MedKoo Cat#: 130224 | Name: AM11095

Description:

WARNING: This product is for research use only, not for human or veterinary use.

AM11095 is an inhibitor of NAAA with demonstrated potential as a cancer therapeutic agent with an IC₅₀ of 20 nM. NAAA is an enzyme responsible for degrading palmitoylethanolamide (PEA), an endogenous lipid mediator with anti-inflammatory and neuroprotective properties. By inhibiting NAAA, AM11095 elevates PEA levels, leading to anti-inflammatory effects. Studies have demonstrated that AM11095 reduces the secretion of pro-inflammatory cytokines such as IL-6 and IL-8, decreases activation of the NF-κB pathway, and inhibits tumor cell migration in triple-negative breast cancer models.

Chemical Structure

AM11095
AM11095
CAS#1831115-37-7 (free base)

Theoretical Analysis

MedKoo Cat#: 130224

Name: AM11095

CAS#: 1831115-37-7 (free base)

Chemical Formula: C18H17FN2O2S

Exact Mass: 344.0995

Molecular Weight: 344.40

Elemental Analysis: C, 62.77; H, 4.98; F, 5.52; N, 8.13; O, 9.29; S, 9.31

Price and Availability

This product is currently not in stock but may be available through custom synthesis. To ensure cost efficiency, the minimum order quantity is 1 gram. The estimated lead time is 2 to 4 months, with pricing dependent on the complexity of the synthesis (typically high for intricate chemistries). Quotes for quantities below 1 gram will not be provided. To request a quote, please click the button below. Note: If this product becomes available in stock in the future, pricing will be listed accordingly.
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Related CAS #
1831115-37-7 (free base) 2387696-99-1 (citrate)
Synonym
AM11095; AM 11095; AM-11095
IUPAC/Chemical Name
5-(3-fluoro-4-methoxyphenyl)-2-(((1s,3s)-3-isothiocyanatocyclobutoxy)methyl)pyridine
InChi Key
GAVRQMDMBSIEDN-IYBDPMFKSA-N
InChi Code
InChI=1S/C18H17FN2O2S/c1-22-18-5-3-12(6-17(18)19)13-2-4-14(20-9-13)10-23-16-7-15(8-16)21-11-24/h2-6,9,15-16H,7-8,10H2,1H3/t15-,16+
SMILES Code
S=C=N[C@@H]1C[C@H](OCC2=NC=C(C3=CC=C(OC)C(F)=C3)C=C2)C1
Appearance
To be determined
Purity
>98% (or refer to the Certificate of Analysis)
Shipping Condition
Shipped under ambient temperature as non-hazardous chemical. This product is stable enough for a few weeks during ordinary shipping and time spent in Customs.
Storage Condition
Dry, dark and at 0 - 4 C for short term (days to weeks) or -20 C for long term (months to years).
Solubility
To be determined
Shelf Life
>2 years if stored properly
Drug Formulation
To be determined
Stock Solution Storage
0 - 4 C for short term (days to weeks), or -20 C for long term (months).
HS Tariff Code
2934.99.9001
More Info

Preparing Stock Solutions

The following data is based on the product molecular weight 344.40 Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which will affect the solvent volumes required to prepare stock solutions.

Recalculate based on batch purity %
Concentration / Solvent Volume / Mass 1 mg 5 mg 10 mg
1 mM 1.15 mL 5.76 mL 11.51 mL
5 mM 0.23 mL 1.15 mL 2.3 mL
10 mM 0.12 mL 0.58 mL 1.15 mL
50 mM 0.02 mL 0.12 mL 0.23 mL
1. Benchama O, Malamas MS, Praveen K, Ethier EC, Williams MK, Makriyannis A, Avraham HK. Inhibition of triple negative breast cancer-associated inflammation and progression by N- acylethanolamine acid amide hydrolase (NAAA). Sci Rep. 2022 Dec 23;12(1):22255. doi: 10.1038/s41598-022-26564-6. PMID: 36564457; PMCID: PMC9789040. 2. Congiu M, Micheli L, Santoni M, Sagheddu C, Muntoni AL, Makriyannis A, Malamas MS, Ghelardini C, Di Cesare Mannelli L, Pistis M. N-Acylethanolamine Acid Amidase Inhibition Potentiates Morphine Analgesia and Delays the Development of Tolerance. Neurotherapeutics. 2021 Oct;18(4):2722-2736. doi: 10.1007/s13311-021-01116-4. Epub 2021 Sep 22. PMID: 34553321; PMCID: PMC8804012. 3. Sagheddu C, Scherma M, Congiu M, Fadda P, Carta G, Banni S, Wood JT, Makriyannis A, Malamas MS, Pistis M. Inhibition of N-acylethanolamine acid amidase reduces nicotine-induced dopamine activation and reward. Neuropharmacology. 2019 Jan;144:327-336. doi: 10.1016/j.neuropharm.2018.11.013. Epub 2018 Nov 12. PMID: 30439418.