CAS 65604-80-0
:(3beta,25R)-spirost-5-en-3-il 6-desossi-alfa-L-mannopiranosil-(1->2)-[beta-D-xilopiranosil-(1->3)]-beta-D-glucopiranoside
Descrizione:
La sostanza chimica nota come "(3beta,25R)-spirost-5-en-3-il 6-desossi-alfa-L-mannopiranosil-(1->2)-[beta-D-xilopiranosil-(1->3)]-beta-D-glucopiranoside," con il numero CAS 65604-80-0, è un glicoside complesso derivato da un telaio steroideo spirostanico. Questo composto presenta un nucleo spirostene, caratterizzato da una struttura steroidea con una configurazione spiro unica, che contribuisce alla sua attività biologica. La presenza di più unità di zucchero, tra cui 6-deossi-alfa-L-mannopiranosilico, beta-D-xilopiranosilico e beta-D-glucopiranosilico, indica la sua classificazione come glicoside, suggerendo potenziali interazioni con sistemi biologici, inclusa l'inibizione o la modulazione delle vie cellulari. La stereochimica, denotata dalle configurazioni 3beta e 25R, gioca un ruolo cruciale nella determinazione dell'orientamento spaziale del composto e, di conseguenza, della sua reattività e funzione biologica. Tali composti sono spesso studiati per le loro proprietà farmacologiche, inclusi effetti anti-infiammatori, anti-cancro o immunomodulatori, rendendoli di interesse nella chimica medicinale e nella ricerca di prodotti naturali.
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]
Sinonimi:- (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
Ordinare per
Purezza (%)
0
100
|
0
|
50
|
90
|
95
|
100
6 prodotti.
(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:C44H70O16Purezza:99%Peso molecolare: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:C44H70O16Purezza:99.77%Colore e forma:SolidPeso molecolare: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:C44H70O16Purezza:Min. 95%Peso molecolare:855.02 g/mol





