Compounds > dicitrinin a
Page last updated: 2024-10-15

dicitrinin a

Description

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

Cross-References

ID SourceID
PubMed CID137629393
CHEMBL ID514105
MeSH IDM0512157

Synonyms (2)

Synonym
CHEMBL514105
dicitrinin a
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Bioassays (11)

Assay IDTitleYearJournalArticle
AID1243499Antimicrobial activity against Vibrio anguillarum by well diffusion method2015Journal of natural products, Sep-25, Volume: 78, Issue:9
Citrifelins A and B, Citrinin Adducts with a Tetracyclic Framework from Cocultures of Marine-Derived Isolates of Penicillium citrinum and Beauveria felina.
AID385146Antioxidant activity assessed as DPPH free radical scavenging activity after 30 mins2008Journal of natural products, Apr, Volume: 71, Issue:4
Citrinin dimers from the halotolerant fungus Penicillium citrinum B-57.
AID616587Cytotoxicity against human KB cells after 72 hrs by SRB assay2011Journal of medicinal chemistry, Aug-25, Volume: 54, Issue:16
Unprecedented citrinin trimer tricitinol B functions as a novel topoisomerase IIα inhibitor.
AID1243500Antimicrobial activity against Vibrio harveyi by well diffusion method2015Journal of natural products, Sep-25, Volume: 78, Issue:9
Citrifelins A and B, Citrinin Adducts with a Tetracyclic Framework from Cocultures of Marine-Derived Isolates of Penicillium citrinum and Beauveria felina.
AID385141Cytotoxicity against mouse NS1 cells2008Journal of natural products, Apr, Volume: 71, Issue:4
Citrinin dimers from the halotolerant fungus Penicillium citrinum B-57.
AID1243506Antimicrobial activity against Vibrio parahaemolyticus by well diffusion method2015Journal of natural products, Sep-25, Volume: 78, Issue:9
Citrifelins A and B, Citrinin Adducts with a Tetracyclic Framework from Cocultures of Marine-Derived Isolates of Penicillium citrinum and Beauveria felina.
AID1243503Antimicrobial activity against Edwardsiella tarda by well diffusion method2015Journal of natural products, Sep-25, Volume: 78, Issue:9
Citrifelins A and B, Citrinin Adducts with a Tetracyclic Framework from Cocultures of Marine-Derived Isolates of Penicillium citrinum and Beauveria felina.
AID1243502Antimicrobial activity against Aeromonas hydrophila by well diffusion method2015Journal of natural products, Sep-25, Volume: 78, Issue:9
Citrifelins A and B, Citrinin Adducts with a Tetracyclic Framework from Cocultures of Marine-Derived Isolates of Penicillium citrinum and Beauveria felina.
AID616588Cytotoxicity against human HL60 cells after 72 hrs by MTT assay2011Journal of medicinal chemistry, Aug-25, Volume: 54, Issue:16
Unprecedented citrinin trimer tricitinol B functions as a novel topoisomerase IIα inhibitor.
AID1243501Antimicrobial activity against Vibrio alginolyticus by well diffusion method2015Journal of natural products, Sep-25, Volume: 78, Issue:9
Citrifelins A and B, Citrinin Adducts with a Tetracyclic Framework from Cocultures of Marine-Derived Isolates of Penicillium citrinum and Beauveria felina.
AID616589Cytotoxicity against human HCT116 cells after 72 hrs by SRB assay2011Journal of medicinal chemistry, Aug-25, Volume: 54, Issue:16
Unprecedented citrinin trimer tricitinol B functions as a novel topoisomerase IIα inhibitor.
[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's0 (0.00)18.2507
2000's2 (40.00)29.6817
2010's3 (60.00)24.3611
2020's0 (0.00)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

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%
Other5 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]
SubstanceRelationship StrengthStudiesTrialsClassesRoles
vincristine
[no description available]		2.0610acetate ester;
formamides;
methyl ester;
organic heteropentacyclic compound;
organic heterotetracyclic compound;
tertiary alcohol;
tertiary amino compound;
vinca alkaloid		antineoplastic agent;
drug;
microtubule-destabilising agent;
plant metabolite;
tubulin modulator
orcinol
orcinol: used as reagent for pentoses, lignin, beet sugar, saccharoses, arabinose & diastase; RN given refers to parent cpd; structure. orcinol : A 5-alkylresorcinol in which the alkyl group is specified as methyl.		2.04105-alkylresorcinol;
dihydroxytoluene		Aspergillus metabolite
paclitaxel
Taxus: Genus of coniferous yew trees or shrubs, several species of which have medicinal uses. Notable is the Pacific yew, Taxus brevifolia, which is used to make the anti-neoplastic drug taxol (PACLITAXEL).		2.0410taxane diterpenoid;
tetracyclic diterpenoid		antineoplastic agent;
human metabolite;
metabolite;
microtubule-stabilising agent
dihydrocitrinone
[no description available]		2.7630
benzofurans
Benzofurans: Compounds that contain a BENZENE ring fused to a furan ring.		2.4620
ascorbic acid
Ascorbic Acid: A six carbon compound related to glucose. It is found naturally in citrus fruits and many vegetables. Ascorbic acid is an essential nutrient in human diets, and necessary to maintain connective tissue and bone. Its biologically active form, vitamin C, functions as a reducing agent and coenzyme in several metabolic pathways. Vitamin C is considered an antioxidant.. L-ascorbic acid : The L-enantiomer of ascorbic acid and conjugate acid of L-ascorbate.. L-ascorbate : The L-enantiomer of ascorbate and conjugate base of L-ascorbic acid, arising from selective deprotonation of the 3-hydroxy group. Required for a range of essential metabolic reactions in all animals and plants.. vitamin C : Any member of a group of vitamers that belong to the chemical structural class called butenolides that exhibit biological activity against vitamin C deficiency in animals. The vitamers include L-ascorbic acid and its salt, ionized and oxidized forms.		2.0410ascorbic acid;
vitamin C		coenzyme;
cofactor;
flour treatment agent;
food antioxidant;
food colour retention agent;
geroprotector;
plant metabolite;
skin lightening agent
citrinin
Citrinin: Antibiotic and mycotoxin from Aspergillus niveus and Penicillium citrinum.		2.9740
ConditionIndicatedRelationship StrengthStudiesTrials