M/Z: 578.2159

Hit 1 annotations: 8-Acetoxypinoresinol 4-glucoside_[M-H2O+NH4]+

在BioDeep NovoCell知识数据库中，参考离子总共被划分为4个级别。

Confirmed: 这个参考离子已经通过手动审计得到确认和验证。
Reliable: 这个参考离子可能在特定的解剖组织环境中高度保守。
Unreliable: 这个参考离子具有较高的排名价值，但缺乏可重复性。
Unavailable: 由于排名价值低且缺乏可重复性，这个参考离子不应用于注释。

Found 5 Reference Ions Near m/z 578.2159

NovoCell ID	m/z	Mass Window	Metabolite	Ranking	Anatomy Context
MSI_000008888 Unreliable	578.2067	578.2067 ~ 578.2067 MzDiff: `none`	5'-(4-Hydroxy-(E)-cinnamoyl) alpha-L-arabinofuranosyl-(1->3)-beta-D-xylopyranosyl-(1->4)-D-xylopyranoside (BioDeep_00000026173) Formula: C24H32O15 (560.1741)	3.22 (100%)	Mus musculus [UBERON:0004645] urinary bladder urothelium
MSI_000008939 Unreliable	578.2159	578.2159 ~ 578.2159 MzDiff: `none`	8-Acetoxypinoresinol 4-glucoside (BioDeep_00000022017) Formula: C28H34O13 (578.1999)	3.19 (100%)	Mus musculus [UBERON:0004645] urinary bladder urothelium
MSI_000024930 Unreliable	578.2062	578.2062 ~ 578.2062 MzDiff: `none`	5'-(4-Hydroxy-(E)-cinnamoyl) alpha-L-arabinofuranosyl-(1->3)-beta-D-xylopyranosyl-(1->4)-D-xylopyranoside (BioDeep_00000026173) Formula: C24H32O15 (560.1741)	1.75 (100%)	Mus musculus [UBERON:0004269] upper arm connective tissue
MSI_000000769 Unavailable	578.2067	578.2067 ~ 578.2067 MzDiff: `none`	5'-(4-Hydroxy-(E)-cinnamoyl) alpha-L-arabinofuranosyl-(1->3)-beta-D-xylopyranosyl-(1->4)-D-xylopyranoside (BioDeep_00000026173) Formula: C24H32O15 (560.1741)	-0.59 (100%)	Mus musculus [CL:0000066] epithelial cell
MSI_000000831 Unavailable	578.2159	578.2159 ~ 578.2159 MzDiff: `none`	8-Acetoxypinoresinol 4-glucoside (BioDeep_00000022017) Formula: C28H34O13 (578.1999)	-0.62 (100%)	Mus musculus [CL:0000066] epithelial cell

Found 1 Sample Hits

Metabolite	Species	Sample
8-Acetoxypinoresinol 4-glucoside Formula: C28H34O13 (578.1999) Adducts: [M-H2O+NH4]+ (Ppm: 12.6)	Mus musculus (Urinary bladder)	HR2MSI_mouse_urinary_bladder - S096 Resolution: 10μm, 260x134 Description Mass spectrometry imaging of phospholipids in mouse urinary bladder (imzML dataset) The spatial distribution of phospholipids in a tissue section of mouse urinary bladder was analyzed by MALDI MS imaging at 10 micrometer pixel size with high mass resolution (using an LTQ Orbitrap mass spectrometer). R, ö, mpp A, Guenther S, Schober Y, Schulz O, Takats Z, Kummer W, Spengler B, Histology by mass spectrometry: label-free tissue characterization obtained from high-accuracy bioanalytical imaging. Angew Chem Int Ed Engl, 49(22):3834-8(2010) Fig. S2: Single ion images of compounds shown in Fig. 1A-B : (upper left to lower right) m/z = 743.5482 (unknown), m/z = 741.5307 (SM (16:0), [M+K]+), m/z = 798.5410 (PC (34:1), [M+K]+), m/z = 616.1767 (heme b, M+), m/z = 772.5253 (PC (32:0), [M+K]+). Stability of determined mass values was in the range of +/- 1 ppm over 22 hours of measurement (Fig. S4), with a standard deviation of 0.56 ppm. Accuracy data were obtained during tissue scanning experiments by monitoring the mass signal at nominal mass 798. The internal lock mass function of the Orbitrap instrument was used for automatic calibration during imaging measurements, using the known matrix-related ion signals at m/z = 137.0233, m/z = 444.0925 and m/z = 716.1246.

Metabolite

Species

Sample

8-Acetoxypinoresinol 4-glucoside

Formula: C28H34O13 (578.1999)
Adducts: [M-H2O+NH4]+ (Ppm: 12.6)

Mus musculus (Urinary bladder)

HR2MSI_mouse_urinary_bladder - S096

Resolution: 10μm, 260x134

Description

Mass spectrometry imaging of phospholipids in mouse urinary bladder (imzML dataset)
The spatial distribution of phospholipids in a tissue section of mouse urinary bladder was analyzed by MALDI MS imaging at 10 micrometer pixel size with high mass resolution (using an LTQ Orbitrap mass spectrometer).

R, ö, mpp A, Guenther S, Schober Y, Schulz O, Takats Z, Kummer W, Spengler B, Histology by mass spectrometry: label-free tissue characterization obtained from high-accuracy bioanalytical imaging. Angew Chem Int Ed Engl, 49(22):3834-8(2010)

Fig. S2: Single ion images of compounds shown in Fig. 1A-B : (upper left to lower right) m/z = 743.5482 (unknown), m/z = 741.5307 (SM (16:0), [M+K]+), m/z = 798.5410 (PC (34:1), [M+K]+), m/z = 616.1767 (heme b, M+), m/z = 772.5253 (PC (32:0), [M+K]+).

Stability of determined mass values was in the range of +/- 1 ppm over 22 hours of measurement (Fig. S4), with a standard deviation of 0.56 ppm. Accuracy data were obtained during tissue scanning experiments by monitoring the mass signal at nominal mass 798. The internal lock mass function of the Orbitrap instrument was used for automatic calibration during imaging measurements, using the known matrix-related ion signals at m/z = 137.0233, m/z = 444.0925 and m/z = 716.1246.