Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My Custom Filters

Edit custom filters

Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1961 1
1962 1
1963 2
1975 2
1977 1
1978 1
1979 1
1981 3
1982 2
1983 3
1984 2
1985 3
1986 2
1987 4
1988 6
1989 2
1990 3
1991 1
1992 2
1993 3
1994 4
1996 1
1997 4
1998 1
1999 1
2000 1
2001 3
2002 1
2003 2
2004 3
2005 5
2006 3
2007 1
2008 2
2009 2
2010 5
2011 2
2012 1
2013 3
2014 2
2015 2
2016 2
2017 3
2018 2
2019 3
2020 2
2021 4
2022 3
2023 3
2024 1
2025 2
2026 0

Publication date

Text availability

Article attribute

Article type

Additional filters

Article Language

Species

Sex

Age

Other

Search Results

115 results

Results by year

Filters applied: . Clear all
Quoted phrase not found in phrase index: "g-collidine"
Page 1
Synthesis of ent-thallusin.
Gao X, Matsuo Y, Snider BB. Gao X, et al. Org Lett. 2006 May 11;8(10):2123-6. doi: 10.1021/ol0605777. Org Lett. 2006. PMID: 16671797 Free PMC article.
[reaction: see text] A three-step route from sclareol oxide (6) to bromo ester 4 in 53% overall yield was achieved using the efficient oxidation of an allylic bromide to an enal with bis(2,4,6-trimethylpyridine)silver(I) hexafluorophosphate in DMSO. St …
[reaction: see text] A three-step route from sclareol oxide (6) to bromo ester 4 in 53% overall yield was achieved using the efficient oxida …
2,4,6-Trimethylpyridine-Derived Vinylene-Linked Covalent Organic Frameworks for Confined Catalytic Esterification.
Meng F, Bi S, Sun Z, Wu D, Zhang F. Meng F, et al. Angew Chem Int Ed Engl. 2022 Nov 2;61(44):e202210447. doi: 10.1002/anie.202210447. Epub 2022 Oct 5. Angew Chem Int Ed Engl. 2022. PMID: 36099563
Following this strategy, two vinylene-linked COFs were constructed using 2,4,6-trimethylpyridine and multi-aldehyde-substituted aromatic derivatives as monomers. ...
Following this strategy, two vinylene-linked COFs were constructed using 2,4,6-trimethylpyridine and multi-aldeh …
Effect of collidine (2,4,6-trimethylpyridine) on rat pineal gland and vas deferens nerves. Further evidence for a monoamine-releasing effect.
Tomsig JL, Pellegrino de Iraldi A. Tomsig JL, et al. Histochemistry. 1988;89(3):301-6. doi: 10.1007/BF00493156. Histochemistry. 1988. PMID: 3403302
In previous work of our laboratory it was demonstrated that collidine (2,4,6-trimethylpyridine) abolishes the core osmiophilia and chromaffin reaction from rat pinal gland and vas deferens nerves. ...
In previous work of our laboratory it was demonstrated that collidine (2,4,6-trimethylpyridine) abolishes …
Melatonin modulates drug-induced acute porphyria.
Lelli SM, Mazzetti MB, San Martín de Viale LC. Lelli SM, et al. Toxicol Rep. 2016 Jan 7;3:141-147. doi: 10.1016/j.toxrep.2015.12.010. eCollection 2016. Toxicol Rep. 2016. PMID: 28959532 Free PMC article.
This work investigated the modulation by melatonin (Mel) of the effects of the porphyrinogenic drugs 2-allyl-2-isopropylacetamide (AIA) and 3,5-diethoxycarbonyl-1,4-dihydro-2,4,6-collidine (DDC) on oxidative environment, glucose biosynthesis and heme p …
This work investigated the modulation by melatonin (Mel) of the effects of the porphyrinogenic drugs 2-allyl-2-isopropylacetamide (AIA) and …
Actinobacteria Warfare Against the Plant Pathogen Sclerotinia sclerotiorum: 2,4,6-Trimethylpyridine Identified as a Bacterial Derived Volatile With Antifungal Activity.
