Page last updated: 2024-12-11

10(9)-hydroxystearic acid

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

Description

It seems like you're asking about **10(S)-hydroxystearic acid**. It's a fatty acid with a hydroxyl group (-OH) at the 10th carbon position. This molecule is interesting due to its biological relevance and potential applications in research.

Here's what makes 10(S)-hydroxystearic acid important:

**1. Biological Relevance:**

* **Found in Nature:** It's found in various organisms, including plants and animals. For example, it's a significant component of certain fats and oils.
* **Potential Role in Cellular Processes:** Studies suggest it might play a role in cell signaling and membrane function. This is because the hydroxyl group can interact with other molecules and influence the structure and behavior of cell membranes.

**2. Research Applications:**

* **Biomaterials and Drug Delivery:** Researchers are exploring its potential as a building block for biocompatible materials and drug delivery systems. Its unique structure and properties, like its ability to form micelles, make it attractive for these applications.
* **Food Science:** 10(S)-hydroxystearic acid's presence in certain foods is being investigated in relation to its potential health benefits or its role in food stability.
* **Synthesis and Chemical Studies:** It's used as a starting material for synthesizing other molecules with potential biological activity.
* **Cosmetic Industry:** It's showing potential use in cosmetic formulations due to its moisturizing and skin-conditioning properties.

**Important Note:** Research into 10(S)-hydroxystearic acid is ongoing. While promising, its exact biological roles and potential applications are still under investigation.

If you have more specific questions about its properties, research findings, or applications in a particular field, please let me know.

10(9)-hydroxystearic acid: structure; RN given refers to parent cpd; see also records for 9-hydroxystearic acid & 10-hydroxystearic acid [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

9-hydroxyoctadecanoic acid : A hydroxyoctadecanoic acid that is octadecanoic acid (stearic acid) which has been substituted by a hydroxy group at position 9. [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 CID9570127
CHEMBL ID1093742
CHEBI ID136638
SCHEMBL ID465907
MeSH IDM0051644

Synonyms (23)

Synonym
9-hydroxyoctadecanoic acid
3384-24-5
CHEBI:136638
AKOS000277649
9-hydroxystearic acid
CHEMBL1093742
octadecanoic acid, 9-hydroxy-
dl-9-hydroxy stearic acid
9-hydroxy-octadecanoic acid
LMFA02000127
10(9)-hydroxystearic acid
25498-28-6
9(or 10)-hydroxyoctadecanoic acid
SCHEMBL465907
AKOS025399398
9-hydroxy stearic acid
18:0(9-oh)
FT-0774903
DTXSID60948393
HY-N11692
CS-0716321
PD150705
F73266
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Drug Classes (1)

ClassDescription
hydroxyoctadecanoic acidA hydroxy fatty acid that is ocatadecanoic acid (stearic acid) in which the aliphatic chain has been substituted by one or more hydroxy groups.
[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]

Bioassays (2)

Assay IDTitleYearJournalArticle
AID464598Inhibition of CRM1 interaction with HIV1 HA-tagged Rev in HeLa cells assessed as inhibition of Rev nuclear export by indirect fluorescent antibody technique2010Bioorganic & medicinal chemistry letters, Mar-15, Volume: 20, Issue:6
Unprecedented NES non-antagonistic inhibitor for nuclear export of Rev from Sida cordifolia.
AID1831923Growth inhibition of human A549 cells at 50 microM measured after 72 hrs by MTT assay2021Journal of medicinal chemistry, 05-13, Volume: 64, Issue:9
Saturated Oxo Fatty Acids (SOFAs): A Previously Unrecognized Class of Endogenous Bioactive Lipids Exhibiting a Cell Growth Inhibitory Activity.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (22)

TimeframeStudies, This Drug (%)All Drugs %
pre-19902 (9.09)18.7374
1990's3 (13.64)18.2507
2000's7 (31.82)29.6817
2010's8 (36.36)24.3611
2020's2 (9.09)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 11.72

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 Index11.72 (24.57)
Research Supply Index3.14 (2.92)
Research Growth Index4.85 (4.65)
Search Engine Demand Index0.00 (26.88)
Search Engine Supply Index0.00 (0.95)

This Compound (11.72)

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%
Other22 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]