Interesting facts
Interesting Facts about 2-(2-methyl-5-nitro-imidazol-1-yl)ethanol
2-(2-methyl-5-nitro-imidazol-1-yl)ethanol is a fascinating compound that merges the worlds of synthetic chemistry and medicinal applications. Here are some intriguing facts:
- Pharmaceutical Significance: One of the most compelling aspects of this compound is its role in the development of pharmaceuticals. Its structure features an imidazole ring, which is pivotal in many bioactive molecules.
- Mechanism of Action: This compound is often studied for its action mechanism in affecting nitroreductase enzymes, which play a critical role in microbial metabolism. This makes it of particular interest for researchers focused on antibiotic drug development.
- Research Potential: Due to its nitro group, it's often researched for its potential as an anti-cancer agent. The nitro-containing compounds have been shown to have unique interactions with cellular components, and ongoing studies continue to explore these pathways.
- Versatile Applications: Beyond pharmaceuticals, compounds similar to 2-(2-methyl-5-nitro-imidazol-1-yl)ethanol are also explored in agriculture, serving as potential herbicides and fungicides, showcasing their versatility.
- Environmental Considerations: As with many nitrogen-containing compounds, understanding the biodegradation and environmental impact of such molecules is critical. Research in this area may address safety and efficacy during active use.
In sum, 2-(2-methyl-5-nitro-imidazol-1-yl)ethanol's diverse potential in medicinal chemistry and its intriguing structural characteristics make it a compound worth following in ongoing research and development.
Synonyms
metronidazole
443-48-1
Flagyl
Metronidazol
2-Methyl-5-nitroimidazole-1-ethanol
Anagiardil
Gineflavir
Deflamon
Orvagil
MetroGel
Novonidazol
Meronidal
Metronidaz
Mexibol
Trichazol
Bayer 5360
Metronidazolo
Acromona
Flagemona
Flagesol
Giatricol
Protostat
Sanatrichom
Takimetol
Trichocide
Trichomol
Trichopol
Tricocet
Trikacide
Trikamon
Trikojol
Trikozol
Trivazol
Vertisal
Wagitran
Arilin
Atrivyl
Danizol
Efloran
Elyzol
Entizol
Flagil
Monagyl
Monasin
Trichex
Trimeks
Vagilen
Vagimid
Bexon
Clont
Eumin
Klion
Klont
MetroCream
MetroLotion
Nalox
neo-Tric
Tricowas B
MetroGel-Vaginal
2-(2-Methyl-5-nitro-1H-imidazol-1-yl)ethanol
Metromidol
Deflamon-wirkstoff
Satric
Tricom
CONT
NIDA
Noritate
Trichopal
Fossyol
Flagyl Er
Methronidazole
Metronidazolum
Flegyl
Metro I.V.
1H-Imidazole-1-ethanol, 2-methyl-5-nitro-
Metrolyl
Vandazole
Zadstat
RP 8823
NSC-50364
Metrolag
Metrotop
Rathimed
1-(2-Hydroxyethyl)-2-methyl-5-nitroimidazole
Metric 21
Tricho cordes
Trichomonacid 'pharmachim'
Tricho-gynaedron
2-(2-methyl-5-nitroimidazol-1-yl)ethanol
Metronidazole in Plastic Container
SC 10295
2-Methyl-1-(2-hydroxyethyl)-5-nitroimidazole
2-Methyl-3-(2-hydroxyethyl)-4-nitroimidazole
Zidoval
