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Merck
CN

72674

1,2-Dioleoyl-sn-glycero-3-phosphoethanolamine, pyrene-labeled

BioReagent, suitable for fluorescence, ≥98.0% (TLC)

Synonym(s):

L-β,γ-Dioleoyl-α-cephaline, pyrene-labeled, N-(1-Pyrenesulfonyl)-1,2-dioleoyl-sn-glycero-3-phosphoethanolamine, Phosphatidylethanolamine 18:1, pyrene-labeled

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About This Item

Empirical Formula (Hill Notation):
C57H86NO10PS
Molecular Weight:
1008.33
UNSPSC Code:
12352200
PubChem Substance ID:
MDL number:
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InChI

1S/C57H86NO10PS/c1-3-5-7-9-11-13-15-17-19-21-23-25-27-29-31-36-54(59)65-46-51(68-55(60)37-32-30-28-26-24-22-20-18-16-14-12-10-8-6-4-2)47-67-69(61,62)66-45-44-58-70(63,64)53-43-41-50-39-38-48-34-33-35-49-40-42-52(53)57(50)56(48)49/h17-20,33-35,38-43,51,58H,3-16,21-32,36-37,44-47H2,1-2H3,(H,61,62)/b19-17+,20-18+/t51-/m1/s1

SMILES string

CCCCCCCC\C=C\CCCCCCCC(=O)OC[C@H](COP(O)(=O)OCCNS(=O)(=O)c1ccc2ccc3cccc4ccc1c2c34)OC(=O)CCCCCCC\C=C\CCCCCCCC

InChI key

VQMRCQVKHOAKOB-YQAYVEMKSA-N

product line

BioReagent

assay

≥98.0% (TLC)

form

powder

fluorescence

λex 323 nm; λem 378 nm in methanol

suitability

suitable for fluorescence

storage temp.

−20°C

Storage Class

13 - Non Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

Regulatory Information

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Woo Jun Shim et al.
Cell systems, 11(6), 625-639 (2020-12-06)
Determining genes that orchestrate cell differentiation in development and disease remains a fundamental goal of cell biology. This study establishes a genome-wide metric based on the gene-repressive trimethylation of histone H3 at lysine 27 (H3K27me3) across hundreds of diverse cell
Clayton E Friedman et al.
Cell stem cell, 23(4), 586-598 (2018-10-06)
Cardiac differentiation of human pluripotent stem cells (hPSCs) requires orchestration of dynamic gene regulatory networks during stepwise fate transitions but often generates immature cell types that do not fully recapitulate properties of their adult counterparts, suggesting incomplete activation of key

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