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851620

D-Norvaline

Name: <SC>D</SC>-Norvaline
Brand: ALDRICH

99%

Synonym(s):

(R)-(−)-2-Aminopentanoic acid

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About This Item

Linear Formula:

CH₃CH₂CH₂CH(NH₂)CO₂H

CAS Number:

2013-12-9

Molecular Weight:

117.15

NACRES:

NA.22

PubChem Substance ID:

24888214

eCl@ss:

32160406

UNSPSC Code:

12352200

EC Number:

217-936-2

MDL number:

MFCD00008097

Beilstein/REAXYS Number:

1721161

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Properties

assay

99%

form

crystals

optical activity

[α]20/D −24°, c = 10 in 5 M HCl

optical purity

ee: 98% (GLC)

reaction suitability

reaction type: solution phase peptide synthesis

mp

>300 °C (lit.)

application(s)

peptide synthesis

SMILES string

CCC[C@@H](N)C(O)=O

InChI

1S/C5H11NO2/c1-2-3-4(6)5(7)8/h4H,2-3,6H2,1H3,(H,7,8)/t4-/m1/s1

InChI key

SNDPXSYFESPGGJ-SCSAIBSYSA-N

Description

Physical form

α-Amino acid analog with unnatural, (R)-configuration

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)

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5-Hydroxyhexanoic Acid Predicts Early Renal Functional Decline in Type 2 Diabetes Patients with Microalbuminuria.

Xiaofang Tang et al.

Kidney & blood pressure research, 44(2), 245-263 (2019-05-10)

Diabetic nephropathy (DN) is a leading cause of end-stage renal disease. Microalbuminuria (MA) is widely used to predict early progressive renal function decline (ERFD) of DN in type 2 diabetes mellitus (T2D) patients, but the sensitivity and specificity of MA

Red fluorescent redox-sensitive biosensor Grx1-roCherry.

Arina G Shokhina et al.

Redox biology, 21, 101071-101071 (2018-12-24)

Redox-sensitive fluorescent proteins (roFPs) are a powerful tool for imaging intracellular redox changes. The structure of these proteins contains a pair of cysteines capable of forming a disulfide upon oxidation that affects the protein conformation and spectral characteristics. To date

Three-dimensional quantitative structure-activity relationship analyses of substrates of the human proton-coupled amino acid transporter 1 (hPAT1).

Iris Thondorf et al.

Bioorganic & medicinal chemistry, 19(21), 6409-6418 (2011-10-01)

The proton-coupled amino acid transporter hPAT1 has recently gained much interest due to its ability to transport small drugs thereby allowing their oral administration. A three-dimensional quantitative structure-activity relationship (3D QSAR) study has been performed on its natural and synthetic

Global Trade Item Number

SKU	GTIN
851620-5G-A	04061833324387