Page last updated: 2024-12-09

aflatoxin b

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

Description

aflatoxin B2: RN given refers to cpd without isomeric designation [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

aflatoxin B2 : An aflatoxin having a hexahydrocyclopenta[c]furo[3',2':4,5]furo[2,3-h]chromene skeleton with oxygen functionality at positions 1, 4 and 11. [Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

Cross-References

ID SourceID
PubMed CID2724360
CHEBI ID48209
SCHEMBL ID14424508
MeSH IDM0025322

Synonyms (40)

Synonym
2,3,6aalpha,8,9,9aalpha-hexahydro-4-methoxycyclopenta[c]furo[3',2':4,5]furo[2,3-h][1]benzopyran-1,11-dione
afb2
(6ar,9as)-4-methoxy-2,3,6a,8,9,9a-hexahydrocyclopenta[c]furo[3',2':4,5]furo[2,3-h]chromene-1,11-dione
CHEBI:48209
aflatoxin-b(2)
(6ar-cis)-2,3,6a,8,9,9a-hexahydro-4-methoxycyclopenta[c]furo[3',2';4,5]furo[2,3-h][1]benzopyran-1,11-dione
2,3,6aalpha,8,9,9aalpha-hexahydro-4-methoxycyclopenta[c]furo[3',2':4,5]furo[2,3-h]chromene-1,11-dione
dihydroaflatoxin b1
2,3,6aalpha,8,9,9aalpha-hexahydro-4-methoxycyclopenta(c)furo(2',3':4,5)furo(2,3-h)chromene-1,11-dione
hsdb 3454
ccris 13
einecs 230-618-8
cyclopenta(c)furo(3',2':4,5)furo(2,3-h)(1)benzopyran-1,11-dione, 2,3,6a-alpha,8,9,9a-alpha-hexahydro-4-methoxy-
2,3,6aalpha,8,9,9aalpha-hexahydro-4-methoxycyclopenta(c)furo(3',2':4,5)furo(2,3-h)(1)benzopyran-1,11-dione
brn 1355115
dihydroaflatoxine b1
cyclopenta(c)furo(3',2':4,5)furo(2,3-h)(1)benzopyran-1,11-dione, 2,3,6aalpha,8,9,9aalpha-hexahydro-4-methoxy-
aflatoxin b2
7220-81-7
5-19-10-00552 (beilstein handbook reference)
7skr7s646p ,
unii-7skr7s646p
aflatoxin b [mi]
aflatoxin b2 [hsdb]
2,3,6aalpha,8,9,9aalpha-hexahydro-4- methoxycyclopenta(c)furo(3',2':4,5)furo(2,3-h)(1)benzopyran- 1,11-dione
cyclopenta(c)furo(3',2':4,5)furo(2,3-h)(1)benzopyran-1,11-dione, 2,3,6a,8,9,9a-hexahydro-4-methoxy-, (6ar-cis)-
cyclopenta(c)furo(3',2':4,5)furo(2,3-h)(1)benzopyran-1,11-dione, 2,3,6a,8,9,9a-hexahydro-4-methoxy-, (6ar,9as)-
DTXSID70222535
SCHEMBL14424508
aflatoxinb2
(6ar-cis)-2,3,6a,8,9,9a-hexahydro-4-methoxycyclopenta[c]furo[3',2'
4,5]furo[2,3-h][1]benzopyran-1,11-dione
(3s,7r)-11-methoxy-6,8,19-trioxapentacyclo[10.7.0.02,9.03,7.013,17]nonadeca-1,9,11,13(17)-tetraene-16,18-dione
aflatoxin b2, from aspergillus flavus
aflatoxin b2, reference material
dl-threo-ritalinic acid lactam
Q26840819
(6ar,9as)-2,3,6a,8,9,9ahexahydro-4-methoxy-cyclopenta[c]furo[3',2':4,5]furo[2,3h][1]benzopyran-1,11-dione
aflatoxin b2 0.5 microg/ml in acetonitrile
cyclopenta[c]furo[3',2':4,5]furo[2,3-h][1]benzopyran-1,11-dione, 2,3,6a,8,9,9a-hexahydro-4-methoxy-, (6ar,9as)-

Research Excerpts

Overview

Alatoxin B1 (AFB1) is a class 1 carcinogen. It is a common food contaminant worldwide with widely uncontrolled human exposure.

ExcerptReferenceRelevance
"Aflatoxin B1 (AFB1) is a class 1 carcinogen and a common food contaminant worldwide with widely uncontrolled human exposure. "( Effect of dietary acids on the formation of aflatoxin B2a as a means to detoxify aflatoxin B1.
Rushing, BR; Selim, MI, 2016
)
2.14

Compound-Compound Interactions

ExcerptReferenceRelevance
"A novel, simple, and rapid method is presented for the analysis of aflatoxin B1, aflatoxin B2, and ochratoxin A in rice samples by dispersive liquid-liquid microextraction combined with LC and fluorescence detection."( Rapid analysis of aflatoxins B1, B2, and ochratoxin A in rice samples using dispersive liquid-liquid microextraction combined with HPLC.
Lai, XW; Liu, CL; Ruan, CQ; Sun, DL; Zhang, H, 2014
)
0.64
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Drug Classes (1)

ClassDescription
aflatoxinAny of a group of related and highly toxic secondary metabolites (mycotoxins) whose main structural feature is a fused coumarin-bis(dihydrofuran) ring system and which are produced by strains of the moulds Aspergillus flavus or A. parasiticus, together with further metabolites of these mycotoxins
[compound class information is derived from Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

Pathways (1)

PathwayProteinsCompounds
aflatoxins B2 and G2 biosynthesis313

Research

Studies (150)

TimeframeStudies, This Drug (%)All Drugs %
pre-199039 (26.00)18.7374
1990's19 (12.67)18.2507
2000's37 (24.67)29.6817
2010's52 (34.67)24.3611
2020's3 (2.00)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 (%)
Trials2 (1.12%)5.53%
Reviews1 (0.56%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other176 (98.32%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]