3-Methylpyridin-2-amine
3-Methylpyridin-2-amine structure
|
Common Name | 3-Methylpyridin-2-amine | ||
|---|---|---|---|---|
| CAS Number | 1603-40-3 | Molecular Weight | 108.141 | |
| Density | 1.1±0.1 g/cm3 | Boiling Point | 220.9±20.0 °C at 760 mmHg | |
| Molecular Formula | C6H8N2 | Melting Point | 29-31 °C(lit.) | |
| MSDS | Chinese USA | Flash Point | 111.7±0.0 °C | |
| Symbol |
GHS06, GHS08 |
Signal Word | Danger | |
|
Synthesis and characterisation of two novel proton transfer compounds and their inhibition studies on carbonic anhydrase isoenzymes.
J. Enzyme Inhib. Med. Chem. 26(1) , 104-14, (2011) Two novel proton transfer compounds were prepared between 2,4-dichloro-5-sulphamoylbenzoic acid (lasamide) (Hsba) and ethylenediamine (en), namely ethane-1,2-diaminium 2,4-dichloro-5-sulphamoylbenzoate (1), and also between Hsba and 2-amino-3-methylpyridine (... |
|
|
Comutagenesis-III. In vitro metabolism of 2-amino-3-methylpyridine: the effect of various potential inhibitors, activators and inducers.
Xenobiotica 27(11) , 1103-11, (1997) 1. The effects of various potential inhibitors, activators and inducers on the metabolism of the comutagen 2-amino-3-methylpyridine (2A3MP) by rabbit hepatic microsomes and S9 supernatants have been studied. 2. The 1-N-oxidation of 2A3MP to 2-amino-3-methylpy... |
|
|
Comutagenesis-I: the in vitro metabolism of 2-amino-3-methylpyridine.
Anticancer Res. 17(5A) , 3485-91, (1997) The metabolism of the comutagen 2-amino-3-methylpyridine has been studied in vitro using rat and rabbit hepatic preparations. 2-Amino-3-methylpyridine-N-oxide, 2-amino-3-hydroxymethylpyridine and 2-amino-5-hydroxy-3-methylpyridine were formed by both rat and ... |
|
|
Comutagenesis-IV in vitro metabolism of the comutagen 2-amino-3-methylpyridine: species differences and metabolic interaction with norharman.
Anticancer Res. 17(6D) , 4479-82, (1997) The metabolism of 2-amino-3-methylpyridine (2A3MP) in vitro has been investigated using the rat, rabbit, dog, marmoset, guinea pig and hamster hepatic microsomes and S9 supernatants (10,000 g fraction). Species differences were observed in the in vitro format... |
|
|
Comutagenesis--V: rapid conversion of 2-hydroxyl-amino-3-methylpyridineto 2-amino-3-methylpyridine by a hepatic S9 preparation.
Eur. J. Drug Metab. Pharmacokinet. 22(4) , 341-4, (1997) The in vitro metabolism of 2-hydroxylamino-3-methylpyridine has been investigated using arochlor 1254 pretreated rat S9 mixtures. 2-Hydroxylamino-3-methylpyridine is rapidly converted to the parent amine 2-amino-3-methylpyridine. No further oxidation products... |