N-Phthaloylglycine

CAS : 4702-13-0

Ref. 3D-FP34542

Informations sur le produit

• Nom: N-Phthaloylglycine
• Synonymes: (1,3-Dihydro-1,3-dioxo-2H-isoindol-2-yl)acetic acid, (1,3-Dioxo-1,3-dihydroisoindol-2-yl)acetic acid, (1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)acetate, (1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)acetic acid, 1,3-Dihydro-1,3-Dioxo-2H-Isoindole-2-Aceticacid, 1,3-Dihydro-1,3-dioxo-2H-isoindole-2-acetic acid, 1,3-Dihydro-1,3-dioxo-2H-isoindoleacetic acid, 1,3-Dioxo-2-isoindolineacetic acid, 2-(1,3-Dioxo-2,3-dihydro-1H-isoindol-2-yl)acetic acid, 2-(1,3-Dioxoisoindol-2-yl)acetic acid, 2-(1,3-Dioxoisoindolin-2-yl)acetic acid, 2-Isoindolineacetic acid, 1,3-dioxo-, 2-Phthalimidoacetic acid, 2-Phthalimidoylacetic acid, 2H-Isoindole-2-acetic acid, 1,3-dihydro-1,3-dioxo-, N-(2-Hydroxy-2-oxoethyl)phthalimide, N-(Carboxymethyl)phthalimide, NSC 10771, NSC 29044, Phthalimidoacetic acid, Phthaloglycine, Phthaloyl glycine, Phthaloylglycine
• CAS: 4702-13-0

Description

N-Phthaloylglycine is a molecule that has the formula HOC(C=O)NHCHCOH. It is reactive and can be used as a model system to study metal coordination. The molecule contains two nitrogen atoms, which are in second-order rate constant with copper ions, and three oxygen atoms. The molecule also has a carbonyl group and chelate ring. N-Phthaloylglycine has been shown to have anticancer effects in vitro and in vivo. Its mechanism of action is not well understood, but it may have an effect on DNA synthesis or DNA repair processes.

• Marque: Biosynth

Propriétés chimiques

• Masse moléculaire: 205.17 g/mol
• Formule: C₁₀H₇NO₄
• Degré de pureté: Min. 99.0 Area-%
• InChI: InChI=1S/C10H7NO4/c12-8(13)5-11-9(14)6-3-1-2-4-7(6)10(11)15/h1-4H,5H2,(H,12,13)
• Code InChI: InChIKey=WQINSVOOIJDOLJ-UHFFFAOYSA-N
• SMILES: O=C(O)CN1C(=O)c2ccccc2C1=O