Yamogenin (Neodiosgenin) is a diastereomer of diosgenin. Yamogenin (Neodiosgenin) antagonizes the activation of the liver X receptor (LXR) in luciferase ligand assay. Yamogenin (Neodiosgenin) inhibits triacylglyceride (TG) accumulation through the suppression of gene expression of fatty acid synthesis in HepG2 hepatocytes.

For the detailed information of yamogenin, the solubility of yamogenin in water, the solubility of yamogenin in DMSO, the solubility of yamogenin in PBS buffer, the animal experiment（test） (test) of yamogenin, the cell expriment (test) of yamogenin, the in vivo, in vitro and clinical trial test of yamogenin, the EC50, IC50,and Affinity of yamogenin,, please contact DC Chemicals.

Medchemexpress, HY-N2078 10mg Yamogenin CAS:512-06-1 Yamogenin (Neodiosgenin) is a diastereomer of diosgenin. Yamogenin (Neodiosgenin) antagonizes the activation of the liver X receptor (LXR) in luciferase ligand assay. Yamogenin (Neodiosgenin) inhibits triacylglyceride (TG) accumulation through the suppression of gene expression of fatty acid synthesis in HepG2 hepatocytes. Purity:>98% Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.

Chinese Factory Supply Best Quality 512-06-1 with Safe Delivery

• Molecular Formula:C27H42O3
• Molecular Weight:414.629
• Appearance/Colour:White Solid 
• Vapor Pressure:2.59E-13mmHg at 25°C 
• Melting Point:193-199°C 
• Refractive Index:1.564 
• Boiling Point:527.1oC at 760 mmHg 
• Flash Point:272.6oC 
• PSA：38.69000 
• Density:1.13g/cm3 
• LogP:5.71390 

(20α,22R,25S)-Spirosta-5-ene-3β-ol(Cas 512-06-1) Usage

InChI:InChI=1/C27H42O3/c1-16-7-12-27(29-15-16)17(2)24-23(30-27)14-22-20-6-5-18-13-19(28)8-10-25(18,3)21(20)9-11-26(22,24)4/h5,16-17,19-24,28H,6-15H2,1-4H3/t16-,17-,19-,20+,21-,22-,23-,24-,25-,26-,27+/m0/s1

512-06-1 Relevant articles

Spirostanol saponins from the rhizomes of Tacca chantrieri and their cytotoxic activity.

Yokosuka, Akihito,Mimaki, Yoshihiro,Sashida, Yutaka

, p. 73 - 78 (2002)

The rhizomes of Tacca chantrieri have be...

OLIGOFURO- AND SPIRO-STANOSIDES OF ASPARAGUS ADSCENDENS

Sharma, S. C.,Sharma, H. C.

, p. 645 - 648 (1984)

Two oligofurostanosides and two spirosta...

Steroidal and pregnane glycosides from the rhizomes of Tacca chantrieri

Yokosuka, Akihito,Mimaki, Yoshihiro,Sashida, Yutaka

, p. 1293 - 1298 (2002)

The rhizomes of Tacca chantrieri have be...

Steroidal saponin from Polygonatum verticillatum

Gvazava,Skhirtladze

, p. 1052 - 1055 (2018/03/21)

New steroidal glycoside 1 was isolated b...

Mild and selective deprotection method of acetylated steroids and diterpenes by dibutyltin oxide

Wang, Shao-Min,Zhang, Yan-Bing,Liu, Hong-Min,Yu, Guo-Bin,Wang, Ke-Rang

, p. 26 - 30 (2007/10/03)

Dibutyltin oxide (DBTO) was first utiliz...

512-06-1 Process route

C₆₃H₁₀₆O₂₂

512-06-1

yamogenin

Conditions

Conditions	Yield
With sulfuric acid; In methanol; water; for 8h; Reflux;

(25S)-spirost-5-en-3-ol 3-O-β-D-glucopyranosyl-(1→3)-[β-D-fucopyranosyl-(1→2)]-β-D-glucopyranosyl-(1→4)-β-D-galactopyranoside

512-06-1

yamogenin

Conditions

Conditions	Yield
With sulfuric acid; In methanol; water; for 8h; Reflux;	23.8 mg

512-06-1 Upstream products

• 
  91327-42-3

  (25S)-spirost-5-en-3β-yl O-β-D-glucopyranosyl-(1→2)-O-[β-D-xylopyranosyl-(1→3)]-O-β-D-glucopyranosyl-(1→4)-β-D-galactopyranoside

• 
  67-56-1

  methanol

• 
  7647-01-0

  hydrogenchloride

• 
  64-17-5

  ethanol

512-06-1 Downstream products

• 
  6808-14-6

  pseudodiosgenin

• 
  4965-78-0

  O-(toluene-4-sulfonyl)-yamogenin

• 
  512-04-9

  diosgenin

• 
  151534-39-3

  3-tert-butyldiphenylsilyldiosgenin