851723-84-7
Chemical Structure
Timapiprant
Synonym(s): OC000459; OC-459
- CAS. Nr.: 851723-84-7
- Formula:C21H17FN2O2
- Molecular Weight:348.37
IUPAC Name: 2-(5-fluoro-2-methyl-3-(quinolin-2-ylmethyl)-1H-indol-1-yl)acetic acid
InChIKey: FATGTHLOZSXOBC-UHFFFAOYSA-N
SMILES: O=C(O)CN1C(C)=C(CC2=NC3=CC=CC=C3C=C2)C4=C1C=CC(F)=C4
Biological Activity: Timapiprant (OC000459) is a potent, selective, and orally active D prostanoid receptor 2 (DP2, also known as CRTH2) antagonist. Timapiprant (OC000459) potently displaces [3H] PGD2 from human recombinant DP2 (Ki=13 nM), rat recombinant DP2 (Ki=3 nM), and human native DP2 (Ki=4 nM). Timapiprant (OC000459) inhibits mast cell activation of Th2 lymphocytes and eosinophils[1].
| Art. -Nr. | Produktname | Reinheit | Beschreibung | Pricing | |||||||||||||||||||
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Timapiprant | 98.03% | Timapiprant (OC000459) is a potent, selective, and orally active D prostanoid receptor 2 (DP2, also known as CRTH2) antagonist. Timapiprant (OC000459) potently displaces [3H] PGD2 from human recombinant DP2 (Ki=13 nM), rat recombinant DP2 (Ki=3 nM), and human native DP2 (Ki=4 nM). Timapiprant (OC000459) inhibits mast cell activation of Th2 lymphocytes and eosinophils. | ||||||||||||||||||||
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Similarity Score 0.90
HY-15342ATimapiprant sodium -
Similarity Score 0.56
HY-16635Setipiprant -
Similarity Score 0.52
HY-116811AZ-11665362 -
Similarity Score 0.51
HY-108564L 655240 -
Similarity Score 0.50
HY-169803L-657926 -
Similarity Score 0.50
HY-106198RLidorestat (Standard) -
Similarity Score 0.50
HY-148969FPPS-IN-1 -
Similarity Score 0.49
HY-W0301202-(1-(4-Fluorobenzyl)-1H-indol-3-yl)acetic acid -
Similarity Score 0.49
HY-106066Dazmegrel -
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