Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C9H11N |
| Molecular Weight | 133.1903 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
NC1CC2=C(C1)C=CC=C2
InChI
InChIKey=LMHHFZAXSANGGM-UHFFFAOYSA-N
InChI=1S/C9H11N/c10-9-5-7-3-1-2-4-8(7)6-9/h1-4,9H,5-6,10H2
| Molecular Formula | C9H11N |
| Molecular Weight | 133.1903 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Carbonic anhydrase inhibitors. Design of anticonvulsant sulfonamides incorporating indane moieties. | 2004 Dec 6 |
|
| Steady-state pharmacokinetics and pharmacodynamics of CHF3381, a novel antineuropathic pain agent, in healthy subjects. | 2005 Apr |
|
| Indantadol, a novel NMDA antagonist and nonselective MAO inhibitor for the potential treatment of neuropathic pain. | 2007 Sep |
|
| Synthesis, dopaminergic profile, and molecular dynamics calculations of N-aralkyl substituted 2-aminoindans. | 2008 Mar 15 |
|
| Synthesis and pharmacological evaluation of schiff bases of 4-(2-aminophenyl)-morpholines. | 2009 Jul |
|
| Analgesic effect of Lepidium sativum Linn. (Chandrashura) in experimental animals. | 2010 Jul |
|
| The neuroprotective mechanism of 1-(R)-aminoindan, the major metabolite of the anti-parkinsonian drug rasagiline. | 2010 Mar |
Patents
| Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 01:41:59 GMT 2023
by
admin
on
Sat Dec 16 01:41:59 GMT 2023
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| Record UNII |
1P810SQ3EY
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| Record Status |
Validated (UNII)
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WIKIPEDIA |
Designer-drugs-2-AI
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1P810SQ3EY
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SUB181269
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2975-41-9
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100000166971
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DTXSID40183902
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221-021-3
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2-Aminoindan
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76310
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| Related Record | Type | Details | ||
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ACTIVE MOIETY |
SD Rats (male)
IN-VIVO
Scientific Literature
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ACTIVE MOIETY |
Analgesic potency (ED50) in male mice (s.c.): 15.0 +/- 1.8 mg/kg (as 2-aminoindane HCL)
IN-VIVO
Scientific Literature
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