Pseudoprotodioscin

CAS : 102115-79-7

Ref. TR-P840188

Informations sur le produit

• Nom: Pseudoprotodioscin
• Synonymes: (3ß,25R)-26-(ß-D-Glucopyranosyloxy)furosta-5,20(22)-dien-3-yl O-6-deoxy-a-L-mannopyranosyl-(1?2)-O-[6-deoxy-a-L-mannopyranosyl-(1?4)]-ß-D-glucopyranoside, Oligofurostanoside A, (3β,25R)-26-(β-<span class="text-smallcaps">D</smallcap>-Glucopyranosyloxy)furosta-5,20(22)-dien-3-yl O-6-deoxy-α-<smallcap>L</smallcap>-mannopyranosyl-(1→2)-O-[6-deoxy-α-<smallcap>L</smallcap>-mannopyranosyl-(1→4)]-β-<smallcap>D</span>-glucopyranoside, Protodioscin, Pseudo-, Pseudo-Protodioscin, Pseudoprototribestin, β-<span class="text-smallcaps">D</smallcap>-Glucopyranoside, (3β,25R)-26-(β-<smallcap>D</smallcap>-glucopyranosyloxy)furosta-5,20(22)-dien-3-yl O-6-deoxy-α-<smallcap>L</smallcap>-mannopyranosyl-(1→2)-O-[6-deoxy-α-<smallcap>L</span>-mannopyranosyl-(1→4)]-

Description

Stability Hygroscopic
Applications Pseduoprotodioscin (CAS# 102115-79-7) is a steroidal saponin extracted from plants such as those of the genus Dioscorea spongiosa II, and exhibits cytotoxic effects against human colorectal carcinoma and gastric cancer cells.
References Ruan, J.; et al.: Shenyang Yaoke Daxue Xuebao, 33, 438 (2016); Liang, F.; et al.: Phytochemistry Letters, 16, 294 (2016).

• Marque: TRC

Propriétés chimiques

• Masse moléculaire: 1029.21
• Formule: C₅₂H₈₄O₂₀
• Couleur/Forme: Neat
• InChI: InChI=1S/C52H84O20/c1-21(20-65-48-43(62)42(61)39(58)33(18-53)70-48)7-10-30-23(3)35-31(68-30)17-29-27-9-8-25-16-26(11-13-51(25,5)28(27)12-14-52(29,35)6)67-50-47(72-49-44(63)41(60)37(56)24(4)66-49)45(64)46(34(19-54)71-50)69-32-15-22(2)36(55)40(59)38(32)57/h8,21-22,24,26-29,31-50,53-64H,7,9-20H2,1-6H3/t21-,22-,24+,26+,27-,28+,29?,31+,32-,33-,34-,35+,36+,37+,38+,39-,40-,41-,42+,43-,44-,45+,46-,47-,48-,49+,50-,51+,52+/m1/s1
• Code InChI: InChIKey=MRIWELQAUFPXCU-QVYNFBSOSA-N
• SMILES: CC1=C(CC[C@@H](C)CO[C@H]2[CH][C@@H](O)[C@H](O)[C@@H](CO)O2)O[C@H]2C[C@H]3[C@@H]4CC=C5CC(O[C@@H]6O[C@H](CO)[C@@H](O[C@@H]7O[C@@H](C)[C@H](O)[C@@H](O)[C@H]7O)[C@H](O)[C@H]6O[C@@H]6O[C@@H](C)[C@H](O)[C@@H](O)[C@H]6O)CC[C@]5(C)[C@H]4CC[C@]3(C)[C@@H]12