Drug Designing: Open Access

Drug Designing: Open Access
Open Access

ISSN: 2169-0138

Drug Designing: Open Access : Citations & Metrics Report

Articles published in Drug Designing: Open Access have been cited by esteemed scholars and scientists all around the world. Drug Designing: Open Access has got h-index 9, which means every article in Drug Designing: Open Access has got 9 average citations.

Following are the list of articles that have cited the articles published in Drug Designing: Open Access.

  2024 2023 2022 2021 2020 2019 2018 2017 2016 2015 2014 2013 2012

Total published articles

22 32 30 31 67 2 5 16 18 12 14 24 6

Research, Review articles and Editorials

0 2 2 24 33 0 4 15 15 12 10 25 6

Research communications, Review communications, Editorial communications, Case reports and Commentary

14 30 27 7 35 2 1 1 3 0 4 3 0

Conference proceedings

0 5 5 0 0 0 124 81 41 56 0 0 58

Citations received as per Google Scholar, other indexing platforms and portals

45 51 54 62 43 41 41 23 48 16 10 5 0
Journal total citations count 456
Journal impact factor 1.70
Journal 5 years impact factor 1.5
Journal cite score 1.57
Journal h-index 9
Journal h-index since 2019 7
Important citations (297)

The essential medicinal chemistry of curcumin

Advancements in novel drug delivery systems and opportunities for indian pharmaceutical companies

Alzheimer?s disease and glucose metabolism

Alzheimer disease: a neurogenetic connection

Nanotechnology: a potential tool in exploring herbal benefits

Advancements in novel drug delivery systems and opportunities for indian pharmaceutical companies

Design, synthesis, characterization and in vitro kinetic study of novel antibacterials prodrugs 2015

Antibacterial predrugs-from 1899 till 2015

Antibacterial activity of novel prodrugs of amoxicillin and cephalexin

Diclofenac codrugs and prodrugs-three decades of design

A solution to aversive tasting drugs for pediatric and geriatric patients

Enzyme models-from catalysis to prodrugs.

From conventional prodrugs to prodrugs designed by molecular orbital methods

Computationally designed prodrugs of statins based on kirby’s enzyme model

Prodrugs design based on inter? and intramolecular chemical processes

The prodrug naming dilemma

Combinatorial designing of novel lead molecules towards the putative drug targets of extreme drug-resistant mycobacterium tuberculosis: a future insight for molecular medicine

Feature optimization in high dimensional chemical space: statistical and data mining solutions

From idea to market: the drug design, development & approval process

Prodrug: design and its applications

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