All Photos(1)



17:1 Lyso PE

1-(10Z-heptadecenoyl)-sn-glycero-3-phosphoethanolamine, chloroform

1-heptadecenoyl-2-hydroxy-sn-glycero-3-phosphoethanolamine; PE(17:1(10Z)/0:0); 110699
Empirical Formula (Hill Notation):
Molecular Weight:


>99% (LPE; may contain up to 10% of the 2-LPE isomer, TLC)


pkg of 1 × 1 mL (856707C-5mg)


5 mg/mL (856707C-5mg)

shipped in

dry ice

storage temp.


SMILES string



5 mL Clear Glass Sealed Ampule (856707C-5mg)


Skull and crossbonesHealth hazard

Signal Word


Hazard Classifications

Acute Tox. 3 Inhalation - Acute Tox. 4 Oral - Aquatic Chronic 3 - Carc. 2 - Eye Irrit. 2 - Repr. 2 - Skin Irrit. 2 - STOT RE 1 - STOT SE 3

Target Organs

Central nervous system

Storage Class Code

6.1D - Non-combustible, acute toxic Cat.3 / toxic hazardous materials or hazardous materials causing chronic effects

WGK Germany


Flash Point(F)

does not flash

Flash Point(C)

does not flash

Certificate of Analysis

Certificate of Origin

Peng Wu et al.
Chinese medicine, 15, 9-9 (2020-01-31)
Our previous clinical evidence suggested that the direct application of "Sanse powder" the main ingredient of "Yiceng" might represent an alternative treatment for knee osteoarthritis. However, the mechanism underlying its effect is poorly understood. In this study, we investigated the...
Tsukasa Yagi et al.
Cancers, 12(1) (2020-01-01)
Ovarian cancer remains a highly lethal disease due to its late clinical presentation and lack of reliable early biomarkers. Protein-based diagnostic markers have presented limitations in identifying ovarian cancer. We tested the potential of phospholipids as markers of ovarian cancer...
Biyu Hou et al.
Life sciences, 245, 117352-117352 (2020-02-02)
The depot-specific differences in lipidome of visceral adipose tissue (VAT) and subcutaneous adipose tissue (SAT) reflect heterogeneity of white adipose tissue (WAT), which plays a central role in its distinct response to outside stimuli. However, the detailed lipidome of depot-specific...
Jordon M Inloes et al.
Biochemistry, 57(39), 5759-5767 (2018-09-18)
Deleterious mutations in the serine hydrolase DDHD domain containing 1 (DDHD1) cause the SPG28 subtype of the neurological disease hereditary spastic paraplegia (HSP), which is characterized by axonal neuropathy and gait impairments. DDHD1 has been shown to display PLA1-type phospholipase...

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