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metabolism and cell protection
InChi: InChI=1S/C24H36O5/c1-5-15(3)24(27)29-21-11-14(2)10-17-7-6-16(4)20(23(17)21)9-8-19-12-18(25)13-22(26)28-19/h6-7
8 nM) very similar to that of Chrysamine-G
Water: 122 mg/mL(200
Smiles: CC(O)C1NC(=O)C(CCCCN)NC(=O)C(CC2=CNC3=CC=CC=C23)NC(=O)C(CC2C=CC=CC=2)NC(=O)C(CC2C=CC=CC=2)NC(=O)C(CC(N)=O)NC(=O)C(CCCCN)NC(=O)C(CSSCC(NC(=O)C(CO)NC(=O)C(CO)NC(=O)C(CC2C=CC=CC=2)NC1=O)C(=O)NC(CCCCN)C(O)=O)NC(=O)C1CCCN1
Luteolin-7-O-β-D-glucopyranoside 064icrotoxinin metabolism and cell protectionLuteolin 7 O D glucopyranoside is one of the chemical constituents of the aerial parts of codonopsis nervosa. Product information CAS Number: 70855 41 3 Molecular Weight: 610. 52 Formula: C27H30O16 Chemical Name: 2 (3,4 dihydroxyphenyl) 5 hydroxy 7 {[(2S,3R,4S,5S,6R) 3,4,5 trihydroxy 6 ({[(2R,3R,4S,5S,6R) 3,4,5 trihydroxy 6 (hydroxymethyl)oxan 2 yl]oxy}methyl)oxan 2 yl]oxy} 4H chromen 4 one Smiles: