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Literature summary for 5.3.99.5 extracted from

  • Kamiya, S.; Matsui, H.; Shirahase, H.; Nakamura, S.; Wada, K.; Kanda, M.; Shimaji, H.; Kakeya, N.
    Thromboxane A2 synthetase inhibitors with histamine H1-blocking activity: synthesis and evaluation of a new series of indole derivatives (1995), Chem. Pharm. Bull., 43, 1692-1695.
    View publication on PubMed

Application

Application Comment Organism
pharmacology the thromboxane A2 synthetase inhibitor 1-[3-(4-benzylhydryl-1-piperazinyl)propyl]-3-(1H-imidazol-1-ylmethyl)-1H-indole-6-carboxylic acid is a candidate anti-asthmatic drug Oryctolagus cuniculus

Inhibitors

Inhibitors Comment Organism Structure
1-[3-(4-Benzylhydryl-1-piperazinyl)propyl]-3-(1H-imidazol-1-ylmethyl)-1H-indole-6-carboxylic acid strong thromboxane synthetase inhibition and H1-blocking activity Oryctolagus cuniculus
N-Substituted 3-(1H-imidazol-1-ylmethyl)indole carboxylic acid derivatives
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Oryctolagus cuniculus

Organism

Organism UniProt Comment Textmining
Oryctolagus cuniculus
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-
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Source Tissue

Source Tissue Comment Organism Textmining
platelet
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Oryctolagus cuniculus
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Substrates and Products (Substrate)

Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
Prostaglandin H2 i.e. PGH2 Oryctolagus cuniculus thromboxane B2 + 12(L)-hydroxy-5,8,10-heptadecatrienoic acid
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