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HPGDS inhibitor 1

HPGDS inhibitor 1 is a potent, selective and orally active Hematopoietic Prostaglandin D Synthase (HPGDS) inhibitor with an IC50s of 0.6 nM and 32 nM in enzyme and cellular assays, respectively. HPGDS inhibitor 1 does not inhibit human L-PGDS, mPGES, COX-1, COX-2, or 5-LOX[1].

Product Specifications

CAS Number

[1033836-12-2]

UNSPSC

12352005

Hazard Statement

H302, H315, H320, H335

Target

PGE synthase

Type

Reference compound

Related Pathways

Immunology/Inflammation

Applications

COVID-19-immunoregulation

Field of Research

Inflammation/Immunology

Assay Protocol

https://www.medchemexpress.com/hpgds-inhibitor-1.html

Purity

99.42

Solubility

DMSO : 50 mg/mL (ultrasonic)

Smiles

O=C(NC1CCN(CC(F)(F)F)CC1)C2=CC=C(C3=CC=CC(F)=C3)N=C2

Molecular Formula

C19H19F4N3O

Molecular Weight

381.37

Precautions

H302, H315, H320, H335

References & Citations

[1]Chris P Carron, et al. Discovery of an Oral Potent Selective Inhibitor of Hematopoietic Prostaglandin D Synthase (HPGDS) . ACS Med Chem Lett. 2010 Feb 2;1 (2) :59-63.

Shipping Conditions

Room Temperature

Storage Conditions

-20°C, 3 years; 4°C, 2 years (Powder)

Scientific Category

Reference compound1

Clinical Information

No Development Reported

Available Sizes

Curated Selection

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