triterpenoid ginsenoside Rg2 0 784.49729 785.025 pubmed:22031031 pubmed:22062806 pubmed:24117771 pubmed:22261865 pubmed:19673396 (3beta,6alpha,12beta)-3,12,20-trihydroxydammar-24-en-6-yl 2-O-(6-deoxy-alpha-L-mannopyranosyl)-beta-D-glucopyranoside C42H72O13 pubmed:23626475 pubmed:12661769 Chikusetsusaponin I CHEBI:77151 (3beta,6alpha,12beta)-3,12,20-trihydroxydammar-24-en-6-yl 2-O-(alpha-L-rhamnopyranosyl)-beta-D-glucopyranoside [H][C@]12C[C@@H](O)[C@]3([H])[C@@]([H])([C@@](C)(O)CCC=C(C)C)CC[C@@]3(C)[C@]1(C)C[C@H](O[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O[C@@H]1O[C@@H](C)[C@H](O)[C@@H](O)[C@H]1O)[C@@]1([H])C(C)(C)[C@@H](O)CC[C@]21C pubmed:24198651 A ginsenoside found in <em>Panax</em> species that is dammarane which is substituted by hydroxy groups at the 3β, 6α, 12β and 20 <em>pro</em>-<i>S</i> positions, in which the hydroxy group at position 6 has been converted to the corresponding α-<small>L</small>-rhamnopyranosyl-(1→2)-β-<small>D</small>-glucopyranoside, and in which a double bond has been introduced at the 24-25 position. Prosapogenin C2 ginsenoside Rg2 reaxys:5720818 metacyc.compound:CPD-15444 chebi_ontology (3beta,6alpha,12beta)-3,12,20-trihydroxydammar-24-en-6-yl 2-O-(6-deoxy-alpha-L-mannopyranosyl)-beta-D-glucopyranoside pubmed:23742679 cas:52286-74-5 (3beta,6alpha,12beta)-3,12,20-trihydroxydammar-24-en-6-yl 2-O-(alpha-L-rhamnopyranosyl)-beta-D-glucopyranoside hmdb:HMDB0035395 InChI=1S/C42H72O13/c1-20(2)11-10-14-42(9,51)22-12-16-40(7)28(22)23(44)17-26-39(6)15-13-27(45)38(4,5)35(39)24(18-41(26,40)8)53-37-34(32(49)30(47)25(19-43)54-37)55-36-33(50)31(48)29(46)21(3)52-36/h11,21-37,43-51H,10,12-19H2,1-9H3/t21-,22-,23+,24-,25+,26+,27-,28-,29-,30+,31+,32-,33+,34+,35-,36-,37+,39+,40+,41+,42-/m0/s1 pubmed:15617510 Ginsenoside C pubmed:20508917 beilstein:6627213 AGBCLJAHARWNLA-DQUQINEDSA-N