CAS 65604-80-0
:(3beta,25R)-spirost-5-en-3-yl 6-deoxy-alpha-L-mannopyranosyl-(1->2)-[beta-D-xylopyranosyl-(1->3)]-beta-D-glucopyranoside
Description:
The chemical substance known as "(3beta,25R)-spirost-5-en-3-yl 6-deoxy-alpha-L-mannopyranosyl-(1->2)-[beta-D-xylopyranosyl-(1->3)]-beta-D-glucopyranoside," with the CAS number 65604-80-0, is a complex glycoside derived from a spirostane steroid framework. This compound features a spirostene core, characterized by a steroid structure with a unique spiro configuration, which contributes to its biological activity. The presence of multiple sugar moieties, including 6-deoxy-alpha-L-mannopyranosyl, beta-D-xylopyranosyl, and beta-D-glucopyranosyl units, indicates its classification as a glycoside, suggesting potential interactions with biological systems, including enzyme inhibition or modulation of cellular pathways. The stereochemistry, denoted by the 3beta and 25R configurations, plays a crucial role in determining the compound's spatial orientation and, consequently, its reactivity and biological function. Such compounds are often studied for their pharmacological properties, including anti-inflammatory, anti-cancer, or immunomodulatory effects, making them of interest in medicinal chemistry and natural product research.
Formula:C44H70O16
InChI:InChI=1/C44H70O16/c1-19-8-13-44(54-17-19)20(2)30-28(60-44)15-26-24-7-6-22-14-23(9-11-42(22,4)25(24)10-12-43(26,30)5)56-41-38(59-40-36(52)34(50)31(47)21(3)55-40)37(33(49)29(16-45)57-41)58-39-35(51)32(48)27(46)18-53-39/h6,19-21,23-41,45-52H,7-18H2,1-5H3/t19-,20+,21+,23+,24-,25+,26+,27-,28+,29-,30+,31+,32+,33-,34-,35-,36-,37+,38-,39+,40+,41-,42+,43+,44-/m1/s1
InChI key:InChIKey=DQYACEDUQHWXQZ-QOYNBSPSSA-N
SMILES:C[C@@]12[C@@]3([C@](C[C@]1([C@]4([C@](CC2)([C@]5(C)C(=CC4)C[C@@H](O[C@H]6[C@H](O[C@H]7[C@H](O)[C@H](O)[C@@H](O)[C@H](C)O7)[C@@H](O[C@H]8[C@H](O)[C@@H](O)[C@H](O)CO8)[C@H](O)[C@@H](CO)O6)CC5)[H])[H])[H])(O[C@@]9([C@H]3C)CC[C@@H](C)CO9)[H])[H]
Synonyms:- (3β,25R)-Spirost-5-en-3-yl O-6-deoxy-α-<span class="text-smallcaps">L</smallcap>-mannopyranosyl-(1→2)-O-[β-<smallcap>D</smallcap>-xylopyranosyl-(1→3)]-β-<smallcap>D</span>-glucopyranoside
- Diosgenin 3-O-[α-<span class="text-smallcaps">L</smallcap>-rhamnopyranosyl-(1→2)][β-<smallcap>D</smallcap>-xylopyranosyl-(1→3)]-β-<smallcap>D</span>-glucopyranoside
- Ophiopogonin D'
- β-<span class="text-smallcaps">D</smallcap>-Glucopyranoside, (3β,25R)-spirost-5-en-3-yl O-6-deoxy-α-<smallcap>L</smallcap>-mannopyranosyl-(1→2)-O-[β-<smallcap>D</span>-xylopyranosyl-(1→3)]-
- Diosgenin 3-O-[α-L-rhamnopyranosyl-(1→2)][β-D-xylopyranosyl-(1→3)]-β-D-glucopyranoside
- β-D-Glucopyranoside, (3β,25R)-spirost-5-en-3-yl O-6-deoxy-α-L-mannopyranosyl-(1→2)-O-[β-D-xylopyranosyl-(1→3)]-
- (3β,25R)-Spirost-5-en-3-yl O-6-deoxy-α-L-mannopyranosyl-(1→2)-O-[β-D-xylopyranosyl-(1→3)]-β-D-glucopyranoside
- (3β,25R)-Spirost-5-en-3-yl 6-deoxy-α-L-mannopyranosyl-(1->
- 3)]-β-D-glucopyranoside
- Diosgenin 3-O-[alpha-L-rhamnopyranosyl-(1-2)][beta-D-xylopyranosyl-(1-3)]-beta-D-glucopyranoside
- (3β,25R)-Spirost-5-en-3-yl 6-deoxy-α-L-mannopyranosyl-(1->2)-[β-D-xylopyranosyl-(1->3)]-β-D-glucopyranoside
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 6 products.
(2S,3R,4R,5R,6S)-2-(((2R,3R,4S,5R,6R)-5-Hydroxy-6-(hydroxymethyl)-2-(((4S,5'R,6aR,6bS,8aS,8bR,9S,10R,11aS,12aS,12bS)-5',6a,8a,9-tetramethyl-1,3,3',4,4',5,5',6,6a,6b,6',7,8,8a,8b,9,11a,12,12a,12b-icosahydrospiro[naphtho[2',1':4,5]indeno[2,1-b]furan-10,2'-pyran]-4-yl)oxy)-4-(((2S,3R,4S,5R)-3,4,5-trihydroxytetrahydro-2H-pyran-2-yl)oxy)tetrahydro-2H-pyran-3-yl)oxy)-6-methyltetrahydro-2H-pyran-3,4,5-triol
CAS:Formula:C44H70O16Purity:99%Molecular weight:855.0170Ophiopogonin D'
CAS:<p>Ophiopogonin D' can activate SIRT1 in a dose-dependent manner. Ophiopogonin D' also noncompetitively inhibits UGT1A6 and UGT1A10.</p>Formula:C44H70O16Purity:99.77%Color and Shape:SolidMolecular weight:855.02Ophiopogonin D'
CAS:<p>Ophiopogonin D is a type of saponin, which is a class of chemical compounds found in various plant species. Saponins are glycoside compounds that occur primarily in the roots, leaves, and seeds of plants. The specific source of Ophiopogonin D is the plant Ophiopogon japonicus, commonly known as dwarf lilyturf or mondo grass. This compound is isolated through extraction and purification processes from the root tubers of the plant.</p>Formula:C44H70O16Purity:Min. 95%Molecular weight:855.02 g/mol





