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About This Item
Empirical Formula (Hill Notation):
C10H12ClN5O4 · 0.5H2O
CAS Number:
Molecular Weight:
310.69
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
205-678-3
MDL number:
Assay:
97%
Form:
powder
InChI
1S/2C10H12ClN5O4.H2O/c2*11-10-14-7(12)4-8(15-10)16(2-13-4)9-6(19)5(18)3(1-17)20-9;/h2*2-3,5-6,9,17-19H,1H2,(H2,12,14,15);1H2/t2*3-,5-,6-,9-;/m11./s1
InChI key
WRURCFOLSGPTMO-IZGCVNAISA-N
SMILES string
O[C@H]1[C@@H](O)[C@H](N(C=N2)C3=C2C(N)=NC(Cl)=N3)O[C@@H]1CO.O[C@H]4[C@@H](O)[C@H](N(C=N5)C6=C5C(N)=NC(Cl)=N6)O[C@@H]4CO.O
assay
97%
form
powder
mp
160 °C (dec.) (lit.)
functional group
chloro, ether
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Brian H Trieu et al.
The Journal of physiology, 593(13), 2889-2907 (2015-04-24)
Extended trains of theta rhythm afferent activity lead to a biphasic response facilitation in field CA1 but not in the lateral perforant path input to the dentate gyrus. Processes that reverse long-term potentiation in field CA1 are not operative in
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