9-stearolic acid

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

Description

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

stearolic acid : An octadecynoic acid having its triple bond 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 Source	ID
PubMed CID	68167
CHEMBL ID	482804
CHEBI ID	28801
SCHEMBL ID	196385
MeSH ID	M0181286

Synonyms (34)

Synonym
9-octadecynoic acid ,
octadec-9-insaeure
9-odya
CHEBI:28801 ,
9-oda
octadec-9-ynoic acid
delta(9)-octadecynoic acid
9a-18:1
stearolsaeure
NCGC00179891-01
MEGXP0_001740
ACON1_002039
C08459
9-stearolic acid
stearolic acid
506-24-1
steariolic acid
LMFA01030455
CHEMBL482804 ,
bdbm50292401
7m9kfa3wku ,
einecs 208-030-8
unii-7m9kfa3wku
FT-0621682
SCHEMBL196385
octadeca-9-ynoic acid
AKOS025117038
mfcd00014386
DTXSID90198647
Q27103903
stearolicacid
CS-0453095
octadecanoic acid-9-yne
PD183458

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

Drug Classes (1)

Class	Description
octadecynoic acid	Any C18, straight-chain, monounsaturated fatty acid having a C#C triple-bond at any position.
[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 (35)

Assay ID	Title	Year	Journal	Article
AID530460	Antifungal activity against Candida albicans ATCC 200955 at 178.6 uM after 48 hrs by CLSI method	2008	Antimicrobial agents and chemotherapy, Jul, Volume: 52, Issue:7	Potent in vitro antifungal activities of naturally occurring acetylenic acids.
AID530714	Antifungal activity against Aspergillus niger ATCC 16404 at 178.6 uM after 48 hrs by CLSI method	2008	Antimicrobial agents and chemotherapy, Jul, Volume: 52, Issue:7	Potent in vitro antifungal activities of naturally occurring acetylenic acids.
AID530440	Antifungal activity against Candida albicans ATCC 60193 at 178.6 uM after 48 hrs by CLSI method	2008	Antimicrobial agents and chemotherapy, Jul, Volume: 52, Issue:7	Potent in vitro antifungal activities of naturally occurring acetylenic acids.
AID531197	Cytotoxicity against human KB cells up to 32 uM by neutral red method	2008	Antimicrobial agents and chemotherapy, Jul, Volume: 52, Issue:7	Potent in vitro antifungal activities of naturally occurring acetylenic acids.
AID530947	Antifungal activity against Trichophyton rubrum ATCC MYA-4438 by CLSI method	2008	Antimicrobial agents and chemotherapy, Jul, Volume: 52, Issue:7	Potent in vitro antifungal activities of naturally occurring acetylenic acids.
AID530953	Antifungal activity against Trichophyton mentagrophytes ATCC MYA-4439 by CLSI method	2008	Antimicrobial agents and chemotherapy, Jul, Volume: 52, Issue:7	Potent in vitro antifungal activities of naturally occurring acetylenic acids.
AID530688	Antifungal activity against Cryptococcus neoformans ATCC 66031 at 178.6 uM after 72 hrs by CLSI method	2008	Antimicrobial agents and chemotherapy, Jul, Volume: 52, Issue:7	Potent in vitro antifungal activities of naturally occurring acetylenic acids.
AID531196	Cytotoxicity against human SK-MEL cells up to 32 uM by neutral red method	2008	Antimicrobial agents and chemotherapy, Jul, Volume: 52, Issue:7	Potent in vitro antifungal activities of naturally occurring acetylenic acids.
AID530729	Antifungal activity against Trichophyton rubrum ATCC 10218 at 178.6 uM after 5 days by CLSI method	2008	Antimicrobial agents and chemotherapy, Jul, Volume: 52, Issue:7	Potent in vitro antifungal activities of naturally occurring acetylenic acids.
AID530433	Antifungal activity against Candida albicans ATCC 14053 at 178.6 uM after 48 hrs by CLSI method	2008	Antimicrobial agents and chemotherapy, Jul, Volume: 52, Issue:7	Potent in vitro antifungal activities of naturally occurring acetylenic acids.
