6-pentadecylsalicylic acid

ChemicalBook > CAS DataBase List > 6-pentadecylsalicylic acid

6-pentadecylsalicylic acid

Product Name: 6-pentadecylsalicylic acid
CAS No.: 16611-84-0
Chemical Name: 6-pentadecylsalicylic acid
Synonyms: Anachardic acid;NSC 623096;NSC 333857;NSC 229596;22:0-Anacardic acid;Anacardic Acid 15:0;(15:0)-Anacardic acid;Cyclogallipharic acid;PENTADECYLSALICYLICACID;Hodrogenated anacardic acid
CBNumber: CB01364624
Molecular Formula: C22H36O3
Formula Weight: 348.52
MOL File: 16611-84-0.mol

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6-pentadecylsalicylic acid Property

Melting point:: 90-91℃
Boiling point:: 474.8±33.0 °C(Predicted)
Density: 1.002
storage temp.: -20°C
solubility: DMSO: ≥20mg/mL
pka: 3.08±0.30(Predicted)
form: White solid
color: white to beige
Stability:: Stable for 1 year from date of purchase as supplied. Solutions in DMSO or ethanol may be stored at -20°C for up to 3 months.
InChIKey: ADFWQBGTDJIESE-UHFFFAOYSA-N
LogP: 9.960 (est)

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Safety

Hazard Codes: Xi
Risk Statements: 36
Safety Statements: 26
WGK Germany: 3

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Hazard and Precautionary Statements (GHS)

Symbol(GHS)

Signal word

Warning

Hazard statements

H315Causes skin irritation

H319Causes serious eye irritation

Precautionary statements

P264Wash hands thoroughly after handling.

P264Wash skin thouroughly after handling.

P280Wear protective gloves/protective clothing/eye protection/face protection.

P302+P352IF ON SKIN: wash with plenty of soap and water.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

P332+P313IF SKIN irritation occurs: Get medical advice/attention.

P337+P313IF eye irritation persists: Get medical advice/attention.

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N-Bromosuccinimide Price

Sigma-Aldrich

Product number: A7236
Product name: Anacardic acid
Packaging: 5mg
Price: $155
Updated: 2024/03/01

Sigma-Aldrich

Product number: 172050
Product name: Anacardic Acid - CAS 16611-84-0 - Calbiochem
Purity: The Anacardic Acid, also referenced under CAS 16611-84-0, modulates the biological activity of Anacardic. This small molecule/inhibitor is primarily used for Cell Structure applications.
Packaging: 10mg
Price: $144
Updated: 2024/03/01

Sigma-Aldrich

Product number: 05506
Product name: (15:0)-Anacardic acid
Purity: analytical standard
Packaging: 10mg
Price: $319
Updated: 2022/05/15

Cayman Chemical

Product number: 13144
Product name: Anacardic Acid
Purity: ≥98%
Packaging: 1mg
Price: $26
Updated: 2024/03/01

Cayman Chemical

Product number: 13144
Product name: Anacardic Acid
Purity: ≥98%
Packaging: 5mg
Price: $48
Updated: 2024/03/01

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6-pentadecylsalicylic acid Chemical Properties,Usage,Production

Description

Anacardic acid, isolated from cashew shells or several other medicinal plants, is the general name given to a family of four different 6-alkyl salicyclic acids having varying degrees of unsaturation in the 15-carbon alkyl chain. These compounds are associated with anti-inflammatory, anti-tumor, molluscicidal, and anti-microbial activity. Literature frequently sites and gives the name anacardic acid to the completely-saturated compound (6-pentadecyl salicylic acid). Anacardic acid inhibits the histone acetyltransferase (HAT) activity of the transcription co-activators p300 and p300/CREB-binding protein-associated factor (PCAF) with IC₅₀ values of 8.5 and 5 μM, respectively. At 25 μmol/L, anacardic acid suppresses NF-κB activation, inhibits IκB-α phosphorylation, and prohibits p65 nuclear translocation in KBM-5 cells.

Uses

Anacardic acid has been used:

as a histone acetylase (HAT) inhibitor to study its effects on rat cortical neurons
as a positive control in acetylation assay in vitro
as an acetylase inhibitor to study its effects on the ribonucleic acid export 1 (Rae-1) protein acetylation that was transfected in human embryonic kidney cells

Uses

Anacardic acid, isolated from cashew shells or several other medicinal plants, is the general name given to a family of four different 6-alkyl salicyclic acids having varying degrees of unsaturation in the 15-carbon alkyl chain. These compounds are associated with anti-inflammatory, anti-tumor, molluscicidal, and anti-microbial activity. Literature frequently sites and gives the name anacardic acid to the completely-saturated compound (6-pentadecyl salicylic acid). Anacardic acid inhibits the histone acetyltransferase (HAT) activity of the transcription co-activators p300 and p300/CREB-binding protein-associated factor (PCAF) with IC50 values of 8.5 and 5 μM, respectively. At 25 μmol/L, anacardic acid suppresses NF-κB activation, inhibits IκB-α phosphorylation, and prohibits p65 nuclear translocation in KBM-5 cells.[Cayman Chemical]

Uses

2-Hydroxy-6-pentadecyl Benzoic Acid, is a compound that is used to treat agriculture from various fruit insects. Derivative of this molecule has been also shown to be a potent activator of human 5-lipoxygenases (5-LOX).

Definition

ChEBI: Anacardic acid is a hydroxybenzoic acid that is salicylic acid substituted by a pentadecyl group at position 6. It is a major component of cashew nut shell liquid and exhibits an extensive range of bioactivities. It has a role as an EC 2.3.1.48 (histone acetyltransferase) inhibitor, an apoptosis inducer, a neuroprotective agent, an EC 3.4.22.69 (SARS coronavirus main proteinase) inhibitor, an anticoronaviral agent, an antibacterial agent, an anti-inflammatory agent and a plant metabolite. It is a hydroxybenzoic acid and a hydroxy monocarboxylic acid. It is functionally related to a salicylic acid.

