Page last updated: 2024-11-06

biotin sulfone

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

Description

Biotin sulfone is a synthetic analog of biotin, a vitamin essential for various metabolic processes. It is known to inhibit biotin-dependent enzymes, particularly carboxylases, by acting as a competitive inhibitor. This inhibition occurs due to the sulfone group replacing the carboxyl group in biotin, which is essential for binding to the enzyme active site. Biotin sulfone's ability to inhibit carboxylases has led to its investigation as a potential therapeutic agent in certain conditions, including cancer and metabolic disorders. Studies have shown that biotin sulfone can suppress the growth of cancer cells and regulate blood glucose levels in diabetic models. However, further research is needed to understand its potential clinical applications and safety profile. The study of biotin sulfone is important as it provides insights into the mechanisms of biotin-dependent enzymes and the potential for developing new therapeutic strategies.'

biotin sulfone: RN given for (3aS-(3aalpha,4beta,6aalpha))-isomer; structure in first source [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

biotin sulfone : A member of the class of biotins that is biotin sulfoxide with a sulfone group replacing the sulfoxide. [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 CID83863
CHEBI ID74092
SCHEMBL ID710629
MeSH IDM0272598

Synonyms (30)

Synonym
5-[(3as,4s,6ar)-5,5-dioxido-2-oxohexahydro-1h-thieno[3,4-d]imidazol-4-yl]pentanoic acid
EN300-24308
5-[(3as,4s,6ar)-2,5,5-trioxo-hexahydro-1h-5lambda6-thieno[3,4-d]imidazolidin-4-yl]pentanoic acid
biotin sulfone
40720-05-6
5-[(3as,4s,6ar)-2,5,5-trioxo-1,3,3a,4,6,6a-hexahydrothieno[3,4-d]imidazol-4-yl]pentanoic acid
AKOS001254221
1h-thieno(3,4-d)imidazole-4-pentanoic acid, hexahydro-2-oxo-, 5,5-dioxide, (3as,4s,6ar)-
unii-22451myq9x
1h-thieno(3,4-d)imidazole-4-pentanoic acid, hexahydro-2-oxo-, 5,5-dioxide, (3as-(3aalpha,4beta,6aalpha))-
22451myq9x ,
C20387
[3as-(3aa,4b,6aa)]-5,5-dioxide-hexahydro-2-oxo-1h-thieno[3,4-d]imidazole-4-pentanoic acid
5,5-dioxide biotin
CHEBI:74092
SCHEMBL710629
QPFQYMONYBAUCY-ZKWXMUAHSA-N
5-((1r,5s,6s)-3,7,7-trioxo-7-thia-2,4-diazabicyclo[3.3.0]oct-6-yl)pentanoic acid
[3as-(3aa,4b,6aa)]- 5,5-dioxide-hexahydro-2-oxo-1h-thieno[3,4-d]imidazole-4-pentanoic acid
[3as-(3aa,4b,6aa)]- 5,5-dioxide-hexahydro-2-oxo-1h-thieno[3,4-d]imidazole-4-pentanoate
Z190662994
Q27144407
HY-113268
CS-0059469
5-((3as,4s,6ar)-5,5-dioxido-2-oxohexahydro-1h-thieno[3,4-d]imidazol-4-yl)pentanoic acid
MS-23928
5-((3as,4s,6ar)-5,5-dioxido-2-oxohexahydro-1h-thieno[3,4-d]imidazol-4-yl)pentanoicacid
1h-thieno[3,4-d]imidazole-4-pentanoic acid, hexahydro-2-oxo-, 5,5-dioxide, (3as,4s,6ar)-
DTXSID301124523
mfcd08444234
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Roles (1)

RoleDescription
metaboliteAny intermediate or product resulting from metabolism. The term 'metabolite' subsumes the classes commonly known as primary and secondary metabolites.
[role 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]

Drug Classes (2)

ClassDescription
biotinsCompounds containing a biotin (5-[(3aS,4S,6aR)-2-oxohexahydro-1H-thieno[3,4-d]imidazol-4-yl]pentanoic acid) skeleton.
sulfoneAn organosulfur compound having the structure RS(=O)2R (R =/= H).
[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]

Research

Studies (10)

TimeframeStudies, This Drug (%)All Drugs %
pre-19904 (40.00)18.7374
1990's2 (20.00)18.2507
2000's1 (10.00)29.6817
2010's3 (30.00)24.3611
2020's0 (0.00)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 20.03

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 moderate demand-to-supply ratio for research on this compound.

MetricThis Compound (vs All)
Research Demand Index20.03 (24.57)
Research Supply Index2.40 (2.92)
Research Growth Index4.80 (4.65)
Search Engine Demand Index15.26 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (20.03)

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%
Other10 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]