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:
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.
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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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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