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
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)
InChIKey: BZAFBWJGAGQBMJ-UHFFFAOYSA-N
Reference
<sup>1</sup>H and <sup>13</sup>C NMR Spectroscopic Analysis of Human Saliva
Profiling of Phenols in Human Fecal Water after Raspberry Supplementation
Metabolite Composition and Bioactivity of<i>Rhizoctonia solani</i>Sclerotial Exudates
Volatile Flavor Components of Corn Tortillas and Related Products
Wasabisides A–E, Lignan Glycosides from the Roots of <i>Wasabia japonica</i>
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
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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
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