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408433

Boc-His-OH

Name: Boc-His-OH
Brand: ALDRICH

99%

Synonym(s):

N_α-(tert-Butoxycarbonyl)-L-histidine, N_α-Boc-L-histidine

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About This Item

Empirical Formula (Hill Notation):

C₁₁H₁₇N₃O₄

CAS Number:

17791-52-5

Molecular Weight:

255.27

NACRES:

NA.22

PubChem Substance ID:

24865569

eCl@ss:

32160406

UNSPSC Code:

12352209

EC Number:

241-768-9

MDL number:

MFCD00065576

Beilstein/REAXYS Number:

755289

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Properties

Quality Level

100

assay

99%

optical activity

[α]20/D +26°, c = 1 in methanol

reaction suitability

reaction type: Boc solid-phase peptide synthesis

mp

195 °C (dec.) (lit.)

application(s)

peptide synthesis

SMILES string

CC(C)(C)OC(=O)N[C@@H](Cc1c[nH]cn1)C(O)=O

InChI

1S/C11H17N3O4/c1-11(2,3)18-10(17)14-8(9(15)16)4-7-5-12-6-13-7/h5-6,8H,4H2,1-3H3,(H,12,13)(H,14,17)(H,15,16)/t8-/m0/s1

InChI key

AYMLQYFMYHISQO-QMMMGPOBSA-N

Description

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Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

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Exploring advantages/disadvantages and improvements in overcoming gene delivery barriers of amino acid modified trimethylated chitosan.

Hao Zheng et al.

Pharmaceutical research, 32(6), 2038-2050 (2014-12-24)

Present study aimed at exploring advantages/disadvantages of amino acid modified trimethylated chitosan in conquering multiple gene delivery obstacles and thus providing comprehensive understandings for improved transfection efficiency. Arginine, cysteine, and histidine modified trimethyl chitosan were synthesized and employed to self-assemble

Transport and signaling via the amino acid binding site of the yeast Gap1 amino acid transceptor.

Griet Van Zeebroeck et al.

Nature chemical biology, 5(1), 45-52 (2008-12-09)

Transporter-related nutrient sensors, called transceptors, mediate nutrient activation of signaling pathways through the plasma membrane. The mechanism of action of transporting and nontransporting transceptors is unknown. We have screened 319 amino acid analogs to identify compounds that act on Gap1

Global Trade Item Number

SKU	GTIN
408433-5G	04061832642055