AID530958	Antifungal activity against Cryptococcus neoformans ATCC 66031 after 72 hrs by CLSI method	2008	Antimicrobial agents and chemotherapy, Jul, Volume: 52, Issue:7	Potent in vitro antifungal activities of naturally occurring acetylenic acids.
AID530720	Antifungal activity against Trichophyton mentagrophytes ATCC 9533 at 178.6 uM after 5 days by CLSI method	2008	Antimicrobial agents and chemotherapy, Jul, Volume: 52, Issue:7	Potent in vitro antifungal activities of naturally occurring acetylenic acids.
AID530707	Antifungal activity against Aspergillus flavus ATCC 204304 at 178.6 uM after 48 hrs by CLSI method	2008	Antimicrobial agents and chemotherapy, Jul, Volume: 52, Issue:7	Potent in vitro antifungal activities of naturally occurring acetylenic acids.
AID530498	Antifungal activity against Candida tropicalis ATCC 750 at 178.6 uM after 48 hrs by CLSI method	2008	Antimicrobial agents and chemotherapy, Jul, Volume: 52, Issue:7	Potent in vitro antifungal activities of naturally occurring acetylenic acids.
AID530472	Antifungal activity against Fluconazole resistant Candida albicans isolate 17 at 178.6 uM after 48 hrs by CLSI method	2008	Antimicrobial agents and chemotherapy, Jul, Volume: 52, Issue:7	Potent in vitro antifungal activities of naturally occurring acetylenic acids.
AID530492	Antifungal activity against Candida parapsilosis ATCC 22019 at 178.6 uM after 48 hrs by CLSI method	2008	Antimicrobial agents and chemotherapy, Jul, Volume: 52, Issue:7	Potent in vitro antifungal activities of naturally occurring acetylenic acids.
AID530682	Antifungal activity against Cryptococcus neoformans ATCC 90113 at 178.6 uM after 72 hrs by CLSI method	2008	Antimicrobial agents and chemotherapy, Jul, Volume: 52, Issue:7	Potent in vitro antifungal activities of naturally occurring acetylenic acids.
AID1525224	Cytotoxicity against mouse L929 cells measured after 48 hrs by MTT assay	2019	Journal of natural products, 05-24, Volume: 82, Issue:5	Antitrypanosomal Activity of Acetogenins Isolated from the Seeds of Porcelia macrocarpa Is Associated with Alterations in Both Plasma Membrane Electric Potential and Mitochondrial Membrane Potential.
AID531199	Cytotoxicity against human SKOV3 cells up to 32 uM by neutral red method	2008	Antimicrobial agents and chemotherapy, Jul, Volume: 52, Issue:7	Potent in vitro antifungal activities of naturally occurring acetylenic acids.
AID530694	Antifungal activity against Aspergillus fumigatus ATCC 204305 at 178.6 uM after 48 hrs by CLSI method	2008	Antimicrobial agents and chemotherapy, Jul, Volume: 52, Issue:7	Potent in vitro antifungal activities of naturally occurring acetylenic acids.
AID530941	Antifungal activity against Trichophyton rubrum ATCC 10218 by CLSI method	2008	Antimicrobial agents and chemotherapy, Jul, Volume: 52, Issue:7	Potent in vitro antifungal activities of naturally occurring acetylenic acids.
AID530962	Antifungal activity against Candida krusei ATCC 6258 after 48 hrs by CLSI method	2008	Antimicrobial agents and chemotherapy, Jul, Volume: 52, Issue:7	Potent in vitro antifungal activities of naturally occurring acetylenic acids.
AID530466	Antifungal activity against Fluconazole resistant Candida albicans isolate 1 at 178.6 uM after 48 hrs by CLSI method	2008	Antimicrobial agents and chemotherapy, Jul, Volume: 52, Issue:7	Potent in vitro antifungal activities of naturally occurring acetylenic acids.
