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Details

Stereochemistry ABSOLUTE
Molecular Formula C9H11N
Molecular Weight 133.1903
Optical Activity ( - )
Defined Stereocenters 1 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 1-AMINOINDANE, (R)-

SMILES

N[C@@H]1CCC2=C1C=CC=C2

InChI

InChIKey=XJEVHMGJSYVQBQ-SECBINFHSA-N
InChI=1S/C9H11N/c10-9-6-5-7-3-1-2-4-8(7)9/h1-4,9H,5-6,10H2/t9-/m1/s1

HIDE SMILES / InChI
Molecular Formula C9H11N
Molecular Weight 133.1903
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 1 / 1
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

Unknown
139594
PubMed

PubMed

TitleDatePubMed
Comparative neuroprotective effects of rasagiline and aminoindan with selegiline on dexamethasone-induced brain cell apoptosis.
2009 Apr
Patents

Patents

04501735
2
05639913
2
05877218
2
05877221
2
05880159
2
05914349
2
05994408
2
06271263
2
06303650
2
06462222
2
06528685
2
06538025
2
06703392
4
07348332
2
07598258
2
07910595
4
07923561
2
07994324
2
08022062
3
08044100
4
08067445
5
08163740
8
08188284
2
08207177
4
08236950
5
08362044
5
08367687
2
08367836
2
08426449
4
08470859
2
08552023
2
08580780
5
08835654
2
JP4782252B2
2
Substance Class Chemical
Created
by admin
on Sat Dec 16 10:52:05 UTC 2023
Edited
by admin
on Sat Dec 16 10:52:05 UTC 2023
Record UNII
I17RC77CJ2
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
1-AMINOINDANE, (R)-
Common Name English
((1R)-2,3-DIHYDRO-1H-INDEN-1-YL)AMINE
Systematic Name English
(1R)-2,3-DIHYDRO-1H-INDEN-1-AMINE
Systematic Name English
1H-INDEN-1-AMINE, 2,3-DIHYDRO-, (1R)-
Systematic Name English
1-AMINOINDAN, (-)-
Systematic Name English
(1R)-2,3-DIHYDRO-1H-INDENE-1-AMINE
Systematic Name English
TV-136
Code English
1-INDANAMINE, (R)-
Systematic Name English
(-)-1-AMINOINDAN
Systematic Name English
Code System Code Type Description
CAS
10277-74-4
Created by admin on Sat Dec 16 10:52:05 UTC 2023 , Edited by admin on Sat Dec 16 10:52:05 UTC 2023
PRIMARY
PUBCHEM
2733933
Created by admin on Sat Dec 16 10:52:05 UTC 2023 , Edited by admin on Sat Dec 16 10:52:05 UTC 2023
PRIMARY
EPA CompTox
DTXSID70370045
Created by admin on Sat Dec 16 10:52:05 UTC 2023 , Edited by admin on Sat Dec 16 10:52:05 UTC 2023
PRIMARY
FDA UNII
I17RC77CJ2
Created by admin on Sat Dec 16 10:52:05 UTC 2023 , Edited by admin on Sat Dec 16 10:52:05 UTC 2023
PRIMARY
Related Record Type Details
Structure of 1-AMINOINDANE
RACEMATE -> ENANTIOMER
Related Record Type Details
Structure of RASAGILINE
PARENT -> METABOLITE
major metabolite, 1(R)-aminoindan, which is not an MAO inhibitor, has been therapeutically active in animal models relevant to Parkinson?s disease
MAJOR
PLASMA
NIH
NCATS
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