Interesting facts
Interesting Facts about 3-Aminobenzamide
3-Aminobenzamide is a fascinating compound in the realm of organic chemistry, often studied for its biological significance and potential applications. Here are some key points to consider:
- Structural Features: This compound consists of a benzene ring substituted with an amino group and a carbonyl group, illustrating the structural diversity found in amides.
- Biological Importance: 3-Aminobenzamide has been extensively researched due to its role in the inhibition of certain enzymes. For instance, it can act as an inhibitor of poly(ADP-ribose) polymerases (PARPs), which are involved in DNA repair mechanisms.
- Pharmaceutical Applications: The compound is being explored in the development of therapeutic agents, especially for conditions like cancer, where targeting DNA repair pathways can enhance the efficacy of chemotherapy.
- Reactivity: Like many amides, 3-Aminobenzamide can undergo various chemical reactions, making it a useful intermediate in organic synthesis. It can be acylated or reacted with different reagents to generate a plethora of derivatives.
- Insights from Literature: According to various studies, “The potential of 3-aminobenzamide in drug design continues to expand as researchers identify novel pathways and interactions.” This underscores its relevance in medicinal chemistry.
- Research Relevance: Ongoing research continues to explore the nuances of 3-aminobenzamide, investigating its interactions and implications in cellular processes.
In summary, 3-Aminobenzamide is more than just a chemical entity; it plays a crucial role in significant biological processes and is an interesting subject for research in drug development and organic synthesis.
Synonyms
3-aminobenzamide
3544-24-9
m-Aminobenzamide
Benzamide, 3-amino-
Benzamide, m-amino-
3-Amino-benzamide
meta-aminobenzamide
3-Aminobenzimide
aniline-3-carboxamide
3-ABA
3-aminobenzoic acid amide
3-carboxamidoaniline
MFCD00007989
3-AB
CCRIS 3925
3-Aminobenzaminde
EINECS 222-586-9
UNII-8J365YF1YH
NSC 36962
3-H2NC6H4CONH2
BRN 2802373
8J365YF1YH
CHEBI:64042
HSDB 7581
NSC-36962
PARP-IN-1
CHEMBL81977
3-NH2-C6H4CONH2
3-(AMINOCARBONYL)ANILINE
3-AMINOBENZAMIDE [HSDB]
DTXSID90188922
4-14-00-01094 (Beilstein Handbook Reference)
(3-(AMINOCARBONYL)PHENYL)AMINE
3-amino benzamide
SR-01000075657
4pml
3AB
Spectrum_001492
Tocris-0788
Spectrum2_001577
Spectrum3_000972
Spectrum4_001096
Spectrum5_001459
3-Aminobenzamide, 97%
Lopac-A-0788
UPCMLD-DP128
3-aminobenzamide (3-ABA)
zerenex e/1009157;
Lopac0_000043
Oprea1_589004
SCHEMBL16070
Benzamide, 3-amino-(9CI)
BSPBio_001432
BSPBio_002603
KBioGR_000152
KBioGR_001512
KBioGR_002355
KBioSS_000152
KBioSS_001972
KBioSS_002358
MLS002153497
DivK1c_000717
INO-1001,3-Aminobenzamide
SPBio_001514
UPCMLD-DP128:001
3-ABA; 3-AB
BCBcMAP01_000186
BDBM27506
HMS502D19
KBio1_000717
KBio2_000152
KBio2_001972
KBio2_002355
KBio2_002720
KBio2_004540
KBio2_004923
KBio2_005288
KBio2_007108
KBio2_007491
KBio3_000303
KBio3_000304
KBio3_001823
KBio3_002834
ABA, 3-
DTXCID50111413
INO-1001 (3-Aminobenzamide)
3-(Aminocarbonyl) Aniline;3-AB
cMAP_000029
NINDS_000717
BCPP000203
Bio1_000466
Bio1_000955
Bio1_001444
Bio2_000152
Bio2_000632
HMS1361H14
HMS1791H14
HMS1989H14
HMS3260I07
HMS3266F08
HMS3402H14
HMS3411L09
HMS3654C08
HMS3656P18
HMS3675L09
BCP27669
NSC36962
3-Aminobenzamide, >=99% (TLC)
Tox21_500043
AB, 3-
BBL027669
CCG-39623
HSCI1_000265
s1132
STK730785
AKOS000118163
BCP9000790
CS-0157
FA71335
LP00043
SDCCGSBI-0050032.P003
IDI1_000717
IDI1_033902
SMP2_000089
Biochem Biophys Res Commun 225: 826
NCGC00015034-01
NCGC00015034-02
NCGC00015034-03
NCGC00015034-04
NCGC00015034-05
NCGC00015034-06
NCGC00015034-07
NCGC00015034-08
NCGC00015034-21
NCGC00024792-01
NCGC00024792-02
NCGC00024792-03
NCGC00024792-04
NCGC00024792-05
NCGC00024792-06
NCGC00260728-01
AC-10266
AS-17352
HY-12022
SMR000375902
SY012693
DB-022254
A0630
EU-0100043
NS00018655
SW219192-1
SW219192-2
EN300-21784
A 0788
PARP-IN-1 (3-aminobenzamide; 3-ABA; 3-AB)
Q4634111
SR-01000075657-1
SR-01000075657-3
Aminobenzamide (3-ABA) [3-aminobenzamide (3-ABA)]
BRD-K08703257-001-01-4
BRD-K08703257-001-12-1
BRD-K08703257-001-13-9
F3377-1722
Z118530082
Zerenex e/1009157; 3-Aminobenzamide; M-aminobenzamide
222-586-9
Solubility of 3-aminobenzamide
3-aminobenzamide (C7H8N2O) is a fascinating compound with specific solubility characteristics that are influenced by its functional groups and molecular structure. Here’s an exploration of its solubility:
In summary, the solubility of 3-aminobenzamide can be described as moderate in water and favorable in polar organic solvents, largely due to its functional groups enhancing interaction with polar media. Understanding these properties can be pivotal for its applications in various chemical processes.