AID1525222	Antitrypanosomal activity against Trypanosoma cruzi trypomastigotes measured after 24 hrs by resazurin dye based assay	2019	Journal of natural products, 05-24, Volume: 82, Issue:5	Antitrypanosomal Activity of Acetogenins Isolated from the Seeds of Porcelia macrocarpa Is Associated with Alterations in Both Plasma Membrane Electric Potential and Mitochondrial Membrane Potential.
AID531201	Cytotoxicity against pig LLC-PK1 cells up to 32 uM by neutral red method	2008	Antimicrobial agents and chemotherapy, Jul, Volume: 52, Issue:7	Potent in vitro antifungal activities of naturally occurring acetylenic acids.
AID531200	Cytotoxicity against African green monkey Vero cells up to 32 uM by neutral red method	2008	Antimicrobial agents and chemotherapy, Jul, Volume: 52, Issue:7	Potent in vitro antifungal activities of naturally occurring acetylenic acids.
AID530726	Antifungal activity against Trichophyton rubrum ATCC MYA-4438 at 178.6 uM after 5 days by CLSI method	2008	Antimicrobial agents and chemotherapy, Jul, Volume: 52, Issue:7	Potent in vitro antifungal activities of naturally occurring acetylenic acids.
AID1525223	Antitrypanosomal activity against Trypanosoma cruzi amastigotes infected in peritoneal macrophages (unknown origin) measured after 48 hrs by resazurin dye based assay	2019	Journal of natural products, 05-24, Volume: 82, Issue:5	Antitrypanosomal Activity of Acetogenins Isolated from the Seeds of Porcelia macrocarpa Is Associated with Alterations in Both Plasma Membrane Electric Potential and Mitochondrial Membrane Potential.
AID530453	Antifungal activity against Candida albicans ATCC 90028 at 178.6 uM after 48 hrs by CLSI method	2008	Antimicrobial agents and chemotherapy, Jul, Volume: 52, Issue:7	Potent in vitro antifungal activities of naturally occurring acetylenic acids.
AID530717	Antifungal activity against Trichophyton mentagrophytes ATCC MYA-4439 at 178.6 uM after 5 days by CLSI method	2008	Antimicrobial agents and chemotherapy, Jul, Volume: 52, Issue:7	Potent in vitro antifungal activities of naturally occurring acetylenic acids.
AID530701	Antifungal activity against Aspergillus fumigatus ATCC 90906 at 178.6 uM after 48 hrs by CLSI method	2008	Antimicrobial agents and chemotherapy, Jul, Volume: 52, Issue:7	Potent in vitro antifungal activities of naturally occurring acetylenic acids.
AID530447	Antifungal activity against Candida albicans ATCC 32354 at 178.6 uM after 48 hrs by CLSI method	2008	Antimicrobial agents and chemotherapy, Jul, Volume: 52, Issue:7	Potent in vitro antifungal activities of naturally occurring acetylenic acids.
AID1525225	Selectivity index, ratio of CC50 for mouse L929 cells to IC50 for Trypanosoma cruzi trypomastigotes	2019	Journal of natural products, 05-24, Volume: 82, Issue:5	Antitrypanosomal Activity of Acetogenins Isolated from the Seeds of Porcelia macrocarpa Is Associated with Alterations in Both Plasma Membrane Electric Potential and Mitochondrial Membrane Potential.
AID531198	Cytotoxicity against human BT549 cells up to 32 uM by neutral red method	2008	Antimicrobial agents and chemotherapy, Jul, Volume: 52, Issue:7	Potent in vitro antifungal activities of naturally occurring acetylenic acids.
AID530479	Antifungal activity against Candida glabrata ATCC 90030 at 178.6 uM after 48 hrs by CLSI method	2008	Antimicrobial agents and chemotherapy, Jul, Volume: 52, Issue:7	Potent in vitro antifungal activities of naturally occurring acetylenic acids.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (8)

