ARCHIV DER PHARMAZIE
ISSN:0365-6233

ARCHIV DER PHARMAZIE

ARCH PHARM
学科领域:医学
是否预警:不在预警名单内
是否OA:
录用周期:约3.0个月
新锐分区:医学3区
年发文量:217
影响因子:3.6
JCR分区:Q2

基本信息

Archiv der Pharmazie - Chemistry in Life Sciences是一份致力于药物和药物化学所有领域研究和开发的国际期刊。重点放在将合成有机化学、结构生物学、分子建模、生物有机化学、天然产物化学、生物化学或分析方法与药学或医学方面(如生物活性)相结合的论文上。本期刊的重点是原创研究论文,但也欢迎其他有科学价值的贡献(如综述、小型综述、亮点、专题讨论会贡献、讨论和论文)。
0365-6233SCIE/Scopus收录
3.6
3.1
2026年3月发布
点击查看历史分区趋势    >
大类学科小类学科Top期刊综述期刊
医学3区
CHEMISTRY, MEDICINAL 药物化学
3区
CHEMISTRY, MULTIDISCIPLINARY 化学:综合
3区
PHARMACOLOGY & PHARMACY 药学
3区
N/A
WOS期刊SCI分区  2024-2025最新升级版
按JIF指标学科分区收集子录JIF分区JIF排名百分位
学科:CHEMISTRY, MEDICINAL
SCIE
Q2
32/72
学科:CHEMISTRY, MULTIDISCIPLINARY
SCIE
Q2
96/239
学科:PHARMACOLOGY & PHARMACY
SCIE
Q2
103/352
按JCR指标学科分区收集子录JCR分区JCR排名百分位
学科:CHEMISTRY, MEDICINAL
SCIE
Q2
30/72
学科:CHEMISTRY, MULTIDISCIPLINARY
SCIE
Q2
65/241
学科:PHARMACOLOGY & PHARMACY
SCIE
Q2
104/353
54
217
14%0约3.0个月-医学-化学综合
8.3%
时间预警情况
2026年03月发布的新锐学术版不在预警名单中
2025年03月发布的2025版不在预警名单中
2024年02月发布的2024版不在预警名单中
2023年01月发布的2023版不在预警名单中
2021年12月发布的2021版不在预警名单中
2020年12月发布的2020版不在预警名单中
76.96%23.2%0.67%
CiteScore:7.00
SJR:0.571
SNIP:1.019
学科类别分区排名百分位
大类:Pharmacology, Toxicology and Pharmaceutics
小类:Pharmaceutical Science
Q1
43 / 185
大类:Pharmacology, Toxicology and Pharmaceutics
小类:Drug Discovery
Q2
47 / 156

期刊高被引文献

Aminopyrazole‐substituted metallophthalocyanines: Preparation, aggregation behavior, and investigation of metabolic enzymes inhibition properties
来源期刊:Archiv der PharmazieDOI:10.1002/ardp.201800292
Synthesis, characterization, biological evaluation, and molecular docking studies of some piperonyl‐based 4‐thiazolidinone derivatives
来源期刊:Archiv der PharmazieDOI:10.1002/ardp.201900304
Synthesis and antimicrobial activity of novel 1,2,3‐triazole‐conjugates of quinazolin‐4‐ones
来源期刊:Archiv der PharmazieDOI:10.1002/ardp.201800302
Interconnection of sulfides and sulfoxides in medicinal chemistry
来源期刊:Archiv der PharmazieDOI:10.1002/ardp.201800248
Quinolone derivatives: Potential anti‐HIV agent—development and application
来源期刊:Archiv der PharmazieDOI:10.1002/ardp.201900045
New 2,4‐disubstituted‐2‐thiopyrimidines as VEGFR‐2 inhibitors: Design, synthesis, and biological evaluation
来源期刊:Archiv der PharmazieDOI:10.1002/ardp.201900089
Synthesis and biological evaluation of novel benzo[c]acridine‐diones as potential anticancer agents and tubulin polymerization inhibitors
来源期刊:Archiv der PharmazieDOI:10.1002/ardp.201800307
Design, synthesis, biological evaluation, and molecular modeling studies of rhodanine derivatives as pancreatic lipase inhibitors
来源期刊:Archiv der PharmazieDOI:10.1002/ardp.201900029
Novel quinoline derivatives carrying nitrones/oximes nitric oxide donors: Design, synthesis, antiproliferative and caspase‐3 activation activities
来源期刊:Archiv der PharmazieDOI:10.1002/ardp.201800270
Artemisinin‐derived dimers as potential anticancer agents: Current developments, action mechanisms, and structure–activity relationships
来源期刊:Archiv der PharmazieDOI:10.1002/ardp.201900240
Design, synthesis, and biological evaluation of new pyrazino[1,2‐a]benzimidazole derivatives as selective cyclooxygenase (COX‐2) inhibitors
来源期刊:Archiv der PharmazieDOI:10.1002/ardp.201800265
Design and synthesis of 1,2,4‐triazolo[1,5‐a]pyrimidine derivatives as PDE 4B inhibitors endowed with bronchodilator activity
来源期刊:Archiv der PharmazieDOI:10.1002/ardp.201900002
Synthesis and anti‐coronavirus activity of a series of 1‐thia‐4‐azaspiro[4.5]decan‐3‐one derivatives
来源期刊:Archiv Der PharmazieDOI:10.1002/ardp.201800330
1H‐1,2,3‐Triazole tethered isatin‐moxifloxacin: Design, synthesis and in vitro anti‐mycobacterial evaluation
来源期刊:Archiv der PharmazieDOI:10.1002/ardp.201900040
Synthesis of novel gefitinib‐based derivatives and their anticancer activity
来源期刊:Archiv der PharmazieDOI:10.1002/ardp.201800381
Pharmacological explorations of eco‐friendly amide substituted (Z)‐β‐enaminones as anti‐breast cancer drugs
来源期刊:Archiv der PharmazieDOI:10.1002/ardp.201800244
Safran
来源期刊:Archiv der PharmazieDOI:10.1002/ardp.18782120438
Synthesis and biological evaluation of sphingosine kinase 2 inhibitors with anti‐inflammatory activity
来源期刊:Archiv der PharmazieDOI:10.1002/ardp.201800298
Identification of dehydroxy isoquine and isotebuquine as promising antileishmanial agents
来源期刊:Archiv der PharmazieDOI:10.1002/ardp.201800281
1,2,4‐Triazole‐conjugated 1,3,4‐thiadiazole hybrid scaffolds: A potent ameliorant of carrageenan‐induced inflammation by lessening proinflammatory mediators
来源期刊:Archiv der PharmazieDOI:10.1002/ardp.201900233
Densely substituted piperidines as a new class of elastase inhibitors: Synthesis and molecular modeling studies
来源期刊:Archiv der PharmazieDOI:10.1002/ardp.201900061
Identification of new NIK inhibitors by discriminatory analysis‐based molecular docking and biological evaluation
来源期刊:Archiv der PharmazieDOI:10.1002/ardp.201800374
Synthesis, molecular docking studies, and biological evaluation of novel alkyl bis(4‐amino‐5‐cyanopyrimidine) derivatives
来源期刊:Archiv der PharmazieDOI:10.1002/ardp.201900027
Discovery to solve multidrug resistance: Design, synthesis, and biological evaluation of novel agents
来源期刊:Archiv der PharmazieDOI:10.1002/ardp.201900127
Microwave‐assisted synthesis of 1‐substituted‐1H‐benzimidazolium salts: Non‐competitive inhibition of human carbonic anhydrase I and II
来源期刊:Archiv der PharmazieDOI:10.1002/ardp.201800325
