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128549-96-2 | 1H-Indole-3-acetamide, N-(20-amino-4-hydroxy-4,8,12,17-tetraazaeicos-1-yl)-
CAS No: 128549-96-2 Catalog No: AG000Y70 MDL No:
Product Description
Catalog Number:
AG000Y70
Chemical Name:
1H-Indole-3-acetamide, N-(20-amino-4-hydroxy-4,8,12,17-tetraazaeicos-1-yl)-
CAS Number:
128549-96-2
Molecular Formula:
C26H47N7O2
Molecular Weight:
489.6971
IUPAC Name:
N-[3-[3-[3-[4-(3-aminopropylamino)butylamino]propylamino]propyl-hydroxyamino]propyl]-2-(1H-indol-3-yl)acetamide
InChI:
InChI=1S/C26H47N7O2/c27-11-5-14-28-12-3-4-13-29-15-6-16-30-17-7-19-33(35)20-8-18-31-26(34)21-23-22-32-25-10-2-1-9-24(23)25/h1-2,9-10,22,28-30,32,35H,3-8,11-21,27H2,(H,31,34)
InChI Key:
LIURIBSBVUMOJS-UHFFFAOYSA-N
SMILES:
NCCCNCCCCNCCCNCCCN(CCCNC(=O)Cc1c[nH]c2c1cccc2)O
Properties
Complexity:
526
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
489.379g/mol
Formal Charge:
0
Heavy Atom Count:
35
Hydrogen Bond Acceptor Count:
7
Hydrogen Bond Donor Count:
7
Isotope Atom Count:
0
Molecular Weight:
489.709g/mol
Monoisotopic Mass:
489.379g/mol
Rotatable Bond Count:
22
Topological Polar Surface Area:
131A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
0.6
Literature
| Title | Journal |
|---|---|
| Reduction in endocannabinoid tone is a homeostatic mechanism for specific inhibitory synapses. | Nature neuroscience 20100501 |
| An inhibitor of TRPV1 channels isolated from funnel Web spider venom. | Biochemistry 20051129 |
| Effects of Na+-Ca2+ exchanger activity on the alpha-amino-3-hydroxy-5-methyl-4-isoxazolone-propionate-induced Ca2+ influx in cerebellar Purkinje neurons. | Neuroscience 20050101 |
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