Belt K, Flematti GR, Bohman B, Chooi H, Roper MM, Dow L, Truman AW, Wilkinson B, Singh KB, Thatcher LF. Belt K, et al. Microb Biotechnol. 2025 Mar;18(3):e70082. doi: 10.1111/1751-7915.70082. Microb Biotechnol. 2025. PMID: 40040294 Free PMC article.
Solid-phase microextraction (SPME) coupled with gas chromatography-mass spectrometry (GC-MS) analysis identified 2,4,6-trimethylpyridine, a compound not identified previously from Actinobacteria, which showed antifungal activity against different isola …
Solid-phase microextraction (SPME) coupled with gas chromatography-mass spectrometry (GC-MS) analysis identified 2,4,6- …
Effects of 4-alkyl analogues of 3,5-diethoxycarbonyl-1,4-dihydro-2,4,6-trimethylpyridine on hepatic cytochrome P-450 heme, apoproteins, and catalytic activities following in vivo administration to rats.
Riddick DS, Park SS, Gelboin HV, Marks GS. Riddick DS, et al. Mol Pharmacol. 1990 Jan;37(1):130-6. Mol Pharmacol. 1990. PMID: 2405248
Various 4-alkyl analogues of 3,5-diethoxycarbonyl-1,4-dihydro-2,4,6-trimethylpyridine (DDC) cause mechanism-based inactivation of cytochrome P-450 (P-450) via heme destruction. ...
Various 4-alkyl analogues of 3,5-diethoxycarbonyl-1,4-dihydro-2,4,6-trimethylpyridine (DDC) cause mechanism-base …
Inactivation of cytochrome P450 and inhibition of ferrochelatase by analogues of 3,5-diethoxycarbonyl-1,4-dihydro-2,4,6-trimethylpyridine with 4-nonyl and 4-dodecyl substituents.
McCluskey SA, Riddick DS, Mackie JE, Kimmett SM, Whitney RA, Marks GS. McCluskey SA, et al. Can J Physiol Pharmacol. 1992 Aug;70(8):1069-74. doi: 10.1139/y92-148. Can J Physiol Pharmacol. 1992. PMID: 1473038
Cytochrome P450- and heme-destructive effects of the 4-nonyl and 4-dodecyl analogues of 3,5-diethoxycarbonyl-1,4-dihydro-2,4,6-trimethylpyridine (DDC) were determined using hepatic microsomal preparations obtained from untreated, beta-naphthoflavone-tr …
Cytochrome P450- and heme-destructive effects of the 4-nonyl and 4-dodecyl analogues of 3,5-diethoxycarbonyl-1,4-dihydro-2,4, …
NMR study of CHN hydrogen bond and proton transfer in 1,1-dinitroethane complex with 2,4,6-trimethylpyridine.
Tupikina EY, Denisov GS, Tolstoy PM. Tupikina EY, et al. J Phys Chem A. 2015 Jan 29;119(4):659-68. doi: 10.1021/jp511493m. Epub 2015 Jan 13. J Phys Chem A. 2015. PMID: 25532047
The intermolecular complex with a CHN hydrogen bond formed by 1,1-dinitroethane (DNE) and 2,4,6-trimethylpyridine (collidine) dissolved in CD2Cl2 was studied experimentally by (1)H NMR spectroscopy at 180-300 K. ...
The intermolecular complex with a CHN hydrogen bond formed by 1,1-dinitroethane (DNE) and 2,4,6-trimethylpyridine …
Irreversible binding of heme to microsomal protein during inactivation of cytochrome P450 by 4-alkyl analogues of 3,5-diethoxycarbonyl-1,4-dihydro-2,4,6-trimethylpyridine.
Riddick DS, Marks GS. Riddick DS, et al. Biochem Pharmacol. 1990 Oct 15;40(8):1915-21. doi: 10.1016/0006-2952(90)90374-t. Biochem Pharmacol. 1990. PMID: 2242024
The porphyrinogenicity of 4-alkyl analogues of 3,5-diethoxycarbonyl-1,4-dihydro-2,4,6-trimethylpyridine (DDC) is related to the process of mechanism-based destruction of cytochrome P450 (P450) heme, accompanied by conversion of heme to N-alkylprotoporp …
The porphyrinogenicity of 4-alkyl analogues of 3,5-diethoxycarbonyl-1,4-dihydro-2,4,6-trimethylpyridine (DDC) is …
115 results