Compounds > pachybasin
Page last updated: 2024-11-08

pachybasin

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

Description

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

Cross-References

ID SourceID
PubMed CID164982
CHEMBL ID2229888
SCHEMBL ID7624909
MeSH IDM0575040

Synonyms (18)

Synonym
2549-78-2
1-hydroxy-3-methylanthracene-9,10-dione
1-hydroxy-3-methyl-9,10-dihydroanthracene-9,10-dione
w9fs8qf9zx ,
unii-w9fs8qf9zx
9,10-anthracenedione, 1-hydroxy-3-methyl-
pachybasin
1-hydroxy-3-methyl-9,10-anthracenedione
AKOS022660296
CHEMBL2229888
SCHEMBL7624909
1-hydroxy-3-methylanthraquinone
DTXSID80180177
1-hydroxy-3-methyl-anthraquinone
EN300-25893672
BS-1311
CS-0113230
HY-N7307
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Bioassays (9)

Assay IDTitleYearJournalArticle
AID1080765Antibacterial activity against Bacillus cereus using 50 uL of compound solution from 500 ug/mL stock solution after 24 hr by agar disk diffusion method2009Journal of agricultural and food chemistry, Aug-26, Volume: 57, Issue:16
Study on the anthraquinones separated from the cultivation of Trichoderma harzianum strain Th-R16 and their biological activity.
AID1080768Antibacterial activity against Pseudomonas aeruginosa using 50 uL of compound solution from 500 ug/mL stock solution after 24 hr by agar disk diffusion method2009Journal of agricultural and food chemistry, Aug-26, Volume: 57, Issue:16
Study on the anthraquinones separated from the cultivation of Trichoderma harzianum strain Th-R16 and their biological activity.
AID1091701Antifungal activity against Botryotinia fuckeliana assessed as growth inhibition at 0.01 to 200 ug/plug2009Letters in applied microbiology, Jun, Volume: 48, Issue:6
Factors affecting the production of Trichoderma harzianum secondary metabolites during the interaction with different plant pathogens.
AID1091702Antifungal activity against Phytophthora cinnamomi assessed as growth inhibition at 0.01 to 200 ug/plug2009Letters in applied microbiology, Jun, Volume: 48, Issue:6
Factors affecting the production of Trichoderma harzianum secondary metabolites during the interaction with different plant pathogens.
AID1080758Antifungal activity against Botryotinia fuckeliana assessed as growth inhibition at 500 ug/mL after 4 days2009Journal of agricultural and food chemistry, Aug-26, Volume: 57, Issue:16
Study on the anthraquinones separated from the cultivation of Trichoderma harzianum strain Th-R16 and their biological activity.
AID1080767Antibacterial activity against Escherichia coli using 50 uL of compound solution from 500 ug/mL stock solution after 24 hr by agar disk diffusion method2009Journal of agricultural and food chemistry, Aug-26, Volume: 57, Issue:16
Study on the anthraquinones separated from the cultivation of Trichoderma harzianum strain Th-R16 and their biological activity.
AID1080766Antibacterial activity against Staphylococcus aureus using 50 uL of compound solution from 500 ug/mL stock solution after 24 hr by agar disk diffusion method2009Journal of agricultural and food chemistry, Aug-26, Volume: 57, Issue:16
Study on the anthraquinones separated from the cultivation of Trichoderma harzianum strain Th-R16 and their biological activity.
AID1080760Antifungal activity against Rhizoctonia solani assessed as growth inhibition at 500 ug/mL after 2 days2009Journal of agricultural and food chemistry, Aug-26, Volume: 57, Issue:16
Study on the anthraquinones separated from the cultivation of Trichoderma harzianum strain Th-R16 and their biological activity.
AID1091700Antifungal activity against Leptosphaeria maculans isolate UWA P11 assessed as growth inhibition at 0.01 to 200 ug/plug2009Letters in applied microbiology, Jun, Volume: 48, Issue:6
Factors affecting the production of Trichoderma harzianum secondary metabolites during the interaction with different plant pathogens.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (7)

TimeframeStudies, This Drug (%)All Drugs %
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's2 (28.57)29.6817
2010's4 (57.14)24.3611
2020's1 (14.29)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 12.72

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 Index12.72 (24.57)
Research Supply Index2.08 (2.92)
Research Growth Index4.80 (4.65)
Search Engine Demand Index0.00 (26.88)
Search Engine Supply Index0.00 (0.95)

This Compound (12.72)

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%
Other7 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]
SubstanceRelationship StrengthStudiesTrialsClassesRoles
emodin
Emodin: Purgative anthraquinone found in several plants, especially RHAMNUS PURSHIANA. It was formerly used as a laxative, but is now used mainly as a tool in toxicity studies.. emodin : A trihydroxyanthraquinone that is 9,10-anthraquinone which is substituted by hydroxy groups at positions 1, 3, and 8 and by a methyl group at position 6. It is present in the roots and barks of numerous plants (particularly rhubarb and buckthorn), moulds, and lichens. It is an active ingredient of various Chinese herbs.		2.7830trihydroxyanthraquinoneantineoplastic agent;
laxative;
plant metabolite;
tyrosine kinase inhibitor
9,10-anthraquinone
9,10-anthraquinone : An anthraquinone that is anthracene in which positions 9 and 10 have been oxidised to carbonyls.		2.1510anthraquinone
chrysophanic acid
chrysophanic acid: RN given refers to parent cpd; structure in Merck, 9th ed, #2260. chrysophanol : A trihydroxyanthraquinone that is chrysazin with a methyl substituent at C-3. It has been isolated from Aloe vera and exhibits antiviral and anti-inflammatory activity.		340dihydroxyanthraquinoneanti-inflammatory agent;
antiviral agent;
plant metabolite
physcione
physcione: structure. physcion : A dihydroxyanthraquinone that is 9,10-anthraquinone bearing hydroxy substituents at positions 1 and 8, a methoxy group at position 3, and a methyl group at position 6. It has been widely isolated and characterised from both terrestrial and marine sources.		2.1710dihydroxyanthraquinoneanti-inflammatory agent;
antibacterial agent;
antifungal agent;
antineoplastic agent;
apoptosis inducer;
hepatoprotective agent;
metabolite
kanamycin sulfate
[no description available]		2.0510aminoglycoside sulfate saltantibacterial drug;
geroprotector
sodium acetate, anhydrous
Sodium Acetate: The trihydrate sodium salt of acetic acid, which is used as a source of sodium ions in solutions for dialysis and as a systemic and urinary alkalizer, diuretic, and expectorant.		2.3110organic sodium saltNMR chemical shift reference compound
harzianolide
harzianolide: from the culture broth of Trichoderma sp. FKI-5513; structure in first source		2.0510
ConditionIndicatedRelationship StrengthStudiesTrials