16948-04-2

16948-04-2 structure

Name: 3-(5-METHYL-FURAN-2-YL)-PROPIONALDEHYDE
Chemical Name: boc-lys(z)-oh dcha
CAS Number: 16948-04-2
Molecular Formula: C₃₁H₅₁N₃O₆
Molecular Weight: 561.75300
Catalog: Biochemical Amino acids and their derivatives Lysine derivative
Create Date: 2018-12-02 17:08:51
Modify Date: 2024-01-22 17:31:20
Boc-Lys(Z)-OH (DCHA) is a involves in synthesis thymosin β4, βg and β6 fragments, and increases E-rosette forming capacity in Lupus Nephritis model. Boc-Lys(Z)-OH (DCHA) involves in synthesis Boc-Lyz-OCH3 and acts as a reagent of peptidyl thrombin inhibitors production[1][2][3].

Name	boc-lys(z)-oh dcha
Synonyms	N-cyclohexylcyclohexanamine,(2S)-2-[(2-methylpropan-2-yl)oxycarbonylamino]-6-(phenylmethoxycarbonylamino)hexanoic acid MFCD00066511 Nalpha-BOC-Nepsilon-CBZ-L-Lysine DCHA EINECS 241-018-0

Description	Boc-Lys(Z)-OH (DCHA) is a involves in synthesis thymosin β4, βg and β6 fragments, and increases E-rosette forming capacity in Lupus Nephritis model. Boc-Lys(Z)-OH (DCHA) involves in synthesis Boc-Lyz-OCH3 and acts as a reagent of peptidyl thrombin inhibitors production[1][2][3].
Related Catalog	Signaling Pathways >> Others >> Others Research Areas >> Inflammation/Immunology
References	[1]. Abiko, et al. Synthesis of six common amino acid sequence fragments of thymosins beta 4, beta 8 and beta 9 and determination of their effects on the low E-rosette forming cells of lupus nephritis patients. Chemical & pharmaceutical bulletin, 1984. [2]. Cal PM, et al. Iminoboronates: a new strategy for reversible protein modification. J Am Chem Soc. 2012 Jun 20;134(24):10299-305. [3]. Van Boeckel, et al. Preparation of peptidyl thrombin inhibitors: World Intellectual Property Organization, WO9807308. 1998-02-26.

Personal Protective Equipment	Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
Safety Phrases	S24/25
RIDADR	NONH for all modes of transport
WGK Germany	3
HS Code	29224985

Precursor 0
DownStream 1
63958-90-7