𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Structure of a novel type steroid glycoside, 18-norspirostanol oligoglycoside

✍ Scribed by T. Nohara; A. Nakano; K. Miyahara; T. Komori; T. Kawasaki


Publisher
Elsevier Science
Year
1975
Tongue
French
Weight
223 KB
Volume
16
Category
Article
ISSN
0040-4039

No coin nor oath required. For personal study only.

✦ Synopsis


Previously it was reported 1) that eight kinds of glycosides of pennogenin, kryptogenin and their related sapogenins were isolated from the fresh rhizomes of Trillium kamtschaticum PG.


📜 SIMILAR VOLUMES


Biologically Active Glycosides from Aste
✍ Itakura, Yoichi ;Komori, Tetsuya ;Kawasaki, Toshio 📂 Article 📅 1983 🏛 John Wiley and Sons 🌐 English ⚖ 767 KB

## Abstract In addition to the already known 3β,6α‐dihydroxy‐5α‐pregn‐9(11)‐en‐20‐one (**1**), 3β,6α,20ξ‐trihydroxy‐5α‐cholest‐9(11)‐en‐23‐one (**2**), 3β,6α,20ξ‐trihydroxy‐24ξ‐methyl‐5α‐cholest‐9(11)‐en‐23‐one (**3**) [isolated in the form of the diacetates **1**′, **2**′, and **3**′ from the enzy

Starfish saponins, part 8. Structure of
✍ R Riccio; L Minale; C Pizza; F Zollo; J Pusset 📂 Article 📅 1982 🏛 Elsevier Science 🌐 French ⚖ 264 KB

A nom2 steroidal glycoside has been isolated from the starfish Protoreaster nodosus. The structure includes a 3B,5a,6B,8B,lScr,24S-hexahydroxysteroidal moiety and a sugar moiety [2-0-methyl-B-D-xylopyranosyl-(1 + 21-a-L-arabinofuranosyZ]which is glycosidicaZZy attached at C-24 of the aglycone.

Veralkamine, a novel type of steroidal a
✍ J. Tomko; A. Vassová; G. Adam; K. Schreiber; E. Höhne 📂 Article 📅 1967 🏛 Elsevier Science 🌐 French ⚖ 267 KB

Some years ago, Tomko et al. (I) isolated a secondary alkaloid, veralkamine, from Veratrum album ssp. lobelianum (Bernh.) Suessenguth. In alteration of a formerly proposed provisional constitution (2) its complete structure has been established by recent chemical and physical reinvestigations includ

Jurine, a novel type of steroidal saponi
✍ K. Schreiber; H. Ripperger 📂 Article 📅 1966 🏛 Elsevier Science 🌐 French ⚖ 244 KB

NEARLY twenty years ago, Marker et al. (1) suggested that the true naturally occurring steroidal saponins synthesized by plants might have an open side chain moiety in which ring closure to the spiroketal structure encountered in the corresponding sapogenins is prevented by conjugation of the hydrox