2-[2-amino-5-(2-methoxyphenyl)pyrimidin-4-yl]-5-[(4-fluorophenyl)methoxy]phenol

AlkaPlorer ID: AK156557

Synonym: None

IUPAC Name: 2-[2-amino-5-(2-methoxyphenyl)pyrimidin-4-yl]-5-[(4-fluorophenyl)methoxy]phenol

Structure

SMILES: COC1=CC=CC=C1C1=CN=C(N)N=C1C1=CC=C(OCC2=CC=C(F)C=C2)C=C1O

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InChI: InChI=1S/C24H20FN3O3/c1-30-22-5-3-2-4-18(22)20-13-27-24(26)28-23(20)19-11-10-17(12-21(19)29)31-14-15-6-8-16(25)9-7-15/h2-13,29H,14H2,1H3,(H2,26,27,28)

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InChIKey: BZAFBWJGAGQBMJ-UHFFFAOYSA-N

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Reference

Integrated Profiling of Fatty Acids, Sterols and Phenolic Compounds in Tree and Herbaceous Peony Seed Oils: Marker Screening for New Resources of Vegetable Oil

<sup>1</sup>H and <sup>13</sup>C NMR Spectroscopic Analysis of Human Saliva

Bioactive components, antioxidant and antimicrobial activities of Paeonia rockii fruit during development

The bioactive compounds and cellular antioxidant activity of Herbaceous peony (<i>Paeonia lactiflora</i> Pall) seed oil from China

Profiling of Phenols in Human Fecal Water after Raspberry Supplementation

Metabolite Composition and Bioactivity of<i>Rhizoctonia solani</i>Sclerotial Exudates

Characterization of tyrosinase inhibitory constituents from the aerial parts of Humulus japonicus using LC-MS/MS coupled online assay

Volatile Flavor Components of Corn Tortillas and Related Products

Wasabisides A–E, Lignan Glycosides from the Roots of <i>Wasabia japonica</i>

Bioassay-Guided Isolation of Constituents of <i>Piper sarmentosum</i> Using a Mitochondrial Transmembrane Potential Assay

Study on the Constituents of Mexican Propolis and Their Cytotoxic Activity against PANC-1 Human Pancreatic Cancer Cells

Chemical Profile of Lipophilic Fractions of Different Parts of Zizyphus lotus L. by GC-MS and Evaluation of Their Antiproliferative and Antibacterial Activities

Ferruginenes A−C from <i>Rhododendron ferrugineum</i> and Their Cytotoxic Evaluation

Stachylines A−D from the Sponge-Derived Fungus <i>Stachylidium</i> sp.

Antitubercular Constituents from the Stem Wood of <i>Cinnamomum </i><i>k</i><i>otoense</i>

Triterpenoid Constituents from the Roots of <i>Paeonia rockii</i> ssp. <i>rockii</i>

The response of <i>Chlamydomonas reinhardtii</i> to nitrogen deprivation: a systems biology analysis

A Metabolite Profiling Approach to Identify Biomarkers of Flavonoid Intake in Humans1–3

Chlorogenic Acid, Quercetin-3-Rutinoside and Black Tea Phenols Are Extensively Metabolized in Humans

PubChem CID: 3758377

SuperNatural Ⅲ: SN0039338

COCONUT: CNP0170195

Source

Species Genus Family Order Class Phylum Kingdom Domain

Properties Information

Molecule Weight: 417.4400000000001

TPSA: 90.49

MolLogP: 4.825100000000004

Number of H-Donors: 2

Number of H-Acceptors: 6

RingCount: 4

Activities Information

Organism Target Name Standard Type Standard Value Standard Units doi

Metabolism Information