P6502
Phosphocreatine disodium salt hydrate
~98%
Synonym(s):
N-(Imino[phosphonoamino]methyl)-N-methylglycine
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About This Item
Linear Formula:
C4H8N3O5PNa2 · x H2O
CAS Number:
Molecular Weight:
255.08 (anhydrous basis)
EC Number:
MDL number:
UNSPSC Code:
12352200
PubChem Substance ID:
Recommended Products
assay
~98%
storage temp.
−20°C
SMILES string
O.[Na+].[Na+].CN(CC(O)=O)C(=N)NP([O-])([O-])=O
InChI
1S/C4H10N3O5P.2Na.H2O/c1-7(2-3(8)9)4(5)6-13(10,11)12;;;/h2H2,1H3,(H,8,9)(H4,5,6,10,11,12);;;1H2/q;2*+1;/p-2
InChI key
KZVYPOKBYRXZKS-UHFFFAOYSA-L
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Biochem/physiol Actions
Phosphocreatine, a high-energy phosphate reservoir in vertebrate and some invertebrate muscles, provides phosphate for ADP-ATP conversion.
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Product No.
Description
Pricing
Storage Class
11 - Combustible Solids
wgk_germany
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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Justin L Sparks et al.
Cell, 176(1-2), 167-181 (2019-01-01)
Covalent DNA-protein cross-links (DPCs) impede replication fork progression and threaten genome integrity. Using Xenopus egg extracts, we previously showed that replication fork collision with DPCs causes their proteolysis, followed by translesion DNA synthesis. We show here that when DPC proteolysis
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