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OSW 1

Known as: 3 beta, 16 beta, 17-alpha-trihydroxy-cholest-5-en-22-one 16-O-(2-O-4-methoxybenzoyl-beta-D-xylopyranosyl)- (1-->3)-(2-O-acetyl-alpha-L-arabinopyranoside), OSW-1 
National Institutes of Health

Related topics

Related topics

1 relation

Broader (1)

Saponins

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2007
2007
New analogues of the potent cytotoxic saponin OSW-1.
Saponin OSW-1 (5e-G2; 3 beta,16 beta,17 alpha-trihydroxycholest-5-en-22-one 16-O-{O-[2-O-(4-methoxybenzoyl)-beta-D-xylopyranosyl… 
Highly Cited
2005
Highly Cited
2005
OSW saponins: facile synthesis toward a new type of structures with potent antitumor activities.
[reaction: see text] OSW saponins, featuring a 16beta,17alpha-dihydroxycholest-22-one aglycon and an acylated beta-D… 
2005
2005
Efficacy of Troxerutin on Streptozotocin-induced Rat Model in the Early Stage of Diabetic Retinopathy
Summary The vascular changes associated with early diabetic retinopathy, which include the formation of microaneurysms and… 
Review
2005
Review
2005
Synthesis of a Highly Potent Antitumor Saponin OSW-1 and its Analogues
Twelve years ago a group of cholestane glycosides was isolated from the bulbs of Ornithogalum saundersiae, a species of the lily… 
2004
2004
Synthesis of analogues of a potent antitumor saponin OSW-1.
2002
2002
Synthesis of a cholestane glycoside OSW-1 with potent cytostatic activity.
Highly Cited
2001
Highly Cited
2001
A new strategy for the stereoselective introduction of steroid side chain via alpha-alkoxy vinyl cuprates: total synthesis of a highly potent antitumor natural product OSW-1.
2000
2000
Steroidal compounds from the Caribbean octocoral Eunicea laciniata.
A previously isolated trihydroxy-gorgosterol derivative (2), a new gorgosterol (3), and the known sterol cholestane-3beta,5alpha… 
1981
1981
A comparison of the effects of 4-catechol oestrogens and 2-pyrogallol oestrogens on prostaglandin synthesis by the rat and human uterus.
1970
1970
[Renal excretion of trihydroxy-ethylrutoside (Venoruton) after parenteral and oral administration].
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