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Key Documents

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05506

Supelco

(15:0)-Anacardic acid

analytical standard

Sinonimo/i:

Anacardic acid, 2-Hydroxy-6-pentadecylbenzoic acid, 22:0-Anacardic acid, 6-Pentadecylsalicylic acid

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About This Item

Formula empirica (notazione di Hill):
C22H36O3
Numero CAS:
16611-84-0
Peso molecolare:
348.52
Numero MDL:
MFCD07368254
Codice UNSPSC:
85151701
ID PubChem:
329748077
NACRES:
NA.24

Grado

analytical standard

Livello qualitativo

100

Saggio

≥95.0% (HPLC)

Durata

limited shelf life, expiry date on the label

applicazioni

food and beverages

Formato

neat

Temperatura di conservazione

2-8°C

Stringa SMILE

CCCCCCCCCCCCCCCc1cccc(O)c1C(O)=O

InChI

1S/C22H36O3/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-16-19-17-15-18-20(23)21(19)22(24)25/h15,17-18,23H,2-14,16H2,1H3,(H,24,25)
ADFWQBGTDJIESE-UHFFFAOYSA-N

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Descrizione generale

(15:0)-Anacardic acid is a mixture of salicylic acid analogues, comprising of a 15 carbon aliphatic side chain in various degrees of unsaturation.

Azioni biochim/fisiol

Anacardic acid is a HAT (Histone Acetyltransferase) inhibitor.

Confezionamento

Bottomless glass bottle. Contents are inside inserted fused cone.

Prodotti consigliati

Find a digital Reference Material for this product available on our online platform ChemisTwin® for NMR. You can use this digital equivalent on ChemisTwin® for your sample identity confirmation and compound quantification (with digital external standard). An NMR spectrum of this substance can be viewed and an online comparison against your sample can be performed with a few mouseclicks. Learn more here and start your free trial.

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

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Certificati d'analisi (COA)

Lot/Batch Number
BCCF5510
BCBX4234
BCBT4382
BCBS3165V
BCBQ0473V

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Uncoupling effect of anacardic acids from cashew nut shell oil on oxidative phosphorylation of rat liver mitochondria.
Toyomizu M, et al.
Life Sciences, 66(3), 229-234 (1999)
Rikke Illum Høgh et al.
FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 34(11), 15531-15546 (2020-10-01)
SCFAs are primarily produced in the colon by bacterial fermentation of nondigestible carbohydrates. Besides providing energy, SCFAs can suppress development of colon cancer. The mechanism, however, remains elusive. Here, we demonstrate that the SCFA propionate upregulates surface expression of the
E Pieterse et al.
Clinical and experimental immunology, 179(1), 68-74 (2014-04-25)
In addition to disturbed apoptosis and insufficient clearance of apoptotic cells, there is recent evidence for a role of neutrophils in the aetiopathogenesis of systemic lupus erythematosus (SLE). In response to various stimuli, neutrophils can rapidly release DNA fibres decorated
Tomohiro Nabekura et al.
Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie, 70, 140-145 (2015-03-18)
Drug efflux transporter P-glycoprotein plays an important role in cancer chemotherapy. The nuclear factor-κB (NF-κB) transcription factors play critical roles in development and progression of cancer. In this study, the effects of natural compounds that can inhibit NF-κB activation on
Mi Ae Kang et al.
International journal of oncology, 46(1), 342-350 (2014-10-24)
The tumor suppressor p53 plays a key role in regulation of the cell cycle, apoptosis and senescence in response to various stresses. We screened a library of 7920 chemical compounds for the p53 activator and identified N-[2-(dimethylamino)ethyl]-2,3-dimethyl-4-oxo-4H-pyrido[1,2-a]thieno[2,3-d]pyrimidine-9-carboxamide (PTP), which significantly
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