Trilloside A

Base Information

• Chemical Name: Trilloside A
• CAS No.: 55659-75-1
• Molecular Formula: C₄₅H₇₂O₁₇
• Molecular Weight: 885.056
• Wikidata: Q105193869
• Mol file: 55659-75-1.mol

Synonyms:Trilloside A;2-[4-Hydroxy-6-(hydroxymethyl)-2-(5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-16-yl)oxy-5-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol;AKOS037515088;FT-0775737

Chemical Property of Trilloside A

Chemical Property:

• Melting Point: 298-300 °C (decomp)
• Boiling Point: °Cat760mmHg
• PKA: 12?+-.0.70(Predicted)
• Flash Point: °C
• PSA: 255.91000
• Density: 1.42g/cm³
• LogP: 0.21410
• XLogP3: 0.8
• Hydrogen Bond Donor Count: 9
• Hydrogen Bond Acceptor Count: 17
• Rotatable Bond Count: 8
• Exact Mass: 884.47695082
• Heavy Atom Count: 62
• Complexity: 1620

Purity/Quality:

99%, ^*data from raw suppliers

Deltonin ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

• Canonical SMILES: CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)CO)O)O)O)O)OC9C(C(C(C(O9)C)O)O)O)C)C)C)OC1

Technology Process of Trilloside A

There total 4 articles about Trilloside A which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

(3β,25R)-spirost-5-en-3-yl O-β-D-glucopyranosyl-(1->3)-O-β-D-glucopyranosyl-(1->4)-O-[α-L-rhamnopyranosyl-(1->2)]-β-D-glucopyranoside → diosgenin 3-O-<α-L-rhamnopyranosyl(1<*>2)>-<β-D-glucopyranosyl(1<*>4)>-β-D-glucopyranoside (53846-52-9,99661-97-9,55659-75-1)

Guidance literature:

With steroidal saponin-β-glucosidase from Aspergillus flavus; In aq. buffer; at 50 ℃; pH=5; Enzymatic reaction;

DOI:10.1016/j.molcatb.2013.09.013

Reference yield:

(25R)-26-[(β-D-glucopyranosyl)oxy]-22α-hydroxyfurost-5-en-3β-yl O-β-D-glucopyranosyl-(1→4)-O-[α-L-rhamnopyranosyl-(1→2)]-β-D-glucopyranoside (1240293-61-1) → D-Glucose (2280-44-6) + diosgenin 3-O-<α-L-rhamnopyranosyl(1<*>2)>-<β-D-glucopyranosyl(1<*>4)>-β-D-glucopyranoside (53846-52-9,99661-97-9,55659-75-1)

Guidance literature:

With β-D-glucosidase; water; acetic acid; In aq. acetate buffer; at 20 ℃; for 13h; Enzymatic reaction;

DOI:10.1021/acs.jafc.1c05782

Reference yield:

(25R)-O-β-D-glucopyranosyl-22-O-methylfurost-5-ene-3β,22ξ,26-triol 3-O-2)-O-<β-D-glucopyranosyl-(1->4)>-β-D-glucopyranoside> (94992-07-1) → diosgenin 3-O-<α-L-rhamnopyranosyl(1<*>2)>-<β-D-glucopyranosyl(1<*>4)>-β-D-glucopyranoside (53846-52-9,99661-97-9,55659-75-1)

Guidance literature:

In water; at 37 ℃; for 4h; almond emulsin;

upstream raw materials:

(25R)-O-β-D-glucopyranosyl-22-O-methylfurost-5-ene-3β,22ξ,26-triol 3-O-2)-O-<β-D-glucopyranosyl-(1->4)>-β-D-glucopyranoside>

(25R)-26-[(β-D-glucopyranosyl)oxy]-22α-hydroxyfurost-5-en-3β-yl O-β-D-glucopyranosyl-(1→4)-O-[α-L-rhamnopyranosyl-(1→2)]-β-D-glucopyranoside

Downstream raw materials:

ophiopogonin C

trillin

diosgenin

(25R)-5-en-spirostane-3β-ol 3-O-β-D-glucopyranosyl-(1→4)-β-D-glucopyranoside

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