetrahydro-1,2,3,13-tetramethoxy-6,7-dimethylbenzo[3,4]cycloocta[1,2-f][1,3]benzodioxole

2 references

based on heuristic

inferred from InChIKey

based on heuristic

inferred from InChI

1 reference

based on heuristic

inferred from InChI

chemical formula

C₂₅H₃₀O₈

0 references

canonical SMILES

O=C(OC1C2=CC=3OCOC3C(OC)=C2C=4C(OC)=C(OC)C(OC)=CC4CC(C)C1C)C

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isomeric SMILES

COc1cc2c(c(OC)c1OC)-c1c(cc3c(c1OC)OCO3)[C@@H](OC(C)=O)[C@@H](C)[C@H](C)C2

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Kadsura heteroclita

2 references

Compounds from Kadsura heteroclita and related anti-HIV activity

Interiotherins C and D, two new lignans from Kadsura interior and antitumor-promoting effects of related neolignans on Epstein-Barr virus activation

Kadsura interior

1 reference

Interiotherins C and D, two new lignans from Kadsura interior and antitumor-promoting effects of related neolignans on Epstein-Barr virus activation

Schisandra propinqua var. sinensis

1 reference

Lignans with anti-HIV activity from Schisandra propinqua var. sinensis.

Identifiers

InChI=1S/C25H30O8/c1-12-8-15-9-17(27-4)22(28-5)24(29-6)19(15)20-16(21(13(12)2)33-14(3)26)10-18-23(25(20)30-7)32-11-31-18/h9-10,12-13,21H,8,11H2,1-7H3/t12-,13+,21+/m1/s1

0 references

QUGMSTJBNZWXQS-BHVCSQLQSA-N

0 references

1 reference

17 September 2022

based on heuristic

inferred from InChIKey

UniChem compound ID

1 reference

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