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Hoodigogenin A from Hoodia gordonii.


ABSTRACT: The title mol-ecule (systematic name: 12-O-?-tigloyl-3?,14?-dihydroxy-pregn-5-en-20-one), C(26)H(38)O(5), isolated from aerial parts of Hoodia gordonii, has its steroid A and C rings in chair conformations, its B ring in a half-chair conformation, and its five-membered ring in an envelope conformation. The OH group at the C/D ring junction forms an intra-molecular hydrogen bond with the keto substituent. The OH group on the A ring forms an inter-molecular hydrogen bond with the tiglate C=O group, propagating [010] chains in the crystal structure.

SUBMITTER: Shukla YJ 

PROVIDER: S-EPMC2962224 | biostudies-other | 2008

REPOSITORIES: biostudies-other

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Hoodigogenin A from Hoodia gordonii.

Shukla Yatin J YJ   Fronczek Frank R FR   Pawar Rahul S RS   Khan Ikhlas A IA  

Acta crystallographica. Section E, Structure reports online 20080731 Pt 8


The title mol-ecule (systematic name: 12-O-β-tigloyl-3β,14β-dihydroxy-pregn-5-en-20-one), C(26)H(38)O(5), isolated from aerial parts of Hoodia gordonii, has its steroid A and C rings in chair conformations, its B ring in a half-chair conformation, and its five-membered ring in an envelope conformation. The OH group at the C/D ring junction forms an intra-molecular hydrogen bond with the keto substituent. The OH group on the A ring forms an inter-molecular hydrogen bond with the tiglate C=O group  ...[more]

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