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About This Item
Empirical Formula (Hill Notation):
C6H13O9P · 2C6H13N
CAS Number:
Molecular Weight:
458.48
PubChem Substance ID:
UNSPSC Code:
12352201
Beilstein/REAXYS Number:
3923086
MDL number:
SMILES string
NC1CCCCC1.NC2CCCCC2.O[C@@H]3[C@@H](O)[C@H](O)[C@H](OP(O)(O)=O)[C@H](O)[C@H]3O
InChI
1S/2C6H13N.C6H13O9P/c2*7-6-4-2-1-3-5-6;7-1-2(8)4(10)6(5(11)3(1)9)15-16(12,13)14/h2*6H,1-5,7H2;1-11H,(H2,12,13,14)/t;;1-,2-,3+,4+,5-,6+
InChI key
IMIHZMWNWGIJKQ-YAUWMCRJSA-N
assay
~95%
form
powder
color
white
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Storage Class
13 - Non Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
Regulatory Information
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Sophie J Bradley et al.
Nature chemical biology, 16(3), 240-249 (2020-02-23)
Cholinesterase inhibitors, the current frontline symptomatic treatment for Alzheimer's disease (AD), are associated with low efficacy and adverse effects. M1 muscarinic acetylcholine receptors (M1 mAChRs) represent a potential alternate therapeutic target; however, drug discovery programs focused on this G protein-coupled
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