1244967-98-3
Chemical Structure
Pizuglanstat
Synonym(s): TAS-205 free base
- CAS No.: 1244967-98-3
- Formula:C27H36N6O4
- Molecular Weight:508.61
IUPAC Name: 4-(1-methyl-1H-pyrrole-2-carbonyl)-N-(4-(4-(morpholine-4-carbonyl)piperidin-1-yl)phenyl)piperazine-1-carboxamide
InChIKey: ZNFJGCDCPYTEKF-UHFFFAOYSA-N
SMILES: O=C(N1CCOCC1)C2CCN(C3=CC=C(NC(N4CCN(C(C5=CC=CN5C)=O)CC4)=O)C=C3)CC2
Biological Activity: Pizuglanstat (Compound 3; TAS-205 free base) is an orally active prostaglandin D synthase inhibitor with an IC50 of 76 nM for human hematopoietic prostaglandin D synthase. Pizuglanstat inhibits the synthesis of PGD2. Pizuglanstat improves experimental allergic rhinitis. Pizuglanstat can be used in the study of muscle regenerative diseases such as muscular dystrophy[1][2][3].
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Pizuglanstat | 99.70% | Pizuglanstat (Compound 3; TAS-205 free base) is an orally active prostaglandin D synthase inhibitor with an IC50 of 76 nM for human hematopoietic prostaglandin D synthase. Pizuglanstat inhibits the synthesis of PGD2. Pizuglanstat improves experimental allergic rhinitis. Pizuglanstat can be used in the study of muscle regenerative diseases such as muscular dystrophy. | ||||||||||||||||||||
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Pizuglanstat (Standard) | ≥98% | Pizuglanstat (Standard) is the analytical standard of Pizuglanstat (HY-109134). This product is intended for research and analytical applications. Pizuglanstat (Compound 3; TAS-205 free base) is an orally active prostaglandin D synthase inhibitor with an IC50 of 76 nM for human hematopoietic prostaglandin D synthase. Pizuglanstat inhibits the synthesis of PGD2. Pizuglanstat improves experimental allergic rhinitis. Pizuglanstat can be used in the study of muscle regenerative diseases such as muscular dystrophy. | ||||||||||||||||||||
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Similarity Score 0.99
HY-109134APizuglanstat hydrate -
Similarity Score 0.58
HY-110167TFC 007 -
Similarity Score 0.56
HY-157567FSI-TN42 -
Similarity Score 0.50
HY-163173TEAD-IN-8 -
Similarity Score 0.49
HY-15259ACP-640186 hydrochloride -
Similarity Score 0.49
HY-15259CP-640186 -
Similarity Score 0.49
HY-122054ABPK-29 hydrochloride -
Similarity Score 0.49
HY-122054BPK-29 -
Similarity Score 0.48
HY-164868SARS-CoV-2-IN-106 -
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References
- [1]. Yoshihiro Urade, et al. Piperazine compound capable of inhibiting prostaglandin D synthase. United States. US8865714B2. 2010-03-08.
- [2]. Aoyagi H, et al. Potential synergistic effects of novel hematopoietic prostaglandin D synthase inhibitor TAS-205 and different types of anti-allergic medicine on nasal obstruction in a Guinea pig model of experimental allergic rhinitis. Eur J Pharmacol. 2020 May 15;875:173030. [Content Brief]
- [3]. Komaki H, et al. Early phase 2 trial of TAS-205 in patients with Duchenne muscular dystrophy. Ann Clin Transl Neurol. 2020 Feb;7(2):181-190. [Content Brief]
