1,3,6-Trihydroxy-7-methoxy-2,8-bis(3-methylbut-2-enyl)-9H-xanthen-9-one
The title compound (trivial name α-mangostin), C24H26O6, isolated from Cratoxylum glaucum, is characterized by a xanthone skeleton of three fused six-membered rings and two 3-methylbut-2-enyl side chains. The three rings in the structure are nearly coplanar, with an r.m.s. deviation for the tricycl...
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Format: | Article |
Language: | English English |
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International Union of Crystallography
2010
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Online Access: | http://psasir.upm.edu.my/id/eprint/12629/1/1.pdf |
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author | Ee, Gwendoline Cheng Lian Mohamed Tahir, Mohamed Ibrahim Silong, Sidik Wei, Chung Sim Huey, Chong Kwong |
author_facet | Ee, Gwendoline Cheng Lian Mohamed Tahir, Mohamed Ibrahim Silong, Sidik Wei, Chung Sim Huey, Chong Kwong |
author_sort | Ee, Gwendoline Cheng Lian |
collection | UPM |
description | The title compound (trivial name α-mangostin), C24H26O6, isolated from Cratoxylum glaucum, is characterized by a xanthone skeleton of three fused six-membered rings and two 3-methylbut-2-enyl side chains. The three rings in the structure are nearly coplanar, with an r.m.s. deviation for the tricyclic ring system of 0.0014 Å. The two 3-methylbut-2-enyl side chains are in (+)-synclinal and (-)-anticlinal conformations. Intramolecular O—H[cdots, three dots, centered]O and C—H[cdots, three dots, centered]O interactions occur. The crystal structure is stabilized by intermolecular O—H[cdots, three dots, centered]O, C—H[cdots, three dots, centered]O and C—H[cdots, three dots, centered]π interactions. |
first_indexed | 2024-03-06T07:25:56Z |
format | Article |
id | upm.eprints-12629 |
institution | Universiti Putra Malaysia |
language | English English |
last_indexed | 2024-03-06T07:25:56Z |
publishDate | 2010 |
publisher | International Union of Crystallography |
record_format | dspace |
spelling | upm.eprints-126292015-09-10T03:42:01Z http://psasir.upm.edu.my/id/eprint/12629/ 1,3,6-Trihydroxy-7-methoxy-2,8-bis(3-methylbut-2-enyl)-9H-xanthen-9-one Ee, Gwendoline Cheng Lian Mohamed Tahir, Mohamed Ibrahim Silong, Sidik Wei, Chung Sim Huey, Chong Kwong The title compound (trivial name α-mangostin), C24H26O6, isolated from Cratoxylum glaucum, is characterized by a xanthone skeleton of three fused six-membered rings and two 3-methylbut-2-enyl side chains. The three rings in the structure are nearly coplanar, with an r.m.s. deviation for the tricyclic ring system of 0.0014 Å. The two 3-methylbut-2-enyl side chains are in (+)-synclinal and (-)-anticlinal conformations. Intramolecular O—H[cdots, three dots, centered]O and C—H[cdots, three dots, centered]O interactions occur. The crystal structure is stabilized by intermolecular O—H[cdots, three dots, centered]O, C—H[cdots, three dots, centered]O and C—H[cdots, three dots, centered]π interactions. International Union of Crystallography 2010 Article PeerReviewed application/pdf en http://psasir.upm.edu.my/id/eprint/12629/1/1.pdf Ee, Gwendoline Cheng Lian and Mohamed Tahir, Mohamed Ibrahim and Silong, Sidik and Wei, Chung Sim and Huey, Chong Kwong (2010) 1,3,6-Trihydroxy-7-methoxy-2,8-bis(3-methylbut-2-enyl)-9H-xanthen-9-one. Acta Crystallographica Section E: Structure Reports Online, 66 (12). pp. 3362-3363. ISSN 1600-5368 http://dx.doi.org/10.1107/S1600536810049123 crystal 10.1107/S1600536810049123 English |
spellingShingle | crystal Ee, Gwendoline Cheng Lian Mohamed Tahir, Mohamed Ibrahim Silong, Sidik Wei, Chung Sim Huey, Chong Kwong 1,3,6-Trihydroxy-7-methoxy-2,8-bis(3-methylbut-2-enyl)-9H-xanthen-9-one |
title | 1,3,6-Trihydroxy-7-methoxy-2,8-bis(3-methylbut-2-enyl)-9H-xanthen-9-one |
title_full | 1,3,6-Trihydroxy-7-methoxy-2,8-bis(3-methylbut-2-enyl)-9H-xanthen-9-one |
title_fullStr | 1,3,6-Trihydroxy-7-methoxy-2,8-bis(3-methylbut-2-enyl)-9H-xanthen-9-one |
title_full_unstemmed | 1,3,6-Trihydroxy-7-methoxy-2,8-bis(3-methylbut-2-enyl)-9H-xanthen-9-one |
title_short | 1,3,6-Trihydroxy-7-methoxy-2,8-bis(3-methylbut-2-enyl)-9H-xanthen-9-one |
title_sort | 1 3 6 trihy droxy 7 meth oxy 2 8 bis 3 methyl but 2 en yl 9h xanthen 9 one |
topic | crystal |
url | http://psasir.upm.edu.my/id/eprint/12629/1/1.pdf |
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