50170
Gly-Asp
≥99.0%
Synonym(s):
Glycyl-L-aspartic acid
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About This Item
Linear Formula:
NH2CH2CONHCH(COOH)CH2COOH
CAS Number:
Molecular Weight:
190.15
UNSPSC Code:
12352209
NACRES:
NA.22
PubChem Substance ID:
EC Number:
225-140-1
Beilstein/REAXYS Number:
1727387
MDL number:
InChI key
SCCPDJAQCXWPTF-VKHMYHEASA-N
InChI
1S/C6H10N2O5/c7-2-4(9)8-3(6(12)13)1-5(10)11/h3H,1-2,7H2,(H,8,9)(H,10,11)(H,12,13)/t3-/m0/s1
SMILES string
NCC(=O)N[C@@H](CC(O)=O)C(O)=O
assay
≥99.0%
optical activity
[α]20/D +12.0±2°, c = 5% in H2O
reaction suitability
reaction type: solution phase peptide synthesis
mp
195-210 °C (dec.)
application(s)
peptide synthesis
Quality Level
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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D S Eggleston et al.
International journal of peptide and protein research, 19(2), 206-211 (1982-02-01)
The crystal structure of the acidic dipeptide glycyl-L-aspartic acid dihydrate, Gly-L-Asp X 2H2O, C6H10N2O5 X 2H2O, has been determined by means of three-dimensional counter X-ray data. The dipeptide crystallizes in space group P212121 of the orthorhombic system with four formula
Florian Rohm et al.
Molecular nutrition & food research, 63(5), e1801094-e1801094 (2018-12-07)
Peptide transporter 1 (PEPT1) function is well understood, yet little is known about its contribution toward the absorption of dietary amino acids in the form of di- and tripeptides. In the present human study, changes in plasma concentrations of a
Hyangmi Kim et al.
Archives of microbiology, 199(4), 597-603 (2016-12-29)
A Gram-negative, aerobic, non-motile, rod-shaped bacterial strain, designated MAB-07
Soo-Il Kim et al.
Phytomedicine : international journal of phytotherapy and phytopharmacology, 79, 153351-153351 (2020-09-29)
Since enhanced bone resorption due to osteoclast differentiation and activation cause skeletal diseases, there is a growing need in therapeutics for combating bone-resorbing osteoclasts. Botanical antioxidants are being increasingly investigated for their health-promoting effects on bone. Edible Cirsium setidens contains
R Chitra et al.
Acta crystallographica. Section C, Crystal structure communications, 63(Pt 1), o11-o13 (2007-01-09)
The title bis(glycyl-L-aspartic acid) oxalate complex {systematic name: bis[2-(2-ammonioacetamido)butanedioic acid] oxalate 0.4-hydrate}, 2C6H11N2O5+.C2O4(2-).4H2O, crystallizes in a triclinic space group with the planar peptide unit in a trans conformation. The asymmetric unit consists of two glycyl-L-aspartic acid molecules with positively charged
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