CAS 104987-36-2: Oenothein B
Description:Oenothein B is a naturally occurring phenolic compound primarily found in the plant genus Oenothera, commonly known as evening primrose. It belongs to a class of compounds known as flavonoids, which are known for their antioxidant properties. Oenothein B is characterized by its unique chemical structure, which includes a flavonoid backbone with specific hydroxyl and methoxy groups that contribute to its biological activity. This compound has garnered interest in pharmacological research due to its potential health benefits, including anti-inflammatory and anticancer properties. Additionally, Oenothein B may play a role in protecting cells from oxidative stress, making it a subject of study in the context of various diseases. Its solubility and stability can vary depending on environmental conditions, which is important for its application in dietary supplements and herbal medicine. Overall, Oenothein B represents a significant area of interest in natural product chemistry and its potential therapeutic applications.
Formula:C68H48O44
InChI:InChI=1S/C68H48O44/c69-11-35-59(111-61(95)15-1-23(71)41(81)24(72)2-15)57-32(80)14-104-64(98)19-9-33(47(87)51(91)39(19)38-18(65(99)109-57)6-28(76)44(84)50(38)90)105-55-21(7-29(77)45(85)53(55)93)67(101)108-36(12-70)60(112-62(96)16-3-25(73)42(82)26(74)4-16)58-31(79)13-103-63(97)17-5-27(75)43(83)49(89)37(17)40-20(66(100)110-58)10-34(48(88)52(40)92)106-56-22(68(102)107-35)8-30(78)46(86)54(56)94/h1-12,31-32,35-36,57-60,71-94H,13-14H2
InChI key:InChIKey=MGFJAOIDAUFIHI-UHFFFAOYSA-N
SMILES:O=CC1OC(=O)C2=CC(O)=C(O)C(O)=C2OC=3C=C4C(=O)OC(C(O)COC(=O)C5=CC(O)=C(O)C(O)=C5C4=C(O)C3O)C(OC(=O)C6=CC(O)=C(O)C(O)=C6)C(OC(=O)C7=CC(O)=C(O)C(O)=C7OC=8C=C9C(=O)OCC(O)C(OC(=O)C%10=CC(O)=C(O)C(O)=C%10C9=C(O)C8O)C1OC(=O)C%11=CC(O)=C(O)C(O)=C%11)C=O
- Synonyms:
- 18,8-(Epoxymethano)-38,30-(ethanoxymethano)-6,9:28,31-dietheno-14H,16H,22H,36H,38H,42H-tetrabenzo[b,k,r,c<sub>1</sub>][1,5,9,17,21,27]hexaoxacyclotetratriacontin, <span class="text-smallcaps">D</span>-glucose deriv.
- <span class="text-smallcaps">D</smallcap>-Glucose, cyclic 4,6-[(1S)-4-(6-carboxy-2,3,4-trihydroxyphenoxy)-4′,5,5′,6,6′-pentahydroxy[1,1′-biphenyl]-2,2′-dicarboxylate] 2-[2-[[(1S)-6,6′-dicarboxy-2,2′,3,3′,4′-pentahydroxy[1,1′-biphenyl]-4-yl]oxy]-3,4,5-trihydroxybenzoate] 3-(3,4,5-trihydroxybenzoate), cyclic ester with <smallcap>D</span>-glucose 3-(3,4,5-trihydroxybenzoate)
- <span class="text-smallcaps">D</smallcap>-Glucose, cyclic 4,6-[4-(6-carboxy-2,3,4-trihydroxyphenoxy)-4′,5,5′,6,6′-pentahydroxy[1,1′-biphenyl]-2,2′-dicarboxylate] 2-[2-[(6,6′-dicarboxy-2,2′,3,3′,4′-pentahydroxy[1,1′-biphenyl]-4-yl)oxy]-3,4,5-trihydroxybenzoate] 3-(3,4,5-trihydroxybenzoate), cyclic ester with <smallcap>D</span>-glucose 3-(3,4,5-trihydroxybenzoate), [2(S),4(S)]-
- D-Glucose, cyclic 4,6-(4-(6-carboxy-2,3,4-trihydroxyphenoxy)-4',5,5',6,6'-pentahydroxy(1,1'-biphenyl)-2,2'-dicarboxylate) 2-(2-((6,6'-dicarboxy-2,2',3,3',4'-pentahydroxy(1,1'-biphenyl)-4-yl)oxy)-3,4,5-trihydroxybenzoate) 3-(3,4,5-trihydroxybenzoate), cyclic ester with D-glucose 3-(3,4,5-trihydroxybenzoate), (2(S),4(S))-
- D-Glucose, cyclic 4,6-[(1S)-4-(6-carboxy-2,3,4-trihydroxyphenoxy)-4′,5,5′,6,6′-pentahydroxy[1,1′-biphenyl]-2,2′-dicarboxylate] 2-[2-[[(1S)-6,6′-dicarboxy-2,2′,3,3′,4′-pentahydroxy[1,1′-biphenyl]-4-yl]oxy]-3,4,5-trihydroxybenzoate] 3-(3,4,5-trihydroxybenzoate), cyclic ester with D-glucose 3-(3,4,5-trihydroxybenzoate)
- D-Glucose, cyclic 4,6-[4-(6-carboxy-2,3,4-trihydroxyphenoxy)-4′,5,5′,6,6′-pentahydroxy[1,1′-biphenyl]-2,2′-dicarboxylate] 2-[2-[(6,6′-dicarboxy-2,2′,3,3′,4′-pentahydroxy[1,1′-biphenyl]-4-yl)oxy]-3,4,5-trihydroxybenzoate] 3-(3,4,5-trihydroxybenzoate), cyclic ester with D-glucose 3-(3,4,5-trihydroxybenzoate), [2(S),4(S)]-
- Oenothein B
- 18,8-(Epoxymethano)-38,30-(ethanoxymethano)-6,9:28,31-dietheno-14H,16H,22H,36H,38H,42H-tetrabenzo[b,k,r,c1][1,5,9,17,21,27]hexaoxacyclotetratriacontin, D-glucose deriv.
