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860345C

Avanti

14:0 PC-d54

1,2-dimyristoyl-d54-sn-glycero-3-phosphocholine, chloroform

别名:

DMPC-D54

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About This Item

经验公式（希尔记法）:
C36H18NO8PD54
CAS号:
78415-49-3
分子量:
732.27
分類程式碼代碼:
51191904
NACRES:
NA.25

化驗

>99% (TLC)

形狀

liquid

包裝

pkg of 1 × 1 mL (860345C-10mg)
pkg of 1 × 4 mL (860345C-100mg)

製造商／商標名

Avanti Research™ - A Croda Brand 860345C

濃度

10 mg/mL (860345C-10mg)
25 mg/mL (860345C-100mg)

運輸包裝

dry ice

儲存溫度

−20°C

SMILES 字串

[O-]P(OCC[N+](C)(C)C)(OC[C@]([H])(OC(C([2H])([2H])C([2H])([2H])C([2H])([2H])C([2H])([2H])C([2H])([2H])C([2H])([2H])C([2H])([2H])C([2H])([2H])C([2H])([2H])C([2H])([2H])C([2H])([2H])C([2H])([2H])C([2H])([2H])[2H])=O)COC(C([2H])([2H])C([2H])([2H])C([2H])([2H

InChI

1S/C36H72NO8P/c1-6-8-10-12-14-16-18-20-22-24-26-28-35(38)42-32-34(33-44-46(40,41)43-31-30-37(3,4)5)45-36(39)29-27-25-23-21-19-17-15-13-11-9-7-2/h34H,6-33H2,1-5H3/t34-/m1/s1/i1D3,2D3,6D2,7D2,8D2,9D2,10D2,11D2,12D2,13D2,14D2,15D2,16D2,17D2,18D2,19D2,20D2,21D2,22D2,23D2,24D2,25D2,26D2,27D2,28D2,29D2

InChI 密鑰

CITHEXJVPOWHKC-RPLUSTTMSA-N

相关类别

一般說明

Deuterated fatty acids experience exchange of the deuteriums on the alpha carbon to the carbonyl, i.e., C2 position, and will therefore be a mixture of compounds that are fully deuterated and partially deuterated at that position.

應用

14:0 PC-d54 is suitable to reconstitute [ILV-13CH3, U-15N, 2H] labeled EmrE in n-dodecyl-β-D-maltopyranoside (DDM) back-exchanged to 1H at the amide positions during nuclear magnetic resonance (NMR) sample preparation. It is also suitable for the preparation of phospholipid liposomes.

包裝

5 mL Clear Glass Sealed Ampule (860345C-100mg)
5 mL Clear Glass Sealed Ampule (860345C-10mg)

法律資訊

Avanti Research is a trademark of Avanti Polar Lipids, LLC

象形圖

Skull and crossbonesHealth hazard
GHS06,GHS08

訊號詞

Danger

危險分類

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

標靶器官

Central nervous system

水污染物質分類（WGK）

WGK 3

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Jess Li et al.
The Journal of biological chemistry, 295(9), 2664-2675 (2020-01-25)
Engineering and bioconjugation of proteins is a critically valuable tool that can facilitate a wide range of biophysical and structural studies. The ability to orthogonally tag or label a domain within a multidomain protein may be complicated by undesirable side
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Vitamin K1 and vitamin K2 play very important biological roles as members of chains of electron transport as antioxidants in membranes and as cofactors for the posttranslational modification of proteins that participate in a number of physiological functions such as
Protonation of a glutamate residue modulates the dynamics of the drug transporter EmrE
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Fusion of Legionella pneumophila outer membrane vesicles with eukaryotic membrane systems is a mechanism to deliver pathogen factors to host cell membranes
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Cellular Microbiology, 17(5), 607-620 (2015)
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Journal of colloid and interface science, 574, 272-284 (2020-04-25)
Over recent years, there has been a rapid development of membrane-mimetic systems to encapsulate and stabilize planar segments of phospholipid bilayers in solution. One such system has been the use of amphipathic copolymers to solubilize lipid bilayers into nanodiscs. The
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