Page last updated: 2024-11-08

anhydrodihydroartemisinin

Description Research Excerpts Clinical Trials Roles Classes Pathways Study Profile Bioassays Related Drugs Related Conditions Protein Interactions Research Growth Market Indicators

Description

anhydrodihydroartemisinin: structure given in first source [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID393517
CHEMBL ID279307
MeSH IDM0237659

Synonyms (23)

Synonym
nsc695575
nsc-695575
anhydrodihydroartemisinin
3r,5as,6r,8as,12r,12ar)-3,4,5,5a,6,7,8,8a-octahydro-3,6,9-trimethyl-3,12-epoxy-12hpyrano[4,3-j]-1,2-benzodioxepin
CHEMBL279307
82596-30-3
anhydro dihydro artemisinin
9,10-anhydrodehydroartemisinin
9,10-anhydro-10-deoxoartemisinin
anhydrodihydroartemisnin
(3r,5as,6r,8as,12r,12ar)-3,4,5,5a,6,7,8,8a-octahydro-3,6,9-trimethyl-3,12-epoxy-12h-pyrano(4,3-j)-1,2-benzodioxepin(+)-9,10
0YH8NQO930 ,
3,12-epoxy-12h-pyrano(4,3-j)-1,2-benzodioxepin, 3,4,5,5a,6,7,8,8a-octahydro-3,6,9-trimethyl-, (3r,5as,6r,8as,12r,12ar)-
unii-0yh8nqo930
artemisinin, anhydrodihydro-
DTXSID50327855
9,10-dehydrodeoxyartemisinin
UKXCIQFCSITOCY-VLDCTWHGSA-N
Q27237351
(1r,4s,5r,8s,12r,13r)-1,5,9-trimethyl-11,14,15,16-tetraoxatetracyclo[10.3.1.04,13.08,13]hexadec-9-ene
(3r,5as,6r,8as,12r,12ar)-3,6,9-trimethyl-4,5,5a,6,7,8,8a,12-octahydro-3h-3,12-epoxy[1,2]dioxepino[4,3-i]isochromene
(1r,4s,5r,8s,12r,13r)-1,5,9-trimethyl-11,14,15,16-tetraoxatetracyclo[10.3.1.0?,??.0?,??]hexadec-9-ene
AKOS040760837

Research Excerpts

Treatment

ExcerptReferenceRelevance
"When anhydrodihydroartemisinin was treated with a Fe(II) salt in acetonitrile-water solution, the same product was generated, together with an isomeric 2-deoxy-4α-hydroxy-anhydrodihydroartemisinin derivative, as expected from the usual homolytic radical opening of the endoperoxide bond previously described for other artemisinin derivatives."( A new derivative detected in accelerated ageing of artesunate-amodiaquine fixed dose combination tablets.
Azerad, R; Bertho, G; Charrier, C; Moneton, P; Petigny, O,
)
0.59
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Bioassays (1)

Assay IDTitleYearJournalArticle
AID159028Antimalarial activity against chloroquine-resistant, mefloquine-sensitive Plasmodium falciparum W22002Journal of medicinal chemistry, Jan-17, Volume: 45, Issue:2
Structure-activity relationships of the antimalarial agent artemisinin. 6. The development of predictive in vitro potency models using CoMFA and HQSAR methodologies.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (5)

TimeframeStudies, This Drug (%)All Drugs %
pre-19900 (0.00)18.7374
1990's1 (20.00)18.2507
2000's3 (60.00)29.6817
2010's0 (0.00)24.3611
2020's1 (20.00)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 12.74

According to the monthly volume, diversity, and competition of internet searches for this compound, as well the volume and growth of publications, there is estimated to be weak demand-to-supply ratio for research on this compound.

MetricThis Compound (vs All)
Research Demand Index12.74 (24.57)
Research Supply Index1.95 (2.92)
Research Growth Index4.69 (4.65)
Search Engine Demand Index0.00 (26.88)
Search Engine Supply Index0.00 (0.95)

This Compound (12.74)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews0 (0.00%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other6 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]