Liquiritigenin → 2',4,4',6'-Tetrahydroxychalcone

HRID 1160625

反応式

HRID 1160625 の反応式
C1C(/C=C/C(C2C=CC(O)=CC=2O)=O)=CC=C(O)C=1.C1C([C@H]2OC3C=C(O)C=CC=3C(=O)C2)=CC=C(O)C=1.[CH:39]1[C:44]([C@H:45]2[O:55][C:54]3[CH:53]=[C:52]([OH:56])[CH:51]=[C:50]([OH:57])[C:49]=3[C:47](=[O:48])[CH2:46]2)=[CH:43][CH:42]=[C:41]([OH:58])[CH:40]=1.C1C(C2C(=O)C3C(O)=CC(O)=CC=3OC=2)=CC=C(O)C=1>>[CH:39]1[C:44](/[CH:45]=[CH:46]/[C:47]([C:49]2[C:50]([OH:57])=[CH:51][C:52]([OH:56])=[CH:53][C:54]=2[OH:55])=[O:48])=[CH:43][CH:42]=[C:41]([OH:58])[CH:40]=1

参加物

5

実験手順

Isoliquiritigenin, liquiritigenin, naringenin and genistein were purchased from Indofine Chemical Co. (Hillsborough, N.J.). Naringenin chalcone was prepared from naringenin as previously described (Shimokoriyama, 1957).

出典と根拠

ORDレコード
ord-45c01546480e49bfbf3d6214a0515ba1
出典データセット
uspto-grants-2010_10
特許番号
US07816507B2

関連ノート

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