(Q104402001)

English

(3R)-5,7-dihydroxy-2H-9',11'-dioxaspiro[1-benzopyran-3,4'-tricyclo[6.3.0.0³,⁶]undecane]-1'(8'),2',6'-trien-4-one

chemical compound

In more languages

Statements

type of chemical entity

0 references

5,7-dihydroxyspiro[2H-chromene-3,4'-9,11-dioxatricyclo[6.3.0.03,6]undeca-1(8),2,6-triene]-4-one

1 reference

based on heuristic

inferred from SMILES

312.063388104 dalton

1 reference

based on heuristic

inferred from SMILES

stereoisomer of

(3S)-5,7-dihydroxyspiro[2H-chromene-3,4'-9,11-dioxatricyclo[6.3.0.03,6]undeca-1(8),2,6-triene]-4-one

2 references

based on heuristic

inferred from InChIKey

based on heuristic

inferred from InChI

chemical formula

C₁₇H₁₂O₆

0 references

canonical SMILES

O=C1C=2C(O)=CC(O)=CC2OCC13C4=CC=5OCOC5C=C4C3

0 references

isomeric SMILES

O=C1c2c(O)cc(O)cc2OC[C@]12Cc1cc3c(cc12)OCO3

0 references

Scilla luciliae

1 reference

Homoisoflavanones from Chionodoxa luciliae

Muscari neglectum

1 reference

Homoisoflavanones from Muscari neglectum

Eucomis schijffii

3 references

Anti-inflammatory activity and QSAR studies of compounds isolated from Hyacinthaceae species and Tachiadenus longiflorus Griseb. (Gentianaceae)

Homoisoflavanones and spirocyclic nortriterpenoids from three Eucomis species: E. comosa, E. schijffii and E. pallidiflora subsp. pole-evansii (Hyacinthaceae)

Vascular myorelaxing activity of isolates from South African Hyacinthaceae partly mediated by activation of soluble guanylyl cyclase in rat aortic ring preparations.

Merwilla natalensis

1 reference

Eucosterol-type nortriterpenoids from Merwilla natalensis.

Merwilla plumbea

1 reference

Eucosterol-type nortriterpenoids from Merwilla natalensis.

Barnardia japonica var. japonica

1 reference

A new homostilbene and two new homoisoflavones from the bulbs of Scilla scilloides

Identifiers

InChI=1S/C17H12O6/c18-9-2-11(19)15-14(3-9)21-6-17(16(15)20)5-8-1-12-13(4-10(8)17)23-7-22-12/h1-4,18-19H,5-7H2/t17-/m0/s1

0 references

SAXOGBBWXWKZKR-KRWDZBQOSA-N

0 references

2 references

17 September 2022

based on heuristic

inferred from InChIKey

matched by identifier from

SAXOGBBWXWKZKR-KRWDZBQOSA-N

UniChem compound ID

1 reference

Sitelinks

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