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Ginsenoside Rh2

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Name

Ginsenoside Rh2

EINECS N/A
CAS No. 78214-33-2 Density 1.19 g/cm3
PSA 139.84000 LogP 4.32480
Solubility N/A Melting Point 139-144 °C
Formula C36H62 O8 Boiling Point 726.4 °C at 760 mmHg
Molecular Weight 622.883 Flash Point 393.1 °C
Transport Information N/A Appearance White powder
Safety 24/25 Risk Codes 22
Molecular Structure Molecular Structure of 78214-33-2 (Ginsenoside Rh2) Hazard Symbols Xn
Synonyms

Dammarane,b-D-glucopyranoside deriv.;(3b,12b)-12,20-Dihydroxydammar-24-en-3-yl b-D-glucopyranoside;20(S)-Ginsenoside Rh2;20(S)-Rh2;3-O-b-D-Glucopyranosyl-20(S)-protopanaxadiol;

Article Data 10

Ginsenoside Rh2 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 Å2; (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 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. It 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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