Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C30H36N4O |
| Molecular Weight | 468.633 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 1 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CC1=CC=C(\C=C\C(=O)NCCCCN2CCN(CC2)C(C3=CC=CC=C3)C4=CC=CC=C4)C=N1
InChI
InChIKey=DVYCNKDRINREMB-WUKNDPDISA-N
InChI=1S/C30H36N4O/c1-25-14-15-26(24-32-25)16-17-29(35)31-18-8-9-19-33-20-22-34(23-21-33)30(27-10-4-2-5-11-27)28-12-6-3-7-13-28/h2-7,10-17,24,30H,8-9,18-23H2,1H3,(H,31,35)/b17-16+
| Molecular Formula | C30H36N4O |
| Molecular Weight | 468.633 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 1 |
| Optical Activity | NONE |
Tagorizine (also known as AL-3264) is a pyridylacrylamidoalkylpiperazine derivative patented by Dainippon Pharmaceutical Co., Ltd as an antiallergic agent. Tagorizine acts as 5-lipoxygenase inhibitor and blocks histamine H1-receptors in isolated guinea pig trachea, inhibits antigen-induced histamine release from isolated rat peritoneal mast cells, and suppress leukotriene production from activated human leukocytes. In preclinical models Tagorizine inhibited the antigen-induced leukotriene production in the abdominal cavity of passively sensitized rats and suppressed the arachidonic acid-induced ear edema in mice.
Approval Year
Targets
| Primary Target | Pharmacology | Condition | Potency |
|---|---|---|---|
Target ID: GO:0006939 Sources: https://www.ncbi.nlm.nih.gov/pubmed/7780684 |
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Target ID: GO:0004051 |
4.9 µM [IC50] | ||
Target ID: CHEMBL231 |
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/7916384
rat 30 100 mg/kg
Route of Administration:
Oral
| Substance Class |
Chemical
Created
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Edited
Mon Mar 31 18:32:03 GMT 2025
by
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Mon Mar 31 18:32:03 GMT 2025
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| Record UNII |
668QM8QJFS
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| Record Status |
Validated (UNII)
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Code | English |
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NCI_THESAURUS |
C1322
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SUB10799MIG
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CHEMBL154139
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668QM8QJFS
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7332
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118420-47-6
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100000082995
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C73066
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6436051
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ACTIVE MOIETY |
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