Timeframe	Studies, This Drug (%)	All Drugs %
pre-1990	0 (0.00)	18.7374
1990's	2 (25.00)	18.2507
2000's	2 (25.00)	29.6817
2010's	2 (25.00)	24.3611
2020's	2 (25.00)	2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 12.42

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.

Metric	This Compound (vs All)
Research Demand Index	12.42 (24.57)
Research Supply Index	2.30 (2.92)
Research Growth Index	4.72 (4.65)
Search Engine Demand Index	0.00 (26.88)
Search Engine Supply Index	0.00 (0.95)

This Compound (12.42)

All Compounds (24.57)

Study Types

Publication Type	This drug (%)	All Drugs (%)
Trials	0 (0.00%)	5.53%
Reviews	0 (0.00%)	6.00%
Case Studies	0 (0.00%)	4.05%
Observational	0 (0.00%)	0.25%
Other	9 (100.00%)	84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Substance	Relationship Strength	Studies	Classes	Roles
lipoamide Lipozyme: lipase from Rhizomucor miehei immobilized on anion exchange resin	1.99	1	dithiolanes; monocarboxylic acid amide	Escherichia coli metabolite; human metabolite; mouse metabolite; Saccharomyces cerevisiae metabolite
1-anilino-8-naphthalenesulfonate 1-anilino-8-naphthalenesulfonate: RN given refers to parent cpd. 8-anilinonaphthalene-1-sulfonic acid : A naphthalenesulfonic acid that is naphthalene-1-sulfonic acid substituted by a phenylamino group at position 8.	1.99	1	aminonaphthalene; naphthalenesulfonic acid	fluorescent probe
5,8,11,14-eicosatetraynoic acid 5,8,11,14-Eicosatetraynoic Acid: A 20-carbon unsaturated fatty acid containing 4 alkyne bonds. It inhibits the enzymatic conversion of arachidonic acid to prostaglandins E(2) and F(2a).	2.04	1	long-chain fatty acid
fluconazole Fluconazole: Triazole antifungal agent that is used to treat oropharyngeal CANDIDIASIS and cryptococcal MENINGITIS in AIDS.. fluconazole : A member of the class of triazoles that is propan-2-ol substituted at position 1 and 3 by 1H-1,2,4-triazol-1-yl groups and at position 2 by a 2,4-difluorophenyl group. It is an antifungal drug used for the treatment of mucosal candidiasis and for systemic infections including systemic candidiasis, coccidioidomycosis, and cryptococcosis.	2.04	1	conazole antifungal drug; difluorobenzene; tertiary alcohol; triazole antifungal drug	environmental contaminant; P450 inhibitor; xenobiotic
ketoconazole 1-acetyl-4-(4-{[2-(2,4-dichlorophenyl)-2-(1H-imidazol-1-ylmethyl)-1,3-dioxolan-4-yl]methoxy}phenyl)piperazine : A dioxolane that is 1,3-dioxolane which is substituted at positions 2, 2, and 4 by imidazol-1-ylmethyl, 2,4-dichlorophenyl, and [para-(4-acetylpiperazin-1-yl)phenoxy]methyl groups, respectively.	2.04	1	dichlorobenzene; dioxolane; ether; imidazoles; N-acylpiperazine; N-arylpiperazine
stearic acid octadecanoic acid : A C18 straight-chain saturated fatty acid component of many animal and vegetable lipids. As well as in the diet, it is used in hardening soaps, softening plastics and in making cosmetics, candles and plastics.	2.5	2	long-chain fatty acid; saturated fatty acid; straight-chain saturated fatty acid	algal metabolite; Daphnia magna metabolite; human metabolite; plant metabolite
undecylenic acid undecylenic acid: a fatty acid with a terminal double bond. 10-undecenoic acid : An undecenoic acid having its double bond in the 10-position. It is derived from castor oil and is used for the treatment of skin problems.. undecenoic acid : A C11, straight-chain fatty acid carrying a C=C double bond at any position.	2.04	1	undecenoic acid	antifungal drug; plant metabolite
acetylene [no description available]	1.99	1	alkyne; gas molecular entity; terminal acetylenic compound
benzonidazole benzonidazole: used in treatment of Chagas' disease. benznidazole : A monocarboxylic acid amide obtained by formal condensation of the carboxy group of (2-nitroimidazol-1-yl)acetic acid with the aromatic amino group of benzylamine. Used for treatment of Chagas disease.	2.21	1	C-nitro compound; imidazoles; monocarboxylic acid amide	antiprotozoal drug
6-octadecynoic acid 6-octadecynoic acid: from the roots of Pentagonia gigantifolia; structure in first source. tariric acid : An octadecynoic acid having its triple bond at position 6.	2.78	3	octadecynoic acid
arachidonic acid icosa-5,8,11,14-tetraenoic acid : Any icosatetraenoic acid with the double bonds at positions 5, 8, 11 and 14.. arachidonate : A long-chain fatty acid anion resulting from the removal of a proton from the carboxy group of arachidonic acid.	2.6	1	icosa-5,8,11,14-tetraenoic acid; long-chain fatty acid; omega-6 fatty acid	Daphnia galeata metabolite; EC 3.1.1.1 (carboxylesterase) inhibitor; human metabolite; mouse metabolite
terbinafine [no description available]	2.04	1	acetylenic compound; allylamine antifungal drug; enyne; naphthalenes; tertiary amine	EC 1.14.13.132 (squalene monooxygenase) inhibitor; P450 inhibitor; sterol biosynthesis inhibitor
cancidas [no description available]	2.04	1
amphotericin b Amphotericin B: Macrolide antifungal antibiotic produced by Streptomyces nodosus obtained from soil of the Orinoco river region of Venezuela.. amphotericin B : A macrolide antibiotic used to treat potentially life-threatening fungal infections.	2.04	1	antibiotic antifungal drug; macrolide antibiotic; polyene antibiotic	antiamoebic agent; antiprotozoal drug; bacterial metabolite
6-nonadecynoic acid 6-nonadecynoic acid: from the roots of Pentagonia gigantifolia; structure in first source	2.04	1

Condition	Indicated	Relationship Strength	Studies	Trials
Adenoma, beta-Cell [description not available]	0	2.25	1	0
Insulinoma A benign tumor of the PANCREATIC BETA CELLS. Insulinoma secretes excess INSULIN resulting in HYPOGLYCEMIA.	0	2.25	1	0

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