N-[3-(4-\{[1-(5-chloro-2,4-dimethoxyanilino)-1-oxopropan-2-yl]sulfanyl\}anilino)-3-oxo-1-phenylprop-1-en-2-yl]benzamide (BioCAD00000506356)
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Metabolite Card
Formula: C33H30ClN3O5S (615.1595)
SMILES: ClC=1C=C(NC(=O)C(SC2=CC=C(NC(=O)C(NC(=O)C3=CC=CC=C3)=CC4=CC=CC=C4)C=C2)C)C(OC)=CC1OC
Synonyms [en]
N-[3-(4-{[1-(5-chloro-2,4-dimethoxyanilino)-1-oxopropan-2-yl]sulfanyl}anilino)-3-oxo-1-phenylprop-1-en-2-yl]benzamide; N-[3-(4-\{[1-(5-chloro-2,4-dimethoxyanilino)-1-oxopropan-2-yl]sulfanyl\}anilino)-3-oxo-1-phenylprop-1-en-2-yl]benzamide; ~{N}-[1-[[4-[2-(5-chloro-2,4-dimethoxy-anilino)-1-methyl-2-oxo-ethyl]sulfanylphenyl]carbamoyl]-2-phenyl-vinyl]benzamide; Q27163018; CHEBI:91012
Last reviewed on 2024-06-28.
Cite this Page
N-[3-(4-\{[1-(5-chloro-2,4-dimethoxyanilino)-1-oxopropan-2-yl]sulfanyl\}anilino)-3-oxo-1-phenylprop-1-en-2-yl]benzamide. 数据之源,洞见之始. SMRUCC genomics institute, a synthetic life researcher from China.
https://biocad_registry.innovation.ac.cn/s/(-)-arctiin
(retrieved
2026-01-03) (CAD Registry RN: BioCAD00000506356). Licensed
under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0).
Note
A member of the class of enamides obtained by formal condensation of the carboxy group of 2-benzamido-3-phenylprop-2-enoic acid with the aromatic amino group of 2-[(4-aminophenyl)sulfanyl]propanoic acid, the carboxy group of which has also undergone formal condensation with the amino group of 5-chloro-2,4-dimethoxyaniline." []
DBLinks
- CAS Registry Number:
- PubChem CID:
- ChEBI: 91012
- HMDB:
- LipidMaps:
- KEGG:
- BioCyc:
- NCBI MeSH:
- Wikipedia:
Other DBLinks
- ChEBI: ChEBI:91012
- Coconut NaturalProduct: CNP0082155.0