(Q27896637)

inferred from SMILES

mass

652.6158318 dalton

1 reference

[(3S,8R,9S,10R,13R,14R,17R)-17-[(2R,5S)-5-ethyl-6-methylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl] hexadecanoate

inferred from SMILES

stereoisomer of

1 reference

inferred from InChI

chemical formula

C₄₅H₈₀O₂

1 reference

Sitosteryl palmitate (English)

21 November 2016

canonical SMILES

CCCCCCCCCCCCCCCC(=O)OC1CCC2(C3CCC4(C(C3CC=C2C1)CCC4C(C)CCC(CC)C(C)C)C)C

1 reference

Sitosteryl palmitate (English)

21 November 2016

isomeric SMILES

CCCCCCCCCCCCCCCC(=O)O[C@H]1CC[C@@]2([C@H]3CC[C@]4([C@H]([C@@H]3CC=C2C1)CC[C@@H]4[C@H](C)CC[C@@H](CC)C(C)C)C)C

1 reference

Constituents of the roots of Boerhaavia diffusa L.I. Examination of sterols and structures of new rotenoids, boeravinones A and B.

Sitosteryl palmitate (English)

21 November 2016

1 reference

Piper betle

2 references

Polyphenols and alkaloids from piper species

Polyphenols and alkaloids from piper species

Vachellia pennatula

1 reference

Terpenes, Coumarins, and Flavones from Acacia pennatula

Angelica archangelica

1 reference

Constituents of the Umbelliferous Plants. I. Constituents of the Root of Angelica archangelica L.

Astilbe chinensis

1 reference

Cytotoxic Pentacyclic Triterpenoids from the Rhizome ofAstilbe chinensis

Astilbe rubra

1 reference

Cytotoxic Pentacyclic Triterpenoids from the Rhizome ofAstilbe chinensis

Crescentia alata

1 reference

Iridoids from Crescentia alata

Zanthoxylum leprieurii

1 reference

The isolation and structure elucidation of some derivatives of dimethylallyl-coumarin, chromone, quinoline, and phenol from Fagara species, and from Cedrelopsis grevei

Trifoliate orange

1 reference

Anti-human immunodeficiency virus-1 constituents of the bark of Poncirus trifoliata

Serenoa repens

1 reference

The contents of sabal fruits and testing of their anti-inflammatory effect

Zingiber officinale

1 reference

Metabolic Profiles of Ginger, A Functional Food, and Its Representative Pungent Compounds in Rats by Ultraperformance Liquid Chromatography Coupled with Quadrupole Time-of-Flight Tandem Mass Spectrometry.

Identifiers

InChI

InChI=1S/C45H80O2/c1-8-10-11-12-13-14-15-16-17-18-19-20-21-22-43(46)47-38-29-31-44(6)37(33-38)25-26-39-41-28-27-40(45(41,7)32-30-42(39)44)35(5)23-24-36(9-2)34(3)4/h25,34-36,38-42H,8-24,26-33H2,1-7H3/t35-,36-,38+,39+,40-,41+,42+,44+,45-/m1/s1

1 reference

Sitosteryl palmitate (English)

21 November 2016

1 reference

Global Substance Registration System

Sitosteryl palmitate (English)

21 November 2016

2 references

UNII

LEB596GYDL

https://commonchemistry.cas.org/detail?cas_rn=2308-85-2

β-sitosteryl palmitate (English)

21 November 2016

7 April 2021

1 reference

sitosterol palmitate (English)

21 November 2016

2 references

Sitosteryl palmitate (English)

21 November 2016

1 reference

1 reference

Human Metabolome Database ID

HMDB0304589

2 references

inferred from InChIKey

UNII

LEB596GYDL

2 references

Global Substance Registration System

UNII

LEB596GYDL

β-sitosteryl palmitate (English)

21 November 2016

http://www.lipidmaps.org/rest/compound/lm_id/LM/all/download

1 reference