General Description

A cell-permeable ginkgolic acid (Cat. No. 345887) analog that inhibits protein SUMO (Cat. Nos. 662037, 662039, and 662042) modification (IC₅₀ = 2.2 μM using RanGAP1-C2 as substrate) in an ATP-dependent manner by selectively targeting SUMO-activating enzyme E1 (Cat. Nos. 662073 and 662074) and interfering with E1-SUMO intermediate formation. Both anacardic acid and ginkgolic acid are shown to effectively decrease overall SUMOylation of 293T cellular proteins in a dose-dependent manner, while neither compound is effective in affecting overall cellular protein ubiquitination or histone H4K8 acetylation in 293T cultures, although anacardic acid is shown to inhibit p300 (Cat. No. 506200) and PCAF (Cat. No. 124026) histone acetyltransferase activities in cell-free acetylase assays (by 82% and 86%, respectively, at 10 μM). Also reported to inhibit the activity of prostaglandin synthase, tyrosinase, and lipoxygenase, as well as to enhance Aurora kinase A (Cat. No. 481413), but not Aurora kinase B, autophosphorylation and kinase activity by inducing conformation change and enhancing ATP binding.

Biochem/physiol Actions

Target IC50: 5 μM against HAT; 8.5 μM against PCAF; 2.2 μM inhibiting protein SUMO modification using RanGAP1-C2 as substrate

in vitro

lncap, a classical metastatic prostate adenocarcinoma cell line, was adopted to study the effect of aa on cell growth, cycles and apoptosis. it was found that 125 m aa significantly inhibited lncap cell proliferation. in addition, the g1/s cell cycles arrest and the apoptosis of lncap cell was induced. further mechanistic study suggested that aa induced cell apoptosis via suppressing p300. [1]

in vivo

diesel exhaust particle- (dep-) induced lung inflammation model was established to study the effect of aa on inflammation in mice. ten days before dep-instillation stimulation, mice were orally pretreated with 50, 150, or 250 mg/kg of aa for thirty days. all doses of aa ameliorated activities of oxidative enzymes. moreover, 50 mg/kg of aa significantly decreased the expression level of tumor necrosis factor in lung. [2]

IC 50

noncompetitively inhibit histone acetyltransferase (hat) activity in prostate cancer with an ic50 value of about 5.0 m.

storage

-20°C

References

1) Balasubramanyam et al. (2003), Small molecule modulators of histone acetyltransferase p300; J. Biol. Chem. 278 19134 2) Sun et al. (2006), Inhibition of histone acetyltransferase activity by anacardic acid sensitizes tumor cells to ionizing radiation; FEBS Lett. 580 4353 3) Wu et al. (2011), Anacardic acid (6-Pentadecylsalicylic acid) Inhibits Tumor Angiogenesis by Targeting Src/FAK/Rho GTPases Signaling Pathway; J. Pharmacol. Exp. Ther. 339 403 4) Omanakuttan et al. (2012), Anacardic acid Inhibits the Catalytic Activity of Matrix Metalloproteinase-2 and Matrix Metalloproteinase-9; Mol. Pharmacol. 82 614 5) Sung et al. (2008), Anacardic acid (6-nonadecyl salicylic acid), an inhibitor of histone acetyltransferase, suppresses expression of nuclear factor-kB- regulated gene products involved in cell survival, proliferation, invasion, and inflammation through inhibition of the inhibitory subunit of nuclear factor-kBα kinase, leading to potentiation of apoptosis; Blood 111 4880

6-pentadecylsalicylic acid Preparation Products And Raw materials

Raw materials

Preparation Products

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View Lastest Price from 6-pentadecylsalicylic acid manufacturers

Shanghai Standard Technology Co., Ltd.

Product: 6-pentadecylsalicylic acid 16611-84-0
Price: US $0.00/mg
Min. Order: 5mg
Purity: ≥98%(HPLC)
Supply Ability: 10 g
Release date: 2020-04-02

16611-84-0, 6-pentadecylsalicylic acidRelated Search:

Ginkgolide A S-Trityl-L-cysteine ZM 447439 AG 490 Ginkgolic Acid C17:2 Ginkgolic acid Ginkgolic Acid C17:1 Tivantinib (ARQ 197) PHA-665752 SGC-CBP30 Trametinib Phenformin hydrochloride JNJ-38877605 Ginkgolide B Ginkgolide C GINKGETIN Ginkgolide J Ginkgolic acid (13:0)

NSC 333857

NSC 623096

Anachardic acid

(15:0)-Anacardic acid

Ginkgolic Acid 15:0 〔Anacardic Acid 15:0〕

Hodrogenated anacardic acid

PENTADECYLSALICYLICACID

6-Pentadecyl-2-hydroxybenzoic acid

Cyclogallipharic acid

Benzoic acid, 2-hydroxy-6-pentadecyl-

Anacardic acid A - Pentadecylsalicylic acid, 6-

Anacardic Acid - CAS 16611-84-0 - Calbiochem

22:0-Anacardic acid

Hydrogenated anacardic acid

NSC 229596

6-pentadecylsalicylic acid USP/EP/BP

Anacardic Acid 15:0

Anacardic Acid (Hydroginkgolic acid)

Ginkgolic acid （C15:0）/Anacardic acid

Bacterial,HATs,inhibit,HAT,Anacardic Acid,Histone Acetyltransferase,Ginkgolic Acid C15:0,Epigenetic Reader Domain,Inhibitor

N-Nitroso Bupivacaine EP Impurity B

16611-84-0

Inhibitors