Catalogue Number
BF-G2016
Analysis Method
HPLC,NMR,MS
Specification
98%
Storage
-20℃
Molecular Weight
622.87
Appearance
White powder
Botanical Source
Panax ginseng,Panax notoginseng,Panax quinqueflius
Structure Type
Terpenoids
Category
Standards;Natural Pytochemical;API
SMILES
CC(=CCCC(C)(C1CCC2(C1C(CC3C2(CCC4C3(CCC(C4(C)C)OC5C(C(C(C(O5)CO)O)O)O)C)C)O)C)O)C
Synonyms
(3β,12β,20R)-12,20-Dihydroxydammar-24-en-3-yl β-D-glucopyranoside/20(R)-Ginsenoside Rh2/20(R)-Ginsenoside-Rh2/b-D-Glucopyranoside, (3b,12b,20R)-12,20-dihydroxydammar-24-en-3-yl/Ginsenoside-Rh2/(R) Ginsenoside Rh2/(3beta,12beta)-12,20-dihydroxydammar-24-en-3-yl beta-d-glucopyranoside/20-(R)-Ginsenoside Rh2/β-D-Glucopyranoside, (3β,12β,20R)-12,20-dihydroxydammar-24-en-3-yl/20(R)-GINSENOSIDERH2/Ginsenoside Rh2, 20(R)-
IUPAC Name
(2R,3R,4S,5S,6R)-2-[[(3S,5R,8R,9R,10R,12R,13R,14R,17S)-12-hydroxy-17-[(2R)-2-hydroxy-6-methylhept-5-en-2-yl]-4,4,8,10,14-pentamethyl-2,3,5,6,7,9,11,12,13,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol
Density
1.19
Solubility
Methanol
Flash Point
393.1±32.9 °C
Boiling Point
726.4±60.0 °C at 760 mmHg
Melting Point
InChl
InChI=1S/C36H62O8/c1-20(2)10-9-14-36(8,42)21-11-16-35(7)27(21)22(38)18-25-33(5)15-13-26(32(3,4)24(33)12-17-34(25,35)6)44-31-30(41)29(40)28(39)23(19-37)43-31/h10,21-31,37-42H,9,11-19H2,1-8H3/t21-,22+,23+,24-,25+,26-,27-,28+,29-,30+,31-,33-,34+,35+,36+/m0/s1
InChl Key
CKUVNOCSBYYHIS-SUEBGMEDSA-N
WGK Germany
RID/ADR
HS Code Reference
2938900000
Personal Projective Equipment
Correct Usage
For Reference Standard and R&D, Not for Human Use Directly.
Meta Tag
provides coniferyl ferulate(CAS#:112246-15-8) MSDS, density, melting point, boiling point, structure, formula, molecular weight etc. Articles of coniferyl ferulate are included as well.>> amp version: coniferyl ferulate
COA
No Article Available.
Description :
20(R)-Ginsenoside Rh2, a matrix metalloproteinase (MMP) inhibitor, acts as a cell antiproliferator. It has anticancer effects via blocking cell proliferation and causing G1 phase arrest. 20(R)-Ginsenoside Rh2 induces apoptosis, and has anti-inflammatory and antioxidative activity[1][2][3].
