Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C10H24N2 |
| Molecular Weight | 172.311 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
NCCCCCCCCCCN
InChI
InChIKey=YQLZOAVZWJBZSY-UHFFFAOYSA-N
InChI=1S/C10H24N2/c11-9-7-5-3-1-2-4-6-8-10-12/h1-12H2
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Synthesis, cytotoxicity, and in vitro antileishmanial activity of mono-t-butyloxycarbonyl-protected diamines. | 2011-11 |
|
| Köln-Timişoara Molecular activity combined models toward interspecies toxicity assessment. | 2009-11-20 |
|
| Guest-directed supramolecular architectures of {W36} polyoxometalate crowns. | 2009-10-05 |
|
| Novel agmatine-containing poly(amidoamine) hydrogels as scaffolds for tissue engineering. | 2005-07-12 |
|
| Adsorption of Co(II), Ni(II), Cu(II), and Zn(II) on hexagonal templated zirconia obtained thorough a sol-gel process: the effects of nanostructure on adsorption features. | 2004-09-01 |
|
| Inclusion networks of a calix[5]arene-based exoditopic receptor and long-chain alkyldiammonium ions. | 2003-10-30 |
|
| Inward rectification by polyamines in mouse Kir2.1 channels: synergy between blocking components. | 2003-07-01 |
|
| Complexation in pseudorotaxanes based on alpha-cyclodextrin and different alpha,omega-diaminoalkanes by NMR diffusion measurements. | 2002-04-19 |
|
| Investigation of the actions and antagonist activity of some polyamine analogues in vivo. | 1998-05 |
Patents
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| Code System | Code | Type | Description | ||
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DTXSID8060953
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646-25-3
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6GPF1OF9Y1
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SUBSTANCE RECORD
