Home Other Building Blocks b-D-Glucopyranoside, (3b,12b)-12-hydroxydammara-20,24-dien-3-yl2-O-b-D-glucopyranosyl-

b-D-Glucopyranoside, (3b,12b)-12-hydroxydammara-20,24-dien-3-yl2-O-b-D-glucopyranosyl-

CAS No.:
494753-69-4
Catalog Number:
AG00DHMR
Molecular Formula:
Molecular Weight:
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Product Description
Catalog Number:
AG00DHMR
Chemical Name:
b-D-Glucopyranoside, (3b,12b)-12-hydroxydammara-20,24-dien-3-yl2-O-b-D-glucopyranosyl-
CAS Number:
494753-69-4
MDL Number:
MFCD28124355
IUPAC Name:
(2S,3R,4S,5S,6R)-2-[(2R,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-2-[[(3S,5R,8R,9R,10R,12R,13R,14R,17S)-12-hydroxy-4,4,8,10,14-pentamethyl-17-(6-methylhepta-1,5-dien-2-yl)-2,3,5,6,7,9,11,12,13,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]oxan-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol
InChI:
InChI=1S/C42H70O12/c1-21(2)10-9-11-22(3)23-12-16-42(8)30(23)24(45)18-28-40(6)15-14-29(39(4,5)27(40)13-17-41(28,42)7)53-38-36(34(49)32(47)26(20-44)52-38)54-37-35(50)33(48)31(46)25(19-43)51-37/h10,23-38,43-50H,3,9,11-20H2,1-2,4-8H3/t23-,24-,25-,26-,27+,28-,29+,30+,31-,32-,33+,34+,35-,36-,37+,38+,40+,41-,42-/m1/s1
InChI Key:
KWDWBAISZWOAHD-MHOSXIPRSA-N
Properties
Complexity:
1370  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
19  
Defined Bond Stereocenter Count:
0
Exact Mass:
766.487g/mol
Formal Charge:
0
Heavy Atom Count:
54  
Hydrogen Bond Acceptor Count:
12  
Hydrogen Bond Donor Count:
8  
Isotope Atom Count:
0
Molecular Weight:
767.01g/mol
Monoisotopic Mass:
766.487g/mol
Rotatable Bond Count:
10  
Topological Polar Surface Area:
199A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
5.4  
Literature
Title Journal
Structural-Activity Relationship of Ginsenosides from Steamed Ginseng in the Treatment of Erectile Dysfunction. The American journal of Chinese medicine 20180101
Metabolomic investigation of the anti-platelet aggregation activity of ginsenoside Rk₁ reveals attenuated 12-HETE production. Journal of proteome research 20121005
Induction of apoptosis by ginsenoside Rk1 in SK-MEL-2-human melanoma. Archives of pharmacal research 20120301
Cholesterol-derived novel anti-apoptotic agents on the structural basis of ginsenoside Rk1. Bioorganic & medicinal chemistry letters 20101201
Autophagy inhibition enhances apoptosis induced by ginsenoside Rk1 in hepatocellular carcinoma cells. Bioscience, biotechnology, and biochemistry 20091001
Anti-tumor activity of the ginsenoside Rk1 in human hepatocellular carcinoma cells through inhibition of telomerase activity and induction of apoptosis. Biological & pharmaceutical bulletin 20080501
Panaxadiol glycosides that induce neuronal differentiation in neurosphere stem cells. Journal of natural products 20070801
Memory enhancing and neuroprotective effects of selected ginsenosides. Archives of pharmacal research 20050301
Three new dammarane glycosides from heat processed ginseng. Archives of pharmacal research 20020801
Properties