Ginsenoside F2 supplier | CasNO.62025-49-4

Name
GINSENOSIDE F2
EINECS
CAS No. 62025-49-4
Article Data8
CAS DataBase
Density 1.303 g/cm³
Solubility
Melting Point
Formula C₄₂H₇₂O₁₃
Boiling Point 871.488 °C at 760 mmHg
Molecular Weight 785.026
Flash Point 480.858 °C
Transport Information
Appearance
Safety
Risk Codes
Molecular Structure
Hazard Symbols
Synonyms Dammarane,b-D-glucopyranoside deriv.;Ginsenoside F2;
PSA 218.99000
LogP 2.14900

Synthetic route

: 52705-93-8
ginsenoside Rd

: 62025-49-4
ginsenoside F2

Conditions

Conditions	Yield
With water at 30℃; Microbiological reaction;	74%
With recombinant β-glucosidase CcBgl1A from Cellulosimicrobium cellulans sp. 21 In aq. phosphate buffer at 30℃; for 2h; pH=5.5; Enzymatic reaction;	62 mg
With Aspergillus oryzae β-galactosidase; water In aq. phosphate buffer at 50℃; for 1h; pH=4.5; Enzymatic reaction;

: 41753-43-9, 132929-86-3
Ginsenoside Rb1

A: 62025-49-4
ginsenoside F2

B: 80321-69-3
3-O-(β-D-glucopyranosyl)-20-O-[β-D-glucopyranosyl-(1→6)-β-D-glucopyranosyl]-3β,12β,20β-trihydroxydammar-24-ene

Conditions

Conditions	Yield
With water at 30℃; for 36h; Microbiological reaction;	A 58% B n/a
With recombinant β-glycosidase from Microbacterium sp. Gsoil 167, Ile184Ala, Ile389Ala, Phe390Ala mutant for 1h; Time; Enzymatic reaction;

: 108194-57-6
3,20-di-O-(2',3',4',6'-tetra-O-acetyl-β-D-glucopyranosyl)dammar-24-en-3β,12β,20S-triol

: 62025-49-4
ginsenoside F2

Conditions

Conditions	Yield
With sodium methylate In methanol Yield given;

: 6892-79-1
(20S)-dammar-24-ene-3α,12β,20-triol

: 62025-49-4
ginsenoside F2

Conditions

Conditions	Yield
Multi-step reaction with 4 steps 1: chromic anhydride / pyridine 2: sodium borohydride / propan-2-ol 3: silver oxide / CH2Cl2 4: 0.1M sodium methoxide / methanol View Scheme
Multi-step reaction with 4 steps 1: chromic anhydride / pyridine 2: sodium borohydride / propan-2-ol 3: silver oxide / CH2Cl2 4: 0.1M sodium methoxide / methanol View Scheme
Multi-step reaction with 4 steps 1: chromic anhydride / pyridine 2: sodium borohydride / propan-2-ol 3: silver oxide / CH2Cl2 4: 0.1M sodium methoxide / methanol View Scheme
Multi-step reaction with 4 steps 1: chromic anhydride / pyridine 2: sodium borohydride / propan-2-ol 3: silver oxide / CH2Cl2 4: 0.1M sodium methoxide / methanol View Scheme

: 6892-79-1, 7755-01-3, 30636-90-9, 38243-15-1, 53368-76-6, 103834-30-6
protopanaxadiol

: 62025-49-4
ginsenoside F2

Conditions

Conditions	Yield
Multi-step reaction with 2 steps 1: silver oxide / CH2Cl2 2: 0.1M sodium methoxide / methanol View Scheme
Multi-step reaction with 2 steps 1: silver oxide / CH2Cl2 2: 0.1M sodium methoxide / methanol View Scheme
Multi-step reaction with 2 steps 1: silver oxide / CH2Cl2 2: 0.1M sodium methoxide / methanol View Scheme
Multi-step reaction with 2 steps 1: silver oxide / CH2Cl2 2: 0.1M sodium methoxide / methanol View Scheme

