AR-9281 - 10mM in DMSO , Epoxide hydratase inhibitor, CAS No.913548-29-5, Epoxide hydratase inhibitor

CAS: 913548-29-5 Cat. No.: A655278 Molecular Weight: 319.44 PubChem CID: 12000797
AVAILABLE TO ORDER
GRADE & PURITY 10mM in DMSO
Storage
Store at -80°C
Shipped In
Dry ice packs + Cold packs
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Size
Status
Price
Qty
1ml
A655278-1ml
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$279.90
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Why this grade

10mM in DMSO for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

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Storage & shipping

Store at -80°C Ships Dry ice packs + Cold packs Check lot-specific COA for exact specifications.

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Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

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Literature proof

Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Overview

AR9281 (APAU) is a potent, selective and orally active soluble epoxide hydrolase (s-EH) inhibitor. AR-9281 can inhibits human sEH (HsEH) and murine sEH (MsEH) with IC 50 values of 13.8 nM and 1.7 nM, respectively. AR9281 can be used for the research of inflammation, hypertension and type 2 diabetes

In Vitro

AR-9281 (APAU) has inhibitory activity for human sEH (HsEH) and murine sEH (MsEH) with IC 50 values of 13.8 nM and 1.7 nM, respectively. MCE has not independently confirmed the accuracy of these methods. They are for reference only.

In Vivo

AR-9281 (APAU) (oral, 150-200 mg/dL, for 6 weeks) enhances the therapeutic effects of EETs, slows progression of hyperglycemia, protects the myocyte structure, and reduces Ca 2+ dysregulation and SERCA remodeling in hyperglycemic rats. MCE has not independently confirmed the accuracy of these methods. They are for reference only. Animal Model: T2DM rat modelDosage: 150-200 mg/dL Administration: oral(drinking), for 6 weeks Result: Attenuated the progressive increase of blood glucose concentration and preserved mitochondrial structure and myofibril morphology in cardiac myocytes. Protected the intracellular Ca 2+ effector system. Had less downregulation of sarco(endo)plasmic reticulum Ca 2+ ATPase (SERCA) and lowed expression of hypertrophic markers.

IC50& Target:IC50: 13.8 nM (HsEH),1.7 nM (MsEH)

Specifications

Specifications & Purity
10mM in DMSO
Biochemical and Physiological Mechanisms
AR9281 (APAU) is a potent, selective and orally active soluble epoxide hydrolase (s-EH) inhibitor. AR-9281 can inhibits human sEH (HsEH) and murine sEH (MsEH) with IC 50 values of 13.8 nM and 1.7 nM, respectively. AR9281 can be used for the research of in
Storage
Store at -80°C
Shipped In
Dry ice packs + Cold packs
This product requires cold chain shipping. Ground and other economy services are not available.
Action Type
INHIBITOR
Mechanism of action
Epoxide hydratase inhibitor
Product Properties
ALogP2.1
Names and Identifiers
Isomeric SMILES CC(=O)N1CCC(CC1)NC(=O)NC23CC4CC(C2)CC(C4)C3
Alternate CAS 913548-29-5
PubChem CID 12000797
MeSH Entry Terms 1-(1-acetyl-piperidine-4-yl)-3-adamantan-1-yl-urea;AR 9281;AR-9281;AR9281
Molecular Weight 319.44

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Associated Targets(Human)
EPHX2 Tchem Bifunctional epoxide hydrolase 2 (9 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
EPHX1 Tchem Epoxide hydrolase 1 (1 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
Certificates(CoA,COO,BSE/TSE and Analysis Chart)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:
Solution Calculators
Reviews

Customer Reviews

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