Interesting facts
Interesting Facts about (1R,2S)-2-phenylcyclopropanamine
(1R,2S)-2-phenylcyclopropanamine is a fascinating compound known for its unique structure and potential applications in various fields. The cyclopropane ring is a three-membered carbon ring that is both strained and reactive, which can lead to interesting chemical behavior. Here are some enticing aspects of this compound:
- Structural Significance: The specific stereochemistry, indicated by the (1R,2S) configuration, plays a vital role in its biological activity. Stereochemistry can greatly influence how molecules interact with biological systems, making it essential in drug development.
- Pharmaceutical Potential: Compounds like (1R,2S)-2-phenylcyclopropanamine are often studied for their activity as neurotransmitter reuptake inhibitors. They may have implications for treating neurological disorders, which makes them a valuable focus of research.
- Reactivity and Synthesis: The presence of the cyclopropane ring in its structure renders the compound quite reactive. This can pave the way for interesting synthetic pathways that lead to new derivatives with enhanced properties.
- Research Insights: Studies on cyclopropane derivatives have shown that they can mimic larger structures in biological systems, allowing researchers to explore new ways to develop targeted therapies.
- Mechanistic Understanding: Investigating the mechanism of action of this compound can lead to deeper insights into how certain drugs work at the molecular level, opening doors for more effective treatments.
As researchers continue to explore the properties and applications of (1R,2S)-2-phenylcyclopropanamine, it is evident that compounds with such unique architectures hold the key to numerous scientific advancements. The journey of uncovering their secrets can lead to innovations not just in chemistry but also in medicine and beyond!
Synonyms
tranylcypromine
155-09-9
95-62-5
Tranilcipromina
Parnitene
Tranylcyprominum
trans-2-Phenylcyclopropylamine
Cyclopropanamine, 2-phenyl-, (1R,2S)-rel-
SKF Trans-385
SKF 385
trans-DL-2-Phenylcyclopropylamine
NSC 80664
UNII-3E3V44J4Z9
CCRIS 3344
HSDB 3404
3E3V44J4Z9
EINECS 205-841-9
BRN 3195803
Tranylcyprominum [INN-Latin]
rac-(1R,2S)-2-phenylcyclopropan-1-amine
Tranilcipromina [INN-Spanish]
DTXSID2023694
3-12-00-02797 (Beilstein Handbook Reference)
Cyclopropanamine, 2-phenyl-, (1S,2R)-
Tranylcyprominum (INN-Latin)
Tranilcipromina (INN-Spanish)
NSC-80664
Tranylcypromin
trans 2 Phenylcyclopropylamine
NSC80664
(1R*,2S*)-2-phenylcyclopropan-1-amine
CHEBI:9652
N06AF04
DTXCID501473942
SKF 385'
(+-)-trans-2-phenylcyclopropylamine
205-841-9
(1R,2S)-2-phenylcyclopropan-1-amine
3721-26-4
(1R,2S)-2-phenylcyclopropanamine
Parnate
Transamine
d-Tranylcypromine
trans-2-phenyl-cyclopropylamine
(1R,2S)-tranylcypromine
(+)-(R)-Tranylcypromine
rel-Tranylcypromine
Jatrosom
l-Tranylcypromine
CHEMBL1179
(1R,2S)-2-phenyl-cyclopropylamine
Racemic Tranylcypromine
trans-(-)-2-Phenylcyclopropanamine
Cyclopropanamine, 2-phenyl-, trans-(.+/-.)-
Cyclopropylamine, 2-phenyl-, trans-(.+/-.)-
MFCD00865363
2-Phenyl-1-aminocyclopropane, trans-
Parnate (Salt/Mix)
(rel)-Tranylcypromine
SKF-trans-385
(1r,2s)-rel-2-phenylcyclopropanamine
2-Phenyl-cyclopropylamine
Cyclopropylamine, 2-phenyl-, (1S-trans)-
(.+/-.)-Tranylcypromine
MFCD00001302
TRANYLCYPROMINE [INN]
Tranylcypromine [INN:BAN]
trans-2-phenylcyclopropan-1-amine
trans amine
trans-amine
Cyclopropanamine, 2-phenyl-, trans-(+-)-
(+/-)-trans-2-phenylcyclopropylamine
(.+/-.)-trans-2-Phenylcyclopropamine
(.+/-.)-trans-2-Phenylcyclopropylamine
GJZ
BRN 2802413
(1R,2S)-rel-2-phenylcyclopropan-1-amine
Cyclopropylamine, 2-phenyl-, trans-(-)-
Cyclopropanamine, 2-phenyl-, (1R-trans)-
Cyclopropylamine, 2-phenyl-, trans-(+-)-
Prestwick0_000173
Prestwick1_000173
Prestwick2_000173
Lopac-P-8511
CBChromo1_000132
TRANYLCYPROMINE [MI]
SCHEMBL34339
TRANYLCYPROMINE [HSDB]
SPBio_001986
TRANYLCYPROMINE [VANDF]
trans-2-phenyl cyclopropylamine
(1R,2S)-trans-tranylcypromine
TRANYLCYPROMINE [WHO-DD]
(Trans)-2-phenylcyclopropanamine
[trans-2-phenylcyclopropyl]amine
CHEBI:94631
cid_2723716
CHEBI:131510
DTXSID201015773
[(trans)-2-phenylcyclopropyl]amine
BDBM50240772
NSC789036
PDSP2_001079
PDSP2_001080
(1R-trans)-2-phenyl-cyclopropanamine
AKOS006282586
(1R,2S)-2-phenyl-1-cyclopropanamine
cyclopropane, trans-1-amino-2-phenyl-
NSC-789036
(1R,2S)-(-)-2-phenylcyclopropylamine
NCGC00015848-01
NCGC00015848-07
NCGC00015848-09
(tranylcypromine)2-Phenyl-cyclopropylamine
AC-15970
BS-50045
DA-77397
CS-0099373
trans-(1R,2S)-2-Phenylcyclopropan-1-amine
EN300-197006
EN300-253001
BRD-K47029922-003-03-4
BRD-K47029922-003-10-9
BRD-K47029922-003-11-7
Solubility of (1R,2S)-2-phenylcyclopropanamine
The solubility of (1R,2S)-2-phenylcyclopropanamine in various solvents can provide crucial insights into its chemical behavior and potential applications. This compound is characterized by its unique cyclopropane structure, which can influence its interaction with solvents.
Key Points on Solubility:
In summary, the solubility of (1R,2S)-2-phenylcyclopropanamine is influenced by various factors, including solvent polarity, temperature, and pH. Understanding these factors can aid in optimizing conditions for reactions or extractions involving this intriguing compound.