: 51116-90-6
12-β-O-hydroxy-20(S)-hydroxydammarane-24-ene-3-one

: 62025-49-4
ginsenoside F2

Conditions

Conditions	Yield
Multi-step reaction with 3 steps 1: sodium borohydride / propan-2-ol 2: silver oxide / CH2Cl2 3: 0.1M sodium methoxide / methanol View Scheme
Multi-step reaction with 3 steps 1: sodium borohydride / propan-2-ol 2: silver oxide / CH2Cl2 3: 0.1M sodium methoxide / methanol View Scheme
Multi-step reaction with 3 steps 1: sodium borohydride / propan-2-ol 2: silver oxide / CH2Cl2 3: 0.1M sodium methoxide / methanol View Scheme
Multi-step reaction with 3 steps 1: sodium borohydride / propan-2-ol 2: silver oxide / CH2Cl2 3: 0.1M sodium methoxide / methanol View Scheme

: 41753-43-9, 132929-86-3
Ginsenoside Rb1

A: 62025-49-4
ginsenoside F2

B: 39262-14-1
compound K

Conditions

Conditions	Yield
With Fusarium sp.,(YMF1.02193) In methanol at 28℃; Microbiological reaction;
With recombinant β-glycosidase from Microbacterium sp. Gsoil 167, Ile184Ala, Ile389Ala, Phe390Ala mutant for 24h; Kinetics; Time; Enzymatic reaction;

: 41753-43-9, 132929-86-3
Ginsenoside Rb1

: 62025-49-4
ginsenoside F2

Conditions

Conditions	Yield
With Fusarium oxysporum(YMF1.02670) In methanol at 28℃; Microbiological reaction;	5 mg
Multi-step reaction with 2 steps 1: water / 36 h / 30 °C / Microbiological reaction 2: water / 72 h / 30 °C / Microbiological reaction View Scheme
With β-galactosidase from Aspergillus saponins; water In methanol at 60℃; for 96h; Enzymatic reaction;

: 80321-69-3
3-O-(β-D-glucopyranosyl)-20-O-[β-D-glucopyranosyl-(1→6)-β-D-glucopyranosyl]-3β,12β,20β-trihydroxydammar-24-ene

: 62025-49-4
ginsenoside F2

Conditions

Conditions	Yield
With water at 30℃; for 72h; Microbiological reaction;

: 11021-13-9, 68406-26-8, 82166-13-0, 82166-14-1, 146987-67-9
Ginsenoside Rb3

A: 62025-49-4
ginsenoside F2

B: 3-O-β-D-glucopyranosyl-20-O-[β-D-xylopyranosyl-(1→6)-β-D-glucopyranosyl]-20(S)-protopanaxadiol

Conditions

Conditions	Yield
With recombinant β-glycosidase from Microbacterium sp. Gsoil 167, wild-type for 120h; Enzymatic reaction;

: 41753-43-9, 132929-86-3
Ginsenoside Rb1

A: 62025-49-4
ginsenoside F2

B: 52705-93-8
ginsenoside Rd

Conditions

Conditions	Yield
With recombinant β-glycosidase from Microbacterium sp. Gsoil 167, wild-type for 24h; Enzymatic reaction;

: 11021-13-9, 68406-26-8, 82166-13-0, 82166-14-1, 146987-67-9
ginsenoside Rb2

A: 62025-49-4
ginsenoside F2

B: 3-O-(β-D-glucopyranosyl)-20-O-[α-L-arabinopyranosyl-(1→6)-β-D-glucopyranosyl]-3β,12β,20β-trihydroxydammar-24-ene

Conditions

Conditions	Yield
With recombinant β-glycosidase from Microbacterium sp. Gsoil 167, Ile184Ala, Ile389Ala, Phe390Ala mutant for 1h; Time; Enzymatic reaction;

