CHEBI:131510 - (1R,2S)-tranylcypromine

Main

ChEBI Ontology

Automatic Xrefs

Reactions

Pathways

Models

ChEBI Name (1R,2S)-tranylcypromine ChEBI ID CHEBI:131510 ChEBI ASCII Name (1R,2S)-tranylcypromine Definition A 2-phenylcyclopropan-1-amine that is the (1R,2S)-enantiomer of tranylcypromine. Stars This entity has been manually annotated by the ChEBI Team. Secondary ChEBI IDs CHEBI:94631 Supplier Information Download Molfile XML SDF Find compounds which contain this structure Find compounds which resemble this structure Take structure to the Advanced Search Formula C9H11N Net Charge 0 Average Mass 133.191 Monoisotopic Mass 133.08915 InChI InChI=1S/C9H11N/c10-9-6-8(9)7-4-2-1-3-5-7/h1-5,8-9H,6,10H2/t8-,9+/m0/s1 InChIKey AELCINSCMGFISI-DTWKUNHWSA-N SMILES [C@H]1(C2=CC=CC=C2)[C@H](N)C1 Roles Classification Chemical Role(s): Bronsted base A molecular entity capable of accepting a hydron from a donor (Bronsted acid). (via organic amino compound ) View more via ChEBI Ontology ChEBI Ontology Outgoing (1R,2S)-tranylcypromine (CHEBI:131510) is a 2-phenylcyclopropan-1-amine (CHEBI:131512) (1R,2S)-tranylcypromine (CHEBI:131510) is conjugate base of (1R,2S)-tranylcypromine(1+) (CHEBI:131517) (1R,2S)-tranylcypromine (CHEBI:131510) is enantiomer of (1S,2R)-tranylcypromine (CHEBI:131511) Incoming tranylcypromine (CHEBI:9652) has part (1R,2S)-tranylcypromine (CHEBI:131510) (1R,2S)-tranylcypromine(1+) (CHEBI:131517) is conjugate acid of (1R,2S)-tranylcypromine (CHEBI:131510) (1S,2R)-tranylcypromine (CHEBI:131511) is enantiomer of (1R,2S)-tranylcypromine (CHEBI:131510) IUPAC Name (1R,2S)-2-phenylcyclopropan-1-amine Synonyms Sources (+)-(R)-Tranylcypromine ChemIDplus (+)-Tranylcypromine ChemIDplus (1R,2S)-2-phenyl-1-cyclopropanamine ChEBI (1R,2S)-trans-tranylcypromine ChEBI d-Tranylcypromine ChemIDplus trans-2-phenylcyclopropan-1-amine ChEBI trans-2-Phenylcyclopropylamine ChemIDplus Manual Xrefs Databases CPD-17678 MetaCyc LSM-5578 LINCS View more database links Registry Numbers Types Sources 2206146 Reaxys Registry Number Reaxys 3721-28-6 CAS Registry Number ChemIDplus Citations Types Sources 27882656 PubMed citation Europe PMC 29542357 PubMed citation Europe PMC Last Modified 15 January 2020