Interesting facts
Interesting Facts about 2-(1H-imidazol-5-yl)ethanamine
2-(1H-imidazol-5-yl)ethanamine, commonly known as a derivative of imidazole, plays a crucial role in various biochemical and pharmacological applications. The unique structure of this compound contributes to its diverse biological activities.
Key Features
- Biological Significance: This compound acts as a precursor for several bioactive molecules and is often utilized in medicinal chemistry for drug development.
- Role in Neurotransmission: Imidazole derivatives, including this compound, are known to interact with neurotransmitter receptors, which can influence neurological processes.
- Research Applications: 2-(1H-imidazol-5-yl)ethanamine has been investigated for its potential use in treating conditions such as anxiety and depression, among other disorders.
- Dynamic Structure: The imidazole ring, a key component of this compound, is notorious for its ability to participate in hydrogen bonding, enabling it to interact with various biomolecules.
The versatility of 2-(1H-imidazol-5-yl)ethanamine exemplifies the intricate relationship between chemical structure and biological function. As researchers continue to explore this compound, we remain hopeful for novel therapeutic insights and applications.
"Understanding the chemical foundations of compounds like 2-(1H-imidazol-5-yl)ethanamine opens doors to innovative solutions in medicine."
Synonyms
histamine
51-45-6
2-(1H-imidazol-5-yl)ethanamine
1H-Imidazole-4-ethanamine
Ergamine
Ergotidine
2-(4-Imidazolyl)ethylamine
5-Imidazoleethylamine
Eramin
Theramine
2-(1H-Imidazol-4-yl)ethanamine
Free histamine
65592-96-3
beta-Aminoethylimidazole
2-Imidazol-4-ylethylamine
Imidazole-4-ethylamine
4-(2-Aminoethyl)-1H-imidazole
Histamine Base
2-(1H-imidazol-4-yl)ethan-1-amine
beta-Aminoethylglyoxaline
4-Imidazoleethylamine
Istamina
Histamine, Free Base
beta-Imidazolyl-4-ethylamine
Ethylamine, 2-imidazol-4-yl-
Imidazole, 4-(2-aminoethyl)-
2-(3H-Imidazol-4-yl)-ethylamine
1H-Imidazole-5-ethanamine
L-histamine
[3H]histamine
Ceplene
NSC 33792
CCRIS 6535
CHEBI:18295
HSDB 3338
beta-aminothethylglyoxaline
L-Histamin base
.beta.-Aminoethylglyoxaline
EINECS 200-100-6
MFCD00005210
NSC-33792
peremin
DTXSID4023125
UNII-820484N8I3
CHEMBL90
.beta.-Aminoethylimidazole
2-(1H-imidazol-5-yl)ethan-1-amine
4-(2-Aminoethyl)imidazole
MLS000069447
DTXCID103125
.beta.-Imidazolyl-4-ethylamine
820484N8I3
2-(1H-Imidazol-4-yl)ethylamine
NSC33792
Histamine [USAN]
Istamina [Italian]
NCGC00015513-04
SMR000059091
HISTAMINE (MART.)
HISTAMINE [MART.]
[2-(1H-imidazol-5-yl)ethyl]amine dihydrochloride
2-(3H-imidazol-4-yl)ethanamine
Histaminum
imidazole, 4(5)-(2-aminoethyl)-
CAS-51-45-6
Histaminum (TN)
Histamine (DCF)
2-imidazol-5-ylethylamine
3h-histamine
imido-
Racemic histamine
1avn
1qft
ALBB-005968
ALEROFF
Histamine (Standard)
Spectrum_000845
HISTAMINE [MI]
HISTAMINE [HSDB]
Opera_ID_1772
Spectrum2_000665
Spectrum3_000452
Spectrum4_000960
Spectrum5_000796
HISTAMINE [VANDF]
Lopac-H-7250
b-Imidazolyl-4-ethylamine
bmse000744
Histamine, >=97.0%
HISTAMINE [WHO-DD]
SCHEMBL2279
748 - Fish based sample
2-(4-Imidazolyl)ethanamine
2-imidazol-4-yl-Ethylamine
Lopac0_000595
WLN: T5M CNJ D2Z
BSPBio_001117
BSPBio_002124
KBioGR_000457
KBioGR_001580
KBioSS_000457
KBioSS_001325
DivK1c_000308
Histamine, analytical standard
SPBio_000729
(1H-imidazol-4-yl)ethylamine
BDBM7966
GTPL1204
GTPL1247
BCBcMAP01_000250
HY-B1204R
KBio1_000308
KBio2_000457
KBio2_001325
KBio2_003025
KBio2_003893
KBio2_005593
KBio2_006461
KBio3_000853
KBio3_000854
KBio3_001344
F411C768-A159-4FC0-A195-291A08BB03AA
2-(1H-Imidazol-5-yl)ethylamine
2-(3H-imidazol-4-yl)ethylamine
NINDS_000308
Bio1_000487
Bio1_000976
Bio1_001465
Bio2_000389
Bio2_000869
ethylamine, 2-(4'-imidazolyl)-
HMS1362G19
HMS1792G19
HMS1990G19
HMS3403G19
HMS3743G03
HMS3885M14
2-(1H-Imidazol-4-yl)-ethylamine
HY-B1204
Tox21_110166
[2-(1H-imidazol-4-yl)ethyl]amine
2-(1H-Imidazol-4-yl)ethanamine #
BBL004932
BDBM50121205
Histamine Dihydrochloride (Salt/Mix)
MFCD00128939
s3968
STK346752
AKOS000274386
AKOS009158347
HISTAMINE FREE BASE CRYSTALLINE
Histamine, base, >=97.0% (NT)
Tox21_110166_1
CCG-204684
CS-4697
DB05381
FS-5386
SDCCGMLS-0066601.P001
SDCCGSBI-0050577.P005
IDI1_000308
IDI1_002144
s10979
SMP1_000151
NCGC00015513-01
NCGC00015513-02
NCGC00015513-03
NCGC00015513-05
NCGC00015513-06
NCGC00015513-07
NCGC00015513-08
NCGC00015513-09
NCGC00015513-10
NCGC00015513-11
NCGC00015513-25
NCGC00093371-02
NCGC00093371-03
NCGC00093371-04
NCGC00093371-05
AC-13185
BP-11484
FH145712
Histamine, Free Base - CAS 51-45-6
SY041787
SBI-0050577.P004
CS-0368357
NS00004684
2-(1H-IMIDAZOL-4-YL)-1-ETHANAMINE
EN300-78991
Histamine, Vetec(TM) reagent grade, >=97%
C00388
D08040
F10913
Q61233
AB00053481_20
AB00053481_21
L000292
BRD-K01674964-001-19-0
BRD-K01674964-300-06-3
BRD-K01674964-300-07-1
BRD-K01674964-300-08-9
BRD-K01674964-316-01-0
Histamine, EuropePharmacopoeia (EP) Reference Standard
F2173-0575
117932-92-0
200-100-6
Solubility of 2-(1H-imidazol-5-yl)ethanamine (C5H9N3)
The solubility of 2-(1H-imidazol-5-yl)ethanamine is influenced by its unique structure as a biogenic amine and an imidazole derivative. This compound demonstrates a number of interesting solubility characteristics:
Overall, the solubility of 2-(1H-imidazol-5-yl)ethanamine showcases the importance of molecular structure in determining solvent interactions. As noted in some studies, “the amine functional groups contribute significantly to its solubility profile,” facilitating interactions with a variety of solvents and environments.