27505
D-Citrulline
≥99.0%, for peptide synthesis
Synonym(s):
(R)-2-Amino-5-ureidopentanoic acid
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About This Item
Empirical Formula (Hill Notation):
C6H13N3O3
CAS Number:
Molecular Weight:
175.19
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352209
MDL number:
Beilstein/REAXYS Number:
1725415
Product Name
D-Citrulline, ≥99.0%
InChI key
RHGKLRLOHDJJDR-SCSAIBSYSA-N
SMILES string
N[C@H](CCCNC(N)=O)C(O)=O
InChI
1S/C6H13N3O3/c7-4(5(10)11)2-1-3-9-6(8)12/h4H,1-3,7H2,(H,10,11)(H3,8,9,12)/t4-/m1/s1
assay
≥99.0%
form
powder
optical activity
[α]20/D −20.5±2.0°, c = 2% in 1 M HCl
reaction suitability
reaction type: solution phase peptide synthesis
application(s)
peptide synthesis
storage temp.
−20°C
Quality Level
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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Sylvain V Costes et al.
PLoS computational biology, 3(8), e155-e155 (2007-08-07)
Several proteins involved in the response to DNA double strand breaks (DSB) form microscopically visible nuclear domains, or foci, after exposure to ionizing radiation. Radiation-induced foci (RIF) are believed to be located where DNA damage occurs. To test this assumption
S V Costes et al.
Mutation research, 704(1-3), 78-87 (2010-01-12)
DNA damage sensing proteins have been shown to localize to the sites of DNA double strand breaks (DSB) within seconds to minutes following ionizing radiation (IR) exposure, resulting in the formation of microscopically visible nuclear domains referred to as radiation-induced
Nikhil Vadhavkar et al.
Radiation research, 182(3), 273-281 (2014-07-31)
In contrast to the classic view of static DNA double-strand breaks (DSBs) being repaired at the site of damage, we hypothesize that DSBs move and merge with each other over large distances (μm). As X-ray dose increases, the probability of
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