aminotipyr
A carboxylic ester resulting from the formal condensation of the carboxy group of 2-amino-6-methylpyridine-3-carboxylic acid with the hydroxy group of {4-[(5-methyl-1,3-thiazol-2-yl)oxy]phenyl}methanol. It is a fungicide developed by Qingdao KingAgroot Chemical Compound Co., Ltd.
Machine-generated and unreviewed. Identity, structure and cross-references come straight from ChEBI's and CARD's own data; no curator has signed off on this record yet.
Classification
Chemical structure
| Molecular formula | C18H17N3O3S |
|---|---|
| Charge | 0 |
| Average mass | 355.419 Da |
| Monoisotopic mass | 355.09906 Da |
| Source | ChEBI |
| InChIKey | FAYVBMMWMRQVMB-UHFFFAOYSA-N |
Cc1ccc(C(=O)OCc2ccc(Oc3ncc(C)s3)cc2)c(N)n1
InChI=1S/C18H17N3O3S/c1-11-3-8-15(16(19)21-11)17(22)23-10-13-4-6-14(7-5-13)24-18-20-9-12(2)25-18/h3-9H,10H2,1-2H3,(H2,19,21)
Also called
- 4-[(5-methyl-1,3-thiazol-2-yl)oxy]benzyl 2-amino-6-methylpyridine-3-carboxylate
- 4-[(5-methylthiazol-2-yl)oxy]benzyl 2-amino-6-methylnicotinate
- 4-[(5-methylthiazol-2-yl)oxy]benzyl 2-amino-6-methylpyridine-3-carboxylate
- [4-[(5-methyl-2-thiazolyl)oxy]phenyl]methyl 2-amino-6-methyl-3-pyridinecarboxylate
- {4-[(5-methyl-1,3-thiazol-2-yl)oxy]phenyl}methyl 2-amino-6-methylpyridine-3-carboxylate
Cross-references
Activity roles
- fungicide
CHEBI:24127
Source concepts
| Source | Native ID | Label | Minted CURIE | Version |
|---|---|---|---|---|
| CHEBI | CHEBI:233987 |
aminotipyr | antibioticmech:chebi-d54c27a0f7 |
2026-08-30 |
Curation history
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SEEDED_FROM_SOURCES
Seeded from data/raw/ inventories (CHEBI)
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RESEEDED_FROM_SOURCES
Re-seeded from updated data/raw/ inventories
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RESEEDED_FROM_SOURCES
Re-seeded from updated data/raw/ inventories