HRID547239

反应详情

EQUATION

反应方程式

REACTANTS

反应物

结构：O=S1(=O)OC(c2ccc(O)cc2)(c2ccc(O)cc2)c2ccccc21

HCID4766

Phenol red

C19H14O5S

HCID79784

Glycine, N-[2-hydroxy-1,1-bis(hydroxymethyl)ethyl]-

C6H13NO5

HCID93573

Tromethamine hydrochloride

C4H12ClNO3

HCID3423265

Sodium Lauryl Sulfate

C12H25NaO4S

$结构：CCOc1ccc(Nc2ccc(/C(=C3\C=CC(=[N+](CC)Cc4cccc(S(=O)(=O)O)c4)C=C3C)c3ccc(N(CC)Cc4cccc(S(=O)(=O)O)c4)cc3C)cc2)cc1$

HCID6333920

未命名化合物

PRODUCTS

生成物

结构：CCCCCCCCCCCCOS(=O)(=O)[O-].O=C(O)CNC(CO)(CO)CO.[Na+]

HCID23667616

未命名化合物

AUXILIARIES

试剂、催化剂与溶剂

溶剂HCID753

Glycerol

C3H8O3

PROCEDURE

实验过程

20 μl 2× Tricine Sample Buffer—Non-reducing (TSB-NR) (300 mM Tris-HCl, pH 8.45, 24% Glycerol, 8% SDS, 0.005% Coomassie Blue G, 0.005% Phenol Red) were added to 20 μl Pre-stained markers (Bio-Rad), and 20 μl per well were used.

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-8563d15ca27b4ed2817cb767ae73f7fc
来源数据集: uspto-grants-2011_05
DOI: 10.6084/m9.figshare.5104873.v1
专利: US07939075B2
来源说明: uspto-grants-2011_05

反应 SMILES

[NH:1]([C:6]([CH2:11][OH:12])([CH2:9][OH:10])[CH2:7][OH:8])[CH2:2][C:3]([OH:5])=[O:4].C(O)C(N)(CO)CO.Cl.[CH3:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH2:31][CH2:32][CH2:33][O:34][S:35]([O-:38])(=[O:37])=[O:36].[Na+:39].CCN(C1C=CC(/C(/C2C=CC(NC3C=CC(OCC)=CC=3)=CC=2)=C2/C=CC(C=C/2C)=[N+](CC2C=CC=C(S(O)(=O)=O)C=2)CC)=C(C)C=1)CC1C=CC=C(S(O)(=O)=O)C=1.C1C=CC2S(=O)(=O)OC(C3C=CC(O)=CC=3)(C3C=CC(O)=CC=3)C=2C=1>OCC(CO)O>[NH:1]([C:6]([CH2:9][OH:10])([CH2:11][OH:12])[CH2:7][OH:8])[CH2:2][C:3]([OH:5])=[O:4].[CH3:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH2:31][CH2:32][CH2:33][O:34][S:35]([O-:38])(=[O:37])=[O:36].[Na+:39]