| Name | transferase |
|---|---|
| Synonyms | 4' phosphopantetheinyl transferase; 4' phosphopantetheinyl transferase; AASD PPT; AASDHPPT; AASDPPT; Alpha aminoadipic semialdehyde dehydrogenase phosphopantetheinyl transferase; Aminoadipate semialdehyde dehydrogenase phosphopantetheinyl transferase; CGI 80… |
| Name | alachlor |
|---|---|
| CAS |
| PubMed | Abstract | RScore(About this table) | |
|---|---|---|---|
| 10552507 | Logusch SJ, Feng PC, Fujiwara H, Hutton WC, Wratten SJ: Enzymatic synthesis of 4-amino-3,5-diethylphenyl a rodent metabolite of alachlor. J Agric Food Chem. 1999 May;47(5):2125-9. ADEPS formation in rodents is associated with the production of other reactive metabolites implicated in alachlor rodent carcinogenesis, making dependable access to an ADEPS standard highly desirable. (14) C- was oxidized by rat liver microsomes to (14) C-4-amino-3,5-diethylphenol, which was further converted to ADEPS via addition of the transferase cofactor -3'--5'- |
31(0,1,1,1) | Details |
| 20120471 | Tilak KS, Raju PW, Butchiram MS: Effects of alachlor on biochemical parameters of the freshwater fish, Channa punctatus (Bloch). J Environ Biol. 2009 May;30(3):420-6. The fresh water fish Channa punctatus (Bloch) were exposed to lethal and sublethal concentrations of a chloroacetanilide herbicide Alachlor and its commercial formulation Lasso 50% Emulsifiable Concentrate EC to study the impacts on some biochemical parameters - the energy dependent sources: such as total proteins and metabolic enzymes: amino transferase (AAT), amino transferase (ALAT), Lactate Dehydrogenase (LDH), Deoxyribonucleic acid (DNA) and Ribonucleic acid (RNA). |
6(0,0,1,1) | Details |
| 7599527 | Holt DC, Lay VJ, Clarke ED, Dinsmore A, Jepson I, Bright SW, Greenland AJ: Characterization of the safener-induced glutathione S-transferase isoform II from maize. Planta. 1995;196(2):295-302. The safener-induced maize (Zea mays S-transferase, GST II (EC 2.5.1.18) and another predominant isoform, GST I, were purified from extracts of maize roots treated with the safeners R-25788 (N,N-diallyl-2-dichloroacetamide) or R-29148 (3-dichloroacetyl-2,2,5-trimethyl-1,3-oxazolidone). The isoforms GST I and GST II are respectively a homodimer of 29-kDa (GST-29) subunits and a heterodimer of 29- and 27-kDa (GST-27) subunits, while GST I is twice as active with 1-chloro-2,4-dinitrobenzene as GST II, GST II is about seven times more active against the herbicide, alachlor. |
1(0,0,0,1) | Details |
| 8812207 | Wilson AG, Thake DC, Heydens WE, Brewster DW, Hotz KJ: Mode of action of thyroid tumor formation in the male Long-Evans rat administered high doses of alachlor. Fundam Appl Toxicol. 1996 Sep;33(1):16-23. Liver and thyroid weights and serum levels of (T3), (T4), and thyroid-stimulating hormone (TSH), as well as hepatic glucuronosyl transferase (UDPGT) activity, were determined at 7, 14, 28, 60, and 120 days of treatment. |
1(0,0,0,1) | Details |