1-(beta-Ethylol)-2-methyl-5-nitro-3-azapyrrole
Flagyl I.V. RTU
1-(2-Hydroxy-1-ethyl)-2-methyl-5-nitroimidazole
Metro I.V. In Plastic Container
Caswell No. 579AA
MFCD00009750
1-Hydroxyethyl-2-methyl-5-nitroimidazole
Metronidazol [INN-Spanish]
Metronidazolum [INN-Latin]
1-(beta-Hydroxyethyl)-2-methyl-5-nitroimidazole
2-(2-methyl-5-nitro-1-imidazolyl)ethanol
CCRIS 410
2-(2-methyl-5-nitro-1H-imidazol-1-yl)ethan-1-ol
NSC 50364
FLAGYL I.V. RTU IN PLASTIC CONTAINER
1-(beta-Oxyethyl)-2-methyl-5-nitroimidazole
HSDB 3129
Imidazole-1-ethanol, 2-methyl-5-nitro-
BAY-5360
NSC69587
EINECS 207-136-1
NSC 69587
NSC-69587
EPA Pesticide Chemical Code 120401
UNII-140QMO216E
RP-8823
BRN 0611683
BAYER-5360
CHEBI:6909
DTXSID2020892
140QMO216E
2-(2-methyl-5-nitro-imidazol-1-yl)ethanol
NSC50364
DTXCID20892
MLS000028590
5-23-05-00063 (Beilstein Handbook Reference)
Metro Gel
PYLERA COMPONENT METRONIDAZOLE
HELIDAC COMPONENT METRONIDAZOLE
giniflavir
NCGC00016446-06
CAS-443-48-1
Metronidazole [USAN:USP:INN:BAN:JAN]
SMR000058175
Metronidazolo [DCIT]
Metronidazol (INN-Spanish)
Metronidazolum (INN-Latin)
METRONIDAZOLE (IARC)
METRONIDAZOLE [IARC]
Mexibol 'silanes'
METRONIDAZOLE (MART.)
METRONIDAZOLE [MART.]
1-(.beta.-Ethylol)-2-methyl-5-nitro-3-azapyrrole
1-(.beta.-Hydroxyethyl)-2-methyl-5-nitroimidazole
METRONIDAZOLE (USP-RS)
METRONIDAZOLE [USP-RS]
Flagyl 375
Trichobrol
Florazole
Mepagyl
Nidagyl
Rosased
METRONIDAZOLE (EP IMPURITY)
METRONIDAZOLE [EP IMPURITY]
METRONIDAZOLE (EP MONOGRAPH)
METRONIDAZOLE (USP IMPURITY)
METRONIDAZOLE [EP MONOGRAPH]
METRONIDAZOLE [USP IMPURITY]
WLN: T5N CNJ A2Q B1 ENW
METRONIDAZOLE (USP MONOGRAPH)
METRONIDAZOLE [USP MONOGRAPH]
Noritate (TN)
Metronidazole (USAN:USP:INN:BAN:JAN)
Metro cream & gel
Flagyl (TN)
WLN: T6NTJ DQ ANU1- ET5N CNJ A1 BNW
SR-01000000244
Polibiotic
Givagil
Metroplex
Nuvessa
Rosaced
Trikhopol
Donnan
Flazol
MetroCleanse
Rosaclear System
Mexibol'silanes'
CB-01-14 MMX
Metro IV
Vandazole (TN)
Metronidazole,(S)
Prestwick_334
metronidazole vaginal
Nuvessa (TN)
2 Methyl 5 nitroimidazole 1 ethanol
IDR-90105
LIKMEZ
Metronidazole250 mg
Metronidazole500 mg
Cimetrol 500LPCI
Metronidazole, BioXtra
Metronidazole (Flagyl)
Spectrum_001035
HELIDAC (Salt/Mix)
2-(2-methyl-5-nitroimidazolyl)ethan-1-ol
Metronidazole (Standard)
Trichomonacid'pharmachim'
Maybridge1_001999
Metronidazole Topical Gel
Opera_ID_1585
Prestwick0_000081
Prestwick1_000081
Prestwick2_000081
Prestwick3_000081
Spectrum2_000883
Spectrum3_000506
Spectrum4_000060
Spectrum5_001289
M0924
METRONIDAZOLE [MI]
CHEMBL137
Metronidazole Topical Cream
METRONIDAZOLE [INN]
METRONIDAZOLE [JAN]
METRONIDAZOLE [HSDB]
METRONIDAZOLE [USAN]
NCIOpen2_000337
SCHEMBL23042
BSPBio_000002
BSPBio_002031
KBioGR_000559
KBioSS_001515
METRONIDAZOLE [VANDF]
Metronidazole250 mg250 mg
Metronidazole500 mg500 mg
MLS000758286
MLS001424018
BIDD:GT0107
DivK1c_000007
SPECTRUM1500412
SPBio_000666
SPBio_001941
