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Ginsenoside Rh2 (78214-33-2)

Identification
Name:Ginsenoside Rh2
Synonyms:(3beta,12beta)-12,20-Dihydroxydammar-24-en-3-yl beta-D-glucopyranoside
CAS:78214-33-2
Molecular Formula: C36H62O8
Molecular Weight: 622.87
InChI: InChI=1/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
Molecular Structure: (C36H62O8) (3beta,12beta)-12,20-Dihydroxydammar-24-en-3-yl beta-D-glucopyranoside
Properties
Density:1.19 g/cm3
Refractive index:1.571
Appearance:White powder
Specification:

The beta-D-Glucopyranoside, (3beta,12beta)-12,20-dihydroxydammar-24-en-3-yl has its cas register number 78214-33-2. And it has other names, such as (3beta,12beta)-12,20-dihydroxydammar-24-en-3-yl beta-d-glucopyranoside; ginsenoside rh2; dihydroxydammar-24-en-3-yl; β-d-glucopyranoside, (3β,12β)-12,20-; r-form-ginsenoside rh2; 12β,20-dihydroxy-5α-dammar-24-en-3β-yl β-d-glucopyranoside; 3β-(β-d-glucopyranosyloxy)dammara-24-ene-12β,20-diol; 3β-(β-d-glucopyranosyl.

The characteristics of this chemical are as below: (1)ACD/LogP: 5.62; (2)# of Rule of 5 Violations: 3; (3)ACD/LogD (pH 5.5): 5.62; (4)ACD/LogD (pH 7.4): 5.62; (5)ACD/BCF (pH 5.5): 10969.9; (6)ACD/BCF (pH 7.4): 10969.83; (7)ACD/KOC (pH 5.5): 27137.27; (8)ACD/KOC (pH 7.4): 27137.09; (9)#H bond acceptors: 8; (10)#H bond donors: 6; (11)#Freely Rotating Bonds: 13; (12)Polar Surface Area: 73.84 ; (13)Index of Refraction: 1.571; (14)Molar Refractivity: 170.7 cm3; (15)Molar Volume: 519.1 cm3; (16)Polarizability: 67.67 ×10-24 cm3; (17)Surface Tension: 54.5 dyne/cm; (18)Density: 1.19 g/cm3; (19)Flash Point: 393.1 °C; (20)Enthalpy of Vaporization: 121.13 kJ/mol; (21)Boiling Point: 726.4 °C at 760 mmHg; (22)Vapour Pressure: 2.31E-24 mmHg at 25°C.

This is a kind of white powder, and it is usually be called as "Cancer buster". It is the extract of Panax ginseng C.A.Mey, and it has the function of obviously resist the growth, breed of cancer cells, and also could induce the cancer cells to differentiate and reverse to the normal cells. Besides, it could improve the resistant cells' toxicity and other pharmacological actives. What's more, it could be applied in pharmaceutics and health protection. It belongs to the product categories which is ginsenoside series.

Additionally, you could convert the following data information to obtain the molecular structure:
(1)SMILES:O([C@@H]2C(C)(C)[C@@H]3CC[C@@]1(C)[C@]4(C)CC[C@H]([C@](O)(C)CC\C=C(/C)C)[C@H]4[C@H](O)C[C@@H]1[C@@]3(C)CC2)[C@@H]5O[C@@H]([C@@H](O)[C@H](O)[C@H]5O)COCopyCopied
(2)InChI:InChI=1/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
(3)InChIKey:CKUVNOCSBYYHIS-IRFFNABBBY

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