170–171° and M+ 428 (CIMS). RS-2 was soluble in ethyl acetate, methanol and water. It responded to all the characteristic color reactions of flavonoids as described earlier. The wavelengths of maximum absorbance in the UV spectrum of the aglycone were at: λmax (MeOH) 272, 345 nm, λmax (NaOMe) 280, 330, 392 nm, λmax (AlCl3) 272, 390, 400 nm, λmax (AlCl3 + HCl) 275, 390, 406 nm, λmax (NaOAc) 286, 345 nm, λmax (NaOAc + H3BO3) 290, 355 nm as depicted in Graph 2. The characteristic

IR band as noticed in the IR spectrum of RS-2(A) and the structural units inferred with the help of available literature selleckchem were used for the structural elucidation of the aglycone as discussed below. Characteristic band at Vmax (KBr) 3400.9 cm−1 in the IR spectrum of the aglycone RS-2(A) indicated the presence of –OH group(s) in Venetoclax it. The RS-2(A) aglycone, underwent acetylation with (Ac2O and Pyridine), to an acetylated

product, m.p. 159–160°, molecular formula C29H30O11 and M+ 554 (CIMS). The estimation of the acetyl group (24.04%) by Weisenberger method as described by Belcher and Godbert confirmed the presence of three –OH groups in RS-2(A). The IR band at Vmax (KBr) 2927.6 cm−1 in the IR spectrum of RS-2 (A) showed the presence of methoxyl group(s) in it. The estimation of methoxyl group (22%) by Zeisel’s method indicated the presence of three methoxyl groups in the aglycone RS-2 (A). Thus based on the above facts, a tentative structure of the aglycone RS-2(A) was assigned in Fig. 1. The bathochromic shift of 45 nm in band I with AlCl3 (relative to MeOH) and 16 nm in band II with NaOAc (relative to MeOH) showed the presence of –OH groups at C-5 and C-7 respectively in RS-2(A). I. RS-2(A) gave a pink colored solution with Mg/HCl, which became blue on addition of NaHCO3 and indicated the presence of –OH group at C-4 in

RS-2(A). As such based on above facts a tentative structure to the aglycone RS-2(A) was assigned in Fig. 2. For establishing the position of the remaining groups the compound was made to undergo cyclization followed by alkaline to oxidation. RS-2(A) under cyclization on heating with HCOOH followed by alkaline oxidation when it yielded a compound, m.p. 179–180°, molecular formula C13H16O4 and M+ 236 (CIMS). The oxidized product was identified as; 8-methoxy-2,2-dimethyl-chroman-6-carboxylic acid by m.m.p. and superimposable spectral analysis and is shown in Fig. 3. Because C-5, C-7, C-4 positions were already occupied with –OH groups, therefore the remaining three methoxyl groups cannot be fixed at these positions in RS-2(A). The position of one of the methoxyl group at C-6 was established by the absence of green precipitate, when aqueous solution of RS-2(A) was treated with SrSO4 (solid). The presence of one methoxyl group at C-3 position was supported by the fact that no bathochromic shift in the band II with AlCl3 was observed, which indicated that there was one-OCH3 group at C-3 in RS-2(A) as depicted in Graph 4.