: 11021-13-9, 68406-26-8, 82166-13-0, 82166-14-1, 146987-67-9
ginsenoside Rb2

A: 62025-49-4
ginsenoside F2

B: 52705-93-8
ginsenoside Rd

Conditions

Conditions	Yield
With recombinant β-glycosidase from Microbacterium sp. Gsoil 167, wild-type for 24h; Enzymatic reaction;

: 11021-13-9, 68406-26-8, 82166-13-0, 82166-14-1, 146987-67-9
ginsenoside Rb2

A: 62025-49-4
ginsenoside F2

B: 39262-14-1
compound K

Conditions

Conditions	Yield
With recombinant β-glycosidase from Microbacterium sp. Gsoil 167, Ile184Ala, Ile389Ala, Phe390Ala mutant for 120h; Kinetics; Enzymatic reaction;

Ginsenoside F2 Specification

The cas register number of Ginsenoside F2 is 62025-49-4. It also can be called as b-D-Glucopyranoside, (3b,12b)-12-hydroxydammar-24-ene-3,20-diyl bis- and the Systematic name about this chemical is (3β,12β)-20-(β-D-glucopyranosyloxy)-12-hydroxydammar-24-en-3-yl β-D-glucopyranoside. It belongs to the Ginseng series.

Physical properties about Ginsenoside F2 are: (1)ACD/LogP: 3.24; (2)# of Rule of 5 Violations: 3; (3)ACD/LogD (pH 5.5): 4; (4)ACD/LogD (pH 7.4): 4; (5)ACD/BCF (pH 5.5): 285; (6)ACD/BCF (pH 7.4): 285; (7)ACD/KOC (pH 5.5): 1987; (8)ACD/KOC (pH 7.4): 1987; (9)#H bond acceptors: 13; (10)#H bond donors: 9; (11)#Freely Rotating Bonds: 19; (12)Polar Surface Area: 218.99 Å²; (13)Index of Refraction: 1.594; (14)Molar Refractivity: 204.424 cm³; (15)Molar Volume: 602.655 cm³; (16)Polarizability: 81.04x10^-24cm³; (17)Surface Tension: 63.767 dyne/cm; (18)Enthalpy of Vaporization: 143.908 kJ/mol.

You can still convert the following datas into molecular structure:
(1)SMILES: O([C@@H]3C(C)(C)[C@@H]4CC[C@@]2(C)[C@]5(C)CC[C@H]([C@](O[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O)(C)CC\C=C(/C)C)[C@H]5[C@H](O)C[C@@H]2[C@@]4(C)CC3)[C@@H]6O[C@@H]([C@@H](O)[C@H](O)[C@H]6O)CO
(2)InChI: InChI=1/C42H72O13/c1-21(2)10-9-14-42(8,55-37-35(51)33(49)31(47)25(20-44)53-37)22-11-16-41(7)29(22)23(45)18-27-39(5)15-13-28(38(3,4)26(39)12-17-40(27,41)6)54-36-34(50)32(48)30(46)24(19-43)52-36/h10,22-37,43-51H,9,11-20H2,1-8H3/t22-,23+,24+,25+,26-,27+,28-,29-,30+,31+,32-,33-,34+,35+,36-,37-,39-,40+,41+,42-/m0/s1
(3)InChIKey: SWIROVJVGRGSPO-JBVRGBGGBD
(4)Std. InChI: InChI=1S/C42H72O13/c1-21(2)10-9-14-42(8,55-37-35(51)33(49)31(47)25(20-44)53-37)22-11-16-41(7)29(22)23(45)18-27-39(5)15-13-28(38(3,4)26(39)12-17-40(27,41)6)54-36-34(50)32(48)30(46)24(19-43)52-36/h10,22-37,43-51H,9,11-20H2,1-8H3/t22-,23+,24+,25+,26-,27+,28-,29-,30+,31+,32-,33-,34+,35+,36-,37-,39-,40+,41+,42-/m0/s1
(5)Std. InChIKey: SWIROVJVGRGSPO-JBVRGBGGSA-N

Product Name

GINSENOSIDE F2

Synthetic route

Ginsenoside F2 Specification

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