verified SJR 0,621 · Q2 • database Scopus / SJR & Web of Science indexed

United States · Elsevier Inc.

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Journal of Inorganic Biochemistry

Journal of Inorganic Biochemistry is a journal indexed in SJR in Biochemistry and Inorganic Chemistry with an H index of 150. It has an SJR impact factor of 0,621 and it has a best quartile of Q2. It is published in English. It has an SJR impact factor of 0,621.

Journal of Inorganic Biochemistry focuses its scope in these topics and keywords: dfc, agent, protein, dependent, exposure, cadmiumsulfide, ferritin, chelating, fihconversion, coordination, ...

ISSN: 0162-0134

Editorial: Elsevier Inc.

Category: Biochemistry

Indexation: verifiedScopus / SJR verifiedWeb of Science

Unclaimed profile — some fields may be incomplete.

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SJR Impact Factor trending_up

0,621 Q2

H-index 150

Tasa de Aceptación pie_chart

22% Selectiva

Fuente Acceptance_Rate

Tiempo a publicación hourglass_top

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Campo Sin dato

Coste de Publicación (APC) payments

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Ruta Non-OA NPD

Metrics

Campos Scimago / CoP — sin series inventadas

Scopus / SJR Web of Science

SJR Impact

0,621

H-index

150

Docs (year)

211

Docs 3y

766

Total refs

13286

Cites 3y

2718

Citable 3y

752

Cites/Doc 2y

3.21

Ref/Doc

62.97

Immediate OA

—

Embargoed OA

NPD

Non OA / Submission

—

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Best articles by citations

Bioinorganic chemistry at the service of microbial systematics: Purification and characterisation of key proteins from sulphate-reducing bacterial strains as a tool for their identification

Urinary excretion of essential metals following intravenous calcium disodium edetate: an estimate of free zinc and zinc status in man

Detection of iron-containing proteins contributing to the cellular labile iron pool by a native electrophoresis metal blotting technique

Design and synthesis of new biomimetic materials

Copper(I) and (II) complexes of tridentate and tetradentate ligands containing a sulfur donor as functional models of dopamine beta-monooxygenase

Coordination ability of digalactosamine, and di- and trigalacturonic acids. Potentiometric and spectroscopic studies of Cu(II) complexes

Complexing of 6-chloropurine with some transition metal ions in aqueous solution

Comparison of the binding behavior of oxaliplatin, cisplatin and analogues to 5'-GMP in the presence of sulfur-containing molecules by means of capillary electrophoresis and electrospray mass spectrometry

Chiral porphyrins and metalloporphyrins: Asymmetric recognition and catalyses

Carbonated hydroxyapatites precipitated in the presence of Ti

Ca(C5H3N4O3)2(H2O)3 - mixed-coordinated calcium hydrogenurate hydrate

Bis-tridentate iron chelating analogues of pyridoxal isonicotinyl hydrazone

SHOW MORE ARTICLES

Biphasic kinetics of Zn2+ removal from Zn metallothionein by nitrilotriacetate are associated with differential reactivity of the two metal clusters

A calorimetric study of 3d metal ions-acyclovir interactions. The 2-hydroxyethoxymethyl group of acyclovir mimics the role of ribose in deoxy-guanosine and guanosine promoting the coordination through N(7)

Binding of metallobleomycins to DNA 10-mers

Bacterial cytochrome c nitrite reductase: new structural and functional aspects1Presented in part at the 5th ISABC, Corfu, Greece, 1999.1

Application of a self-modeling curve resolution approach to the study of solvent effects on the acid-base and copper(II)-complexing behavior of polyuridylic acid

Antioxidant effect of copper(II) on photosensitized lipid peroxidation

Announcing ''Focused Review Articles''

An MCD spectroscopic study of the molybdenum active site in sulfite oxidase: insight into the role of coordinated cysteine

An in vitro study of the use of chelating agents in cleaning nickel contaminated human skin: An alternative approach to preventing nickel allergic contact dermatitis

An examination of the binding of aluminum to protein and mineral components of bone and teeth

Activities and relative affinities of divalent metals in unmodified and phosphorothioate-substituted hammerhead ribozymes

A mechanistic study of the oxidation of disulfides using Rh2S2 cyclic compounds

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