
CAS 163061-74-3: (1S,2S)-1-Amino-2-indanol
Formula:C9H11NO
InChI:InChI=1S/C9H11NO/c10-9-7-4-2-1-3-6(7)5-8(9)11/h1-4,8-9,11H,5,10H2/t8-,9-/m0/s1
InChI key:InChIKey=LOPKSXMQWBYUOI-IUCAKERBSA-N
SMILES:N[C@H]1C=2C(C[C@@H]1O)=CC=CC2
Synonyms:- (1S,2S)-1-Amino-2-indanol
- 1H-Inden-2-ol, 1-amino-2,3-dihydro-, (1S-trans)-
- 1H-Inden-2-ol, 1-amino-2,3-dihydro-, (1S,2S)-
- (1S,2S)-1-Amino-2,3-dihydro-1H-inden-2-ol
- trans-(1S,2S)-1-Amino-2-indanol
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Found 5 products.
(1S,2S)-(+)-1-Amino-2-indanol
CAS:(1S,2S)-(+)-1-Amino-2-indanolPurity:97%Color and Shape:White-Pale Yellow SolidMolecular weight:149.19g/mol(1S,2S)-(+)-Trans-1-amino-2-indanol
CAS:(1S,2S)-(+)-Trans-1-amino-2-indanol is the enantiomer of (1R,2R)-(-)-trans-1-amino-2-indanol. It is an inhibitor of the viral protein kinase that is responsible for the viral DNA replication cycle. (1S,2S)-(+)-trans-1-amino-2-indanol blocks the activity of a pump that transports ions across cellular membranes. The compound has been shown to be effective against herpes simplex virus type 1 and hepatitis C virus in cell culture studies. The antiviral effect of (1S,2S)-(+)-trans-1-amino-2-indanol may be due to its ability to inhibit the pump that transports ions across cellular membranes. This inhibition leads to an increase in intracellular sodium levels which causes cells to swell and burst.Formula:C9H11NOPurity:Min. 95%Molecular weight:149.19 g/molRef: 3D-FT44521
Discontinued product(1S,2S)-(+)-trans-1-Amino-2-indanol
CAS:Purity:99.0%Color and Shape:SolidMolecular weight:149.19299316406251H-Inden-2-ol, 1-amino-2,3-dihydro-, (1S,2S)-
CAS:Formula:C9H11NOPurity:97%Color and Shape:SolidMolecular weight:149.18974(1S,2S)-(+)-1-Amino-2-indanol
CAS:Formula:C9H11NOPurity:>98.0%(GC)Color and Shape:White to Orange to Green powder to crystalMolecular weight:149.19