METRONIDAZOLE [WHO-DD]
METRONIDAZOLE [WHO-IP]
BPBio1_000004
Flagyl I.V. RTU (Salt/Mix)
BCBcMAP01_000184
GTPL10914
HMS500A09
HMS547C19
HY-B0318R
KBio1_000007
KBio2_001515
KBio2_004083
KBio2_006651
KBio3_001531
A01AB17
D06BX01
G01AF01
J01XD01
Metronidazole (JP17/USP/INN)
MSK5554
P01AB01
Metronidazole, analytical standard
NINDS_000007
HMS1568A04
HMS1920N19
HMS2051G07
HMS2090B19
HMS2091F14
HMS2095A04
HMS2231E11
HMS3373O05
HMS3393G07
HMS3655E22
HMS3712A04
Pharmakon1600-01500412
METRONIDAZOLE [ORANGE BOOK]
BCP13757
HY-B0318
LAC39247
Metronidazole Vaginal Gel, 0.75%
Tox21_110441
Tox21_202413
Tox21_302794
BBL005452
BDBM50375309
CCG-40016
FP-250
NSC757118
s1907
STK177359
Metronidazole 2.0 mg/ml in Methanol
AKOS000269646
AKOS005169650
Tox21_110441_1
AM01526
DB00916
KS-5140
NC00020
NSC-757118
IDI1_000007
METRONIDAZOLE COMPONENT OF PYLERA
SMP1_000189
USEPA/OPP Pesticide Code: 120401
METRONIDAZOLE COMPONENT OF HELIDAC
NCGC00016446-01
NCGC00016446-02
NCGC00016446-03
NCGC00016446-04
NCGC00016446-05
NCGC00016446-07
NCGC00016446-08
NCGC00016446-09
NCGC00016446-11
NCGC00016446-12
NCGC00016446-17
NCGC00022059-03
NCGC00022059-04
NCGC00022059-05
NCGC00256513-01
NCGC00259962-01
AC-23968
SY002821
SBI-0051447.P003
DB-051212
Metronidazole, SAJ first grade, >=99.0%
AB00052046
NS00000210
SW196613-4
EN300-16851
C07203
D00409
AB00052046-17
AB00052046_18
AB00052046_19
A826552
imidazole, 1-(2-hydroxyethyl)-2-methyl-5-nitro-
Metronidazole, VETRANAL(TM), analytical standard
Q169569
2-(2-Methyl-5-nitro-1H-imidazol-1-yl)ethanol #
SR-01000000244-4
SR-01000000244-5
BRD-K52020312-001-05-2
BRD-K52020312-001-15-1
BRD-K52020312-001-25-0
BRD-K52020312-001-26-8
METRONIDAZOLE BENZOATE IMPURITY A [EP IMPURITY]
Z87001124
F1773-0073
Metronidazole, certified reference material, TraceCERT(R)
Metronidazole, British Pharmacopoeia (BP) Reference Standard
Metronidazole, European Pharmacopoeia (EP) Reference Standard
Metronidazole, United States Pharmacopeia (USP) Reference Standard
Metronidazole, Pharmaceutical Secondary Standard; Certified Reference Material
207-136-1
56010-45-8
Solubility of 2-(2-methyl-5-nitro-imidazol-1-yl)ethanol
The solubility of 2-(2-methyl-5-nitro-imidazol-1-yl)ethanol (C6H9N3O3) is influenced by its chemical structure and functional groups. This compound features a nitro group and an imidazole ring, which can significantly affect its interaction with solvents.
Factors Affecting Solubility:
As a general observation, compounds like 2-(2-methyl-5-nitro-imidazol-1-yl)ethanol may exhibit a moderate solubility in polar solvents, while showing reduced solubility in non-polar solvents. This behavior is often summarized with the phrase:
This means that the solubility of this compound can be significantly higher in polar environments compared to non-polar ones, making it essential to consider the solvent choice when dealing with such chemical substances.