Antileismanial activity, mechanism of action study and molecular docking of 1,4‐bis(substituted benzalhydrazino)phthalazines
来源期刊:Archiv der PharmazieDOI:10.1002/ardp.201800299
Novel calcitriol analogue with an oxolane group: In vitro, in vivo, and in silico studies
来源期刊:Archiv der PharmazieDOI:10.1002/ardp.201800315
Design, synthesis, and molecular docking studies of novel pyrazolyl 2‐aminopyrimidine derivatives as HSP90 inhibitors
来源期刊:Archiv der PharmazieDOI:10.1002/ardp.201900063
Efficient synthesis of meso‐substituted porphyrins and molecular docking as potential new antioxidant and cytotoxicity agents
来源期刊:Archiv der PharmazieDOI:10.1002/ardp.201800221
Synthesis, antibacterial evaluation, and DNA gyrase inhibition profile of some new quinoline hybrids
来源期刊:Archiv der PharmazieDOI:10.1002/ardp.201900086
Chemical structure modifications and nano‐technology applications for improving ADME‐Tox properties, a review
来源期刊:Archiv der PharmazieDOI:10.1002/ardp.201800213
Enantioselective synthesis and biological investigation of tetrahydro‐β‐carboline‐based HDAC6 inhibitors with improved solubility
来源期刊:Archiv der PharmazieDOI:10.1002/ardp.201900026
G protein‐coupled receptor binding and pharmacological evaluation of indole‐derived thiourea compounds
来源期刊:Archiv der PharmazieDOI:10.1002/ardp.201900218
Design, synthesis and biological evaluation of 6‐substituted quinolines derived from cabozantinib as c‐Met inhibitors
来源期刊:Archiv der PharmazieDOI:10.1002/ardp.201900101
Synthesis and antiageing properties of antioxidant pseudopeptides designed based on the bioisostere principle
来源期刊:Archiv der PharmazieDOI:10.1002/ardp.201800354
Quinolone derivatives and their antifungal activities: An overview
来源期刊:Archiv der PharmazieDOI:10.1002/ardp.201800382
Novel N‐(1‐thia‐4‐azaspiro[4.5]decan‐4‐yl)carboxamide derivatives as potent and selective influenza virus fusion inhibitors
来源期刊:Archiv der PharmazieDOI:10.1002/ardp.201900028
Synthesis, docking studies, and pharmacological evaluation of 5HT2C ligands containing the N′‐cyanoisonicotinamidine or N′‐cyanopicolinamidine nucleus
来源期刊:Archiv der PharmazieDOI:10.1002/ardp.201800373
Bi‐heterocyclic benzamides as alkaline phosphatase inhibitors: Mechanistic comprehensions through kinetics and computational approaches
来源期刊:Archiv der PharmazieDOI:10.1002/ardp.201800278
Novel ketoprofen–antioxidants mutual codrugs as safer nonsteroidal anti‐inflammatory drugs: Synthesis, kinetic and pharmacological evaluation
来源期刊:Archiv der PharmazieDOI:10.1002/ardp.201800339
Synthesis and mycobacterial evaluation of 5‐substituted‐6‐acetyl‐2‐amino‐7‐methyl‐5,8‐dihydropyrido‐[2,3‐d]pyrimidin‐4(3H)‐one derivatives
来源期刊:Archiv der PharmazieDOI:10.1002/ardp.201900068
Design and synthesis of imidazolidinone derivatives as potent anti‐leishmanial agents by bioisosterism
来源期刊:Archiv der PharmazieDOI:10.1002/ardp.201800290
Discovery and biological evaluation of novel G protein‐coupled receptor 119 agonists for type 2 diabetes
来源期刊:Archiv der PharmazieDOI:10.1002/ardp.201800267
Exploration of the structure–activity relationship and druggability of novel oxazolidinone‐based compounds as Gram‐negative antibacterial agents
来源期刊:Archiv der PharmazieDOI:10.1002/ardp.201900129
Sulfonylpiperazines based on a flavone as antioxidant and cytotoxic agents
来源期刊:Archiv der PharmazieDOI:10.1002/ardp.201900051
Synthesis and biological evaluation of heteroalicyclic cyanoguanidines at histamine receptors
来源期刊:Archiv der PharmazieDOI:10.1002/ardp.201900107
Bioassay of ferulic acid derivatives as influenza neuraminidase inhibitors
来源期刊:Archiv der PharmazieDOI:10.1002/ardp.201900174
Identification of novel selective Mtb‐DHFR inhibitors as antitubercular agents through structure‐based computational techniques
来源期刊:Archiv der PharmazieDOI:10.1002/ardp.201900287
Jod.
来源期刊:Archiv der PharmazieDOI:10.1002/ardp.18270210339
Targeting HIV‐TB coinfection by developing novel piperidin‐4‐substituted imines: Design, synthesis, in vitro and in silico studies
来源期刊:Archiv der PharmazieDOI:10.1002/ardp.201800358

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