Basic information
- CAS
149341-39-9- Standard SMILES
CN(C(=O)Cc1ccc(Cl)c(Cl)c1)C1CCCCC1N1CCCC1- InChIKey
VQLPLYSROCPWFF-UHFFFAOYSA-N- Molecular formula
- C19H26Cl2N2O
- Average molar mass
- 369.3 g/mol
- Monoisotopic mass
- 368.1422188
Overview
2-(3,4-dichlorophenyl)-N-methyl-N-[2-(1-pyrrolidinyl)cyclohexyl]acetamide is a member of acetamides.
Names & identifiers
- Preferred name
- 3,4-Dichloro-N-methyl-N-(2-(1-pyrrolidinyl)cyclohexyl)benzeneacetamide
- IUPAC
- 2-(3,4-dichlorophenyl)-N-methyl-N-(2-pyrrolidin-1-ylcyclohexyl)acetamide
Names & synonyms
149341-39-93,4-dichloro-N-methyl-N-[2-(1-pyrrolidinyl)cyclohexyl]benzeneacetamide3,4-Dichloro-N-methyl-N-(2-(1-pyrrolidinyl)cyclohexyl)benzeneacetamideRefChem:270853Talactoferrin Alfa2-(3,4-dichlorophenyl)-N-methyl-N-(2-pyrrolidin-1-ylcyclohexyl)acetamideSCHEMBL332192CHEMBL290543BDBM86547CHEBI:103981DTXSID101155047CAS_135349
Show more names
NSC_135349L000607BRD-A12822115-003-01-6Q271812192-(3,4-dichlorophenyl)-N-methyl-N-[2-(1-pyrrolidinyl)cyclohexyl]acetamide3,4-dichloro-N-methyl-N-[2-(1-pyrrolidinyl)-cyclohexyl]-benzeneacetamide2-(3,4-dichlorophenyl)-N-methyl-N-[2-(pyrrolidin-1-yl)cyclohexyl]acetamide
Database identifiers
- CAS
149341-39-9、308240-58-6- PubChem CID
- 5619
- DTXSID
DTXSID101155047- ChEMBL
CHEMBL290543- ChEBI
CHEBI:103981
Properties
Computed structural properties
- XLogP
- 4.4
- Topological polar surface area
- 23.6 Ų
- Hydrogen bond donors
- 0
- Hydrogen bond acceptors
- 2
- Rotatable bonds
- 4
- Heavy atoms
- 24
- Formal charge
- 0
- Complexity
- 428
Chemistry & industry
Pharmacology
Mechanism of Action
Oral talactoferrin stimulated the production of the immunostimulatory cytokine IL-18 in mice, increasing IL-18 levels both in the gut and in systemic circulation. Oral talactoferrin was also shown to stimulate the activity of NK cells and to increase the production and activity of key circulating immune cells.
Related reactions
0 records
No reaction records under the current filter.
Compound notes
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